JPH0729490B2 - Optical information recording medium - Google Patents

Optical information recording medium

Info

Publication number
JPH0729490B2
JPH0729490B2 JP61029328A JP2932886A JPH0729490B2 JP H0729490 B2 JPH0729490 B2 JP H0729490B2 JP 61029328 A JP61029328 A JP 61029328A JP 2932886 A JP2932886 A JP 2932886A JP H0729490 B2 JPH0729490 B2 JP H0729490B2
Authority
JP
Japan
Prior art keywords
recording medium
carbon atoms
dye
recording
recording layer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP61029328A
Other languages
Japanese (ja)
Other versions
JPS62187085A (en
Inventor
敏之 管野
均 渡辺
広平 浜西
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsubishi Rayon Co Ltd
Original Assignee
Mitsubishi Rayon Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Mitsubishi Rayon Co Ltd filed Critical Mitsubishi Rayon Co Ltd
Priority to JP61029328A priority Critical patent/JPH0729490B2/en
Priority to US07/011,896 priority patent/US4908294A/en
Priority to DE19873704601 priority patent/DE3704601A1/en
Publication of JPS62187085A publication Critical patent/JPS62187085A/en
Publication of JPH0729490B2 publication Critical patent/JPH0729490B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G11INFORMATION STORAGE
    • G11BINFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
    • G11B7/00Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
    • G11B7/24Record carriers characterised by shape, structure or physical properties, or by the selection of the material
    • G11B7/241Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
    • G11B7/242Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers
    • G11B7/244Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only
    • G11B7/249Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing organometallic compounds
    • GPHYSICS
    • G11INFORMATION STORAGE
    • G11BINFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
    • G11B7/00Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
    • G11B7/24Record carriers characterised by shape, structure or physical properties, or by the selection of the material
    • G11B7/241Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
    • G11B7/242Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers
    • G11B7/244Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only
    • G11B7/246Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing dyes
    • G11B7/247Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing dyes methine or polymethine dyes
    • G11B7/2472Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing dyes methine or polymethine dyes cyanine
    • GPHYSICS
    • G11INFORMATION STORAGE
    • G11BINFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
    • G11B7/00Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
    • G11B7/24Record carriers characterised by shape, structure or physical properties, or by the selection of the material
    • G11B7/241Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
    • G11B7/242Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers
    • G11B7/244Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only
    • G11B7/246Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing dyes
    • G11B7/248Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing dyes porphines; azaporphines, e.g. phthalocyanines
    • GPHYSICS
    • G11INFORMATION STORAGE
    • G11BINFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
    • G11B7/00Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
    • G11B7/24Record carriers characterised by shape, structure or physical properties, or by the selection of the material
    • G11B7/241Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
    • G11B7/252Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers
    • G11B7/253Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of substrates
    • G11B7/2531Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of substrates comprising glass
    • GPHYSICS
    • G11INFORMATION STORAGE
    • G11BINFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
    • G11B7/00Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
    • G11B7/24Record carriers characterised by shape, structure or physical properties, or by the selection of the material
    • G11B7/241Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
    • G11B7/252Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers
    • G11B7/253Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of substrates
    • G11B7/2533Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of substrates comprising resins

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、レーザ、特に半導体レーザによる書き込み、
再生記録がなされる光メモリ媒体に関する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to writing by a laser, particularly a semiconductor laser,
The present invention relates to an optical memory medium for reproducing and recording.

〔従来技術および問題点〕[Prior art and problems]

一般に光ディスクは、基板上に設けた薄膜記録層に形成
された光学的に検出可能な小さな(例えば約1μm)ピ
ットをらせん状又は円形のトラック形態にして高密度情
報を記憶することができる。この様なディスクに情報を
書込むには、レーザ感応層の表面に集速したレーザを走
査し、このレーザ光線が照射された表面のみにピットを
形成し、このピットをらせん状又は円形トラック等の形
態で形成する。この感応層はレーザエネルギーを吸収し
て光学的に検出可能なピットを形成できる。例えばヒー
トモード記録方式では記録層がレーザエネルギーを吸収
してその照射部分が局部的に加熱され融解蒸発あるいは
凝集等の物理的変化を起こし非照射部分との間に光学的
差異(例えば反射率、吸収率等)を生じさせて読み取る
ことによって検出される。この様な光記録媒体としてこ
れまでアルミニウム蒸着膜などの金属薄膜、ビスマス薄
膜、テルル系薄膜やカルコゲナイド系非晶質ガラス膜な
どの無機物質が提案されている。
In general, an optical disc can store high density information by forming a small (for example, about 1 μm) optically detectable pit formed in a thin film recording layer provided on a substrate into a spiral or circular track form. In order to write information on such a disc, the surface of the laser sensitive layer is scanned with a focused laser to form pits only on the surface irradiated with this laser beam, and the pits are formed into spiral or circular tracks. It is formed in the form of. This sensitive layer can absorb laser energy to form optically detectable pits. For example, in the heat mode recording method, the recording layer absorbs laser energy and the irradiated portion is locally heated to cause a physical change such as melting, evaporation, or aggregation, and an optical difference (for example, reflectance, The absorption rate, etc.) is generated and read. As such optical recording media, inorganic substances such as metal thin films such as aluminum vapor deposition films, bismuth thin films, tellurium thin films and chalcogenide amorphous glass films have been proposed so far.

