Transfer of azo dyes having a pyridine coupling component

The present invention relates to a novel process for transferring azo dyes having a diaminopyridine-based coupling component from a substrate to a plastic-coated paper with the aid of a thermal printing head.
In thermotransfer printing processes, a transfer sheet which contains a thermally transferable dye in one or more binders with or without suitable assistants on a substrate is heated from the back with a thermal printing head in short heat pulses (duration: fractions of a second), as a result of which the dye migrates out of the transfer sheet and diffuses into the surface coating of a receiving medium. The essential advantage of this process is that control of the amount of dye to be transferred (and hence of the color gradation) is easily possible by adjusting the energy to be supplied to the thermal printing head.
In general, color recording is carried out using the three subtractive primaries yellow, magenta and cyan (and in certain cases black). To facilitate optimal color recording, the dyes must have the following properties:
(i) ready thermal transferability,
(ii) low migration tendency within or on the surface coating of the receiving medium at room temperature,
(iii) high thermal and photochemical stability and resistance to moisture and chemical substances,
(iv) suitable hues for subtractive color mixing,
(v) a high molar adsorption coefficient,
(vi) resistance to crystallization in the course of storage of the transfer sheet and
(vii) ready industrial accessibility.
These requirements are from experience very difficult to meet at one and the same time.
For this reason most of the known cyan dyes used for thermal transfer printing do not meet the required range of properties.
There is prior art concerning dyes used in thermotransfer printing processes. For instance, EP-A-216,483 and EP-A-258,856 describe azo dyes from thiophene-based diazo components and aniline-based coupling components.
Furthermore, EP-A-218,397 describes thiophene- and aniline-based disazo dyes for this purpose.
JP-A-30,392/1985 teaches the use of azo dyes which have a diazo component based on 5-aminothia-2,4-diazole and a coupling component based on aniline.
Finally, JP-A-227,092/1986 discloses the used of azo dyes whose diazo and coupling components come from the aniline series.

It is an object of the present invention to provide a process for the transfer of dyes where the dyes should ideally meet all the abovementioned requirements (i) to (vii).
We have found that this object is achieved in an advantageous manner by transferring azo dyes from a substrate to a plastic-coated paper by diffusion with the aid of a thermal printing head on using a substrate on which there are one or more azo dyes of the formula I ##STR2## where
R.sup.1, R.sup.2 and R.sup.3 are identical or different and each is independently of the others alkyl, alkoxyalkyl, alkanoyloxyalkyl, alkoxycarbonyloxyalkyl or alkoxycarbonylalkyl, which each may have up to 20 carbon atoms and be substituted by phenyl, C.sub.1 -C.sub.4 -alkylphenyl, C.sub.1 -C.sub.4 -alkoxyphenyl, halophenyl, benzyloxy, C.sub.1 -C.sub.4 -alkylbenzyloxy, C.sub.1 -C.sub.4 -alkoxybenzyloxy, halobenzyloxy, halogen, hydroxyl or cyano, or are each hydrogen, unsubstituted or C.sub.1 -C.sub.15 -alkyl-, C.sub.1 -C.sub.15 -alkoxy-, halogen- or benzyloxy-substituted phenyl, unsubstituted or C.sub.1 -C.sub.15 -alkyl-, C.sub.1 -C.sub.15 -alkoxy, halo- gen- or benzyloxy-substituted cyclohexyl or a radical of the formula II
[--Y--O].sub.m --R.sup.5 8c (II)
where 3
Y is C.sub.2 -C.sub.6 -alkylene,
m is 1, 2, 3, 4, 5, or 6 and
R.sup.5 is C.sub.1 -C.sub.4 -alkyl or unsubstituted or C.sub.1 -C.sub.4 -alkyl- or C.sub.1 -C.sub.4 -alkoxy-substituted phenyl,
R.sup.4 is C.sub.1 -C.sub.4 -alkyl and
D is the radical of a diazo component.
The radical D in the formula I is derived for example from a diazo component which comes from the aniline, phenylazoanline, aminothiophene, phenylazoaminothiophene, aminothiazole, phenylazoaminothiazole, aminoisothiazole or aminothiadiazole series.
Preference is given to the use of dyes of the formula I where the radical D is derived for example from a diazo component D-NH.sub.2 of the formula ##STR3## where
R.sup.7, R.sup.8 and R.sup.9 are identical or different and each is independently of the others alkyl, alkoxyalkyl, alkoxycarbonylalkyl or alkanoyloxyalkyl, which may each have up to 12 carbon atoms, hydrogen, cyano, halogen, nitro, or a radical of the formula II
[--Y--O].sub.m R.sup.5 (II),
where Y, R.sup.5 and m are each as defined above, or a radical of the formula --CO--OR.sup.17, --CO--NR.sup.17 R.sup.18, --SO.sub.2 --R.sup.17, --SO.sub.2 --OR.sup.17 or --SO.sub.2 --NR.sup.17 R.sup.18, where R.sup.17 and R.sup.18 are identical or different and each is independently of the other alkyl, alkoxyalkyl, alkoxycarbonylalkyl or alkanoyloxyalkyl, which may each have up to 12 carbon atoms, hydrogen or a radical of the formula II
[--Y--O].sub.m --R.sup.5 (II),
where Y, R.sup.5 and m are each as defined above,
R.sup.10 is hydrogen, chlorine, cyano, C.sub.1 -C.sub.8 -alkyl, C.sub.1 -C.sub.8 -alkoxy, C.sub.1 -C.sub.8 -alkylthio, alkoxyalkyl of up to 8 carbon atoms, phenyl, which may be substituted by C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy or benzyloxy, benzyl, benzyloxy or a radical of the formula --CO--OR.sup.17 or --CO--NR.sup.17 R.sup.18 where R.sup.17 and R.sup.18 are each as defined above,
R.sup.11 is hydrogen, cyano, nitro or a radical of the formula --CO--OR.sup.17 or --CO--NR.sup.17 R.sup.18 where R.sup.17 and R.sup.18 are each as defined above,
R.sup.12 is cyano, nitro, formyl or a radical of the formula ##STR4## where
R.sup.17 and R.sup.18 are each as defined above,
R.sup.13 R.sup.14 are identical or different and each is independently of the other hydrogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy, chlorine, cyano, nitro or a radical of the formula --CO--OR.sup.17 or --CO--NR.sup.17 R.sup.18 where R.sup.17 and R.sup.18 are each as defined above,
R.sup.15 is hydrogen, C.sub.1 -C.sub.4 -alkyl or chlorine, and
R.sup.16 is cyano or a radical of the formula --CO--OR.sup.17 or --CO--NR.sup.17 R.sup.16 where R.sup.17 and R.sup.18 are each as defined above.
