Patent Grant
8871304
The present invention relates to a novel (amide amino alkane) metal compound, and a method of producing a metal-containing thin film on an object by a chemical vapor deposition method (hereinafter, referred to as CVD method) using the metal compound.
In recent years, various metal-containing thin films have been researched and developed as materials in the field of semiconductors, electronic components, and the like.
Conventionally, various magnesium compounds such as bis(cyclopentadienyl)magnesium, magnesium alkoxide and magnesium diketonato, for example, have been known as magnesium compounds to be used for the formation of magnesium-containing thin film (See Patent Documents 1 to 2). Among them, bis(cyclopentadienyl)magnesium, and analogs thereof are relatively frequently employed. Meanwhile, bis(amide amino alkane) magnesium compounds have been known and used as a catalyst, and a material for the production of medicines, agricultural chemicals, and the like, for example (See Non-Patent Documents 1 to 2).
There have been proposed, as cobalt compounds to be used for the formation of thin film, bis(acetylacetonato)cobalt (See, for example, Non-Patent Document 3), bis(dipivaloylmethanato)cobalt (See, for example, Non-Patent Document 4), octacarbonyl dicobalt (See, for example, Non-Patent Document 5 and Patent Document 3), cobalt cyclopentadienyl dicarbonyl (See, for example, Non-Patent Document 6 and Patent Document 4) and bis(trimethylsilyl cyclopentadienyl)cobalt (See, for example, Patent Document 5), bis(N,N′-diisopropylacetoamidinato)cobalt (See, for example, Patent Document 6, Patent Document 7 and Non-Patent Document 7) and bis(N-t-butyl-N′-ethylpropionamidinato)cobalt (See, for example, Patent Document 8 and Non-Patent Document 8), for example.
There have been proposed, as manganese compounds to be used for the formation of thin film, bis(dipivaloylmethanato)manganese (See, for example, Patent Document 9), bis(ethylcyclopentadienyl)manganese (See, for example, Patent Documents 9 and 10), bis(N,N′-diisopropylacetoamidinato)manganese (See, for example, Patent Document 11) and bis(N,N′-diisopropylpentaneamidinato)manganese (See, for example, Patent Documents 12 and 13 and Non-Patent Documents 9 and 10), for example.
There have been proposed, as zinc compounds to be used for the formation of thin film, bis(acetylacetonato)zinc (See, for example, Patent Documents 14 and 15), for example.
There have been proposed, as metal compounds to be used for the formation of iron-containing thin film, nickel-containing thin film or lanthanum-containing thin film, bis(N,N′-diisopropylacetoamidinato)iron, bis(N,N′-diisopropylacetoamidinato)nickel and tris(N,N′-diisopropyl-2-t-butylamidinato)lanthanum (See, for example, Patent Document 11), for example.
Patent Document 1: JP-A-2002-170993
Patent Document 2: JP-A-2005-298874
Patent Document 3: US 2005/0130417 A1
Patent Document 4: US 2006/0157863 A1
Patent Document 5: WO 2008/111499 A1
Patent Document 6: WO 2004/046417 A1
Patent Document 7: WO 2009/088522 A1
Patent Document 8: JP-A-2010-524264
Patent Document 9: WO 2010/116889 A1
Patent Document 10: WO 2011/037090 A1
Patent Document 11: JP-A-2010-156058
Patent Document 12: WO 2009/117670 A1
Patent Document 13: WO 2011/050073 A1
Patent Document 14: JP-A-2009-277357
Patent Document 15: JP-A-2003-31846
Non-patent Document 1: Eur. J. Solid State Inorg. Chem., p. 241 (1993)
Non-patent Document 2: Tetrahedron Lett., p. 4175 (2004)
Non-patent Document 3: Japanese Journal of Applied Physics, vol. 36, p. 705 (1997)
Non-patent Document 4: Chemistry of Materials, vol. 13, p. 588 (2001)
Non-patent Document 5: Thin Solid Films, vol. 485, p. 95 (2005)
Non-patent Document 6: Japanese Journal of Applied Physics, vol. 46, p. 173 (1997)
Non-patent Document 7: Journal of The Electrochemical Society, vol. 157, D10-D15 (2010)
Non-patent Document 8: Dalton Transactions, p. 2592-2597 (2008)
Non-patent Document 9: Journal of The Electrochemical Society, vol. 157, D341-D345 (2010)
Non-patent Document 10: Journal of The Electrochemical Society, vol. 158, D248-D253 (2011)
Non-patent Document 11: Jpn. J. Appl. Phys. 1114 (2004)
However, the conventional metal compounds to be used for the formation of thin film do not necessarily have optimal properties such as steam pressure, heat stability and reactivity for the formation of metal-containing thin film, and it may be that no metal compounds are adequate for the formation of metal-containing thin film. Accordingly, there is a need for metal compounds having all properties such as steam pressure, heat stability and reactivity satisfying the requirements.
An object of the present invention is to solve the above-mentioned problems, and to provide a metal compound which is suitable for industrial use and from which a metal-containing thin film may be produced on an object by a simple method, and more specifically, a metal compound which is suitable for the formation of metal-containing thin film by a CVD method. Another object of the present invention is to provide a method of producing a metal-containing thin film using the metal compound.
The present invention relates to the following items:
[1] An (amide amino alkane) metal compound represented by the formula (1):
wherein
M represents a metal atom;
R1 represents a linear, branched or cyclic alkyl group having 1 to 6 carbon atoms;
R2 and R3 may be the same as, or different from each other, and each independently represents a linear or branched alkyl group having 1 to 3 carbon atoms, or R2 and R3 may form a substituted or unsubstituted 5- or 6-membered ring together with the nitrogen atom to which they are bound;
Z represents a linear or branched alkylene group having 1 to 10 carbon atoms (a part of which may optionally form a ring); and
n represents a number of the ligands, which is equal to the valence of the metal (M), and represents an integer of from 1 to 3;
with the proviso that
the metal compounds in which M is Li (Lithium), Be (Beryllium), Ge (Germanium) or Nd (Neodymium) are excluded;
the metal compounds in which M is Mg (Magnesium) and R1 is methyl group are excluded;
the metal compounds in which M is Zn (Zinc) and R1 is methyl group are excluded;
the metal compounds in which M is Bi (Bismuth) and R1 is t-butyl group are excluded; and
in cases where n is two or greater, two or more ligands may be the same as, or different from each other.
[2] The (amide amino alkane) metal compound as described in [1], wherein M is sodium, magnesium, manganese, iron, cobalt, nickel, zinc, yttrium, lanthanum, or indium.
[3] The (amide amino alkane) metal compound as described in [1], wherein Z is a linear or branched alkylene group having 1 to 5 carbon atoms, or a group represented by the formula:
wherein
Z1 represents a linear alkylene group having 1 to 3 carbon atoms; and
R represents a linear or branched alkyl group having 1 to 6 carbon atoms, or a cycloalkyl group having 3 to 6 carbon atoms.
[4] A method of producing an (amide amino alkane) metal compound as described in [1], which is represented by the formula (1):
wherein M, R1, R2, R3, Z and n are defined as above;
comprising a step of:
reacting a mono- or di-alkyl metal compound represented by the formula (2a) or (2b):
R4M (2a)
R4R5M (2b)
wherein
M represents a metal atom; and
R4 and R5 may be the same as, or different from each other, and each independently represents a linear or branched alkyl group having 1 to 10 carbon atoms:
with a di-amino alkane compound represented by the formula (3):
wherein R1, R2, R3 and Z are defined as above.
[5] A method of producing an (amide amino alkane) metal compound as described in [1], which is represented by the formula (1):
wherein M, R1—, R2, R3, Z and n are defined as above;
comprising steps of
reacting an alkyl alkali metal compound represented by the formula (4a);
R4A (4a)
wherein
R4 represents a linear or branched alkyl group having 1 to 10 carbon atoms; and
A represents an alkali metal atom;
or an alkali metal with a di-amino alkane compound represented by the formula (3):
wherein R1, R2, R3 and Z are defined as above;
to form a (amide amino alkane) alkali metal compound represented by the formula (5):
wherein R1, R2, R3, A and Z are defined as above; and
reacting the (amide amino alkane) alkali metal compound with a metal halide compound represented by the formula (6):
MXn (6)
wherein
M represents a metal atom;
X represents a halogen atom; and
n represents a number of the halogen atoms, which is equal to the valence of the metal (M), and represents an integer of from 1 to 3.
[6] A method of producing an (amide amino alkane) metal compound as described in [1], which is represented by the formula (1):
wherein R1, R2, R3, M, Z and n are defined as above;
comprising a step of:
reacting a metal represented by the formula (7):
M (7)
wherein
M represents a metal atom, and is defined as above;
with a di-amino alkane compound represented by the formula (3):
wherein R1, R2, R3 and Z are defined as above.
[7] A method of producing a metal-containing thin film by a chemical vapor deposition method, wherein an (amide amino alkane) metal compound as described in [1] is used as a source.
[8] A material for forming a metal-containing thin film, comprising an (amide amino alkane) metal compound as described in [1].
According to the present invention, there may be provided a novel (amide amino alkane) metal compound, including bis(amide amino alkane) magnesium compound, bis(amide amino alkane) cobalt compound, bis(amide amino alkane) manganese compound and bis(amide amino alkane) zinc compound, which is particularly suitable for the production/formation of metal-containing thin film by a CVD method. In addition, a metal-containing thin film may be produced with good film-forming performance by a CVD method using the metal compound.
The (amide amino alkane) metal compound, including bis(amide amino alkane) magnesium compound, bis(amide amino alkane) cobalt compound, bis(amide amino alkane) manganese compound and bis(amide amino alkane) zinc compound, is useful as a material for the formation of metal-containing thin film, including magnesium-containing thin film, cobalt-containing thin film, manganese-containing thin film and zinc-containing thin film, respectively, and is useful as a catalyst, and a material for the production of medicines, agricultural chemicals, and the like, for example.
The (amide amino alkane) metal compound of the present invention is represented by the above formula (1).
In the formula (1), M represents a metal atom (excluding Be (beryllium), Ge (germanium) and Nd (neodymium)), and may be, for example, lithium, sodium, magnesium, manganese, iron, cobalt, nickel, zinc, yttrium, lanthanum, or indium.
R1 represents a linear, branched or cyclic alkyl group having 1 to 6 carbon atoms such as methyl, ethyl, n-propyl, isopropyl, cyclopropyl, s-butyl, t-butyl, cyclobutyl, t-pentyl, neopentyl, cyclopentyl and cyclohexyl. R1 may be preferably a linear or branched alkyl group having 1 to 6 carbon atoms, more preferably a linear or branched alkyl group having 1 to 5 carbon atoms. In one embodiment, R1 may be more preferably a linear or branched alkyl group having 2 to 5 carbon atoms, more preferably a linear or branched alkyl group having 3 to 5 carbon atoms, particularly preferably isopropyl, s-butyl, t-butyl or t-pentyl.
The cases where R1 is methyl group when M is Mg (magnesium), however, are excluded. The cases where R1 is methyl group when M is Zn (zinc) are excluded. The cases where R1 is t-butyl group when M is Bi (bismuth) are excluded.
