JP2009066895A - Optical information recording medium and information recording method - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an optical information recording medium capable of carrying out high density recording and reproduction of information by short wavelength laser beam irradiation and having a good shelf life. <P>SOLUTION: The optical information recording medium has a recording layer mainly composed of a coloring matter compound expressed by a general formula (I-1), on a substrate. In the general formula (I-1), E<SP>1</SP>and E<SP>2</SP>are atomic groups required to form a conjugated double bond chain, and Y<SP>1</SP>and -(E<SP>1</SP>)-, and Y<SP>2</SP>and -(E<SP>2</SP>)- are atomic groups required to form carbocyclic or heterocyclic rings respectively. X<SP>1</SP>is O or NR<SP>1</SP>, and X<SP>2</SP>is O or -NR<SP>2</SP>or NR<SP>3</SP>R<SP>4</SP>. R<SP>1</SP>-R<SP>4</SP>are substituents or hydrogen, and X and Y are 0 or 1. <P>COPYRIGHT: (C)2009,JPO&INPIT

Description

  The present invention relates to an optical information recording medium and an information recording / reproducing method capable of recording and reproducing information using a laser beam. In particular, the present invention relates to a heat mode type optical information recording medium suitable for recording information using a short wavelength laser beam having a wavelength of 440 nm or less.

  Conventionally, a write-once type CD (so-called CD-R) is known as an optical information recording medium (optical disc) capable of recording information only once with a laser beam. In its typical structure, a recording layer containing an organic dye, a light reflecting layer made of metal such as gold, and a protective layer made of resin are provided in this order on a transparent disk-like substrate. Information recording on this CD-R is performed by irradiating the CD-R with a near-infrared laser beam (usually a laser beam having a wavelength near 780 nm), and the irradiated portion of the recording layer emits the light. Information is recorded by absorbing and locally raising the temperature, causing physical or chemical changes (eg, pit generation) to change its optical properties. On the other hand, information is read (reproduced) by irradiating a laser beam having the same wavelength as that of the recording laser beam. The information is reproduced by detecting the difference in reflectance from (). Furthermore, a DVD-R that enables high-density recording using visible laser light (630 nm to 680 nm) as a recording laser has been put into practical use. Since DVD-R uses laser light having a shorter wavelength than CD-R as recording laser light, higher-density recording is possible than CD-R. Therefore, in recent years, DVD-R has secured its position as a large-capacity recording medium to some extent.

Recently, networks such as the Internet and high-definition TV are rapidly spreading. In addition, there is an increasing demand for a large-capacity recording medium for recording image information inexpensively and easily, with the upcoming broadcast of HDTV (High Definition Television). However, it cannot be said that the above-mentioned CD-R and DVD-R have a recording procedure large enough to meet future requirements. Therefore, development of an optical disc having a higher recording capacity by improving the recording density by using a laser beam having a wavelength shorter than that of the DVD-R is underway. For example, as such an optical disk, an optical recording disk called a Blu-ray system using a 405 nm blue laser has been put on the market. For example, Patent Documents 1 to 22 disclose porphyrin compounds, azo dyes, metal azo dyes, quinophthalone dyes, trimethine cyanine dyes, dicyanovinylphenyl skeletons as information recording and reproducing methods by irradiation with a short wavelength laser beam such as a blue laser. An information recording / reproducing method for recording / reproducing information by irradiating a blue (wavelength 400 to 430 nm, 488 nm) or blue-green (wavelength 515 nm) laser light onto an optical disk using a dye, a coumarin compound, a naphthalocyanine compound, etc., There has been proposed an information recording / reproducing method for recording / reproducing information by irradiating an optical disk using an oxonol dye as a dye of a recording layer with a laser beam of 550 nm or less.
Japanese Patent Laid-Open No. 11-53758 JP 2001-287460 A JP 2001-287465 A JP 2001-253171 A JP 2001-39034 A JP 2000-318313 A JP 2000-318312 A JP 2000-280621 A JP 2000-280620 A JP 2000-263939 A JP 2000-222772 A JP 2000-222771 A JP 2000-218940 A JP 2000-158818 A JP 2000-149320 A JP 2000-108513 A JP 2000-113504 A JP 2002-301870 A JP 2001-287465 A US Patent Application Publication No. 2002/76648 JP 2003-94828 A JP 2001-71638 A

However, according to the study by the present inventors, in the optical disk using the dye described in Patent Documents 1 to 21, the short wavelength recording characteristics are still not at a sufficiently satisfactory level.
On the other hand, the optical disk using the oxonol dyes disclosed in Patent Document 22 has been required to further improve the light resistance although the short wavelength recording characteristics can be secured to a certain level.
In general, a BD optical disc is stored with the label side (the side opposite to the recording layer) facing up. This is because Blu-ray discs have a light-reflective layer between the substrate and the recording layer, so if stored with the label side up, room light, natural light, etc. are blocked by the light-reflective layer before reaching the recording layer. Because it is done. However, if the reflective layer is thick, the pre-groove on the reflective layer becomes narrower than the pre-groove on the substrate, making it difficult to obtain sufficient characteristics (modulation degree). As a countermeasure, it is conceivable to make the groove of the substrate itself wide and deep in consideration of the narrowing of the groove of the substrate. However, since the track pitch is narrow (preferably 330 nm ≧) in a high-density recording optical disc such as a Blu-ray disc as compared with the track pitch (720 nm) of DVD-R, it is not desirable for molding to have a wide groove on the substrate. . Therefore, in order to obtain the necessary groove width when the track pitch is narrowed in order to increase the recording density, it is desirable that the thickness of the reflective layer is as thin as possible within the range where the reflectance can be obtained. On the other hand, if the reflective layer is made thin, the light transmittance of the reflective layer increases, so that the light blocking property by the reflective layer decreases during storage. Therefore, in order to maintain the storage stability of the recording layer, it is necessary to use a dye having excellent light resistance as a recording dye. Further, if the reflective layer is made thin, the reflectance becomes lower than that of a sufficiently thick reflective layer, which is disadvantageous in terms of recording sensitivity. Therefore, as the reflective layer is made thinner in order to increase the recording density, it is required to improve the light resistance of the dye and to increase the sensitivity of the recording layer itself in order to compensate for the decrease in sensitivity due to the thinner reflective layer.

  Accordingly, an object of the present invention is to provide an optical information recording medium which can record and reproduce information at high density by irradiation with a short wavelength laser beam, particularly a laser beam having a wavelength of 440 nm or less, and has good storage stability.

  As a result of intensive studies in order to achieve the above object, the present inventors have found that a dye compound represented by the following general formula (I-1), a dye compound formed from the compound and a counter ion, and the compound The present inventors have found that a metal complex compound containing as a ligand has excellent information recording / reproduction characteristics by irradiation with a short wavelength laser beam and has excellent light resistance, and has completed the present invention.

[一般式(I-1)中、Ｅ¹およびＥ²は、それぞれ独立に、共役二重結合鎖を完成するために必要な原子団を表し、ｘおよびyは、それぞれ独立に０または１を表し、Ｙ¹は、C-(E¹)x-Cで表される部分構造とともに炭素環または複素環を形成するために必要な原子団を表し、Ｙ²は、C=(E²)y=Cで表される部分構造とともに炭素環または複素環を形成するために必要な原子団を表し、Ｘ¹はＯまたはＮＲ¹を表し、Ｘ²はＯ^-、^-ＮＲ²またはＮＲ³Ｒ⁴を表し、Ｒ¹、Ｒ²、Ｒ³およびＲ⁴は、それぞれ独立に置換基または水素原子を表す。Ｒ¹が置換基を表す場合、Ｒ¹はＹ¹とC-(E¹)x-Cとによって形成される炭素環または複素環と縮環した環を形成してもよく、Ｒ²が置換基を表す場合、Ｒ²はＹ²とC=(E²)y=Cとによって形成される炭素環または複素環と縮環した環を形成してもよく、Ｒ³、Ｒ⁴が置換基を表す場合、Ｒ³、Ｒ⁴はそれぞれＹ²とC=(E²)y=Cとによって形成される炭素環または複素環と縮環した環を形成してもよい。]
[２]前記基板は、少なくとも一方の面にトラックピッチ５０〜５００ｎｍのプレグルーブを有し、該プレグルーブを有する面上に前記記録層を有する[１]に記載の光情報記録媒体。
[３]前記基板と前記記録層との間に光反射層を有する[１]または[２]に記載の光情報記録媒体。
[４]前記基板、前記光反射層、前記記録層、バリア層、および保護層をこの順に有する[３]に記載の光情報記録媒体。
[５]波長４４０ｎｍ以下のレーザー光を照射することにより情報を記録するために使用される[１]〜[４]のいずれかに記載の光情報記録媒体。
[６][１]〜[５]のいずれかに記載の光情報記録媒体に、波長４４０ｎｍ以下のレーザー光を照射することにより情報を記録する情報記録方法。 That is, the above object has been achieved by the following means.
[1] An optical information recording medium having a recording layer containing a dye compound on a substrate,
The dye compound includes a dye compound represented by the following general formula (I-1), a compound represented by the following general formula (I-1), and a counter ion in an amount capable of neutralizing the charge of the compound. An optical information recording medium comprising a dye compound and at least one dye compound selected from the group consisting of a compound represented by the following general formula (I-1) and a metal complex dye compound containing a metal ion or a metal oxide ion.