Any alkyl in the abovementioned formula can be linear or branched.
Y is for example ethylene, 1,2-or 1,3-propylene, 1,2-, 1,3- 1,4- or 2,3-butylene, pentamethylene, hexamethylene or 2-methylpentamethylene.
R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.7, R.sup.8, R.sup.9, R.sup.10, R.sup.13, R.sup.14, R.sup.15, R.sup.17 and R.sup.18 are each for example methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl or tert-butyl.
R.sup.1, R.sup.2, R.sup.3, R.sup.7, R.sup.8, R.sup.9, R.sup.10, R.sup.17 and R.sup.18 are each further for example pentyl, isopentyl, neopentyl, tert-pentyl, hexyl, 2-methylpentyl, heptyl, octyl, 2-ethylhexyl or isooctyl.
R.sup.1, R.sup.2, R.sup.3, R.sup.7, R.sup.8, R.sup.9, R.sup.17 and R.sup.18 are each further for example nonyl, isononyl, decyl, isodecyl, undecyl or dodecyl.
R.sup.1, R.sup.2 and R.sup.3 are each further for example tridecyl, isotridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl or eicosyl. (The terms isooctyl, isononyl, isodecyl and isotridecyl are trivial names due to alcohols obtained by the oxo process (cf. Ullmanns Enzyklopadie der technischen Chemie, 4th edition, volume 7, pages 215-217 and volume 11, pages 435 and 436).)
R.sup.1, R.sup.2, R.sup.3, R.sup.7, R.sup.8, R.sup.9, R.sup.17 and R.sup.18 are each further for example 2-methoxyethyl, 2-ethoxyethyl, 2-propoxyethyl, 2-butoxyethyl, 2- or 3-methoxypropyl, 2- or 3-ethoxpropyl, 2- or 3-propoxypropyl, 2- or 3-butoxypropoyl, 4-methoxybutyl, 4-ethoxybutyl, 4-butoxybutyl, 4-(2-ethylhexyloxy)butyl, 8-methoxyoctyl or 8-butoxyoctyl.
R.sup.10, R.sup.13 and R.sup.14 are each further for example methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy or sec-butoxy.
R.sup.10 is further for example pentyloxy, isopentyloxy, neopentyloxy, hexyloxy, heptyloxy, octyloxy, 2-ethylhexyloxy, methylthio, ethylthio, propylthio, isopropylthio, butylithio, pentylthio, hexylthio, heptylthio, octylthio or 2-ethylhexylthio.
R.sup.1, R.sup.2 and R.sup.3 are each further for example benzyl, 1-or 2-phenylethyl, ##STR5##
The radicals R.sup.7, R.sup.8, R.sup.9, R.sup.17 and R.sup.18 are each subject to the corresponding exemplifying observations above.
Preference is given to using in the process according to the invention a substrate on which there are one or more azo dyes of the formula I where
R.sup.1, R.sup.2 and R.sup.3 are each independently of the others hydrogen, alkyl or alkoxyalkyl, each of which may have up to 15 carbon atoms and be substituted by phenyl, C.sub.1 -C.sub.4 -alkylphenyl, C.sub.1 -C.sub.4 -alkoxyphenyl or cyano, or a radical of the formula III
[--(CH.sub.2).sub.3 --O].sub.p [--CH.sub.2 --CH.sub.2 --O]--R.sup.5 (III),
where
n is 1, 2, 3 or 4,
p is 0 or 1 and
R.sup.5 is C.sub.1 -C.sub.4 -alkyl or phenyl, and R.sup.4 is methyl.
Particular preference is given to the novel process using a substrate on which there are one or more azo dyes of the formula I where the radical D is derived from a diazo component conforming to the formula IVa, IVb, IVd or IVf where R.sup.7, R.sup.8 and R.sup.9 are each independently of the others alkyl, alkoxyalkyl, alkoxycarbonylalkyl or alkanoyloxyalkyl, which may each have up to 10 carbon atoms, hydrogen, cyano, halogen, nitro or a radical of the formula --CO--OR.sup.19, --CO--NR.sup.19 R.sup.20, --SO.sub.2 --R.sup.19, --SO.sub.2 --OR.sup.19 or SO.sub.2 --NR.sup.19 R.sup.20 where R.sup.19 and R.sup.20 are each independently of the other alkyl, alkoxyalkyl, alkoxycarbonylalkyl or alkanoyloxyalkyl, which may each have up to 10 carbon atoms, hydrogen or a radical of the formula 1
[ (II),
where R.sup.5 and n are each as defined above.
