JPH0348843A - Optical recording medium and manufacture of same - Google Patents
Optical recording medium and manufacture of sameInfo
- Publication number
- JPH0348843A JPH0348843A JP1185517A JP18551789A JPH0348843A JP H0348843 A JPH0348843 A JP H0348843A JP 1185517 A JP1185517 A JP 1185517A JP 18551789 A JP18551789 A JP 18551789A JP H0348843 A JPH0348843 A JP H0348843A
- Authority
- JP
- Japan
- Prior art keywords
- compound
- optical recording
- light
- recording medium
- state
- 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.)
- Pending
Links
- 230000003287 optical effect Effects 0.000 title claims abstract description 20
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- 150000001875 compounds Chemical class 0.000 claims abstract description 20
- 238000010521 absorption reaction Methods 0.000 claims abstract description 16
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 claims abstract description 3
- 125000005131 dialkylammonium group Chemical group 0.000 claims abstract 2
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract 2
- 150000002148 esters Chemical class 0.000 claims abstract 2
- 229930195729 fatty acid Natural products 0.000 claims abstract 2
- 239000000194 fatty acid Substances 0.000 claims abstract 2
- 239000000203 mixture Substances 0.000 claims abstract 2
- 150000003839 salts Chemical class 0.000 claims abstract 2
- 125000005472 straight-chain saturated fatty acid group Chemical class 0.000 claims abstract 2
- 238000000034 method Methods 0.000 claims description 12
- 230000001678 irradiating effect Effects 0.000 claims description 6
- 239000011248 coating agent Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- 239000000975 dye Substances 0.000 abstract description 8
- HPEUJPJOZXNMSJ-UHFFFAOYSA-N Methyl stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC HPEUJPJOZXNMSJ-UHFFFAOYSA-N 0.000 abstract description 6
- CAMHHLOGFDZBBG-UHFFFAOYSA-N epoxidized methyl oleate Natural products CCCCCCCCC1OC1CCCCCCCC(=O)OC CAMHHLOGFDZBBG-UHFFFAOYSA-N 0.000 abstract description 3
- OGQYPPBGSLZBEG-UHFFFAOYSA-N dimethyl(dioctadecyl)azanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC OGQYPPBGSLZBEG-UHFFFAOYSA-N 0.000 abstract description 2
- 238000000862 absorption spectrum Methods 0.000 description 8
- 230000002776 aggregation Effects 0.000 description 3
- 238000004220 aggregation Methods 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 239000000693 micelle Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- -1 saturated fatty acid ester Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
- Optical Record Carriers And Manufacture Thereof (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明CAL 情報記録用の光ディスクなどに利用さ
れる光学記録媒体及びその製造方法に関する。DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to an optical recording medium used for optical discs for recording information and a method for manufacturing the same.
従来の技術
有機材料を記録体とする光学記録媒体の1つとして、色
素分子の特徴的な分子集合状態である会合体を利用した
ものがある。その会合状態のうち、鋭い(ピーク波長半
値幅の狭い)吸収スペクトルを示すj会合体を利用した
光学記録媒体が報告されており、その薄膜化方法として
ラングミュア−プロジェット(以下LBと略す)法を利
用する方法力(例えばア7°ライビ・フィシ゛フクス・
レター49巻(1986年)第1677頁から第167
9頁(Appl、 Phys、 Lett、 19(1
986)PP1677〜1679)に発表されていも
このような光学記録媒体への記録は ピーク吸収波長に
一致する波長のレーザ光を照射し 熱モードによって吸
収スペクトル中の対応するピークが消失すも そのピー
クの有無によって記録が行なわれ そのピークの吸収強
度の検出によって再生が行なわれる。2. Description of the Related Art One type of optical recording medium using an organic material as a recording medium utilizes an aggregate, which is a characteristic molecular aggregation state of dye molecules. Among these association states, an optical recording medium using a j-aggregate that exhibits a sharp absorption spectrum (narrow peak wavelength half-width) has been reported, and the Langmuir-Prodgett (hereinafter abbreviated as LB) method is used to thin the film. How to use the power (e.g.
Letter Volume 49 (1986) Pages 1677 to 167
9 pages (Appl, Phys, Lett, 19(1)
986) PP1677-1679)
Recording on such an optical recording medium is performed by irradiating a laser beam with a wavelength that matches the peak absorption wavelength, and although the corresponding peak in the absorption spectrum disappears due to the thermal mode, recording is performed depending on the presence or absence of that peak. Regeneration is performed by detecting the intensity.