[In General Formula (I-1), E ¹ and E ² each independently represent an atomic group necessary to complete a conjugated double bond chain, and x and y each independently represents 0 or 1 Y ¹ represents an atomic group necessary for forming a carbocycle or a heterocycle with a partial structure represented by C- (E ¹ ) xC, and Y ² represents C = (E ² ) y = C in conjunction with the partial structure represented represents an atomic group necessary to form a carbocyclic or heterocyclic ring, X ¹ represents O or NR ^1, X ² is O ^{-, -} represents NR ² or NR ³ R ⁴ , R ¹ , R ² , R ³ and R ⁴ each independently represents a substituent or a hydrogen atom. When R ¹ represents a substituent, R ¹ may form a condensed ring with a carbocycle or a heterocycle formed by Y ¹ and C- (E ¹ ) xC, and R ² represents a substituent. When represented, R ² may form a condensed ring with a carbocycle or a heterocycle formed by Y ² and C = (E ² ) y = C, and R ³ and R ⁴ represent a substituent. In this case, R ³ and R ⁴ may each form a ring condensed with a carbocyclic or heterocyclic ring formed by Y ² and C = (E ² ) y = C. ]
[2] The optical information recording medium according to [1], wherein the substrate has a pregroove with a track pitch of 50 to 500 nm on at least one surface, and the recording layer on the surface having the pregroove.
[3] The optical information recording medium according to [1] or [2], wherein a light reflecting layer is provided between the substrate and the recording layer.
[4] The optical information recording medium according to [3], including the substrate, the light reflecting layer, the recording layer, the barrier layer, and the protective layer in this order.
[5] The optical information recording medium according to any one of [1] to [4], which is used for recording information by irradiating a laser beam having a wavelength of 440 nm or less.
[6] An information recording method for recording information by irradiating the optical information recording medium according to any one of [1] to [5] with a laser beam having a wavelength of 440 nm or less.

  According to the present invention, it is possible to obtain an optical information recording medium that exhibits good recording characteristics and good light-resistant storage stability. In particular, since the above effect can be obtained by using a laser having a shorter wavelength than in the case of CD-R and DVD-R, a higher-density information recording medium and a recording / reproducing method can be provided.

[Optical information recording medium]
The optical information recording medium of the present invention has a recording layer containing a dye compound on a substrate. The dye compound contained in the recording layer includes (i) a dye compound represented by the general formula (I-1), (ii) a compound represented by the general formula (I-1) and neutralizing the charge of the compound And at least one dye compound selected from the group consisting of: (iii) a metal complex dye compound containing a compound represented by the general formula (I-1) as a ligand; including. The optical information recording medium of the present invention is suitable as an optical disk for high-density recording in which information is recorded by a short wavelength laser such as Blu-ray Disc (BD) or HD-DVD.
The high-density recording optical disc generally has a structural feature that the track pitch is narrower than that of a conventional write-once optical disc. In addition, a BD-structured optical disc has a reflective layer and a recording layer in this order on a substrate, and further has a relatively thin protective layer (generally called a cover layer) on the recording layer. And has a different layer structure. Therefore, in the optical information recording medium corresponding to the short wavelength laser, the dye used as the recording dye for the conventional write-once optical information recording medium such as CD-R, DVD-R, etc. due to the difference in the layer structure is sufficient. It was a problem that a good recording / reproduction characteristic could not be obtained.
On the other hand, the present inventors have newly found that the dye compound can exhibit good recording / reproducing characteristics in the short wavelength laser compatible optical information recording medium, and further has excellent light resistance. The optical information recording medium of the present invention containing the dye compound in the recording layer has good light resistance, and good recording / reproduction characteristics can be obtained by irradiation with laser light having a short wavelength (for example, a wavelength of 440 nm or less). In particular, the optical information recording medium of the present invention is suitable as a BD medium.
Hereinafter, the optical information recording medium of the present invention will be described in more detail.

Dye compound represented by formula (I-1)

In general formula (I-1), E ¹ and E ² each independently represent an atomic group necessary for completing a conjugated double bond chain. The conjugated double bond chain formed by E ^1, for example, -CH = CH -, - CH = CH-CH = CH -, - CH = C (CH 3) - and the like can be exemplified, E ² Examples of the conjugated double bond chain formed by ═CH—CH═, ═CH—CH═CH—CH═, ═CH—C (CH ₃ ) — and the like can be mentioned.

  x and y each independently represents 0 or 1, and is preferably 0.

Y ¹ represents an atomic group necessary for forming a carbocyclic or heterocyclic ring together with a partial structure represented by C- (E ¹ ) xC, and Y ² is represented by C = (E ² ) y = C. Represents an atomic group necessary for forming a carbocyclic or heterocyclic ring together with the partial structure. Bound to ^{Y 1 [-C (= NR)} - (E 1) x -C (= X 1) -] ( hereinafter, for convenience, in .W ¹ called W ^1, R is formula (I- represent) a corresponding partial structure of 1) binds to ^{Y 2 [-C (-NR ')} = (E 2) y = C (-X 2) -]. ( hereinafter, for convenience, W ^{2. In} W ¹ , R ′ represents a corresponding partial structure in the general formula (I-1)) and is in a conjugated state, and is represented by Y ¹ and C- (E ¹ ) xC. A carbocycle or a heterocycle formed by a partial structure represented by Y ² and C = (E ² ) y = C, each of which is a resonance structure. Is considered. The carbocycle and heterocycle are preferably 4- to 7-membered rings, particularly preferably 5-membered or 6-membered rings. Moreover, as a hetero atom which forms a heterocyclic ring, a boron atom (B), a nitrogen atom (N), an oxygen atom (O), a sulfur atom (S), a selenium atom (Se), and a tellurium atom (Te) are preferable. A nitrogen atom (N), an oxygen atom (O), and a sulfur atom (S) are particularly preferable.

  Each of the carbocycle and the heterocycle may further form a condensed ring with another 4- to 7-membered ring, and these may further have a substituent. Examples of the substituent include the following. A substituted or unsubstituted linear, branched or cyclic alkyl group having 1 to 18 carbon atoms (preferably 1 to 8 carbon atoms) (eg, methyl group, ethyl group, propyl group, isopropyl group, n-butyl) Group, isobutyl group, sec-butyl group, t-butyl group, cyclohexyl group, methoxyethyl group, ethoxycarbonylethyl group, cyanoethyl group, diethylaminoethyl group, hydroxyethyl group, chloroethyl group, acetoxyethyl group, trifluoromethyl group, etc. ); C2-C18 (preferably C2-C8) alkenyl group (e.g., vinyl group); C2-C18 (preferably C2-C8) alkynyl group (e.g., ethynyl group, etc.) A substituted or unsubstituted aryl group having 6 to 18 carbon atoms (preferably 6 to 10 carbon atoms) (eg, phenyl group, 4-methylphenol group, 4 A methoxyphenyl group, a 4-carboxyphenyl group, a 3,5-dicarboxyphenyl group, etc.); a substituted or unsubstituted aralkyl group having 7 to 18 carbon atoms (preferably 7 to 12 carbon atoms) (eg, benzyl group, carboxy group) A benzyl group or the like; a substituted or unsubstituted acyl group having 2 to 18 carbon atoms (preferably 2 to 8 carbon atoms) (eg, acetyl group, propionyl group, butanoyl group, chloroacetyl group, etc.); (Preferably having 1 to 8 carbon atoms) substituted or unsubstituted alkyl or arylsulfonyl group (eg, methanesulfonyl group, p-toluenesulfonyl group, etc.); having 1 to 18 carbon atoms (preferably having 1 to 8 carbon atoms) Alkylsulfinyl group (eg, methanesulfinyl group, ethanesulfinyl group, octanesulphinyl group, etc.); C 2-18 (preferably carbon 2-8) alkoxycarbonyl group (eg, methoxycarbonyl group, ethoxycarbonyl group, butoxycarbonyl group, etc.); aryloxycarbonyl group (eg, phenoxycarbonyl) having 7-18 carbon atoms (preferably 7-12 carbon atoms) Group, 4-methylphenoxycarbonyl group, 4-methoxyphenylcarbonyl group, etc.); a substituted or unsubstituted alkoxy group having 1 to 18 carbon atoms (preferably 1 to 8 carbon atoms) (eg, methoxy group, ethoxy group, n -Butoxy group, methoxyethoxy group, etc.); C6-C18 (preferably C6-C10) substituted or unsubstituted aryloxy group (eg, phenoxy group, 4-methoxyphenoxy group, etc.); C1 -18 (preferably 1-8 carbon atoms) alkylthio group (eg, methylthio group, ethylthio group, etc.); Preferably an arylthio group having 1 to 8 carbon atoms (eg, phenylthio group); a substituted or unsubstituted acyloxy group having 2 to 18 carbon atoms (preferably having 2 to 8 carbon atoms) (eg, an acetoxy group, ethylcarbonyloxy) Group, cyclohexylcarbonyloxy group, benzoyloxy group, chloroacetyloxy group, etc.); substituted or unsubstituted sulfonyloxy group having 1 to 18 carbon atoms (preferably 1 to 8 carbon atoms) (eg, methanesulfonyloxy group, etc.) A substituted or unsubstituted carbamoyloxy group having 2 to 18 carbon atoms (preferably 2 to 8 carbon atoms) (eg, methylcarbamoyloxy group, diethylcarbamoyloxy, etc.); an unsubstituted amino group, or 1 to 18 carbon atoms; A substituted amino group (preferably having 1 to 8 carbon atoms) (eg, methylamino group, dimethylamino group, diethylamino group) , Anilino group, methoxyphenylamino group, chlorophenylamino group, pyridylamino group, methoxycarbonylamino group, n-butoxycarbonylamino group, phenoxycarbonylamino group, phenylcarbamoylamino group, ethylthiocarbamoylamino group, methylsulfamoylamino group , Phenylsulfamoylamino group, ethylcarbonylamino group, ethylthiocarbonylamino group, cyclohexylcarbonylamino group, benzoylamino group, chloroacetylamino group, methanesulfonylamino group, benzenesulfonylamino group, etc.); carbon number 1-18 Amide group (preferably having 1 to 8 carbon atoms) (eg, acetamido group, acetylmethylamide group, acetyloctylamide group, etc.); Is an unsubstituted ureido group (eg, unsubstituted ureido group, methylureido group, ethylureido group, dimethylureido group, etc.); a substituted or unsubstituted carbamoyl having 1 to 18 carbon atoms (preferably 1 to 8 carbon atoms) Group (eg, unsubstituted carbamoyl group, methylcarbamoyl group, ethylcarbamoyl group, n-butylcarbamoyl group, t-butylcarbamoyl group, dimethylcarbamoyl group, morpholinocarbamoyl group, pyrrolidinocarbamoyl group, etc.); unsubstituted sulfamoyl group Or a substituted sulfamoyl group having 1 to 18 carbon atoms (preferably 1 to 8 carbon atoms) (eg, methylsulfamoyl group, phenylsulfamoyl group, etc.); halogen atom (eg, fluorine atom, chlorine atom, bromine atom, etc.) ); Hydroxyl group; mercapto group; nitro group; cyano group; carboxyl group; sulfo group; Suphono group (eg, diethoxyphosphono, etc.); heterocyclic group (eg, oxazole ring, benzoxazole ring, thiazole ring, benzothiazole ring, imidazole ring, benzimidazole ring, indolenine ring, pyridine ring, morpholine ring, piperidine Ring, pyrrolidine ring, sulfolane ring, furan ring, thiophene ring, pyrazole ring, pyrrole ring, chroman ring, and coumarin ring).