Particular preference is further given to the novel process using a substrate in which there are one or more azo dyes of the formula I where the radical D is derived from a diazo component conforming to the formula IVc where
R.sup.10 is hydrogen, chlorine, C.sub.1 -C.sub.8 -alkyl, unsubstituted C.sub.1 -C.sub.4 -alkyl- or C.sub.1 -C.sub.4 -alkoxy-substituted phenyl or benzyl,
R.sup.11 is cyano or a radical of the formula --CO--OR.sup.19 or --CO--NR.sup.19 R.sup.20 where R.sup.19 and R.sup.20 are each as defined above, and
R.sup.12 is a radical of the formula ##STR6## where R.sup.19 and R.sup.20 are each as defined above.
Preference is further given to the novel process using a substrate on which there are one or more azo dyes of the formula I where the radical D is derived from a diazo component conforming to the formula IVe where
R.sup.10 is hydrogen, chlorine, C.sub.1 -C.sub.8 -alkyl, unsubstituted or C.sub.1 -C.sub.4 -alkyl- or C.sub.1 -C.sub.4 -alkkoxy-substituted phenyl or benzyl and
R.sup.12 is cyano, nitro, formyl or a radical of the formula --CO--OR.sup.19 where R.sup.19 is as defined above.
Preference is further given to the novel process using a substrate on which there are one or more azo dyes of the formula I where the radical D is derived from a diazo component conforming to the formual IVg where
R.sup.10 is C.sub.1 -C.sub.8 -alkyl, C.sub.1 -C.sub.8 -alkoxy, alkoxyalkyl, of up to 8 carbon atoms, unsubstituted or C.sub.1 -C.sub.4 -alkyl- or C.sub.1 -C.sub.4 -alkoxy-substituted phneyl, benzyl or benzyloxy and
R.sup.11 is cyano, nitro or a radical of the formula --CO--OR.sup.19 where R.sup.19 is as defined above.
Preference is furter given to the novel process using a substrate on which there are one or more azo dyes of the formula I where the radical D is derived from a diazo component conforming to the formula IVc where
R.sup.10 is hydrogen, chlorine, C.sub.1 -C.sub.8 -alkyl, C.sub.1 -C.sub.8 -alkoxy, alkoxyalkyl of up to 8 carbon atoms, unsubstituted or C.sub.1 -C.sub.4 -alkyl- or C.sub.1 -C.sub.4 -alkoxy-substituted phneyl, benzyl or a radical of the formula --CO--OR.sup.19 where R.sup.19 is as defined above,
R.sup.11 is cyano or a radical of the formula --CO--OR.sup.19 where R.sup.19 is as defined above, and
R.sup.12 is cyano, nitro, formyl or a radical of the formula --CO--OR.sup.19 where R.sup.19 is as defined above.
Particularly good results are obtained on using a substrate on which there are one or more azo dyes of the formula I where the radical D is derived from a diazo component conforming to the formula IVa, IVb, IVc, IVd, IVe, IVf or IVg where R.sup.19 and (if present) R.sup.20 are each hydrogen or C.sub.1 -C.sub.5 -alkyl.
Particularly favorable results are further obtained on using a substrate on which there are one or more azo dyes of the formula I where the radical D is derived from a diazo component conforming to the formula V ##STR7## where R.sup.7 is as defined above.
The dyes of the formula I are known per se or can be obtained by methods known per se.
Compared with the dyes used in existing processes, the dyes transferred in the process according to the invention are notable in general for improved migration properties in the receiving medium at room temperature, more ready thermal transferability, higher photochemical stability, easier industrial accessibility, better resistance to moisture and chemical substances, higher color strength, better solubility, higher purity of hue and in particular by substantially higher light fastness.
It is further surprising that the dyes of the formula I are readily transferable despite their relatively high molecular weight.
To prepare the dye substrate required for the novel process, the dyes are incorporated in a suitable organic solvent, for example chlorobenzene, isobutanol, methyl ethyl ketone, methylene chloride, toluene, tetrahydrofuran or a mixture thereof, with one or more binders with or without assistants to give a printing ink. This ink preferably contains the dye in a molecularly dispersed, ie. dissolved, form. The printing ink is applied to the inert substrate by knife coating and dried in air. Suitable binders are all resins or polymer materials which are soluble in organic solvents and are capable of holding the dye on the inert substrate in an abrasion-resistant bond. Preference is given to binders which, after the printing ink has dried in air, hold the dye in a clear, transparent film without visible crystallization of the dye.
Examples of such binders are cellulose derivatives, for example methylcellulose, ethylcellulose, ethylhydroxyethylcellulose, hydroxypropylcellulose, cellulose acetate or cellulose acetobutyrate, starch, alginates, alkyd resins, vinyl resins, polyvinyl alcohol, polyvinyl acetate, polyvinyl butyrate or polyvinylpyrrolidones. Other possibilities as binders are polymers and copolymers of acrylates or derivatives thereof, such as polyacrylic acid, polymethyl methacrylate or styrene/acrylate copolymers, polyester resins, polyamide resins, polyurethane resins or natural CH resins, such as gum arabic. Further suitable binders are described in DE-A-3,524,519.
Preferred binders are ethylcellulose and ethylhydroxyethylcellulose.
The ratio of binder to dye preferably varies from 5:1 to 1:1.
