Patent Application
20100046344
This application claims the benefit of priority to Japanese Patent Application No. 2007-16321 filed on Jan. 26, 2007, which is expressly incorporated herein by reference in its entirety.
The present invention relates to an optical recording medium, and more particularly, to an optical recording medium having a recording layer for recording music data and the like, and a visible information recording layer for recording visible information to identify recorded data. The present invention further relates to a method of recording visible information on the optical recording medium.
Optical information recording media (optical disks) on which information can be recorded once by means of a laser beam are known. Such optical disks include recordable CDs (known as “CD-Rs”) and recordable digital versatile disks (known as “DVD-Rs”).
Optical disks, having a label on which visible information (such as the song titles of music data recorded on the recording side, titles for identifying recorded data, and the like) is printed that is adhered on the opposite side from the side on which music data and the like are recorded, are known. Such optical disks are prepared by using a printer or the like to print in advance titles and the like on a round label sheet, which is then adhered on the opposite side from the optical disk recording side.
However, in addition to an optical disk drive, a printer is required when preparing an optical disk with a label on the surface of which are recorded desired visible images such as titles. Accordingly, a complex operation is required, for example, after using an optical disk drive to record data on the recording surface of a given optical disk, it is necessary to remove the optical disk from the optical disk drive and attach the label sheet that has been printed by the printer separately prepared. Accordingly, optical recording media have been proposed that permit the use of laser markers on the opposite surface from the recording surface to vary the contrast between the surface and the background and indicate information (for example, see Japanese Unexamined Patent Publication (KOKAI) Heisei No. 11-66617, which is expressly incorporated herein by reference in its entirety). The use of such a method permits the printing of a desired image on the label surface of an optical disk with an optical disk drive without separate preparation of printers and the like. However, this method affords low sensitivity and requires the use of a high-power gas laser such as a carbon dioxide gas laser. The visible image that is formed by such a laser beam is of low contrast and affords poor visibility. Further, there are problems in that when manufacturing a coating-use ink employing a dye for image formation, the dye does not have adequate solubility in the ink solvent, and the dye in the image-forming layer crystallizes over long periods of time.
Under such circumstances, the object of the present invention is to provide an optical recording medium permitting the recording of visible information with high contrast and good visibility, and more particularly, to provide an optical recording medium permitting the recording of visible information with high contrast and good visibility with the laser beam that is used to record information in the recording layer.
The present inventors conducted extensive research into achieving the above-stated objects, and discovered that by employing a prescribed dye in the visible information recording layer of an optical recording medium, it was possible to form visible information with high contrast and good visibility.
The present invention relates to an optical recording medium (referred to as “Optical recording medium 1” or “Medium 1”, hereinafter) comprising a visible information recording layer on a support, wherein the visible information recording layer comprises a dye denoted by the following general formula (1):
wherein, in general formula (1), each of R1, R2, and R3 independently denotes a hydrogen atom or a monovalent substituent, A1 denotes an atom group forming a heterocyclic ring with carbon atoms bonded at either end, and B1 denotes an atom group forming a heterocyclic ring with a carbon atom and a nitrogen atom at either end.
According to one embodiment, the dye denoted by general formula (1) is a dye denoted by the following general formula (2):
wherein, in general formula (2), R1, R2, and R3 are defined identically with R1, R2, and R3 in general formula (1), respectively, each of R5, R6, and R7 independently denotes a hydrogen atom or a monovalent substituent, each of R4 and R8 independently denotes a monovalent substituent, n1 denotes an integer ranging from 0 to 4, and n2 denotes an integer ranging from 0 to 5.
The present invention further relates to an optical recording medium (referred to as “Optical recording medium 2” or “Medium 2”, hereinafter) comprising a visible information recording layer on a support, wherein the visible information recording layer comprises a dye denoted by the following general formula (3):
wherein, in general formula (3), each of R11, R13, and R14 independently denotes a hydrogen atom or a monovalent substituent, R12 denotes a monovalent substituent, A2 denotes an atom group forming a heterocyclic ring with carbon atoms bonded at either end, and n3 denotes an integer ranging from 0 to 4.
The present invention further relates to an optical recording medium (referred to as “Optical recording medium 3” or “Medium 3”, hereinafter) comprising a visible information recording layer on a support, wherein the visible information recording layer comprises a dye denoted by the following general formula (4):
wherein, in general formula (4), D denotes a diazonium salt-derived arocyclic group or aromatic heterocyclic group, each of R16 and R17 independently denotes a hydrogen atom or a monovalent substituent, R15 denotes a monovalent substituent, and n4 denotes an integer ranging from 0 to 4.
The present invention further relates to an optical recording medium (referred to as “Optical recording medium 4” or “Medium 4”, hereinafter) comprising a visible information recording layer on a support, wherein the visible information recording layer comprises a dye denoted by the following general formula (5):
wherein, in general formula (5), A3 denotes an atom group forming a heterocyclic ring with carbon atoms bonded at either end, EWG1 denotes an electron-withdrawing group, R18 denotes a monovalent substituent, each of R19 and R20 independently denotes a hydrogen atom or a monovalent substituent, and n5 denotes an integer ranging from 0 to 4.
The present invention further relates to an optical recording medium (referred to as “Optical recording medium 5” or “Medium 5”, hereinafter) comprising a visible information recording layer on a support, wherein the visible information recording layer comprises a dye denoted by the following general formula (6):
wherein, in general formula (6), each of R51 and R52 independently denotes a monovalent substituent, n8 denotes an integer ranging from 0 to 5, and n9 denotes an integer ranging from 0 to 4.
The present invention further relates to an optical recording medium (referred to as “Optical recording medium 6” or “Medium 6”, hereinafter) comprising a visible information recording layer on a support, wherein the visible information recording layer comprises a dye denoted by the following general formula (7):
wherein, in general formula (7), R64 denotes a hydrogen atom or a monovalent substituent, R61 denotes a monovalent substituent, each of R63 and R62 independently denotes a hydrogen atom, substituted or unsubstituted alkyl group, substituted or unsubstituted aryl group, or substituted or unsubstituted heterocyclic group, and n10 denotes an integer ranging from 0 to 4.
The present invention further relates to an optical recording medium (referred to as “Optical recording medium 7” or “Medium 7”, hereinafter) comprising a visible information recording layer on a support, wherein the visible information recording layer comprises a dye denoted by the following general formula (8):
wherein, in general formula (8), each of R71 and R73 independently denotes a hydrogen atom or a monovalent substituent, each of R72 and R74 independently denotes a monovalent substituent, nil denotes an integer ranging from 0 to 4, and n12 denotes an integer ranging from 0 to 2.
The present invention further relates to an optical recording medium (referred to as “Optical recording medium 8” or “Medium 8”, hereinafter) comprising a visible information recording layer on a support, wherein the visible information recording layer comprises a dye denoted by the following general formula (9):
wherein, in general formula (9), R81 denotes a hydrogen atom or a monovalent substituent, each of R82 and R84 independently denotes a monovalent substituent, n13 denotes an integer ranging from 0 to 4, and n14 denotes an integer ranging from 0 to 2.
The present invention further relates to an optical recording medium (referred to as “Optical recording medium 9” or “Medium 9”, hereinafter) comprising a visible information recording layer on a support, wherein the visible information recording layer comprises a dye denoted by the following general formula (10):
wherein, in general formula (10), each of R111 and R113 independently denotes a hydrogen atom or a monovalent substituent, each of R112 and R114 independently denotes a monovalent substituent, n18 denotes an integer ranging from 0 to 4, and n19 denotes an integer ranging from 0 to 2.
According to one embodiment, the above monovalent substituent is a halogen atoms, or a substituted or unsubstituted alkyl groups, alkenyl groups, alkynyl groups, aryl groups, heterocyclic groups, cyano groups, alkoxy groups, aryloxy groups, acyloxy groups, carbamoyloxy groups, alkoxycarbonyloxy groups, aryloxycarbonyloxy groups, amino groups, acylamino groups, aminocarbonylamino groups, alkoxycarbonylamino groups, aryloxycarbonylamino groups, sulfamoylamino groups, alkylsulfonylamino groups, arylsulfonylamino groups, alkylthio groups, sulfamoyl groups, alkylsulfinyl groups, arylsulfinyl groups, alkylsulfonyl groups, arylsulfonyl groups, acyl groups, aryloxycarbonyl groups, alkoxycarbonyl groups, carbamoyl groups, arylazo groups, heterocyclic azo groups or imido groups.
According to one embodiment, in the general formula (2), R1 denotes a hydrogen atom, R2 denotes a hydrogen atom, R3 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, R4 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, R5 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, R1 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, R7 denotes a substituted or unsubstituted dialkylamino group having 1 to 12 carbon atoms, R8 denotes a substituted or unsubstituted alkoxycarbonyl group having 1 to 6 carbon atoms or a chlorine atom, n1 denotes an integer ranging from 0 to 3, and n2 denotes an integer ranging from 0 to 3.
According to one embodiment, in the general formula (3), A2 denotes 2-pyrazoline-5-one comprising a substituent, R11 denotes a hydrogen atom, R12 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms or a substituted or unsubstituted alkoxy group having 1 to 6 carbon atoms, R13 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, R14 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, and n3 is 0 or 1.
According to one embodiment, in the general formula (4), D denotes a monovalent group derived from an isothiazole ring comprising a substituent or a monovalent group derived from a 1,3,4-thiadiazole ring comprising a substituent, R15 denotes an acylamino group, R16 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, R17 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, and n4 denotes an integer ranging from 0 to 4.
According to one embodiment, in the general formula (5), A3 denotes 2-pyrazoline-5-one comprising a substituent, EWG1 denotes a cyano group, R18 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms or a substituted or unsubstituted alkoxy group having 1 to 6 carbon atoms, R19 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, R20 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, and n5 denotes an integer ranging from 0 to 4.
According to one embodiment, in the general formula (6), R51 denotes an alkyl group having 1 to 6 carbon atoms, R52 denotes a substituted or unsubstituted carbamoyl group or aryloxycarbonyl group having 6 to 10 carbon atoms or alkoxycarbonyl group having 1 to 6 carbon atoms, n8 denotes an integer ranging from 0 to 3, and n9 denotes an integer ranging from 0 to 3.
According to one embodiment, in the general formula (7), R61 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, R62 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, R63 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, R64 denotes a hydrogen atom, and n10 denotes an integer ranging from 0 to 4.
According to one embodiment, in the general formula (8), R71 denotes a hydrogen atom, R72 denotes a substituted or unsubstituted aryloxy group having 6 to 12 carbon atoms, R73 denotes a hydrogen atom, n11 denotes 0, and n12 denotes an integer ranging from 0 to 2.
