JPH04370599A - Optical recording medium - Google Patents
Optical recording mediumInfo
- Publication number
- JPH04370599A JPH04370599A JP3148910A JP14891091A JPH04370599A JP H04370599 A JPH04370599 A JP H04370599A JP 3148910 A JP3148910 A JP 3148910A JP 14891091 A JP14891091 A JP 14891091A JP H04370599 A JPH04370599 A JP H04370599A
- Authority
- JP
- Japan
- Prior art keywords
- molecule
- recording medium
- temperature
- optical recording
- phase transition
- 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.)
- Granted
Links
- 230000003287 optical effect Effects 0.000 title claims abstract description 21
- 150000001875 compounds Chemical class 0.000 claims abstract description 14
- 230000007704 transition Effects 0.000 claims abstract description 9
- 230000001747 exhibiting effect Effects 0.000 claims description 5
- 230000035945 sensitivity Effects 0.000 abstract description 10
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 abstract description 9
- 229940067606 lecithin Drugs 0.000 abstract description 9
- 235000010445 lecithin Nutrition 0.000 abstract description 9
- 239000000787 lecithin Substances 0.000 abstract description 9
- VKOBVWXKNCXXDE-UHFFFAOYSA-N icosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCC(O)=O VKOBVWXKNCXXDE-UHFFFAOYSA-N 0.000 abstract description 7
- 238000006243 chemical reaction Methods 0.000 abstract description 6
- 239000000203 mixture Substances 0.000 abstract description 5
- 238000006317 isomerization reaction Methods 0.000 abstract description 4
- 230000005284 excitation Effects 0.000 abstract description 3
- 238000010438 heat treatment Methods 0.000 abstract description 3
- CITHEXJVPOWHKC-UUWRZZSWSA-N 1,2-di-O-myristoyl-sn-glycero-3-phosphocholine Chemical group CCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCC CITHEXJVPOWHKC-UUWRZZSWSA-N 0.000 abstract description 2
- 239000012528 membrane Substances 0.000 abstract 1
- 239000010408 film Substances 0.000 description 6
- 230000008859 change Effects 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 238000000862 absorption spectrum Methods 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 230000001678 irradiating effect Effects 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 230000001443 photoexcitation Effects 0.000 description 2
- IENILPMDTHYRMT-UHFFFAOYSA-N 4-nitro-6-[2-(1,3,3-trimethylindol-2-ylidene)ethylidene]cyclohexa-2,4-dien-1-one Chemical compound CC1(C)C2=CC=CC=C2N(C)C1=CC=C1C=C([N+]([O-])=O)C=CC1=O IENILPMDTHYRMT-UHFFFAOYSA-N 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000008033 biological extinction Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000006862 quantum yield reaction Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は光記録媒体に関するもの
であり、フォトクロミック化合物と熱的相転移を示す化
合物を累積することにより、記録速度及び記録感度に優
れた光記録媒体を提供するものである。[Field of Industrial Application] The present invention relates to an optical recording medium, and provides an optical recording medium with excellent recording speed and recording sensitivity by accumulating a photochromic compound and a compound exhibiting a thermal phase transition. be.
【0002】0002
【従来の技術】フォトクロミック化合物を用いた光記録
媒体は、薄膜作製過程での成膜性及び膜質を向上させる
ために、脂肪酸等の化合物を添加する場合が多い。2. Description of the Related Art In optical recording media using photochromic compounds, compounds such as fatty acids are often added in order to improve film formability and film quality during the thin film manufacturing process.
【0003】フォトクロミック化合物は、高分解能、多
重記録性等の多くの利点を有するが、感度が不十分であ
るため、未だ光記録媒体に応用されていない。Although photochromic compounds have many advantages such as high resolution and multi-recordability, they have not yet been applied to optical recording media because of insufficient sensitivity.
【0004】フォトクロミック材料を実用化する際、光
記録媒体に対して速い書き込み速度が要求される。この
速度は分子の異性化速度、異性化量子収率及び吸光係数
に依存し、分子設計等の有機分子合成技術の開発が積極
的に行われている。[0004] When putting photochromic materials into practical use, a high writing speed is required for optical recording media. This rate depends on the isomerization rate, isomerization quantum yield, and extinction coefficient of the molecule, and organic molecule synthesis techniques such as molecular design are being actively developed.
