US2005240019A1PendingUtilityA1
Styryl dyes
Assignee: KABAYUSHI KAISHI HAYASHIBARA SPriority: Dec 2, 1999Filed: Apr 11, 2005Published: Oct 27, 2005
Est. expiryDec 2, 2019(expired)· nominal 20-yr term from priority
G11B 7/247G11B 7/2467G11B 7/248G11B 7/2472G11B 7/245G11B 7/2463Y10S430/146G11B 7/246G11B 7/2478G11B 7/2475C09B 23/145G11B 2007/24612G11B 7/2531G11B 7/259G11B 7/2495
50
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Claims
Abstract
The present invention provides styryl dyes which have absorption maxima at a wavelength of 400 nm or less and are sensitive to a laser beam with a wavelength of 450 nm or less, light absorbents and optical recording media which comprise the styryl dyes, and a process for producing the styryl dyes which comprises reacting with an aldehyde compound a quaternary ammonium salt of nitrogen atom containing heterocyclic compound having an active methyl or active methylene group.
Claims
exact text as granted — not AI-modified1 . A styryl dye represented by Formula 1:
Formula 1:
wherein in Formula 1, φ 1 represents a heterocycle represented by any one of Formulae 2 to 8; φ 2 represents an optionally substituted aromatic ring or heterocycle; R 1 represents a hydrogen atom, an aliphatic hydrocarbon group, ether group, acyl group, halogen, or cyano group, and the aliphatic hydrocarbon group, ether group, and acyl group may have a substituent; X − represents a counter ion; and “n” is a number of X − to balance the electric charge in the styryl dye:
throughout Formulae 2 to 7, A represents an optionally substituted monocyclic or polycyclic aromatic ring or heterocycle; when A is not present in Formulae 2 to 7, a substituent similar to A is in position filled by A; throughout Formulae 2 to 8, R 2 represents an optionally substituted aliphatic hydrocarbon group and R 3 represents a hydrogen or an optionally substituted aliphatic hydrocarbon group which is identical to or different from R 2 .
2 . The styryl dye of claim 1 , wherein said φ 2 is a nitrogen atom containing heterocycle which forms an ammonium salt.
3 . The styryl dye of claim 1 wherein said counter ion is an organic metal complex anion with a light-resistant improving ability.
4 . The styryl dye of claim 1 which has an absorption maximum at a wavelength of 400 nm or less.
5 . The styryl dye of claim 1 which substantially absorbs a visible light with a wavelength of 450 nm or less when formed in a thin layer.
6 . A process for producing the styryl dye of claim 1 comprising reacting a compound, represented by Formula 9 having φ 1 and R 1 corresponding to Formula 1, with a compound represented by Formula 10 having φ 2 corresponding to Formula 1.
7 . The styryl dye of claim 2 , wherein said counter ion is an organic metal complex anion with a light-resistant improving ability.
8 . The styryl dye of claim 2 which has an absorption maximum at a wavelength of 400 nm or less.
9 . The styryl dye of claim 3 which has an absorption maximum at a wavelength of 400 nm or less.
10 . The styryl dye of claim 2 which substantially absorbs visible light with a wavelength of 450 nm or less when formed in thin layer.
11 . The styryl dye of claim 3 which substantially absorbs visible light with a wavelength of 450 nm or less when formed in thin layer.
12 . The styryl dye of claim 4 which substantially absorbs visible light with a wavelength of 450 nm or less when formed in thin layers.Join the waitlist — get patent alerts
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