According to one embodiment, in the general formula (9), R81 denotes a hydrogen atom, R82 denotes an aryloxy group, n13 denotes 0, and n14 denotes 1 or 2.
According to one embodiment, in the general formula (10), R111 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms or a substituted or unsubstituted aryl group having 6 to 10 carbon atoms, R113 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms or a substituted or unsubstituted aryl group having 6 to 10 carbon atoms, n18 is 0, and n19 is 0.
According to one embodiment, the visible information recording layer further comprises a cyanine dye denoted by the general formula (I):
wherein, in general formula (1), each of Za31 and Za32 independently denotes an atom group forming a carbon ring or heterocyclic ring, each of R100, R101, R102, R103, R104, R105, R106, R107, and R108 independently denotes a hydrogen atom or a monovalent substituent, each of X1 and X2 independently denotes a carbon atom or a hetero atom, Ka denotes 2 or 3, plural R102s and R103s present may be identical or different, and Q denotes a monovalent anion.
According to one embodiment, the optical recording medium further comprises a recording layer capable of recording and/or reproducing information by irradiation of a laser beam. The optical recording medium may comprise a first support, the recording layer, a reflective layer, the visible information recording layer, and a second support in this order.
According to one embodiment, the optical recording medium is disk-shaped.
An another aspect of the present invention relates to a method of recording visible information on the visible information recording layer of the optical recording medium comprising a recording layer capable of recording and/or reproducing information by irradiation of a laser beam. In the method of recording visible information, the visible information is recorded by using the same laser bean as that used in recording information on the recording layer.
An another aspect of the present invention relates to a method of recording visible information on the visible information recording layer of the optical recording medium being disk-shaped. In the method of recording visible information, the visible information is recorded by using a laser beam that oscillates in a radial direction of the optical recording medium as well as is irradiated plural times on approximately identical paths.
According to the present invention, an optical recording medium permitting the recording of visible information with high contrast and good visibility can be provided. Further, the dye employed in the present invention has adequate solubility in the solvent, so the optical recording medium is readily manufactured. Since the visible information recording layer comprising the dye has good stability over time, an optical recording medium with good storage properties can be provided. Further, the dye is suited to systems of forming images by new recording methods differing from common digital data recording, and permits the formation of visible information with high contrast, sharpness, and good resistance to light in such systems.
Further, the image that is drawn in the visible information recording layer is required to exhibit the desired color tones that are intended by the user. To achieve this, a recording medium for image drawing is demanded that employs dyes having various color tones. According to the present invention, it is possible to create an optical recording medium exhibiting desired sharp color tones with high contrast by selecting dyes having various color tones that are suitable to image drawing and by selecting multiple dyes with different color tones to adjust the mix ratio.
The present invention will be described in further detail below.
[Optical Recording Medium]
All the optical recording media 1 to 9 of the present invention comprise a visible information recording layer on a support, and comprises a given dye in the visible information recording layer. Dyes comprised in the visible information recording layer of each optical recording medium will be described in order below.
<Dyes>
Medium 1
Medium 1 comprises the dye denoted by the following general formula (1) in the visible information recording layer.
In general formula (1), each of R1, R2, and R3 independently denotes a hydrogen atom or a monovalent substituent. The monovalent substituent will be described in greater detail. Examples of the monovalent substituent are: halogen atoms, alkyl groups (including cycloalkyl and bicycloalkyl groups), alkenyl groups (including cycloalkenyl and bicycloalkenyl groups), alkynyl groups, aryl groups, heterocyclic groups, cyano groups, alkoxy groups, aryloxy groups, acyloxy groups, carbamoyloxy groups, alkoxycarbonyloxy groups, aryloxycarbonyloxy groups, amino groups (including anilino groups), acylamino groups, aminocarbonylamino groups, alkoxycarbonylamino groups, aryloxycarbonylamino groups, sulfamoylamino groups, alkylsulfonylamino groups, arylsulfonylamino groups, alkylthio groups, sulfamoyl groups, alkylsulfinyl groups, arylsulfinyl groups, alkylsulfonyl groups, arylsulfonyl groups, acyl groups, aryloxycarbonyl groups, alkoxycarbonyl groups, carbamoyl groups, arylazo groups, heterocyclic azo groups, and imido groups. These groups may comprise substituents. Each of these groups will be described in greater detail below.
Examples of the above halogen atoms are fluorine, chlorine, bromine, and iodine atoms. Of these, chlorine and iodine atoms are desirable, and chlorine atoms are preferred.
The above alkyl groups include substituted and unsubstituted cycloalkyl and bicycloalkyl groups, as well as linear and branched substituted and unsubstituted alkyl groups. The number of carbon atoms in these linear and branched substituted and unsubstituted alkyl groups desirably falls within a range of 1 to 30. Specific examples thereof are methyl, ethyl, n-propyl, isopropyl, t-butyl, n-octyl, eicosyl, 2-chloroethyl, 2-cyanoethyl, or 2-ethylhexyl groups. The number of carbon atoms in the above substituted and unsubstituted cycloalkyl groups desirably falls within a range of 3 to 30. Specific examples thereof are cyclohexyl groups, cyclopentyl groups, and 4-n-dodecylcyclohexyl groups. A bicycloalkyl group having 5 to 30 carbon atoms, that is, a monovalent group in the form of a bicycloalkane having 5 to 30 carbon atoms from which a hydrogen atom has been removed, is desirable as the above substituted or unsubstituted bicycloalkyl group. Specific examples thereof are bicyclo[1,2,2]heptane-2-yl and bicyclo[2,2,2]octane-3-yl. Alkyl groups comprising an even larger number of cyclic structures, such as a tricyclic structure, are included. The alkyl groups in the substituents described further below (such as the alkyl group in an alkylthio group) also denote alkyl groups based on the above concept.
The above alkenyl groups include substituted and unsubstituted cycloalkenyl and bicycloalkenyl groups, as well as linear, branched, and cyclic substituted and unsubstituted alkenyl groups. The number of carbon atoms in these linear, branched, and cyclic substituted and unsubstituted alkenyl groups desirably falls within a range of 2 to 30. Specific examples thereof are vinyl, allyl, prenyl, geranyl, and oleyl groups. A substituted or unsubstituted cycloalkenyl group having 3 to 30 carbon atoms, that is, a monovalent group in the form of a cycloalkene having 3 to 30 carbon atoms from which a hydrogen atom has been removed, is desirable as the above substituted or unsubstituted cycloalkenyl group. Specific examples thereof are 2-cycloheptene-1-yl and 2-cyclohexene-1-yl. A substituted or unsubstituted bicycloalkenyl group having 5 to 30 carbon atoms, that is, a monovalent group in the form of a bicycloalkene having a single double bond from which a hydrogen atom has been removed is desirable as the above substituted or unsubstituted bicycloalkenyl group. Specific examples thereof are bicyclo[2,2,1]hepto-2-ene-1-yl and bicyclo[2,2,2]octo-2-ene-4-yl.
By way of example, the above alkynyl group is a substituted or unsubstituted alkynyl group having 2 to 30 carbon atoms, specific examples of which are ethynyl and propargyl groups.
The above aryl groups are, for example, substituted or unsubstituted aryl groups having 6 to 30 carbon atoms. Specific examples thereof are phenyl, p-tolyl, naphthyl, m-chlorophenyl, and o-hexadecanoylaminophenyl groups.
Examples of the above heterocyclic groups are monovalent groups in the form of five or six-membered, substituted or unsubstituted, aromatic or nonaromatic heterocyclic compounds from which a hydrogen atom has been removed. The rings in these groups may be further condensed. Five or six-membered aromatic heterocyclic groups having 3 to 30 carbon atoms are preferred. Examples of heterocyclic groups, irrespective of substitution position, are monovalent groups corresponding to pyridine, pyrazine, pyridazine, pyrimidine, triazine, quinoline, isoquinoline, quinazoline, cinnoline, phthalazine, quinoxaline, pyrrole, indole, furan, benzofuran, thiophene, benzothiophene, pyrazole, imidazole, benzimidazole, triazole, oxazole, benzoxazole, thiazole, benzothiazole, isothiazole, benzisothiazole, thiadiazole, isooxazole, benzisooxazole, pyrrolidine, piperidine, piperazine, imidazolidine, thiazoline, and the like.
The above alkoxy groups include substituted and unsubstituted alkoxy groups. The substituted and unsubstituted alkoxy groups desirably have 1 to 30 carbon atoms. Examples of these alkoxy groups are: methoxy, ethoxy, isopropoxy, n-octyloxy, methoxyethoxy, hydroxyethoxy, and 3-carboxypropoxy groups.
The above aryloxy groups are desirably substituted or unsubstituted aryloxy groups having 6 to 30 carbon atoms. Examples of these aryloxy groups are: phenoxy, 2-methylphenoxy, 4-t-butylphenoxy, 3-nitrophenoxy, and 2-tetradecanoylaminophenoxy groups.
The above acyloxy groups are desirably formyloxy groups, substituted or unsubstituted alkylcarbonyloxy groups having 2 to 30 carbon atoms, or substituted or unsubstituted arylcarbonyloxy groups having 6 to 30 carbon atoms. Examples of these acyloxy groups are formyloxy, acetyloxy, pivaloyloxy, stearoyloxy, benzoyloxy, and p-methoxyphenylcarbonyloxy groups.
The above carbamoyloxy groups are desirably substituted or unsubstituted carbamoyloxy groups having 1 to 30 carbon atoms. Examples of these carbamoyloxy groups are N,N-dimethylcarbamoyloxy, N,N-diethylcarbamoyloxy, morpholinocarbonyloxy, N,N-di-n-octylaminocarbonyloxy, and N-n-octylcarbamoyloxy groups.
The above alkoxycarbonyloxy groups are desirably substituted or unsubstituted alkoxycarbonyloxy groups having 2 to 30 carbon atoms. Examples of these alkoxycarbonyloxy groups are methoxycarbonyloxy, ethoxycarbonyloxy, t-butoxycarbonyloxy, and n-octylcarbonyloxy groups.
The above aryloxycarbonyloxy groups are desirably substituted or unsubstituted aryloxycarbonyloxy groups having 7 to 30 carbon atoms. Examples of these aryloxycarbonyloxy groups are phenoxycarbonyloxy, p-methoxyphenoxycarbonyloxy, and p-n-hexadecyloxyphenoxycarbonyloxy groups.