[式中、＊は結合部位を示す。]
の具体例としては、以下のものが挙げられる。下記例示式中、Ｒａ、Ｒｂ、ＲｃおよびＲｄは、それぞれ独立に水素原子または置換基を表す。＊は連結部位を表す。また、一般式(I-1)中、下記部分構造：

[式中、＊は結合部位を示す。]
の具体例としては、下記例示式の共鳴構造を挙げることができる。 In the general formula (I-1), the following partial structure:

[In the formula, * represents a binding site. ]
Specific examples of these include the following. In the following exemplary formula, Ra, Rb, Rc and Rd each independently represent a hydrogen atom or a substituent. * Represents a linking site. In the general formula (I-1), the following partial structure:

[In the formula, * represents a binding site. ]
As specific examples, there can be mentioned the resonance structures of the following illustrative formulas.

  In the above exemplified formula, preferred carbocycles or heterocycles are A-8, A-9, A-10, A-11, A-12, A-13, A-14, A-16, A-17, A. -36, A-39, A-41, A-54, A-57, A-65, A-66. More preferably, it is shown by A-8, A-9, A-10, A-13, A-14, A-16, A-17, A-57, A-65, A-66. Most preferably, it is shown by A-9, A-10, A-13, A-17, A-57, A-65.

  In the above exemplary formulas, Ra, Rb, Rc and Rd are each independently a hydrogen atom or a substituent, and examples of the substituent include the following. A substituted or unsubstituted linear, branched or cyclic alkyl group having 1 to 18 carbon atoms (preferably 1 to 8 carbon atoms) (eg, methyl group, ethyl group, propyl group, isopropyl group, n-butyl) Group, isobutyl group, sec-butyl group, t-butyl group, cyclohexyl group, methoxyethyl group, ethoxycarbonylethyl group, cyanoethyl group, diethylaminoethyl group, hydroxyethyl group, chloroethyl group, acetoxyethyl group, trifluoromethyl group, etc. ); C2-C18 (preferably C2-C8) alkenyl group (e.g., vinyl group); C2-C18 (preferably C2-C8) alkynyl group (e.g., ethynyl group, etc.) A substituted or unsubstituted aryl group having 6 to 18 carbon atoms (preferably 6 to 10 carbon atoms) (eg, phenyl group, 4-methylphenol group, 4 A methoxyphenyl group, a 4-carboxyphenyl group, a 3,5-dicarboxyphenyl group, etc.); a substituted or unsubstituted aralkyl group having 7 to 18 carbon atoms (preferably 7 to 12 carbon atoms) (eg, benzyl group, carboxy group) A benzyl group or the like; a substituted or unsubstituted acyl group having 2 to 18 carbon atoms (preferably 2 to 8 carbon atoms) (eg, acetyl group, propionyl group, butanoyl group, chloroacetyl group, etc.); (Preferably having 1 to 8 carbon atoms) substituted or unsubstituted alkyl or arylsulfonyl group (eg, methanesulfonyl group, p-toluenesulfonyl group, etc.); having 1 to 18 carbon atoms (preferably having 1 to 8 carbon atoms) Alkylsulfinyl group (eg, methanesulfinyl group, ethanesulfinyl group, octanesulphinyl group, etc.); C 2-18 (preferably carbon 2-8) alkoxycarbonyl group (eg, methoxycarbonyl group, ethoxycarbonyl group, butoxycarbonyl group, etc.); aryloxycarbonyl group (eg, phenoxycarbonyl) having 7-18 carbon atoms (preferably 7-12 carbon atoms) Group, 4-methylphenoxycarbonyl group, 4-methoxyphenylcarbonyl group, etc.); a substituted or unsubstituted alkoxy group having 1 to 18 carbon atoms (preferably 1 to 8 carbon atoms) (eg, methoxy group, ethoxy group, n -Butoxy group, methoxyethoxy group, etc.); C6-C18 (preferably C6-C10) substituted or unsubstituted aryloxy group (eg, phenoxy group, 4-methoxyphenoxy group, etc.); C1 -18 (preferably 1-8 carbon atoms) alkylthio group (eg, methylthio group, ethylthio group, etc.); Preferably an arylthio group having 1 to 8 carbon atoms (eg, phenylthio group); a substituted or unsubstituted acyloxy group having 2 to 18 carbon atoms (preferably having 2 to 8 carbon atoms) (eg, an acetoxy group, ethylcarbonyloxy) Group, cyclohexylcarbonyloxy group, benzoyloxy group, chloroacetyloxy group, etc.); substituted or unsubstituted sulfonyloxy group having 1 to 18 carbon atoms (preferably 1 to 8 carbon atoms) (eg, methanesulfonyloxy group, etc.) A substituted or unsubstituted carbamoyloxy group having 2 to 18 carbon atoms (preferably 2 to 8 carbon atoms) (eg, methylcarbamoyloxy group, diethylcarbamoyloxy group, etc.); an unsubstituted amino group, or 1 to 1 carbon atoms; 18 (preferably having 1 to 8 carbon atoms) substituted amino group (eg, methylamino group, dimethylamino group, diethylamino group) Group, anilino group, methoxyphenylamino group, chlorophenylamino group, pyridylamino group, methoxycarbonylamino group, n-butoxycarbonylamino group, phenoxycarbonylamino group, phenylcarbamoylamino group, ethylthiocarbamoylamino group, methylsulfamoylamino group Group, phenylsulfamoylamino group, ethylcarbonylamino group, ethylthiocarbonylamino group, cyclohexylcarbonylamino group, benzoylamino group, chloroacetylamino group, methanesulfonylamino group, benzenesulfonylamino group, etc.); An amide group having 18 (preferably 1 to 8 carbon atoms) (eg, acetamido group, acetylmethylamide group, acetyloctylamide group, etc.); substitution of 1 to 18 carbon atoms (preferably 1 to 8 carbon atoms) Or an unsubstituted ureido group (eg, an unsubstituted ureido group, a methylureido group, an ethylureido group, a dimethylureido group, etc.); a substituted or unsubstituted group having 1 to 18 carbon atoms (preferably 1 to 8 carbon atoms) Carbamoyl group (eg, unsubstituted carbamoyl, methylcarbamoyl, ethylcarbamoyl, n-butylcarbamoyl group, t-butylcarbamoyl group, dimethylcarbamoyl group, morpholinocarbamoyl group, pyrrolidinocarbamoyl group, etc.); unsubstituted sulfamoyl group or carbon A substituted sulfamoyl group having 1 to 18 (preferably 1 to 8 carbon atoms) (eg, methylsulfamoyl group, phenylsulfamoyl group, etc.); halogen atom (eg, fluorine atom, chlorine atom, bromine atom); Hydroxyl group; mercapto group; nitro group; cyano group; carboxyl group; sulfo group; Group (eg, diethoxyphosphono); heterocyclic group (eg, oxazole ring, benzoxazole ring, thiazole ring, benzothiazole ring, imidazole ring, benzimidazole ring, indolenine ring, pyridine ring, morpholine ring, piperidine Ring, pyrrolidine ring, sulfolane ring, furan ring, thiophene ring, pyrazole ring, pyrrole ring, chroman ring, and coumarin ring).

