Internally doped high chloride {100} tabular grain emulsions

FIELD OF THE INVENTION
The invention relates to photography. More specifically, the invention relates to photographic silver halide emulsions.
BACKGROUND OF THE INVENTION
a. Definition of Terms
All references to periods and groups within the periodic table of elements are based on the format of the periodic table adopted by the American Chemical Society and published in the Chemical and Engineering News, Feb. 4, 1985, p. 26. In this form the prior numbering of the periods was retained, but the Roman numeral numbering of groups and the A and B group designations (having opposite meanings in the U.S. and Europe) were replaced by a simple left to right 1 through 18 numbering of the groups.
The term "dopant" is employed herein to designate any element or ion other than silver or halide incorporated in a face centered silver halide crystal lattice.
The term "metal" in referring to elements includes all elements other than those of the following atomic numbers: 2, 5-10, 14-18, 33-36, 52-54, 85 and 86.
The term "Group VIII metal" refers to an element from period 4, 5 or 6 and any one of groups 8 to 10 inclusive.
The term "Group VIII noble metal" refers to an element from period 5 or 6 and any one of groups 8 to 10 inclusive.
The term "palladium triad metal" refers to an element from period 5 and any one of groups 8 to 10 inclusive.
The term "platinum triad metal" refers to an element from period 6 and any one of groups 8 to 10 inclusive.
The term "halide" is employed in its conventional usage in silver halide photography to indicate chloride, bromide or iodide.
The term "pseudohalide" refers to groups known to approximate the properties of halides--that is, monovalent anionic groups sufficiently electronegative to exhibit a positive Hammett sigma value at least equaling that of a halide--e.g., CN.sup.-, OCN.sup.-, SCN.sup.-, SeCN.sup.-, TeCN.sup.-, N.sub.3.sup.-, C(CN).sub.3.sup.- and CH.sup.-.
The term "C--C, H--C or C--N--H organic" refers to groups that contain at least one carbon-to-carbon bond, at least one carbon-to-hydrogen bond or at least one carbon-to-nitrogen-to-hydrogen bond sequence.
The terms "high chloride" as applied to silver halide grains and emulsions indicates a chloride concentration of greater than 50 mole percent, based on silver.
The term "{100} tabular grain(s)" refers to tabular grain(s) that contain parallel major faces lying in {100} crystal planes.
In referring to grains and emulsions that contain more than one halide, the halides are recited in order of ascending concentrations.
To avoid repetition, it is understood that all references to photographic emulsions are to negative-working photographic emulsions, except as otherwise indicated.
Research Disclosure is published by Kenneth Mason Publications, Ltd., Dudley House, 12 North St., Emsworth, Hampshire P010 7DQ, England
(b) Prior Art
Maskasky U.S. Pat. Nos. 5,264,337 and 5,292,632 and Brust et al EPO 0 534 395 disclose high chloride {100} tabular grain emulsions.
Research Disclosure, Vol. 176, Dec. 1978, Item 17643, Section I, sub-section A, states that "sensitizing compounds, such as compounds of copper, thallium, lead, bismuth, cadmium and Group VIII noble metals, can be present during precipitation of silver halide" emulsions. The quoted passage is followed by citations to demonstrate the general knowledge of the art that metals incorporated as dopants in silver halide grains during precipitation are capable of acting to improve grain sensitivity.
Research Disclosure, Vol. 308, Dec. 1989, Item 308119, Section I, sub-section D, states that "compounds of metals such as copper, thallium, lead, mercury, bismuth, zinc, cadmium, rhenium, and Group VIII metals (e.g., iron, ruthenium, rhodium, palladium, osmium, iridium and platinum) can be present during the precipitation of silver halide" emulsions. The quoted passage is essentially cumulative with Research Disclosure 17643, Section I, sub-section A, except that the metals have been broadened beyond sensitizers to include those that otherwise modify photographic performance when included as dopants during silver halide precipitation.
Research Disclosure 308119, sub-section D, proceeds further to point out a fundamental change that occurred in the art between the 1978 and 1989 publication dates of these silver halide photography surveys. Research Disclosure 308119, I-D states further:
The metals introduced during grain nucleation and/or growth can enter the grains as dopants to modify photographic properties, depending on their level and location within the grains. When the metal forms a part of a coordination complex, such as a hexacoordination complex or a tetracoordination complex, the ligands can also be occluded within the grains. Coordination ligands, such as halo, aquo, cyano, cyanate, thiocyanate, nitrosyl, thionitrosyl, oxo, and carbonyl ligands are contemplated and can be relied upon to vary emulsion properties further.
Although it was known for many years that the photographic performance of silver halide emulsions can be modified by the introduction of dopant metal ions during grain precipitation, it was generally assumed that the anion paired with the metal ion, except when it happened to be a halide ion, did not enter the grain structure and that the counterion selection was unrelated to photographic performance. Janusonis et al U.S. Pat. No. 4,835,093; McDugle et al U.S. Pat. Nos. 4,933,272, 4,981,781 and 5,037,732; Marchetti et al U.S. Pat. No. 4,937,180; and Keevert et al U.S. Pat. No. 4,945,035 were the first to demonstrate that ligands capable of forming coordination complexes with dopant metal ions are capable of entering the grain crystal structure and producing modifications of photographic performance that are not realized by incorporation of the transition metal ion alone. In each of these patents emphasis is placed on the fact that the coordination complex steric configuration allows the metal ion in the complex to replace a silver ion in the crystal lattice with the ligands replacing adjacent halide ions.
Thereafter, by hindsight, it was realized that earlier disclosures of the addition of dopant metal ions, either as simple salts or as coordination complexes, had inadvertently disclosed useful ligand incorporations. Of these inadvertent teachings, the incorporation of iron hexacyanide during grain precipitation is the most notable and is illustrated by Shiba et al U.S. Pat. No. 3,790,390; Ohkubo et al U.S. Pat. No. 3,890,154; Iwaosa et al U.S. Pat. No. 3,901,711 and Habu et al U.S. Pat. No. 4,173,483.
Ohya et al European patent-application 0 513 748 A1, published Nov. 19, 1992, discloses photographic silver halide emulsions precipitated in the presence of a metal complex having an oxidation potential of from -1.34 V to +1.66 V and a reduction potential not higher than -1.34 V and chemically sensitized in the presence of a gold-containing compound. On page 2 of the patent a table of illustrative complexes satisfying the oxidation and reduction potentials are listed. This listing includes, in addition to the complexes consisting of halide and pseudohalide ligands, K.sub.2 [Fe(EDTA)], where EDTA is an acronym for ethylenediaminetetraacetic acid. In a preferred variation it is taught to employ in combination with a required metal complex an iridium containing compound. Examples of useful iridium compounds include, in addition to simple halide salts and coordination complexes containing halide ligands, hexaamine iridium (III) salt (i.e., a [(NH.sub.3).sub.6 Ir].sup.+3 salt), hexaamine iridium (IV) salt (i.e., a [(NH.sub.3).sub.6 Ir].sup.+4 salt), a trioxalate iridium (III) salt and a trioxalate iridium (IV) salt. While offering a somewhat broader selection of ligands for use with the metals disclosed, Ohya et al does not attach any importance to ligand selection and does not address whether ligands are or are not incorporated into the grain structures during precipitation.
Ohkubo et al U.S. Pat. No. 3,672,901 (hereinafter designated Ohkubo et al '901) discloses silver halide precipitation in the presence of iron compounds. Ohkubo et al states, "Specific examples include: ferrous arsenate, ferrous bromide, ferrous carbonate, ferrous chloride, ferrous citrate, ferrous fluoride, ferrous formate, ferrous gluconate, ferrous hydroxide, ferrous iodide, ferrous lactate, ferrous oxalate, ferrous phosphate, ferrous succinate, ferrous sulfate, ferrous thiocyanate, ferrous nitrate, ammonium ferrous sulfate, potassium hexacyanoferrate (II), potassium pentacyanoamine-ferrate (II), basic ferric acetate, ferric albuminate, ammonium ferric acetate, ferric bromide, ferric chloride, ferric chromate, ferric citrate, ferric fluoride, ferric formate, ferric glycero phosphate, ferric hydroxide, acidic ferric phosphate, sodium ferric ethylenedinitrilotetraacetate, sodium ferric pyrophosphate, ferric thiocyanate, ferric sulfate, ammonium ferric sulfate, guanidine ferric sulfate, ammonium ferric citrate, potassium hexacyanoferrate (III), tris(dipyridyl) iron (III) chloride, potassium ferric pentacyanonitrosyl, and hexaurea iron (III) chloride. The only compounds reported in the Examples are hexacyanoferrate (II) and (III) and ferric thiocyanate.
Hayashi U.S. Pat. No. 5,112,732 discloses useful results to be obtained in internal latent image forming direct positive emulsions precipitated in the presence of potassoium ferrocyanide, potassium ferricyanide or an EDTA iron complex salt. Doping with iron oxalate is-demonstrated to be ineffective. "While the art has heretofore achieved useful photographic performance modifications through adding dopant metal salts and coordination complexes during grain precipitation, the photographic effects that have heretofore been achieved have been attributable to the dopant metal alone or to the metal dopant in combination with coordination complex ligands chosen from only a few restricted categories: halo, pseudohalo, aquo, nitrosyl, thionitrosyl, carbonyl and oxo ligands.
Prior to the present invention reported introductions during grain precipitation of metal coordination complexes containing organic ligands have not demonstrated photographically useful modifying effects attributable to the presence of the organic ligands, and, in fact, such coordination complexes have limited the photographic modifications that would be expected from introducing the metal in the form of a simple salt. Performance modification failures employing ethylenediamine and trioxalate metal coordination complexes of types analogous to those suggested by Ohya et al and Ohkubo et al '901 are presented below as comparative Examples.
Bigelow U.S. Pat. No. 4,092,171 discloses increasing the sensitivity of silver halide emulsions by introducing "at any stage of preparation of the silver halide emulsion, e.g., during the precipitation of the silver halides, after the washing step and redispersion stage, during digestion, or as a final addition just prior to coating" an organo-phosphine chelate of a palladium or platinum metal salt. Only tetracoordination complexes of platinum and palladium are disclosed.
RELATED PATENT APPLICATIONS
Olm et al U.S. Ser. No. 08/091,148, filed Jul. 13, 1994, titled INTERNALLY DOPED SILVER HALIDE EMULSIONS AND PROCESS FOR THEIR PREPARATION, now U.S. Pat. No. 5,360,712, commonly assigned, discloses silver halide emulsions doped with metal hexacoordination complexes having at least one H--C, C--C or C--N--H organic ligand and at least half of the metal coordination sites occupied by halide pseudohalide ligands. The metal forming the complex is chosen from periods 4, 5 and 6 and groups 3 to 13 of the periodic table of elements.
House et al U.S. Ser. No. 08/112,489, filed Aug. 25, 1993, titled HIGH CHLORIDE TABULAR GRAIN EMULSIONS AND PROCESSES FOR THEIR PREPARATION, now U.S. Pat. No. 5,520,938, commonly assigned and now allowed, discloses high chloride {100} tabular grain emulsions, their preparation and uses in photography.
Chang et al U.S. Ser. No. 08/215,072, filed Mar. 18, 1994, titled HIGH CHLORIDE {100} TABULAR GRAIN EMULSIONS--IMPROVED EMULSIONS AND IMPROVED PRECIPITATION PROCESSES, now abandoned in favor of U.S. Ser. No. 08/235,532, filed Jun. 3, 1994, commonly assigned, discloses that delaying iodide introduction until after the initiation of grain nucleation increases the proportion of total grain projected area accounted for by high chloride {100} tabular grains. The projected area of the {100} tabular grains can exceed 95 percent of total grain projected area.
SUMMARY OF THE INVENTION
The present invention has for the first time introduced during high chloride {100} tabular grain precipitation dopant metal coordination complexes containing one or more organic ligands and obtained modifications in photographic performance that can be attributed specifically to the presence of the organic ligand or ligands. The result is to provide the art with additional and useful means for tailoring photographic performance to meet specific application requirements.
In one aspect this invention is directed to a photographic silver halide emulsion comprised of a silver halide tabular grain population (a) bounded by {100} major faces having adjacent edge ratios of less than 10, (b) containing at least 50 mole percent chloride, based on total silver forming the grain population, (c) accounting for greater than 50 percent of total grain projected area, (d) having a thickness of less than 0.3 .mu.m, (e) having an average aspect ratio of at least 2, and (f) exhibiting a face centered cubic crystal lattice structure containing a hexacoordination complex of a metal chosen from periods 4, 5 and 6 and groups 3 to 14 inclusive of the periodic table of elements in which one or more organic ligands each containing at least one carbon-to-carbon bond, hydrogen-to-carbon bond or carbon-to-nitrogen-to-hydrogen bonding system occupy up to half the metal coordination sites in the coordination complex and at least half of the metal coordination sites in the coordination complex are provided by halogen or pseudohalogen ligands.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
High chloride {100} tabular grain emulsions have only recently become available to the photographic art. These emulsions contain a silver halide tabular grain population (a) bounded by {100} major faces having adjacent edge ratios of less than 10, (b) containing at least 50 mole percent chloride, based on total silver forming the grain population, (c) accounting for greater than 50 percent of total grain projected area, (d) having a thickness of less than 0.3 .mu.m, (e) having an average aspect ratio of at least 2, and (f) exhibiting a face centered cubic crystal lattice structure. These emulsions satisfy a long standing need in the art for high chloride tabular grain emulsions that exhibit the inherent tabular grain stability that is imparted by the presence of tabular grain with (100) major faces. The advantages of tabular grain emulsions are well documented in the art and include improved speed-granularity relationships, increased covering power both on an absolute basis and as a function of binder hardening, more rapid developability, increased thermal stability, increased separation of native and spectral sensitization imparted imaging speeds, and improved image sharpness in both mono- and multi-emulsion layer formats. The advantages of high chloride emulsions include increased rates of processing, the higher ecological compatibility of chloride ions as opposed to other halide ions in spent processing solutions, the higher processing solution seasoning tolerances with chloride ions as opposed to other halide ions in solution, and the reduced native sensitivity to visible light exhibited by high chloride emulsions, which can be reflected by lower levels blue contamination in forming minus-blue exposure records.
High chloride {100} tabular grains have square or rectangular major faces. The adjacent edges of the major faces are specified to have length ratios of less than 10 so that they are clearly distinguished from rod-like grains. In practice the high chloride tabular grains typically have {100} major face adjacent edge ratios of less than 5 and, preferably, less than 2.
High chloride {100} tabular grain emulsions by definition have a chloride content of greater than 50 mole percent, based on total silver forming the tabular grains, preferably contain at least 70 mole percent chloride, and optimally contain at least 90 mole percent chloride. The emulsions can be pure silver chloride emulsions. Alternatively, they can contain minor amounts of bromide and/or iodide ions. The face centered cubic crystal lattice structure of the high chloride {100} tabular grains allows for silver bromide to form the balance of the grain structure not provided by silver chloride. Silver iodide can be present up to its solubility limit in the high chloride face centered cubic crystal lattice. Rarely is silver iodide present in a concentration above 20 mole percent, and iodide is more typically limited to concentrations of less than 10 molar percent. In a specifically preferred form of the invention the presence of iodide during the early stages of grain formation are relied upon to produce {100} tabular grains; therefore silver iodochloride tabular grain compositions are specifically contemplated. Only very minor amounts of iodide are, however, required for this purpose, with useful iodide concentrations of about 0.01 mole percent being contemplated, but preferably iodide concentrations of at least 0.05 mole percent are preferred.