The above amino groups include arylamino groups. These amino groups are desirably substituted or unsubstituted alkylamino groups having 1 to 30 carbon atoms, or substituted or unsubstituted arylamino groups having 6 to 30 carbon atoms. Examples of these amino groups are amino, methylamino, dimethylamino, anilino, N-methylanilino, diphenylamino, hydroxyethylamino, carboxyethylamino, sulfoethylamino, and 3,5-dicarboxyanilino groups.
The above acylamino groups are desirably formylamino groups, substituted or unsubstituted alkylcarbonylamino groups having 1 to 30 carbon atoms, or substituted or unsubstituted arylcarbonylamino groups having 6 to 30 carbon atoms. Examples of these acylamino groups are formylamino, acetylamino, pivaloylamino, lauroylamino, benzoylamino, and 3,4,5-tri-n-octyloxyphenylcarbonylamino groups.
The above aminocarbonylamino groups are desirably substituted or unsubstituted aminocarbonylamino groups having 1 to 30 carbon atoms. Examples of these aminocarbonylamino groups are: carbamoylamino, N,N-dimethylaminocarbonylamino, N,N-diethylaminocarbonylamino, and morpholinocarbonylamino groups.
The above alkoxycarbonylamino groups are desirably substituted or unsubstituted alkoxycarbonylamino groups having 2 to 30 carbon atoms. Examples of these alkoxycarbonylamino groups are methoxycarbonylamino, ethoxycarbonylamino, t-butoxycarbonylamino, n-octadecyloxycarbonylamino, and N-methylmethoxycarbonyl-amino groups.
The above aryloxycarbonylamino groups are desirably substituted or unsubstituted aryloxycarbonylamino groups having 7 to 30 carbon atoms. Examples of these aryloxycarbonylamino groups are phenoxycarbonylamino, p-chlorophenoxy-carbonylamino, and m-n-octyloxyphenoxycarbonylamino groups.
The above sulfamoylamino groups are desirably substituted or unsubstituted sulfamoylamino groups having 0 to 30 carbon atoms. Examples of these sulfamoylamino groups are: sulfamoylamino, N,N-dimethylaminosulfonylamino, and N-n-octylaminosulfonylamino groups.
The above alkylsulfonylamino groups are desirably substituted or unsubstituted alkylsulfonylamino groups having 1 to 30 carbon atoms. The above arylsulfonylamino groups are desirably substituted or unsubstituted arylsulfonylamino groups having 6 to 30 carbon atoms. Examples of these alkylsulfonylamino and arylsulfonylamino groups are: methylsulfonylamino, butylsulfonylamino, phenylsulfonylamino, 2,3,5-trichlorophenylsulfonylamino, and p-methylphenylsulfonylamino groups.
The above alkylthio groups are desirably substituted or unsubstituted alkylthio groups having 1 to 30 carbon atoms. Examples of these alkylthio groups are: methylthio, ethylthio, and n-hexadecylthio groups.
The above sulfamoyl groups are desirably substituted or unsubstituted sulfamoyl groups having 0 to 30 carbon atoms. Examples of these sulfamoyl groups are: N-ethylsulfamoyl, N-(3-dodecyloxypropyl)sulfamoyl, N,N-dimethylsulfamoyl, N-acetylsulfamoyl, N-benzoylsulfamoyl, and N—(N′-phenylcarbamoyl)sulfamoyl groups.
The above alkylsulfinyl groups are desirably substituted or unsubstituted alkylsulfinyl groups having 1 to 30 carbon atoms. The above arylsulfinyl groups are desirably substituted or unsubstituted arylsulfinyl groups having 6 to 30 carbon atoms. Examples of these alkyl and arylsulfinyl groups are: methylsulfinyl, ethylsulfinyl, phenylsulfinyl, and p-methylphenylsulfinyl groups.
The above alkylsulfinyl groups are desirably substituted or unsubstituted alkylsulfonyl groups having 1 to 30 carbon atoms. The above arylsulfonyl groups are desirably substituted or unsubstituted arylsulfonyl groups having 6 to 30 carbon atoms. Examples of these alkyl and arylsulfonyl groups are methylsulfonyl, ethylsulfonyl, phenylsulfonyl, and p-toluenesulfonyl groups.
The above acyl groups are desirably formyl groups, substituted or unsubstituted alkylcarbonyl groups having 2 to 30 carbon atoms, substituted or unsubstituted arylcarbonyl groups having 7 to 30 carbon atoms, or substituted or unsubstituted heterocyclic carbonyl groups that have 4 to 30 carbon atoms and are bonded to the carbonyl group through the carbon atom. Examples of these acyl groups are: acetyl, pivaloyl, 2-chloroacetyl, stearoyl, benzoyl, p-n-octyloxyphenylcarbonyl, 2-pyridylcarbonyl, and 2-furylcarbonyl groups.
The above aryloxycarbonyl groups are desirably substituted or unsubstituted aryloxycarbonyl groups having 7 to 30 carbon atoms. Examples of these aryloxycarbonyl groups are phenoxycarbonyl, o-chlorophenoxycarbonyl, m-nitrophenoxycarbonyl, and p-t-butylphenoxycarbonyl groups.
The above alkoxycarbonyl groups are desirably substituted or unsubstituted alkoxycarbonyl groups having 2 to 30 carbon atoms. Examples of these alkoxycarbonyl groups are methoxycarbonyl, ethoxycarbonyl, t-butoxycarbonyl, and n-octadecyloxycarbonyl groups.
The above carbamoyl groups are desirably substituted or unsubstituted carbamoyl groups having 1 to 30 carbon atoms. Examples of these carbamoyl groups are: carbamoyl, N-methylcarbamoyl, N,N-dimethylcarbamoyl, N,N-di-n-octylcarbamoyl, and N-(methylsulfonyl)carbamoyl groups.
Examples of the above aryl and heterocyclic azo groups are: phenylazo, 4-methoxyphenylazo, 4-pivaloylaminophenylazo, and 2-hydroxy-4-propanoylphenylazo groups.
Examples of the above imido groups are N-succinimide and N-phthalimide groups.
Each of R1 and R2 desirably independently denotes a hydrogen atom, substituted or unsubstituted alkyl group, substituted or unsubstituted alkenyl group, substituted or unsubstituted aryl group, substituted or unsubstituted heterocyclic group, substituted or unsubstituted acylamino group, substituted or unsubstituted aminocarbonylamino group, substituted or unsubstituted alkoxycarbonylamino group, or substituted or unsubstituted amino group, preferably denoting a hydrogen atom or a substituted or unsubstituted alkyl group.
R3 desirably denotes a hydrogen atom, substituted or unsubstituted alkyl group, substituted or unsubstituted alkenyl group, substituted or unsubstituted aryl group, or substituted or unsubstituted heterocyclic group, preferably denoting a hydrogen atom or a substituted or unsubstituted alkyl group.
In general formula (1), A1 denotes an atom group forming a heterocyclic ring with carbon atoms bonded at either end. A1 denotes an atom group forming an acidic nucleus. It is defined in James, ed., The Theory of the Photographic Process, 4th Edition, Macmillan, 1977, p. 198, and F. M. Harmer, Heterocyclic Compounds—Cyanine Dyes and Related Compounds, John Wiley & Sons, New York, London, 1964 Annual (which are expressly incorporated herein by reference in their entirety), and A1 desirably denotes an atom group forming a five or six-membered nitrogen-containing heterocyclic ring. These may be further condensed with a benzene ring, benzofuran ring, pyridine ring, pyrrole ring, indole ring, thiophene ring, or the like. Specific examples are nuclei in the form of 2-pyrazoline-5-one, pyrazolidine-3,5-dione, imidazoline-5-one, hydantoin, 2 or 4-thiohydantoin, 2-iminooxazolidine-4-one, 2-oxazoline-5-one, 2-thiooxazoline-2,4-dione, isorhodanine, rhodanine, indane-1,3-dione, thiophene-3-one, thiophene-3-one-1,1-dioxide, indoline-2-one, indoline-3-one, 2-oxoindazolium, 5,7-dioxo-6,7-dihydrothiazolo[3,2-a]pyrimidine, 3,4-dihydroisoquinoline-4-one, 1,3-dioxane-4,6-dione, barbituric acid, 2-thiobarbituric acid, coumarin-2,4-dione, indazoline-2-one, pyrido[1,2-a]pyrimidine-1,3-dione, pyrazolo[1,5-b]quinazolone, pyrazolopyridone, 3-dicyanomethylidenyl-3-phenylpropionitrile, and Meldrum's acid, with 2-pyrazoline-5-one being desirable. These may further comprise substituents.
In general formula (1), B1 denotes an atom group forming a heterocyclic ring with a carbon atom and a nitrogen atom at either end. B1 denotes an atom group forming a five or six-membered nitrogen-containing heterocyclic ring. These may be further condensed with a benzene ring, benzofuran ring, pyridine ring, pyrrole ring, indole ring, thiophene ring, or the like. Examples of B1 are: an oxazole nucleus having 3 to 25 carbon atoms (such as 2-3-methyloxazolyl), a thiazole nucleus having 3 to 25 carbon atoms (such as 2-3-methylthiazolyl), an imidazole nucleus having 3 to 25 carbon atoms (such as 2-1,3-diethylimidazolyl), an indolenine nucleus having 10 to 30 carbon atoms (such as 3,3-dimethylindolenine), a quinoline nucleus having 9 to 25 carbon atoms (such as 2-1-methylquinolyl), a selenazole nucleus having 3 to 25 carbon atoms (such as 2-3-methylbenzoselenazolyl), a pyridine nucleus having 5 to 25 carbon atoms (such as 2-pyridyl), a thiazoline nucleus, an oxazoline nucleus, a selenazoline nucleus, a tellurazoline nucleus, a tellurazole nucleus, a benzotellurazole nucleus, an imidazoline nucleus, an imidazo[4,5-quinoxaline] nucleus, an oxadiazole nucleus, a thiadiazole nucleus, a tetrazole nucleus, and a pyrimidine nucleus. These may further comprise substituents.
The dye denoted by the above general formula (1) is desirably the dye denoted by the following general formula (2).
General formula (2) will be described in detail below.
In general formula (2), R1, R2, and R3 are defined identically with R1, R2, and R3 in general formula (1), respectively. Each of R5, R6, and R7 independently denotes a hydrogen atom or a monovalent substituent. Each of R4 and R8 independently denotes a monovalent substituent. Examples of these monovalent substituents are the substituents described for R1, R2, and R3 above. n1 denotes an integer ranging from 0 to 4, and n2 denotes an integer ranging from 0 to 5.
