JP2937281B2 - Third-order nonlinear optical material - Google Patents
Third-order nonlinear optical materialInfo
- Publication number
- JP2937281B2 JP2937281B2 JP9609692A JP9609692A JP2937281B2 JP 2937281 B2 JP2937281 B2 JP 2937281B2 JP 9609692 A JP9609692 A JP 9609692A JP 9609692 A JP9609692 A JP 9609692A JP 2937281 B2 JP2937281 B2 JP 2937281B2
- Authority
- JP
- Japan
- Prior art keywords
- nonlinear optical
- optical material
- order nonlinear
- light
- order
- 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 - Fee Related
Links
Description
【0001】[0001]
【産業上の利用分野】本発明は、オプトエレクトロニク
ス、光情報処理、光通信等の分野において有用な三次非
線形光学材料に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a third-order nonlinear optical material useful in fields such as optoelectronics, optical information processing, and optical communication.
【0002】[0002]
【従来の技術およびその問題点】非線形光学材料は、レ
ーザー光の強電界下、二次以上の非線形応答を示す材料
であって、周波数変換、発振、スイッチング等の光信号
処理において重要な素材である。特に、三次非線形光学
材料は、光が有する高速性、並列性という優れた特性を
十分に発揮させた次世代の光通信、情報処理における基
幹素材として注目されている。2. Description of the Related Art A nonlinear optical material is a material that exhibits a second-order or higher nonlinear response under a strong electric field of laser light, and is an important material in optical signal processing such as frequency conversion, oscillation, and switching. is there. In particular, tertiary nonlinear optical materials are attracting attention as key materials in next-generation optical communication and information processing that fully exhibit the excellent characteristics of light, such as high speed and parallelism.
【0003】この非線形光学材料のうち、有機非線形光
学材料は、従来の無機非線形光学材料に比べて高速応答
性で非線形光学定数の大きいものが存在するため、特に
重要である。[0003] Among these nonlinear optical materials, organic nonlinear optical materials are particularly important because some of them have high-speed response and a large nonlinear optical constant as compared with conventional inorganic nonlinear optical materials.
【0004】現在、三次の効果の大きい有機非線形材料
は、ポリジアセチレン[特に、PTS:2,4−ヘキ
サジイン−1,6−ビス(p−トルエンスルホナー
ト)]、ポリアセチレンに代表されるπ共役高分子系
と、アミノニトロスチルベン(特に、DEANS:
N,N−ジエチル−4−アミノ−4’−ニトロスチルベ
ン)に代表される、ドナー・アクセプターを非対称に置
換した低分子系の2種に分類できる。At present, organic non-linear materials having a large tertiary effect include polydiacetylene [particularly, PTS: 2,4-hexadiyne-1,6-bis (p-toluenesulfonate)] and π-conjugated materials represented by polyacetylene. Molecular systems and aminonitrostilbenes (especially DEANS:
N, N-diethyl-4-amino-4'-nitrostilbene), which are classified into two types of low molecular weight systems in which donors and acceptors are asymmetrically substituted.
【0005】のπ共役高分子系非線形性は、価電子帯
の自由電子の分極を根源としているため、無機半導体と
極めて類似した欠点、すなわち、狭いバンドギャップに
基づいた共鳴効果による応答速度の低下から逃れられな
い。また、のドナー・アクセプター非対称置換低分子
系は、現状(DEANS)以上に効果を大きくしようと
すると分子内電荷移動による吸収帯の長波長化によっ
て、と同様の欠点を露呈する。The non-linearity of the π-conjugated polymer system is based on the polarization of free electrons in the valence band. Therefore, the defect is very similar to that of an inorganic semiconductor, that is, the response speed decreases due to the resonance effect based on a narrow band gap. Can not escape. Further, the donor-acceptor asymmetrically substituted low-molecular-weight system exhibits the same drawbacks as an attempt to increase the effect beyond the current state (DEANS) by increasing the wavelength of the absorption band due to intramolecular charge transfer.