R2 and R3 may be the same as, or different from each other, and each independently represents a linear or branched alkyl group having 1 to 3 carbon atoms such as methyl, ethyl, n-propyl and isopropyl, or R2 and R3 may form a substituted or unsubstituted 5- or 6-membered ring together with the nitrogen atom to which they are bound. R2 and R3 may be preferably an alkyl group having 1 to 2 carbon atoms (methyl, ethyl) and may also preferably form a substituted or unsubstituted 5-membered ring, more preferably a unsubstituted 5-membered ring, together with the nitrogen atom to which they are bound. R2 and R3 may be particularly preferably methyl or ethyl.
Z represents a linear or branched alkylene group having 1 to 10 carbon atoms (a part of which may optionally form a ring). Z may be preferably a linear or branched alkylene group having 1 to 10 carbon atoms which does not contain a cycloalkyl group, although a part of Z may form a ring, that is, Z may contain a cycloalkyl group such as cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl,
Z may be preferably a linear or branched alkylene group having 1 to 5 carbon atoms such as methylene, ethylene, trimethylene, methylethylene, 1,2-dimethylethylene, 1,1-dimethylethylene, tetraethylene, 2-methyltrimethylene and hexamethylene.
In cases where Z is a linear alkylene group, Z may be more preferably an alkylene group having 1 to 3 carbon atoms, particularly preferably an alkylene group having 2 carbon atoms (ethylene).
In cases where Z is a branched alkylene group, Z may be preferably, for example, a group represented by the formula:
wherein Z1 represents a linear alkylene group having 1 to 3 carbon atoms, and R represents a linear or branched alkyl group having 1 to 6 carbon atoms, or a cycloalkyl group having 3 to 6 carbon atoms.
Z1 represents a linear alkylene group having 1 to 3 carbon atoms such as methylene, ethylene and trimethylene, for example, and may be preferably methylene.
R represents a linear or branched alkyl group having 1 to 6 carbon atoms such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, s-butyl, t-butyl, heptyl and hexyl, or a cycloalkyl group having 3 to 6 carbon atoms such as cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl, for example, and may be preferably a linear or branched alkyl group having 1 to 6 carbon atoms, more preferably a linear or branched alkyl group having 1 to 4 carbon atoms, more preferably a linear alkyl group having 1 to 3 carbon atoms, particularly preferably methyl.
In one preferred embodiment of this type, Z1 may be methylene, and R may be a linear alkyl group having 1 to 3 carbon atoms, more preferably methyl.
Z may be preferably a linear or branched alkylene group having 1 to 10 carbon atoms which does not contain a ring (cycloalkyl group), more preferably a linear or branched alkylene group having 1 to 5 carbon atoms, and may be particularly preferably an alkylene group having 1 to 5 carbon atoms, more preferably having 1 to 3 carbon atoms, more preferably having 2 carbon atoms (linear alkylene group), or an alkylene group having 2 carbon atoms to which one or two alkyl groups having 1 to 3 carbon atoms, more preferably methyl, are bound (branched alkylene group). In the branched alkylene group, two alkyl groups may be bound to one carbon atom in the alkylene group, or may be bound to different carbon atoms, and two alkyl groups may be the same as, or different from each other.
In the formula (1), n represents a number of the ligands, which is equal to the valence of the metal (M), and n is generally an integer of from 1 to 3.
In cases where n is two or greater, two or more ligands may be the same as, or different from each other. In cases where the ligand is a mixture of two or more different types of ligands, a plurality of complexes may be formed.
In one preferred embodiment of the present invention, R1 may be an alkyl group having 2 to 5 carbon atoms, more preferably an alkyl group having 3 to 5 carbon atoms, and R2 and R3 may be an alkyl group having 1 to 2 carbon atoms, and Z may be an alkylene group having 1 to 3 carbon atoms.
In another preferred embodiment of the present invention, R1 may be an alkyl group having 1 to 5 carbon atoms, and R2 and R3 may be an alkyl group having 1 to 2 carbon atoms, and Z may be a group represented by the formula:
wherein Z1 represents an alkylene group having 1 to 3 carbon atoms, and R represents a linear or branched alkyl group having 1 to 4 carbon atoms.
Specific examples of the (amide amino alkane) metal compound of the present invention include the compounds represented by the following formulas (1) to (498). In the formulas, M represents a metal atom, and n represents a number of the ligands, which is equal to the valence of the metal (M). In addition, o and p represent a number of each of ligands, and the sum (o+p) is equal to the valence of the metal (M).
Specific examples of the bis(amide amino alkane) magnesium compound of the present invention include the compounds represented by the following formulas (4) to (18).
Specific examples of the bis(amide amino alkane) cobalt compound of the present invention include the compounds represented by the following formulas (6) to (20) and (1a) to (1u).
Specific examples of the bis(amide amino alkane) manganese compound of the present invention include the compounds represented by the following formulas (6) to (27).
The (amide amino alkane) metal compound of the present invention such as bis(amide amino alkane) magnesium compound and (amide amino alkane) lithium compound, in particular, may be synthesized by a method (hereinafter, sometimes referred to as “Reaction (I) of the present invention”) in which an (amide amino alkane) metal compound (1) is synthesized by reacting a mono- or di-alkyl metal compound (2a) or (2b) such as di-alkyl magnesium compound and alkyl lithium compound with a di-amino alkane compound (3) as shown in the following scheme.
wherein
The mono- or di-alkyl metal compound to be used in the Reaction (I) of the present invention is represented by the above formula (2a) or (2b). In the formulas (2a) and (2b), R4 and R5 may be the same as, or different from each other, and each independently represents a linear or branched alkyl group having 1 to 10 carbon atoms such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, t-butyl, n-pentyl, t-pentyl, neopentyl and n-decyl.
The mono- or di-alkyl metal compound to be used in the Reaction (I) of the present invention may be a commercially available product, and may be prepared from a metal, simple substance, such as metallic magnesium as a starting material by a known method. A mono- or di-alkyl metal compound represented by the formula (2a) or (2b) in which R4 and R5 are n-butyl or ethyl, including di(n-butyl) magnesium and n-butyl ethyl magnesium, may be suitably used.
The di-amino alkane compound to be used in the Reaction (I) of the present invention is represented by the above formula (3). In the formula (3), R1, R2, R3 and Z correspond to R1, R2, R3 and Z in the formula (1), respectively, and are defined as above.
Accordingly, preferable examples of the di-amino alkane compound to be suitably used in the Reaction (I) of the present invention include 1-isopropylamino-2-dimethylaminoethane, 1-cyclopropylamino-2-dimethylaminoethane, 1-(t-butylamino)-2-dimethylaminoethane, 1-isobutylamino-2-dimethylaminoethane, 1-dimethylamino-2-(t-pentylamino)ethane, 1-isopropylamino-3-dimethylaminopropane, 1-(t-butylamino)-3-dimethylaminopropane, (isopropylamino)(dimethylamino)methane and (t-butylamino)(dimethylamino)methane.
The di-amino alkane compound to be used in the Reaction (I) of the present invention may be a commercially available product, and may be prepared by a combination of known methods. A method in which the compound is prepared by the reduction reaction of hydrochloride of halogenated alkane having mono-alkyl amine and “di-alkyl amino group” in its structure, or the corresponding imine compound, for example, may be preferably employed.
The amount of the di-amino alkane compound to be used may be preferably from 1.5 mole to 3.0 mole, more preferably from 1.8 mole to 2.2 mole, per mole of the mono- or di-alkyl metal compound.
The Reaction (I) of the present invention may be preferably conducted in an organic solvent. The organic solvent to be used is not limited as long as it does not inhibit the reaction. Examples thereof include ethers such as diethyl ether, tetrahydrofuran, dimethoxyethane and dioxane; aliphatic hydrocarbons such as hexane, heptane, octane, cyclohexane, methylcyclohexane and ethylcyclohexane; and aromatic hydrocarbons such as toluene and xylene. An ether, an aliphatic hydrocarbon, or a mixture of an ether and an aliphatic hydrocarbon may be suitably used. These organic solvents may be used alone or in combination of two or more types thereof.
The amount of the organic solvent to be used may be preferably from 1 g to 100 g, more preferably from 1 g to 10 g, per gram (g) of the mono- or di-alkyl metal compound.
The Reaction (I) of the present invention may be conducted, for example, by a method in which the reaction is conducted while mixing and stirring the mono- or di-alkyl metal compound, the di-amino alkane compound and an organic solvent. The reaction temperature may be preferably from −20° C. to 120° C., more preferably from 0° C. to 100° C. There are no particular restrictions to the reaction pressure.
The (amide amino alkane) metal compound, which is the desired product, may be obtained by the Reaction (I) of the present invention. After the completion of the reaction, the synthesized (amide amino alkane) metal compound may be isolated/purified by a known method such as extraction, filtration, concentration, distillation, sublimation, recrystallization and column chromatography.
The (amide amino alkane) metal compound, which is the desired product of the present invention, and the di-alkyl magnesium compound, which is the starting material, are often unstable to moisture and oxygen in the atmosphere. Accordingly, the reaction operation, the post-treatment of the reaction solution, and the like may be preferably conducted under anhydrous conditions or under inert gas atmosphere.
The (amide amino alkane) metal compound of the present invention may be synthesized by reacting a metal with a di-amino alkane compound in the same way as in the above-described process in which the mono- or di-alkyl metal compound is used, except that the metal is used instead of the mono- or di-alkyl metal compound.
wherein M, R1, R2, R3 and Z are defined as above.
The (amide amino alkane) metal compound of the present invention such as bis(amide amino alkane) cobalt compound, bis(amide amino alkane) manganese compound, bis(amide amino alkane) zinc compound, bis(amide amino alkane) iron compound, bis(amide amino alkane) nickel compound, tris(amide amino alkane) indium compound, tris(amide amino alkane) yttrium compound and tris(amide amino alkane) lanthanum compound, in particular, may be synthesized by a method as shown in the following scheme, and more specifically, a method in which an (amide amino alkane) metal compound (1) is prepared by reacting an alkyl alkali metal compound (4a) or an alkali metal (4b) with a di-amino alkane compound (3) to form an (amide amino alkane) alkali metal compound (5) (hereinafter, sometimes referred to as “Reaction (A)”), and then reacting this compound with a metal halide compound (6) such as di-halogeno cobalt compound and di-halogeno manganese compound (hereinafter, sometimes referred to as “Reaction (B)”). Hereinafter, the combination of the Reaction (A) and the Reaction (B) is sometimes referred to as “Reaction (II) of the present invention”.
wherein
The alkyl alkali metal compound to be used in the Reaction (A) of the present invention is represented by the above formula (4a). In the formula (4a), R4 represents a linear or branched alkyl group having 1 to 10 carbon atoms such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, t-butyl, n-pentyl, t-pentyl, neopentyl and n-decyl, and A represents an alkali metal such as lithium atom, sodium atom and potassium atom. These alkyl alkali metal compounds may be used alone or in combination of two or more types thereof.
As the alkyl alkali metal compound, lithium methyl or lithium n-butyl may be suitably used.
In addition, an alkali metal (4b) may be used instead of the alkyl alkali metal compound (4a).
The di-amino alkane compound to be used in the Reaction (A) of the present invention is represented by the above formula (3). In the formula (3), R1, R2, R3 and Z correspond to R1, R2, R3 and Z in the formula (1), respectively, and are defined as above.