Each of R4 and R8 desirably independently denotes a halogen atom, alkyl group, alkenyl group, alkynyl group, aryl group, heterocyclic group, cyano group, alkoxy group, aryloxy group, acyloxy group, carbamoyloxy group, alkoxycarbonyloxy group, aryloxycarbonyloxy group, amino group, acylamino group, aminocarbonylamino group, alkoxycarbonylamino group, aryloxycarbonylamino group, sulfamoylamino group, alkylsulfonylamino group, arylsulfonylamino group, alkylthio group, sulfamoyl group, alkylsulfinyl group, arylsulfinyl group, alkylsulfonyl group, arylsulfonyl group, acyl group, aryloxycarbonyl group, alkoxycarbonyl group, or carbamoyl group; preferably denotes a hydrogen atom, halogen atom, alkyl group, alkenyl group, aryl group, heterocyclic group, alkoxy group, aryloxy group, acyloxy group, carbamoyloxy group, alkoxycarbonyloxy group, aryloxycarbonyloxy group, amino group, acylamino group, aminocarbonylamino group, alkoxycarbonylamino group, aryloxycarbonylamino group, alkylthio group, acyl group, aryloxycarbonyl group, alkoxycarbonyl group, or carbamoyl group; more preferably denotes a halogen atom, substituted or unsubstituted alkyl group, substituted or unsubstituted alkenyl group, substituted or unsubstituted aryl group, substituted or unsubstituted heterocyclic group; and still more preferably, denotes a substituted or unsubstituted alkyl group.
R5 and R6 are desirably identical to R1 and R2 in general formula (1). Each preferably independently denotes a hydrogen atom, substituted or unsubstituted alkyl group, substituted or unsubstituted alkenyl group, substituted or unsubstituted aryl group, or substituted or unsubstituted heterocyclic group; and more preferably denotes a hydrogen atom or substituted or unsubstituted alkyl group.
R7 desirably denotes a hydrogen atom, substituted or unsubstituted alkyl group, substituted or unsubstituted alkenyl group, substituted or unsubstituted aryl group, substituted or unsubstituted heterocyclic group, substituted or unsubstituted amino group, or substituted or unsubstituted acylamino group; and preferably denotes a hydrogen atom, substituted or unsubstituted alkyl group, substituted or unsubstituted aryl group, substituted or unsubstituted amino group, or substituted or unsubstituted acylamino group.
In desirable substituent combinations of the dye denoted by general formula (2), it is desirable for at least one of the various substituents to be one of the above desirable groups, preferable for more of the various substituents to be from among the above desirable groups, and more preferable for all of the substituents to be from among the above desirable groups.
The following combination is an example of a specific desirable combination: a combination in which R1 denotes a hydrogen atom, R2 denotes a hydrogen atom, R3 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, R4 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, R5 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, R6 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, R7 denotes a substituted or unsubstituted dialkylamino group having 1 to 12 carbon atoms, R8 denotes a substituted or unsubstituted alkoxycarbonyl group having 1 to 6 carbon atoms or a chlorine atom, n1=0 to 3, n2=0 to 3. The following combination is an example of a preferred combination: a combination in which R1 denotes a hydrogen atom, R2 denotes a hydrogen atom, R3 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, R5 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, R6 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, R7 denotes a substituted or unsubstituted dialkylamino group having 1 to 12 carbon atoms, n1=0, and n2=0.
Medium 2
Medium 2 comprises the dye denoted by the following general formula (3) in the visible information recording layer.
In general formula (3), each of R11, R13, and R14 independently denotes a hydrogen atom or a monovalent substituent, and R12 denotes a monovalent substituent. Examples of the monovalent substituents are those described for R1, R2, and R3 above. A2 denotes an atom group forming a heterocyclic ring with carbon atoms bonded at either end. n3 denotes an integer ranging from 0 to 4.
R11 is desirably identical to R1 in general formula (1); is preferably a hydrogen atom or a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms; and is more preferably a hydrogen atom.
R12 is desirably identical to R4 and R8 in general formula (2); and is preferably a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, or a halogen atom.
Specific desirable examples of R13 and R14 are the substituents described for R3 of general formula (1). Preferred examples are hydrogen atoms and substituted or unsubstituted alkyl groups having 1 to 6 carbon atoms.
The substituents described for A1 in general formula (1) are examples of A2. The same holds true for specific desirable examples.
In desirable substituent combinations of the dye denoted by general formula (3), it is desirable for at least one of the various substituents to be one of the above desirable groups, preferable for more of the various substituents to be from among the above desirable groups, and more preferable for all of the substituents to be from among the above desirable groups.
The following combination is an example of a specific desirable combination: a combination in which A2 denotes 2-pyrazoline-5-one comprising a substituent, R11 denotes a hydrogen atom, R12 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms or a substituted or unsubstituted alkoxy group having 1 to 6 carbon atoms, R13 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, R14 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, and n3=0 to 2. The following combination is an example of a preferred combination: a combination in which A2 denotes 2-pyrazoline-5-one comprising a substituent, R11 denotes a hydrogen atom, R12 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms or a substituted or unsubstituted alkoxy group having 1 to 6 carbon atoms, R13 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, R14 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, and n3=0 or 1.
Medium 3
Medium 3 comprises the dye denoted by the following general formula (4) in the visible information recording layer.
In general formula (4), D denotes a diazonium salt-derived arocyclic group or aromatic heterocyclic group; each of R16 and R17 independently denotes a hydrogen atom or a monovalent substituent; and R15 denotes a monovalent substituent. Examples of the monovalent substituent are those described for R1, R2, and R3 above. n4 denotes an integer ranging from 0 to 4.
D denotes a diazonium salt-derived, substituted or unsubstituted arocyclic group or substituted or unsubstituted aromatic heterocyclic group. That is, D is a diazo component. The term “diazo component” means a partial structure that can be incorporated by converting a heterocyclic compound or a benzene derivative having a substituent in the form of an amino group into a diazo compound (diazonium salt) and causing it to undergo a diazo coupling reaction with a coupler. This is a concept that is frequently employed in the field of azo dyes. In other words, it is a substituent in the form of a heterocyclic compound substituted with an amino group capable of undergoing a diazo conversion reaction, or a benzene derivative, that has been converted to a monovalent group by removing the amino group.
Examples of the aromatic heterocyclic group, irrespective of substitution position, are pyrrole, pyrazole, triazole, thiazole, isothiazole, benzothiazole, 1,3,4-thiadiazole, 1,2,4-thiadiazole, oxazole, benzooxazole, imidazole, benzoisothiazole, thiophene, benzothiophene, pyridine, pyridazine, pyrimidine, pyrazine, indole, quinoline, purine, carbazole, and acrylidine rings. Desirable examples are monovalent groups derived from isothiazole, 1,3,4-thiadiazole, and 1,2,4-thiadiazole rings. The various heterocyclic rings may further comprise substituents, and may be condensed.
D desirably denotes the group described in the following group (1) of heterocyclic groups.
In above group (1) of heterocyclic groups, each of Ra, Rb, Rd, and Re independently denotes a hydrogen atom or a monovalent substituent. Examples of the monovalent substituent are identical to the substituents given by way of example as substituents for R1, R2, and R3.
D preferably denotes the group selected from the following group (2) of heterocyclic groups.
In each group in the above group (2) of heterocyclic groups, Ra, Rb, and Rc are defined as Ra, Rb, and Rc in each group in the above group (1) of heterocyclic groups, and the desirable substituents are identical thereto.
In the various groups in above groups (1) and (2) of heterocyclic groups, Ra desirably denotes a hydrogen atom, or substituted or unsubstituted alkyl group, substituted or unsubstituted aryl group, substituted or unsubstituted heterocyclic group; and preferably denotes a substituted or unsubstituted alkyl group or substituted or unsubstituted aryl group. Each of Rb, Rc, Rd, and Re desirably independently denotes a hydrogen atom, substituted or unsubstituted alkyl group, substituted or unsubstituted alkenyl group, substituted or unsubstituted aryl group, substituted or unsubstituted heterocyclic group, substituted or unsubstituted acyl group, cyano group, carbamoyl group, or alkoxycarbonyl group; and more preferably denotes a hydrogen atom, substituted or unsubstituted alkyl group, substituted or unsubstituted aryl group, substituted or unsubstituted heterocyclic group, or cyano group.
In general formula (4), R15 is desirably identical to R4 in general formula (1); preferably denotes an alkyl group, alkoxy group, amino group, acylamino group, aminocarbonylamino group, alkoxycarbonylamino group, aryloxycarbonylamino group, sulfamoylamino group, or alkyl or arylsulfonylamino group.
Desirable examples of R16 and R17 are the substituents described for R3 in general formula (1), with hydrogen atoms or substituted or unsubstituted alkyl groups having 1 to 6 carbon atoms being preferred.
In combinations of desirable substituents of the dye denoted by general formula (4), it is desirable for at least one of the various substituents to be one of the above desirable groups, preferable for more of the various substituents to be from among the above desirable groups, and more preferable for all of the substituents to be from among the above desirable groups.
The following combination is an example of a specific desirable combination: a combination in which D denotes a monovalent group derived from an isothiazole ring comprising a substituent or a monovalent group derived from a 1,3,4-thiadiazole ring comprising a substituent; R15 denotes an acylamino group; R16 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms; R17 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms; and n4=0 to 4. The following combination is an example of a preferred combination: a combination in which D denotes a monovalent group derived from an isothiazole ring comprising a substituent or a monovalent group derived from a 1,3,4-thiadiazole ring comprising a substituent, R15 denotes an acylamino group, R16 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, R17 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, n4=1, with the substitution position of R15 being the o-position relative to the azo group.
Medium 4
Medium 4 comprises the dye denoted by the following general formula (5) in the visible information recording layer.
In general formula (5), A3 denotes an atom group forming a heterocyclic ring with carbon atoms bonded at either end, EWG1 denotes an electron-withdrawing group, R18 denotes a monovalent substituent, and each of R19 and R20 independently denotes a hydrogen atom or a monovalent substituent. Examples of the monovalent substituent are those given in the description of R1, R2, and R3 above. n5 denotes an integer ranging from 0 to 4.
The substituents described for A1 in general formula (1) are specific examples of A3. The same applies for desirable specific examples.