  Ra, Rb, Rc and Rd may be connected to each other to form a carbocyclic or heterocyclic ring. Examples of the carbocycle include saturated or unsaturated 4- to 7-membered carbocycles such as a cyclohexyl ring, a cyclopentyl ring, a cyclohexene ring, and a benzene ring. Examples of the heterocyclic ring include saturated or unsaturated 4- to 7-membered heterocyclic rings such as a piperidine ring, piperazine ring, morpholine ring, tetrahydrofuran ring, furan ring, thiophene ring, pyridine ring, and pyrazine ring. it can. These carbocycles or heterocycles may be further substituted. Further, examples of the group which can be substituted include those exemplified as the substituents represented by Ra, Rb, Rc and Rd.

The dye compound comprising the compound represented by the general formula (I-1) and a counter ion in an amount capable of neutralizing the charge of the compound The compound represented by the general formula (I-1) does not contain a counter ion. It can exist as a dye compound in a state, or it can exist as a dye compound in a state containing a counter ion in an amount capable of neutralizing the charge of the compound. As a dye compound containing a counter ion, a dye compound represented by the following general formula (I-2) containing a compound represented by the general formula (I-1) and a counter ion represented by (M) n Can be mentioned.

  In the general formula (I-2), the details of the structure corresponding to the general formula (I-1) are as described above. In general formula (I-2), M represents a cation or an anion, preferably a cation. n represents the number of counter ions necessary for neutralizing the charge of the whole molecule, and is in the range of 1 to 4, for example.

  When M is a cation, examples of the cation represented by M include hydrogen ions, sodium ions, potassium ions, lithium ions, calcium ions, iron ions, copper ions and other metal ions, metal complex ions, ammonium ions, Examples include pyridinium ion, oxonium ion, sulfonium ion, phosphonium ion, selenonium ion, iodonium ion, and the like. Preferably, it is a quaternary ammonium ion.

  Quaternary ammonium is generally a tertiary amine (eg, trimethylamine, triethylamine, tributylamine, triethanolamine, N-methylpyrrolidine, N-methylpiperidine, N, N-dimethylpiperazine, triethylenediamine, N, N, N ', N'-tetramethylethylenediamine, etc.) or nitrogen-containing heterocycle (pyridine ring, picoline ring, 2,2'-bipyridyl ring, 4,4'-bipyridyl ring, 1,10-phenanthroline ring, quinoline ring, oxazole ring , Thiazole ring, N-methylimidazole ring, pyrazine ring, tetrazole ring, etc.) can be obtained by alkylation (Menstokin reaction), alkenylation, alkynylation or arylation.

  The quaternary ammonium ion represented by M is preferably a quaternary ammonium ion composed of a nitrogen-containing heterocyclic ring, particularly preferably a quaternary pyridinium ion.

  Specific examples of the dye compound represented by the general formula (I-1) and the dye compound represented by the general formula (I-2) are shown below, but the present invention is not limited thereto.

［上記式中、＊は窒素原子との結合部位を示す。］

[In the above formula, * represents a bonding site with a nitrogen atom. ]

Metal Complex Dye Compound In a metal complex dye compound containing a compound represented by the general formula (I-1) as a ligand, the coordination in the case where the compound of the general formula (I-1) forms a coordinate bond with a metal species. the position points, X ^1, X ^2, and Y ¹ and Y ² of the nitrogen atoms connecting is preferably at least 2 or more places.

  The metal species to which the compound represented by the general formula (I-1) is coordinated is any metal ion or metal oxide ion capable of complexing with the compound represented by the general formula (I-1). However, it is preferably a divalent or trivalent transition metal ion from the viewpoint of the stability of the complex. Specific examples include Ni ion, Cu ion, Co ion, Zn ion, Al ion, Fe ion, Pd ion, Cr ion and Mn ion, preferably Ni ion, Cu ion, Co ion and Zn ion. Fe ions, particularly preferably nickel ions or copper ions. In addition, even if the metal complex compound which makes the pigment compound represented by general formula (I-1) a ligand has a ligand other than the pigment compound represented by general formula (I-1). Good.

  Although the specific example of the said metal complex pigment | dye compound is given to the following, this invention is not limited to these. In each structural formula, a bond represented by a dotted line means a coordinate bond.

  The dye compound represented by the general formula (I-1) and the dye compound represented by the general formula (I-2) in which the compound represented by the general formula (I-2) forms a salt with a counter ion are generally used. , Nitrosating the corresponding active methylene compound (for example, the acidic nucleus corresponding to A1 to A76), and further condensation reaction with another equivalent of the corresponding active methylene compound (for example, the acidic nucleus corresponding to A1 to A76) Can be synthesized. Specifically, for the nitrosation of an active methylene compound, for example, nitrite (for example, sodium nitrite, potassium nitrite, etc.) or nitrosylsulfuric acid can be used. (For example, triethylamine, pyridine) A catalyst or a dehydrating agent such as acetic anhydride can be used. Moreover, you may perform a nitrosation process and a condensation reaction process continuously by one-pot.

  In addition, the metal complex dye compound containing a compound represented by the general formula (I-1) as a ligand is composed of a compound represented by the general formula (I-1) and a metal salt (eg, nickel acetate, perchloric acid). (Nickel, copper acetate, copper chloride, zinc acetate, cobalt acetate, etc.) can be easily synthesized in a solvent. At this time, for the purpose of increasing the coordination power by dissociating active hydrogen of the compound represented by the general formula (I-1) to form an anionic ligand, an organic base (for example, triethylamine, diethylamine) is used in the reaction system. , Quinoline, etc.) or an inorganic base (eg lithium hydroxide, sodium carbonate, potassium carbonate, etc.) may be added.

  The optical information recording medium of the present invention comprises (i) a dye compound represented by the general formula (I-1), (ii) a compound represented by the general formula (I-1) and a compound of the compound as a recording dye. At least one selected from the group consisting of a dye compound containing a counter ion in an amount capable of neutralizing electric charge, and (iii) a metal complex dye compound containing a compound represented by formula (I-1) as a ligand It is also possible to include two or more of these dye compounds. Moreover, you may use together the said pigment compound and pigment compounds other than this. The content of the dye compound in the recording layer is, for example, in the range of 1 to 100% by mass, preferably in the range of 70 to 100% by mass, and more preferably in the range of 80 to 100% with respect to the total mass of the recording layer. It is in the range of 100% by mass, and most preferably in the range of 90-100% by mass.

  When a dye other than the dye compound is used as the dye component, the dye preferably has an absorption in a short wavelength region having a wavelength of 440 nm or less, for example. Examples of such dyes include, but are not limited to, azo dyes, azo metal complex dyes, phthalocyanine dyes, oxonol dyes, and cyanine dyes.

  In the optical information recording medium of the present invention, the recording layer containing the dye compound is a layer capable of recording information by irradiation with laser light. Here, recording of information by laser light irradiation means that the portion of the recording layer irradiated with the laser light changes its optical characteristics. The change in the optical properties is caused by the portion of the recording layer irradiated with the laser light absorbing the light and locally raising the temperature, causing a physical or chemical change (for example, generation of pits). It is thought that. Reading (reproduction) of information recorded on the recording layer does not change from the portion (recording portion) where the optical characteristics of the recording layer have changed by, for example, irradiating laser light having the same wavelength as the recording laser light. This can be done by detecting a difference in optical characteristics such as reflectance from the portion (unrecorded portion). The dye compound represented by the general formula (I-1) has, for example, absorptivity with respect to laser light having a wavelength of 440 nm or less. Thus, the optical information recording medium of the present invention having a recording layer containing a dye compound having an absorptivity in a short wavelength region can be recorded by a short wavelength laser such as a Blu-ray optical disk using a 405 nm blue laser. It is suitable as a large capacity optical disk. The method for recording information on the optical information recording medium of the present invention will be described later.

  The optical information recording medium of the present invention has at least the recording layer on the substrate, and may further have a light reflecting layer, a protective layer, etc. in addition to the recording layer.

As the substrate used in the present invention, various materials used as substrate materials for conventional optical information recording media can be arbitrarily selected and used. As the substrate, a transparent disk-shaped substrate is preferably used.
Specifically, glass; acrylic resin such as polycarbonate and polymethyl methacrylate; vinyl chloride resin such as polyvinyl chloride and vinyl chloride copolymer; epoxy resin; amorphous polyolefin; polyester; metal such as aluminum; These may be used together if desired.
Among the materials, thermoplastic resins such as amorphous polyolefin and polycarbonate are preferable, and polycarbonate is particularly preferable from the viewpoints of moisture resistance, dimensional stability, and low price. When these resins are used, the substrate can be manufactured by injection molding.
The thickness of the substrate is generally in the range of 0.7 to 2 mm, preferably in the range of 0.9 to 1.6 mm, and more preferably 1.0 to 1.3 mm.
An undercoat layer can also be formed on the substrate surface on the side where the light reflecting layer described later is provided for the purpose of improving flatness and adhesion.

Examples of the material for the undercoat layer include polymethyl methacrylate, acrylic acid / methacrylic acid copolymer, styrene / maleic anhydride copolymer, polyvinyl alcohol, N-methylol acrylamide, styrene / vinyl toluene copolymer, chlorosulfone. Polymer materials such as chlorinated polyethylene, nitrocellulose, polyvinyl chloride, chlorinated polyolefin, polyester, polyimide, vinyl acetate-vinyl chloride copolymer, ethylene-vinyl acetate copolymer, polyethylene, polypropylene, polycarbonate; silane coupling agents And the like.
The undercoat layer is formed by dissolving or dispersing the above materials in an appropriate solvent to prepare a coating solution, and then applying this coating solution to the substrate surface by a coating method such as spin coating, dip coating, or extrusion coating. can do.
The thickness of the undercoat layer is generally in the range of 0.005 to 20 μm, and preferably in the range of 0.01 to 10 μm.