Accordingly, specific examples of the di-amino alkane compound to be suitably used in the Reaction (A) of the present invention include 1-ethylamino-2-dimethylaminoethane, 1-isopropylamino-2-dimethylaminoethane, 1-(t-butylamino)-2-dimethylaminoethane, 1-isobutylamino-2-dimethylaminoethane, 1-dimethylamino-2-(t-pentylamino)ethane, 1-isopropylamino-3-dimethylaminopropane, 1-(t-butylamino)-3-dimethylaminopropane, (isopropylamino)(dimethylamino)methane, (t-butylamino)(dimethylamino)methane, 1-methylamino-2-dimethylaminopropane, 1-ethylamino-2-dimethylaminopropane, 1-isopropylamino-2-dimethylaminopropane, 1-(t-butylamino)-2-dimethylaminopropane, 1-(s-butylamino)-2-dimethylaminopropane, 1-isobutylamino-2-dimethylaminopropane and 1-(t-pentylamino)-2-dimethylaminopropane.
The di-amino alkane compound to be used in the Reaction (A) of the present invention may be a commercially available product, and may be prepared by a combination of known methods. A method in which the compound is prepared by the reduction reaction of hydrochloride of halogenated alkane having mono-alkyl amine and “di-alkyl amino group” in its structure, or the corresponding imine compound, for example, may be preferably employed.
The amount of the di-amino alkane compound to be used may be preferably from 1.5 mole to 3.0 mole, more preferably from 1.8 mole to 2.2 mole, per mole of the alkyl alkali metal compound or the alkali metal.
The Reaction (A) of the present invention may be preferably conducted in an organic solvent. The organic solvent to be used is not limited as long as it does not inhibit the reaction. Examples thereof include ethers such as diethyl ether, tetrahydrofuran, dimethoxyethane and dioxane; aliphatic hydrocarbons such as hexane, heptane, octane, cyclohexane, methylcyclohexane and ethylcyclohexane; and aromatic hydrocarbons such as toluene and xylene. An ether, an aliphatic hydrocarbon, or a mixture of an ether and an aliphatic hydrocarbon may be suitably used. These organic solvents may be used alone or in combination of two or more types thereof.
The amount of the organic solvent to be used may be preferably from 1 g to 100 g, more preferably from 1 g to 10 g, per gram (g) of the alkyl alkali metal compound or the alkali metal.
The Reaction (A) of the present invention may be conducted, for example, by a method in which the reaction is conducted while stirring a mixture of the di-amino alkane compound and an organic solvent, to which a solution (which may be a suspension) of the alkyl alkali metal compound or alkali metal in an organic solvent is added. The reaction temperature may be preferably from −78° C. to 120° C., more preferably from −20° C. to 60° C. There are no particular restrictions to the reaction pressure.
(Reaction (B): Synthesis of (amide amino alkane) Metal Compound (1))
The metal halide compound to be used in the Reaction (B) of the present invention, including di-halogeno cobalt compound, di-halogeno manganese compound, di-halogeno zinc compound, di-halogeno iron compound, di-halogeno nickel compound, tri-halogeno indium compound, tri-halogeno yttrium compound and tri-halogeno lanthanum compound, is represented by the above formula (6). In the formula (6), X represents a halogen atom such as fluorine atom, chlorine atom, bromine atom and iodine atom.
Preferable examples of the metal halide compound to be suitably used include metal chloride such as cobalt(II) chloride, manganese(II) chloride, zinc(II) chloride, iron(II) chloride, nickel(II) chloride, indium(III) chloride, yttrium(III) chloride and lanthanum(III) chloride; metal bromide such as cobalt(II) bromide, manganese(II) bromide, zinc(II) bromide, iron(II) bromide, nickel(II) bromide, indium(III) bromide, yttrium(III) bromide and lanthanum(III) bromide; and metal iodide such as cobalt(II) iodide, manganese(II) iodide, zinc(II) iodide, iron(II) iodide, nickel(II) iodide, indium(III) iodide, yttrium(III) iodide and lanthanum(III) iodide.
The amount of the metal halide compound to be used may be preferably from 0.25 mole to 0.75 mole, more preferably from 0.4 mole to 0.6 mole, per mole of the (amide amino alkane) alkali metal compound.
The Reaction (B) of the present invention may be preferably conducted in an organic solvent. The organic solvent to be used is not limited as long as it does not inhibit the reaction. Examples thereof include ethers such as diethyl ether, tetrahydrofuran, dimethoxyethane and dioxane; aliphatic hydrocarbons such as hexane, heptane, octane, cyclohexane, methylcyclohexane and ethylcyclohexane; and aromatic hydrocarbons such as toluene and xylene. An ether, an aliphatic hydrocarbon, or a mixture of an ether and an aliphatic hydrocarbon may be suitably used. These organic solvents may be used alone or in combination of two or more types thereof.
The amount of the organic solvent to be used may be preferably from 1 g to 100 g, more preferably from 1 g to 10 g, per gram (g) of the (amide amino alkane) alkali metal compound.
The Reaction (B) of the present invention may be conducted, for example, by a method in which the reaction is conducted while stirring a mixture of the metal halide compound and an organic solvent, to which a solution of the (amide amino alkane) alkali metal compound, which is prepared by the Reaction (A), in an organic solvent is added. The reaction temperature may be preferably from −78° C. to 120° C., more preferably from −20° C. to 60° C. There are no particular restrictions to the reaction pressure.
The (amide amino alkane) metal compound, which is the desired product, may be obtained by the Reaction (B) of the present invention. After the completion of the reaction, the synthesized (amide amino alkane) metal compound may be isolated/purified by a known method such as extraction, filtration, concentration, distillation, sublimation, recrystallization and column chromatography, for example.
The same solvent may be used for conducting the Reactions (A) and (B) of the present invention, for example. The reaction solution obtained by the Reaction (A) may be used for the Reaction (B) without any treatment, or without isolating/purifying the (amide amino alkane) alkali metal compound (5) produced as a result of the Reaction (A), to continuously synthesize the (amide amino alkane) metal compound.
The (amide amino alkane) metal compound, which is the desired product, the alkyl alkali metal compound, which is the starting material, and the (amide amino alkane) alkali metal compound, which is the synthetic intermediate, are often unstable to moisture and oxygen in the atmosphere. Accordingly, the reaction operation, the post-treatment of the reaction solution, and the like may be preferably conducted under anhydrous conditions or under inert gas atmosphere. In addition, the starting material, solvent, and the like may be preferably dehydrated or dried prior to being used.
A metal-containing thin film may be formed with good film-forming performance by a CVD method, for example, using the (amide amino alkane) metal compound of the present invention.
A metal-containing thin film may be vapor-deposited on an object by a known CVD method and atomic layer deposition method (ALD method). A metal-containing thin film may be vapor-deposited on an object, for example, by feeding the vapor of the (amide amino alkane) metal compound onto the heated object under atmospheric or reduced pressure, together with a hydrogen source (a reducing gas such as hydrogen, ammonia, and the like, for example), a nitrogen source (nitrogen, ammonia, and the like, for example) or an oxygen source (for example, an oxidizing gas such as oxygen, ozone, and the like; water; alcohols such as methanol, ethanol, n-propyl alcohol, isopropyl alcohol, n-butyl alcohol, and the like). The gas (including a vaporized liquid) may be diluted with an inert gas, and the like. A metal-containing thin film may be also vapor-deposited by a plasma CVD method in which the similar material is fed.
In the CVD method, the (amide amino alkane) metal compound needs to be vaporized for the formation of thin film. A method of vaporizing the (amide amino alkane) metal compound to be employed in the present invention may be, for example, a method in which the (amide amino alkane) metal compound is filled or fed into a vaporizing chamber, and then vaporized therein, or alternatively, a method (solution method) in which a solution prepared by diluting the (amide amino alkane) metal compound with a suitable solvent (Examples thereof include aliphatic hydrocarbons such as hexane, cyclohexane, methylcyclohexane, ethylcyclohexane, heptane and octane; aromatic hydrocarbons such as toluene, ethyl benzene and xylene; and ethers such as glyme, diglyme, triglyme, dioxane and tetrahydrofuran) is fed into a vaporizing chamber with a liquid feed pump, and then vaporized therein.
As for the vapor-deposition conditions in the case where a metal-containing thin film is vapor-deposited using the (amide amino alkane) metal compound of the present invention, for example, the pressure in the reaction system may be preferably from 1 Pa to 200 kPa, the temperature of the object on which the film is formed may be preferably from 50° C. to 900° C., more preferably from 100° C. to 600° C., and the temperature at which the (amide amino alkane) metal compound is vaporized may be preferably from 0° C. to 250° C., more preferably from 30° C. to 200° C.
When a metal-containing thin film is vapor-deposited, the percentage of an oxygen source (an oxidizing gas, water vapor or alcohol vapor, or a mixture thereof, for example), a nitrogen source (nitrogen gas, ammonia gas, or a mixture thereof, for example) or a reducing gas (hydrogen gas or ammonia gas, or a mixture thereof, for example) to the total amount of the gases may be preferably from 3 vol % to 99 vol %, more preferably from 5 vol % to 98 vol %.
The present invention will be more specifically described below with reference to the Examples. However, the scope of the present invention should not be limited to these Examples.
Under argon atmosphere, into a 100 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 5.5 g (0.23 mol) of metallic magnesium and 20 ml of diethyl ether. And then, 3.0 g (21 mmol) of bromobutane was slowly dropped into the flask. Subsequently, 180 ml of diethyl ether and 25 g (0.18 mol) of bromobutane were slowly dropped into the flask, and the mixture was reacted while stirring at 40° C. for 2 hours. And then, 55 g (0.62 mol) of dioxane was added to the reaction solution, and the mixture was reacted while stirring at 40° C. for 2 hours. After the completion of the reaction, under argon atmosphere, the reaction solution was filtrated, and the filtrate was concentrated under reduced pressure. The resultant concentrate was heated and dried under vacuum, to provide 22 g of dibutyl magnesium. (Isolation yield: 80%)
Into a 50 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 6.0 g (0.10 mol) of isopropylamine and 5 ml of water. And then, while maintaining the solution temperature within a range of from 30° C. to 50° C., 10 ml of aqueous solution of 5.0 g (35 mmol) of 2-(dimethylamino)ethyl chloride hydrochloride was slowly dropped into the flask, and the mixture was stirred for 2 hours. Subsequently, 10 ml of aqueous solution of 2.8 g (70 mmol) of sodium hydroxide was slowly dropped into the flask in an ice bath, and the mixture was reacted for 10 minutes. After the completion of the reaction, the reaction solution was subjected to extraction with 25 ml of hexane twice, and the hexane layer was concentrated under reduced pressure. The resultant concentrate was distilled under reduced pressure (65° C., 4.0 kPa), to provide 1.4 g of 1-isopropylamino-2-dimethylaminoethane. (Isolation yield: 31%)
The reaction was conducted in the same way as in Reference Example A2, except that 7.3 g (0.10 mol) of t-butylamine was used instead of isopropylamine. Then, the reaction solution was concentrated, and the resultant concentrate was distilled under reduced pressure (60° C., 2.4 kPa), to provide 1.8 g of 1-(t-butylamino)-2-dimethylaminoethane. (Isolation yield: 36%)
The reaction was conducted in the same way as in Reference Example A2, except that 7.3 g (0.10 mol) of s-butylamine was used instead of isopropylamine. Then, the reaction solution was concentrated, and the resultant concentrate was distilled under reduced pressure (65° C., 2.0 kPa), to provide 1.7 g of 1-(s-butylamino)-2-dimethylaminoethane. (Isolation yield: 34%)
The reaction was conducted in the same way as in Reference Example A2, except that 5.5 g (35 mmol) of 3-(dimethylamino)propyl chloride hydrochloride was used instead of 5.0 g (35 mmol) of 2-(dimethylamino)ethyl chloride hydrochloride. Then, the reaction solution was concentrated, and the resultant concentrate was distilled under reduced pressure (60° C., 0.80 kPa), to provide 2.2 g of (t-butyl)(3-(dimethylamino)propylamine. (Isolation yield: 40%)
Into a 50 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 16 g (0.22 mol) of t-butylamine, 5.0 g (35 mmol) of 2-(dimethylamino)ethyl chloride hydrochloride and 1 ml of water. And then, the mixture was reacted at 70° C. for 10 hours. After the completion of the reaction, the reaction solution was subjected to extraction with 25 ml of hexane twice, and the hexane layer was concentrated under reduced pressure. The resultant concentrate was distilled under reduced pressure (60° C., 2.4 kPa), to provide 3.0 g of 1-(t-butylamino)-2-dimethylaminoethane. (Isolation yield: 60%)
Under argon atmosphere, into a 25 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 0.69 g (5.0 mmol) of dibutyl magnesium prepared in Reference Example A1 and 10 ml of heptane. And then, 1.3 g (10 mmol) of 1-isopropylamino-2-dimethylaminoethane prepared in Reference Example A2 was slowly dropped into the flask, and the mixture was reacted while stirring at 90° C. for 6 hours. After the completion of the reaction, the reaction solution was concentrated, and the resultant concentrate was distilled under reduced pressure (80° C., 13 Pa), to provide 1.3 g of bis(1-isopropylamide-2-dimethylaminoethane-N,N′) magnesium as a colorless and transparent liquid. (Isolation yield: 92%) The compound was maintained at 25° C. for several hours, to change into a white solid.