EWG1 denotes an electron-withdrawing group with a Hammett substituent constant σp value of equal to or greater than 0. EWG1 desirably denotes an electron-withdrawing group with a σp value of equal to or greater than 0.30, preferably an electron-withdrawing group with a σp value of equal to or greater than 0.45, and more preferably, an electron-withdrawing group with a σp value of equal to or greater than 0.60. Examples of electron-withdrawing groups with σp values of equal to or greater than 0.60 are: nitro, cyano, methanesulfonyl, trifluoromethanesulfonyl, trifluoroacetyl, dimethylaminosulfonyl, and sulfamoyl groups. Examples of electron-withdrawing groups with σp values of equal to or greater than 0.45 are: alkoxycarbonyl, acyl, and carboxy groups. Examples of electron-withdrawing groups with σp values of equal to or greater than 0.30 are sulfo and carbamoyl groups. Cyano, carboxyl, alkoxycarbonyl, and carbamoyl groups are preferred. Cyano, alkoxycarbonyl, and carbamoyl groups are of greater preference. And cyano and carbamoyl groups are the groups of greatest preference.
A brief description will be given of the value of Hammett's substituent constant σp. The validity of the Hammett's equation, an empirical equation proposed by L. P. Hammett in 1935 for quantitatively stating the effect of a substituent on the equilibrium or reaction of a benzene derivative, is widely recognized today. The values of the substituent constants σp and σm are calculated using the Hammett's equation. These values can be seen in many common treatises, and are described in detail in J. A. Dean, ed., Lange's Handbook of Chemistry, 12th Ed., 1979 (McGraw-Hill) and The Domain of Chemistry, Supplemental Edition No. 122, pp. 96-103, 1979 (Nankodo), for example. The contents thereof are expressly incorporated herein by reference in their entirety. In the present specification, the various substituents are limited or described by Hammett's substituent constant σp. However, this does not mean that they are limited to substituents for which values exist in the literature and can be found in the above-cited treatises; when the value has not been given in the literature, but has been determined based on Hammett's equation, substituents included within the given range are covered. The above general formulas include compounds that are not benzene derivatives; however, the value of σp is employed irrespective of substitution position as a measure of the electron activity of a substituent. The σp value is employed with this meaning in the present specification.
Desirable examples of R18 are the substituents described for R4 and R8 in general formula (2). Alkyl groups having 1 to 6 carbon atoms and alkoxy groups having 1 to 6 carbon atoms are preferred.
Desirable examples of R19 and R20 are the substituents described for R3 in general formula (1). Each preferably independently denotes a hydrogen atom, substituted or unsubstituted alkyl group, substituted or unsubstituted aryl group, or substituted or unsubstituted heterocyclic group, and more preferably denotes a hydrogen atom or substituted or unsubstituted alkyl group.
In desirable substituent combinations of the dye denoted by general formula (5), it is desirable for at least one of the various substituents to be one of the above desirable groups, preferable for more of the various substituents to be from among the above desirable groups, and more preferable for all of the substituents to be from among the above desirable groups.
The following combination is an example of a specific desirable combination: a combination in which A3 denotes 2-pyrazoline-5-one comprising a substituent, EWG1 denotes a cyano group, R18 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms or a substituted or unsubstituted alkoxy group having 1 to 6 carbon atoms, R19 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, R20 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, and n5=0 to 4. The following combination is an example of a preferred combination: a combination in which A3 denotes 2-pyrazoline-5-one comprising a substituent, EWG1 denotes a cyano group, R19 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, R20 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, and n5=0.
Medium 5
Medium 5 comprises the dye denoted by the following general formula (6) in the visible information recording layer.
In general formula (6), each of R51 and R52 independently denotes a monovalent substituent. Examples of the monovalent substituent are those described for R1, R2, and R3 above. n8 denotes an integer ranging from 0 to 5, and n9 denotes an integer ranging from 0 to 4.
Examples of R51 are the substituents described for R4 and R8 in general formula (2). A hydrogen atom or an alkyl group having 1 to 6 carbon atoms is preferred, with an alkyl group having 1 to 6 carbon atoms being of greater preference.
Examples of R52 are the substituents described for R4 and R8 in general formula (2). Aryloxycarbonyl groups having 6 to 10 carbon atoms, alkoxycarbonyl groups having 1 to 6 carbon atoms, and substituted and unsubstituted carbamoyl groups are desirable, with substituted carbamoyl groups being preferred.
In desirable substituent combinations of the dye denoted by general formula (6), it is desirable for at least one of the various substituents to be one of the above desirable groups, preferable for more of the various substituents to be from among the above desirable groups, and more preferable for all of the substituents to be from among the above desirable groups.
The following combination is an example of a specific desirable combination: a combination in which R51 denotes an alkyl group having 1 to 6 carbon atoms; R52 denotes a substituted or unsubstituted carbamoyl group or aryloxycarbonyl group having 6 to 10 carbon atoms or alkoxycarbonyl group having 1 to 6 carbon atoms; n8=0 to 3, and n9=0 to 3. The following combination is an example of a preferred combination: a combination in which R51 denotes an alkyl group having 1 to 6 carbon atoms; R52 denotes a substituted or unsubstituted carbamoyl group or aryloxycarbonyl group having 6 to 10 carbon atoms or alkoxycarbonyl group having 1 to 6 carbon atoms; n8=0 to 2; and n9=0 to 2. The following combination is an example of a combination of greater preference: a combination in which R51 denotes an alkyl group having 1 to 6 carbon atoms; R52 denotes a substituted or unsubstituted carbamoyl group or aryloxycarbonyl group having 6 to 10 carbon atoms or alkoxycarbonyl group having 1 to 6 carbon atoms; n8=0 to 1; and n9=0 to 2.
Medium 6
Medium 6 comprises the dye denoted by the following general formula (7) in the visible information recording layer.
In general formula (7), R64 denotes a hydrogen atom or a monovalent substituent, and R61 denotes a monovalent substituent. Examples of these monovalent substituents are those described for R1, R2, and R3 above. Each of R63 and R62 independently denotes a hydrogen atom, substituted or unsubstituted alkyl group, substituted or unsubstituted aryl group, or substituted or unsubstituted heterocyclic group. n10 denotes an integer ranging from 0 to 4.
Examples of R64 are the substituents described for R1 and R2 in general formula (1); the same holds true for desirable examples. A hydrogen atom or alkyl group having 1 to 6 carbon atoms is preferred, with a hydrogen atom being of greater preference.
Examples of R61 are the substituents described for R4 and R8 in general equation (2); the same holds true for desirable examples. An alkyl group having 1 to 6 carbon atoms is preferred, and an alkyl group having 1 to 6 carbon atoms is of greater preference.
Examples of R62 and R63 are the substituents described for R3 in general formula (1); the same holds true for desirable examples. A hydrogen atom or a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms is preferred.
In desirable substituent combinations of the dye denoted by general formula (7), it is desirable for at least one of the various substituents to be one of the above desirable groups, preferable for more of the various substituents to be from among the above desirable groups, and more preferable for all of the substituents to be from among the above desirable groups.
The following combination is an example of a specific desirable combination: a combination in which R61 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms; R62 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms; R63 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms; R64 denotes a hydrogen atom; and n10=0 to 4. The following combination is an example of a preferred combination: a combination in which R61 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms; R62 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms; R63 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms; R64 denotes a hydrogen atom; and n10=0 to 1.
Medium 7
Medium 7 comprises the dye denoted by the following general formula (8) in the visible information recording layer.
In general formula (8), each of R71 and R73 independently denotes a hydrogen atom or a monovalent substituent. Each of R72 and R74 independently denotes a monovalent substituent. Examples of these monovalent substituents are the substituents described for R1, R2, and R3 above. n11 denotes an integer ranging from 0 to 4 and n12 denotes an integer ranging from 0 to 2.
Examples of R71 and R73 are the substituents described for R3 in general formula (1); the same holds true for desirable examples. A hydrogen atom or substituted or unsubstituted alkyl group having 1 to 6 carbon atoms is preferred, with a hydrogen atom being of greater preference.
Examples of R72 and R74 are the substituents described for R4 and R8 in general formula (2). Alkoxy groups, aryloxy groups, acyloxy groups, carbamoyloxy groups, alkoxycarbonyloxy groups, and aryloxycarbonyloxy groups are desirable, and alkoxy groups and aryloxy groups are preferred. Each group may comprise substituents.
In desirable substituent combinations of the dye denoted by general formula (8), it is desirable for at least one of the various substituents to be one of the above desirable groups, preferable for more of the various substituents to be from among the above desirable groups, and more preferable for all of the substituents to be from among the above desirable groups.
The following combination is an example of a specific desirable combination in general formula (8): a combination in which R71 denotes a hydrogen atom; R72 denotes a substituted or unsubstituted aryloxy group having 6 to 12 carbon atoms; R73 denotes a hydrogen atom; n11=0; and n12=0 to 2. The following combination is an example of a preferred combination: a combination in which R71 denotes a hydrogen atom; R72 denotes a substituted or unsubstituted aryloxy group having 6 to 12 carbon atoms; R73 denotes a hydrogen atom; n11=0; and n12=2.
Medium 8
Medium 8 comprises the dye denoted by the following general formula (9) in the visible information recording layer.
In general formula (9), R81 denotes a hydrogen atom or a monovalent substituent, and each of R82 and R84 independently denotes a monovalent substituent. Examples of these monovalent substituents are those described for R1, R2, and R3 above. n13 denotes an integer ranging from 0 to 4 and n14 denotes an integer ranging from 0 to 2.
Examples of R81 are the substituents described for R3 in general formula (1); the same holds true for desirable examples. A hydrogen atom or substituted or unsubstituted alkyl group having 1 to 6 carbon atoms is preferred, and a hydrogen atom is of greater preference.
Examples of R82 and R84 are the substituents described for R4 and R8 in general formula (2). Alkoxy groups, aryloxy groups, acyloxy groups, carbamoyloxy groups, alkoxycarbonyloxy groups, and aryloxycarbonyloxy groups are preferred, and alkoxy and aryloxy groups are of greater preference. Each group may comprise substituents.
In desirable substituent combinations of the dye denoted by general formula (9), it is desirable for at least one of the various substituents to be one of the above desirable groups, preferable for more of the various substituents to be from among the above desirable groups, and more preferable for all of the substituents to be from among the above desirable groups.
The following combination is an example of a specific desirable combination in general formula (9): a combination in which R81 denotes a hydrogen atom; R82 denotes an aryloxy group, n13=0, and n14=1 to 2. The following combination is an example of a preferred combination: a combination in which R81 denotes a hydrogen atom, R82 denotes an aryloxy group, n13=1, and n14=0. The following combination is an example of a combination of greater preference: a combination in which R81 denotes a hydrogen atom, R82 denotes an aryloxy group, n13=0, and n14=1, with R82 being substituted at the o-position relative to the amino group.
Medium 9
Medium 9 comprises the dye denoted by the following general formula (10) in the visible information recording layer.