これらは、蒸着法、スパッタ法などにより薄膜が得ら
れ、近赤外域でも光吸収を有するため半導体レーザが使
用できうという長所があるが、反面反射率が大きく、し
かも熱伝導率が大きく比熱も大きい等の欠点あがる。特
に反射率が大きいということは、レーザ光のエネルギー
を有効に利用できないので記録に要する光エネルギーが
大きくなり、大出力レーザ光線を必要とする。その結
果、記録装置が大型かつ高価になると云う欠点がある。
また、テルル、ビスマス、セレン等の薄膜では毒性を有
するという欠点がある。このような事から、近年吸収性
の選択ができ、吸収率が大きく、さらに熱伝導が小さ
く、加えて生産性が良く且つ毒性が低いことから色素薄
膜を記録層として適用した光学メモリ媒体の研究提案が
なされて来ている。代表的色素としてはシアニン系色素
(特開昭58−112790)、アントラキノン系色素(特開昭
58−224448)、ナフトキノン系色素(特開昭58−22479
3)及びフタロシアニン系色素(特開昭60−48396)等が
あり、これらを単独又は自己酸化性樹脂との併用から成
る化合物をスピンナー塗布、ディッピング法、プラズマ
法又は真空蒸着法等により、基板上に形成した光記録媒
体である。この色素薄膜系は上記長所を有し、特にシア
ニン系色素は構造的に近赤外に吸収波長をもたせること
が可能であり、しかも溶剤に対する溶解性及び融点が低
い等の長所を有することから多く検討がなされている。
反面、光劣化、熱に対して不安定及び湿度劣化等があ
り、長期保存性及び再生安定性(読み出し光に対する安
定性)等に問題があると従来言われており、これらの問
題について種々の改良案が出されている。具体的には、
記録層上に保護膜を設けること(特開昭55−22961,57−
66541)、酸素による退色防止物質を混合すること(特
開昭59−55795)、長波長域に光吸収を有する金属錯体
を添加すること(特開昭59−215892)等が提案されてい
る。しかしながら、これらの提案によっても問題を十分
に解決しておらず、更に添加剤による成膜性や反射率、
吸収率の低下という問題が生じる。
These have the advantage that a semiconductor laser can be used because a thin film can be obtained by a vapor deposition method, a sputtering method, or the like and have light absorption in the near infrared region, but on the other hand, they have a large reflectance and a large thermal conductivity and a high specific heat. The drawbacks such as big ones rise. In particular, the fact that the reflectance is large means that the energy of the laser light cannot be effectively utilized, so that the light energy required for recording becomes large and a high-power laser beam is required. As a result, there is a drawback that the recording apparatus becomes large and expensive.
Further, a thin film of tellurium, bismuth, selenium, etc. has a drawback that it has toxicity. Therefore, in recent years, it has been possible to select absorptivity, the absorptance is large, the thermal conductivity is small, the productivity is low, and the toxicity is low. Suggestions are coming. Representative dyes include cyanine dyes (JP-A-58-112790), anthraquinone dyes (JP-A-58-112790).
58-224448), naphthoquinone dyes (JP-A-58-22479)
3) and phthalocyanine dyes (JP-A-60-48396), etc., and a compound consisting of them alone or in combination with an auto-oxidizing resin is applied on a substrate by spinner coating, dipping method, plasma method or vacuum deposition method. The optical recording medium is formed on. This dye thin film system has the above-mentioned advantages, and in particular, the cyanine dye is structurally capable of having an absorption wavelength in the near infrared, and has many advantages such as low solubility in a solvent and low melting point. Consideration is being made.
On the other hand, there are problems such as long-term storage stability and reproduction stability (stability against readout light) due to photodegradation, heat instability, humidity deterioration, etc. An improvement plan has been issued. In particular,
Providing a protective film on the recording layer (JP-A-55-22961,57-
66541), mixing an anti-fading substance with oxygen (JP-A-59-55795), and adding a metal complex having light absorption in the long wavelength region (JP-A-59-215892). However, even these proposals have not sufficiently solved the problem, and the film-forming property and reflectance by the additive,
There is a problem that the absorption rate is lowered.

こうしたことから、記録密度及び反射性の点より下記一
般式に示すシアニン系色素を用いた塗布型記録媒体が注
目されている。
From these points, a coating type recording medium using a cyanine dye represented by the following general formula has attracted attention in terms of recording density and reflectivity.