色素分子の会合状態として(友 三量体 三量体など多
くの会合体が知られている。特に 半値幅の狭(\ 鋭
い吸収スペクトルを示すものとして(表金合体のピーク
吸収波長が単量体の吸収ピーク波長よりも長波長側にシ
フトしたJ会合体 および短波長側にシフトしたH(ま
たはHo、以下合わせてHと記す)会合体が知られてい
も
L B法は有機超薄膜形成方法であり、光学記録媒体の
記録層の膜厚制御に優れているばかりでなく、色素分子
の会合状態制御にも優れていも発明が解決しようとする
課題
色素のJ会合体を利用した光学記録媒体において(上
従来は記録状態の消去方法として高湿度処鳳 熱処虱
溶媒処理など雰囲気処理が用いられていた そのた敢
消去・記録を同時に行なうオーバーライド方式の適用が
できなかっ八本発明(よ このような従来技術の課題を
解決することを目的とする。Many aggregates, such as trimers, are known as associated states of dye molecules. In particular, they exhibit narrow half-widths (\ sharp absorption spectra) (the peak absorption wavelength of the metal alloy is monomeric). Even though J aggregates shifted to longer wavelengths than the absorption peak wavelength of the body and H (or Ho, hereinafter referred to collectively as H) aggregates shifted to shorter wavelengths are known, the LB method can form ultra-thin organic films. Optical recording using J-aggregates of dyes is a method that is not only excellent in controlling the film thickness of the recording layer of an optical recording medium, but also excellent in controlling the association state of dye molecules. In the medium (top
Conventionally, the method of erasing the recorded state was to use a high-humidity heat treatment.
Atmospheric treatments such as solvent treatment were used.
The present invention aims to solve these problems of the prior art.
課題を解決するための手段
媒体中においである分子集合状態と他の分子集合状態と
力丈 それらの形成割合が逆比例的鳳 状態の移行を生
じる化合物があも 本発明(よ この移行を光照射によ
って制御するものであって、吸収波長の異なる2つ以上
の分子集合状態を有する化合物へ 1つの分子集合状態
の吸収に対応する波長の光を照射することで記録を行な
((さらに他の1つの分子集合状態に対応する波長の光
を照射することで消去を行なう光学記録媒体である。Means for Solving the Problems The ratio of formation of one molecular assembly state to another molecular assembly state and strength in a medium is inversely proportional to each other. It is controlled by irradiation, and recording is performed by irradiating a compound that has two or more molecular assembly states with different absorption wavelengths with light of a wavelength corresponding to the absorption of one molecular assembly state ((and other methods). This is an optical recording medium that performs erasing by irradiating light with a wavelength corresponding to one molecular aggregation state.
分子集合状態として(よ 結晶形風 ラメラ、 ミセル
などがある力(分子の会合体を利用する。As a state of molecular assembly (like crystal form, lamellae, micelles, etc.) there are forces (using aggregates of molecules).
作用
記録層(、−ある分子集合状態に対応する光を照射する
と光吸収による状態移行を生じて、もう−方の分子集合
状態の割合が増えも そのたべ 吸収極大の強度は前者
が減少し 後者が増大すムこの時を記録状態とすム 連
間 吸収の増大した分子集合状態に対応する波長の光を
ある光強度で照射すると、初期の状態に移行すも この
ケースが消去に対応することなる。Action recording layer (-When irradiated with light corresponding to a certain molecular assembly state, a state transition occurs due to light absorption, and the proportion of the other molecular assembly state increases.However, the intensity of the absorption maximum decreases in the former and the latter When the molecular assembly state with increased absorption is irradiated with light of a wavelength corresponding to the molecular assembly state at a certain light intensity, the state shifts to the initial state. This case corresponds to erasure. Become.
更(へ 具体的に説明すも 分子集合状態としての会合
体の[NH会合体とJ会合体を利用すムH会合体は単量
体の吸収極大波長よりも短波長側に半値幅の狭いピーク
を示LA J会合体は長波長側に半値幅の狭いピークを
示す。信号として吸収極大波長における吸収強度を利用
するた八 波長での分離が明瞭になる。Further, to give a more specific explanation, the association as a state of molecular assembly [NH association and J association are utilized. The LAJ aggregate shows a peak with a narrow half-width on the long wavelength side.Separation at eight wavelengths becomes clear because the absorption intensity at the absorption maximum wavelength is used as a signal.