The high chloride {100} tabular grain emulsions preferably account for at least 70 percent of total grain projected area and optimally greater than 90 percent of total grain projected area.
The high chloride {100} tabular grains contemplated for determination of these projected areas are those that exhibit thicknesses of less than 0.3 .mu.m. The tabular grains preferably have thicknesses of less than 0.2 .mu.m. In one specifically contemplated for of the invention the high chloride {100} tabular grains can have mean thicknesses of less than 0.07 .mu.m. Such emulsions are referred to in the art as "ultrathin" tabular grain emulsions. Mean grain thicknesses as low as 0.02 .mu.m or even 0.01 .mu.m have been disclosed in the art.
To realize the advantages of tabular grain shape it is contemplated that the tabular grain population will in all instances have an average aspect ratio of at least 2. Preferred tabular grain emulsions exhibit an average aspect ratio of at least 5. Optimally the average aspect ratio is greater than 8. Average aspect ratio is obtained from the relationship:
ECD.div.t (I)
where
ECD is the mean equivalent circular diameter of the {100} tabular grains, measured in micrometers (.mu.m) and
t is the mean thickness of the {100} tabular grains, measured in micrometers (.mu.m). Considering the mean thicknesses of the tabular grains noted above and that their mean ECD's can range up to 10 .mu.m, but are typically 5 .mu.m or less, it is apparent that extremely high average aspect ratios for the high chloride {100} tabular grain emulsions are feasible.
Another way of looking at the properties imparted by tabular grain shape is to consider mean tabularity, defined by the following relationship:
ECD.div.t.sup.2 (II)
where
ECD and t are as previously defined.
Mean tabularities preferably are greater than 25 and preferably greater than 100. Mean tabularities of 1000 or more are contemplated.
High chloride {100} tabular grain emulsions and their preparation are disclosed by Maskasky U.S. Pat. Nos. 5,264,337, 5,275,930 and 5,275,632; Brust et al EPO 0 534 395; House et al U.S. Ser. No. 112,489, filed Aug. 25, 1993, now allowed; Szajewski U.S. Ser. No. 08/034,061, filed Mar. 22, 1993, now allowed; Brust et al U.S. Ser. No. 08/048,434, filed Apr. 16, 1993, now allowed; the disclosures of which are here incorporated by reference, both for their emulsion and emulsion preparation teachings and for teachings of further photographic features used in combination.
The present invention has achieved modifications of photographic performance in high chloride {100} tabular grain emulsions that can be specifically attributed to the presence during grain precipitation of metal hexacoordination complexes containing one or more C--C, H--C or C--N--H organic ligands. The photographic effectiveness of these organic ligand metal complexes is attributed to the recognition of criteria for selection never previously appreciated by those skilled in the art.
The complexes are chosen from among hexacoordination complexes to favor steric compatibility with the face centered cubic crystal structures of high chloride {100} tabular grains. Metals from periods 4, 5 and 6 and groups 3 to 14 inclusive of the periodic table of elements are known to form hexacoordination complexes and are therefore specifically contemplated. Preferred metals for inclusion in the coordination complexes are Group VIII metals. Non-noble Group VIII metals (i.e., the period 4 Group VIII metals) are contemplated for grain incorporation, with iron being a specifically preferred dopant metal. Noble Group VIII metals (those from the palladium and platinum triads) are contemplated, with ruthenium and rhodium being specifically preferred period 5 metal dopants and iridium being a specifically preferred period 6 dopant.
Further defining the coordination complexes are the ligands they contain. The coordination complexes contain a balance of halide and/or pseudohalide ligands (that is, ligands of types well known to be useful in photography) and organic ligands. To achieve performance modification attributable to the presence of the C--C, C--H or C--N--H organic ligands at least half of the coordination sites provided by the metal ions must be satisfied by pseudohalide, halide or a combination of halide and pseudohalide ligands and at least one of the coordination sites of the metal ion must be occupied by an organic ligand. When the C--C, C--H or C--N--H organic ligands occupy all or even the majority of coordination sites in the complex, photographic modifications attributable to the presence of the organic ligand have not been identified.
A surprising discovery has been that the selection of the C--C, C--H or C--N--H organic ligands is not limited by steric considerations in the manner indicated by Janusonis et al, McDugle et al, Marchetti et al and Keevert et al, all cited above. Whereas each of these patents teach replacing a single halide ion the crystal lattice structure with a nonhalide ligand occupying exactly the same lattice position, C--C, C--H or C--N--H organic ligands of varied steric configurations have been observed to be effective. While it seems plausible that the smaller C--C, C--H or C--N--H organic ligands lend themselves to one-for-one displacement of halide ions in the crystal lattice structure, the demonstration of the effectiveness of larger C--C, C--H or C--N--H organic ligands and C--C, C--H or C--N--H organic ligands of varied steric forms clearly demonstrates a much broader tolerance for geometrical configuration divergence of the host face centered cubic crystal lattice structure and the ligands of the metal dopant coordination complexes than had heretofore been thought feasible. In fact, the variation of steric forms of C--C, C--H or C--N--H organic ligands observed has led to the conclusion that neither the steric form nor size of the C--C, C--H or C--N--H organic ligand is in itself a determinant of photographic utility.
Metal hexacoordination complexes suitable for use in the practice of this invention have at least one C--C, H--C or C--N--H organic ligand and at least half of the metal coordination sites occupied by halide or pseudohalide ligands. A variety of such complexes are known. The specific embodiments are listed below. Formula acronyms are defined at their first occurrence.
MC-1
[Sc(NCS).sub.3 (py).sub.3 ]
py=pyridine
Tris(pyridine)tris(thiocyanato) scandium (III)
Reported by G. Wilkinson, R. D. Gillard and J. A. McCleverty (eds.), Comprehensive Coordination Chemistry, Pergamon 1987.
MC-2
[M(Cl.sub.3)(1,10-phenanthroline)(H.sub.2 O)]
M=La, Ce, Pr, Nd, Sa
Aquotrichloro(1,10-phenanthroline) lanthanide (III)
Reported by F. A. Hart and F. P. Laming, J. Inorg. Nucl. Chem., 26, 579 (1964).
MC-3
(Et.sub.4 N)[TiCl.sub.4 (MeCN).sub.2 ]
Et=ethyl, Me=methyl
Tetraethylammonium bis(acetonitrile) tetrachloro titanium (III)
Reported by B. T. Russ and G. W. A. Fowles, Chem. Comm., 1, 19 (1966).
MC-4
(R.sub.4 N)[TiCl.sub.14 (EtO)(MeCN)]
EtO=CH.sub.3 CH.sub.2 O
MC-4a R=Me
Tetramethylammonium (acetonitrile)ethoxytetrachloro titanate (IV)
MC-4b R=Et
Tetraethylammonium (acetonitrile)ethoxytetrachloro titanate (IV)
a-b Reported by F. Von Adalbert, Z. Anorg. Allgem. Chem., 338, 147 (1965).
MC-5
(Et.sub.4 N)[TiCl.sub.15 (MeCN)]
Tetraethylammonium (acetonitrile)pentachloro titanate (IV)
Reported by J. M. Kolthoff and F. G. Thomas, J. Electrochem. Soc., 111, 1065 (1964).
MC-6
Pyridinium [V(NCS).sub.4 (py).sub.2 ]
Pyridinium bis(pyridine)tetra(thiocyanato) vanadate (III)
Reported by R. J. H. Clark, Comprehensive Inorganic Chemistry, Vol. 3, pp. 544-545, edited by A. F. Trotman-Dickerson, Pergoman Press, Oxford, 1973.
MC-7
(Et.sub.4 N)[VCl.sub.4 (MeCN).sub.2 ]
Tetraethylammonium bis(acetonitrile) tetrachloro vanadate (III) Pyridinium
Reported by R. J. H. Clark, Comprehensive Inorganic Chemistry, Vol. 3, pp. 544-545, edited by A. F. Trotman-Dickerson, Pergoman Press, Oxford, 1973.
MC-8
[WCl.sub.4 (en)]
en=ethylenediamine
(Ethylenediamine)tetrachloro tungsten (IV) Reported by C. D. Kennedy and R. D. Peacock, J. Chem. Soc., 3392 (1963).
MC-9
(Bu.sub.4 N)[Cr(NCO).sub.4 (en)]
Bu=butyl Tetrabutylammonium
(ethylenediamine)tetra(cyanato) chromate (III)
Reported by E. Blasius and G. Klemm, Z. Anorg. Allgem. Chem., 428, 254 (1977).
MC-10
(Bu.sub.4 N)[Cr(NCO).sub.4 (1,2-propanediamine)]
Tetrabutylammonium tetra(cyanato) (1,2-propanediamine) chromate (III)
Reported by E. Blasius and G. Klemm, Z. Anorg. Allgem. Chem., 443, 265 (1978).
MC-11
(Bu.sub.4 N)[Cr(NCO).sub.4 (1,2-cyclohexanediamine)]
Tetrabutylammonium tetra(cyanato)(1,2-cyclohexanediamine) chromate (III)
Reported by E. Blasius and G. Klemm, Z. Anorg. Allgem. Chem., 443, 265 (1978).
MC-12
[ReOCl.sub.3 (en)]
Trichloro (ethylenediamine)oxo rhenium (V)
Reported by D. E. Grove and G. Wilkinson, J. Chem. Soc. (A), 1224 (1966).
MC-13
[ReI.sub.4 (py).sub.2 ]
Tetraiodobis(pyridine) rhenium (IV)
Reported by R. Colton, R. Levitus and G. Wilkinson, J. Chem. Soc., 4121 (1960).
MC-14
Na.sub.3 [Fe(CN).sub.5 L]
MC-14a L=(py)
Sodium pentacyano(pyridine) ferrate (II)
MC-14b L=pyrazine=(pyz)
Sodium pentacyano(pyrazine) ferrate (II)
MC-14c L=4,4'-bipyridine
Sodium pentacyano (4,4'-bipyridine) ferrate (II)
MC-14d L=3,3'-dimethyl-4,4'-bipyridine
Sodium pentacyano(3,3'-dimethyl-4,4'-bipyridine) ferrate (II)
MC-14e L=3,8-phenanthroline
Sodium pentacyano(3,8-phenanthroline) ferrate (II)
MC-14f L=2,7-diazapyrene
Sodium pentacyano(2,7 -diazapyrene) ferrate (II)
MC-14g L=1,4-bis(4-pyridyl)butadiyne]
Sodium pentacyano[1,4-bis(4-pyridyl)butadiyne]ferrate (II)
a-g Reported by G-H. Lee, L. D. Ciana, A. Haim, J. Am. Chem. Soc., 111, 1235-41 (1989).
MC-14h L=(4-py)pyridinium
Sodium pentacyano(4-pyridylpyridinium) ferrate (II)
MC-14i L=1-methyl-4-(4-py)pyridinium
Sodium pentacyano[1-methyl-4-(4-pyridyl) pyridium] ferrate (II)
MC-14j L=N-Me-pyrazinium
Sodium pentacyano(N-methylpyrazinium) ferrate (II)
MC-14k L=4-Cl(py)
Sodium pentacyano(4-chloropyridino) ferrate (II)
h-k Reported by H. E. Toma and J. M. Malin, Inorg. Chem. 12, 1039 (1973).
MC-141 L=Ph.sub.3 P
Ph=phenyl
Sodium pentacyano(triphenylphosphine) ferrate (II)
Reported by M. M. Monzyk and R. A. Holwerda, Polyhedron, 9, 2433 (1990).
MC-14m L=thiourea
Sodium pentacyano(thiourea) ferrate (II)
MC-14n L=pyrazole
Sodium pentacyano(pyrazole) ferrate (II)
MC-14o L=imidazole
Sodium pentacyano(imidazole) ferrate (II)
m-o Reported by C. R. Johnson, W. W. Henderson and R. E. Shepherd, Inorg. Chem., 23, 2754 (1984).
MC-14p L=MeNH.sub.2
Sodium pentacyano(methylamine) ferrate (II)
MC-14q L=Me.sub.2 NH
Sodium pentacyano(dimethylamine) ferrate (II)
MC-14r L=Me.sub.3 NH
Sodium pentacyano(trimethylamine) ferrate (II)
MC-14s L=EtNH.sub.2
Sodium pentacyano(ethylamine) ferrate (II)
MC-14t L=BuNH.sub.2
Sodium pentacyano(butylamine) ferrate (II)
MC-14u L=cyclohexylamine
Sodium pentacyano(cyclohexylamine) ferrate (II)
MC-14v L=piperidine
Sodium pentacyano(piperidine) ferrate (II)
MC-14x L=aniline
Sodium pentacyano(aniline) ferrate (II)
MC-14y L=morpholine
Sodium pentacyano(morpholine) ferrate (II)
MC-14y L=ethanolamine
Sodium pentacyano(ethanolamine) ferrate (II)
p-y Reported by N. E. Klatz, P. J. Aymoneno, M. A. Blesa and J. A. Olabe, Inorg. Chem. 17, 556 (1978).
MC-14z L=P(OBu).sub.3
Sodium pentacyano(tributylphosphite)
ferrate (II)
MC-14aa L=P(Bu).sub.3
Sodium pentacyano[(tributyl)phosphine]
ferrate (II)
z-aa Reported by V. H. Inouye, E. Fluck, H. Binder and S. Yanagisawa, Z. Anorg. Allgem. Chem., 483, 75-85 (1981).
MC-14bb L=p-nitroso-N,N-dimethylaniline
Sodium pentacyano(p-nitroso-N, N-dimethylaniline) ferrate (II)
MC-14cc L=nitrosobenzene
Sodium pentacyano(nitrosobenzene) ferrate (II)
MC-14dd L=4-CN-(py)
Sodium pentacyano (4-cyanopyridine)
ferrate (II) -bb-dd Reported by Z. Bradic, M. Pribanic and S. Asperger, J. Chem. Soc., 353 (1975).
MC-14ee L=3[(H.sub.5 C.sub.2).sub.2 NC(0)](py)
Sodium pentacyano(nicotinamide) ferrate (II)
MC-14ff L=4-[NH.sub.2 NHC(0)](py)
Sodium pentacyano(isonicotinoylhydrazine) ferrate (II)
MC-14gg L=3-CHO-(py)
Sodium pentacyano(nicotinaldehyde) ferrate (II)
MC-14hh L=3-NH.sub.2 C(0)](py)
Sodium pentacyano (nicotinamide) ferrate (II)
MC-14ii L=4-[NH.sub.2 C(O)](py)
Sodium pentacyano(isonicotinamide) ferrate (II)
MC-14jj L=3-[.sup.- OC(O)](py)
Sodium pentacyano(nicotinato) ferrate (II)
MC-14kk L=4-[.sup.- OC(O)](py)
Sodium pentacyano(isonicotinato) ferrate (II)
MC-14ll L=3-[.sup.- OC(O)CH.sub.2 NHC(O)](py)
Sodium Pentacyano(nicotinoylglycinato) ferrate (II)
MC14mm L=[H.sub.2 NC(O)](pyz)
Sodium pentacyano(pyrazineamide) ferrate (II)
MC-14nn L=(pyz)-mono-N-oxide
Sodium pentacyano(pyrazinemono-N-oxide) ferrate (II)
ee-nn Reported by P. J. Morando, U. I. E. Bruyere and M. A. Blesa, Transition Metal Chem., 8, 99 (1983).