【0006】[0006]
【問題点を解決するための手段】本発明の目的は、前記
問題点を解決し、高速・高応答の光非線形応答を示す有
機非線形光学材料を提供することにある。本発明は、下
記一般式[I]で表される化合物を含有してなる三次非
線形光学材料に関する。SUMMARY OF THE INVENTION It is an object of the present invention to solve the above-mentioned problems and to provide an organic nonlinear optical material exhibiting a high-speed and high-response optical nonlinear response. The present invention relates to a third-order nonlinear optical material containing a compound represented by the following general formula [I].
【0007】[0007]
【化2】 Embedded image
【0008】本発明による有機非線形光学材料の主要な
特徴は、吸収の長波長化を抑制して応答速度の低下を防
いでいる上に、従来になく大きな三次の非線形光学効果
を有する点である。これは、非線形光学効果を大きくし
ようとすると、π共役の拡大や電荷移動の増大による吸
収の長波長化を伴うという従来技術の欠点を、π共役系
を芳香環3個(イミダゾール環を含む)に抑え、イミダ
ゾール環の有する電子供与性を利用した分子内電荷移動
効果により解決した。The main features of the organic nonlinear optical material according to the present invention are that it has a longer third-order nonlinear optical effect than ever before, while suppressing a longer wavelength of absorption to prevent a decrease in response speed. . This has the disadvantage of increasing the wavelength of absorption due to an increase in π-conjugation and an increase in charge transfer when trying to increase the nonlinear optical effect. The disadvantage of the prior art is that the π-conjugated system has three aromatic rings (including imidazole rings). The problem was solved by the intramolecular charge transfer effect utilizing the electron donating property of the imidazole ring.
【0009】イミダゾールをπ共役系として用いること
により吸収を短波長にとどめることができ、さらに2位
のフェニル基への電子受容基の導入による三次の非線形
光学効果の向上も確認された。また、フェナンスロ
[9,10−d]イミダゾール基を用いることで分子の
平面性をよくし、分子量を上げることなくπ共役系を広
げ、三次の非線形性を向上させた。By using imidazole as a π-conjugated system, it was possible to limit the absorption to a short wavelength, and it was also confirmed that the third-order nonlinear optical effect was improved by introducing an electron accepting group into the 2-position phenyl group. Further, by using a phenanthro [9,10-d] imidazole group, the planarity of the molecule was improved, the π-conjugate system was expanded without increasing the molecular weight, and the third-order nonlinearity was improved.
【0010】[0010]
【実施例】以下に、実施例を示す。 合成例1Embodiments are described below. Synthesis Example 1
【0011】[0011]
【化3】 Embedded image
【0012】フェナントラキノン0.01mol、p−ニトロ
アルデヒド0.01molと酢酸アンモニウム15.5gを100mlの
酢酸に加え、1時間加熱還流した。反応後の溶液に水を
加えて結晶を析出させた。次いで、濾過、洗浄、乾燥
し、ピリジンと水との混合液から再結晶して、2−
(4’−ニトロフェニル)−フェナンスロ[9,10−
d]イミダゾールを得た。[0012] 0.01 mol of phenanthraquinone, 0.01 mol of p-nitroaldehyde and 15.5 g of ammonium acetate were added to 100 ml of acetic acid, and the mixture was heated under reflux for 1 hour. Water was added to the solution after the reaction to precipitate crystals. Then, it was filtered, washed, dried, and recrystallized from a mixture of pyridine and water to give 2-
(4′-nitrophenyl) -phenanthro [9,10-
d] Imidazole was obtained.