In general formula (10), each of R111 and R113 independently denotes a hydrogen atom or a monovalent substituent, each of R112 and R114 independently denotes a monovalent substituent, n18 denotes an integer ranging from 0 to 4, and n19 denotes an integer ranging from 0 to 2. Examples of these monovalent substituents are those described for R1, R2, and R3 above.
Examples of R111 and R113 are the substituents described for R3 in general formula (1); the same holds true for desirable examples. Hydrogen atoms, substituted or unsubstituted alkyl groups having 1 to 6 carbon atoms, and substituted or unsubstituted aryl groups are preferred.
Examples of R112 and R114 are the substituents described for R4 and R8 in general formula (2); the same holds true for desirable examples.
In desirable substituent combinations of the dye denoted by general formula (10), it is desirable for at least one of the various substituents to be one of the above desirable groups, preferable for more of the various substituents to be from among the above desirable groups, and more preferable for all of the substituents to be from among the above desirable groups.
The following combination is an example of a specific desirable combination: a combination in which R111 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms or a substituted or unsubstituted aryl group having 6 to 10 carbon atoms; R113 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms or a substituted or unsubstituted aryl group having 6 to 110 carbon atoms; n18=0; and n19=0. The following combination is an example of a preferred combination: a combination in which R111 denotes a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms; R113 denotes a substituted or unsubstituted aryl group having 6 to 10 carbon atoms; n18=0; and n19=0.
Examples of the substituent when the various above-described substituents are substituted are the monovalent substituents described for R1, R2, and R3 above.
Specific examples of the dyes denoted by the above general formulas (1) to (10) are given below. However, the dyes employed in the present invention are not limited to the following examples.
Some of the dyes denoted by general formulas (1) to (10) are available as commercial products. Those that are not commercially available can be synthesized in accordance with the methods described in the following literature: U.S. application Ser. No. 07/059,442; Specifications of U.S. Pat. No. 3,770,370, Japanese Unexamined Patent Publication (KOKAI) No. 2004-51873, German Patent No. 2,316,755, Japanese Unexamined Patent Publication (KOKAI) Heisci No. 7-137455; Japanese Unexamined Patent Publication (KOKAI) Showa No. 61-31292; J. Chem. Soc. Perkin Transfer I, 1977, 2047; and Chapman, Merocyanine Dye-Donor Element Used in Thermal Dye Transfer. The contents thereof are expressly incorporated herein by reference in their entirety.
<Visible Information Recording Medium>
The optical recording media 1 to 9 of the present invention contain the various dyes in a visible recording layer. In the present invention, it is possible to employ the individual dyes singly, or in combinations of two or more. The dyes denoted by general formulas (1), (2), (3), (6), and (7) are yellow dyes. The dyes denoted by general formulas (4), (5), (8), and (9) are magenta dyes. And the dye denoted by general formula (10) is a cyan dye. In the present invention, suitable dyes can be combined for use as needed based on a desired tone. The various above dyes can absorb the laser beam that is irradiated, resulting in photo-thermal conversion. The heat that is generated can degrade the dye, reducing absorption of light in the visible light region. Thus, a difference in tone can be produced relative to regions in which color is exhibited by undegraded dye, thereby making it possible to form visible information such as an image in the visible information recording layer.
Each of the above dyes desirably has absorbance of equal to or greater than 0.01 (desirably 0.1 to 1.0) for a laser beam in the wavelength region of 400 to 850 nm. The above absorbance of the dye contained in the visible information recording layer can permit the recording with good clarity of visible information such as text, images, and patterns by irradiation with a laser beam.
The visible information recording layer can contain dyes other than the above dyes. The dyes that are employed in combination can be suitably selected based on the desired tone. Examples of dyes that are desirable for forming images with good clarity and high contrast are the cyanine dyes of general formula (I) below.
In general formula (I), each of Za31 and Za32 independently denotes an atom group forming a carbon ring or heterocyclic ring.
A substituted or unsubstituted six-membered aromatic ring is desirable as the carbon ring that is formed. The aromatic ring may be substituted with substituents. Examples of the substituents are the substituents given by way of example for R1, R2, and R3 in general formula (1). Specific examples of carbon rings are substituted or unsubstituted benzene rings and substituted or unsubstituted naphthalene rings. Benzene rings are desirable.
A substituted or unsubstituted six-membered aromatic heterocyclic ring is desirable as the heterocyclic ring that is formed. Examples of substituents are those given by way of example for R1, R2, and R3 in general formula (1). A substituted or unsubstituted pyridine ring is desirable as a heterocyclic ring.
The ring structure formed by Za31 and Za32 is more desirably a carbon ring than a heterocyclic ring.
Each of R100 and R101 independently denotes a hydrogen atom or a monovalent substituent. Examples of monovalent substituents denoted by R100 and R101 are those described above for R1, R2, and R3 in general formula (1). R100 and R101 desirably denote linear or branched, substituted or unsubstituted alkyl groups. The alkyl groups desirably have 1 to 10, preferably 2 to 5, carbon atoms.
Each of R102, R103, R104, R105, R106, R107 and R108 independently denotes a hydrogen atom or a monovalent substituent. Examples of these monovalent substituents are those set forth above for R1, R2, and R3 in general formula (1).
R102, R103, and R104 desirably denote hydrogen atoms or alkyl groups having 1 to 6 carbon atoms; preferably denote hydrogen atoms or alkyl groups having 1 to 4 carbon atoms; and more preferably denote hydrogen atoms.
R105, R106, R107, and R108 desirably denote linear or branched substituted or unsubstituted alkyl groups. The alkyl groups desirably have 1 to 6, preferably 1 to 4, carbon atoms.
Each of X1 and X2 independently denotes a carbon atom or a hetero atom. Examples of the hetero atom are nitrogen, sulfur, and oxygen atoms. Oxygen and sulfur atoms are desirable, and sulfur atoms are preferred. X1 and X2 more desirably denote carbon atoms than hetero atoms.
Ka denotes 2 or 3, desirably 2. The plural R102s and R103s that are present may be identical or different.
Q denotes a monovalent anion. Examples of monovalent anions are halogen ions and perchloric acid ions. Halogen ions are desirable.
Specific examples of cyanine dyes denoted by general formula (1) are given below. However, the present invention is not limited to the specific examples given below.
Some of the above cyanine dyes are commercially available. Detailed methods of synthesizing cyanine dyes are described in Cyanine Dyes and Related Compounds, John Wjley & Sons, New York, London, released in 1964, in the series entitled The Chemistry of Heterocyclic Compounds, which is expressly incorporated herein by reference in its entirety.
The visible information recording layer can be formed by coating a coating liquid prepared by dissolving the dyes in a solvent. Any of the various solvents suitable for use in the preparation of coating liquids for recording layers, described further below, may be employed. The details of other additives, the coating method, and the like, are as set forth further below for the recording layer.
The above dyes preferably constitute the principal component of the above visible information recording layer. In the present invention, the term “principal component” means that the content of the dye (total content of dyes when plural dyes are employed) is equal to or greater than 50 mass percent of the total solid component of the visible information recording layer. The dye content of the visible information recording layer preferably constitutes equal to or greater than 80 percent mass, more preferably 90 to 100 mass percent.
When employing the cyanine dye denoted by general formula (1) in combination with dyes denoted by general formulas (1) to (10), it's better to set the mixing ratio so that the reflectance of the optical recording medium at the wavelength of the laser employed in recording is within the specified range of the system. In particular, when drawing an image with the red laser employed with DVD disks, it is desirable to employ a mixture such that the dye of general formula (1) constitutes 5 to 30 mass percent of the total dye in the visible information recording layer, with 10 to 20 mass percent being preferred. The dyes denoted by general formulas (1), (2), (3), (6), and (7) are yellow dyes and do not absorb in the red region. Thus, they cannot absorb laser energy when drawing an image with a red laser. When employing such a laser, recording is conducted by using dyes having absorption in the red range. The cyanine dye of general formula (I) is particularly desirable as a dye for combined use in such cases.
The thickness of the visible information recording layer is preferably 0.01 to 200 micrometers, more preferably 0.05 to 150 micrometers, and further preferably, 0.1 to 50 micrometers. The ratio of the thickness of the visible information recording layer to that of the recording layer (thickness of visible information recording layer/thickness of recording layer) preferably ranges from 1/100 to 100/1, more preferably from 1/10 to 10/1.
The visible information that is recorded on the visible information recording layer means information that can be identified visually, including all visibly recognizable information such as characters (strings), patterns, and graphics. Examples of character information is: information specifying allowed users, information specifying possible use periods, information specifying frequency of use, rental information, information specifying resolution, information specifying layers, information specifying users, copyright information, copyright number information, manufacturer information, manufacturing date information, sale date information, information on store where sold or seller, use set number information, information specifying a region, information specifying language, information specifying applications, information on the product user, and information on use numbers.
<Layer Structure>
The optical recording medium of the present invention may comprise, for example, a first support, a recording layer capable of recording and/or reproducing information by the irradiation of a laser beam, a reflective layer, a visible information recording layer, and a second support in this order. However, the layer structure of the optical recording medium of the present invention is not specifically limited other than that there be a visible information recording layer on a support and that the visible information recording layer comprises the above-described dye. A variety of layer structures are thus possible.
The optical recording medium 10 shown in
The following are examples of the layer structure of the optical recording medium of the present invention:
(1) The first layer structure, as shown in
(2) The second layer structure, not shown in the drawing, is comprised of a first support 16, on which are sequentially formed a recording layer 18, a first reflective layer 20, and an adhesive layer 22. On adhesive layer 22 are provided a visible information recording layer 14 and a second support 26.
(3) The third layer structure, not shown in the drawing, is comprised of a first support 16, on which are sequentially formed a recording layer 18, a first reflective layer 20, a protective layer, and an adhesive layer 22. On adhesive layer 22 are provided a visible information recording layer 14 and a second support 26.
(4) The fourth layer structure, not shown in the drawing, is comprised of a first support 16, on which are sequentially formed a recording layer 18, a first reflective layer 20, a first protective layer, an adhesive layer 22, and a second protective layer. On the second protective layer are provided a visible information recording layer 14 and a second support 26.
(5) The fifth layer structure, not shown, is comprised of a first support 16, on which are sequentially formed a recording layer 18, a first reflective layer 20, a first protective layer, an adhesive layer 22, a second protective layer, and a second reflective layer 24. On second reflective layer 24 are provided a visible information recording layer 14 and a second support 26.
