Indole compound, optical filter and optical recording material
AssigneeAdeka Corporation
InventorSatoshi Yanagisawa
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AssigneeAdeka Corporation
InventorSatoshi Yanagisawa
Estimating the term…
An indole compound represented by general formula (I): wherein R1 and R2 each represent a hydrogen atom, a hydrocarbon group having 1 to 30 carbon atoms or a substituent represented by general formula (II); R3 and R4 each represent an alkyl group having 1 to 10 carbon atoms, an alkoxy group having 1 to 10 carbon atoms or an aryl group having 6 to 30 carbon atoms; R5, R6, R7, and R8 each represent a hydrogen atom, a hydrocarbon group having 1 to 30 carbon atoms, a halogen atom, a hydroxyl group, a nitro group, a cyano group, NHR or NR′R″; R, R′, and R″ each represent an alkyl group having 1 to 10 carbon atoms, or R′ and R″ are taken together to form a ring; R5 and R6, R6 and R7, or R7 and R8 may be taken together to form a ring; Anq− represents a q-valent anion; q represents 1 or 2; and p represents a coefficient necessary to maintain charge neutrality.
An optical filter containing an indole compound represented by general formula (I):
An optical recording medium comprising a substrate and an optical recording layer on the substrate, wherein the optical recording layer is formed from an optical recording material comprising an indole compound represented by general formula (I):
Dependencies are inferred from the claim text.
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Filters: absorbing filters
With substituted hydrocarbon radicals attached to carbon atoms of the hetero ring: radicals substituted by nitrogen atoms, not forming part of a…
Containing two hetero rings: directly linked by a ring-member-to-ring-member bond
Comprising organic materials only: containing dyes
About 1 year 1 month of term left · ends 1 Dec 2027 (estimated)
This invention relates to a novel indole compound, an optical filter, and an optical recording medium. The indole compound is useful as an optical element and the like. The indole compound is particularly useful as an ultraviolet (UV) absorber incorporated into an optical filter for application to image displays. It is also useful as an optical recording material for use in optical recording media capable of high density optical writing and reading with low energy lasers having wavelengths in the visible to near infrared regions.
Optical recording media have been widespread generally because of their superiority such as high recording capacity and non-contact write/read system. Recordable optical disks such as WORMs, CD-Rs, and DVD-Rs record information by irradiating a very small area of the optical recording layer with a focused laser beam to change the properties of the irradiated area and reproduce the recorded information making use of the difference in reflected light quantity between the recorded area and the non-recorded area.
Wavelengths of semiconductor lasers used in writing and reading information on the currently available optical disks of the type described are in the ranges of 750 to 830 nm for CD-Rs and of 620 to 690 nm for DVD-Rs. In pursuit of a further increased capacity, optical disks using shorter wavelength lasers have been under study. For example, those using a write wavelength of 380 to 420 nm have been studied.
The indole compound and the optical filter and optical recording material containing the indole compound will be described in detail with reference to their preferred embodiments.
The indole compound of the invention is described first.
In general formula (I), examples of the hydrocarbon group having 1 to 30 carbon atoms represented by R1, R2, R5, R6, R7, and R8 include alkyl groups, such as methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, tert-butyl, isobutyl, amyl, isoamyl, tert-amyl, hexyl, cyclohexyl, cyclohexylmethyl, 2-cyclohexylethyl, heptyl, isoheptyl, tert-heptyl, n-octyl, isooctyl, tert-octyl, 2-ethylhexyl, nonyl, isononyl, decyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, and octadecyl; alkenyl groups, such as vinyl, 1-methylethenyl, 2-methylethenyl, propenyl, butenyl, isobutenyl, pentenyl, hexenyl, heptenyl, octenyl, decenyl, pentadecenyl, and 1-phenylpropen-3-yl; phenyl; naphthyl; alkylaryl groups, such as 2-methylphenyl, 3-methylphenyl, 4-methylphenyl, 4-vinylphenyl, 3-isopropylphenyl, 4-isopropylphenyl, 4-butylphenyl, 4-isobutylphenyl, 4-tert-butylphenyl, 4-hexylphenyl, 4-cyclohexylphenyl, 4-octylphenyl, 4-(2-ethylhexyl)phenyl, 4-stearylphenyl, 2,3-dimethylphenyl, 2,4-dimethylphenyl, 2,5-dimethylphenyl, 2,6-dimethylphenyl, 3,4-dimethylphenyl, 3,5-dimethylphenyl, 2,4-di-t-butylpheyl, and cyclohexylphenyl; arylalkyl groups, such as benzyl, phenethyl, 2-phenylpropan-2-yl, diphenylmethyl, triphenylmethyl, styryl, and cinnamyl; and the above recited hydrocarbon groups interrupted by an ether and/or a thioether linkage, such as 2-methoxyethyl, 3-methoxypropyl, 4-methoxybutyl, 2-butoxyethyl, methoxyethoxyethyl, methoxyethoxyethoxyethyl, 3-methoxybutyl, 2-phenoxyethyl, 3-phenoxypropyol, 2-methylthioethyl, and 2-phenylthioethyl. These hydrocarbon groups may be substituted, e.g., with an alkoxy group, an alkenyl group, a nitro group, a cyano group, or a halogen group. When the hydrocarbon group is substituted with one or more groups selected from alkoxy groups, alkenyl groups, and a cyano group, the total carbon atom number of the hydrocarbon group inclusive of the substituent(s) is 30 at the most.