〔但し、式中のAはO,S,Se,C、Xはハロゲン陰イオン,B
F4 -,ClO4 -、Rはアルキルを示す〕 しかしながら、上記一般式で表わされるシアニン系色素
についても成膜性、熱光安定性に欠けるという本質的な
問題を有する。成膜性については、メチン連鎖数(n)
の増加により溶剤溶解性が低下すること、両端の複素環
の種類及び置換基の種類により溶解性が変わることが知
られている。熱光安定性については、メチン連鎖数が増
加する程、熱、光に対して不安定になり、酸化劣化も起
こり易くなること、複素環の種類により熱、光に対する
安定性が異なることが知られている。
[However, A in the formula is O, S, Se, C, X is a halogen anion, B
F 4 , ClO 4 , and R represent alkyl] However, the cyanine dye represented by the above general formula also has an essential problem that it lacks film-forming properties and heat and light stability. Membrane chain number (n)
It is known that the solubility of the solvent decreases due to an increase in the amount of the solvent, and that the solubility changes depending on the types of heterocycles and the substituents at both ends. Regarding thermophotostability, it is known that the more the number of methine chains increases, the more unstable it is to heat and light, and the more likely it is to undergo oxidative deterioration, and that the stability to heat and light differs depending on the type of heterocycle. Has been.

本発明は、上記事情に鑑みなされたもので、高い反射率
と高い記録感度を有し、光学的信号の書き込み、再生を
安定して行なうことが可能で、かつ再生時の光や日光、
湿度に対する安定性の高い無公害の光学的情報記録媒体
を提供しようとするものである。
The present invention has been made in view of the above circumstances, has a high reflectance and a high recording sensitivity, it is possible to write and reproduce an optical signal stably, and light and sunlight at the time of reproduction,
It is intended to provide a pollution-free optical information recording medium having high stability against humidity.

〔問題点を解決するための手段及び作用〕 本発明は、下記一般式にて表わされる有機色素を含む記
録層を備えることを特徴とする光情報記録媒体である。
[Means and Actions for Solving Problems] The present invention is an optical information recording medium comprising a recording layer containing an organic dye represented by the following general formula.

ただし、式中のR1は炭素数1〜6のアルキル基、アラル
キル基またはフェニル基、R2は水素原子、ハロゲン原
子、炭素数1〜6のアルキル基、 (Ph;フェニル基)または (R3;炭素数1〜6のアルキル基)、Xはパークロレー
ト、フルオロボレート、アイオダイド、クロライド、ブ
ロマイド、p−トルエンスルフォネートから選ばれる陰
イオン、Yは炭素数1〜18のアルキル基、フェニル基、
−R4OR5、−R4COR5、−R4COOR5(R4;炭素数1〜20のアルキレン基、R5;炭素数1〜18の
アルキル基またはフェニル基)、Zはインドールを構成
するベンゼン環に付加されるベンゼン環を示す。本発明
に用いる有機色素は、メチン連鎖中に で表わされるペンタ環を導入することにより、特開昭59
−85791号に開示された のようなメチン連鎖のみから構成されたシアニン色素に
比べて耐熱性、耐光性が向上し、より耐保存性、再生劣
化特性に優れた記録層を形成できる。前記ペンタ環に導
入されるR2は、既述のとおりであるが、特にハロゲン原
子を用いた場合、Cl,Br又はアルキル基を用いた場合、
炭素数1〜3のものが好ましい。
However, in the formula, R 1 is an alkyl group having 1 to 6 carbon atoms, an aralkyl group or a phenyl group, R 2 is a hydrogen atom, a halogen atom, an alkyl group having 1 to 6 carbon atoms, (Ph; phenyl group) or (R 3 ; alkyl group having 1 to 6 carbon atoms), X is an anion selected from perchlorate, fluoroborate, iodide, chloride, bromide and p-toluenesulfonate, Y is an alkyl group having 1 to 18 carbon atoms , Phenyl group,
-R 4 OR 5 , -R 4 COR 5 , -R 4 COOR 5 , (R 4 ; alkylene group having 1 to 20 carbon atoms, R 5 ; alkyl group having 1 to 18 carbon atoms or phenyl group), Z represents a benzene ring added to the benzene ring constituting indole. The organic dye used in the present invention has a methine chain By introducing a penta ring represented by
Disclosed in −85791 The heat resistance and the light resistance are improved as compared with the cyanine dye composed only of the methine chain, and a recording layer having more excellent storage resistance and reproduction deterioration characteristics can be formed. R 2 introduced into the penta ring is as described above, especially when a halogen atom is used, when Cl, Br or an alkyl group is used,
Those having 1 to 3 carbon atoms are preferable.

また、本発明に用いる有機色素は、インドールを構成す
るベンゼン環にZとしてのベンゼン環を付加させること
により、特開昭59−150795号、特開昭58−194595号に開
示された、例えば のようなインドールを構成するベンゼン環が未置換もし
くはアルキル基で置換された有機色素に比べて疎水性が
高められ、耐環境性の要素の1つである耐湿性を向上で
きる。
The organic dye used in the present invention is disclosed in JP-A-59-150795 and JP-A-58-194595, for example, by adding a benzene ring as Z to the benzene ring constituting indole. The hydrophobicity is enhanced as compared with an organic dye in which the benzene ring constituting the indole is unsubstituted or substituted with an alkyl group, and moisture resistance, which is one of the elements of environmental resistance, can be improved.