Additionally, bis(1-isopropylamide-2-dimethylaminoethane-N,N′) magnesium was a novel compound, which had the following properties:
1H-NMR (tetrahydrofuran-d8, δ (ppm)); 2.99 (4H, t, 5.8 Hz), 2.85 (2H, sept, 6.3 Hz), 2.61 (4H, t, 5.8 Hz), 2.35 (12H, s), 1.01 (12H, d, 6.3 Hz)
Melting point; 53-55° C.
The reaction was conducted in the same way as in Example A1, except that 1.4 g (10 mmol) of 1-(t-butylamino)-2-dimethylaminoethane prepared in Reference Example A3 was used instead of 1-isopropylamino-2-dimethylaminoethane. Then, the reaction solution was concentrated, and the resultant concentrate was sublimed under reduced pressure (90° C., 13 Pa), to provide 1.2 g of bis(1-(t-butylamide)-2-dimethylaminoethane-N,N′) magnesium as a white solid. (Isolation yield: 77%)
Additionally, bis(1-(t-butylamide)-2-dimethylaminoethane-N,N′) magnesium was a novel compound, which had the following properties:
1H-NMR (tetrahydrofuran-d8, δ (ppm)); 3.00 (4H, t, 5.8 Hz), 2.58 (4H, t, 5.8 Hz), 2.34 (12H, s), 1.08 (18H, s)
Melting point; 90-93° C.
The reaction was conducted in the same way as in Example A1, except that 1.4 g (10 mmol) of 1-(s-butylamino)-2-dimethylaminoethane prepared in Reference Example A4 was used instead of 1-isopropylamino-2-dimethylaminoethane. Then, the reaction solution was concentrated, and the resultant concentrate was distilled under reduced pressure (90° C., 13 Pa), to provide 1.4 g of bis(1-(s-butylamide)-2-dimethylaminoethane-N,N′) magnesium as a colorless and transparent liquid. (Isolation yield: 90%)
Additionally, bis(1-(s-butylamide)-2-dimethylaminoethane-N,N′) magnesium was a novel compound, which had the following properties:
1H-NMR (tetrahydrofuran-d8, δ (ppm)); 2.98 (6H, m), 2.60 (4H, m), 2.35 (12H, s), 1.53 (2H, m), 1.16 (2H, m), 1.00 (6H, m), 0.85 (6H, m)
The reaction was conducted in the same way as in Example A1, except that 1.2 g (10 mmol) of 1-ethylamino-2-dimethylaminoethane (commercially available product) was used instead of 1-isopropylamino-2-dimethylaminoethane. Then, the reaction solution was concentrated, and the resultant concentrate was distilled under reduced pressure (110° C., 13 Pa), to provide 0.90 g of bis(1-ethylamide-2-dimethylaminoethane-N,N′) magnesium as a colorless and transparent liquid. (Isolation yield: 71%)
Additionally, bis(1-ethylamide-2-dimethylaminoethane-N,N′) magnesium was a novel compound, which had the following properties:
1H-NMR (tetrahydrofuran-d8, δ (ppm)); 2.93 (4H, br), 2.90 (4H, br), 2.63 (4H, br), 2.15 (12H, br), 1.00 (6H, br)
The reaction was conducted in the same way as in Example A1, except that 1.4 g (10 mmol) of 1-ethylamino-2-diethylaminoethane (commercially available product) was used instead of 1-isopropylamino-2-dimethylaminoethane. Then, the reaction solution was concentrated, and the resultant concentrate was distilled under reduced pressure (130° C., 13 Pa), to provide 1.0 g of bis(1-ethylamide-2-diethylaminoethane-N,N′) magnesium as a colorless and transparent liquid. (Isolation yield: 60%)
Additionally, bis(1-ethylamide-2-diethylaminoethane-N,N′) magnesium was a novel compound, which had the following properties:
1H-NMR (tetrahydrofuran-d8, δ (ppm)); 2.97 (4H, br), 2.78 (8H, br), 2.45 (8H, br), 1.10 (6H, br), 0.96 (12H, br)
The reaction was conducted in the same way as in Example A1, except that 1.6 g (10 mmol) of (t-butyl)(3-(dimethylamino)propylamine prepared in Reference Example A5 was used instead of 1-isopropylamino-2-dimethylaminoethane. Then, the reaction solution was concentrated, and the resultant concentrate was distilled under reduced pressure (90° C., 13 Pa), to provide 1.4 g of bis(1-(t-butylamide)-3-dimethylaminopropane-N,N′) magnesium as a colorless and transparent liquid. (Isolation yield: 76%)
Additionally, bis(1-(t-butylamide)-3-dimethylaminopropane-N,N′) magnesium was a novel compound, which had the following properties:
1H-NMR (tetrahydrofuran-d8, δ (ppm)); 3.04 (4H, t, 5.8 Hz), 2.51 (4H, t, 5.8 Hz), 2.39 (12H, s), 1.60 (4H, m), 1.10 (18H, s)
Melting point; 110-114° C.
The vapor-deposition tests were conducted by the CVD method, using bis(1-isopropylamide-2-dimethylaminoethane-N,N′)magnesium (magnesium compound (6)) obtained in Example A1, to evaluate the film-forming performance.
The apparatus shown in
The vapor-deposition conditions and the film properties were as follows.
(Vapor-deposition Conditions)
(Film Properties (XPS-Depth Measurement))
(Vapor-deposition Test; Formation of Magnesium-Containing Thin Film)
The vapor-deposition tests were conducted by the CVD method in the same way as in Example A7, using bis(cyclopentadienyl)magnesium, to evaluate the film-forming performance. The vapor-deposition conditions and the film properties were as follows. The vapor-deposition tests were conducted under the conditions where the amount of the raw material fed was equal to the amount of the raw material fed in Example A7 by adjusting the various conditions.
(Vapor-deposition Conditions)
(Film Properties (XPS-Depth Measurement))
The results revealed that a high-quality magnesium-containing thin film (magnesium oxide film), which does not contain impurities such as carbon atom and nitrogen atom, might be formed using the bis(amide amino alkane) magnesium compound of the present invention.
Under argon atmosphere, into a 50 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 2.15 g (16.5 mmol) of 1-isopropylamino-2-dimethylaminoethane and 15 ml of hexane. And then, while maintaining the solution temperature at 0° C., 10 ml (16.5 mmol) of 1.65 mol/l n-butyl lithium/hexane solution was slowly dropped into the flask, and the mixture was reacted while stirring at the same temperature for 30 minutes and at 20° C. for 2 hours. After the completion of the reaction, the reaction solution was concentrated under reduced pressure. The resultant concentrate was dried under vacuum, to provide 2.13 g of (1-isopropylamide-2-dimethylaminoethane-N,N′)lithium. (Isolation yield: 95%)
Additionally, (1-isopropylamide-2-dimethylaminoethane-N,N′) lithium had the following properties:
1H-NMR (tetrahydrofuran-d8, δ (ppm)); 2.95 (2H, t, 6.0 Hz), 2.91 (1H, quint, 6.2 Hz), 2.44 (2H, t, 6.0 Hz), 2.18 (6H, s), 0.99 (6H, d, 6.2 Hz)
Under argon atmosphere, into a 50 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 0.500 g (3.85 mmol) of cobalt(II) chloride (pre-dried anhydride) and 10 ml of tetrahydrofuran. And then, these were mixed and the mixture was stirred for 2 hours. Subsequently, while maintaining the solution temperature at 0° C., 10 ml of solution of 1.05 g (7.71 mmol) of 1-isopropylamide-2-dimethylaminoethane-N,N′) lithium, which was prepared in the same way as in Reference Example B1, in tetrahydrofuran was slowly dropped into the flask. And then, the mixture was reacted while stirring at 20° C. for 6 hours. After the completion of the reaction, the reaction solution was concentrated under reduced pressure. To the resultant concentrate was added 50 ml of hexane. And then, the mixture was stirred. The mixture was filtrated, and the filtrate was concentrated under reduced pressure. And then, the resultant concentrate was distilled under reduced pressure (80° C., 13.3 Pa), to provide 1.0 g of (bis(1-isopropylamide-2-dimethylaminoethane-N,N′) cobalt(II) as a dark green solid. (Isolation yield: 80%)
Additionally, bis(1-isopropylamide-2-dimethylaminoethane-N,N′) cobalt(II) was a novel compound, which had the following properties:
Melting point; 68-69° C.
Cobalt content determined by inductively coupled plasma (ICP) analysis; 19.2 wt % (calculated value; 18.6 wt %)
Under argon atmosphere, into a 50 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 2.59 g (16.5 mmol) of 1-s-butylamino-2-dimethylaminoethane prepared in Reference Example A4 and 15 ml of hexane. And then, while maintaining the mixture solution at 0° C., 10 ml (16.5 mmol) of 1.65 mold n-butyl lithium/hexane solution was slowly dropped into the flask. After the dropping, the mixture solution was stirred at 0° C. for 30 minutes, and then the mixture was reacted while stirring at 20° C. for 2 hours. After the completion of the reaction, the reaction solution was concentrated under reduced pressure. The resultant concentrate was dried under vacuum, to provide 1-s-butylamide-2-dimethylaminoethane-N,N′) lithium. Additionally, 1-s-butylamide-2-dimethylaminoethane-N,N′) lithium was used for the subsequent reaction without any purification.