  The surface on which the recording layer of the substrate is formed is usually provided with unevenness (pregroove) representing information such as tracking guide grooves or address signals. In order to achieve a higher recording density, the optical information recording medium of the present invention preferably uses a substrate on which a narrower track pitch is formed than CD-R and DVD-R. Details such as a preferable range of the track pitch will be described later.

  Preferred embodiments of the optical information recording medium of the present invention include the following embodiments (1) and (2).

Aspect (1): Optical information recording medium having a write-once recording layer containing a dye and a cover layer having a thickness of 0.01 to 0.5 mm in order from the substrate side on a substrate having a thickness of 0.7 to 2 mm Aspect (2): Optical information having a write-once recording layer containing a dye and a protective substrate having a thickness of 0.1 to 1.0 mm in order from the substrate side on a substrate having a thickness of 0.1 to 1.0 mm. recoding media

  In aspect (1), it is preferable that the track pitch of the pregroove formed on the substrate is 50 to 500 nm, the groove width is 25 to 250 nm, and the groove depth is 5 to 150 nm. In aspect (2), the substrate It is preferable that the track pitch of the pregroove formed is 200 to 600 nm, the groove width is 50 to 300 nm, the groove depth is 30 to 200 nm, and the wobble amplitude is 10 to 50 nm.

[Optical Information Recording Medium of Aspect (1)]
The optical information recording medium of aspect (1) is an aspect having at least a substrate, a write-once recording layer, and a cover layer, and is a so-called BD-structured optical disk. A specific example of the optical information recording medium of aspect (1) is shown in FIG. A first optical information recording medium 10A shown in FIG. 1 has a first light reflecting layer 18, a first write-once recording layer 14, a barrier layer 20, and a first adhesive layer or a first adhesive on a first substrate 12. It has the layer 22 and the cover layer 16 in this order.
Below, the material which comprises these is demonstrated one by one.

In the substrate of the substrate mode (1), pregrooves (guide grooves) having a shape in which the track pitch, groove width (half width), groove depth, and wobble amplitude are all within the following ranges are formed. . This pre-groove is provided to achieve a higher recording density than CD-R and DVD-R. For example, the optical information recording medium of the present invention is used as a medium corresponding to a blue-violet laser. It is suitable for use.

  The track pitch of the pregroove is in the range of 50 to 500 nm, and the upper limit is preferably 420 nm or less, more preferably 370 nm or less, and further preferably 330 nm or less. Further, the lower limit is preferably 100 nm or more, more preferably 200 nm or more, and further preferably 260 nm or more. If the track pitch is 50 nm or more, the pregroove can be formed accurately, and the occurrence of crosstalk can be avoided. If the track pitch is 500 nm or less, high-density recording can be performed.

  The groove width (half width) of the pregroove is in the range of 25 to 250 nm, and the upper limit value is preferably 200 nm or less, more preferably 170 nm or less, and further preferably 150 nm or less. Further, the lower limit is preferably 50 nm or more, more preferably 80 nm or more, and further preferably 100 nm or more. If the groove width of the pregroove is 25 nm or more, the groove can be sufficiently transferred at the time of molding, and further, an increase in error rate at the time of recording can be suppressed. Furthermore, it is possible to avoid the occurrence of crosstalk due to the spread of pits formed during recording.

  The groove depth of the pregroove is in the range of 5 to 150 nm, and the upper limit is preferably 100 nm or less, more preferably 70 nm or less, and further preferably 50 nm or less. Further, the lower limit is preferably 10 nm or more, more preferably 20 nm or more, and further preferably 28 nm or more. If the groove depth of the pregroove is 5 nm or more, a sufficient recording modulation degree can be obtained, and if it is 150 nm or less, a high reflectance can be obtained.

In addition, the groove inclination angle of the pregroove is preferably 80 ° or less, more preferably 70 ° or less, still more preferably 60 ° or less, and particularly preferably 50 ° or less. preferable. Further, the lower limit value is preferably 20 ° or more, more preferably 30 ° or more, and further preferably 40 ° or more.
If the groove inclination angle of the pregroove is 20 ° or more, a sufficient tracking error signal amplitude can be obtained, and if it is 80 ° or less, the moldability is good.

In the write-once recording layer of write-once recording layer mode (1), a dye is dissolved in a suitable solvent together with a binder or the like or without using a binder, and a coating solution is prepared. Or after apply | coating on the light reflection layer mentioned later and forming a coating film, it can form by drying. Here, the write-once recording layer may be a single layer or a multilayer. In the case of a multilayer structure, the step of applying the coating liquid is performed a plurality of times.
The concentration of the dye in the coating solution is generally in the range of 0.01 to 15% by mass, preferably in the range of 0.1 to 10% by mass, more preferably in the range of 0.5 to 5% by mass, most preferably. It is the range of 0.5-3 mass%.

Solvents used for preparing the coating solution include, for example, esters such as butyl acetate, ethyl lactate and cellosolve acetate; ketones such as methyl ethyl ketone, cyclohexanone and methyl isobutyl ketone; chlorinated hydrocarbons such as dichloromethane, 1,2-dichloroethane and chloroform. Amides such as dimethylformamide; hydrocarbons such as methylcyclohexane; ethers such as tetrahydrofuran, ethyl ether and dioxane; alcohols such as ethanol, n-propanol, isopropanol and n-butanol diacetone alcohol; 2,2,3,3- Fluorinated solvents such as tetrafluoro-1-propanol; glycol agents such as ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, propylene glycol monomethyl ether And the like can be given; le compound.
Solvents can be used alone or in combination of two or more in consideration of the solubility of the dye used. In the coating solution, various additives such as a binder, an antioxidant, a UV absorber, a plasticizer, and a lubricant may be added according to the purpose.

Examples of the coating method include a spray method, a spin coating method, a dip method, a roll coating method, a blade coating method, a doctor roll method, and a screen printing method.
At the time of application, the temperature of the coating solution is preferably in the range of 23 to 50 ° C, more preferably in the range of 24 to 40 ° C, and particularly preferably in the range of 23 to 38 ° C.

The thickness of the write-once recording layer is preferably 100 nm or less, more preferably 70 nm or less, still more preferably 50 nm or less, and 40 nm or less on the land (convex portion in the substrate). It is particularly preferred. The lower limit is preferably 5 nm or more, more preferably 10 nm or more, and particularly preferably 20 nm or more.
Further, the thickness of the write-once recording layer is preferably 200 nm or less, more preferably 150 nm or less, and still more preferably 100 nm or less on the groove (the concave portion in the substrate). The lower limit is preferably 20 nm or more, more preferably 30 nm or more, and further preferably 40 nm or more.
Further, the ratio of the thickness of the write-once recording layer on the land / the thickness of the write-once recording layer on the groove is preferably 0.3 or more, more preferably 0.4 or more, and 5 or more is more preferable, and 0.55 or more is particularly preferable. The upper limit value is preferably less than 0.9, more preferably 0.8 or less, still more preferably 0.7 or less, and particularly preferably 0.6 or less.

  The write-once recording layer can contain various anti-fading agents in order to further improve the light resistance of the write-once recording layer. Examples of the antifading agent include organic oxidants and singlet oxygen quenchers. As the organic oxidizing agent used as an anti-fading agent, compounds described in JP-A-10-151861 are preferable. As the singlet oxygen quencher, those described in publications such as known patent specifications can be used. Specific examples thereof include JP-A Nos. 58-175893, 59-81194, 60-18387, 60-19586, 60-19586, 60-35054, 60-36190, 60-36191, 60-44554, 60-44555, 60-44389, 60-44390, 60-54892, 60-47069, 63-20995, JP Listed in publications such as Nos. 4-25492, 1-38680, and 6-26028, German Patent No. 350399, and the Chemical Society of Japan, October 1992, page 1141 Can do. Preferred examples of the singlet oxygen quencher include compounds represented by the following general formula (A).

In the general formula (A), R ²¹ represents an alkyl group which may have a substituent, and Q ⁻ represents an anion.

In the general formula (A), R ²¹ is an optionally substituted alkyl group having 1 to 8 carbon atoms, and an unsubstituted alkyl group having 1 to 6 carbon atoms is preferable. Examples of the substituent for the alkyl group include halogen atoms (eg, F, Cl), alkoxy groups (eg, methoxy group, ethoxy group), alkylthio groups (eg, methylthio group, ethylthio group), acyl groups (eg, acetyl group, Propionyl group), acyloxy group (eg, acetoxy group, propionyloxy group), hydroxy group, alkoxycarbonyl group (eg, methoxycarbonyl group, ethoxycarbonyl group), alkenyl group (eg, vinyl group), aryl group (eg, phenyl) Group, naphthyl group). Among these, a halogen atom, an alkoxy group, an alkylthio group, and an alkoxycarbonyl group are preferable. Preferable examples of the anion of Q ⁻ include ClO ₄ ⁻ , AsF ₆ ⁻ , BF ₄ ⁻ , and SbF ₆ ⁻ .

  Examples of compounds represented by formula (A) (compound numbers A-1 to A-8) are shown in the following table.

  The amount of the antifading agent such as the singlet oxygen quencher used is usually in the range of 0.1 to 50% by mass, preferably in the range of 0.5 to 45% by mass, more preferably relative to the amount of the dye. Is in the range of 3-40% by weight, particularly preferably in the range of 5-25% by weight.