更に、本発明に用いる有機色素はインドールに既述した
置換基Yが導入された構造であるが、Yとしてアルキル
基、アラルキル基を導入すると比較的耐湿性、耐熱性の
向上がなされ、Yとして−R4COR5,−R4OR5,−R4COOR5
導入すると溶剤溶解性、成膜性の向上がなされる。こう
したことから、置換基Yは記録媒体の構成、目的により
適宜選択すればよい。
Further, the organic dye used in the present invention has a structure in which the above-mentioned substituent Y is introduced into indole. However, when an alkyl group or an aralkyl group is introduced as Y, relative humidity resistance and heat resistance are relatively improved, and -R 4 COR 5, -R 4 OR 5, solvent solubility when introducing -R 4 COOR 5, improvement in film-forming properties are made. Therefore, the substituent Y may be appropriately selected depending on the structure and purpose of the recording medium.

上記一般式にて表わされる色素を具体的に例示すると、
下記構造式(1)〜(13)に示すもの等が挙げられる。
Specifically exemplifying the dye represented by the above general formula,
Examples include those represented by the following structural formulas (1) to (13).

上記一般式で表わされる色素を含む記録層は、該色素を
酢酸エチル、トルエン、アセトン、メチルイソブチルケ
トン、塩化メチレン、アルコール等の溶剤に溶解してス
ピンナー法、ディッピング法、ドクターブレード法、ロ
ールコータ法等により基板上に薄膜を形成することによ
り得られる。この記録層の厚さは、薄い程、記録感度が
高くなるが、反射率が膜厚に依存するために、10nm〜10
00nm、好ましくは30nm〜500nmの範囲にすることが適切
である。また、基板としてはガラス、プラスチック、金
属等の一般に用いられるものが使用可能であるが、アク
リル樹脂、ポリカーボネート、ポリオレフィン、ポリエ
ステル、ポリイミドのフィルムでもよい。
The recording layer containing the dye represented by the above general formula is prepared by dissolving the dye in a solvent such as ethyl acetate, toluene, acetone, methyl isobutyl ketone, methylene chloride or alcohol, and spinner method, dipping method, doctor blade method, roll coater. It is obtained by forming a thin film on a substrate by a method or the like. The thinner the recording layer, the higher the recording sensitivity, but the reflectance depends on the film thickness.
It is suitable to have a range of 00 nm, preferably 30 nm to 500 nm. Further, as the substrate, a commonly used one such as glass, plastic, metal, etc. can be used, but an acrylic resin, polycarbonate, polyolefin, polyester or polyimide film may be used.

記録層は上述した方法により形成される。更に色素にバ
インダ樹脂を1〜40重量%、好ましくは3〜20重量%添
加することにより、膜形成することができ、成膜性、耐
熱性、耐湿性を向上させることができる。ここに用いる
バインダ樹脂としては、例えばアクリル、エステル、ニ
トロセルロース、エチレン、プロピレン、カーボネー
ト、エチレンテレフタレート、エポキシ、ブチラール、
塩化ビニル、酢酸ビニル、スチレン等の単独重合体、こ
れらの共重合体等を挙げることができる。
The recording layer is formed by the method described above. Furthermore, by adding a binder resin to the dye in an amount of 1 to 40% by weight, preferably 3 to 20% by weight, a film can be formed, and film formability, heat resistance and moisture resistance can be improved. Examples of the binder resin used here include acrylic, ester, nitrocellulose, ethylene, propylene, carbonate, ethylene terephthalate, epoxy, butyral,
Examples thereof include homopolymers of vinyl chloride, vinyl acetate, styrene and the like, and copolymers thereof.

また、上記バインダ樹脂の代りに他の色素を混入させる
か、又は色素層を重ねた多層構造にすることによって成
膜性の向上や耐熱、耐湿、耐光性を向上させることがで
き、ひいては高密度、高感度で再生劣化等のない耐久性
の優れた光情報記録媒体を得ることができる。この場
合、他の色素を積層して耐熱性、耐湿性、耐光性を向上
させることも可能である。ここに用いる色素としては、
例えばシアニン色素、メロシアニン色素、アントラキノ
ン色素、トリフェニルメタン色素、キサンテン系色素、
フタロシアニン系色素等を挙げることができる。
Further, it is possible to improve the film-forming property and heat resistance, humidity resistance, and light resistance by mixing other dyes instead of the binder resin or by forming a multilayer structure in which dye layers are stacked, and consequently high density. Thus, it is possible to obtain an optical information recording medium having high sensitivity and excellent durability without deterioration of reproduction. In this case, other dyes may be laminated to improve heat resistance, humidity resistance and light resistance. As the dye used here,
For example, cyanine dye, merocyanine dye, anthraquinone dye, triphenylmethane dye, xanthene dye,
Examples thereof include phthalocyanine dyes.

例えば下記一般式(A),(B)にて表わされるアミン
化合物や下記一般式(C)にて表わされるジチオレート
金属鎖体を添加し、光,酸素,水分による記録層の光学
特性の劣化を防止することも可能である。
For example, an amine compound represented by the following general formulas (A) and (B) or a dithiolate metal chain represented by the following general formula (C) is added to prevent deterioration of the optical characteristics of the recording layer due to light, oxygen and water. It is also possible to prevent it.