MC-14oo L=4-Ph(py)
Sodium pentacyano(4-phenylpyridine) ferrate (II)
MC-14pp L=pyridazine
Sodium pentacyano(pyridazine) ferrate (II)
MC-14qq L=pyrimidine
Sodium pentacyano(pyrimidine) ferrate (II)
oo-qq Reported by D. K. LaVallee and E. B. Fleischer, J. Am. Chem. Soc., 94 (8), 2583 (1972).
MC-14rr L=Me.sub.2 SO
Sodium pentacyano(dimethylsulfoxide) ferrate (II)
Reported by H. E. Toma, J. M. Malin and E. Biesbrecht, Inorg. Chem., 12, 2884 (1973).
MC-14ss L=2-chloropyrazine
Sodium pentacyano(2-chloropyrazine) ferrate (II)
MC-15
K.sub.3 [Ru(CN).sub.5 L]
MC-15a L=(pyz)
Potassium pentacyano(pyrazine) ruthenate (II)
Reported by C. R. Johnson and R. E. Shepherd, Inorg. Chem., 22, 2439 (1983).
MC-15b L=methylpyrazinium
Potassium pentacyano(methylpyrazinium) ruthenate (II)
MC-15c L=imidazole
Potassium pentacyano (imidazole) ruthenate (II)
MC-15d L=4-pyridylpyridinium
Potassium pentacyano(4-pyridylpyridinium) ruthenate (II)
MC-15e L=4,4'-bipyridine
Potassium pentacyano(4,4'-bipyridine) ruthenate (II)
MC-15f L=Me.sub.2 SO
Potassium pentacyano(dimethylsulfoxide) ruthenate (II)
MC-15g L=(py)
Potassium pentacyano(pyridine) ruthenate (II)
MC-15h L=4-[.sup.- OC(O)](py)
Potassium pentacyano(isonicotinato) ruthenate (II)
b-h Reported by M. A. Hoddenbagh and D. A. McCartney, Inorg. Chem., 25, 2099 (1986).
MC-16
K.sub.2 [Co(CN).sub.5 L]
MC-16a L=Me
Potassium pentacyano(methyl) cobaltate (III)
MC-16b L=Et
Potassium pentacyano(ethyl) cobaltate (III)
MC-16c L=tolyl
Potassium pentacyano(tolyl) cobaltate (III)
MC-16d L=acetamide
Potassium pentacyano(acetamide) cobaltate (III)
MC-16e L=--CH.sub.2 C(O)O.sup.-
Potassium pentacyano(acetato) cobaltate (III)
MC-16f L=--CH.sub.2 C(O)OCH.sub.3
Potassium pentacyano (methylacetato) cobaltate (III)
MC-16g L=--CH.sub.2 CH.sub.2 C(O)OCH.sub.3 Me
Potassium pentacyano (methylproponato) cobaltate (III)
a-g Reported by J. Halpern and J. P. Maher, J. Am. Chem. Soc., 87, 5361 (1965).
MC-17
K[Co(CN).sub.4 (en)]
Potassium tetracyano(ethylenediamine)
cobaltate (III)
Reported by K. Ohkawa, J. Fujita and Y. Shimura, Bulletin of the Chemical Society of Japan, 42, 3184-9 (1969).
MC-18
Ba[Co(CN).sub.4 (tn)]
(tn)=trimethylenediamine
Barium tetracyano(trimethylenediamine)
cobaltate (III)
Reported by K. Ohkawa, J. Fujita and Y. Shimura, Bulletin of the Chemical Society of Japan, 42, 3184-9 (1969).
MC-19
[RhL.sub.3 Cl.sub.3 ]
MC-19a L=MeCN
Tris(acetonitrile)trichloro rhodium (III)
MC-19b L=PhCN
Tris(benzonitrile)trichloro rhodium (III)
a-b Reported by G. Beech and G. Marr, J. Chem. Soc. (A) , 2904 (1970).
MC-20
Na.sub.2 [RhCl.sub.5 (SMe.sub.2)]
Sodium pentachloro(dimethylsulfide) rhodate (III)
Reported by S. J. Anderson, J. R. Barnes, P. L. Goggin and R. S. Goodfellow, J. Chem. Res. (M), 3601 (1978).
MC-21
cis,trans-[RhX.sub.4 (SMe.sub.2).sub.2 ]
X=halo
cis or trans-Tetrahalobis(dimethylsulfide) rhodate (III)
Reported by S. J. Anderson, J. R. Barnes, P. L. Goggin and R. S. Goodfellow, J. Chem. Res. (M), 3601 (1978).
MC-22
mer,fac-[RhX.sub.3 (SMe.sub.2).sub.3 ]
met or fac-Trihalotris(dimethylsulfide) rhodate (III)
Reported by S. J. Anderson, J. R. Barnes, P. L. Goggin and R. S. Goodfellow, J. Chem. Res. (M), 3601 (1978).
MC-23
cis, trans-[N(C.sub.3 H.sub.7).sub.4 ][RhCl.sub.4 (Me.sub.2 SO).sub.2 ]
Tetrapropylammonium tetrachloro
bis(dimethylsulfoxide) rhodium (III)
Reported by Y. N. Kukushkin, N. D. Rubtsora and N. Y. Irannikova, Russ. J. Inorg. Chem. ( Trans. Ed. ), 15, 1032 (1970).
MC-24
[RhCl.sub.3 (Me.sub.2 SO).sub.3 ]
Trichlorotris (di
methylsulfoxide) rhodium (III)
Reported by Y. N. Kukushkin, N. D. Rubtsora and N. Y. Irannikova, Russ. J. Inorg. Chem. (Trans. Ed.), 15, 1032 (1970).
MC-25
K[RhCl.sub.4 L]
MC-25a L=1,10-phenanthroline
Potassium tetrachloro( 1,10-phenanthroline ) rhodate (III )
MC-25b L=5-methyl (1,10-phenanthroline)
Potassium tetrachloro[5-methyl(1,10-phenanthroline)]rhodate (III)
MC-25c L=5,6-dimethyl (1,10-phenanthroline)
Potassium tetrachloro[5,6-dimethyl-1,10-phenanthroline)]rhodate (III)
MC-25d L=5-bromo(1,10-phenanthroline)
Potassium tetrachloro[5-bromo(1,10-phenanthroline)]rhodate (III)
MC-25e L=5-chloro(1,10-phenanthroline)
Potassium tetrachloro[5-chloro(1,10-phenanthroline)]rhodate (III)
MC-25f L=5-nitro(1,10-phenanthroline)
Potassium tetrachloro[5-nitro(1,10-phenanthroline)]rhodate (III)
MC-25g L=4,7-diphenyl(1,10-phenanthroline
Potassium tetrachloro(1,10-phenanthroline) rhodate (III)
a-g Reported by R. J. Watts and J. Van Houten, J. Am. Chem. Soc., 96, 4334 (1974).
MC-26
K[IrX.sub.4 (en)]
MC-26a X=Cl
Potassium tetrachloro(ethylenediamine) iridate (III)
MC-26b X=Br
Potassium tetrabromo(ethylenediamine) iridate (III)
a-b Reported by I. B. Barnovskii, R. E. Sevast'ynova, G. Y. Mazo and V. I. Nefadov, Russ. J. of Inorg. Chem., (Trans. Ed. ) 19, 1974.
MC-27
K[IrCl.sub.x (MeCN).sub.v ]
MC-27a x=4, y=2
Potassium tetrachlorobis(acetonitrile) iridate (III)
MC-27b x=5, y=1
Potassium pentachloro(acetonitrile) iridate (III)
a-b Reported by B. D. Catsikis and M. L. Good, Inorg. Nucl. Chem. Lett., 9, 1129-30 (1973).
[N(Me).sub.4 ][IrCl.sub.4 (MeSCH.sub.2 CH.sub.2 SMe)]
MC-28
Tetramethylammonium tetrachloro(2,5-dithiahexane) iridate (III)
Reported by D. J. Gulliver, W. Levason, K. G. Smith and M. J. Selwood, J. Chem. Soc. Dalton trans, 1872-8 (1980).
MC-29
K.sub.m [IrX.sub.x (pyz).sub.v L.sub.n ]
MC-29a X=Cl, m=2, n=0, x=5, y=1
Potassium pentachloro (pyrazine) iridate (III)
MC-29b X=Cl, m=2, n=0, x=4, y=2, cis isomer
Potassium tetrachlorobiscis(pyrazine) iridate (III)
MC-29c X=Cl, m=1, n=0, x=4, y=2, trans isomer
Potassium tetrachlorobis trans(pyrazine) iridate (III)
MC-29d X=Cl, m=1, n=0, x=3, y=3
Potassium trichlorotris(pyrazine) iridate (III)
a-d Reported by P. Lareze, C. R. Acad. Sc. Paris, 261, 3420 (1965).
MC-30
K.sub.m [IK.sub.2 [IrCl.sub.5 (pyrimidine)]
Potassium pentachloro(pyrimidine) iridate (III)rX.sub.x (pyz).sub.v L.sub.n ]
Reported by F. Larese and L. Bokobza-Sebagh, C. R. Acad. Sc. Paris, 277, 459 (1973).
MC-31 p2 K.sub.4 [Ir.sub.2 Cl.sub.10 (pyz)]
Potassium decachloro(.mu.-pyrazine) bis[pentachloroiridate (III)]
Reported by F. Lareze, C. R. Acad. Sc. Paris, 282, 737 (1976).
MC-32
K.sub.m [IrCl.sub.x (py).sub.v L.sub.n ]
MC-32a m=2, n=0, x=5, y=1
Potassium pentachloro(pyridine) iridate (III)
MC-32b m=1, n=0, x=4, y=2
Potassium tetrachlorobis(pyridine) iridate (III)
MC-32c m=0, n=0, x=3, y=3
Trichlorotris(pyridine) iridate (III)
MC-32d L=pyridazine, m=0, n=1, x=5, y=0
Potassium pentachloro(pyridazine) iridate (III)
a-d Reported by G. Rio and F. Larezo, Bull. Soc. Chim. France, 2393 (1975).
MC-32e L=(C.sub.2 O.sub.4), m=2, n=1, x=3, y=1
Potassium trichloro(oxalate)(pyridine) iridate (III)
Reported by Y. Inamura, Bull. Soc. China, 7, 750 (1940).
MC-32f L=(HOH), m=0, n=1, x=3, y=2
Trichloromonoaquo(pyridine iridium (III)
Reported by M. Delepine, Comptes Rendus, 200, 1373 (1935).
MC-33
K.sub.3 [IrCl.sub.4 (C.sub.2 O.sub.4)]
Potassium tetrachlorooxalato iridate (III)
Reported by A. Duffour, Comptes Rendus, 152, 1393 (1911).
MC-34
[In(thiourea).sub.3 (NCS).sub.3 ]
Tris(isothiocyanato)trithiourea indium (III)
Reported by S. J. Patel, D. B. Sowerby and D. G. Tuck, J. Chem. Soc. (A), 1188 (1967).
MC-35
[In(dimac).sub.3 (NCS).sub.3 ]
dimac=N,N-dimethylacetamide
Tris (N,N-dimethylacetamide)tris(isothiocyanato) indium (III)
Reported by S. J. Patel, D. B. Sowerby and D. G. Tuck, J. Chem. Soc. (A), 1188 (1967).
MC-36
[Et.sub.4 N].sub.2 [Me.sub.m Sn(SCN).sub.n ]
MC-36a m=2, n=4
Tetraethylammonium dimethyltetra(isothiocyanato) stannate
MC-36b m=1, n=5
Tetraethylammonium methylpenta(isothiocyanato) stannate
a-b Reported by A. Cassal, R. Portanova and Barbieri, J. Inorg. Nucl. Chem., 27, 2275 (1965).
MC-37
Na.sub.6 [Fe.sub.2 (CN).sub.10 (pyz)]
Sodium decacyano(.mu.-pyrazine) diferrate (II)
Reported by J. M. Malin, C. F. Schmitt, H. E. Toma, Inorg. Chem., 14, 2924 (1975)
MC-38
Na.sub.6 [Fe.sub.2 (CN).sub.10 (.mu.-4,4'-bipyridine)]
Sodium decacyano(.mu.-4,4-bipyridine) diferrate (II)
Reported by J. E. Figard, J. V. Paukstelis, E. F. Byrne and J. D. Peterson, J. Am. Chem. Soc., 99, 8417 (1977).
MC-39
Na.sub.6 [Fe.sub.2 (CN).sub.10 L]
L=trans-1,2-bis(4-pyridyl)ethylene
Sodium decacyano [.mu.-trans-1,2-bis (4-pyridyl)ethylene]diferrate (II)
Reported by N. E. Katz, An. Quim. Set. B, 77(2), 154-6.
MC-40
Na.sub.5 [(CN).sub.5 FeLCo(CN).sub.5 ]
MC-40a L=(pyz)
Sodium decacyano(.mu.-pyrazine) ferrate (II) cobaltate (III)
MC-40b L=4,4'-bipyridine
Sodium decacyano(.mu.-4,4'-bipyridine)ferrate (II) cobaltate (III)
MC-40c L=4-cyanopyridine
Sodium decacyano(.mu.-4-cyanopyridine)ferrate (II) cobaltate (III)
Reported by K. J. Pfenning, L. Lee, H. D. Wohlers and J. D. Peterson, Inorg. Chem., 21, 2477 (1982).
In addition to the illustrative known compounds, compounds not located in the literature have been synthesized and employed in the practice of the invention. These compounds include the following:
MC-41
K2[IrCl.sub.5 (thiazole)]
Potassium pentchloro(thiazole) iridate (III)
MC-42
Na.sub.3 K.sub.2 [IrCl.sub.5 (pyz)Fe(CN).sub.5 ]
Potassium sodium pentachloro iridate (III)
(.mu.-pyrazine) pentacyanoferrate (II)
MC-43
K.sub.5 [IrCl.sub.5 (pyz)Ru(CN).sub.5 ]
Potassium pentachloroiridate (III)
(.mu.-pyrazine) pentacyano ruthenate (II)
MC-44
Na3K.sub.3 [Fe(CN).sub.5 (pyz)Ru(CN).sub.5 ]
Potassium sodium decacyano(.mu.-pyrazine) ferrate (II) ruthenate (II)
MC-45
K.sub.2 [Rh(CN).sub.5 (thiazole)]
Potassium pentacyano (thiazole) rhodate (III)
MC-46
Na.sub.4 [Rh.sub.2 Cl.sub.10 (pyz)]
Sodium decachloro(pyrazine) rhodate (III)
MC-47
Rh[Cl.sub.3 (oxazole).sub.3 ]
Trichlorotris(oxazole) rhodium (III)
MC-48
Na.sub.3 [Fe(CN).sub.5 TQ]
TQ=(5-triazolo[4,3-a]quinoline)
Sodium pentacyano(5-triazolo[4,3-a]quinoline) ferrate (II)
Preparations of these compounds are presented below.
Generally any C--C, H--C or C--N--H organic ligand capable of forming a dopant metal hexacoordination complex with at least half of the metal coordination sites occupied by halide or pseudohalide ligands can be employed. This, of course, excludes coordination complexes such as metal ethylenediaminetetraacetic acid (EDTA) complexes, since EDTA itself occupies six coordination sites and leaves no room for other ligands. Similarly, tris(oxalate) and bis(oxalate) metal coordination complexes occupy too many metal coordination sites to allow the required inclusion of other ligands.