Possible assistants are release agents as described in EP-A-227,092, EP-A-192,435 and the patent applications cited therein and also particularly organic additives which stop the transfer dye from crystallizing in the course of storage or heating of the inked ribbon, for example cholesterol or vanillin.
Inert substrates are for example tissue, blotting or parchment paper or plastics films of high heat stability, for example uncoated or metal-coated polyester, polyamide or polyimide. The inert substrate may additionally be coated on the side facing the thermal printing head with a lubricant, or slipping, layer in order to prevent adhesion of the thermal printing head to the substrate material. Suitable lubricants are described for example in EP-A-216,483 and EP-A-277,095. The thickness of the dye substrate is in general from 3 to 30 .mu.m, preferably from 5 to 10 .mu.m.
Suitable dye receiver layers are basically all temperature stable plastics layers having an affinity for the dyes to be transferred whose glass transition temperature should- preferably be in the temperature range 50.degree. C. <Tg <100.degree. C. Examples are modified polycarbonates or polyesters. Suitable recipes for the receiver layer composition are described in detail for example in EP-A-227,094, EP-A-133,012, EP-A-133,011, EP-A-111,004, JP-A-199,997/1986, JP-A-283,595/1986, JP-A-237,694/1986 and JP-A-127,392/1986.
Transfer is effected by means of a thermal printing head which must be heatable to a temperature .gtoreq.300.degree. C. for the dye transfer to take place within the time interval t: 0 <t <15 msec. On heating, the dye migrates out of the transfer sheet and diffuses into the surface coating of the receiving medium.
Details of the preparation may be found in the Examples, where percentages are by weight, unless otherwise stated.
Transfer of dyes
To be able to test the transfer characteristics of the dyes in a quantitative and simple manner, the thermotransfer was carried out with large hotplates instead of a thermal printing head, with the transfer temperature being varied within the range 70.degree. C. <T <120.degree. C. and the transfer time being set at 2 minutes.
(A) General recipe for coating the substrate with dye:
X g of binder are dissolved at from 40.degree. to 50.degree. C. in 8 ml of 8:2 v/v toluene/ethanol. A solution of 0.25 g of dye (and any cholesterol as assistant) in 5 ml of tetrahydrofuran was added by stirring. The print paste thus obtained was smoothed down with an 80 .mu.m knife on a sheet of polyester film (thickness: 6-10 .mu.m) and dried with a hair dryer. (The weight ratio of dye:binder:assistant, from which the absolute amount of binder and assistant can be derived, is given for each case in the tables.)
(B) Testing of thermal transferability
The dyes used were tested in the following manner:
The polyester sheet donor containing the dye under test on the coated front was placed face down on commercial Hitachi Color Video Print Paper (receiver) and pressed down. Donor/receiver were then wrapped in aluminum foil and heated between two hotplates at different temperatures T (within the temperature range 70.degree. C. <T <120.degree. C.). The amount of dye diffusing into the bright plastics layer of the receiver is proportional to the optical density (=absorbance A). The latter was determined photometrically. If the logarithm of the absorbance A of the colored receiver papers measured within the temperature range from 80.degree.to 110.degree. C. is plotted against the corresponding reciprocal absolute-temperature, the result is a straight line whose slope gives the activation energy .DELTA.E.sub.T for the transfer experiment: ##EQU1##
To complete the characterization, the plots additionally reveal the temperature T*[.degree. C.] at which the absorbance A of the dyed receiver papers attains the value 2.
The dyes mentioned in the Tables below were processed according to (A), and the resulting dye-coated substrates were tested in respect of their transfer characteristics by (B). The Tables list in each case the thermotransfer parameters T* and .DELTA.E.sub.T, the absorption maximum of the dyes .lambda..sub.max (measured in methylene chloride), the binders used and the weight ratio of dye: binder:assistant.
The abbreviations have the following meanings: B =binder (EC=ethylcellulose, EHEC=ethylhydroxyethylcellulose, ethylcellulose, AC =cellulose acetobutyrate, MIX mixture of polyvinyl butyrate and ethylcellulose in a weight ratio of 2:1)
D =dye
Chol =cholesterol (assistant)
TABLE 1__________________________________________________________________________ ##STR8## No.Example R.sup.1 R.sup.2 R.sup.3 [nm].lambda.max B Chol. D:B:Chol. [.degree.C. ##STR9##__________________________________________________________________________1 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.3 C.