記録光と消去光の波長が異なるた八 2つの光源を使用
すも 消去においても光照射で行なうことができるたべ
この化合物を使用した光学記録媒体においては 2レ
ーザビームによるオーバーライド方式を適用できる。Even though two light sources are used, since the wavelengths of the recording light and erasing light are different, erasing can also be performed by light irradiation.In optical recording media using this compound, an override method using two laser beams can be applied.
実施例
以下へ 本発明の実施例について図面を参照しながら説
明する。Embodiments Below, embodiments of the present invention will be described with reference to the drawings.
用いた化合物(訳 前記に示した構造のシアニン色素と
ジオクタデシル−ジメチルアンモニウムとを1対1に塩
形成させた化合へ あるいはその化合物と直鎖飽和脂肪
酸エステルであるステアリン酸メチルとを1対2に混合
した化合物である。本例(よ ステアリン酸メチルと混
合した系の化合物で実施した例である。この化合物の単
量体の吸収極大G友 550nmであム この化合物は
二量未三量&H会合&J会合体などの複数の会合体を形
成すも
光学記録媒体の製造方法として(上 記録層の厚さの制
御法 および作製プロセスにおける会合状態の制御を実
施するため置 LB法を使用ずム水相は1回蒸留水を用
いて、水温的16\ 圧縮速度10mm/minで圧縮
した後へ 累積速度10rnm/minで累積を行なっ
t、6 LB法の特徴として、単分子膜に加える表面圧
によって会合状態を制御できも この化合物の単分子膜
に対しては 気水界面において表面圧15mN/mを加
えることで、安定な分子集合状態としてH会合体とJ会
合体の2つの会合状態だけを形成することかできる。The compound used (translation: To the compound in which the cyanine dye with the structure shown above and dioctadecyl-dimethylammonium are salted in a 1:1 ratio, or the compound and methyl stearate, which is a linear saturated fatty acid ester, are formed in a 1:2 ratio) This is an example of a compound mixed with methyl stearate.The absorption maximum of the monomer of this compound is 550 nm. As a manufacturing method for optical recording media that forms multiple aggregates such as &H and J aggregates (see above), there is a method for controlling the thickness of the recording layer and the state of association in the manufacturing process without using the LB method. The aqueous phase is compressed using single-distilled water at a hydrothermal temperature of 16 \ at a compression speed of 10 mm/min, and then accumulated at a cumulative speed of 10 nm/min. Although the association state can be controlled by pressure, by applying a surface pressure of 15 mN/m at the air-water interface to a monomolecular film of this compound, two association states, H-aggregate and J-aggregate, can be established as stable molecular assembly states. Can only be formed.
第1図(A)は 累積時の表面圧15mN/mで累積し
た記録層の吸収スペクトルであ4 第2図(よ 作製し
た光学記録媒体の構造図であ4H会合体の吸収極大の波
長は430nm、J会合体は638 nmであも 光源
としては 記録光の波長430nm、消去光の波長64
0 nmの色素レーザを使用する。記録エネルギーはI
OmJ/cm2・パルス 消去エネルギーは30mJ/
cm2・パルスであム 第1図(B)は記録状態の吸収
スペクト瓜 Cは消去状態の吸収スペクトルであム 記
録光 消去光の照射によってそれぞれの状態を繰り返し
再現でき九
発明の効果
以上述べたように 本発明により、 1種の記録層中の
異なる分子集合状態を利用し 光によって記録・消去を
行なえる光学記録媒体を提供できる。Figure 1 (A) shows the absorption spectrum of the recording layer accumulated at a surface pressure of 15 mN/m. The wavelength of the recording light is 430 nm, and the wavelength of the J aggregate is 638 nm.As a light source, the wavelength of the recording light is 430 nm, and the wavelength of the erasing light is 64 nm.
A 0 nm dye laser is used. The recording energy is I
OmJ/cm2・Pulse Erasing energy is 30mJ/
Figure 1 (B) shows the absorption spectrum of the recorded state. C shows the absorption spectrum of the erased state. Recording light Each state can be repeatedly reproduced by irradiation with the erasing light. According to the present invention, it is possible to provide an optical recording medium in which recording and erasing can be performed using light by utilizing different molecular aggregation states in one type of recording layer.