【0005】[0005]
【発明が解決しようとする課題】脂肪酸等の化合物は、
単に良好にフォトクロミック化合物を基板上に累積する
ためだけに光記録媒体に添加されたものであり、媒体の
記録速度及び記録感度の上昇に対して何ら影響を与えて
いるものではない。[Problem to be solved by the invention] Compounds such as fatty acids are
It is added to the optical recording medium simply to satisfactorily accumulate the photochromic compound on the substrate, and does not have any effect on increasing the recording speed and recording sensitivity of the medium.
【0006】フォトクロミック化合物に対する記録速度
及び感度の上昇は、個々のフォトクロミック分子に関し
て行われているが、個々の分子よりも記録安定性の点で
優れる分子会合体に関しては全く行われていない。Although improvements in the recording speed and sensitivity of photochromic compounds have been made for individual photochromic molecules, no efforts have been made for molecular aggregates, which have better recording stability than individual molecules.
【0007】[0007]
【課題を解決するための手段】本発明はフォトクロミッ
ク反応を利用した光記録に対して高速度及び高感度に書
き込みを行なう媒体を提供するものである。その記録媒
体は、、以下の特性を持つフォトクロミズムを示す有機
分子(以下、分子A、分子B、及び分子会合体JB)及
び熱的相転移を示す有機分子(以下、分子C)を用いる
。分子Aは光励起L1により分子会合体形成能を持つ分
子Bに異性化する。分子Bは加熱により分子会合体JB
を形成する。分子会合体JBは光励起L2により分子A
に戻る。一方、分子Cは温度T1ではある相状態P1で
存在する。分子Cは温度T1から温度T2(T1<T2
)の間で相転移を行ない、温度T2では別の相状態P2
で存在する。SUMMARY OF THE INVENTION The present invention provides a medium for optical recording that utilizes photochromic reactions and allows writing at high speed and sensitivity. The recording medium uses organic molecules exhibiting photochromism (hereinafter referred to as molecule A, molecule B, and molecular association JB) and organic molecules exhibiting thermal phase transition (hereinafter referred to as molecule C) having the following characteristics. Molecule A is isomerized into molecule B having the ability to form molecular aggregates by photoexcitation L1. Molecule B becomes molecular association JB by heating
form. Molecular association JB becomes molecule A by photoexcitation L2
Return to On the other hand, molecule C exists in a certain phase state P1 at temperature T1. Molecule C changes from temperature T1 to temperature T2 (T1<T2
), and at temperature T2, a different phase state P2 occurs.
exists in
【0008】分子Cと分子会合体JBを図1に示す構造
で累積した光記録媒体は、温度T1と温度T2の間で光
照射による媒体の吸収特性、即ち変化速度が急激に異な
る。In an optical recording medium in which molecules C and molecular aggregates JB are accumulated in the structure shown in FIG. 1, the absorption characteristics of the medium due to light irradiation, that is, the rate of change, differ sharply between temperatures T1 and T2.
【0009】本発明は、フォトクロミック化合物の単分
子膜間に熱的相転移を示す化合物の単分子膜を挿入して
累積することにより、書き込み速度及び感度に優れた光
記録媒体を提供する。The present invention provides an optical recording medium with excellent writing speed and sensitivity by inserting and accumulating a monomolecular film of a compound exhibiting thermal phase transition between monomolecular films of photochromic compounds.
【0010】0010
【作用】分子Cと分子会合体JBを交互に累積した光記
録媒体OM1の分子会合体JBは、光励起L2により分
子Cの相状態P1とP2で著しく異なる崩壊挙動を示し
、分子Cのある相状態では分子Cを累積していない光記
録媒体OM2の分子会合体JBの崩壊と比較して、多く
の該分子が異性化する。[Operation] The molecular association JB of the optical recording medium OM1, in which molecules C and molecular associations JB are alternately accumulated, exhibits significantly different decay behavior in the phase states P1 and P2 of the molecule C due to optical excitation L2, and the phase state with the molecule C In this state, compared to the collapse of the molecular association JB of the optical recording medium OM2 in which molecules C are not accumulated, many molecules C are isomerized.
【0011】従って、分子Cと分子会合体JBを累積し
た光記録媒体は、多くの該分子が異性化する分子Cの相
状態を利用することにより、高速度及び高速度な書き込
みが可能となる。[0011] Therefore, an optical recording medium in which the molecule C and the molecular association JB are accumulated can perform high-speed and high-speed writing by utilizing the phase state of the molecule C in which many of the molecules are isomerized. .