Into a 300 mL-volume flask equipped with a stirrer and a thermometer were placed 20.6 g (143 mmol) of 2-(dimethylamino)ethane chloride hydrochloride and 74.0 g (859 mmol) of t-pentylamine. And then, the mixture was heated to reflux for 8 hours. After the completion of the reaction, the reaction mixture was filtrated and washed with 100 ml of hexane twice, and the hexane layer was concentrated under reduced pressure. The resultant concentrate was distilled under reduced pressure (120° C., 11.0 kPa), to provide 13.5 g of 1-t-pentylamino-2-dimethylaminoethane. (Isolation yield: 60%)
Under argon atmosphere, into a 100 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 1.07 g (8.25 mmol) of anhydrous cobalt(II) chloride and 20 ml of tetrahydrofuran. And then, the mixture was stirred for 2 hours. Subsequently, while maintaining the solution temperature at 0° C., 20 ml of solution of 1-s-butylamide-2-dimethylaminoethane-N,N′) lithium, which was prepared in Reference Example B2, in tetrahydrofuran was slowly dropped into the flask. And then, the mixture was reacted while stirring at 20° C. for 6 hours. After the completion of the reaction, the reaction solution was concentrated under reduced pressure. To the resultant concentrate was added 100 ml of hexane. And then, the mixture was stirred. The mixture was filtrated, and the filtrate was concentrated under reduced pressure. And then, the resultant concentrate was distilled under reduced pressure (90° C., 13.3 Pa), to provide 0.8 g of (bis(1-s-butylamide-2-dimethylaminoethane-N,N′)cobalt as a dark green liquid. (Isolation yield: 27%)
Additionally, bis(1-s-butylamide-2-dimethylaminoethane-N,N′) cobalt was a novel compound, which had the following properties:
Co content determined by ICP analysis; 16.03 wt % (calculated value; 17.06 wt %)
Under argon atmosphere, into a 50 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 2.69 g (16.5 mmol) of 1-t-pentylamino-2-dimethylaminoethane prepared in Reference Example B3 and 15 ml of hexane. And then, while maintaining the mixture solution at 0° C., 10 ml (16.5 mmol) of 1.65 mol/l n-butyl lithium/hexane solution was slowly dropped into the flask. After the dropping, the mixture solution was stirred at 0° C. for 30 minutes, and then the mixture was reacted while stirring at 20° C. for 2 hours. After the completion of the reaction, the reaction solution was concentrated under reduced pressure. The resultant concentrate was dried under vacuum, to provide 1-t-pentylamide-2-dimethylaminoethane-N,N′ lithium. Additionally, 1-t-pentylamide-2-dimethylaminoethane-N,N′ lithium was used for the subsequent reaction without any purification.
Under argon atmosphere, into a 100 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 1.07 g (8.25 mmol) of anhydrous cobalt(II) chloride and 20 ml of tetrahydrofuran. And then, the mixture was stirred for 2 hours. Subsequently, while maintaining the solution temperature at 0° C., 20 ml of solution of 1-t-pentylamide-2-dimethylaminoethane-N,N′) lithium, which was prepared in Reference Example B4, in tetrahydrofuran was slowly dropped into the flask. And then, the mixture was reacted while stirring at 20° C. for 6 hours. After the completion of the reaction, the reaction solution was concentrated under reduced pressure. To the resultant concentrate was added 100 ml of hexane. And then, the mixture was stirred. The mixture was filtrated, and the filtrate was concentrated under reduced pressure. And then, the resultant concentrate was distilled under reduced pressure (100° C., 13.3 Pa), to provide 1.45 g of (bis(1-t-pentylamide-2-dimethylaminoethane-N,N′)cobalt as a dark green liquid. (Isolation yield: 47%)
Additionally, bis(1-t-pentylamide-2-dimethylaminoethane-N,N′) cobalt was a novel compound, which had the following properties:
Co content determined by ICP analysis; 15.80 wt % (calculated value; 15.80 wt %)
Under argon atmosphere, into a 100 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 1.07 g (8.25 mmol) of anhydrous cobalt(II) chloride and 20 ml of tetrahydrofuran. And then, the mixture was stirred for 2 hours. Subsequently, while maintaining the solution temperature at 0° C., 20 ml of solution of 1-t-butylamide-2-dimethylaminoethane-N,N′) lithium, which was prepared in Reference Example D3, in tetrahydrofuran was slowly dropped into the flask. And then, the mixture was reacted while stirring at 20° C. for 6 hours. After the completion of the reaction, the reaction solution was concentrated under reduced pressure. To the resultant concentrate was added 100 ml of hexane. And then, the mixture was stirred. The mixture was filtrated, and the filtrate was concentrated under reduced pressure. And then, the resultant concentrate was distilled under reduced pressure (95° C., 13.3 Pa), to provide 1.2 g of (bis(1-t-butylamide-2-dimethylaminoethane-N,N′) cobalt as a dark green solid. (Isolation yield: 42%)
Additionally, bis(1-t-butylamide-2-dimethylaminoethane-N,N′) cobalt was a novel compound, which had the following properties:
Co content determined by ICP analysis; 16.5 wt % (calculated value; 17.1 wt %)
The vapor-deposition tests were conducted by the CVD method, using bis(1-isopropylamide-2-dimethylaminoethane-N,N′)cobalt(II) (cobalt compound (8)) obtained in Example B1, to evaluate the film-forming performance.
The apparatus shown in
The vapor-deposition conditions and the film properties were as follows. The rectangular substrate of 6 mm×20 mm was used as the substrate on which the film was vapor-deposited.
(Vapor-deposition Conditions)
(Film Properties (SEM and XPS-Depth Measurement))
The vapor-deposition tests were conducted by the CVD method in the same way as in Example B5, using bis(1-s-butylamide-2-dimethylaminoethane-N,N′) cobalt(II) (cobalt compound (10)) obtained in Example B2, to evaluate the film-forming performance. The vapor-deposition conditions and the film properties were as follows.
(Vapor-deposition Conditions)
(Film Properties (SEM and XPS-Depth Measurement))
(Vapor-deposition Test; Formation of Cobalt-containing Thin Film)
The vapor-deposition tests were conducted by the CVD method in the same way as in Example B5, using bis(N-t-butyl-N′-ethylpropionamidinato) cobalt (the compound disclosed in Patent Document 8), to evaluate the film-forming performance. The vapor-deposition conditions and the film properties were as follows.
(Vapor-deposition Conditions)
(Film Properties (SEM and XPS-Depth Measurement))
The results revealed that the bis(amide amino alkane) cobalt compound of the present invention might be a material from which a cobalt-containing thin film might be formed in a short time (high film-forming rate), and from which a high-quality cobalt-containing thin film, which does not contain impurities such as carbon atom and nitrogen atom, might be formed.
Into a 300 mL-volume flask equipped with a stirrer and a thermometer were placed 25.0 g (158 mmol) of 2-(dimethylamino)propane chloride hydrochloride, 56.1 g (949 mmol) of isopropylamine and 3 ml of water. And then, the mixture was reacted while stirring at 40-50° C. for 10 hours. After the completion of the reaction, the reaction mixture was filtrated and washed with 200 ml of hexane, and the hexane layer was concentrated under reduced pressure. The resultant concentrate was distilled under reduced pressure (105° C., 13.3 kPa), to provide 18.2 g of a mixture of 1-isopropylamino-2-dimethylaminopropane and 2-isopropylamino-1-dimethylaminopropane (mixture ratio 8:2). (Isolation yield: 82%)
Additionally, the mixture of 1-isopropylamino-2-dimethylaminopropane and 2-isopropylamino-1-dimethylaminopropane had the following properties:
1H-NMR (CDCl3, δ (ppm)); 0.89 (3H, s, for major isomer), 0.97 (3H, s, for minor isomer), 1.05, 1.07 (each 3H, each d, J=6.3 Hz, for major isomer), 1.05, 1.10 (each 3H, each d, J=6.3 Hz, for minor isomer), 1.52 (1H, drs), 2.19 (6H, s, for minor isomer), 2.20 (6H, s, for major isomer), 2.48 (2H, d, J=6.8 Hz, for major isomer), 2.50 (2H, d, J=6.8 Hz, for minor isomer), 2.68-2.89 (2H, m)
Under argon atmosphere, into a 50 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 2.15 g (16.5 mmol) of the mixture of 1-isopropylamino-2-dimethylaminopropane and 2-isopropylamino-1-dimethylaminopropane (mixture ratio 8:2) prepared in Reference Example C1, and 15 ml of hexane. And then, while maintaining the mixture solution at 0° C., 10 ml (16.5 mmol) of 1.65 mol/l n-butyl lithium/hexane solution was slowly dropped into the flask. After the dropping, the mixture solution was stirred at 0° C. for 30 minutes, and then the mixture was reacted while stirring at 20° C. for 2 hours. After the completion of the reaction, the reaction solution was concentrated under reduced pressure. The resultant concentrate was dried under vacuum, to provide a mixture of 1-isopropylamide-2-dimethylaminoethane-N,N′) lithium and 2-isopropylamide-1-dimethylaminoethane-N,N′)lithium.
Additionally, the mixture of 1-isopropylamide-2-dimethylaminoethane-N,N′) lithium and 2-isopropylamide-1-dimethylaminoethane-N,N′)lithium was used for the subsequent reaction without any treatment.
Under argon atmosphere, into a 100 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 1.07 g (8.25 mmol) of anhydrous cobalt(II) chloride and 20 ml of tetrahydrofuran. And then, the mixture was stirred for 2 hours. Subsequently, while maintaining the solution temperature at 0° C., 20 ml of solution of the mixture of 1-isopropylamide-2-dimethylaminoethane-N,N′) lithium and 2-isopropylamide-1-dimethylaminoethane-N,N′) lithium, which was prepared in Reference Example C2, in tetrahydrofuran was slowly dropped into the flask. And then, the mixture was reacted while stirring at 20° C. for 6 hours. After the completion of the reaction, the reaction solution was concentrated under reduced pressure. To the resultant concentrate was added 100 ml of hexane. And then, the mixture was stirred. The mixture was filtrated, and the filtrate was concentrated under reduced pressure. And then, the resultant concentrate was distilled under reduced pressure (95° C., 13.3 Pa), to provide 1.9 g of a mixture of bis(1-isopropylamide-2-dimethylaminopropane-N,N′) cobalt, bis(2-isopropylamide-1-dimethylaminopropane-N,N′) cobalt and (1-isopropylamide-2-dimethylaminopropane-N,N′)(2-isopropylamide-1-dimethylaminopropane-N,N′) cobalt as a dark brown solid. (Isolation yield: 67%)
Additionally, the mixture of bis(1-isopropylamide-2-dimethylaminopropane-N,N′) cobalt, bis(2-isopropylamide-1-dimethylaminopropane-N,N′) cobalt and (1-isopropylamide-2-dimethylaminopropane-N,N′)(2-isopropylamide-1-dimethylaminopropane-N,N′) cobalt was a novel compound, which had the following properties:
Melting point; 90° C.