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 544 EC - 1:4 106 172 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 543 EC - 1:4 109 143 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.3 H.sub.6 OCH.sub.3 544 EHE - 1:4 105 124 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.3 H.sub.6 OCH.sub.3 544 AC - 1:4 110 165 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.3 H.sub.6 OCH.sub.3 EC - 1:3 96 246 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 543 EHEC - 1:4 109 137 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 543 EC + 1:4:0.75 92 258 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 543 EC - 1:2 91 249 H C.sub.3 H.sub.6 OCH.sub.3 C.sub.3 H.sub.6 O(C.sub.2 H.sub.4 O).sub.2 C.sub.2 H.sub.5 532 EC - 1:4 113 2110 H C.sub.3 H.sub.6 O(C.sub.2 H.sub.4 O).sub.2 CH.sub.3 C.sub.6 H.sub.5 547 EC + 1:4:0.75 111 2511 H C.sub.3 H.sub.6 OCH.sub.3 C.sub.3 H.sub.6 O(C.sub.2 H.sub.4 O).sub.2 CH.sub.3 533 EC + 1:4:0.75 93 1912 H C.sub.3 H.sub.6 OCH.sub.3 C.sub.3 H.sub.6 O(C.sub.2 H.sub.4 O).sub.2 CH.sub.3 533 EHEC + 1:4:0.75 90 2813 H C.sub.3 H.sub.6 OCH.sub.3 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.4 H.sub.9 534 EC + 1:4:0.75 96 2314 H C.sub.3 H.sub.6 OCH.sub.3 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.4 H.sub.9 534 EHEC + 1:4:0.75 92 3115 H C.sub.3 H.sub.6 O(C.sub.2 H.sub.4 O).sub.2 C.sub.4 H.sub.9 C.sub.3 H.sub.6 OCH.sub.3 535 EC - 1:2 95 3116 H C.sub.3 H.sub.6 O(C.sub.2 H.sub.4 O).sub.2 C.sub.4 H.sub.9 C.sub.3 H.sub.6 OCH.sub.3 535 EC - 1:4 101 2417 H C.sub.3 H.sub.6 O(C.sub.2 H.sub.4 O).sub.2 C.sub.4 H.sub.9 C.sub.3 H.sub.6 OCH.sub.3 535 EC + 1:4:0.75 95 2418 H C.sub.2 H.sub.4 OC.sub.4 H.sub.9 C.sub.2 H.sub.4 OC.sub.4 H.sub.9 530 EC + 1:4:0.75 102 2119 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.3 H.sub.6OCOCH.sub.3 528 EC + 1:4 130 2020 H C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.4 H.sub.9 C.sub.2 H.sub.5 530 EC + 1:5:0.7521 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.2 H.sub.4 OCH.sub.3 541 EC + 1:4:0.75 97 2522 H C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.4 H.sub.9 C.sub.3 H.sub.6 OCH.sub.3 534 EC + 1:4:0.5 88 2023 H C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.4 H.sub.9 C.sub.3 H.sub.6 OCH.sub.3 534 EC + 1:4:0.75 88 3224 H C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.4 H.sub.9 C.sub.3 H.sub.6 OCH.sub.3 534 EC + 1:4:1.0 85 2525 H C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.4 H.sub.9 C.sub.3 H.sub.6 OCH.sub.3 534 EC - 1:4 94 2026 H C.sub.3 H.sub.6 O(C.sub.2 H.sub.4 O).sub.2 C.sub.4 H.sub.9 C.sub.5 H.sub.10 CN 532 EC - 1:4 100 2327 H C.sub.4 H.sub.9 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 534 EC - 1:4 127 1128 C.sub.2 H.sub.5 C.sub.3 H.sub.6 OCH.sub.3 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 545 MIX - 1:4 119 1829 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.3 H.sub.6 OCOCH.sub.3 541 MIX - 1:4 107 9.0__________________________________________________________________________
TABLE 2__________________________________________________________________________ ##STR10## No.Example R.sup.1 R.sup.2 R.sup.3 [nm].lambda.max B Chol. D:B:Chol. [.degree.C. ##STR11##__________________________________________________________________________30 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C(CH.sub.3).sub.2 C.sub.2 H.sub.5 534 EC + 1:4:0.75 100 3231 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.2 H.sub.4 OCH.sub.3 534 EC + 1:4:0.75 104 2632 H ##STR12## ##STR13## 530 EC + 1:4:0.75 101 2933 C.sub.2 H.sub.5 C.sub.2 H.sub.5 (CH.sub.2).sub.3 OCH.sub.3 536 EC + 1:4:0.75 97 2734 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.3 H.sub.6 OCOCH.sub.3 534 EC + 1:4:0.75 94 2335 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 534 EC - 1:4 110 2636 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 534 EHE - 1:4 104 1737 H C.sub.3 H.sub.6 OCH.sub.3 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.4 H.sub.9 532 EC - 1:4 115 1938 H C.sub.3 H.sub.6 OCH.sub.3 C.sub.3 H.sub.6 O(C.sub.2 H.sub.4 O).sub.2 C.sub.4 H.sub.9 532 EC - 1:4 110 2539 H C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 H 515 EC + 1:4:0.75 115 2140 H C.sub.2 H.sub.6 OC.sub.2 H.sub.4 OC.sub.2 H.sub.5 H 514 EC + 1:4:0.75 109 3141 H C.sub.3 H.sub.6 OC.sub.4 H.sub.8 OC.sub.4 H.sub.9 H 515 EC + 1:4:0.75 106 3242 H C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OCH.sub.3 H 515 EC + 1:4:0.75 108 3043 H C.sub.3 H.sub.6 OC.sub.4 H.sub.8 OC.sub.2 H.sub.5 H 515 EC + 1:4:0.75 106 3044 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 537 EC + 1:4:0.75 98 2145 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.3 H.sub.6 OC.sub.2 H.sub.5 534 EC - 1:4 113 2446 H C.sub.3 H.sub.6 O(C.sub.2 H.sub.4 O).sub.2 C.sub.4 H.sub.9 513 EC - 1:4 113 2747 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 536 EC - 1:4 112 1948 C.sub.2 H.sub.5 C.sub.3 H.sub.6 OCH.sub.3 C.sub.3 H.sub.6 OCH.sub.3 537 MIX - 1:4 105 1349 C.sub.2 H.sub.5 C.sub.3 H.sub.6 OCH.sub.3 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 537 EC - 1:4 98 20__________________________________________________________________________
TABLE 3__________________________________________________________________________ ##STR14## No.Example R.sup.1 R.sup.2 R.sup.3 [nm].lambda.max B Chol. D:B:Chol: [.degree.C.]T* ##STR15##__________________________________________________________________________50 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.3 H.sub.6 OC.sub.2 H.sub.5 522 EC + 1:4:0.75 92 28__________________________________________________________________________
TABLE 4__________________________________________________________________________ ##STR16## No.Example R.sup.1 R.sup.2 R.sup.3 [nm].lambda.max B Chol. D:B:Chol. [.degree.C.]T* ##STR17##__________________________________________________________________________51 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.3 H.sub.6 OCH.sub.3 522 EC + 1:4:0.75 84 2152 H C.sub.6 H.sub.5 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OCH.sub.3 524 EC + 1:4:0.75 100 3253 H ##STR18## C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OCH.sub.3 532 EC + 1:4:0.75 93 2254 H C.sub.3 H.sub.6 OC.sub.4 H.sub.8 OC.sub.2 H.sub.5 H 494 EC + 1:4:0.75 90 21__________________________________________________________________________