但し、式中のR1,R2,R4,R5は炭素数1〜6のアルキル
基、R3 で、Rは炭素数1〜6のアルキル基を示す。
However, in the formula, R 1 , R 2 , R 4 , and R 5 are alkyl groups having 1 to 6 carbon atoms, and R 3 is And R represents an alkyl group having 1 to 6 carbon atoms.

但し、式中のRは水素原子又は炭素数1〜6のアルキル
基、Xは過塩素酸イオン、弗化硼素酸素イオン、ヘキサ
フルオロ酸イオン等の陰イオン、mは0又は1,2の整
数、Aは前記m=0,1の時、 (n=1又は2)、 m=2の時 を示す。こうしたアミン化合物としては、例えば市販さ
れているIRG−002,IRG−003(いずれも日本化薬(株)
製商品名)等がある。
However, R in the formula is a hydrogen atom or an alkyl group having 1 to 6 carbon atoms, X is an anion such as perchlorate ion, boron fluoride oxygen ion, hexafluoroacid ion, etc., m is an integer of 0 or 1, 2. , A is the above m = 0,1, (N = 1 or 2), when m = 2 Indicates. Examples of such amine compounds include commercially available IRG-002 and IRG-003 (both manufactured by Nippon Kayaku Co., Ltd.).
Product name) etc.

但し、式中のR1〜R4はアルキル基又はフェニル基、X,Y
は水素、アルキル基、ハロゲン基、MはNi,Co,Fe,Cr等
の金属を示すものである。かかる金属錯体としては、例
えばPA1001〜1006(いずれも三井東圧ファイン(株)製
商品名)、Ni−ビス(o−キシレン−4,5ジオール)テ
トラ(t−ブチル)アンモニウム塩等がある。
However, R 1 to R 4 in the formula are alkyl groups or phenyl groups, X, Y
Represents hydrogen, an alkyl group, a halogen group, and M represents a metal such as Ni, Co, Fe and Cr. Examples of such metal complexes include PA1001 to 1006 (all are trade names manufactured by Mitsui Toatsu Fine Co., Ltd.), Ni-bis (o-xylene-4,5diol) tetra (t-butyl) ammonium salt, and the like.

なお、上記一般式の色素を含む記録層の他に必要に応じ
て中間層、保護層を設けることができる。中間層は、接
着性の向上と共に酸素、水分からの保護の目的で設けら
れ、主に樹脂又は無酸化合物から形成される。樹脂とし
ては、例えば塩化ビニル、酢酸ビニル、アクリル、エス
テル、ニトロセルロース、カーボネート、エポキシ、エ
チレン、プロピレン、ブチラール等の単独もしくは共重
合体等を用いることができ、必要に応じて酸化防止剤、
紫外光吸収剤、レベリング剤や撥水剤等を含有させるこ
とが可能である。これらは、スピンナー法、ディッピン
グ法、ドクターブレード法により形成される。無機化合
物としては、例えばSiO2,SiO,Al2O3,SnO2,MgF2等が用い
られ、イオンビーム、電子ビーム、スパッタ法により薄
膜が形成される。前記保護層も中間層と同様の構成をと
り、光、酸素、水分からの記録層の保護、傷、ホコリ等
からの保護のために用いられる。
Incidentally, in addition to the recording layer containing the dye of the above general formula, an intermediate layer and a protective layer can be provided if necessary. The intermediate layer is provided for the purpose of improving adhesiveness and protection from oxygen and moisture, and is mainly formed of a resin or an acid-free compound. As the resin, for example, vinyl chloride, vinyl acetate, acryl, ester, nitrocellulose, carbonate, epoxy, ethylene, propylene, butyral homopolymers or copolymers can be used, and if necessary, an antioxidant,
It is possible to contain an ultraviolet light absorber, a leveling agent, a water repellent, and the like. These are formed by a spinner method, a dipping method, or a doctor blade method. As the inorganic compound, for example, SiO 2 , SiO, Al 2 O 3 , SnO 2 , MgF 2 or the like is used, and a thin film is formed by an ion beam, an electron beam or a sputtering method. The protective layer also has the same structure as the intermediate layer and is used for protection of the recording layer from light, oxygen and moisture, and protection from scratches, dust and the like.

次に、本発明の光情報記録媒体の構成例について図面を
参照して説明する。
Next, a configuration example of the optical information recording medium of the present invention will be described with reference to the drawings.

第1図は、光情報記録媒体の基本構成を示すもので、基
板1上に一般式の色素を含む記録層2を設けた構造であ
る。記録、再生はレーザ光3を集光レンズにより記録層
2上に0.8〜1.5μmの大きさのスポットに集光して行な
われる。記録再生のレーザ光3は、記録層2から照射し
てもよいが、基板1が透明な材料からなる場合には基板
1側から照射する方が一般的に汚れやゴミの影響を少な
くできる。
FIG. 1 shows the basic structure of an optical information recording medium, which has a structure in which a recording layer 2 containing a dye of the general formula is provided on a substrate 1. Recording and reproduction are performed by condensing the laser beam 3 on the recording layer 2 into a spot having a size of 0.8 to 1.5 μm by a condenser lens. The recording / reproducing laser beam 3 may be irradiated from the recording layer 2, but when the substrate 1 is made of a transparent material, irradiation from the substrate 1 side can generally reduce the influence of dirt and dust.