By definition, to be considered C--C, H--C or C--N--H organic a ligand must include at least one carbon-to-carbon bond, at least one carbon-to-hydrogen bond or at least one hydrogen-to-nitrogen-to-carbon bond linkage. A simple example of a C--C, H--C or C--N--H organic ligand classifiable as such solely by reason of containing a carbon-to-carbon bond is an oxalate (--O(O)C--C(O)O--) ligand. A simple example of a C--C, H--C or C--N--H organic ligand classifiable as such solely by reason of containing a carbon-to-hydrogen bond is a methyl (--CH.sub.3) ligand. A simple example of a C--C, H--C or C--N--H organic ligand classifiable as such solely by reason of containing a hydrogen-to-nitrogen-to-carbon bond linkage is a ureido [--HN--C(O)--NH--] ligand. All of these ligands fall within the customary contemplation of organic ligands. The C--C, H--C or C--N--H organic ligand definition excludes compounds lacking organic characteristics, such as ammonia, which contains only nitrogen-to-hydrogen bonds, carbon dioxide, which contains only carbon-to-oxygen bonds, and cyanide which contains only carbon-to-nitrogen bonds.
The realization of useful photographic performance modifications through the use of C--C, H--C or C--N--H organic ligands is based on performance comparisons and is independent of any particular theory. By comparing the organic ligand definition bonding requirements with the bonds present in ligands heretofore reported to have been incorporated in silver halide grain structures, it is recognized that the definitionally required bonding present in the C--C, H--C or C--N--H organic ligands differentiates them structurally from known ligand dopants. The balancing of halide and pseudohalide ligands with one or more organic ligands to achieve useful photographic effects is consistent with the halide and pseudohalide ligands occupying halide ion lattice sites in the crystal structure. On the other hand, the diversity of size and steric forms of the organic ligands shown to be useful supports the position that photographic effectiveness extends beyond the precepts of prior substitutional models. It is now specifically contemplated that C--C, H--C or C--N--H organic ligand effectiveness can be independent of size or steric configuration and is limited only by their availability in metal dopant ion hexacoordination complexes. Nevertheless, since there is no known disadvantage for choosing organic ligands based on host crystal lattice steric compatibility or approximations of steric compatibility nor have any advantages been identified for increasing ligand size for its own sake, the preferred organic ligand selections discussed below are those deemed most likely to approximate host crystal lattice compatibility. In other words, while the precept of host crystal lattice matching as an essential prerequisite of ligand utility has been discredited, there are significant advantages to be gained by selecting C--C, H--C or C--N--H organic ligands on the basis of their exact or approximate conformation to the host crystal lattice.
In general preferred individual C--C, H--C or C--N--H organic ligands contain up to 24 (optimally up to 18) atoms of sufficient size to occupy silver or halide ion sites within the grain structure. Stated another way, these organic ligands preferably contain up to 24 (optimally up to 18) nonmetallic atoms. Since hydrogen atoms are sufficiently small to be accommodated interstitially within a silver halide face centered cubic crystal structure, the hydrogen content of the organic ligands poses no selection restriction. While these organic ligands can contain metallic ions, these also are readily sterically accommodated within the crystal lattice structure of silver halide, since metal ions are, in general, much smaller than nonmetallic ions of similar atomic number. For example, silver ion (atomic number 47) is much smaller than bromide ion (atomic number 35). In the overwhelming majority of instances the C--C, H--C or C--N--H organic ligands consist of hydrogen and nonmetallic atoms selected from among carbon, nitrogen, oxygen, fluorine, sulfur, selenium, chlorine and bromine. The steric accommodation of iodide ions within silver bromide face centered cubic crystal lattice structures is well known in photography. Thus, even the heaviest non-metallic atoms, iodine and tellurium, can be included within the organic ligands, although their occurrence is preferably limited (e.g., up to 2 and optimally only 1) in any single organic ligand.
Referring to the illustrations of C--C, H--C or C--N--H organic ligand containing coordination complexes above, it is apparent that a wide variety of organic ligands are available for selection. C--C, H--C or C--N--H organic ligands can be selected from among a wide range of organic families, including substituted and unsubstituted aliphatic and aromatic hydrocarbons, secondary and tertiary amines (including diamines and hydrazines), phosphines, amides (including hydrazides), imides, nitriles, aldehydes, ketones, organic acids (including free acids, salts and esters), sulfoxides, and aliphatic and aromatic heterocycles including chalcogen (i.e., oxygen, sulfur, selenium and tellurium) and pnictide (particularly nitrogen) hetero ring atoms. The following are offered as nonlimiting illustrations of preferred C--C, H--C or C--N--H organic ligand categories:
Aliphatic hydrocarbon ligands containing up to 10 (most preferably up to 6) nonmetallic (e.g., carbon) atoms, including linear, branched chain and cyclic alkyl, alkenyl, dialkenyl, alkynyl and dialkynyl ligands.
Aromatic hydrocarbon ligands containing 6 to 14 ring atoms (particularly phenyl and naphthyl).
Aliphatic azahydrocarbon ligands containing up to 14 nonmetallic (e.g., carbon and nitrogen) atoms. The term "azahydrocarbon" is employed to indicate nitrogen atom substitution for at least one, but not all, of the carbon atoms. The most stable and hence preferred azahydrocarbons contain no more than one nitrogen-to-nitrogen bond. Both cyclic and acyclic azahydrocarbons are particularly contemplated.
Aliphatic and aromatic nitriles containing up to 14 carbon atoms, preferably up to 6 carbon atoms.
Aliphatic ether and thioether ligands, the latter also being commonly named as thiahydrocarbons in a manner analogous to azahydrocarbon ligands. Both cyclic and acyclic ethers and thioethers are contemplated.
Amines, including diamines, most preferably those containing up to 12 (optimally up to 6) nonmetal (e.g., carbon) atoms per nitrogen atom organic substituent. Note that the amines must be secondary or tertiary amines, since a primary amine (H.sub.2 N--), designated by the term "amine" used alone, does not satisfy the organic ligand definition.
Amides, most preferably including up to 12 (optimally up to 6) nonmetal (e.g., carbon) atoms.
Aldehydes, ketones, carboxylates, sulfonates and phosphonates (including mono and dibasic acids, their salts and esters) containing up to 12 (optimally up to 7) nonmetal (e.g., carbon) atoms.
Aliphatic sulfoxides containing up to 12 (preferably up to 6) nonmetal (e.g., carbon) atoms per aliphatic moiety.
Aromatic and aliphatic heterocyclic ligands containing up to 18 ring atoms with heteroatoms typically being selected from among pnictides (e.g., nitrogen) and chalcogens (e.g., oxygen, sulfur, selenium and tellurium). The heterocylic ligands contain at least one five or six membered heterocyclic ring, with the remainder of the ligand being formed by ring substituents, including one or more optional pendant or fused carbocyclic or heterocyclic rings. In their simplest form the heterocycles contain only 5 or 6 non-metallic atoms. Exemplary nonlimiting illustrations of heterocyclic ring structures include furans, thiophenes, azoles, diazoles, triazoles, tetrazoles, oxazoles, thiazoles, imidazoles, azines, diazines, triazines, as well as their bis (e.g., bipyridine) and fused ring counterparts (e.g., benzo- and napthoanalogues). When a nitrogen hetero atom is present, each of trivalent, protonated and quaternized forms are contemplated. Among specifically preferred heterocyclic ring moieties are those containing from 1 to 3 ring nitrogen atoms and azoles containing a chalcogen atom.
All of the above C--C, H--C or C--N--H organic ligands can be either substituted or unsubstituted. Any of a broad range of stable and synthetically convenient substituents are contemplated. Halide, pseudohalide, hydroxyl, nitro and organic substituents that are linked directly or through divalent oxygen, sulfur or nitrogen linkages are specifically contemplated, where the organic substituents can be simple or composite forms of the types of organic substituents named above.
The requirement that at least one of the coordination complex ligands be a C--C, H--C or C--N--H organic ligand and that half of the ligands be halide or pseudohalide ligands permits one or two of the ligands in hexacoordination complexes to be chosen from among ligands other than organic, halide and pseudohalide ligands. For example, nitrosyl (NO), thionitrosyl (NS), carbonyl (CO), oxo (0) and aquo (HOH) ligands are all known to form coordination complexes that have been successfully incorporated in silver halide grain structures. These ligands are specifically contemplated for inclusion in the coordination complexes satisfying the requirements of the invention.
In general any known dopant metal ion hexacoordination complex containing the required balance of halo and/or pseudohalo ligands with one or more C--C, H--C or C--N--H organic ligands can be employed in the practice of the invention. This, of course, assumes that the coordination complex is structurally stable and exhibits at least very slight water solubility under silver halide precipitation conditions. Since silver halide precipitation is commonly practiced at temperatures ranging down to just above ambient (e.g., typically down to about 30.degree. C.), thermal stability requirements are minimal. In view of the extremely low levels of dopants that have been shown to be useful in the art only extremely low levels of water solubility are required.
The C--C, H--C or C--N--H organic ligand containing coordination complexes satisfying the requirements above can be present during silver halide emulsion precipitation in any conventional level known to be useful for the metal dopant ion. Evans U.S. Pat. No. 5,024,931, discloses effective doping with coordination complexes containing two or more Group VIII noble metals at concentrations that provide on average two metal dopant ions per grain. To achieve this, metal ion concentrations of 10.sup.-10 M are provided in solution, before blending with the emulsion to be doped. Typically useful metal dopant ion concentrations, based on silver, range from 10.sup.-10 to 10.sup.-3 gram atom per mole of silver. A specific concentration selection is dependent upon the specific photographic effect sought. For example, Dostes et al Defensive Publication T962,004 teaches metal ion dopant concentrations ranging from as low as 10.sup.-10 gram atom/Ag mole for reducing low intensity reciprocity failure and kink desensitization in negative-working emulsions; Spence et al U.S. Pat. Nos. 3,687,676 and 3,690,891 teach metal ion dopant concentrations ranging as high as 10.sup.3 gram atom/Ag mole for avoidance of dye desensitization. While useful metal ion dopant concentrations can vary widely, depending upon the halide content of the grains, the metal ion dopant selected, its oxidation state, the specific ligands chosen, and the photographic effect sought, concentrations of less than 10.sup.-6 gram atom/Ag mole are contemplated for improving the performance of surface latent image forming emulsions without significant surface desensitization. Concentrations of from 10.sup.-9 to 10.sup.-6 gram atom/Ag mole have been widely suggested. Graphic arts emulsions seeking to employ metal dopants to increase contrast with incidental or even intentionally sought speed loss often range somewhat higher in metal dopant concentrations than other negative-working emulsions, with concentrations of up to 10.sup.-4 gram atom/Ag mole being common. For internal electron trapping, as is commonly sought in direct-positive emulsions, concentrations of greater than 10.sup.-6 gram atom/Ag mole are generally taught, with concentrations in the range of from 10.sup.-6 to 10.sup.-4 gram atom/Ag mole being commonly employed. For complexes that contain a single metal dopant ion molar and gram atom concentrations are identical; for complexes containing two metal dopant ions gram atom concentrations are twice molar concentrations; etc. Following the accepted practice of the art, stated dopant concentrations are nominal concentrations--that is, they are based on the dopant and silver added to the reaction vessel prior to and during emulsion precipitation.
The C--C, H--C or C--N--H organic ligand containing metal hexacoordination complexes can be introduced during emulsion precipitation employing procedures well known in the art. The coordination complexes can be present in the dispersing medium present in the reaction vessel before grain nucleation. More typically the coordination complexes are introduced at least in part during precipitation through one of the halide ion or silver ion jets or through a separate jet. Typical types of coordination complex introductions are disclosed by Janusonis et al, McDugle et al, Keevert et al, Marchetti et al and Evans et al, each cited above and here incorporated by reference. Another technique, demonstrated in the Examples below, for coordination complex incorporation is to precipitate Lippmann emulsion grains in the presence of the coordination complex followed by ripening the doped Lippmann emulsion grains onto host grains.
It is preferred to defer introduction of the C--C, H--C or C--N--H organic ligand containing metal hexacoordination complex until after tabular grain growth has commenced. Deferring dopant addition at the very outset of precipitation avoids complicating the modifications in grain structure necessary to initiate tabular grain growth. To observe a significant advantage for deferred dopant addition, it is generally preferred to defer dopant introduction until at least about 0.5 percent, most preferably at least 1 percent, of total silver has been precipitated as a minimum. As the percentage of total silver introduced prior to dopant introduction increases the potential influence of the dopant on the final configuration of the grain structure is diminished. For this reason, where compatible with the photographic effect sought to be achieved, it is preferred to defer dopant introduction until at least 20 percent, most preferably at least 50 percent of total silver been precipitated.
In one preferred form of the invention iodide is relied upon to initiate the formation of {100} tabular grains in the emulsion. It has been observed that {100} tabular grains account for a higher proportion of total grain projected area in the completed emulsions when iodide introduction is delayed. The grain nucleation step is initiated when a silver jet is opened to introduce silver into the dispersing medium. Iodide ion is preferably withheld from the dispersing medium until after the onset of grain nucleation. Preferably iodide ion introduction is delayed until at least 0.005 percent of the total silver used to form the emulsion has been introduced into the dispersing medium. Preferred results (high chloride {100} tabular grain projected areas of greater than 95 percent of total grain projected area in the completed emulsions) can be realized when iodide introduction is initiated in the period ranging from 0.01 to 3 (optimally 1.5) percent of total silver introduced.
In addition to the general utility of C--C, H--C or C--N--H organic ligand containing metal hexacoordination dopants to improve the performance of high chloride {100} tabular grain emulsions, specific applications have been observed that are particularly advantageous.
Rhodium hexahalides represent one well known and widely employed class of dopants employed to increase photographic contrast. Generally the dopants have been employed in concentration ranges of 10.sup.-6 to 10.sup.-4 gram atom of rhodium per mole of silver. Rhodium dopants have been employed in all silver halides exhibiting a face centered cubic crystal lattice structure. However, a particularly useful application for rhodium dopants is in graphic arts emulsions. Graphic arts emulsions typically contain at least 50 mole percent chloride based on silver and preferably contain more than 90 mole percent chloride.
One difficulty that has been encountered using rhodium hexahalide dopants is that they exhibit limited stability, requiring care in selecting the conditions under which they are employed. It has been discovered that the substitution of a C--C, H--C or C--N--H organic ligand for one or two of the halide ligands in rhodium hexahalide results in a more stable hexacoordination complex. Thus, it is specifically contemplated to substitute rhodium complexes of the type disclosed in this patent application for rhodium hexahalide complexes that have heretofore been employed in doping photographic emulsions.
In another specific application, it is recognized that spectral sensitizing dye, when adsorbed to the surface of a silver halide grain, allows the grain to absorb longer wavelength electromagnetic radiation. The longer wavelength photon is absorbed by the dye, which is in turn adsorbed to the grain surface. Energy is thereby transferred to the grain allowing it to form a latent image.
While spectral sensitizing dyes provide the silver halide grain with sensitivity to longer wavelength regions, it is quite commonly stated that the dyes also act as desensitizers. By comparing the native sensitivity of the silver halide grains with and without adsorbed spectral sensitizing dye it is possible to identify a reduction in native spectral region sensitivity attributable to the presence of adsorbed dye. From this observation as well as other, indirect observations it is commonly accepted that the spectral sensitizing dyes also are producing less than their full theoretical capability for sensitization outside the spectral region of native sensitivity.
