Optical recording medium and compound used for the same

• US 20070054084A1
• Filed: 10/08/2004
• Published: 03/08/2007
• Est. Priority Date: 10/10/2003
• Status: Abandoned Application

• Current Assignee: Yamamoto Chemicals, Inc.
• Original Assignee: Mitsui Chemicals Incorporated (Mitsui Chemicals)
• Inventors: Ueno, Keiji, Ishida, Tsutomu, Usui, Hideo, Shiozaki, Hiroyoshi, Ogiso, Akira, Miyasato, Masataka
• Application Number:
  US10/575,239
• Publication Number:
  US 20070054084A1
• Time in Patent Office: Days
• US Class Current: 428/64.400
• CPC Class Codes: G01N 33/54346 Nanoparticles
• CPC Class Codes: G11B 7/24038 Multiple laminated recording layers

Abstract

An optical recording medium wherein the percentage change (|[a²−a¹]/a¹|×100) of the recording layer thickness (a²) at the recorded site of recording layer (A) after recorded with laser light compared with the recording layer thickness (a¹) at unrecorded site of said recording layer (A) is less than 25% and the amount of change (|a²−a¹|) of the recording layer thickness (a²) at recorded site of said recording layer (A) after recorded with laser light compared with the recording layer thickness (a¹) at unrecorded site of said recording layer (A) is controlled to be less than 15 nm. The optical recording medium can enable recording and playback with high quality using laser of 300 nm to 900 nm. Also provided is a compound comprising a six-membered ring structure composed of four carbon atoms and two nitrogen atoms and a bonded substituted or unsubstituted amino group.

Claims

1. An optical recording medium containing at least one recording layer (A) capable of recording and playback with a laser light, wherein said recording layer (A) contains at least one kind of organic compound,

wherein the percentage change (|[a²−

a¹]/a¹|×

100) of the recording layer thickness (a²) at the recorded site of said recording layer (A) after recorded with a laser light compared with the recording layer thickness (a¹) at unrecorded site of said recording layer (A) is less than 25%, and the amount of change (|a²−

a¹|) of the recording layer thickness (a²) at recorded site of said recording layer (A) after recorded with laser light compared with the recording layer thickness (a¹) at unrecorded site of said recording layer (A) is less than 15 nm.

2. The optical recording medium according to claim 1, wherein said recording layer (A) is able to be formed by a coating method.

3. The optical recording medium according to claim 2, wherein the organic compound is organic compound (B) that comprises a six-membered ring structure composed of four carbon atoms and two nitrogen atoms and a bonded substituted or unsubstituted amino group.

4. The optical recording medium according to claim 3, wherein the recording laser power is 6 mW or lower.

5. The optical recording medium according to claim 3, wherein organic compound (B) is a tautomer and one of the tautomeric structures of organic compound (B) is represented by general formula (0):

(wherein ring A⁰ represents a substituted or unsubstituted carbocyclic aromatic ring or a substituted or unsubstituted heterocyclic aromatic ring;

R^A and R^B represent a hydrogen atom or a substituent;

X⁰ represents a divalent substituent;

Y⁰ represents a substituted or unsubstituted amino group; and

m⁰ represents the number of Y⁰).

6. The optical recording medium according to claim 5, wherein organic compound (B) is a tautomer and one of the tautomeric structures of organic compound (B) is represented by general formula (1):

(wherein ring A and ring B represent a substituted or unsubstituted carbocyclic aromatic ring or a substituted or unsubstituted heterocyclic aromatic ring;

R represents a hydrogen atom or a substituent;

X represents a divalent substituent;

Y represents a substituted or unsubstituted amino group; and

m represents the number of Y).

7. The optical recording medium according to claim 6, wherein organic compound (B) is a tautomer and one of the tautomeric structures of organic compound (B) is represented by general formula (2):

(wherein ring C represents a substituted or unsubstituted carbocyclic aromatic ring or a substituted or unsubstituted heterocyclic aromatic ring;

X′

represents a divalent substituent, each of R⁰-R⁶ represents independently a hydrogen atom or a substituent;

m′

represents the number of R⁵;

n′

represents the number of R⁶;

at least one group selected from R¹-R⁴ is a substituted or unsubstituted amino group;

in a combination among R¹-R⁴ and a combination of R⁵ and R⁶, each substituent within each combination may independently bond via a linkage group to form a ring structure together with the atom to which it bonds; and

each of m′ and

n′

represents 0 or an integer of 1 or more).

