Organic electroluminescent device and process for producing the same

Claim 2

An organic thin-film electroluminescent device comprising: electrodes, at least one of the electrodes being transparent; and interposed between said electrodes, at least one layer selected from the group consisting of an electroluminescent layer, a charge injecting/transporting layer and a layer capable of electroluminescence and charge injection/transportation, said at least one layer formed out of a thin film of network polymers having a network structure and obtained by a vapor deposition polymerization process, wherein the thin film is composed of polymers each having oxadiazole units.

Claim 3

The organic thin-film electroluminescent device as claimed in claim 1, which is prepared by a process which comprises: providing monomer A consisting of a bifunctional monomer represented by the following formula (I) and monomer B consisting of a polyfunctional monomer represented by the following formula (II) or a mixture of the polyfunctional monomer and a bifunctional monomer represented by the following formula (III): ##STR28## wherein: m is an integer of 3 or greater, each of R 1 and R 3 may be the same or different from each other and independently represents a divalent organic group, R 2 represents an m-valent organic group, provided that m is an integer of 3 or greater, a represents a group selected from a carboxylic acid halide group, a carbohydrazide group and a silylated carbohydrazide group represented by the following formula: ##STR29## wherein R represents an alkyl or aryl group having not more than 6 carbon atoms, provided that, when a is a carboxylic acid halide group, each of b and c is a carbohydrazide group or a silylated carbohydrazide group represented by the above formula (IV) and that, when a is a carbohydrazide group or a silylated carbohydrazide group represented by the above formula (IV), b and c are respective carboxylic acid halide; evaporating the monomers A and B from respective separate vapor sources in vacuum so that a thin film of polyoxadiazole precursors is formed between electrodes, at least one of which is transparent; and heating the thin film at 100 to 400° C. in vacuum or an inert gas, thereby converting the polyoxadiazole precursors to polyoxadiazoles so that an electroluminescent layer and/or a charge injecting/transporting layer is formed out of the thin film of the polyoxadiazoles.

Claim 4

The organic thin-film electroluminescent device as claimed in claim 2, wherein at least one of the groups represented by R 1 , R 2 and R 3 is a group derived from an aromatic tertiary amine or an aromatic tertiary diamine.

Claim 5

The organic thin-film electroluminescent device as claimed in claim 1, which is prepared by a process which comprises: subjecting a carboxylic acid derivative represented by the following formula: ##STR30## wherein X represents a divalent organic group and Y represents a halogen atom; and a silylated dicarbohydrazide represented by the formula: ##STR31## wherein Z represents a divalent organic group and R represents an alkyl or aryl group having not more than 6 carbon atoms, to a vapor deposition polymerization on a surface to be vapor deposited, thereby forming a thin film of polymers each having a repeating unit represented by the formula: ##STR32## wherein X, Z and R are as defined above; and heating the thin film at 100 to 400° C. in vacuum or an inert gas, thereby forming an electroluminescent layer and/or a charge injecting/transporting layer composed of a thin film of polyoxadiazoles each having a repeating unit represented by the formula: ##STR33## wherein X and Z are as defined above.

Claim 6

The organic thin-film electroluminescent device as claimed in claim 4, wherein the vapor deposition polymerization is performed using the carboxylic acid derivative and the silylated dicarbohydrazide in a molar ratio of 1:1 to 1:30 and wherein the temperature of the surface on which the thin film of the polymers each having the repeating unit represented by the above formula (X) is formed by the vapor deposition polymerization ranges from -50 to 200° C.

Claim 7

The organic thin-film electroluminescent device as claimed in claim 4, wherein the vapor deposition polymerization of the carboxylic acid derivative and the silylated dicarbohydrazide is performed at a pressure of 10 -2 to 10 -4 Pa under which the carboxylic acid derivative and the silylated dicarbohydrazide are each evaporated at a rate of at least 10 -10 mol/cm 2 .sec at 40 to 400° C.

Claim 8

The organic thin-film electroluminescent device as claimed in claim 4, wherein the R of the formula (IX) represents a group selected from the group consisting of methyl, ethyl, n-propyl, iso-propyl, n-butyl, isobutyl, sec-butyl and phenyl groups.

Claim 9

The organic thin-film electroluminescent device as claimed in claim 4, wherein each of X and Z represents an organic group containing an aromatic ring or an alkylene group having 2 to 50 carbon atoms which contain conjugated π-electrons.

Claim 10

The organic thin-film electroluminescent device as claimed in claim 8, wherein each of X and Z represents any of a vinylene group, a phenylene group, a biphenylene group and a divalent group derived from triphenylamine, each unsubstituted or substituted with a group selected form the group consisting of alkyl, allyl, aryl and aralkyl groups.