Layer structures (1) to (5) are merely examples. These layer structures need not necessarily be in the above-stated sequences; some replacement is possible. Partial omission is also possible. Further, each layer may be constituted of a single layer or multiple layers.
When the optical recording medium of the present invention is a CD-R, it is preferably comprised of a first support 16, in the form of a transparent disk 1.2±0.2 mm in thickness on which are formed pregrooves 28 (see
(1) An optical information recording medium comprised of two laminated members, each of which is comprised of a first support 16 in the form of a transparent disk 0.6±0.1 mm in thickness on which are formed pregrooves 28 at a track pitch of 0.6 to 0.9 micrometer, on which are sequentially provided a recording layer 18 and a light-reflecting layer, the two laminated members being bonded with their respective recording layers 18 facing inward, with a visible information recording layer 14 that is 1.2±0.2 mm in thickness being formed on at least the first support 16 of one of the two.
(2) An optical information recording medium comprised of a laminated member being comprised of a first support 16 in the form of a transparent disk 0.6±0.1 mm in thickness on which are formed pregrooves 28 at a track pitch of 0.6 to 0.9 micrometer, on which are formed a recording layer 18 and a light-reflecting layer; and a transparent disk-shaped protective support of the same shape as the disk-shaped first support 16 of the laminated member, the laminated member and the protective support being bonded with the recording layer 18 facing inward, with a visible information recording layer 14 that is 1.2±0.2 mm in thickness being provided on the support of at least one of the two. In the above DVD-R optical information recording media, a configuration is also possible in which a protective layer is further provided on the light-reflecting layer.
Each of the above-mentioned layers and support will be sequentially described below.
<Recording Layer>
The recording layer in the optical recording medium of the present invention is a layer that is capable of recording and/or reproducing information when irradiated with a laser beam. The recording layer is a layer that can record encoded information such as digital information. For example, it may be of a recording (preferably a dye recording), phase-changing, or photomagnetic type; there is no specific limitation. However, a dye type is desirable.
Specific examples of the dyes contained in a dye-type recording layer are cyanine dyes, oxonol dyes, metal complex dyes, azo dyes, and phthalocyanine dyes. The dyes described in Japanese Unexamined Patent Publication (KOKAI) Heisei Nos. 4-74690, 8-127174, 11-53758, 11-334204, 11-334205, 11-334206, and 11-334207; and Japanese Unexamined Patent Publication (KOKAI) Nos. 2000-43423, 2000-108513, and 2000-158818 may also be suitably employed. The contents of the above publications are expressly incorporated herein by reference in their entirety.
The above recording layer can be formed by dissolving a recording substance such as a dye in a suitable solvent along with a binder or the like to prepare a coating liquid, coating the coating liquid to a support to form a coating, and then drying the coating. The concentration of the recording substance in the coating liquid generally falls within a range of 0.01 to 15 mass percent, preferably within a range of 0.1 to 10 mass percent, more preferably within a range of 0.5 to 5 mass percent, and further preferably, within a range of 0.5 to 3 mass percent.
The recording layer may be formed by a method such as vapor deposition, sputtering, CVD, or solvent coating. Of these, the use of solvent coating is desirable. In that case, the coating liquid is prepared by dissolving optionally desired quenchers, binders, and the like along with the dyes in a solvent. Next, the coating liquid is coated to the surface of a support to form a coating. The coating is then dried, yielding the recording layer.
Examples of solvents that are suitable for use in the coating liquid are: esters such as butyl acetate, ethyl lactate, and Cellosolve acetate; ketones such as methyl ethyl ketone, cyclohexanol, and methyl isopropyl ketone; chlorinated hydrocarbons such as dichloromethane, 1,2-dichloroethane, and chloroform; amides such as dimethyl formamide; hydrocarbons such as methyl cyclohexane; ethers such as dibutylether, diethylether, tetrahydrofuran, and dioxane; alcohols such as ethanol, n-propanol, isopropanol, n-butanol, and diacetone alcohol; fluorine-based solvents such as 2,2,3,3-tetrafluoropropanol; and glycol ethers such as ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, and propylene glycol monomethyl ether.
These solvents may be employed singly or in combinations of two or more, taking into account the solubility of the dyes employed. To the coating liquid may be further added various additives such as oxidation inhibitors, UV absorbants, plasticizers, and lubricants based on the objective.
Examples of suitable binders when employing a binder are: natural organic polymeric substances such as gelatins, cellulose derivatives, dextran, rosin, and rubber; hydrocarbon resins such as polyethylene, polypropylene, polystyrene, and polyisobutylene; vinyl resins such as polyvinyl chloride, polyvinylidene chloride, and copolymers of polyvinyl chloride and polyvinyl acetate; acrylic resins such as polymethyl acrylate and polymethyl methacrylate; and synthetic organic polymers such as initial condensates of thermosetting resins such as polyvinyl alcohol, chlorinated polyethylene, epoxy resins, bunayral resins, rubber derivatives, and phenol formaldehyde resins.
When employing a binder in the recording layer, the quantity employed generally falls within a range of 0.01 to 50 times, preferably 0.1 to 5 times of the mass of dye.
Examples of methods of coating the above solvent coating are spraying, spin coating, dipping, roll coating, blade coating, using a doctor roll, and screen printing. Recording layer 18 may be a single layer or multiple layers. The thickness of recording layer 18 generally falls within a range of 10 to 500 nm, preferably within a range of 15 to 300 nm, and more preferably, within a range of 20 to 150 nm.
To enhance the photoresistance of the recording layer, various antifading agents may be incorporated. Singlet oxygen quenchers are generally employed as antifading agents. Known singlet oxygen quenchers that are described in publications such as patent specifications may be employed. Antifading agents such as singlet oxygen quenchers are normally employed in a quantity falling within a range of 0.1 to 50 mass percent, preferably within a range of 0.5 to 45 mass percent, more preferably within a range of 3 to 40 mass percent, and furter preferably, within a range of 5 to 25 mass percent of the mass of the dyes.
Specific examples of materials included in phase changing-type recording layers are: Sb—Te alloy, Ge—Sb—Te alloy, Pd—Ge—Sb—Te alloy, Nb—Ge—Sb—Te alloy, Pd—Nb—Ge—Sb—Te alloy, Pt—Ge—Sb—Te alloy, Co—Ge—Sb—Te alloy, In—Sb—Te alloy, Ag—In—Sb—Te alloy, Ag—V—In—Sb—Te alloy, and Ag—Ge—In—Sb—Te alloy. The thickness of a phase changing-type recording layer 18 is preferably 10 to 50 nm, more preferably 15 to 30 nm. A phase changing-type recording layer may be formed by a vapor thin-film deposition method such as sputtering, vacuum deposition or the like.
<First Support>
First support 16 in the optical recording medium shown in
First support 16 is preferably 0.1 to 1.2 mm, more preferably 0.2 to 1.1 mm, in thickness.
To improve smoothness, increase adhesion, and prevent alteration of recording layer 18, an undercoating layer may be provided on the outer surface side (side on which pregrooves 28 are formed) of first support 16 on the side where recording layer 18 is provided.
Examples of the material used in the undercoating layer are: polymethyl methacrylate, acrylic acid—methacrylic acid copolymer, styrene—maleic anhydride copolymer, polyvinyl alcohol, N-methylol acrylamide, styrene—vinyl toluene copolymer, chlorosulfonated polyethylene, nitrocellulose, polyvinyl chloride, chlorinated polyolefin, polyester, polyimide, vinyl acetate—vinyl chloride copolymer, ethylene—vinyl acetate copolymer, polyethylene, polypropylene, polycarbonate, other polymeric substances, and surface-modifying agents such as silane coupling agents. The undercoating layer may be formed by preparing a coating liquid by dissolving or dispersing the above substance in a suitable solvent and coating the coating liquid by a coating method such as spin coating, dip coating, or extrusion coating to the surface of first support 16.
The thickness of the undercoating layer generally falls within a range of 0.005 to 20 micrometers, preferably within a range of 0.01 to 10 micrometers.
<First Reflective Layer>
As shown in
<Adhesive Layer>
As shown in
The material included in adhesive layer 22 is preferably a photosetting resin. Of these, to prevent warping of the disk, a material with a low contraction rate upon curing is preferable. Examples of such thermosetting resins are UV-setting resins (UV-setting adhesives) such as “SD-640” and “SD-347” manufactured by Dainippon Ink and Chemicals, Inc. To impart elasticity, the thickness of adhesive layer 22 preferably falls within a range of 1 to 1,000 micrometers, more preferably a range of 5 to 500 micrometers, and further preferably, within a range of 10 to 100 micrometers.
<Second Support>
As shown in
<Protective Layers>
Protective layers can be provided to physically and chemically protect first reflective layer 20, recording layer 18 and the like. In forms similar to the manufacturing of DVD-R optical recording media, that is, for configurations in which two supports (including cases where one of which is second support 26) are bonded with recording layer 18 facing inward, the formation of a protective layer is not necessarily required.
Examples of materials employed in protective layers are: inorganic substances such as ZnS, ZnS—SiO2, SiO, SiO2, MgF2, SnO2, and Si3N4; and organic substances such as thermoplastic resins, thermosetting resins, and UV-setting resins.
When employing thermoplastic or thermosetting resins, a coating liquid can be prepared by dissolving the resins in a suitable solvent and then coating and drying the coating liquid to form a protective layer. A UV-setting resin can be coated as is, or dissolved in a suitable solvent to prepare a coating liquid, which is then coated, then irradiated to cure the resin, forming a protective layel Various additives, such as antistatic agents, oxidation inhibitors, and UV absorbants, can be added to the coating liquid based on the objective. Protective layers generally range from 0.1 micrometer to 1 mm in thickness.
The optical recording medium of the present invention can be applied as the optical recording medium comprising recording portions (pits) in which reproducible information is recorded by laser beam, that is so-called a read-only optical information recording medium.
[Method of Recording Visible Information]
The first method of recording visible information of the present invention (referred to as “recording method I”, hereinafter) is the method of recording visible information on the visible information recording layer of the optical recording medium of the present invention, wherein the visible information is recorded by using the same laser bean as that used in recording on the recording layer.
The second method of recording visible information of the present invention (referred to as “recording method II”, hereinafter) is the method of recording visible information on the visible information recording layer of the disk-shaped optical recording medium of the present invention, wherein the visible information is recorded by using a laser beam that oscillates in a radial direction of the optical recording medium as well as is irradiated plural times on approximately identical paths. In recording method II, visible information is preferably recorded by using the same laser beam as that used in recording on the recording layer, as in recording method I.
Recording methods I and II are sometimes collectively referred to as the “recording method of the present invention” hereinafter.