【0012】0012
【実施例】以下、本発明の実施例を詳説するが、本発明
はこれに限定されるものではない。[Examples] Examples of the present invention will be described in detail below, but the present invention is not limited thereto.
【0013】[0013]
【化1】[Chemical formula 1]
【0014】[0014]
【化2】[Case 2]
【0015】記録媒体として用いたJB膜は、上式1に
示すスピロピランとアラキジン酸の混合物(1:1)、
上式2に示すL−α−ホスファチジルコリン,ジミリス
トイル(以下、レシチンと略す)とアラキジン酸の混合
物(1:1)をそれぞれpH7の水面上に展開し、垂直
浸漬法で交互に20層累積することにより作製する。有
機分子会合体(J会合体)は、365nmの紫外光を2
0分間照射し、フォトクロミック反応によりフォトメロ
シアニンに異性化した後、40℃で20分間加熱するこ
とにより形成させる。The JB film used as a recording medium is a mixture of spiropyran and arachidic acid (1:1) shown in the above formula 1,
A mixture (1:1) of L-α-phosphatidylcholine, dimyristoyl (hereinafter abbreviated as lecithin) and arachidic acid shown in the above formula 2 is spread on the water surface of pH 7, and 20 layers are accumulated alternately by vertical immersion method. It is prepared by Organic molecular associations (J-aggregates) absorb 365 nm ultraviolet light at 2
After irradiating for 0 minutes and isomerizing to photomerocyanine by photochromic reaction, it is formed by heating at 40° C. for 20 minutes.
【0016】また、上記記録媒体と比較するために、上
式1に示すスピロピランとアラキジン酸の混合物(1:
1)を同様に10層累積したLB膜を作成し、J会合体
を形成させた。In addition, for comparison with the above recording medium, a mixture of spiropyran and arachidic acid (1:
An LB film was prepared by stacking 10 layers in the same manner as in 1), and a J aggregate was formed.
【0017】J会合体の崩壊は、波長615nm、繰り
返し10Hz、パルス幅200psの窒素レーザ励起の
色素レーザを用いて行なった。J会合体に対して所定時
間レーザを照射して吸収を測定する操作を数回繰り返す
ことにより、J会合体崩壊過程での吸収スペクトルの経
時変化を測定し、反応速度定数を求めた。なお、吸収ス
ペクトルの変化量は、590nmから700nmまでの
J会合体の吸収曲線の積分値の変化量として求めた。The collapse of the J-aggregate was carried out using a dye laser excited by a nitrogen laser with a wavelength of 615 nm, a repetition rate of 10 Hz, and a pulse width of 200 ps. By repeating the operation of irradiating the J-aggregate with a laser for a predetermined period of time and measuring its absorption several times, the change in the absorption spectrum over time during the J-aggregate disintegration process was measured, and the reaction rate constant was determined. The amount of change in the absorption spectrum was determined as the amount of change in the integral value of the absorption curve of the J aggregate from 590 nm to 700 nm.
【0018】図2は記録媒体の書き込み温度特性を示し
、図中、白丸はスピロピランJ会合体とレシチンを交互
に累積した本実施例による記録媒体による特性、黒丸は
従来のスピロピランJ会合体の媒体による特性を示す。
スピロピランJ会合体は、少なくとも10℃から40℃
の温度領域で熱異性化を示さない。スピロピランJ会合
体とレシチンを交互に累積した媒体は、30℃付近に屈
曲点を示し、傾きがその前後の温度で大きく異なった。
一方、従来のスピロピランJ会合体の媒体は、明確な屈
曲点を示さなかった。FIG. 2 shows the writing temperature characteristics of the recording medium. In the figure, white circles indicate the characteristics of the recording medium according to this embodiment in which spiropyran J aggregates and lecithin were alternately accumulated, and black circles indicate the characteristics of the conventional medium of spiropyran J aggregates. shows the characteristics according to The spiropyran J aggregate is at least 10°C to 40°C.
It does not exhibit thermal isomerization in the temperature range of . The medium in which spiropyran J aggregates and lecithin were alternately accumulated showed a bending point around 30°C, and the slope differed greatly at temperatures before and after that point. On the other hand, the conventional spiropyran J aggregate medium did not show a clear inflection point.