Cobalt content determined by inductively coupled plasma (ICP) analysis; 16.4 wt % (calculated value; 17.06 wt %)
Into a 200 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 12.0 g (75.9 mmol) of the mixture of 1-isopropylamino-2-dimethylaminopropane and 2-isopropylamino-1-dimethylaminopropane (mixture ratio 8:2) prepared in Reference Example C1, and 50 ml of methanol. And then, the mixture was stirred and heated to 60-70° C. Subsequently, a solution of 13.7 g (151.8 mmol) of oxalic acid and 60 ml of methanol was slowly dropped into the flask, and then the mixture was reacted while stirring at 20° C. for 1 hour. The reaction mixture solution was filtrated, and the filtrate was concentrated under reduced pressure. To the resultant concentrate were added 100 ml of water and 17.0 g (303.6 mmol) of potassium hydroxide. And then, the mixture was subjected to extraction with 50 ml of chloroform three times, and the extract was concentrated under reduced pressure. The resultant concentrate was distilled under reduced pressure (105° C., 13.3 kPa), to provide 7.6 g of 1-isopropylamino-2-dimethylaminopropane. (Isolation yield: 76%)
Additionally, 1-isopropylamino-2-dimethylaminopropane had the following properties. The purity was 100%©, determined by 1H-NMR.
1H-NMR (CDCl3, δ (ppm)); 0.89 (3H, s), 1.05, 1.07 (each 3H, each d, J=6.3 Hz), 1.75 (1H, drs), 2.20 (6H, s), 2.49 (2, d, J=6.8 Hz), 2.68-2.83 (2H, m)
Under argon atmosphere, into a 50 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 2.15 g (16.5 mmol) of 1-isopropylamino-2-dimethylaminopropane prepared in Reference Example C3, and 15 ml of hexane. And then, while maintaining the mixture solution at 0° C., 10 ml (16.5 mmol) of 1.65 mold n-butyl lithium/hexane solution was slowly dropped into the flask. After the dropping, the mixture solution was stirred at 0° C. for 30 minutes, and then the mixture was reacted while stirring at 20° C. for 2 hours. After the completion of the reaction, the reaction solution was concentrated under reduced pressure. The resultant concentrate was dried under vacuum, to provide (1-isopropylamide-2-dimethylaminopropane-N,N′) lithium.
Additionally, (1-isopropylamide-2-dimethylaminopropane-N,N′) lithium was used for the subsequent reaction without any treatment.
Under argon atmosphere, into a 100 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 1.07 g (8.25 mmol) of anhydrous cobalt(II) chloride and 20 ml of tetrahydrofuran. And then, the mixture was stirred for 2 hours. Subsequently, while maintaining the solution temperature at 0° C., 20 ml of solution of 1 isopropylamide-2-dimethylaminopropane-N,N′)lithium, which was prepared in Reference Example C4, in tetrahydrofuran was slowly dropped into the flask. And then, the mixture was reacted while stirring at 20° C. for 6 hours. After the completion of the reaction, the reaction solution was concentrated under reduced pressure. To the resultant concentrate was added 100 ml of hexane. And then, the mixture was stirred. The mixture was filtrated, and the filtrate was concentrated under reduced pressure. And then, the resultant concentrate was distilled under reduced pressure (95° C., 13.3 Pa), to provide 1.2 g of bis(1-isopropylamide-2-dimethylaminopropane-N,N′) cobalt as a dark brown solid. (Isolation yield: 43%)
Into a 300 mL-volume flask equipped with a stirrer and a thermometer were placed 25.0 g (158 mmol) of 2-(dimethylamino)propane chloride hydrochloride and 69.4 g (949 mmol) of s-butylamine. And then, the mixture was reacted while stirring at 80-90° C. for 10 hours. After the completion of the reaction, the reaction mixture was filtrated and washed with 200 ml of hexane, and the hexane layer was concentrated under reduced pressure. The resultant concentrate was distilled under reduced pressure (110° C., 11 kPa), to provide 21.7 g of a mixture of 1-(s-butylamino)-2-dimethylaminopropane and 2-s-butylamino-1-dimethylaminopropane (mixture ratio 8:2). (Isolation yield: 87%)
Additionally, the mixture of 1-(s-butylamino)-2-dimethylaminopropane and 2-s-butylamino-1-dimethylaminopropane had the following properties:
1H-NMR (CDCl3, δ (ppm)); 0.95 (9H, m), 1.29 (1H, m), 1.50 (1H, m), 1.70 (1H, br), 2.20 (6H, s), 2.48 (3H, m), 2.73 (1H, m)
Under argon atmosphere, into a 50 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 2.65 g (16.5 mmol) of the mixture of 1-(s-butylamino)-2-dimethylaminopropane and 2-s-butylamino-1-dimethylaminopropane (mixture ratio 8:2) prepared in Reference Example C5, and 15 ml of hexane. And then, while maintaining the mixture solution at 0° C., 10 ml (16.5 mmol) of 1.65 mol/l n-butyl lithium/hexane solution was slowly dropped into the flask. After the dropping, the mixture solution was stirred at 0° C. for 30 minutes, and then the mixture was reacted while stirring at 20° C. for 2 hours. After the completion of the reaction, the reaction solution was concentrated under reduced pressure. The resultant concentrate was dried under vacuum, to provide a mixture of 1-(s-butylamide)-2-dimethylaminopropane-N,N′) lithium and 2-(s-butylamide)-1-dimethylaminopropane-N,N′)lithium.
Additionally, the mixture of 1-(s-butylamide)-2-dimethylaminopropane-N,N′)lithium and 2-(s-butylamide)-1-dimethylaminopropane-N,N′)lithium was used for the subsequent reaction without any treatment.
Under argon atmosphere, into a 100 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 1.07 g (8.25 mmol) of anhydrous cobalt(II) chloride and 20 ml of tetrahydrofuran. And then, the mixture was stirred for 2 hours. Subsequently, while maintaining the solution temperature at 0° C., 20 ml of solution of the mixture of 1-(s-butylamide)-2-dimethylaminopropane-N,N′) lithium and 2-(s-butylamide)-1-dimethylaminopropane-N,N′) lithium, which was prepared in Reference Example C6, in tetrahydrofuran was slowly dropped into the flask. And then, the mixture was reacted while stirring at 20° C. for 6 hours. After the completion of the reaction, the reaction solution was concentrated under reduced pressure. To the resultant concentrate was added 100 ml of hexane. And then, the mixture was stirred. The mixture was filtrated, and the filtrate was concentrated under reduced pressure. And then, the resultant concentrate was distilled under reduced pressure (105° C., 13.3 Pa), to provide 2.1 g of a mixture of (bis(1-(s-butylamide)-2-dimethylaminopropane-N,N′) cobalt, (bis(2-(s-butylamide)-1-dimethylaminopropane-N,N′) cobalt and (1-(s-butylamide)-2-dimethylaminopropane-N,N′)(2-(s-butylamide)-1-dimethylaminopropane-N,N′) cobalt as a dark brown liquid. (Isolation yield: 68%)
Additionally, the mixture of bis(1-(s-butylamide)-2-dimethylaminopropane-N,N′)cobalt, bis(2-(s-butylamide)-1-dimethylaminopropane-N,N′)cobalt and (1-(s-butylamide)-2-dimethylaminopropane-N,N′)(2-(s-butylamide)-1-dimethylaminopropane-N,N′) cobalt was a novel compound, which had the following properties:
Cobalt content determined by inductively coupled plasma (ICP) analysis; 15.3 wt % (calculated value; 15.8 wt %)
Into a 300 mL-volume flask equipped with a stirrer and a thermometer were placed 25.0 g (158 mmol) of 2-(dimethylamino)propane chloride hydrochloride, 69.4 g (949 mmol) of t-butylamine and 3 ml of water. And then, the mixture was reacted while stirring at 60° C. for 10 hours. After the completion of the reaction, the reaction mixture was filtrated and washed with 200 ml of hexane, and the hexane layer was concentrated under reduced pressure. The resultant concentrate was distilled under reduced pressure (120° C., 12 kPa), to provide 19.2 g of a mixture of 1-t-butylamino-2-dimethylaminopropane and 2-t-butylamino-1-dimethylaminopropane (mixture ratio 8:2). (Isolation yield: 77%)
Additionally, the mixture of 1-t-butylamino-2-dimethylaminopropane and 2-t-butylamino-1-dimethylaminopropane had the following properties:
1H-NMR(CDCl3, δ (ppm)); 0.89 (3H, t, 6.5 Hz), 1.10 (9H, s), 1.40 (1H, brs), 2.18 (6H, s), 2.38 (1H, m), 2.53 (1H, t, 11.0 Hz), 2.48 (3H, m), 2.67-2.77 (1H, m)
Under argon atmosphere, into a 50 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 3.15 g (19.9 mmol) of the mixture of 1-t-butylamino-2-dimethylaminopropane and 2-t-butylamino-1-dimethylaminopropane (mixture ratio 8:2) prepared in Reference Example C7, and 15 ml of hexane. And then, while maintaining the mixture solution at 0° C., 10 ml (16.5 mmol) of 1.65 mol/l n-butyl lithium/hexane solution was slowly dropped into the flask. After the dropping, the mixture solution was stirred at 0° C. for 30 minutes, and then the mixture was reacted while stirring at 20° C. for 2 hours. After the completion of the reaction, the reaction solution was concentrated under reduced pressure. The resultant concentrate was dried under vacuum, to provide a mixture of 1-t-butylamide-2-dimethylaminopropane-N,N′)lithium and 2-t-butylamide-1-dimethylaminopropane-N,N′)lithium.
Additionally, the mixture of 1-t-butylamide-2-dimethylaminopropane-N,N′) lithium and 2-t-butylamide-1-dimethylaminopropane-N,N′) lithium was used for the subsequent reaction without any treatment.
Under argon atmosphere, into a 100 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 1.07 g (8.25 mmol) of anhydrous cobalt(II) chloride and 20 ml of tetrahydrofuran. And then, the mixture was stirred for 2 hours. Subsequently, while maintaining the solution temperature at 0° C., 20 ml of solution of the mixture of 1-t-butylamide-2-dimethylaminopropane-N,N′) lithium and 2-t-butylamide-1-dimethylaminopropane-N,N′) lithium, which was prepared in Reference Example C8, in tetrahydrofuran was slowly dropped into the flask. And then, the mixture was reacted while stirring at 20° C. for 6 hours. After the completion of the reaction, the reaction solution was concentrated under reduced pressure. To the resultant concentrate was added 100 ml of hexane. And then, the mixture was stirred. The mixture was filtrated, and the filtrate was concentrated under reduced pressure. And then, the resultant concentrate was distilled under reduced pressure (115° C., 13.3 Pa), to provide 2.9 g of a mixture of bis(1-t-butylamide-2-dimethylaminopropane-N,N′) cobalt, bis(2-t-butylamide-1-dimethylaminopropane-N,N′)cobalt and (1-t-butylamide-2-dimethylaminopropane-N,N′)(2-t-butylamide-1-dimethylaminopropane-N,N′) cobalt as a dark brown solid. (Isolation yield: 94%)
Additionally, the mixture of bis(1-t-butylamide-2-dimethylaminopropane-N,N′) cobalt, bis(2-t-butylamide-1-dimethylaminopropane-N,N′) cobalt and (1-t-butylamide-2-dimethylaminopropane-N,N′)(2-t-butylamide-1-dimethylaminopropane-N,N′) cobalt was a novel compound, which had the following properties:
Melting point; 90° C.