TABLE 5__________________________________________________________________________ ##STR19## No.Example R.sup.1 R.sup.2 R.sup.3 [nm].lambda.max B Chol. D:B:Chol. [.degree.C.]T* ##STR20##__________________________________________________________________________55 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 527 EC + 1:2:0.75 100 3056 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.3 H.sub.6 OC.sub.2 H.sub.5 526 EC + 1:2:0.75 91 2957 H C.sub.6 H.sub.5 C.sub.3 H.sub.6 O(C.sub.2 H.sub.4 O).sub.2 CH.sub.3 527 EC + 1:4:0.75 116 2458 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 ##STR21## 527 EC + 1:4:0.75 108 2759 H C.sub.3 H.sub.6 O(C.sub.2 H.sub.4 O).sub.2 CH.sub.3 C.sub.6 H.sub.5 528 EC - 1:4 127 20__________________________________________________________________________
TABLE 6__________________________________________________________________________ ##STR22## ##STR23## R.sup.1 R.sup.2 R.sup.3 ##STR24## B Chol. D:B:Chol. ##STR25## ##STR26##__________________________________________________________________________60 H C.sub.6 H.sub.5 C.sub.3 H.sub.6 O(C.sub.2 H.sub.4 O).sub.2 CH.sub.3 557 EC + 1:2:0.75 107 2261 H C.sub.3 H.sub.6 OCHCH.sub.3 CH.sub.2 OCH.sub.3 H 537 EC + 1:4:0.75 101 3062 H C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.2 H.sub.5 H 534 EC + 1:4:0.75 95 2363 H C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.4 H.sub.9 H 537 EC + 1:4:0.75 107 2964 C.sub.3 H.sub.7 C.sub.3 H.sub.7 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 565 EC - 1:4 106 2065 H CH.sub.2 CH.sub.2 OCOCH.sub.3 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 547 MIX - 1:4 116 14__________________________________________________________________________
TABLE 7__________________________________________________________________________ ##STR27## ##STR28## R.sup.1 R.sup.2 R.sup.3 ##STR29## B Chol. D:B:Chol. ##STR30## ##STR31##__________________________________________________________________________66 H C.sub.3 H.sub.6 OC.sub.4 H.sub.8 OC.sub.4 H.sub.9 H 515 EC + 1:4:0.75 102 2467 H C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.4 H.sub.9 H 514 EC + 1:4:0.75 100 32__________________________________________________________________________
TABLE 8__________________________________________________________________________ ##STR32## ##STR33## R.sup.1 R.sup.2 R.sup.3 ##STR34## B Chol. D:B:Chol. ##STR35## ##STR36##__________________________________________________________________________68 H C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.4 H.sub.9 C.sub.2 H.sub.5 519 EC + 1:4:0.75 97 2669 H C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.4 H.sub.9 C.sub.3 H.sub.6 OC.sub.4 H.sub.8 OC.sub.4 H.sub.9 526 EC + 1:4:0.75 96 24__________________________________________________________________________
TABLE 9__________________________________________________________________________ ##STR37## ##STR38## R.sup.1 R.sup.2 R.sup.3 ##STR39## B Chol. D:B:Chol. ##STR40## ##STR41##__________________________________________________________________________70 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.3 H.sub.6 OCH.sub.3 534 EC - 1:4 112 2471 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub. 3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 534 EC - 1:4 112 24__________________________________________________________________________
TABLE 10__________________________________________________________________________ ##STR42## ##STR43## R.sup.1 R.sup.2 R.sup.3 ##STR44## B Chol. D:B:Chol. ##STR45## ##STR46##__________________________________________________________________________72 H C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.2 H.sub.5 H 520 EC + 1:4:0.75 98 2073 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.3 H.sub.6 OC.sub. 4 H.sub.8 OC.sub.4 H.sub.9 545 EC + 1:4:0.75 96 25__________________________________________________________________________
TABLE 11__________________________________________________________________________ ##STR47## ##STR48## R.sup.1 R.sup.2 R.sup.3 ##STR49## B Chol. D:B:Chol. ##STR50## ##STR51##__________________________________________________________________________74 H CH(C.sub.2 H.sub.5)CH.sub.2 OCH.sub.3 CH(C.sub.2 H.sub.5)CH.sub.2 OCH.sub.3 502 EC + 1:4:0.75 95 2275 H CH(C.sub.2 H.sub.5)CH.sub.2 OCH.sub.3 CH(CH.sub.3).sub.2 503 EC + 1:4:0.75 100 24__________________________________________________________________________
TABLE 12__________________________________________________________________________ ##STR52## ##STR53## R.sup.1 R.sup.2 R.sup.3 ##STR54## B Chol. D:B:Chol. ##STR55## ##STR56##__________________________________________________________________________76 H C.sub.6 H.sub.5 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OCH.sub.3 442 EC - 1:4 107 26__________________________________________________________________________
TABLE 13__________________________________________________________________________ ##STR57## / R.sup.1# R.sup.2 R.sup.3 BS Chol. D:B:Chol. ##STR60## ##STR61##__________________________________________________________________________77 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.3 H.sub.6 OC.sub.2 H.sub.5 619 EC + 1:4:0.75 100 2978 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub. 3 H.sub.6 OCH.sub.3 619 EC + 1:4:0.75 110 2679 C.sub.2 H.sub.4 OC.sub.2 H.sub.4 OC.sub.2 H.sub.5 C.sub.2 H.sub.4 OC.sub.2 H.sub.4 OC.sub.2 H.sub.5 C.sub.3 H.sub.6 OCH.sub.3 618 EC - 1:4 123 17__________________________________________________________________________