Claim 11

The organic thin-film electroluminescent device as claimed in claim 4, wherein the number of repeating units represented by (X) in polymer and the number of repeating units represented by (XI) in the polyoxadiazole each range from 5 to 1000.

Claim 12

The organic thin-film electroluminescent device as claimed in claim 1, wherein a first of said electrodes is formed of Mg, Ag, In, Ca or Al as the negative electrode, and a second of said electrodes is formed of indium tin oxide or gold as the positive electrode.

Claim 13

The organic thin-film electroluminescent device as claimed in claim 1, wherein said electroluminescent layer has a thickness of 100 to 2000 Å.

Claim 14

A process of preparing the organic thin-film electroluminescent device of claim 1, the process comprising: providing monomer A consisting of a bifunctional monomer represented by the following formula (I) and monomer B consisting of a polyfunctional monomer represented by the following formula (II) or a mixture of the polyfunctional monomer and a bifunctional monomer represented by the following formula (III): ##STR34## wherein: m is an integer of 3 or greater, each of R 1 and R 3 may be the same or different from each other and independently represents a divalent organic group, R 2 represents an m-valent organic group, provided that m is an integer of 3 or greater, a represents a group selected from a carboxylic acid halide group, a carbohydrazide group and a silylated carbohydrazide group represented by the following formula: ##STR35## wherein R represents an alkyl or aryl group having not more than 6 carbon atoms, provided that, when a is a carboxylic acid halide group, each of b and c is a carbohydrazide group or a silylated carbohydrazide group represented by the above formula (IV) and that, when a is a carbohydrazide group or a silylated carbohydrazide group represented by the above formula (IV), b and c are respective carboxylic acid halide; evaporating the monomers A and B from respective separate vapor sources in vacuum so that a thin film of polyoxadiazole precursors is formed between electrodes, at least one of which is transparent; and heating the thin film at 100 to 400° C. in vacuum or an inert gas, thereby converting the polyoxadiazole precursors to polyoxadiazoles so that an electroluminescent layer and/or a charge injecting/transporting layer is formed out of the thin film of the polyoxadiazoles.

Claim 15

The process as claimed in claim 13, wherein at least one of the groups represented by R 1 , R 2 and R 3 is a group derived from an aromatic tertiary amine or an aromatic tertiary diamine.

Claim 16

A process for preparing the organic thin-film electroluminescent device of claim 1, the process comprising: subjecting a carboxylic acid derivative represented by the following formula: ##STR36## wherein X represents a divalent organic group and Y represents a halogen atom; and a silylated dicarbohydrazide represented by the formula: ##STR37## wherein Z represents a divalent organic group and R represents an alkyl or aryl group having not more than 6 carbon atoms, to a vapor deposition polymerization on a surface to be vapor deposited, thereby forming a thin film of polymers each having a repeating unit represented by the formula: ##STR38## wherein X, Z and R are as defined above; and heating the thin film at 100 to 400° C. in vacuum or an inert gas, thereby forming an electroluminescent layer and/or a charge injecting/transporting layer composed of a thin film of polyoxadiazoles each having a repeating unit represented by the formula: ##STR39## wherein X and Z are as defined above.

Claim 17

The process as claimed in claim 15, wherein the vapor deposition polymerization is performed using the carboxylic acid derivative and the silylated dicarbohydrazide in a molar ratio of 1:1 to 1:30 and wherein the temperature of the surface on which the thin film of the polymers each having the repeating unit represented by the above formula (X) is formed by the vapor deposition polymerization ranges from -50 to 200° C.

Claim 18

The process as claimed in claim 15, wherein the vapor deposition polymerization of the carboxylic acid derivative and the silylated dicarbohydrazide is performed at a pressure of 10 -2 to 10 -4 Pa under which the carboxylic acid derivative and the silylated dicarbohydrazide are each evaporated at a rate of at least 10 -10 mol/cm 2 .sec at 40 to 400° C.

Claim 19

The process as claimed in claim 15, wherein the R of the formula (IX) represents a group selected from the group consisting of methyl, ethyl, n-propyl, iso-propyl, n-butyl, isobutyl, sec-butyl and phenyl groups.

Claim 20

The process as claimed in claim 15, wherein each of X and Z represents an organic group containing an aromatic ring or an alkylene group having 2 to 50 carbon atoms which contain conjugated π-electrons.

Claim 21

The process as claimed in claim 19, wherein each of X and Z represents any of a vinylene group, a phenylene group, a biphenylene group and a divalent group derived from triphenylamine, each unsubstituted or substituted with a group selected form the group consisting of alkyl, allyl, aryl and aralkyl groups.