Cobalt content determined by inductively coupled plasma (ICP) analysis; 15.0 wt % (calculated value; 15.8 wt %)
The vapor-deposition tests were conducted by the CVD method in the same way as in Example B5, using the cobalt compound obtained in Example C1, to evaluate the film-forming performance. The vapor-deposition conditions and the film properties were as follows.
(Vapor-deposition Conditions)
Cobalt raw material; the cobalt compound obtained in Example C1
(Mixture of bis(1-isopropylamide-2-dimethylaminopropane-N,N′) cobalt (compound (1c)), bis(2-isopropylamide-1-dimethylaminopropane-N,N′) cobalt (compound (1j)) and (1-isopropylamide-2-dimethylaminopropane-N,N′)(2-isopropylamide-1-dimethylaminopropane-N,N′) cobalt (compound (N)))
(Film Properties (SEM and XPS-Depth Measurement)
The vapor-deposition tests were conducted by the CVD method in the same way as in Example B5, using the cobalt compound obtained in Example C2, to evaluate the film-forming performance. The vapor-deposition conditions and the film properties were as follows.
(Vapor-deposition Conditions)
Cobalt raw material; the cobalt compound obtained in Example C2
(Bis(1-isopropylamide-2-dimethylaminopropane-N,N′)cobalt (Compound (1c))
(Film Properties (SEM and XPS-Depth Measurement))
The vapor-deposition tests were conducted by the CVD method in the same way as in Example B5, using the cobalt compound obtained in Example C3, to evaluate the film-forming performance. The vapor-deposition conditions and the film properties were as follows.
(Vapor-deposition Conditions)
Cobalt raw material; the cobalt compound obtained in Example C3
(Mixture of bis(1-(s-butylamide)-2-dimethylaminopropane-N,N′) cobalt (Compound (1e)), bis(2-(s-butylamide)-1-dimethylaminopropane-N,N′) cobalt (Compound (1l)) and (1-(s-butylamide)-2-dimethylaminopropane-N,N′)(2-(s-butylamide)-1-dimethylaminopropane-N,N′)cobalt (Compound (1s))
(Film Properties (SEM and XPS-Depth Measurement))
The vapor-deposition tests were conducted by the CVD method in the same way as in Example B5, using the cobalt compound obtained in Example C4, to evaluate the film-forming performance. The vapor-deposition conditions and the film properties were as follows.
(Vapor-deposition Conditions)
Cobalt raw material; the cobalt compound obtained in Example C4
(Mixture of bis(1-t-butylamide-2-dimethylaminopropane-N,N′)cobalt (Cobalt Compound (1d)), bis(2-t-butylamide-1-dimethylaminopropane-N,N′) cobalt (Cobalt Compound (1k)) and (1-t-butylamide-2-dimethylaminopropane-N,N′)(2-t-butylamide-1-dimethylaminopropane-N,N′)cobalt (Cobalt Compound (1r))
(Film Properties (SEM and XPS-Depth Measurement))
(Vapor-deposition Test; Formation of Cobalt-containing Thin Film)
The vapor-deposition tests were conducted by the CVD method in the same way as in Example B5, using bis(N-t-butyl-N′-ethylpropionamidinato) cobalt (the compound disclosed in Patent Document 8), to evaluate the film-forming performance. The vapor-deposition conditions and the film properties were as follows.
(Vapor-deposition Conditions)
Cobalt compound; bis(N-t-butyl-N′-ethylpropionamidinato) cobalt (the compound disclosed in Patent Document 8)
(Film Properties (SEM and XPS-Depth Measurement))
The results revealed that the bis(amide amino alkane) cobalt compound of the present invention might be a material from which a cobalt-containing thin film might be formed in a short time (high film-forming rate), and from which a high-quality cobalt-containing thin film, which does not contain impurities such as carbon atom and nitrogen atom, might be formed.
Under argon atmosphere, into a 50 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 2.1 g (16 mmol) of 1-isopropylamino-2-dimethylaminoethane and 15 ml of hexane. And then, while maintaining the solution temperature at 0° C., 10 ml (16 mmol) of 1.6 mol/l n-butyl lithium/hexane solution was slowly dropped into the flask, and the mixture was reacted while stirring at the same temperature for 30 minutes and at 20° C. for 2 hours. After the completion of the reaction, the reaction solution was concentrated under reduced pressure. The resultant concentrate was dried under vacuum, to provide 2.1 g of (1-isopropylamide-2-dimethylaminoethane-N,N′)lithium. (Isolation yield: 94%)
Additionally, (1-isopropylamide-2-dimethylaminoethane-N,N′) lithium had the following properties:
1H-NMR (tetrahydrofuran-d8, δ (ppm)); 2.95 (2H, t, 6.0 Hz), 2.91 (1H, quint, 6.2 Hz), 2.44 (2H, t, 6.0 Hz), 2.18 (6H, s), 0.99 (6H, d, 6.2 Hz)
Under argon atmosphere, into a 50 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 0.48 g (3.8 mmol) of manganese(II) chloride (pre-dried anhydride) and 10 ml of tetrahydrofuran. And then, these were mixed and the mixture was stirred for 2 hours. Subsequently, while maintaining the solution temperature at 0° C., 10 ml of solution of 1.0 g (7.6 mmol) of (1-isopropylamide-2-dimethylaminoethane-N,N′) lithium, which was prepared in the same way as in Reference Example D1, in tetrahydrofuran was slowly dropped into the flask. And then, the mixture was reacted while stirring at 20° C. for 6 hours. After the completion of the reaction, the reaction solution was concentrated under reduced pressure. To the resultant concentrate was added 50 ml of hexane. And then, the mixture was stirred. The mixture was filtrated, and the filtrate was concentrated under reduced pressure. And then, the resultant concentrate was distilled under reduced pressure (80° C., 13.3 Pa), to provide 1.0 g of (bis(1-isopropylamide-2-dimethylaminoethane-N,N′) manganese(II) as a light brown liquid. (Isolation yield: 84%)
Additionally, bis(1-isopropylamide-2-dimethylaminoethane-N,N′) manganese(II) was a novel compound, which had the following properties:
Manganese content determined by inductively coupled plasma (ICP) analysis; 17.7 wt % (calculated value; 17.5 wt %)
The reaction was conducted in the same way as in Reference Example D1, except that 2.3 g (16 mmol) of 1-(t-butylamino)-2-dimethylaminoethane was used instead of 1-isopropylamino-2-dimethylaminoethane, to provide 2.4 g of 1-(t-butylamino)-2-dimethylaminoethane-N,N′)lithium. (Isolation yield: 96%)
The reaction was conducted in the same way as in Example D1, except that 10 ml of solution of 1.1 g (7.6 mmol) of 1-(t-butylamino)-2-dimethylaminoethane-N,N′) lithium in tetrahydrofuran was used instead of the solution of (1-isopropylamide-2-dimethylaminoethane-N,N′)lithium in tetrahydrofuran. Then, the reaction solution was concentrated, and the resultant concentrate was sublimed under reduced pressure (90° C., 13 Pa), to provide 1.1 g of bis(1-(t-butylamide)-2-dimethylaminoethane-N,N′) manganese as a light greenish brown solid. (Isolation yield: 85%)
Additionally, bis(1-(t-butylamide)-2-dimethylaminoethane-N,N′) manganese(II) was a novel compound, which had the following properties:
Melting point; 70-71° C.
Manganese content determined by inductively coupled plasma (ICP) analysis; 16.5 wt % (calculated value; 16.1 wt %)
The vapor-deposition tests were conducted by the CVD method, using bis(1-(t-butylamide)-2-dimethylaminoethane-N,N′) manganese(II) (manganese compound (9)) obtained in Example D2, to evaluate the film-forming performance.
The apparatus shown in
The vapor-deposition conditions and the film properties were as follows. The rectangular substrate of 6 mm×20 mm was used as the substrate on which the film was vapor-deposited.
(Vapor-deposition Conditions 1)
Manganese raw material; bis(1-(t-butylamide)-2-dimethylaminoethane-N,N′) manganese(II) (Manganese Compound (9)
(Film Properties (SEM and XPS-Depth Measurement, and Resistivity Determined by Four-Probe Method)
(Vapor-deposition Conditions 2)
Ammonia gas flow rate; 10 sccm
(Film Properties (Appearance Observation))
(Vapor-deposition Test; Formation of Manganese-Containing Thin Film)
The vapor-deposition tests were conducted by the CVD method in the same way as in Example D3, using bis(N,N′-diisopropylpentaneamidinato) manganese (the compound disclosed in Non-Patent Documents 9 and 10), to evaluate the film-forming performance. The vapor-deposition conditions and the film properties were as follows.
(Vapor-deposition Conditions 3)
A film was not formed under the conditions substantially similar to Example D3 (Vapor-deposition conditions 3).
(Vapor-deposition Conditions 4)
(Film Properties (Film Thickness, and Resistivity Determined by Four-Probe Method)
The results revealed that the bis(amide amino alkane) manganese compound of the present invention might be a material from which a manganese-containing thin film might be formed at a lower temperature and in a short time (high film-forming rate), and from which a high-quality manganese-containing thin film having a lower resistivity (which does not contain impurities such as carbon atom) might be formed.
Under argon atmosphere, into a 50 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 0.52 g (3.8 mmol) of zinc(II) chloride (pre-dried anhydride) and 10 ml of tetrahydrofuran. And then, these were mixed and the mixture was stirred for 2 hours. Subsequently, while maintaining the solution temperature at 0° C., 10 ml of solution of 1.0 g (7.6 mmol) of (1-isopropylamide-2-dimethylaminoethane-N,N′) lithium, which was prepared in the same way as in Reference Example D1, in tetrahydrofuran was slowly dropped into the flask. And then, the mixture was reacted while stirring at 20° C. for 6 hours. After the completion of the reaction, the reaction solution was concentrated under reduced pressure. To the resultant concentrate was added 50 ml of hexane. And then, the mixture was stirred. The mixture was filtrated, and the filtrate was concentrated under reduced pressure. And then, the resultant concentrate was distilled under reduced pressure (80° C., 13.3 Pa), to provide 1.1 g of (bis(1-isopropylamide-2-dimethylaminoethane-N,N′) zinc(II) as a colorless and transparent liquid. (Isolation yield: 89%)
Additionally, bis(1-isopropylamide-2-dimethylaminoethane-N,N′) zinc(II) was a novel compound, which had the following properties:
1H-NMR (tetrahydrofuran-d8, δ (ppm)); 3.01 (4H, t, 6.0 Hz), 2.91 (2H, quint, 6.2 Hz), 2.52 (4H, t, 6.0 Hz), 2.27 (12H, s), 1.03 (12H, d, 6.2 Hz)
Zinc content determined by inductively coupled plasma (ICP) analysis; 19.8 wt % (calculated value; 20.2 wt %)
The reaction was conducted in the same way as in Example E1, except that 10 ml of solution of 1.1 g (7.6 mmol) of 1-(t-butylamino)-2-dimethylaminoethane-N,N′)lithium, which was prepared in the same way as in Reference Example D2, in tetrahydrofuran was used instead of the solution of (1-isopropylamide-2-dimethylaminoethane-N,N′) lithium in tetrahydrofuran. Then, the reaction solution was concentrated, and the resultant concentrate was sublimed under reduced pressure (90° C., 13 Pa), to provide 1.2 g of bis(1-(t-butylamide)-2-dimethylaminoethane-N,N′) zinc(II) as a white solid. (Isolation yield: 90%)
Additionally, bis(1-(t-butylamide)-2-dimethylaminoethane-N,N′) zinc(II) was a novel compound, which had the following properties:
1H-NMR (tetrahydrofuran-d8, δ (ppm)); 3.03 (4H, t, 6.0 Hz), 2.50 (4H, t, 6.0 Hz), 2.26 (12H, s), 1.11 (18H, s)
Melting point; 98-100° C.