The cover layer of the cover layer mode (1) is usually bonded on the write-once recording layer described above or on the barrier layer as shown in FIG. 1 via an adhesive or an adhesive.
The cover layer is not particularly limited as long as it is a transparent film, but is not limited to acrylic resins such as polycarbonate and polymethyl methacrylate; vinyl chloride resins such as polyvinyl chloride and vinyl chloride copolymers; epoxy resins; amorphous polyolefins Polyester; cellulose triacetate or the like is preferably used, and among them, polycarbonate or cellulose triacetate is more preferably used.
Note that “transparent” means that the transmittance is 80% or more with respect to light used for recording and reproduction.

Further, the cover layer may contain various additives as long as the effects of the present invention are not hindered. For example, a UV absorber for cutting light having a wavelength of 400 nm or less and / or a dye for cutting light having a wavelength of 500 nm or more may be contained.
Further, as the surface physical properties of the cover layer, it is preferable that the surface roughness is 5 nm or less for both the two-dimensional roughness parameter and the three-dimensional roughness parameter.
Further, from the viewpoint of the concentration of light used for recording and reproduction, the birefringence of the cover layer is preferably 10 nm or less.

The thickness of the cover layer can be appropriately determined according to the wavelength and NA of the laser light irradiated for recording and reproduction, but is within the range of 0.01 to 0.5 mm in the present invention. It is preferable that the thickness is in the range of 0.05 to 0.12 mm.
The total thickness of the cover layer and the layer made of an adhesive or a pressure-sensitive adhesive is preferably 0.09 to 0.11 mm, and more preferably 0.095 to 0.105 mm.
The light incident surface of the cover layer may be provided with a protective layer (hard coat layer 44 in the embodiment shown in FIG. 1) for preventing the light incident surface from being damaged when the optical information recording medium is manufactured. Good.

  As an adhesive used for bonding the cover layer to the write-once recording layer or the barrier layer, it is preferable to use, for example, a UV curable resin, an EB curable resin, a thermosetting resin, and the like, and in particular, use a UV curable resin. Is preferred. When a UV curable resin is used as an adhesive, the UV curable resin may be used as it is or dissolved in an appropriate solvent such as methyl ethyl ketone or ethyl acetate to prepare a coating solution, which may be supplied from the dispenser to the coated surface. . Further, in order to prevent warpage of the produced optical information recording medium, it is preferable that the UV curable resin constituting the adhesive layer has a small curing shrinkage rate. Examples of such UV curable resins include UV curable resins such as “SD-640” manufactured by Dainippon Ink and Chemicals, Inc.

  For example, a predetermined amount of the adhesive is applied onto a surface to be bonded (for example, the surface of the barrier layer), and a cover layer is placed thereon, and then the adhesive is applied by spin coating to the surface to be bonded and the cover layer. It is preferable to make it harden | cure after expanding so that it may become uniform between. The thickness of the adhesive layer made of such an adhesive is preferably in the range of 0.1 to 100 μm, more preferably in the range of 0.5 to 50 μm, and still more preferably in the range of 10 to 30 μm.

  As the pressure-sensitive adhesive used for bonding the cover layer, acrylic, rubber-based, or silicon-based pressure-sensitive adhesives can be used, and acrylic-based pressure-sensitive adhesives are preferable from the viewpoint of transparency and durability. . As such an acrylic pressure-sensitive adhesive, 2-ethylhexyl acrylate, n-butyl acrylate and the like are the main components, and in order to improve cohesion, short-chain alkyl acrylates and methacrylates such as methyl acrylate, ethyl acrylate, and methyl methacrylate are used. And acrylic acid, methacrylic acid, acrylamide derivatives, maleic acid, hydroxylethyl acrylate, glycidyl acrylate, and the like, which can be crosslinking points with the crosslinking agent, are preferably used. The glass transition temperature (Tg) and the crosslinking density can be changed by appropriately adjusting the mixing ratio and type of the main component, the short chain component, and the component for adding a crosslinking point.

  As a crosslinking agent used together with the said adhesive, an isocyanate type crosslinking agent is mentioned, for example. Such isocyanate-based crosslinking agents include tolylene diisocyanate, 4,4′-diphenylmethane diisocyanate, hexamethylene diisocyanate, xylylene diisocyanate, naphthylene-1,5-diisocyanate, o-toluidine isocyanate, isophorone diisocyanate, triphenylmethane triisocyanate, and the like. Isocyanates, products of these isocyanates with polyalcohols, and polyisocyanates formed by condensation of isocyanates can be used. Commercially available products of these isocyanates include Coronate L, Coronate HL, Coronate 2030, Coronate 2031, Millionate MR, Millionate HTL manufactured by Nippon Polyurethane; Takenate D-102 and Takenate D-110N manufactured by Takeda Pharmaceutical Co., Ltd. , Takenate D-200, Takenate D-202; Death Module L, Death Module IL, Death Module N, Death Module HL;

  The pressure-sensitive adhesive may be uniformly applied in a predetermined amount on the surface to be bonded (for example, the surface of the barrier layer), and after the cover layer is placed thereon, it may be cured, or one side of the cover layer in advance. Alternatively, a predetermined amount may be uniformly applied to form an adhesive coating film, the coating film may be bonded to the surface to be bonded, and then cured. Moreover, you may use the commercially available adhesive film in which the adhesive layer was previously provided for the cover layer. The thickness of the pressure-sensitive adhesive layer made of such a pressure-sensitive adhesive is preferably in the range of 0.1 to 100 μm, more preferably in the range of 0.5 to 50 μm, and still more preferably in the range of 10 to 30 μm.

The optical information recording medium of the other layer mode (1) may have other arbitrary layers in addition to the essential layers as long as the effects of the present invention are not impaired. As other arbitrary layers, for example, a label layer having a desired image formed on the back surface of the substrate (the non-formation surface side opposite to the side on which the write-once recording layer is formed), or the substrate and write-once type A light reflection layer (details will be described later) provided between the recording layer, a barrier layer (details will be described later) provided between the write-once recording layer and the cover layer, the light reflection layer and the write-once recording layer, And an interface layer provided between the two. Here, the label layer can be formed using an ultraviolet curable resin, a thermosetting resin, a heat drying resin, or the like.
The essential and optional layers described above may be a single layer or a multilayer structure.

  In the optical information recording medium of aspect (1), a light reflecting layer is formed between the substrate and the write-once recording layer in order to increase the reflectivity with respect to the laser beam and to provide the function of improving the recording / reproducing characteristics. It is preferable.

The light reflecting layer can be formed on the substrate by, for example, vacuum deposition, sputtering, or ion plating with a light reflecting material having a high reflectance with respect to laser light.
The thickness of the light reflecting layer is generally in the range of 10 to 300 nm and preferably in the range of 20 to 200 nm.
The reflectance is preferably 70% or more.

  As a light reflective material having a high reflectance, Mg, Se, Y, Ti, Zr, Hf, V, Nb, Ta, Cr, Mo, W, Mn, Re, Fe, Co, Ni, Ru, Rh, Pd , Ir, Pt, Cu, Ag, Au, Zn, Cd, Al, Ga, In, Si, Ge, Te, Pb, Po, Sn, Bi, and the like, and metal and semi-metal or stainless steel. These light reflecting materials may be used alone, or may be used in combination of two or more kinds or as an alloy. Among these, Cr, Ni, Pt, Cu, Ag, Au, Al, and stainless steel are preferable. Particularly preferred is Au, Ag, Al or an alloy thereof, and most preferred is Au, Ag or an alloy thereof.

Barrier layer (intermediate layer)
In the optical information recording medium of aspect (1), it is preferable to form a barrier layer between the write-once recording layer and the cover layer as shown in FIG.
The barrier layer can be provided for improving the storage stability of the write-once recording layer, improving the adhesion between the write-once recording layer and the cover layer, adjusting the reflectivity, adjusting the thermal conductivity, and the like.
The material used for the barrier layer is not particularly limited as long as it is a material that transmits light used for recording and reproduction and can express the above functions. For example, in general, It is preferable to use a material that does not cause corrosion due to contact with a reflective layer material such as a gas or moisture, a material that does not cause corrosion in a wet heat environment, and a dielectric material. preferable.
Specifically, a material made of nitride, oxide, carbide, sulfide, etc. such as Zn, Si, Ti, Te, Sn, Mo, Ge is preferable. MoO ₂ , GeO ₂ , TeO, SiO ₂ , TiO ₂ , ZuO, SnO ₂ , ZnO—Ga ₂ O ₃ , Nb ₂ O ₅ and Ta ₂ O ₅ are preferred, and SnO ₂ , ZnO—Ga ₂ O ₃ , SiO ₂ , Nb ₂ O ₅ and Ta ₂ O ₅ are more preferred.

The barrier layer can be formed by a vacuum film forming method such as vacuum deposition, DC sputtering, RF sputtering, or ion plating. Among these, it is more preferable to use sputtering.
The thickness of the barrier layer is preferably in the range of 1 to 200 nm, more preferably in the range of 2 to 100 nm, and still more preferably in the range of 3 to 50 nm.