It has been observed quite unexpectedly that increased spectral sensitivity of emulsions containing adsorbed spectral sensitizing dyes can be realized when the silver halide grains are doped with a group 8 metal dopant forming a hexacoordination complex containing at least one C--C, H--C or C--N--H organic ligand and pseudohalide ligands containing Hammett sigma values more positive than 0.50. The following pseudohalide meta Hammett sigma values are exemplary: CN 0.61, SCN 0.63 and SeCN 0.67. The meta Hammett sigma values for bromo, chloro and iodo ligands are in the range of from 0.35 to 0.39. The surprising effectiveness of the pseudohalide ligand containing complexes as compared to those that contain halide ligands is attributed to the greater electron withdrawing capacity of the pseudohalide ligands satisfying the stated Hammett sigma values. Further, the sensitizing effect has shown itself to be attainable with spectral sensitizing dyes generally accepted to have desensitizing properties either as the result of hole or electron trapping. On this basis it has been concluded that the dopants are useful in all latent image forming spectrally sensitized emulsions. The dopant can be located either uniformly or non-uniformly within the grains. For maximum effectiveness the dopants are preferably present within 500 .ANG. of the grain surface, and are optimally separated from the grain surface by at least 50 .ANG.. Preferred metal dopant ion concentrations are in the range of from 10.sup.-6 to 10.sup.-9 gram atom/Ag mole.
In another form it is contemplated to employ cobalt coordination complexes satisfying the requirements of the invention to reduce photographic speed with minimal (<5%) or no alteration in photographic contrast. One of the problems that is commonly encountered in preparing photographic emulsions to satisfy specific aim characteristics is that, in adjusting an emulsion that is objectionable solely on the basis of being slightly too high in speed for the specific application, not only speed but the overall shape of the characteristic curve is modified.
It has been discovered quite unexpectedly that cobalt hexacoordination complexes satisfying the general requirements of the invention are capable of translating a characteristic curve along the log E (E=lux-second) exposure axis without significantly altering the shape of the characteristic curve. Specifically, contrast and minimum and maximum densities can all be maintained while decreasing sensitivity by doping. Preferred cobalt complexes are those that contain, in addition to one or two C--C, H--C or C--N--H organic ligands occupying up to two coordination sites, pseudohalide ligands that exhibit Hammett sigma values of that are more positive than 0.50. The cobalt complex can be uniformly or non-uniformly distributed within the grains. Cobalt concentrations are preferably in the range of from 10.sup.-6 to 10.sup.-9 gram atom/Ag mole.
In still another specific application of the invention it has been observed that group 8 metal coordination complexes satisfying the requirements of the invention that contain as the C--C, H--C or C--N--H organic ligand an aliphatic sulfoxide are capable of increasing the speed of high (>50 mole %) chloride emulsions and are capable of increasing the contrast of high (>50 mole %) bromide emulsions. Preferred aliphatic sulfoxides include those containing up to 12 (most preferably up to 6) nonmetal (e.g., carbon) atoms per aliphatic moiety. The coordination complex can occupy any convenient location within the grain structure and can be uniformly or non-uniformly distributed. Preferred concentrations of the group 8 metal are in the range of from 10.sup.-6 to 10.sup.-9 gram atom/Ag mole.
In still another specific application of the invention it has been observed that anionic [IrX.sub.x L.sub.y ] hexacoordination complexes, where X is Cl or Br, x is 4 or 5, L is a C--C, H--C or C--N--H organic ligand, and y is 1 or 2, are surprisingly effective in reducing high intensity reciprocity failure (HIRF). As herein employed HIRF is a measure of the variance of photographic properties for equal exposures, but with exposure times ranging from 10.sup.-1 to 10.sup.-4 second. Improvements in HIRF are observed in doping all face centered cubic lattice structure silver halide grains, but the most striking improvements have been observed in high (>50 mole %) chloride emulsions. Preferred organic ligands are aromatic heterocycles of the type previously described. The most effective organic ligands are azoles, with optimum results having been achieved with thiazole ligands.
Also found to be unexpectedly useful in reducing HIRF are anionic [IrX.sub.5 LMX'.sub.5 ] hexacoordination complexes, where X and X' are independently Cl or Br, M is a group 8 metal, and L is a C--C, H--C or C--N--H organic bridging ligand, such as a substituted or unsubstituted aliphatic or aromatic diazahydrocarbon. Specifically preferred bridging organic ligands include H.sub.2 N--R--NH.sub.2, where R is a substituted or unsubstituted aliphatic or aromatic hydrocarbon containing from 2 to 12 nonmetal atoms, as well as substituted or unsubstituted heterocycles containing two ring nitrogen atoms, such as pyrazine, 4,4'-bipyridine, 3,8'-phenanthroline, 2,7'-diazapyrene and 1,4'-[bis(4-pyridyl)]butadiyne.
The iridate complexes identified above for use in reducing HIRF are useful in all photographic silver halide grains containing a face centered cubic crystal lattice structure. Exceptional performance has been observed in high chloride (>50 mole %) grain structures. The complex can be located either uniformly or non-uniformly within the grains. Concentrations preferably range from 10.sup.-6 to 10.sup.-9 gram atom Ir/Ag mole.

This other specifically advantageous combinations are illustrated in the Examples below.
Apart from the features that have been specifically described the emulsions of the invention and their use in photographic elements can take any convenient-conventional form. A summary of conventional variations in photographic emulsions, their preparation, the photographic elements in which they are incorporated and their use is provided in Research Disclosure, Item 308119 cited above and here incorporated by reference. The following sections are considered particularly relevant:
II. Emulsion washing;
III. Chemical sensitization;
IV. Spectral sensitization and desensitization;
V. Brighteners;
VI. Antifoggants and stabilizers;
VII. Color materials;
VIII. Absorbing and scattering materials
IX. Vehicles and vehicle extenders
X. Hardeners
XI. Coating aids
XII. Plasticizers and lubricants
XIII. Antistatic layers
XIV. Methods of addition
XV. Coating and drying procedures
XVI. Matting agents
XVII. Supports
XVIII. Exposure
XIX. Processing
XX. Developing agents
XXI. Development modifiers
XXII. Physical development systems
XXIII. Image-transfer systems
XXIV. Dry development systems
Preparations
Since the preparation of metal coordination complexes can be undertaken by the procedures described in the articles in which they are reported, cited above, preparations are provided for only those metal coordination complexes for which no source citation is listed.
Preparation of MC-14ss
[Fe(CN).sub.5 (2-chloropyrazine)].sup.3- : Ten grams of chloropyrazine were added to 10 mL of water and the solution cooled to ice temperature. Three grams of Na.sub.3 Fe(CN).sub.5 (NH.sub.3).3H.sub.2 O were dissolved in 20 mL of degassed and chilled water and then added dropwise from a chilled dropping funnel into the chloropyrazine solution over a 15 min period. The reaction was stirred for 1 hr, after which the mixture was poured into 750 mL of cold acetone. A reddish material precipitated and was decanted and washed twice with cold acetone. The material was dried with a nitrogen flow. The entire reaction and drying were performed in the dark. A red-purple product in the amount of 2.88 g was obtained. The purity was determined using nuclear magnetic resonance (NMR) spectroscopy.
Preparation of MC-41
[IrCl.sub.5 (thiazole)].sup.2- : Two tenths gram of K.sub.2 IrCl.sub.5 (H.sub.2 O) was reacted with 2 mL thiazole (Aldrich) in 20 mL H.sub.2 O and stirred for 3 days. The solution was then evaporated to a small volume and precipitated by adding to 50 mL ethanol. The precipitate was filtered and washed with ethanol. The identity of this compound was confirmed by infrared (IR), ultraviolet and visible (UV/Vis) and NMR spectroscopies and carbon, hydrogen and nitrogen (CHN) chemical analyses.
Preparation of MC-42
[IrCl.sub.5 (pyz)Fe(CN).sub.5].sup.5- : Na.sub.3 K.sub.2 [IrCl.sub.5 (pyrazine)Fe(CN).sub.5 ] was prepared by reacting equimolar amounts of K.sub.2 [IrCl.sub.5 (pyrazine)] and Na.sub.3 [Fe(CN).sub.5 (NH.sub.3)].3H.sub.2 O in a small amount of H.sub.2 O at room temperature for 24 hours. The volume was decreased with flowing nitrogen, and ethyl alcohol added to precipitate the final product. The product was assigned a formula of Na.sub.3 K.sub.2 [IrCl.sub.5 (pyrazine)Fe(CN).sub.5 ] by IR, UV/VIS and NMR spectroscopies and by CHN chemical analyses.
Preparation of MC-43
[IrCl.sub.5 (pyz)Ru(CN).sub.5].sup.5- : The mixed metal dimer K.sub.5 [IrCl.sub.5 (pyrazine)Ru(CN).sub.5 ] was prepared by reacting equimolar amounts of K.sub.3 [Ru(CN).sub.5 (pyrazine)] and K.sub.2 [IrCl.sub.5 (H.sub.2)] in a small amount of H.sub.2 O in a hot water bath at 80 C. for 2 hours. The volume was partially reduced with flowing nitrogen, and ethyl alcohol was added to precipitate the final product. The dimer was recrystallized by dissolving in a minimum amount of water and precipitated with ethyl alcohol. The product was assigned as K.sub.5 [IrCl.sub.5 (pyrazine)Ru(CN).sub.5 ] by IR, UV/VIS, and NMR spectroscopies and by CHN chemical analyses.
Preparation of MC-44
[Ru(CN).sub.5 (pyz)Fe(CN).sub.5 ].sup.6- : Na.sub.3 K.sub.3 [Ru(CN).sub.5 (pyrazine)Fe(CN).sub.5 ] was similarly prepared by stirring equimolar amounts of K.sub.3 [Ru(CN).sub.5 (pyrazine)] and Na.sub.3 [Fe(CN).sub.5 (NH.sub.3)].3H.sub.2 O in a small amount of H.sub.2 O at room temperature for 24 hours. The volume was decreased with flowing nitrogen, and ethyl alcohol added to precipitate the final product. The product was assigned as Na.sub.3 K.sub.3 [Ru(CN).sub.5 (pyrazine)Fe(CN).sub.5 ] by IR, UV/VIS and NMR spectroscopies and by CHN chemical analyses.
Preparation of MC-45
[Rh(CN).sub.5 (thiazole)].sup.2- : The synthesis of this compound was similar to literature methods described by G. L. Geoffroy, M. S. Wrighton, G. S. Hammond and H. B. Gray [Inorg. Chem. 13(2), 430-434, (1974)] with slight changes as described here. One half gram of K.sub.3 [Rh(CN).sub.6 ] was dissolved in 100 mL H.sub.2 O and adjusted to a pH of 2 with HClO.sub.4. This solution was irradiated with a mercury lamp in a quartz tube for 24 hours. The solution was then evaporated down to 5 mL and chilled. The KClO.sub.4 was filtered and 1 mL of thiazole in 1 mL of ethanol was added. This solution was again irradiated with the Hg lamp, this time for an hour The volume was reduced, and ethanol was added to produce the final product. The precipitate which was formed was filtered and washed with ethanol. The identity of the compound was confirmed by IR, UV/Vis and NMR spectroscopies.
Preparation of MC-46
[Rh.sub.2 Cl.sub.10 (pyz)].sup.4- : Na.sub.4 [Rh.sub.2 Cl.sub.10 (pyrazine)] was prepared by reacting Na.sub.3 RhCl.sub.6.12H.sub.2 O with pyrazine in a 2 to 1.05 (5% excess pyrazine) molar ratio at 100 C. in a minimum amount of H.sub.2 O for 1 hour. Acetone was added to the cooled solution to give an oil and an orange colored liquid with some suspended solid material which was decanted. The oil was washed several times with acetone and decanted. The acetone was removed with a N.sub.2 flow to give a sticky red substance which was then air dried in an oven at 100 C. for 1 hour to give a dark red material. This was recrystallized twice by dissolving in a minimum amount of H.sub.2 O and precipitated with ethyl alcohol. The final material was filtered, washed with ethyl alcohol, and air dried. The product was assigned as Na.sub.4 [Rh.sub.2 Cl.sub.10 (pyrazine)] by IR, UV/Vis and NMR spectroscopies and by CHN chemical analyses.
Preparation of MC-47
[RhCl.sub.13 (oxazole).sub.3 ]: 0.5 g of (NH.sub.4).sub.2 [RhCl.sub.5 (H.sub.2 O)] was reacted with 0.5 mL oxazole in 15 mL H.sub.2 O for 3 days. The solution was then added to a large amount of acetone whereupon a white precipitate appeared. The precipitate (NH.sub.4 Cl) was filtered off. A yellow solid was obtained after evaporating the solvent from the filtrate. This yellow solid was washed with cold acetone in which it was slightly soluble. Slow evaporation of the acetone solution provided bright yellow crystals. The yellow product was assigned as RhCl.sub.13 (oxazole).sub.3 by Infrared, UV/Vis, and NMR spectroscopies and CHN chemical analysis.
Preparation of MC-48
[Fe(CN).sub.5 TQ].sup.3- : The synthesis of this compound is similar to reported methods of various Na.sub.x Fe(CN).sub.5 L compounds [H. E. Toma and J. M. Malin, Inorg. Chem. 12(5), 1039-1045, (1973)]. One half gram of Na.sub.3 [Fe(CN).sub.5 (NH.sub.3)].3H.sub.2 O was dissolved in 5 mL H.sub.2 O and added to 0.26 g of s-triazolo [4,3-a] quinoline in 5 mL ethanol. The solution was mixed for 1 week then evaporated to 2 mL and precipitated by adding to ethanol. This provided an oil and a light brown precipitate. The precipitate was filtered and the solution was decanted from the oil. The oil was dissolved in a small amount of water and added to a large excess of ethanol. This afforded more brown precipitate. The precipitates were washed with ethanol and analyzed using IR, UV/Vis and NMR spectroscopies and CHN chemical analysis.
Background Examples
The invention can be better appreciated by reference to the following background examples. The background examples demonstrate the effects of C--C, C--H and C--N--H organic ligand metal hexacoordination complexes in high chloride grains structures. Although the background examples do not demonstrate the specific invention claimed in that the high chloride grains are not {100} tabular grains, the background examples are useful in demonstrating performance modifying properties of the dopants.
Comparative Dopants
Except for comparative dopant complexes CD-7 and CD-8, the comparative dopant (CD) complexes listed in Table I below were purchased from commercial sources. CD-7 and CD-8 were prepared as reported by M. Delephine, Ann. Chim., 19, 145 (1923). EDTA=ethylenediaminetetraacetic acid
TABLE I______________________________________CD-1 EDTACD-2 [Fe(EDTA)].sup.-1CD-3 [IrCl.sub.6 ].sup.-2CD-4 K.sub.2 C.sub.2 O.sub.4.H.sub.2 OCD-5 [Fe(CN).sub.6 ].sup.-4CD-6 [Fe(C.sub.2 O.sub.4).sub.3 ].sup.-3CD-7 [cis-IrCl.sub.2 (C.sub.2 O.sub.4).sub.2 ].sup.-3CD-8 [Ir(C.sub.2 O.sub.4).sub.2 ].sup.-3______________________________________
Background Example 1
The purpose of this example is to demonstrate the incorporation C--C, H--C or C--N--H organic ligands within a high chloride silver halide grain structure.
An emulsion B19 was prepared as described below in the B Series of Background Examples, doped with 43.7 molar parts per million (mppm) of dopant MC-14c.
Electron paramagnetic resonance (EPR) spectroscopic measurements were made on emulsion B19 at temperatures between 5.degree. and 300.degree. K., using a standard X-band homodyne EPR spectrometer and standard cryogenic and auxiliary equipment, such as that described in Electron Spin Resonance, 2nd Ed., A Comprehensive Treatise on Experimental Techniques, C. P. Poole, Jr., John Wiley & Sons, New York, 1983. These measurements provided detailed structural information about the microscopic environment of the dopant ion, and, in this background example, showed that all or most of the iron added during precipitation was incorporated in the silver chloride grain crystal structure in the Fe(II) valence state, and all of the incorporated Fe(II) ions had their ligands intact so that [Fe(CN).sub.5 bipyridyl)].sup.3- replaced a [AgCl.sub.6 ].sup.5- moiety.