Zinc content determined by inductively coupled plasma (ICP) analysis; 18.5 wt % (calculated value; 18.6 wt %)
The vapor-deposition tests were conducted by the CVD method in the same way as in Example D3, using (bis(1-isopropylamide-2-dimethylaminoethane-N,N′) zinc(II)) obtained in Example E1, to evaluate the film-forming performance. The vapor-deposition conditions and the film properties were as follows.
(Vapor-deposition Conditions 1)
Zinc raw material; the zinc compound obtained in Example E1
(bis(1-isopropylamide-2-dimethylaminoethane-N,N′) zinc(II))
(Film Properties (XPS-Depth Measurement))
(Vapor-deposition Test; Formation of Zinc-Containing Thin Film)
The vapor-deposition tests were conducted by the CVD method in the same way as in Example E3, using bis(acetylacetonato)zinc (the compound disclosed in Patent Document 14), to evaluate the film-forming performance. The vapor-deposition conditions and the film properties were as follows.
(Vapor-deposition Conditions 2)
A film was not formed under the conditions substantially similar to Example E3 (Vapor deposition conditions 2).
(Vapor-deposition Conditions 3)
(Film Properties (XPS-Depth Measurement)
The results revealed that a high-quality zinc-containing thin film (zinc oxide film), which does not contain impurities such as carbon atom and nitrogen atom, might be formed using the bis(amide amino alkane) zinc compound of the present invention.
Under argon atmosphere, into a 50 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 0.48 g (3.8 mmol) of iron(II) chloride (pre-dried anhydride) and 10 ml of tetrahydrofuran. And then, these were mixed and the mixture was stirred for 2 hours. Subsequently, while maintaining the solution temperature at 0° C., 10 ml of solution of 1.0 g (7.6 mmol) of 1-isopropylamide-2-dimethylaminoethane-N,N′) lithium, which was prepared in the same way as in Reference Example D1, in tetrahydrofuran was slowly dropped into the flask. And then, the mixture was reacted while stirring at 20° C. for 6 hours. After the completion of the reaction, the reaction solution was concentrated under reduced pressure. To the resultant concentrate was added 50 ml of hexane. And then, the mixture was stirred. The mixture was filtrated, and the filtrate was concentrated under reduced pressure. And then, the resultant concentrate was distilled under reduced pressure (80° C., 13.3 Pa), to provide 1.0 g of (bis(1-isopropylamide-2-dimethylaminoethane-N,N′) iron(II) as a brown transparent liquid. (Isolation yield: 84%)
Additionally, (bis(1-isopropylamide-2-dimethylaminoethane-N,N′) iron(II) was a novel compound, which had the following properties:
Iron content determined by inductively coupled plasma (ICP) analysis; 18.2 wt % (calculated value; 17.8 wt %)
The reaction was conducted in the same way as in Example E2, except that 0.49 g (3.8 mmol) of nickel(II) chloride was used instead of zinc(II) chloride. Then, the reaction solution was concentrated, and the resultant concentrate was sublimed under reduced pressure (90° C., 13 Pa), to provide 0.80 g of bis(1-(t-butylamide)-2-dimethylaminoethane-N,N′) nickel as a brown solid. (Isolation yield: 61%)
Additionally, bis(1-(t-butylamide)-2-dimethylaminoethane-N,N′) nickel(II) was a novel compound, which had the following properties:
Melting point; 90-92° C.
Nickel content determined by inductively coupled plasma (ICP) analysis; 17.4 wt %© (calculated value; 17.0 wt %)
The reaction was conducted in the same way as in Reference Example D1, except that 1.6 g (16 mmol) of 1-methylamino-2-dimethylaminoethane was used instead of 1-isopropylamino-2-dimethylaminoethane, to provide 1.6 g of (1-methylamide-2-dimethylaminoethane-N,N′)lithium. (Isolation yield: 92%)
Under argon atmosphere, into a 50 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 0.84 g (3.8 mmol) of indium(III) chloride (pre-dried anhydride) and 10 ml of tetrahydrofuran. And then, these were mixed and the mixture was stirred for 2 hours. Subsequently, while maintaining the solution temperature at 0° C., 10 ml of solution of 1.1 g (11 mmol) of (1-methylamide-2-dimethylaminoethane-N,N′) lithium, which was prepared in Reference Example H1, in tetrahydrofuran was slowly dropped into the flask. And then, the mixture was reacted while stirring at 20° C. for 6 hours. After the completion of the reaction, the reaction solution was concentrated under reduced pressure. To the resultant concentrate was added 50 ml of hexane. And then, the mixture was stirred. The mixture was filtrated, and the filtrate was concentrated under reduced pressure. And then, the resultant concentrate was distilled under reduced pressure (130° C., 13.3 Pa), to provide 1.2 g of tris(1-methylamide-2-dimethylaminoethane-N,N′)indium(III) as a light yellow semi-solid (wax). (Isolation yield: 75%)
Additionally, tris(1-methylamide-2-dimethylaminoethane-N,N′) indium(III) was a novel compound, which had the following properties:
1H-NMR (tetrahydrofuran-d8, δ (ppm)); 2.95 (6H, t, 5.6 Hz), 2.83 (9H, s), 2.44 (6H, t, 5.6 Hz), 2.26 (18H, s)
Indium content determined by inductively coupled plasma (ICP) analysis; 26.8 wt % (calculated value; 27.5 wt %)
Under argon atmosphere, into a 50 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 0.21 g (9.0 mmol) of metallic sodium, 1.0 g (10 mmol) of 1-methylamino-2-dimethylaminoethane, 1.4 g (20 mmol) of isoprene and 25 ml of hexane at 20° C. And then, the mixture was stirred at the same temperature for 20 hours. After the completion of the reaction, under argon atmosphere, the reaction solution was filtrated, and the precipitate was washed with 20 ml of hexane. And then, the precipitate was dried under vacuum, to provide 0.9 g of (1-methylamide-2-dimethylaminoethane-N,N′) sodium. (Isolation yield: 80%)
Additionally, (1-methylamide-2-dimethylaminoethane-N,N′)sodium was a novel compound, which had the following properties:
1H-NMR (tetrahydrofuran-d8, δ (ppm)); 2.98 (2H, t, 6.0 Hz), 2.97 (3H, s), 2.42 (2H, t, 6.0 Hz), 2.16 (6H, s)
Under argon atmosphere, into a 50 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 0.74 g (3.8 mmol) of yttrium(III) chloride (pre-dried anhydride) and 10 ml of tetrahydrofuran. And then, these were mixed and the mixture was stirred for 2 hours. Subsequently, while maintaining the solution temperature at 0° C., 10 ml of solution of 1.4 g (11 mmol) of (1-methylamide-2-dimethylaminoethane-N,N′) sodium, which was prepared in Example I1, in tetrahydrofuran was slowly dropped into the flask. And then, the mixture was reacted while stirring at 20° C. for 6 hours. After the completion of the reaction, the reaction solution was concentrated under reduced pressure. To the resultant concentrate was added 50 ml of hexane. And then, the mixture was stirred. The mixture was filtrated, and the filtrate was concentrated under reduced pressure. And then, the resultant concentrate was distilled under reduced pressure (140° C., 13.3 Pa), to provide 0.60 g of (tris(1-methylamide-2-dimethylaminoethane-N,N′) yttrium(III) as a light yellow semi-solid (wax). (Isolation yield: 40%)
Additionally, tris(1-methylamide-2-dimethylaminoethane-N,N′) yttrium(III) was a novel compound, which had the following properties:
1H-NMR (tetrahydrofuran-d8, δ (ppm)); 2.49 (6H, t, 6.0 Hz), 2.30 (9H, s), 2.26 (6H, t, 6.0 Hz), 2.14 (18H, s)
Yttrium content determined by inductively coupled plasma (ICP) analysis; 21.9 wt % (calculated value; 22.7 wt %)
Under argon atmosphere, into a 50 mL-volume flask equipped with a stirrer, a thermometer and a dropping funnel were placed 1.97 g (3.8 mmol) of lanthanum(III) iodide (pre-dried anhydride) and 20 ml of tetrahydrofuran. And then, these were mixed and the mixture was stirred for 2 hours. Subsequently, while maintaining the solution temperature at 0° C., 10 ml of solution of 1.4 g (11 mmol) of (1-methylamide-2-dimethylaminoethane-N,N′) sodium, which was prepared in Example I1, in tetrahydrofuran was slowly dropped into the flask. And then, the mixture was reacted while stirring at 20° C. for 6 hours. After the completion of the reaction, the reaction solution was concentrated under reduced pressure. To the resultant concentrate was added 50 ml of hexane. And then, the mixture was stirred. The mixture was filtrated, and the filtrate was concentrated under reduced pressure. And then, the resultant concentrate was distilled under reduced pressure (140° C., 13.3 Pa), to provide 0.50 g of (tris(1-methylamide-2-dimethylaminoethane-N,N′)lanthanum(III) as a light yellow semi-solid (wax). (Isolation yield: 30%)
Additionally, tris(1-methylamide-2-dimethylaminoethane-N,N′) lanthanum(III) was a novel compound, which had the following properties:
1H-NMR (tetrahydrofuran-d8, δ (ppm)); 2.90 (6H, t, 6.0 Hz), 2.84 (9H, s), 2.70 (6H, t, 6.0 Hz), 2.31 (18H, s)
Lanthanum content determined by inductively coupled plasma (ICP) analysis; 30.2 wt % (calculated value; 31.4 wt %)
According to the present invention, there may be provided a novel (amide amino alkane) metal compound from which a metal-containing thin film may be produced by a simple method. There may be also provided a method of producing a metal-containing thin film on an object by a CVD method using the metal compound. The (amide amino alkane) metal compound of the present invention is suitable for the formation of metal-containing thin film by a CVD method, and therefore is suitable for industrial use.
The bis(amide amino alkane) magnesium compound is useful as a material for the formation of magnesium-containing thin film, a polymerization catalyst, and a material for the production of medicines, agricultural chemicals, and the like, for example. The bis(amide amino alkane) cobalt compound is useful as a material for the formation of cobalt-containing thin film, a polymerization catalyst, and a material for the production of medicines, agricultural chemicals, and the like, for example.
The bis(amide amino alkane) manganese compound is useful as a material for the formation of manganese-containing thin film, a polymerization catalyst, and a material for the production of medicines, agricultural chemicals, and the like, for example. The bis(amide amino alkane) zinc compound is useful as a material for the formation of manganese-containing thin film, a polymerization catalyst, and a material for the production of medicines, agricultural chemicals, and the like, for example.
(
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| Number | Date | Country | |
|---|---|---|---|
| 20130273250 A1 | Oct 2013 | US |