TABLE 14__________________________________________________________________________ ##STR62## Example No. R.sup.1 R.sup.2 R.sup.3 .lambda.max [nm] B Chol. D:B:Chol. T* [.degree.C.] ##STR63##__________________________________________________________________________80 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.2 H.sub.4 OCH.sub.3 508 EC + 1:4:0.75 94 3181 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.3 H.sub.6 OC.sub.2 H.sub.5 515 EC - 1:2 86 2882 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.3 H.sub.6 OC.sub.2 H.sub.5 515 EC + 1:4:0.75 93 3083 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.3 H.sub.6 OCH.sub.3 508 EC - 1:2 89 1784 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.3 H.sub.6 OCH.sub.3 508 EC + 1:4:0.75 95 2585 H C.sub.2 H.sub.4 OC.sub.4 H.sub.9 C.sub.2 H.sub.4 OC.sub.4 H.sub.9 505 EC - 1:4 109 3086 H C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.4 H.sub.9 C.sub.3 H.sub.6 OCH.sub.3 504 EC - 1:4 103 2687 H C.sub.3 H.sub.6 O(C.sub.2 H.sub.4 O).sub.2 C.sub.4 H.sub.9 C.sub.3 H.sub.6 OCH.sub.3 497 EC - 1:4 105 30__________________________________________________________________________
TABLE 15__________________________________________________________________________ ##STR64## Example No. R.sup.1 R.sup.2 R.sup.3 .lambda.max [nm] B Chol. D:B:Chol. T* [.degree.C.] ##STR65##__________________________________________________________________________88 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.3 H.sub.6 O.sub.2 H.sub.4 OC.sub.6 H.sub.5 548 EC - 1:4 123 15__________________________________________________________________________
TABLE 16__________________________________________________________________________ ##STR66## Example No. R.sup.1 R.sup.2 R.sup.3 .lambda.max [nm] B Chol. D:B:Chol. T* [.degree.C.] ##STR67##__________________________________________________________________________89 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.3 H.sub.6 OCH.sub.3 555 EC - 1:4 110 2390 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.3 H.sub.6 OC.sub.2 H.sub.5 558 EC - 1:4 111 18__________________________________________________________________________
TABLE 17__________________________________________________________________________ ##STR68## Example No. R.sup.1 R.sup.2 R.sup.3 .lambda.max [nm] B Chol. D:B:Chol. T* [.degree.C.] ##STR69##__________________________________________________________________________91 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.3 H.sub.6 OC.sub.2 H.sub.5 614 EC - 1:4 104 3592 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 615 EC - 1:4 100 2593 C.sub.2 H.sub.5 C.sub.2 H.sub.5 (CH.sub.2).sub.4 OC.sub.4 H.sub.9 614 EC - 1:4 108 2494 C.sub.3 H.sub.7 C.sub.3 H.sub.7 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 618 MIX - 1:4 118 1395 C.sub.3 H.sub.7 C.sub.3 H.sub.7 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 618 EC - 1:4 100 30__________________________________________________________________________
TABLE 18__________________________________________________________________________ ##STR70## Example No. X R.sup.1 R.sup.2 R.sup.3 .lambda.max [nm] B Chol. D:B:Chol. T* [.degree.C.] ##STR71##__________________________________________________________________________96 C.sub.4 H.sub.9 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.3 H.sub.6 OC.sub.2 H.sub.5 598 EC - 1:4 117 2897 C.sub.4 H.sub.9 C.sub.3 H.sub.7 C.sub. 3 H.sub.7 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 601 EC - 1:4 127 16__________________________________________________________________________
TABLE 19__________________________________________________________________________ ##STR72## Example No. R.sup.1 R.sup.2 R.sup.3 .lambda.max [nm] B Chol. D:B:Chol. T* [A = 1] [.degree.C.] ##STR73##__________________________________________________________________________ 98 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.3 H.sub.6 OH.sub.3 601 EC - 1:4 127 16 99 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 601 EC - 1:4 129 15100 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 607 EC - 1:4 124 15101 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.4 H.sub.9 605 EC + 1:4:0,75 98 21__________________________________________________________________________
TABLE 20__________________________________________________________________________ ##STR74## Example No. R.sup.1 R.sup.2 R.sup.3 .lambda.max [nm] B Chol. D:B:Chol. T* [.degree.C.] ##STR75##__________________________________________________________________________102 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.3 H.sub.6 OCH.sub.3 517 EC + 1:4:0.75 84 15103 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 518 EC + 1:4:0.75 87 20104 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 504 EC + 1:4:0.75 97 22105 H C.sub.2 H.sub.4 OCONHC.sub.4 H.sub.9 C.sub.2 H.sub.5 501 EC + 1:4:0.75 111 24__________________________________________________________________________
TABLE 21__________________________________________________________________________ ##STR76## Example No. R.sup.1 R.sup.2 R.sup.3 .lambda.max [nm] B Chol. D:B:Chol. T* [.degree.C.] ##STR77##__________________________________________________________________________106 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 531 EC - 1:4 107 16__________________________________________________________________________