第2図は、基板1と記録層2の間に中間層4を、記録層
2上に保護層5を夫々設けた構造のものである。
FIG. 2 shows a structure in which an intermediate layer 4 is provided between the substrate 1 and the recording layer 2 and a protective layer 5 is provided on the recording layer 2.

第3図は、同一構成の2枚の媒体を記録層2が互いに対
向するようにスペーサ6を介して配置させたものであ
る。なお、第3図中の7はエアーギャップ、8はスピン
ドル穴である。かかる構成によれば、特性的に良好であ
り、更に記録層2への汚れやゴミの影響を抑制できる利
点を有する。
In FIG. 3, two media having the same structure are arranged with a spacer 6 so that the recording layers 2 face each other. In FIG. 3, 7 is an air gap and 8 is a spindle hole. According to such a configuration, there are advantages that the characteristics are good and the influence of dirt and dust on the recording layer 2 can be suppressed.

更に、前述した第1図〜第3図の構成において、Al,Ag
等及びその他の反射膜を基板と記録層の間に設けてもよ
い。
Furthermore, in the structure shown in FIGS. 1 to 3 described above, Al, Ag
Etc. and other reflective films may be provided between the substrate and the recording layer.

〔発明の実施例〕Example of Invention

以下、本発明の実施例を詳細に説明する。 Hereinafter, examples of the present invention will be described in detail.

実施例1 上述した構造式(2)の色素をメチルエチルケトンで溶
解し、2%溶液とした後、これをスピンナーコータで厚
さ1.2mmのガラス基板上に塗布、乾燥して厚さ75nmの記
録層を形成して記録媒体を製造した。
Example 1 The dye of structural formula (2) described above was dissolved in methyl ethyl ketone to form a 2% solution, which was then coated on a 1.2 mm-thick glass substrate with a spinner coater and dried to form a 75 nm-thick recording layer. To form a recording medium.

実施例2 上述した構造式(4)の色素をメチルエチルケトンで溶
解し、2%溶液とした後、これをスピンナーコータで厚
さ1.2mmのガラス基板上に塗布、乾燥して厚さ70nmの記
録層を形成して記録媒体を製造した。
Example 2 The dye of structural formula (4) described above was dissolved in methyl ethyl ketone to form a 2% solution, which was then coated on a 1.2 mm-thick glass substrate with a spinner coater and dried to form a 70 nm-thick recording layer. To form a recording medium.

実施例3 上述した構造式(5)の色素を塩化メチレンで溶解して
2%溶液とした後、これをスピンナーコータで厚さ1.2m
mのガラス基板上に塗布、乾燥して厚さ70nmの記録層を
形成して記録媒体を製造した。
Example 3 The dye of structural formula (5) described above was dissolved in methylene chloride to give a 2% solution, which was then applied to a spinner coater to give a thickness of 1.2 m.
A recording medium was manufactured by coating a 70-nm-thick glass substrate and drying it to form a 70-nm-thick recording layer.

実施例4 上述した構造式(7)の色素を塩化メチレンで溶解し、
2%溶液とした後、これをスピンナーコータで厚さ1.3m
mのガラス基板上に塗布、乾燥して厚さ75nmの記録層を
形成し、記録媒体を製造した。
Example 4 The dye of structural formula (7) above was dissolved in methylene chloride,
After making a 2% solution, use a spinner coater to make the thickness 1.3m.
A recording medium having a thickness of 75 nm was formed by coating on a m glass substrate and drying to form a recording medium.

実施例5 上述した構造式(10)の色素に、バインダ樹脂としての
アクリル樹脂(三菱レーヨン社製:ダイヤナールBR−6
0)を10重量%添加し、これをメチルエチルケトンで溶
解して3%溶液とした後、この溶液をスピンナーコータ
で厚さ1.2mmのガラス基板上に塗布、乾燥して厚さ90nm
の記録層を形成して記録媒体を製造した。
Example 5 An acrylic resin (manufactured by Mitsubishi Rayon Co., Ltd .: Dianal BR-6) as a binder resin was added to the dye of the structural formula (10) described above.
0) was added at 10% by weight and dissolved in methyl ethyl ketone to form a 3% solution, which was then applied on a 1.2 mm thick glass substrate with a spinner coater and dried to a thickness of 90 nm.
A recording layer was formed to produce a recording medium.