第1図(よ 本発明の光学記録媒体の一実施例の記録層
の吸収スペクトルを示すグラフであって、同図(A)は
記録層の形成初期を示し 同図(B)は記録状態を示し
同図(C)は消去状態の吸収スペクトルを示すグラフ
、第2図(友 本発明の光学記録媒体の一実施例の構造
図を示す断面図である。FIG. 1 is a graph showing the absorption spectrum of the recording layer of an embodiment of the optical recording medium of the present invention, in which (A) shows the initial stage of formation of the recording layer, and (B) shows the recording state. FIG. 2 (C) is a graph showing an absorption spectrum in an erased state, and FIG.
Claims (5)
る化合物を備え、その1つの分子集合状態の吸収に対応
する波長の光を照射することで記録が行われ、さらに他
の1つの分子集合状態に対応する波長の光を照射するこ
とで消去が行なわれるものであることを特徴とする光学
記録媒体。(1) Recording is performed by irradiating a compound with two or more molecular assembly states with different absorption wavelengths and irradiating it with light of a wavelength corresponding to the absorption of one of the molecular assembly states. An optical recording medium characterized in that erasing is performed by irradiating light with a wavelength corresponding to a collective state.
求項1記載の光学記録媒体。(2) The optical recording medium according to claim 1, wherein the molecular assembly state is an aggregate.
有する色素化合物であることを特徴とする請求項2記載
の光学記録媒体、(3) The optical recording medium according to claim 2, wherein the compound having an aggregate is a dye compound having a J aggregate and an H aggregate;
記に示す構造のシアニン色素とジアルキルアンモニウム
とを塩形成させた化合物、あるいはその化合物と直鎖飽
和脂肪酸エステルとの混合物であることを特徴とする光
学記録媒体。 ▲数式、化学式、表等があります▼(4) The dye compound having the characteristics described in claim 3 is a compound obtained by forming a salt of a cyanine dye and dialkyl ammonium having the structure shown below, or a mixture of the compound and a straight chain saturated fatty acid ester. Characteristic optical recording media. ▲Contains mathematical formulas, chemical formulas, tables, etc.▼
体の記録層を基板上へ被覆する方法がラングミュア−ブ
ロジェット法であることを特徴とする光学記録媒体の製
造方法。(5) A method for manufacturing an optical recording medium, characterized in that the method for coating a substrate with the recording layer of the optical recording medium according to any one of claims 1 to 4 is a Langmuir-Blodgett method.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1185517A JPH0348843A (en) | 1989-07-18 | 1989-07-18 | Optical recording medium and manufacture of same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1185517A JPH0348843A (en) | 1989-07-18 | 1989-07-18 | Optical recording medium and manufacture of same |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0348843A true JPH0348843A (en) | 1991-03-01 |
Family
ID=16172174
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1185517A Pending JPH0348843A (en) | 1989-07-18 | 1989-07-18 | Optical recording medium and manufacture of same |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0348843A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100441862B1 (en) * | 2001-11-07 | 2004-07-27 | 허무회 | A stick |
EP1734080A1 (en) * | 2004-03-30 | 2006-12-20 | Taiyoyuden Co., Ltd. | Monomethine dye compound, optical information recording medium utilizing the compound and process for producing the same |
JP2008010100A (en) * | 2006-06-30 | 2008-01-17 | Nara Institute Of Science & Technology | Pigment aggregation-forming pigment, composition containing pigment aggregation, and information recording/reproducing system by using structural conversion of pigment aggregation |
-
1989
- 1989-07-18 JP JP1185517A patent/JPH0348843A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100441862B1 (en) * | 2001-11-07 | 2004-07-27 | 허무회 | A stick |
EP1734080A1 (en) * | 2004-03-30 | 2006-12-20 | Taiyoyuden Co., Ltd. | Monomethine dye compound, optical information recording medium utilizing the compound and process for producing the same |
EP1734080A4 (en) * | 2004-03-30 | 2009-08-05 | Taiyo Yuden Kk | Monomethine dye compound, optical information recording medium utilizing the compound and process for producing the same |
JP2008010100A (en) * | 2006-06-30 | 2008-01-17 | Nara Institute Of Science & Technology | Pigment aggregation-forming pigment, composition containing pigment aggregation, and information recording/reproducing system by using structural conversion of pigment aggregation |
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