[Optical Information Recording Medium of Aspect (2)]
The optical information recording medium of aspect (2) has at least a substrate, a write-once recording layer, and a protective substrate, and is preferably a bonded optical information recording medium, which is an optical disk called a so-called HD-DVD. is there. The typical layer structure is as follows.
(1) The first layer configuration is a configuration in which a write-once recording layer, a light reflection layer, and an adhesive layer are sequentially formed on a substrate, and a protective substrate is provided on the adhesive layer.
(2) The second layer configuration is a configuration in which a write-once recording layer, a light reflection layer, a protective layer, and an adhesive layer are sequentially formed on a substrate, and a protective substrate is provided on the adhesive layer.
(3) The third layer configuration is a configuration in which a write-once recording layer, a light reflection layer, a protective layer, an adhesive layer, and a protective layer are sequentially formed on a substrate, and a protective substrate is provided on the protective layer.
(4) In the fourth layer configuration, a write-once recording layer, a light reflecting layer, a protective layer, an adhesive layer, a protective layer, and a light reflecting layer are sequentially formed on a substrate, and a protective substrate is provided on the light reflecting layer. It is a configuration.
(5) The fifth layer configuration is a configuration in which a write-once recording layer, a light reflection layer, an adhesive layer, and a light reflection layer are sequentially formed on a substrate, and a protective substrate is provided on the light reflection layer.
Note that the layer configurations (1) to (5) above are merely examples, and the layer configuration is not limited to the order described above, but may be partially replaced or may be partially omitted. The write-once recording layer may also be formed on the protective substrate side. In this case, an optical information recording medium capable of recording and reproducing from both sides is obtained. Furthermore, each layer may be composed of one layer or a plurality of layers.

  Of the above, the optical information recording medium of aspect (2) will be described in detail below, taking as an example a configuration having a write-once recording layer, a light reflection layer, an adhesive layer, and a protective substrate in this order from the substrate side. . A specific example of the optical information recording medium having the above configuration is shown in FIG. A second optical information recording medium 10B shown in FIG. 2 includes a second write-once recording layer 26, a second light reflecting layer 30, a second adhesive layer 32, and a protective substrate 28 on a second substrate 24. Have in order.

The substrate in the substrate mode (2) is formed with a pregroove (guide groove) having a shape in which all of the track pitch, groove width (half width), groove depth, and wobble amplitude are in the following ranges. . This pre-groove is provided to achieve a higher recording density than CD-R and DVD-R. For example, the optical information recording medium of the present invention is used as a medium corresponding to a blue-violet laser. It is suitable for use.

  The track pitch of the pregroove is in the range of 200 to 600 nm, and the upper limit value is preferably 500 nm or less, and more preferably 450 nm or less. The lower limit is preferably 300 nm or more, more preferably 330 nm or more, and still more preferably 370 nm or more. If the track pitch is 200 nm or more, the pregroove can be formed accurately, and further, the occurrence of crosstalk can be avoided. If the track pitch is 600 nm or less, high-density recording can be performed.

  The groove width (half width) of the pregroove is in the range of 50 to 300 nm, and the upper limit value is preferably 250 nm or less, more preferably 200 nm or less, and further preferably 180 nm or less. Further, the lower limit value is preferably 100 nm or more, more preferably 120 nm or more, and further preferably 140 nm or more. If the groove width of the pregroove is 50 nm or more, the groove can be sufficiently transferred at the time of molding, and further, an increase in error rate at the time of recording can be suppressed. It is possible to avoid the occurrence of crosstalk due to the spread of, and to obtain a sufficient degree of modulation.

  The groove depth of the pregroove is in the range of 30 to 200 nm, and the upper limit value is preferably 170 nm or less, more preferably 140 nm or less, and further preferably 120 nm or less. The lower limit is preferably 40 nm or more, more preferably 50 nm or more, and further preferably 60 nm or more. If the groove depth of the pregroove is 30 nm or more, a sufficient recording modulation degree can be obtained, and if it is 200 nm or less, a high reflectance can be obtained.

  The thickness of the substrate is generally in the range of 0.1 to 1.0 mm, preferably in the range of 0.2 to 0.8 mm, and more preferably in the range of 0.3 to 0.7 mm.

  An undercoat layer can be formed on the surface of the substrate on the side where a write-once recording layer, which will be described later, is provided for the purpose of improving flatness and adhesion. The details are as described above.

Details regarding the write-once recording layer in the write-once recording layer aspect (2) are the same as those of the write-once recording layer in aspect (1).

In the light reflection layer mode (2), a light reflection layer can be formed on the write-once recording layer in order to increase the reflectivity with respect to the laser light and to provide the function of improving the recording / reproducing characteristics. Details regarding the light reflecting layer of the aspect (2) are the same as those of the light reflecting layer of the aspect (1).

In the adhesive layer mode (2), an adhesive layer may be provided between the light reflecting layer and the protective substrate in order to improve the adhesion between the light reflecting layer and the protective substrate described later.
As a material constituting the adhesive layer, a photo-curing resin is preferable, and among them, a material having a small curing shrinkage rate is preferable in order to prevent warping of the disk. Examples of such a photocurable resin include UV curable resins (UV curable adhesives) such as “SD-640” and “SD-347” manufactured by Dainippon Ink, Inc.
Further, the thickness of the adhesive layer is preferably in the range of 1 to 1000 μm in order to give elasticity.

The protective substrate (dummy substrate) in the protective substrate mode (2) can be made of the same material and the same shape as the substrate described above. The thickness of the protective substrate is generally in the range of 0.1 to 1.0 mm, preferably in the range of 0.2 to 0.8 mm, and preferably in the range of 0.3 to 0.7 mm. More preferred. Note that when a recording medium having a plurality of recording layers is manufactured, layers such as a pregroove, a write-once recording layer, and a reflective layer may be provided on the protective substrate side. This method is sometimes called an inverse stack method. For the recording layer formed on the protective substrate side, the recording / reproducing wavelength may be the same as or different from that of the recording layer provided on the substrate that is not the protective substrate. Specifically, the material of each layer such as the track pitch, groove shape, additional recording layer material, reflective layer material, and undercoat layer material may be the same or different between the plurality of recording layers.

Depending on the layer structure of the optical information recording medium of the protective layer mode (2), a protective layer may be provided for the purpose of physically and chemically protecting the light reflecting layer, the write-once recording layer, and the like.
Examples of materials used for the protective layer include inorganic substances such as ZnS, ZnS—SiO ₂ , SiO, SiO ₂ , MgF ₂ , SnO ₂ , and Si ₃ N ₄ , thermoplastic resins, thermosetting resins, and UV curable materials. Organic substances such as resins can be mentioned.
The protective layer can be formed, for example, by bonding a film obtained by plastic extrusion onto the light reflecting layer via an adhesive. Moreover, you may provide by methods, such as vacuum evaporation, sputtering, and application | coating.

Further, when a thermoplastic resin or a thermosetting resin is used as the protective layer, it is also formed by dissolving these in an appropriate solvent to prepare a coating solution, and then applying and drying the coating solution. be able to. When forming a protective layer using a UV curable resin, after preparing the coating solution by dissolving the UV curable resin as it is or in an appropriate solvent, the coating solution is applied and irradiated with UV light. It can also be formed by curing. In these coating liquids, various additives such as an antistatic agent, an antioxidant, and a UV absorber may be added according to the purpose.
The thickness of the protective layer is generally in the range of 0.1 μm to 1 mm.

The optical information recording medium of the other layer mode (2) may have other arbitrary layers in addition to the above layers as long as the effects of the present invention are not impaired. The details of other optional layers are the same as those of the other layers of the aspect (1).

[Information recording method]
Furthermore, the present invention relates to a method for recording information on an optical information recording medium having a recording layer on a substrate. In the information recording method of the present invention, information is recorded on the recording layer by irradiating the optical information recording medium of the present invention with laser light having a wavelength of 440 nm or less.

Information is recorded on the optical information recording medium of the above-described preferred embodiment (1) or embodiment (2), for example, as follows.
First, recording light such as semiconductor laser light is irradiated from the substrate side or the protective layer side while rotating the optical information recording medium at a constant linear velocity (for example, 0.5 to 10 m / second) or a constant angular velocity. . By this light irradiation, the optical characteristics of the laser light irradiated portion change and information is recorded. In the embodiment shown in FIG. 1, a recording laser beam 46 such as a semiconductor laser beam is irradiated from the cover layer 16 side through a first objective lens 42 (for example, a numerical aperture NA is 0.85). By the irradiation of the laser beam 46, the write-once recording layer 14 absorbs the laser beam 46 and the temperature rises locally, causing a physical or chemical change (for example, generation of pits) to change its optical characteristics. Thus, it is considered that information is recorded. Similarly, in the embodiment shown in FIG. 2, a recording laser beam 46 such as a semiconductor laser beam is irradiated from the second substrate 24 side through a second objective lens 48 having a numerical aperture NA of, for example, 0.65. By the irradiation of the laser beam 46, the second write-once recording layer 26 absorbs the laser beam 46 and the temperature rises locally, causing a physical or chemical change (for example, generation of pits) to change its optical characteristics. By changing, it is considered that information is recorded.

In the present invention, it is preferable to record information by irradiating a laser beam having a wavelength of 440 nm or less. As the recording light, a semiconductor laser light having an oscillation wavelength in the range of 440 nm or less is preferably used, and as a preferable light source, a blue-violet semiconductor laser light having an oscillation wavelength in the range of 390 to 440 nm (more preferably 390 to 415 nm) is used. A blue-violet SHG laser beam having a center oscillation wavelength of 425 nm, which is a half wavelength of an infrared semiconductor laser beam having a center oscillation wavelength of 850 nm, can be given. In particular, it is preferable to use a blue-violet semiconductor laser beam having an oscillation wavelength in the range of 390 to 415 nm in terms of recording density. The information recorded as described above is reproduced by irradiating a semiconductor laser beam from the substrate side or the protective layer side while rotating the optical information recording medium at the same constant linear velocity as above and detecting the reflected light. Can be performed.
The other details of the information recording method of the present invention are as described for the optical information recording medium of the present invention.