実施例6 上述した構造式(13)の色素と赤外線吸収剤(日本化薬
社製商品名:IRG−003)とを重量比で3:1の割合にて混合
し、これをメチルエチルケトンで溶解して2%溶液とし
た後、この溶液をスピンナーコータで厚さ1.2mmのガラ
ス基板上に塗布、乾燥して厚さ75nmの記録層を形成して
記録媒体を製造した。
Example 6 The dye of structural formula (13) described above and an infrared absorber (trade name: IRG-003 manufactured by Nippon Kayaku Co., Ltd.) were mixed at a weight ratio of 3: 1 and dissolved with methyl ethyl ketone. To a 2% solution, the solution was applied onto a 1.2 mm-thick glass substrate with a spinner coater and dried to form a recording layer having a thickness of 75 nm to manufacture a recording medium.

実施例7 上述した構造式(12)の色素と下記構造式(14)の色素
とを重量比で2:1の割合で混合し、これを実施例1と同
様に溶解し、基板上に塗布、乾燥して厚さ70nmの記録層
を形成し、記録媒体を製造した。
Example 7 The dye of the above structural formula (12) and the dye of the following structural formula (14) were mixed at a weight ratio of 2: 1, dissolved in the same manner as in Example 1, and applied onto a substrate. Then, it was dried to form a recording layer having a thickness of 70 nm, and a recording medium was manufactured.

実施例8 実施例1と同様な方法によりガラス基板上に構造式
(3)の色素からなる厚さ60nmの記録層を形成した後、
この記録層上に下記構造式(15)に示すアルミニウムナ
フタロシアニンを真空度1.0×10-5Torrの条件下で真空
加熱蒸着して厚さ30nmの反射性保護層を形成し、記録媒
体を製造した。
Example 8 After a recording layer having a thickness of 60 nm made of the dye of structural formula (3) was formed on a glass substrate by the same method as in Example 1,
Aluminum naphthalocyanine represented by the following structural formula (15) is vacuum-heat-deposited on the recording layer under the condition of a vacuum degree of 1.0 × 10 -5 Torr to form a reflective protective layer with a thickness of 30 nm, and a recording medium is manufactured. did.

比較例1 下記構造式(I)の色素を塩化メチレンで溶解して2%
溶液とした後、この溶液をスピンナーコータで厚さ1.2m
mのガラス基板上に塗布し、乾燥して厚さ70nmの記録層
を形成し、記録媒体を製造した。
Comparative Example 1 A dye of the following structural formula (I) was dissolved in methylene chloride to obtain 2%.
After making a solution, this solution is 1.2m thick with a spinner coater.
A recording medium was manufactured by applying it on a glass substrate of m and drying it to form a recording layer having a thickness of 70 nm.

比較例2 下記構造式(II)の色素を比較例1と同様な方法で溶解
し、ガラス基板上に塗布、乾燥して厚さ70nmの記録層を
形成し、記録媒体を製造した。
Comparative Example 2 A dye having the following structural formula (II) was dissolved in the same manner as in Comparative Example 1, coated on a glass substrate and dried to form a recording layer having a thickness of 70 nm, to manufacture a recording medium.

比較例3 下記構造式(III)の色素を比較例1と同様な方法で溶
解し、ガラス基板上に塗布、乾燥して厚さ70nmの記録層
を形成し、記録媒体を製造した。
Comparative Example 3 A dye having the following structural formula (III) was dissolved in the same manner as in Comparative Example 1, coated on a glass substrate and dried to form a recording layer having a thickness of 70 nm, to manufacture a recording medium.

比較例4 下記構造式(IV)の色素を比較例1と同様な方法で溶解
し、ガラス基板上に塗布、乾燥して厚さ70nmの記録層を
形成し、記録媒体を製造した。
Comparative Example 4 A dye having the following structural formula (IV) was dissolved in the same manner as in Comparative Example 1, coated on a glass substrate and dried to form a recording layer having a thickness of 70 nm, and a recording medium was manufactured.

しかして、本実施例1〜8及び比較例1〜4の記録媒体
の記録層について、記録層側より波長830nmの光に対す
る反射率を分光度計により測定した。また、各記録層に
ついて波長830nmの光に対する吸光度を測定した。更
に、波長830nmの半導体レーザ光を媒体面出力7mWとなる
ように直径1.2μmのスポットに集光し、この集光レー
ザ光を各記録媒体の基板側からその移動速度を9m/secの
条件下で1MHzの信号を書き込み、同レーザ光で再生出力
0.4mWで再生を行なって記録感度(記録エネルギー閾
値)及び再生信号のC/N値を測定した。更に、本実施例
1〜8及び比較例1〜4の記録媒体を50℃、95%の雰囲
気下に150時間放置し、放置前後の吸光度低下率、反射
率低下率を測定する耐熱湿性試験を行なった。各記録媒
体に25℃、60%の雰囲気で500Wタングステン光を50cmへ
だてて100時間照射し、タングステン光の照射前後での
吸光度低下率、反射率低下率を測定する耐光試験を行な
った。これらの結果を下記表に示した。
Then, with respect to the recording layers of the recording media of Examples 1 to 8 and Comparative Examples 1 to 4, the reflectance for light having a wavelength of 830 nm from the recording layer side was measured by a spectrophotometer. In addition, the absorbance of light having a wavelength of 830 nm was measured for each recording layer. Furthermore, a semiconductor laser beam with a wavelength of 830 nm is focused on a spot with a diameter of 1.2 μm so that the medium surface output is 7 mW, and this focused laser beam is moved from the substrate side of each recording medium at a moving speed of 9 m / sec. 1MHz signal is written by and reproduced by the same laser light
Recording was performed at 0.4 mW and the recording sensitivity (recording energy threshold) and the C / N value of the reproduced signal were measured. Further, the recording media of Examples 1 to 8 and Comparative Examples 1 to 4 were left to stand in an atmosphere of 50 ° C. and 95% for 150 hours, and a heat and humidity test was conducted to measure the rate of decrease in absorbance and the rate of decrease in reflectance before and after standing. I did. Each recording medium was irradiated with 500 W tungsten light at 50 ° C. in an atmosphere of 25 ° C. and 60% for 100 hours, and a light resistance test was performed to measure the rate of decrease in absorbance and the rate of decrease in reflectance before and after irradiation with tungsten light. The results are shown in the table below.