TABLE 22__________________________________________________________________________ ##STR78## No.Example R.sup.1 R.sup.2 R.sup.3 [nm].lambda.max B Chol. D:B:Chol. [.degree.C.]T* ##STR79##__________________________________________________________________________107 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.3 H.sub.6 OCH.sub.3 555 EC - 1:4 118 16__________________________________________________________________________
TABLE 23__________________________________________________________________________ ##STR80## No.Example R.sup.1 R.sup.2 R.sup.3 [nm].lambda.max B Chol. D:B:Chol. [.degree.C.]T* ##STR81##__________________________________________________________________________108 H ##STR82## C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OCH.sub.3 532 EC - 1:4 102 15__________________________________________________________________________
TABLE 24__________________________________________________________________________ ##STR83## No.Example R.sup.1 R.sup.2 R.sup.3 [nm].lambda.max B Chol. D:B:Chol. [.degree.C.]T* ##STR84##__________________________________________________________________________109 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 535 MIX - 1:4 87 21110 C.sub.2 H.sub.5 C.sub.3 H.sub.6 OCH.sub.3 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 537 MIX - 1:4 91 19__________________________________________________________________________
TABLE 25__________________________________________________________________________ ##STR85## No.Example R.sup.1 R.sup.2 R.sup.3 R.sup.10 [nm].lambda.max B Chol. D:B:Chol. [.degree.C.]T* ##STR86##__________________________________________________________________________111 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 H 595 MIX - 1:4 118 16112 C.sub.2 H.sub. 5 C.sub.2 H.sub.5 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 CH.sub.3 598 MIX - 1:4 122 14__________________________________________________________________________
TABLE 26__________________________________________________________________________ ##STR87## No.Example R.sup.1 R.sup.2 R.sup.3 R.sup.13 R.sup.14 [nm].lambda.max B Chol. D:B:Chol. [.degree.C.]T* ##STR88##__________________________________________________________________________123 H C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OCH.sub.3 C.sub.6 H.sub.5 H H 495 EC + 1:4:0.75 113 32__________________________________________________________________________
TABLE 27__________________________________________________________________________ ##STR89## No.Example R.sup.1 R.sup.2 R.sup.3 R.sup.10 [nm].lambda.max B Chol. D:B:Chol. [.degree.C.]T* ##STR90##__________________________________________________________________________114 H C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OCH.sub.3 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 CH.sub.3 540 MIX - 1:4 109 14__________________________________________________________________________
TABLE 28__________________________________________________________________________ ##STR91## No.Example R.sup.1 R.sup.2 R.sup.3 [nm].lambda.max B Chol. D:B:Chol. [.degree.C.]T* ##STR92##__________________________________________________________________________115 H C.sub.3 H.sub.6 OCH(CH.sub.3).sub.2 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 544 MIX - 1:4 107 20116 H C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OCH.sub.3 C.sub.3 H.sub.6 OC.sub.2 H.sub.4 OC.sub. 544.sub.5 MIX - 1:4 106 17__________________________________________________________________________
TABLE 29__________________________________________________________________________ ##STR93## No.Example R.sup.1 R.sup.2 R.sup.3 [nm].lambda.max B Chol. D:B:Chol. [.degree.C.]T* ##STR94##__________________________________________________________________________117 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.3 H.sub.6 OC.sub.2 H.sub.5 601 EC - 1:4 126 17__________________________________________________________________________
TABLE 30__________________________________________________________________________ ##STR95## No.Example R.sup.1 R.sup.2 R.sup.3 R [nm].lambda.max B Chol. D:B:Chol. [.degree.C.]T* ##STR96##__________________________________________________________________________118 H C.sub.3 H.sub.6 OCH.sub.3 C.sub.3 H.sub.6 OCH.sub.3 C.sub.2 H.sub.4 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 511 EC - 1:4 121 17119 H C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.3 C.sub.2 H.sub.4 OC.sub.2 H.sub.4 OC.sub.6 H.sub.5 510 EC - 1:4 108 24120 H C.sub.3 H.sub.6 OCH.sub.3 C.sub.3 H.sub.6 OCH.sub.3 C.sub.2 H.sub.4 OC.sub.3 H.sub.7 520 EC - 1:4 113 24121 H C.sub.3 H.sub.6 OCH.sub.3 C.sub.3 H.sub.6 OCH.sub.3 C.sub.2 H.sub.4 OCH.sub.2 C.sub.6 H.sub.5 521 EC + 1:4:0.75 102 29122 H C.sub.3 H.sub.6 OCH.sub.3 C.sub.3 H.sub.6 OCH.sub.3 CH.sub.2 OCH.sub.3 523 EC + 1:4:0.75 121 15__________________________________________________________________________

Number	Date	Country
258856	Jul 1979	EPX
111004	Jun 1984	EPX
340722	Aug 1989	EPX
3330155	Mar 1985	DEX
30392	Apr 1985	JPX
199997	Feb 1986	JPX
237694	Feb 1986	JPX
227092	Aug 1986	JPX
127392	Sep 1986	JPX
283595	Sep 1986	JPX
2259882	Oct 1977	GBX
2159971	Dec 1985	GBX

Transfer of azo dyes having a pyridine coupling component

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