【0019】試料温度40℃に於いて反応速度数を1パ
ルスのレーザエネルギー密度に対してプロットしたのが
図3(a)である。スピロピランJ会合体とレシチンを
交互に累積した媒体(図中、白丸)は、従来のスピロピ
ランJ会合体の媒体(図中、黒丸)と比較して、J会合
体の崩壊が著しく速かった。一方、図3(b)から明ら
かなように、試料温度10℃の場合、レーザエネルギー
密度に対するJ会合体崩壊は両者の媒体の間で大きな挙
動の違いが見られなかった。FIG. 3(a) shows the reaction rate number plotted against the laser energy density of one pulse at a sample temperature of 40°C. In the medium in which spiropyran J-aggregates and lecithin were alternately accumulated (white circles in the figure), the J-aggregates disintegrated significantly faster than in the conventional medium of spiropyran J-aggregates (black circles in the figure). On the other hand, as is clear from FIG. 3(b), when the sample temperature was 10° C., there was no significant difference in the behavior of the J-aggregate collapse with respect to the laser energy density between the two media.
【0020】図4は、ここで用いたレシチンのDSC測
定結果を示す。ここで用いたレシチンは、25℃付近で
相転移を起こすことが分かった。FIG. 4 shows the DSC measurement results of lecithin used here. It was found that the lecithin used here undergoes a phase transition at around 25°C.
【0021】以上のことから、スピロピランJ会合体の
光記録媒体は、レシチンを交互に累積することにより、
記録媒体の書き込み速度及び感度の著しい向上が見られ
た。[0021] From the above, the optical recording medium of the spiropyran J aggregate can be obtained by alternately accumulating lecithin.
A significant improvement in the writing speed and sensitivity of the recording medium was observed.
【0022】[0022]
【発明の効果】本発明によれば、フォトクロミック反応
を利用した光記録媒体に対して、熱的相転移を示す化合
物を交互に累積することにより、高速度及び高感度に書
き込みができる。According to the present invention, writing can be performed at high speed and sensitivity on an optical recording medium that utilizes a photochromic reaction by alternately accumulating compounds that exhibit a thermal phase transition.
【0023】ここで、本発明は、高速度及び高感度に書
き込みを行なうことができる光記録媒体を提案するばか
りでなく、次世代の光連想記憶素子の記録媒体として利
用可能なものである。The present invention not only proposes an optical recording medium on which writing can be performed at high speed and sensitivity, but also can be used as a recording medium for next-generation optical content addressable memory elements.
【図1】本発明の光記録媒体の累積構造モデル図である
。FIG. 1 is a cumulative structural model diagram of an optical recording medium of the present invention.
【図2】本発明による実施例と従来例の書き込み温度特
性図である。FIG. 2 is a diagram of write temperature characteristics of an embodiment according to the present invention and a conventional example.
【図3】本発明による実施例と従来例の有機分子会合体
崩壊に及ぼすレーザ照射エネルギーの影響を示す図であ
る。FIG. 3 is a diagram showing the influence of laser irradiation energy on the collapse of organic molecule aggregates in an example according to the present invention and a conventional example.
【図4】レシチンのDSC測定結果を示す図である。FIG. 4 is a diagram showing the results of DSC measurement of lecithin.
Claims (1)
、熱的相転移を示す化合物単分子膜を挿入して累積され
てなることを特徴とする光記録媒体。1. An optical recording medium characterized in that a monomolecular film of a compound exhibiting thermal phase transition is inserted and accumulated between monomolecular films of photochromic compounds.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3148910A JP2768567B2 (en) | 1991-06-20 | 1991-06-20 | Optical recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3148910A JP2768567B2 (en) | 1991-06-20 | 1991-06-20 | Optical recording medium |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04370599A true JPH04370599A (en) | 1992-12-22 |
JP2768567B2 JP2768567B2 (en) | 1998-06-25 |
Family
ID=15463398
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3148910A Expired - Fee Related JP2768567B2 (en) | 1991-06-20 | 1991-06-20 | Optical recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2768567B2 (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6426848A (en) * | 1987-07-23 | 1989-01-30 | Agency Ind Science Techn | Optical recording medium |
JPH01148590A (en) * | 1987-12-07 | 1989-06-09 | Agency Of Ind Science & Technol | Optical recording medium |
-
1991
- 1991-06-20 JP JP3148910A patent/JP2768567B2/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6426848A (en) * | 1987-07-23 | 1989-01-30 | Agency Ind Science Techn | Optical recording medium |
JPH01148590A (en) * | 1987-12-07 | 1989-06-09 | Agency Of Ind Science & Technol | Optical recording medium |
Also Published As
Publication number | Publication date |
---|---|
JP2768567B2 (en) | 1998-06-25 |
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