IP Library Granted Patent US 7,642,036
Granted Patent B2
US 7,642,036 · App. 11/205,078 · Granted Jan 5, 2010

Azo-metal chelate dye and optical recording medium

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Quick Facts
Patent No.
US 7,642,036
App. No.
11/205,078
Granted
Jan 5, 2010
Kind
B2
Abstract

The azo-metal chelate dye to which the present invention is applied is a compound formed as follows: for example, 1,3,4-thiadiazole ring is selected as the diazo component; the diazo component is combined with a coupler component having condensed rings including a fluorine-substituted alkylsulfonylamino group and an amino group, to form an azo dye compound; and the azo dye compound forms chelate bonds with at least one metal selected from the group consisting of Co, Ni, Cu and Pd. Here, two absorption bands (OD 1 and OD 2 ) are seen in the absorption spectrum, which is measured in a range of 400 to 800 nm wavelengths. The azo-metal chelate dye is characterized in that the optical density ratio (OD 2 /OD 1 ) of the two absorption bands is greater than 1.25. By using this azo-metal chelate dye, an optical recording medium capable of high-speed recording is provided.

Claims (17)

1. A method comprising recording on an optical recording medium with a laser at a wavelength of from 633 to 680 nm, wherein the optical recording medium comprises a grooved substrate, a reflecting layer, a recording layer, and an optional protection layer, wherein the recording layer comprises an azo-metal chelate dye comprising an azo dye compound and a metal, wherein the azo-metal chelate dye has a OD 2 /OD 1 value of greater than 1.25, which is measured by the following method:

(1) after adding 20 mg of azo-metal chelate dye into 2 g of an octafluoropentanol (OFP) solvent, supersonic dispersion is performed at temperatures between 50° C. and 65° C. for 60 minutes to obtain a solution A, and the solution A is then cooled to room temperature (25±5° C.) to obtain a solution B;

(2) the solution B is applied onto a polycarbonate substrate by spin coating at a rotating speed of 800 rpm, and the substrate onto which the elution B has been spin coated is then annealed at 80° C. for 5 minutes,

the substrate thus obtained, onto which the solution B has been spin coated, being referred to as a coated substrate A;

(3) the absorption spectrum of the coated substrate A is measured in a range of 400 to 800 nm; and

(4) concerning the absorption peaks seen in a range of 500 to 700 nm in the obtained absorption spectrum, the absorption peak at which the optical density is the greatest and the absorption peak at which the optical density is the second greatest are selected, the optical density at the peak on the long wavelength side is defined as OD 2 and the optical density at the peak on the short wavelength side is defined as OD 1 , and the OD 2 /OD 1 value is calculated,

wherein the azo dye compound is represented by the following formula (1):

(where R 1 represents a hydrogen atom or an ester group represented as CO 2 R 3 , R 3 represents a straight or branched chain alkyl group which may be substituted or a cycloalkyl group which may be substituted, R 2 represents a straight or branched chain alkyl group which may be substituted, at least one of X 1 and X 2 represents an NHSO 2 Y group, Y represents a straight or branched chain alkyl group which is substituted with at least two fluorine atoms, R 4 and R 5 independently represents a hydrogen atom or a straight or branched chain alkyl group which may be substituted, and R 6 , R 7 , R 8 and R 9 independently represents a hydrogen atom or a alkyl group having 1 to 2 carbon atoms).

2. The method according to claim 1 , wherein the metal is at least one selected from the group consisting of Ni, Co, Cu and Pd.

3. The method according to claim 1 , wherein the azo-metal chelate dye exhibits the absorption maximum at wavelengths equal to or shorter than 650 nm with regard to the applied light.

4. The method according to claim 1 , wherein the azo-metal chelate dye has a maximum absorption at a wavelength of 700 nm or less.

5. The method according to claim 1 , wherein the azo-metal chelate dye has a maximum absorption at a wavelength of from 650 to 500 nm.

6. The method according to claim 1 , wherein the azo-metal chelate dye has a OD 2 /OD 1 value of 1.29 or more.

7. The method according to claim 1 , wherein the metal is at least Ni.

8. The method according to claim 1 , wherein recording is carried out at a speed approximately 28 m/s or more.

9. The method according to claim 1 , wherein recording is carried out with a laser at a wavelength of 660 nm.

10. The method according to claim 1 , wherein recording is carried out at 8×-speed.

Assignments (7)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 23, 2020
From: MITSUBISHI CHEMICAL MEDIA CO., LTD.
To: CMC MAGNETICS CORPORATION
Reel/Frame 051688/0598 →
CHANGE OF NAME Recorded Nov 11, 2019
From: MITSUBISHI KAGAKU MEDIA CO., LTD.
To: MITSUBISHI CHEMICAL MEDIA CO., LTD.
Reel/Frame 050978/0091 →
CHANGE OF ADDRESS Recorded Nov 11, 2019
From: MITSUBISHI KAGAKU MEDIA CO., LTD.
To: MITSUBISHI KAGAKU MEDIA CO., LTD.
Reel/Frame 050977/0911 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 20, 2009
From: MITSUBISHI CHEMICAL CORPORATION
To: MITSUBISHI KAGAKU MEDIA CO., LTD.
Reel/Frame 022429/0244 →
CORPORATE ADDRESS CHANGE Recorded Jan 21, 2009
From: MITSUBISHI CHEMICAL CORPORATION
To: MITSUBISHI CHEMICAL CORPORATION
Reel/Frame 022126/0470 →
CORPORATE ADDRESS CHANGE Recorded Jan 21, 2009
From: MITSUBISHI KAGAKU MEDIA CO., LTD.
To: MITSUBISHI KAGAKU MEDIA CO., LTD.
Reel/Frame 022128/0827 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 4, 2005
From: SATAKE, KENICHI; NAITOU, YUKO; SHODA, HISASHI; SUZUKI, YUKI
To: MITSUBISHI CHEMICAL CORPORATION; MITSUBISHI KAGAKU MEDIA CO., LTD.
Reel/Frame 017189/0092 →