No EPR signals were observed from the doped sample unless it was exposed to light or strong oxidants, such as gaseous chlorine. After exposure to band-to-band light excitation (365 nm) between 260.degree. K. and room temperature, EPR signals were observed at 5.degree.-8.degree. K. These signals were not observed from the undoped control sample after light exposure. Discernible in these signals were powder pattern lineshapes like those typically observed from a randomly oriented ensemble of low symmetry paramagnetic species in a powder or frozen solution. The strongest powder patterns had g.sub.1 features at 2,924 (Site I), 2,884 (Site II) and 2.810 (Site III), each with a linewidth at half maximum of 1.0.+-.0.1 mT, shown below to be from four distinct kinds of [Fe(CN).sub.5 (bipyridyl)].sup.2- complexes in which the metal ions have low spin d.sup.5 electronic configurations.
By analogy to previous studies of substitutional low spin d.sup.5 transition metal complexes in the silver halides and structurally related crystals, such as described in D. A. Corrigan, R. S. Eachus, R. E. Graves and M. T. Olm, J. Chem. Phys. 70, 5676 (1979) for (RuCl.sub.6).sup.3- centers in AgCl and (RuBr).sub.6.sup.3- centers in AgBr, and R. S. Eachus and M. T. Olm, Rad. Elf. 73, 69 (1983) for (OSCl.sub.6).sup.3- in AgCl and (OsBr.sub.6).sup.3- centers in AgBr, these [Fe(CN).sub.5 (bipyridyl)].sup.2- complexes differ in the arrangement of the associated silver ion vacancies which are necessary to provide charge neutrality in the silver chloride lattice. The g2 feature corresponding to the major structural center (Site I) was at 2,286. The other three g.sub.2 signals were at 2,263 (Site II), 2,213 (Site III) and 2,093 (Site IV). The value of g.sub.3 for the major [Fe(CN).sub.5 (bipyridyl)].sup.2- complex in AgCl (Site I) was found to be 1.376. The g.sub.3 features from the three secondary bipyridyl complexes were not resolved in our experiments. The g values determined for the [Fe(CN).sub.5 (bipyridyl)].sup.2- complex with silver ion vacancies present in the highest concentration (Site I) are consistent with the assignment to a rhombic, low spin Fe(III) complex substituting for (AgCl.sub.6).sup.5- in the cubic silver chloride lattice.
The powder pattern EPR spectrum was also observed after the doped, unexposed silver chloride emulsion was placed in an oxidizing atmosphere of chlorine gas. The observations that this pattern was absent before exposure and was produced by the oxidizing atmosphere confirmed that the [Fe(CN).sub.5 (bipyridyl)] complex dopant was incorporated with the metal ion in the Fe(II) state, which is invisible to EPR measurements, and that the Fe(II) ion trapped a hole (was oxidized) to produce the Fe(III) oxidation state during exposure to chlorine or light.
It was established that the dopant was incorporated primarily as [Fe(CN).sub.5 (bipyridyl)].sup.3- with the ligands surrounding the ferrous ion intact by comparing the observed EPR spectra with those obtained upon doping silver chloride powders with the most chemically-feasible ligand-exchanged contaminants of the dopant salt that might be produced during synthesis of the dopant or precipitation of the emulsion. The species [Fe(CN).sub.6 ].sup.4-, [Fe(CN).sub.5 (H.sub.2 O)].sup.3- [Fe(CN).sub.5 Cl].sup.4- and [Fe.sub.2 (CN).sub.10 ].sup.6- were investigated. The EPR spectra of the corresponding Fe(III) species produced in the silver chloride grains by band-to-band excitation or exposure to chlorine were quite distinct from those assigned to the four [Fe(CN).sub.5 (bipyridyl)].sup.2- dopant complexes.
From the foregoing it was concluded that the bipyridyl ligand was sufficiently stable in aqueous solution to minimize its exchange with chloride or water during coprecipitation. Considering the observation of a well-resolved EPR powder pattern from the doped emulsion, the high yields of the low spin Fe(III) photoproducts, and the propensity of low spin Fe(III) ions for six-fold coordination, it is clear that [Fe(CN).sub.5 (bipyridyl)].sup.3- is incorporated substitutionally in silver chloride, replacing a [AgCl.sub.6 ].sup.5- moiety. Despite the presence of the bulky organic ligand, it is not occluded as a separate phase or adsorbed as a surface species.
A Series Background Examples
These background examples have as their purpose to demonstrate the effectiveness of coordination complexes of rhodium and at least one organic ligand to increase the contrast of regular cubic grain high chloride silver bromochloride emulsions.
Emulsion A1 was prepared as follows:
______________________________________Solution A:Gelatin (bone) 180 gD. W. 7200 gSolution B:1.2N in Sodium bromide2.8N in Sodium chlorideSolution C2.0N Silver nitrateSolution DGelatin (bone) 180 gD. W. 1000 g______________________________________
Solution A was adjusted to a pH of 3 at 35.degree. C., and pAg was adjusted to 7.87 with a NaCl solution. Solutions B and C were run into solution A with stirring. Solutions B and C were run in at rates of about 17.3 and 30 mL/min, respectively, for the first 3 minutes. The addition rate of solution C was then ramped from 30 to 155 mL/min and solution B was ramped from 17.3 to 89.3 mL/min in 12.5 min. Solutions C and B were then run in at 155 mL/min and 89.3 mL/min respectively for 21 min. The pAg was controlled at 7.87 during the addition of solutions B and C. The temperature was then raised to 40.degree. C. and the pAg adjusted to 8.06. The emulsion was washed until the pAg measured 7.20. The emulsion was concentrated and solution D was added. The pAg was adjusted to 7.60 and the pH adjusted to 5.5.
The AgCl.sub.0.70 Br.sub.0.30 emulsions prepared had a narrow distribution of grain sizes and morphologies; emulsion grains were cubic shape with edge lengths of 0.17 .mu.m.
Emulsion A1 was chemically sensitized by the addition of 0.812 mg/Ag mole of 4,4'-phenyl- disulfide diacetanilide from methanolic solution, 13.35 .times.10.sup.-6 mole/Ag mole of 1,3-di(carboxymethyl)-1,3-dimethyl-2-thiourea disodium monohydrate and 8.9.times.10.sup.-6 mole/Ag mole potassium tetrachloroaurate(III), followed by a digestion for 10 minutes at 65.degree. C.
Emulsion A2 was prepared and sensitized as for emulsion A1, except that the salt solution was modified so as to introduce a total of 0.14 mppm of dopant anion MC-46 through the entire emulsion grain.
Photographic Comparison
Coatings of each of the above optimally sensitized emulsions were made at 21.5 mg Ag/dm.sup.2 and 54 mg gelatin/dm.sup.2 with a gelatin overcoat layer made at 10.8 mg gelatin/dm.sup.2 a surfactant and a hardener, on a cellulose acetate support. Some coatings of each sensitized emulsion were exposed for 0.1 second to 365 nm on a standard sensitometer and then developed for 6 minutes in a hydroquinone-Elon.TM.(N-methyl-p-aminophenol hemisulfate) surface developer at 21.degree. C.
The photographic parameters of emulsions A1 and A2 are shown in Table A-I. It can be seen that dopant MC-46 was useful for increasing emulsion contrast and for reducing Dmin.
TABLE A-I______________________________________Dmin, Log Relative Speed times 100 and Contrast forEmulsions EEmulsion Dopant D.sub.min Speed Contrast______________________________________A1 none 0.04 235 3A2 MC-46 0.03 171 3.6______________________________________
B Series Background Examples
These background examples have as their purpose to demonstrate the effectiveness of coordination complexes of iridium and/or iron and at least one organic ligand to increase speed and reduce reciprocity failure of regular cubic grain silver chloride emulsions.
Control Emulsion B1 was prepared in the absence of any dopant salt. A reaction vessel containing 5.7 liters of a 3.95% by weight gelatin solution was adjusted to 46.degree. C., pH of 5.8 and a pAg of 7.51 by addition of a NaCl solution. A solution of 1.2 grams of 1,8-dihydroxy-3,6-dithiaoctane in 50 mL of water was then added to the reaction vessel. A 2M solution of AgNO.sub.3 and a 2M solution of NaCl were simultaneously run into the reaction vessel with rapid stirring, each at a flow rate of 249 mL/min. with controlled pAg of 7.51. The double jet precipitation continued for 21.5 minutes, after which the emulsion was cooled to 38.degree. C., washed to a pAg of 7.26, and then concentrated. Additional gelatin was introduced to achieve 43.4 grams of gelatin/Ag mole, and the emulsion was adjusted to pH of 5.7 and pAg of 7.50. The resulting silver chloride emulsion had a cubic grain morphology and a 0.34 .mu.m average edge length.
Emulsion B2 was prepared similarly as Emulsion B1, except as follows: During the precipitation, an iridium containing dopant was introduced via dissolution into the chloride stream in a way that introduced a total of 0.32 mppm of dopant MC-27a into the outer 93% to 95% of the grain volume. A shell of pure silver chloride (5% of the grain volume) was then precipitated to cover the doped band.
Emulsion B3 was precipitated as described for Emulsion B2, except that dopant MC-27a was added at a level of 0.16 ppm into the outer 93% to 95% of the grain volume.
Emulsion B4 was precipitated as described for Emulsion B2, except that dopant MC-32d was introduced at a total level of 0.32 mppm into the outer 93% to 95% of the grain volume. Analyses for iridium incorporation were performed by ion coupled plasma mass spectrophotometry (ICP-MS). The iridium levels in this emulsion were at least as high as those detected in a comparative emulsion doped with the conventional iridium dopant anions, (IrCl.sub.6).sup.3- or (IrC.sub.6).sup.2-.
Emulsion B5 was precipitated as described for Emulsion B2, except that dopant MC-32d was introduced at a total level of 0.10 mppm into the outer 93% to 95% of the grain volume.
Emulsion B6 was precipitated as described for Emulsion B2, except that MC-41 was introduced at a total level of 0.32 mppm into the outer 93% to 95% of the grain volume. Analyses for iridium incorporation were performed by ICP-MS. The iridium levels in this emulsion were at least as high as those detected in comparative emulsions prepared doped with the conventional iridium dopant anions, (IrCl.sub.6).sup.3- or (IrCl.sub.6).sup.2-.
Emulsion B7 was precipitated as described for Emulsion B2, except that dopant MC-41 was introduced at a total level of 0.16 mppm into the outer 93% to 95% of the grain volume.
Emulsion B8 was precipitated as described for Emulsion B2, except that dopant MC-31 was introduced at a total level of 0.16 mppm into the outer 93% to 95% of the grain volume.
Emulsion B9 was precipitated as described for Emulsion B2, except that dopant MC-29a was introduced at a total level of 0.32 mppm into the outer 93% to 95% of the grain volume. The iridium levels in this emulsion were at least as high as those detected in a comparative emulsions doped with the conventional iridium dopant anions, (IrCl.sub.6).sup.3- or (IrCl.sub.6).sup.2-.
Emulsion B10 was precipitated as described for Emulsion B2, except that dopant MC-29b was introduced at a total level of 0.32 mppm into the outer 93% to 95% of the grain volume.
Emulsion B11 was precipitated as described for Emulsion B2, except that dopant MC-29c was introduced at a total level of 0.32 mppm into the outer 93% to 95% of the grain volume.
Emulsion B12 was precipitated as described for Emulsion B2, except that dopant MC-42 was introduced at a total level of 0.32 mppm into the outer 93% to 95% of the grain volume.
Emulsion B13 was precipitated as described for Emulsion B2, except that dopant MC-43 was introduced at a total level of 0.32 mppm into the outer 93% to 95% of the grain volume.
Emulsion B14 was precipitated as described for Emulsion B2, except that dopant MC-14rr was introduced at a total level of 25 mppm into the outer 79.5% to 92% of the grain volume.
Emulsion B15 was precipitated as described for Emulsion B2, except that dopant MC-14rr was introduced at a total level of 43.7 mppm into the outer 7.9% to 95% of the grain volume. Analysis of this emulsion by ICP-AES showed that, within experimental error, the incorporated Fe level was the same as in similarly prepared emulsions doped with the conventional dopant anion [Fe(CN).sub.6 ].sup.4-.
Emulsion B16 was precipitated as described for Emulsion B2, except that EDTA (CD-1) was introduced as a dopant at a total level of 43.7 mppm into the outer 7.9% to 95% of the grain volume. Analysis of this emulsion by ICP-AES showed that the Fe level was less than the detection limit of this technique (3 mppm Fe in AgCl).
Emulsion B17 was precipitated as described for Emulsion B2, except that dopant Fe(EDTA)(CD-2) was introduced at a total level of 43.7 mppm into the outer 7.9% to 95% of the grain volume. Analysis of this emulsion by ICP-AES showed that the Fe level was less than the detection limit of this technique (3 mppm Fe in AgCl).
Emulsion B18 was precipitated as described for Emulsion B2, except that dopant [Fe(CN).sub.6 ].sup.4- (CD-5) was introduced at a total level of 21.8 mppm into the outer 7.9% to 95% of the grain volume.
Emulsion B19 was precipitated as described for Emulsion B2, except that dopant MC-14c was introduced through a third jet from a 0.1 molar aqueous KClO.sub.4 solution and at a total level of 43.7 mppm into the outer 7.9% to 95% of the grain volume. The emulsion was studied by EPR spectroscopy, and the results were as described above in background Example 1.
Emulsion B20 was precipitated as described for emulsion B2, except that dopant MC-41 was introduced at a total level of 21.8 mppm into the outer 7.9 to 95% of the grain volume. This emulsion was examined by EPR spectroscopy, as described in background Example 1, in order to demonstrate the incorporation of organic ligands within the silver halide grain structure. Exposure of the emulsion B20 at between 180.degree. and 240.degree. K. produced a distinct EPR spectrum, with well resolved iridium and chlorine hyperfine structure. The spectrum could unequivocally be assigned to an iridium (II) ion at a silver position in the silver halide lattice. The EPR g-values were as follows: g.sub.1 =2.911.+-.0.001, g.sub.2 =2.634.+-.0.001, g.sub.3 =1,871.+-.0.001. These are significantly different from those measured previously for (IrCl.sub.6).sup.4- in a AgCl matrix (g.sub.1 =g.sub.2 =2.772.+-.0.001, g.sub.3 =1.883.+-.0.,001) or for (IrCl.sub.5 H.sub.2 O).sup.3- in a AgCl matrix (g.sub.1 =3.006.+-.0.001, g.sub.2 =2.702.+-.0.001, g.sub.3 .ltoreq.2.0. Since no EPR signals from these possible contaminants were observed in emulsion B20, it was concluded that the dopant complex MC-41, (IrCl.sub.5 thiazole).sup.2-, was incorporated intact. On exposure 9.7 [IrCl.sub.5 (thiazole)].sup.2- trapped an electron to give [IrCl.sub.5 (thiazole)].sub.3-, which was detected by EPR.