〔発明の効果〕 以上詳述した如く、本発明によれば高い反射率と高い記
録感度を有し、光学的信号の書き込み、再生を安定して
行なうことが可能で、かつ再生光や日光、湿度に対する
安定性の高い無公害の光情報記録媒体を提供できる。
[Effects of the Invention] As described in detail above, according to the present invention, it has a high reflectance and a high recording sensitivity, and writing and reproduction of optical signals can be stably performed, and reproduction light and sunlight, It is possible to provide a pollution-free optical information recording medium having high stability against humidity.

【図面の簡単な説明】[Brief description of drawings]

第1図〜第3図は、夫々本発明の光情報記録媒体を示す
概略図である。 1……基板、2……記録層、3……レーザ光、4……中
間層、5……保護層、6……スペーサ。
1 to 3 are schematic views showing the optical information recording medium of the present invention. 1 ... Substrate, 2 ... Recording layer, 3 ... Laser light, 4 ... Intermediate layer, 5 ... Protective layer, 6 ... Spacer.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】下記一般式にて表わされる有機色素を含む
記録層を備えることを特徴とする光情報記録媒体。 ただし、式中のR1は炭素数1〜6のアルキル基、アラル
キル基またはフェニル基、R2は水素原子、ハロゲン原
子、炭素数1〜6のアルキル基、 (Ph;フェニル基)または (R3;炭素数1〜6のアルキル基)、Xはパークロレー
ト、フルオロボレート、アイオダイド、クロライド、ブ
ロマイド、p−トルエンスルフォネートから選ばれる陰
イオン、Yは炭素数1〜18のアルキル基、フェニル基、
−R4OR5、−R4COR5、−R4COOR5(R4;炭素数1〜20のアルキレン基、R5;炭素数1〜18の
アルキル基またはフェニル基)、Zはインドールを構成
するベンゼン環に付加されるベンゼン環を示す。
1. An optical information recording medium comprising a recording layer containing an organic dye represented by the following general formula. However, in the formula, R 1 is an alkyl group having 1 to 6 carbon atoms, an aralkyl group or a phenyl group, R 2 is a hydrogen atom, a halogen atom, an alkyl group having 1 to 6 carbon atoms, (Ph; phenyl group) or (R 3 ; alkyl group having 1 to 6 carbon atoms), X is an anion selected from perchlorate, fluoroborate, iodide, chloride, bromide and p-toluenesulfonate, Y is an alkyl group having 1 to 18 carbon atoms , Phenyl group,
-R 4 OR 5 , -R 4 COR 5 , -R 4 COOR 5 , (R 4 ; alkylene group having 1 to 20 carbon atoms, R 5 ; alkyl group having 1 to 18 carbon atoms or phenyl group), Z represents a benzene ring added to the benzene ring constituting indole.
JP61029328A 1986-02-13 1986-02-13 Optical information recording medium Expired - Lifetime JPH0729490B2 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP61029328A JPH0729490B2 (en) 1986-02-13 1986-02-13 Optical information recording medium
US07/011,896 US4908294A (en) 1986-02-13 1987-02-06 Optical information recording medium
DE19873704601 DE3704601A1 (en) 1986-02-13 1987-02-13 RECORD CARRIER FOR OPTICAL DATA

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61029328A JPH0729490B2 (en) 1986-02-13 1986-02-13 Optical information recording medium

Publications (2)

Publication Number Publication Date
JPS62187085A JPS62187085A (en) 1987-08-15
JPH0729490B2 true JPH0729490B2 (en) 1995-04-05

Family

ID=12273165

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61029328A Expired - Lifetime JPH0729490B2 (en) 1986-02-13 1986-02-13 Optical information recording medium

Country Status (1)

Country Link
JP (1) JPH0729490B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04112480U (en) * 1991-03-18 1992-09-30 ヒロセ電機株式会社 Horizontal connector structure
JP4781123B2 (en) * 2006-02-16 2011-09-28 株式会社Adeka Optical filter

Also Published As

Publication number Publication date
JPS62187085A (en) 1987-08-15

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