In recording method I, the same laser beam (laser beam 12 in
In the recording method of the present invention, the recording of visible information such as images on the visible information recording layer and the recording of optical information on the recording layer can be conducted with a single optical disk drive (recording device) functioning to record on both layers. When a single optical disk drive is employed in this manner, following recording on either the visible information recording layer or the recording layer, the disk can be flipped over for recording on the other layer. For example, the optical disk drives described in Japanese Unexamined Patent Publication (KOKAI) Nos. 2003-203348 and English language family member US 2003/0117932 A1, 2003-242750 and the like can be employed as optical disk drives having the function of recording visible information on the visible information recording layer. The contents of the above publications are expressly incorporated herein by reference in their entirety.
When recording visible information on the visible information recording layer, the optical recording medium and the laser pickup can be moved relatively along the surface of the optical recording medium by the recording device. The laser beam can synchronize with this relative movement, and the laser beam can be modulated based on image data such as characters or drawings to be formed as images and directed onto the visible information recording layer to record a visible image. Such a configuration, for example, is described in Japanese Unexamined Patent Publication (KOKAI) No. 2002-203321 and English language family member U.S. Pat. No. 7,015,939, and the like. The contents of the above publications are expressly incorporated herein by reference in their entirety.
In ordinary digital data recording, a laser beam is normally irradiated once over a roughly elliptical path. Generally, in the course of forming pits in the dye recording layer, the formation of pits producing adequate reflectance and an adequate degree of modulation for identification by the drive is considered important. Thus, dyes yielding adequate reflectance and an adequate degree of modulation by this single pass of the laser beam are selected as the dye in the dye recording layer.
By contrast, the system described in Japanese Unexamined Patent Publication (KOKAI) No. 2002-203321 has been proposed as a new method of image formation. In this system, a laser beam is irradiated plural times over roughly the same paths to record visible information such as an image on a visible information recording layer containing dye. Further, although the laser beam cannot be oscillated in a radial direction of the optical disk since the positions at which bits are radially formed are specified on common optical disks, in the above system, the laser beam oscillates in a radial direction of the optical disk and irradiated plural times over approximately the same paths to form visible information. The dyes employed in the present invention are all suited to this system and permit the formation by the above-described recording method of sharp visible information of high contrast and good resistance to light.
The above-mentioned image forming method will be described below in detail with reference to
First, as shown in
Subsequently, the optical disk is rotated once and returned to a circumferential reference position, a feed motor or the like displaces the laser beam source outward by the amount Δr of a prescribed pitch, and the laser power is switched to a prescribed high output at various circumferential image formation positions indicated by the image data for the corresponding radial position to form an image. Subsequently, this operation is repeated and the laser beam source is sequentially displaced outward by a prescribed pitch Δr each time around to form an image.
In the above image forming method, radial positions where there are no image formation spots are not scanned and the laser beam source is moved directly to the next radial location of an image formation spot to form an image. The larger pitch Δr is, the greater the gaps that are generated in the image that is formed, even in images that should normally be formed so as to be connected radially. The gaps can be rendered inconspicuous by reducing pitch Δr, but the number of passes required to form an image over the entire label surface increases and the time required for image formation ends up increasing. In the device described in Japanese Unexamined Patent Publication (KOKAI) No. 2002-203321, an oscillating signal (sine waves, chopping waves, or the like) generated by an oscillating signal generation circuit during image formation is used to drive a tracking actuator, causing an object lens to oscillate in a radial direction of the disk. In this manner, the laser beam is made to vibrate in a radial direction of the disk, permitting image formation in which there is no gap (or a small gap) even for a relatively large pitch Δr. The frequency of the oscillating signal can be set to about several kHz, for example. Pitch Δr can be set to about 50 to 100 micrometers, for example.
Japanese Unexamined Patent Publication (KOKAI) No. 2002-203321 can be referenced for details of the above image forming method.
The recording device that records the optical information (digital information) on the recording layer comprises at least a laser pickup emitting a laser beam and a rotating mechanism that causes the optical recording medium to rotate, and is capable of recording on and reproducing from the recording layer by irradiating a laser beam from the laser pickup toward the recording layer of the optical recording medium while the latter is being rotated. Such a recording device configuration is known.
The recording of information (digital information) on the recording layer will be described below. In the case of a dye-type recording layer, a laser beam is irradiated by the laser pickup while rotating an unrecorded optical recording medium described above at a prescribed linear recording speed. The irradiated beam is absorbed by the dye in the recording layer, causing the temperature to rise locally. A desired void (bit) is generated, thereby changing the optical characteristics to record information.
When forming a single bit, the recording waveform of the laser beam can be either a series of pulses or a single pulse. The ratio to the length (the bit length) actually being recorded is important.
The pulse width of the laser beam preferably falls within a range of 20 to 95 percent, more preferably a range of 30 to 90 percent, and further preferably a range of 35 to 85 percent, of the bit length actually being recorded. When the recording waveform is a series of pulses, it means that the sum of the pulses falls within the above-stated range.
The power of the laser beam varies with the linear recording speed. At a linear recording speed of 3.5 m/s, the power preferably falls within a range of 1 to 100 mW, more preferably within a range of 3 to 50 mW, and further preferably within a range of 5 to 20 mW. When the linear recording speed is doubled, the range of the power of the laser beam is preferably adjusted 21/2-fold. To increase the recording density, the NA of the object lens employed in the pickup is preferably equal to or greater than 0.55, more preferably equal to or greater than 0.6. In the present invention, a semiconductor laser having an oscillation wavelength falling within a range of 350 to 850 nm can be employed as the recording beam.
The case of a phase changing-type recording layer will be described below. In a phase changing type, the recording layer is comprised of the above-described substances and a laser beam is irradiated to change the phase back and forth between a crystalline phase and an amorphous phase. During information recording, a concentrated laser beam pulse is briefly irradiated, partially melting the phase changing recording layer. The melted portion is rapidly cooled by heat dispersion and solidifies, forming an amorphous recording mark. During deletion, the recording mark portion is irradiated by the laser beam, heating it to a temperature below the melting point of the recording layer but above its crystallization temperature. It is then gradually cooled, causing the amorphous recording mark to crystallize and return to an unrecorded state.
The present invention will be further described below based on Examples. However, the present invention is not limited to the embodiments described in Examples.
Example 1 of the optical information recording medium has the layer structure shown in
A first support 16 that was 0.6 mm in thickness, 120 mm in diameter, and had spiral (helical) grooves (130 nm deep, 300 nm in width, with a track pitch of 0.74 micrometers) was formed out of polycarbonate resin by injection molding.
Subsequently, a coating liquid was prepared by dissolving 1.5 g each of the two oxonol dyes indicated below in 100 mL of 2,2,3,3-tetrafluoro-1-propanol. The coating liquid was coated by spin coating to the surface of first support 16 on which pregrooves 28 had been formed, yielding a recording layer 18.
Next, silver was sputtered onto recording layer 18 to form a first reflective layer 20 that was 120 nm in thickness, UV-curing resin (SD318, made by Dainippon Ink and Chemicals, Inc.) was coated by spin coating, and UV radiation was irradiated to cure the resin, forming a first protective layer that was 10 micrometers in thickness. The above steps yielded a first disk.
To form a visible information recording layer 14, 1.0 g of the following dye (1)-1 and 0.2 g of the following dye (A) were dissolved in 100 mL of 2,2,3,3-tetrafluoro-1-propanol to prepare a coating liquid for visible information recording layer. The coating liquid for visible information recording layer was spin coated on a second support 26 that was 0.6 mm in thickness and 120 mm in diameter to form a visible information recording layer 14.
Next, silver was sputtered onto visible information recording layer 14 to form a second reflective layer 24 that was 120 nm in thickness, UV-curing resin (SD318, made by Dainippon Ink and Chemicals, Inc.) was coated by spin coating, and UV radiation was irradiated to cure the resin, forming a second protective layer that was 10 micrometers in thickness. The above steps yielded a second disk.
The first and second disks were bonded together to form a single disk by the following steps. First, a slow-acting cationic polymerization adhesive (SDK7000, made by Sony Chemicals Corp.) was printed by screen printing on both the first protective layer of the first disk and the second protective layer of the second disk. A printing plate with a mesh size of 300 was used for the screen printing. Next, immediately after using a metal halide lamp to irradiate UV radiation, the first and second disks were bonded on their protective layer sides. Pressure was applied from both sides and left in place for 5 minutes to prepare the optical recording medium of Example 1.
With the exception that the dyes employed in the visible information recording layer were changed to the dyes indicated in Table 2, optical recording media were manufactured in the same manner as in Example 1.
(Contrast Evaluation)
Recording was conducted in the following manner with the optical recording media prepared in Examples 1 to 9.
Using the recording device (the laser being a semiconductor laser with a wavelength of 660 nm) having a laser pickup emitting a laser beam and a rotation mechanism rotating the optical recording medium described in Japanese Unexamined Patent Publication (KOKAI) No. 2002-203321, while relatively moving the laser pickup along the surface of the optical recording medium, the semiconductor laser beam was synchronized with the relative movement and modulated based on desired image data. Under conditions of a linear speed of 3.5 m/s and a recording power of 8 mW, the focused laser beam was irradiated onto visible information recording layer 14 to record a visible image. At the time, the laser beam was oscillated in a radial direction of the optical disk and irradiated in plural times on approximately the identical paths to record the visible information. With the optical recording medium being rotated by the rotation mechanism, it is possible for the laser pickup of the recording layer 18 to irradiate the laser beam and record electronic information.
The absolute reflectance of portions of the visible information recording layer exposed to the laser and portions unexposed to the laser was measured for each of the optical recording media on which visible images had been recorded as set forth above.
The following equation was then used to calculate the Sv, and the contrast was evaluated according to the following evaluation criteria.
U(λ): Spectral reflectivity of the portion unexposed to the laser beam [%]
<Standards for Evaluation>
5 (Excellent contrast): equal to or greater than 0.25
4 (Good contrast): equal to or greater than 0.20 but less than 0.25
3 (Practically sufficient contrast): equal to or greater than 0.15 but less than 0.20
2 (Insufficient contrast): equal to or greater than 0.10 but less than 0.15
1 (Poor contrast): less than 0.10
As shown in Table 2, the contrast of the visible information recording layer was good and sharp image recording was possible in the optical recording media of Examples 1 to 11. In addition, recording media on which images with various colors could be drawn were obtained by selecting the combination of dyes.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2007-016321 | Jan 2007 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2007/061700 | 6/11/2007 | WO | 00 | 7/24/2009 |