  EXAMPLES Hereinafter, the present invention will be described more specifically with reference to examples, but the present invention is not limited to the examples.

[Synthesis Example 1: Synthesis of Exemplified Compound (B-1)]
The exemplary compound (B-1) was synthesized according to the following schemes (1) to (3). Other compounds can be synthesized similarly.

(Explanation of Scheme 1)
After 10.2 g of Compound 1 was added to 70 ml of ethanol, 6 ml of an aqueous solution of 2.8 g of sodium nitrite was added dropwise. After heating to reflux for 45 minutes, the reaction mixture was ice-cooled and the amber crystals produced were collected by filtration. This was neutralized in dilute hydrochloric acid water to obtain 9.4 g of Compound 2 .

(Explanation of Scheme 2)
2.5 g of Compound 2 and 2.25 g of Compound 1 were added to 10 ml of acetic anhydride, 1.25 ml of triethylamine was added, and the mixture was stirred at 60 ° C. for 2 hours. The reaction mixture was opened in water, and the extract with ethyl acetate was purified by silica gel column chromatography to obtain 2.5 g of compound 3 .

(Explanation of Scheme 3)
Compound 3 Compound 4 1.4 g of methanol solution 10ml of 2.5g was added, to room temperature after heating under reflux for 2 hours then cooled, resulting crystals were filtered, thereby obtaining Exemplified Compound (B-1) 3.0g. The solution absorption maximum wavelength was 485 nm (in tetrafluoropropanol).

[Synthesis Example 2: Synthesis of Exemplified Compound (C-1)]
Exemplary compound (C-1) was synthesized according to the following scheme.

0.3 g of Compound 3 obtained in Synthesis Example 1 was dissolved in 3 ml of methanol, 0.08 ml of triethylamine and 0.11 g of nickel perchlorate hexahydrate were added, and the mixture was heated to reflux for 1 hour. After cooling to room temperature, the resulting crystals were collected by filtration and washed with water to obtain 0.4 g of exemplary compound (C-1). The identification results are shown below.
MS (Posi) = 1088

[Examples 1 to 20]
<Manufacture of optical information recording media>
(Production of substrate)
Thickness 1.1 mm, outer diameter 120 mm, inner diameter 15 mm, spiral pre-groove (track pitch: 320 nm, groove width: on-groove width 120 nm, groove depth: 35 nm, groove inclination angle: 65 °, wobble amplitude: 20 nm) An injection-molded substrate made of a polycarbonate resin was prepared. Mastering of the stamper used at the time of injection molding was performed using laser cutting (351 nm).

(Formation of light reflection layer)
APC light reflecting layer (Ag: 98.1 mass%, Pd: 0.9 mass) as a vacuum film-forming layer having a film thickness of 100 nm by DC sputtering in an Ar atmosphere using a Cube manufactured by Unaxis Co. %, Cu: 1.0 mass%). The film thickness of the light reflecting layer was adjusted by the sputtering time.

(Formation of write-once recording layer)
1 g of each compound shown in Table 2 was added and dissolved in 100 ml of 2,2,3,3-tetrafluoropropanol to prepare a dye-containing coating solution. And the prepared pigment | dye containing coating liquid was apply | coated on the conditions of 23 degreeC and 50% RH, changing the rotation speed to 300-4000 rpm with a spin coat method on the light reflection layer. Thereafter, it was stored at 23 ° C. and 50% RH for 1 hour to form a write-once recording layer. The formed recording layer had a thickness of 45 nm on the groove and 25 nm on the land.

  After the write-once recording layer was formed, annealing treatment was performed in a clean oven. The annealing treatment was performed by supporting the substrate on a vertical stack pole while leaving a gap with a spacer, and holding at 80 ° C. for 1 hour.

(Formation of barrier layer)
After that, on the write-once recording layer, using Cubes made by Unaxis, consisting of ZnO—Ga ₂ O ₃ (ZnO: Ga ₂ O ₃ = 7: 3 (mass ratio)) by RF sputtering in an Ar atmosphere. A barrier layer having a thickness of 10 nm was formed.

(Covering the cover layer)
As the cover layer, a polycarbonate film (Teijin Pure Ace, thickness: 80 μm) having an inner diameter of 15 mm and an outer diameter of 120 mm and coated with an adhesive on one side, the thickness of the adhesive layer and the polycarbonate film is used. The total thickness was set to 100 μm.
Then, the cover layer was placed on the barrier layer so that the barrier layer and the pressure-sensitive adhesive layer were in contact with each other, and the cover layer was pressed and pressed with a pressing member.
Thereby, the optical information recording media of Examples 1 to 20 were manufactured.

(Comparative Examples 1-4)
Optical information recording media were produced in the same manner as in Examples 1 to 20, except that the following comparative compounds (A) to (D) were used as the recording layer dye.

<Evaluation of optical information recording media>
C / N (Carrier to Noise Ratio) Evaluation Using a recording / reproduction evaluation machine (Pulstec Corporation: DDU1000) in which an OK 405 nm laser and NA 0.85 pickup were loaded from the cover layer side on the manufactured optical information recording medium, clock frequency 66 MHz Then, a 0.16 μm signal (2T) was recorded and reproduced at a linear velocity of 5.28 m / s, and C / N (after recording) was measured with a spectrum analyzer (Pulstech MSG2). Recording was done on the groove. Furthermore, after the produced optical information recording medium was irradiated with 140,000 lux xenon light from the cover layer side for 24 hours, the same measurement was performed. The results are shown in Table 2. Here, when the C / N (after recording) is 25 dB or more, the reproduction signal intensity is sufficient, which is practically preferable.

  From the results of Table 2, the dye compound represented by the general formula (I-1), the dye compound formed by salt formation of the compound represented by the general formula (I-1) with a counter ion, or the general formula (I-1 The recording media of Examples 1 to 20 having a recording layer containing a metal complex dye compound containing a compound represented by the above formula as a ligand show a higher reproduction signal intensity than the recording media of Comparative Examples 1 to 4. Further, it can be seen that the light-resistant storage stability is also good.

  The optical information recording medium of the present invention is suitable as an optical information recording medium for high-density recording such as a Blu-ray optical disk.

It is a schematic sectional drawing which shows an example of the optical information recording medium of this invention. It is a schematic sectional drawing which shows an example of the optical information recording medium of this invention.

Explanation of symbols

DESCRIPTION OF SYMBOLS 10A ... 1st optical information recording medium 10B ... 2nd optical information recording medium 12 ... 1st board | substrate 14 ... 1st write-once recording layer 16 ... cover layer 18 ... 1st light reflection layer 20 ... Barrier layer 22 ... 1st adhesion layer 24 ... Second substrate 26 ... Second write-once recording layer 28 ... Protective substrate 30 ... Second light reflecting layer 32 ... Second adhesive layer 44 ... Hard coat layer

Claims (6)

An optical information recording medium having a recording layer containing a dye compound on a substrate,
The dye compound includes a dye compound represented by the following general formula (I-1), a compound represented by the following general formula (I-1), and a counter ion in an amount capable of neutralizing the charge of the compound. An optical information recording medium comprising a dye compound and at least one dye compound selected from the group consisting of a metal complex dye compound containing a compound represented by the following general formula (I-1) as a ligand.

[In General Formula (I-1), E ¹ and E ² each independently represent an atomic group necessary to complete a conjugated double bond chain, and x and y each independently represents 0 or 1 Y ¹ represents an atomic group necessary for forming a carbocycle or a heterocycle with a partial structure represented by C- (E ¹ ) xC, and Y ² represents C = (E ² ) y = C in conjunction with the partial structure represented represents an atomic group necessary to form a carbocyclic or heterocyclic ring, X ¹ represents O or NR ^1, X ² is O ^{-, -} represents NR ² or NR ³ R ⁴ , R ¹ , R ² , R ³ and R ⁴ each independently represents a substituent or a hydrogen atom. When R ¹ represents a substituent, R ¹ may form a condensed ring with a carbocycle or a heterocycle formed by Y ¹ and C- (E ¹ ) xC, and R ² represents a substituent. When represented, R ² may form a condensed ring with a carbocycle or a heterocycle formed by Y ² and C = (E ² ) y = C, and R ³ and R ⁴ represent a substituent. In this case, R ³ and R ⁴ may each form a ring condensed with a carbocyclic or heterocyclic ring formed by Y ² and C = (E ² ) y = C. ] The optical information recording medium according to claim 1, wherein the substrate has a pregroove having a track pitch of 50 to 500 nm on at least one surface, and the recording layer is provided on the surface having the pregroove. The optical information recording medium according to claim 1, further comprising a light reflecting layer between the substrate and the recording layer. The optical information recording medium according to claim 3, comprising the substrate, the light reflecting layer, the recording layer, the barrier layer, and the protective layer in this order. The optical information recording medium according to claim 1, which is used for recording information by irradiating a laser beam having a wavelength of 440 nm or less. An information recording method for recording information by irradiating the optical information recording medium according to any one of claims 1 to 5 with a laser beam having a wavelength of 440 nm or less.

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