Emulsion B21 was precipitated as described for emulsion B2, except that dopant MC-29a was introduced at a total level of 21.8 mppm into the outer 7.9 to 95% of the grain volume. The emulsion was examined by EPR spectroscopy, as described in background Example 1. Exposure of emulsion B21 at 210.degree. K. produced a distinctive EPR spectrum with well resolved indium and chlorine hyperfine structure. The spectrum could unequivocally be assigned to an iridium (II) ion at a silver position the silver halide lattice. The EPR parameters were as follows: g.sup.1 =3.043.+-.0.001, g.sub.2 =2.503.+-.0.001 and g.sub.3 =1.823.+-.0.005. These were significantly different from those measured previously for (IrCl.sub.6).sup.4- or (IrCl.sub.5 H.sub.2 O).sub.3- in a AgCl matrix (see parameters listed above). Since no EPR signatures from these possible contaminants were observed in emulsion F.sub.21, it was concluded that dopant complex MC-29a, [IrCl.sub.5 (pyrazine)].sup.2-, was incorporated intact. On exposure, [IrCl.sub.5 (pyrazine)] .sup.2- trapped an electron to give [IrCl.sub.5 (pyrazine)].sup.3-, which was detected by EPR.
The resulting emulsions were each divided into several portions.
Those portions designated portions (I) were chemically and spectrally sensitized by the addition of 30 mg/Ag mole of a colloidal dispersion of gold sulfide followed by digestion at 60.degree. C. for 30 minutes. Following digestion each portion I was cooled to 40.degree. and 300 mg/mole of 1-(3-acetamidophenyl)-5-mercaptotetrazole were added and held for 10 minutes, followed by 20 mg/mole of red spectral sensitizing dye anhydro-3-ethyl-9,11-neopentylene-3'-(3-sulfopropyl)thiadicarbocyanine hydroxide (Dye C) and a 20 minute hold.
Those portions designated portions (Ia) were treated as for portions (I), except that no dye was added and the final 20 minute hold was eliminated.
Those portions designated portions (II) were chemically and spectrally sensitized as described for portions (I), except that 50 rather than 30 mg/Ag mole of a colloidal dispersion of gold sulfide was added for each emulsion.
Those portions designated portions (III) were chemically and spectrally sensitized by the addition of aurous bis(1,4,5,-triazolium-1,2,4-trimethyl-3-thiolate) tetrafluoroborate, at 5, 7.5 or 10 mg per silver mole and di(carboxymethyl)dimethyl thiourea, at 0.75 mg per silver mole followed by heat digestion and antifoggant and dye addition as described for portions (I).
Portions (IV) were chemically and spectrally sensitized by the addition of 8.4 mg/Ag mole of a colloidal dispersion of gold sulfide, followed by digestion at 30 minutes at 60.degree. C. The emulsion was then treated as for portion I, except that 1.3 grams of KBr per silver mole were added prior to the dye addition.
Photographic Comparison
Sensitized portions (I, Ia, II and III) of the B series emulsions described above were coated onto cellulose acetate film support at 21.53 mg/dm.sup.2 silver chloride and 53.92 mg/dm.sup.2 gelatin. A gelatin overcoat layer comprised of 10.76 mg/dm.sup.2 gelatin and a hardener, bis(vinylsulfonylmethyl) ether, at a level of 1.5% by wt., based of total gelatin. Samples of these coated photographic elements were evaluated by exposure for 1/10 second to 365 nm radiation, followed by development for 12 minutes in Kodak DK-50.TM. developer. Additionally, samples of the coatings were evaluated for reciprocity failure by giving them a series of calibrated (total energy) white light exposures ranging from 1/10,000th of a second to 10 seconds, followed by development as above.
Sensitized portions (IV) of the B series emulsions described above were coated onto a photographic paper support at silver and gel levels of 1.83 and 8.3 mg/dm.sup.2, respectively. A gelatin overcoat containing 4.2 mg/dm.sup.2 of Coupler C.sub.1 and 1.5% by weight based on total gelatin of the hardener bis(vinylsulfonylmethyl) ether was applied over the emulsion. ##STR1## These coated photographic elements were evaluated by exposure for 1/10 second followed by development for 45 seconds in Kodak Ektacolor RA-4.TM. developer.
Additionally, the coatings were evaluated for reciprocity by giving them a series of calibrated (total energy) white light exposures ranging from 1/10,000th of a second to 10 seconds, followed by development as above. In Tables B-I, B-II and B-III high intensity reciprocity failure (HIRF) and low intensity reciprocity failure (LIRF) are reported as the difference between relative log speeds times 100 measured a minimum density plus 0.15 optical density obtained at exposures of 10.sup.-4 and 10.sup.-1 second for HIRF and 10.sup.-1 and 10 seconds for LIRF. In all reciprocity failure investigations, regardless of the exact measurement points selected for comparison, ideal performance is for no speed difference--e.g., HIRF or LIRF are ideally zero or as near zero as attainable.
TABLE B-I______________________________________Emulsion Dopant Sensitization HIRF LIRF______________________________________B1 control I 24 21B2 MC-27a I 12 17B3 MC-27a I 14 19B5 MC-32d I 10 14B6 MC-41 I 0 6B7 MC-41 I 2 14B8 MC-31 I 14 15B9 MC-29a I 3 20 B10 MC-29b I 14 18 B11 MC-29c I 15 19 B12 MC-42 I 2 19 B13 MC-43 I 23 22______________________________________
TABLE B-II______________________________________Emulsion Dopant Sensitization HIRF LIRF______________________________________B1 control II 26 16B2 MC-27a II 15 15B3 MC-27a II 16 14______________________________________
TABLE B-III______________________________________Emulsion Dopant Sensitization HIRF LIRF______________________________________B1 control III, 10 19 13 mg/mole Au(I) saltB5 MC-34d III, 10 13 9 mg/mole Au(I) saltB7 MC-41 III, 5 1 5 mg/mole Au (I) salt______________________________________
TABLE B-IV______________________________________Reciprocity Data for Format IV Sensiti- Speed Shoulder .DELTA. Toe .DELTA.Emulsion Dopant zation RF.sup.a density.sup.b density.sup.c______________________________________B1 control IV -40 -0.33 0.11B2 MC-27a IV -36 -0.05 0.04B4 MC-32d IV -29 -0.23 0.03B6 MC-41 IV -27 -0.23 0.07B7 MC-41 IV -33 -0.20 0.09B8 MC-33 IV -27 -0.38 0.13______________________________________ .sup.a = Speed RF is taken as the speed difference of equivalent exposure (intensity .times. time) of 0.1 and 100 sec duration. Zero is the ideal difference. .sup.b = Shoulder A density is the difference in density at a point 0.3 log E slow of the 1.0 optical density speed point for two equivalent exposures, the first of 0.1 sec duration and the second of 100 sec duration. Zero is the ideal difference. .sup.c = Toe .DELTA. density is the difference in density at a point 0.3 log E fast of the 1.0 optical density speed point for two equivalent exposures, the first of 0.1 sec duration and the second of 100 sec duration. Zero is the ideal difference.
TABLE B-V______________________________________Emul- Sensiti- Relative Log Esion Dopant zation Dmin (inertial)______________________________________B1 control I 0.06 150B14 MC-14rr I 0.04 164B16 EDTA (CD-1) I 0.06 154B17 [Fe(EDTA)].sup.1- (CD-2) I 0.07 151B18 [Fe(CN)6].sup.4- (CD-5) I 0.06 161B1 control Ia 0.06 167B14 MC-14rr Ia 0.04 191B16 CD-1 Ia 0.06 172B17 CD-2 Ia 0.07 172B18 CD-5 Ia 0.06 170______________________________________
The photographic characteristics of emulsions B are given in Tables B-I, B-II, B-III, B-IV and B-V. For portions III, the best Au(I) level for each emulsion was chosen based on the photographic results and these are the results shown in Table B-III.
Tables B-I, B-II, B-III and B-IV show significant reductions in HIRF to be produced by the incorporation as a grain dopant of iridium complexes containing an acetonitrile, pyridazine, thiazole or pyrazine ligand. Additionally these complexes are capable of significantly reducing LIRF.
The results in Table B-IV show that an iron pentacyano complex containing an organic ligand is capable of producing performance characteristics in the emulsion that are superior to those obtained using an iron hexacyanide complex as a dopant. Further, it is demonstrated that EDTA used alone or as a ligand for iron does not produce the performance advantages demonstrated for the dopant satisfying the requirements of the invention. Cl Series Background Examples
These examples demonstrate that ripening Lippmann silver bromide emulsions doped with coordination complexes satisfying the requirements of the invention onto silver chloride cubic grain emulsions produces doped emulsions with improved reciprocity, thermal stability and latent image keeping properties.
The series C emulsions used conventional precipitation techniques employing thioether silver halide ripening agents of the type disclosed in McBride U.S. Pat. No. 3,271,157.
Substrate Emulsion S1 was prepared as follows: A reaction vessel containing 8.5 liters of a 2.8% by weight gelatin aqueous solution and 1.8 grams of 1,8-dihydroxy-3,6-dithiaoctane was adjusted to a temperature of 68.3.degree. C., pH of 5.8 and a pAg of 7.35 by addition of NaCl solution. A 3.75molar solution containing 1658.0 grams of AgNO.sub.3 in water and a 2.75 molar solution containing 570.4 grams of NaCl in water were simultaneously run into the reaction vessel with rapid stirring, each at a flow rate of 84 mL/min. The double jet precipitation continued for 31 minutes at a controlled pAg of 7.35. A total of 9.76 moles of silver chloride were precipitated, the silver chloride having a cubic morphology of 0.6 .mu.m average cube length.
A series of Lippmann bromide carrier emulsions were prepared as a means of introducing the dopant complex into the emulsion grain during the chemical/spectral sensitization step.
Undoped Lippmann control Emulsion L1 was prepared as follows: A reaction vessel containing 4.0 liters of a 5.6% by weight gelatin aqueous solution was adjusted to a temperature of 40.degree. C., pH of 5.8 and a pAg of 8.86 by addition of AgBr solution. A 2.5 molar solution containing 1698.7 grams of AgNO.sub.3 in water and a 2.5 molar solution containing 1028.9 grams of NaBr in water were simultaneously run into the reaction vessel with rapid stirring, each at a constant flow rate of 200 mL/min. The double jet precipitation continued for 3 minutes at a controlled pAg of 8.86, after which the double jet precipitation was continued for 17 minutes during which the pAg was decreased linearly from 8.86 to 8.06. A total of 10 moles of silver bromide (Lippmann bromide) was precipitated, the silver bromide having average grain sizes of 0.05 .mu.m.
Emulsion L2 was prepared exactly as Emulsion L1, except a solution of 0.217 gram of [IrC.sub.6 ].sup.2- (CD-3) in 25 mL water was added at a constant flow rate beginning at 50% and ending at 90% of the precipitation This triple jet precipitation produced 10 moles of a 0.05 .mu.m particle diameter emulsion.
Emulsion L3 was prepared exactly as Emulsion L1, except a solution of 0.528 gram of MC-29a in 25 mL water was added at a constant flow rate beginning at 50% and ending at 90% of the precipitation. This triple jet precipitation produced 10 moles of a 0.05 .mu.m particle diameter emulsion.
Emulsion L4 was prepared exactly as Emulsion L1, except a solution of 0.488 gram of MC-31 in 25 mL water was added at a constant flow rate beginning at 50% and ending at 90% of the precipitation. This triple jet precipitation produced 10 moles of a 0.05 .mu.m particle diameter emulsion.
Doped and chemically and spectrally sensitized emulsions were prepared as follows:
Control Emulsion C1 was prepared as follows: A 50 millimole (mmole) sample of Emulsion S1 was heated to 40.degree. C. and spectrally sensitized by the addition of 14 milligrams (mg) of the blue spectral sensitizing dye, Dye D, anhydro-5-chloro-3,3'-di(3-sulfopropyl)naphtho[1,2-d]thiazolothiacyanine hydroxide triethylammonium salt.
This was followed by the addition of 0.45 mmoles of Emulsion L1. The temperature was raised to 60.degree. C. to accelerate recrystallization of the Lippmann bromide onto the grain surfaces of Emulsion C1. To the emulsion were added 0.13 mg of sodium thiosulfate and 9.5 mg of 4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene, and the emulsion was held at 60.degree. C. for 30 to 50 minutes until optimal chemical sensitization was achieved. Addition of 1-(3-acetamidophenyl)-5-mercaptotetrazole followed to complete the finishing operation.
Comparative and background example emulsions, identified in Table C-I, were prepared as described for emulsion C1, except that the 0.45 mmole of Emulsion L1 used for emulsion C1 was replaced by equivalent amounts of a combination of emulsion L1 and emulsions L2, L3 or L4 as outlined in Table C-I.
TABLE C-I__________________________________________________________________________Component Emulsions used in preparation of C Series Emulsions Total amount Nominal of Lippmann Amount of Dopant Dopant level Emulsion Amount of L# complex in EmulsionEmulsion (mmole) L1 (mmole) (mmole) incorporated (mppm)__________________________________________________________________________C2a comp. 0.45 0.40 0.05, L2 CD-3 5C2b comp. 0.45 0.35 0.10, L2 CD-3 10C2c comp. 0.45 0.30 0.15, L2 CD-3 15C3a 0.45 0.40 0.05, L3 MC-29a 5C3b 0.45 0.35 0.10, L3 MC-29a 10C3c 0.45 0.30 0.15, L3 MC-29a 15C4a 0.45 0.40 0.05, L4 MC-31 5C4b 0.45 0.35 0.10, L4 MC-31 10C4c 0.45 0.30 0.15, L4 MC-31 15__________________________________________________________________________
The emulsions were coated on a photographic paper support as disclosed in U.S. Pat. No. 4,994,147 at 0.28 gram/m.sup.2 silver with 0.002 gram/m.sup.2 of 2,4-dihydroxy-4-methyl-1-piperidinocyclopenten-3-one and 0.02 gram/m.sup.2 of KCl and 1.08 gram/m.sup.2 yellow dye-forming coupler C2: ##STR2## to give a layer with 0.166 gram/m.sup.2 gelatin. A 1.1 gram/m.sup.2 gelatin protective overcoat was applied along with a bisvinylsulfone gelatin hardener.
The coatings were exposed through a step tablet to a 3000.degree. K. light source for various exposure times and processed as recommended in "Using KODAK EKTACOLOR RA Chemicals", Publication No. Z-130, published by Eastman Kodak Co., 1990, the disclosure of which is here incorporated by reference.
The photographic parameters obtained for these emulsions are shown in Tables C-II and C-III:
TABLE C-II__________________________________________________________________________Speed, Reciprocity and Keeping Parameters for Emulsions C Nominal Dopant complex Dopant level in Speed.sup.a for incorporated in Emulsion G 100 sec IncubationEmulsion # Emulsion G (mppm) exposure Speed RF .DELTA. speed.sup.b__________________________________________________________________________C1 control none 0 154 -61 17C3a MC-29a 5 135 -44 14C3b MC-29a 10 123 -29 13C3c MC-29a 15 116 -30 14C4a MC-31 5 152 -63 14C4b MC-31 10 147 -57 19C4c MC-31 15 143 -48 17__________________________________________________________________________ .sup.a = Speed is based on the light exposure required to obtain an optical density of 1.0. .sup.b = Incubation .DELTA. speed is the speed difference between a coating stored for 3 weeks at 49.degree. C. and 50% relative humidity conditions and a check coating stored at -18.degree. C. and 50% relative humidity conditions. Ideally the difference should be zero.