8. The optical recording medium according to claim 7, wherein organic compound (B) is a tautomer and one of the tautomeric structures of organic compound (B) is represented by general formula (3):

(wherein ring D represents a substituted or unsubstituted carbocyclic aromatic ring or a substituted or unsubstituted heterocyclic aromatic ring;

X″

represents a divalent substituent, each of R⁷-R¹² represents independently a hydrogen atom or a substituent;

at least one group selected from R⁸-R¹¹ is a substituted or unsubstituted amino group; and

each of R⁸-R¹¹ may independently bond via a linkage group to form a ring structure together with the carbon atom to which it bonds).

9. The optical recording medium according to claim 8, wherein organic compound (B) is a tautomer and one of the tautomeric structures of organic compound (B) is represented by general formula (4):

(wherein each of R¹³-R²⁵ represents independently a hydrogen atom or a substituent; and

in a combination among R¹⁴-R¹⁸ and a combination among R²¹-R²⁵, each substituent within each combination may independently bond via a linkage group to form a ring structure together with the carbon atom and/or nitrogen atom to which it bonds).

10. The optical recording medium according to claim 9, wherein organic compound (B) is a tautomer and one of the tautomeric structures of organic compound (B) is represented by general formula (5):

(wherein each of R²⁶-R³⁵ represents independently a hydrogen atom or a substituent; and

in a combination among R²⁶-R³⁰ and a combination among R³¹-R³⁵, each substituent within each combination may independently bond via a linkage group to form a ring structure together with the carbon atom and/or nitrogen atom to which it bonds).

11. The optical recording medium according to claim 10, wherein at least one group among R³¹-R³⁵ is a substituted alkoxy group having a heterocyclic residue containing at least one heteroatom.

12. The optical recording medium according to claim 10, wherein the atoms constituting each substituent represented by R²⁶-R³⁵ are selected from a carbon atom, a hydrogen atom, a nitrogen atom, a sulfur atom, and an oxygen atom.

13. The optical recording medium according to claim 1, wherein the recording layer (A) contains at least one kind of organic compound that absorbs said laser light and has a temperature at which the color changes by heat.

14. The optical recording medium according to claim 1, wherein the recording layer (A) contains at least one kind of organic compound that absorbs said laser light and forms a crystalline state exothermically when an amorphous state is heated.

15. The optical recording medium according to claim 1, wherein said recording layer (A) contains at least one kind of organic compound which exhibits maximum absorption wavelength (λ

max²) in said recording layer (A) after recording that is different from that (λ

max¹) before recording in said recording layer (A) by irradiation with recording laser light.

16. The optical recording medium according to claim 1, wherein said recording layer (A) contains at least one kind of organic compound that, upon irradiation with a laser light with a recording/playback wavelength of λ

0, exhibits a refraction index n2 and an extinction coefficient k2 after recording that are different from the refraction index n1 and the extinction coefficient k1 of said recording layer (A) at λ

0 before recording.

17. The optical recording medium according to claim 1, wherein the maximum absorption wavelength of the organic compound in solution is shifted to the shorter wavelength when it forms a thin film state of the recording layer.

23. The optical recording medium according to claim 2, wherein the recording laser power is 6 mW or lower.

24. The optical recording medium according to claim 1, wherein the recording laser power is 6 mW or lower.

18. A compound represented by general formula (5)

(wherein each of R²⁶-R³⁵ represents independently a hydrogen atom or a substituent;

and in a combination among R²⁶-R³⁰ and a combination among R³¹-R³⁵, each substituent within each combination may independently bond via a linkage group to form a ring structure together with the carbon atom and/or nitrogen atom to which it bonds).

21. A composition comprising at least one kind of compound represented by general formula (5) of claim 18.

19. A quinazolin-4-one compound represented by general formula (6) having a disubstituted amino group at any of positions 5-8 in the quinazoline-4-ring:

(wherein each of R³⁶-R⁴¹ represents independently a hydrogen atom or a substituent).

20. A process for producing of the quinazolin-4-one compound represented by general formula (6) of claim 19 by reacting a compound represented by the following general formula (7) and a compound represented by general formula (8) and/or general formula (9):

(wherein R³⁶-R⁴¹ represent the same group as R³⁶-R⁴¹ in formula (6); and

Z¹ and Z² represent a leaving group).

22. An optical recording medium comprising a recording layer (A) capable of recording/playback with a laser light on a substrate, wherein the recording layer (A) contains at least one kind of organic compound, wherein recording can be carried out by heat generated on irradiation of said recording layer (A) with recording laser light of 6 mW or lower and/or by the laser light without giving mechanical deformation to the substrate.