TABLE C-III__________________________________________________________________________Heat Sensitivity and Latent Image Keeping Parameters for Emulsions GDopant Nominalcomplex Dopant level inincorporated Emuls. G Heat Sensitivity .DELTA..sup.a Latent Image Keeping .DELTA..sup.dEmulsion # in Emuls. G (mppm) Speed.sup.b Toe.sup.b,c Speed.sup.b Toe.sup.b,c__________________________________________________________________________C1 control none 0 25 -0.06 -2 -0.02C2a comp. CD-3 5 8 0 14 -0.01C2b comp. CD-3 10 8 0 23 -0.09C2c comp. CD-3 15 9 -0.02 32 -.12C3a MC-29a 5 13 -0.05 2 -0.01C3b MC-29a 10 9 -0.01 1 -0.01C3c MC-29a 15 8 -0.02 3 -0.02C4a MC-31 5 20 -0.09 1 -0.02C4b MC-31 10 16 -0.06 1 -0.01C4c MC-31 15 11 -0.03 2 -0.01__________________________________________________________________________ .sup.a = Heat sensitivity .DELTA. measures the effect of temperature differences (40.degree. C. versus 20.degree. C.) at the time of exposure, taken as the difference in sensitometry. .sup.b = Speed and Toe measured for a 0.1 sec exposure .sup.c = Toe is the density of the sensitometric curve at an exposure scale value 0.3 log E less than that of the 1.0 optical density speed point. .sup.d = Latent Image keeping Change is the effect of delay time between exposure and processing, taken as the (30' vs. 30") difference in sensitometry.
The results in Tables C-II and C-III demonstrate that emulsions doped with coordination complexes containing iridium and pyrazine have improved reciprocity performance and, unlike comparison dopant [IrCl.sub.6 ](CD-3), show good heat sensitivity and latent image keeping properties.
Examples
Camera Film Emulsion Examples
The following emulsions were chosen to demonstrate the utility of the emulsions of the invention when employed in a camera speed color negative film.
Control Emulsion D1
This emulsion is an undoped control high chloride, {100} tabular grain emulsion control prepared using iodide during nucleation, a combination iodide and chloride dump after nucleation and a higher iodide band inserted in the grain structure during growth by a single rapid addition of a soluble iodide salt.
A 4.3 L solution containing 0.87% by weight of low methionine gelatin (<12 .mu.moles methionine per gram of gelatin), 0.0057M sodium chloride and an antifoamant was provided to a stirred reaction vessel at 45.degree. C. While the solution was vigorously stirred, 68 mL of a 0.024M potassium iodide solution were added. This was followed by the addition of 22.5 mL of 4M silver nitrate containing 0.08 mg mercuric chloride per mole of silver nitrate and 22.5 mL of a 4M sodium chloride solution. The silver and chloride solutions were added simultaneously each at a rate of 45 mL/min. This was followed by the addition of 9.75 L of a solution containing 0.00037M potassium iodide and 0.0058M sodium chloride at 45.degree. C. over a 3-min timeframe. Following a 3-min hold, a 4M silver nitrate solution containing 0.08 mg mercuric chloride per mole of silver nitrate and a 4M sodium chloride solution were added simultaneously each at 15 mL/min for 5 minutes, followed by a linear acceleration from 15 mL/min to 42.6 mL/min over 46 minutes while maintaining the pAg at 7.1. The pAg was adjusted to 1.8 by running the 4.0M sodium chloride solution at 15 mL/min for 5 minutes. This was followed by a 30 minute hold, the subsequent addition of the 4M silver nitrate solution at 15 mL/min for 5 minutes, the subsequent addition of 75 mL of a 0.45M potassium iodide solution, and a 20 minute hold. Following the hold, the 4M silver and chloride solutions were added simultaneously at 15 mL/min for 8 minutes while maintaining pAg at 7.1. The emulsion was then treated with a sodium chloride solution to achieve a pAg of 7.6 and then ultrafiltration washed to a pAg of 7.2. After ultrafiltration, 180 g of low methionine gelatin was added, and the emulsion was adjusted to a pAg of 7.2 with sodium chloride.
The resulting emulsion was a high chloride {100} tabular grain silver halide emulsion containing 0.6 mole percent iodide with the balance of the halide being chloride. Greater than 50 percent of total grain projected area was accounted for by {100} tabular grains having a ratio of adjacent tabular grain major face edge lengths of less than 2. The emulsion exhibited an average equivalent circular diameter (ECD) of 0.88 .mu.m and a mean grain thickness of 0.08 .mu.m.
Control Emulsion D2
This emulsion represents a control in which a high chloride {100} tabular grain emulsion otherwise similar to Control Emulsion D1 was doped with control dopant CD3.
A doped control emulsion containing CD3 at 0.2 mg/mole of silver was prepared in an identical manner to Control Emulsion D1, except that the dopant was added during the precipitation in a band from 80.8 to 82.8% of the silver. Except for the inclusion of dopant, the grains of Control Emulsion D2 were identical to those of Control Emulsion D1.
Example Emulsion D3
This emulsion was prepared to demonstrate the effect of replacing one of the chloride ligands in the iridium hexachloride coordination complex employed in preparing Control Emulsion D2 with a thiazole ligand.
The doped example emulsion was prepared identically to Control Emulsion D2, except that MC-41 was substituted for K.sub.3 IrCl.sub.6. Except for the inclusion of dopant, the grains of Example Emulsion D3 were identical to those of Control Emulsion D1.
Sensitization of emulsions
The emulsions were each optimally sulfur and gold sensitized in the presence of a green spectral sensitizing dye. Thereafter 70 mg/mole of 1-(3-acetamidophenyl)-5-mercaptotetrazole (APMT) was added, and the emulsion was chill set.
Photographic comparisons
Each sensitized emulsion was coated on a film support including an antihalation layer at 10.76 mg/dm.sup.2 of silver and 9.68 mg/dm.sup.2 of cyan dye forming coupler C3 and 32.28 mg/dm.sup.2 of gelatin. This layer was overcoated with 43.04 mg/dm.sup.2 of gelatin and the entire coating was hardened with bis (vinylsulfonylmethyl) ether at 1.75% by weight of the total coated gelatin. ##STR3##
Coated samples were exposed with 365 line radiation for 0.02 second using a step wedge. Other samples of the coatings were evaluated for reciprocity by giving them a series of calibrated (total energy) white light exposures ranging from 10.sup.-5 second to 10 seconds. The exposed coatings were processed in the Kodak Flexicolor.TM. C-41 color negative process.
The results are summarized in Table D-I
TABLE D-I__________________________________________________________________________ Dopant HIRF LIRF % Ag 10.sup.-5 to 10.sup.-2 10.sup.31 2 to 1Emulsion LOCATION D min SPEED GAMMA Dmax sec sec__________________________________________________________________________D1 NONE 0.07 154 2.96 3.42 8 -9D2 80.8 to 82.8 0.07 103 2.59 2.73 11 -5D3 80.8 to 82.8 0.09 127 3.12 3.25 9 -6__________________________________________________________________________
The data demonstrate that [Ir(Cl).sub.6 ].sup.2- (Emulsion D-2) reduces low intensity reciprocity failure (LIRF), but at the cost of increasing high intensity reciprocity failure (HIRF) and reducing both speed and contrast. Ir(Cl.sub.5)thiazole (MC-41) (Emulsion D-3) is also effective in reducing LIRF, but exhibits superior speed and contrast and HIRF as compared to [Ir(Cl).sub.6 ].sup.2- (Emulsion D-2).
Color Paper Emulsion Examples
The examples which follow have as their purpose to demonstrate the utility of the emulsions of the invention in color paper applications.
Control Emulsion E-1
This is an undoped control emulsion.
A 4590 mL solution containing 3.52% by weight of low methionine gelatin, 0.0056M sodium chloride and 1.00.times.10.sup.-3 potassium iodide was provided in a stirred reaction vessel at 40.degree. C. While the solution was vigorously stirred, 90 mL of 2.0M silver nitrate and 90 mL of 1.99M sodium chloride were added simultaneously at a rate of 180 mL/min each. The mixture was held for 3 minutes with the temperature remaining at 40.degree. C. Following the hold, a 0.5M silver nitrate solution and a 0.5M sodium chloride solution were added simultaneously at 24 mL/min for 40 minutes followed by a linear acceleration form 24 mL/min to 37.1 mL/min over 70 minutes, while maintaining the pAg at 6.85. Following the linear acceleration a 0.75M silver chloride solution and a 0.75M sodium chloride solution were added simultaneously at 37.1 mL/min for 90 minutes, while maintaining the pAg at 6.85. The pAg was then adjusted to 7.9 with sodium chloride then washed using ultrafiltration to a pAg of 7.2. The emulsion pAg was then adjusted to 7.55 with sodium chloride.
The resulting emulsion was a high chloride {100} tabular grain emulsion containing 0.11 mole percent iodide with the balance of halide being chloride. The {100} tabular grains having a ratio of adjacent major face edge lengths of less than 2 accounted for greater than 50 percent of total grain projected area. The emulsion grains had an average ECD of 1.59 .mu.m and a mean grain thickness of 0.14 .mu.m.
Sensitization of Emulsions
Emulsion E-1 was sensitized to blue light by the following procedure: A quantity of the emulsion was melted at 40.degree. C., 580 mg/mole Ag of sensitizing dye Dye D were added to the tabular emulsion followed by a 20 minute hold. Aurous sulfide was added at 2.4 mg/mole Ag followed by a 5 minute hold. The temperature was then raised to 60.degree. C. and held for 40 minutes after which the temperature was lowered to 40.degree. C. and 120 mg/mole Ag of APMT was added and held for 10 minutes then the emulsion was chill set.
Photographic Comparisons
The sensitized emulsion was coated on a resin coated paper support at 2.8 mg/dm.sup.2 of silver along with 11 mg/dm.sup.2 of yellow dye forming coupler C2 and 8.2 mg/dm.sup.2 of gelatin.
The coatings were evaluated for white light sensitivity by exposing the coatings for 0.1 second using a step wedge sensitometer with a 3000.degree. K. tungsten lamp. The coatings were processed using the Kodak RA-4.TM. color paper process. Dye density was measured using standard reflection geometry and status A filtration.
Example Emulsion E2
This emulsion was prepared, coated and tested identically to Control Emulsion E1, except that 0.05 mg/mole Ag of MC-41 was added as the grain volume was being increased from 95 to 100 percent of its final volume. The variation in doping had no effect on the physical form of the grains obtained.
The results are summarized below in Table E-I.
TABLE E-I__________________________________________________________________________ HIRF LIRF SPEED 0.02 TO 0.1 TO 100EMULSION DMIN AT D = 1.0 CONTRAST DMAX 0.1 SEC SEC__________________________________________________________________________E1 0.13 200 2.91 2.47 -1 -8E2 0.13 206 2.46 2.45 3 4__________________________________________________________________________
From Table E-I it is apparent that Example Emulsion E2 exhibits reduced low intensity reciprocity failure and increased speed by 0.06 log E, where E is measured in lux-seconds. Thus, dopant MC-41 was effective.
Example Emulsion E3
Example Emulsion E3 was prepared, coated and tested identically to Example Emulsion E2, except that the concentration of MC-41 was increased to 0.2 mg/mole Ag and was added while the grains were being grown from 93 to 95 percent of their final volume. The variation in doping had no effect on the physical form of the grains obtained.
Control Emulsion E4
Control Emulsion E4 was prepared, coated and tested identically to Example Emulsion E3, except that K.sub.2 IrCl.sub.6 was substituted for MC-41. The variation in doping had no effect on the physical form of the grains obtained.
The-results are summarized in Table E-II.
TABLE E-II__________________________________________________________________________ HIRF LIRF SPEED 0.02 TO 0.1 TO 100EMULSION DMIN AT D = 1.0 CONTRAST DMAX 0.1 SEC SEC__________________________________________________________________________E4 0.11 161 2.50 2.40 2 -9E3 0.13 176 2.69 2.40 1 9__________________________________________________________________________
From Table E-II it is apparent that example emulsion E3 has increased speed and contrast compared to control emulsion E4 and does not demonstrate the low intensity speed loss (+9 vs -9) of E4.
Example Emulsion E5
This emulsion was prepared, coated and tested identically to Control Emulsion E1, except that 5 ppm of MC-14ss was added as the grain volume was being increased from 4.3 to 95 percent of its final volume. The variation in doping had no effect on the physical form of the grains obtained.
Example Emulsion E6
This emulsion was prepared, coated and tested identically to Control Emulsion E1, except that 5 ppm of MC-14rr was added as the grain volume was being increased from 4.3 to 95 percent of its final volume. The variation in doping had no effect on the physical form of the grains obtained.
Example Emulsion E7
This emulsion was prepared, coated and tested identically to Control Emulsion E1, except that 5 ppm of MC-14c was added as the grain volume was being increased from 4.3 to 95 percent of its final volume. The variation in doping had no effect on the physical form of the grains obtained.
The results are summarized in Table E-III.
TABLE E-III______________________________________ SPEED ATEMULSION DMIN D = 1.0 CONTRAST DMAX______________________________________E1 0.13 200 2.91 2.47E5 0.13 216 2.71 2.43E6 0.11 209 2.74 2.40______________________________________
From Table E-III it is apparent that example Emulsions E5 and E6 demonstrated higher speed compared to the undoped Control Emulsion E1. Thus, dopants MC-14rr and MC-14ss were effective.
TABLE E-IV______________________________________EMULSION LIRF 0.1 TO 100 SEC______________________________________E1 -8E7 -5______________________________________
From Table E-IV it is apparent that Example Emulsion E7 demonstrated reduced LIRF compared to the undoped control Emulsion E1. Thus; dopant MC-14c was effective.
Example Emulsion E8
This emulsion was prepared, coated and tested identically to Control Emulsion E1, except that 5 ppm of MC-14j was added as the grain volume was being increased from 4.3 to 90 percent of its final volume. The variation in doping had no effect on the physical form of the grains obtained.
This example demonstrates the ability of dopant MC-14j to improve photographic speed in the upper scale, shoulder, of the photographic curve upon a very high intensity (equal energy) exposure. Shoulder HIRF is expressed as relative speed differences between that obtained from a 10.sup.-5 second exposure and that obtained from a 0.01 second exposure measured at a shoulder density of Dmin +1.35. The ideal value of shoulder HIRF is zero, indicating that there is no change in shoulder speed with high intensity exposure. The results are summarized in Table E-V.
TABLE E-V__________________________________________________________________________ SPEED SHOULDER HIRFEMULSION DMIN AT D = 1.0 CONTRAST DMAX 10.sup.-5 to 10.sup.-2 SEC__________________________________________________________________________E1 0.13 200 2.91 2.47 -19E8 0.11 204 2.72 2.45 +1__________________________________________________________________________
From Table E-V it is apparent that Example Emulsion E8 has dramatically decreased shoulder HIRF compared to the undoped Control Emulsion E1. Thus, dopant MC-14j was effective.
The invention has been described in detail with particular reference to preferred embodiments thereof, but it will be understood that variations and modifications can be effected within the spirit and scope of the invention.

Number	Name	Date
3672901	Ohkubo et al.	Jun 1972
3790390	Shiba et al.	Feb 1974
3890154	Ohkubo et al.	Jun 1975
3901711	Iwaosa et al.	Aug 1975
4092171	Bigelow	May 1989
4173483	Habu et al.	Nov 1979
4835093	Janusonis et al.	May 1989
4933272	McDugle et al.	Jun 1990
4937180	Marchetti et al.	Jun 1990
4945035	Keevert, Jr. et al.	Jul 1990
4981781	McDugle et al.	Jan 1991
5037732	McDugle et al.	Aug 1991
5112732	Hayashi et al.	May 1992
5264337	Maskasky	Nov 1993
5292632	Maskasky	Mar 1994
5320938	House et al.	Jun 1994
5360712	Olm et al.	Nov 1994

Internally doped high chloride {100} tabular grain emulsions

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