【0013】実施例1 合成例1で得られた2−(4’−ニトロフェニル)−フ
ェナンスロ[9,10−d]イミダゾールを用いて、図
1に示す偏光・非線形定数測定装置により、三次非線形
光学特性の測定を行った。光源には、QスイッチNd:
YAGレーザー1の第3高調波(355nm)励起によ
る色素レーザー2を用い、この出力光をポンプ光11と
プローブ光21に分け、各々偏光子P1、偏光子P2に
より直線偏光にされる。プローブ光21は、試料3を通
った後、検光子P3により消光されている。ここで、ポ
ンプ光11とプローブ光21の偏光面を45°の角度を
なすようにし、試料3に照射した。検光子P3を透過し
た光を分光器4を通して光電子倍増管5で検出した。そ
の結果、CS2 の80倍の三次非線形光学効果が認めら
れた。Example 1 Using 2- (4′-nitrophenyl) -phenanthro [9,10-d] imidazole obtained in Synthesis Example 1, a third-order nonlinearity was measured by a polarization and nonlinearity constant measuring apparatus shown in FIG. Optical properties were measured. The light source has a Q switch Nd:
Using a dye laser 2 excited by the third harmonic (355 nm) of the YAG laser 1, this output light is divided into pump light 11 and probe light 21 and is linearly polarized by polarizers P1 and P2, respectively. After passing through the sample 3, the probe light 21 is quenched by the analyzer P3. Here, the sample 3 was irradiated with the polarization plane of the pump light 11 and the probe light 21 at an angle of 45 °. The light transmitted through the analyzer P3 was detected by the photomultiplier tube 5 through the spectroscope 4. As a result, a third-order nonlinear optical effect 80 times that of CS 2 was observed.
【図1】図1は、偏光・非線形定数測定装置の概略図で
ある。FIG. 1 is a schematic diagram of a polarization / nonlinear constant measuring apparatus.
───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.6,DB名) G02F 1/35 504 CA(STN)──────────────────────────────────────────────────続 き Continued on front page (58) Field surveyed (Int.Cl. 6 , DB name) G02F 1/35 504 CA (STN)
Claims (1)
有してなる三次非線形光学材料。 【化1】 1. A third-order nonlinear optical material comprising a compound represented by the following general formula [I]. Embedded image
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9609692A JP2937281B2 (en) | 1992-03-24 | 1992-03-24 | Third-order nonlinear optical material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9609692A JP2937281B2 (en) | 1992-03-24 | 1992-03-24 | Third-order nonlinear optical material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH05273618A JPH05273618A (en) | 1993-10-22 |
| JP2937281B2 true JP2937281B2 (en) | 1999-08-23 |
Family
ID=14155866
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9609692A Expired - Fee Related JP2937281B2 (en) | 1992-03-24 | 1992-03-24 | Third-order nonlinear optical material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2937281B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7442716B2 (en) | 2004-12-17 | 2008-10-28 | Merck Frosst Canada Ltd. | 2-(phenyl or heterocyclic)-1H-phenantrho[9,10-d]imidazoles as mPGES-1 inhibitors |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE445672T1 (en) | 2005-03-14 | 2009-10-15 | Basf Se | NEW POLYMERS |
| CA2657231A1 (en) | 2006-07-14 | 2008-01-17 | Ciba Holding Inc. | Novel electroluminescent polymers for electronic applications |
-
1992
- 1992-03-24 JP JP9609692A patent/JP2937281B2/en not_active Expired - Fee Related
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7442716B2 (en) | 2004-12-17 | 2008-10-28 | Merck Frosst Canada Ltd. | 2-(phenyl or heterocyclic)-1H-phenantrho[9,10-d]imidazoles as mPGES-1 inhibitors |
| US7943649B2 (en) | 2004-12-17 | 2011-05-17 | Merck Frosst Canada Ltd. | 2-(phenyl or heterocyclic)-1H-phenantrho[9,10-d]imidazoles as mPGES-1 inhibitors |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH05273618A (en) | 1993-10-22 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4717508A (en) | Organic nonlinear optical substrates | |
| Saadon et al. | Nonlinear optical properties of new organotellurium compounds containing azomethine and azo groups under CW laser illumination | |
| US4707303A (en) | High performance nonlinear optical substrates | |
| US4720355A (en) | Organic nonlinear optical substrates | |
| JP2937281B2 (en) | Third-order nonlinear optical material | |
| Faccini et al. | Enhanced poling efficiency in highly thermal and photostable nonlinear optical chromophores | |
| Beaudin et al. | Synthesis and properties of Zwitterionic nonlinear optical chromophores with large hyperpolarizability for poled polymer applications | |
| JP2937280B2 (en) | Third-order nonlinear optical material | |
| JP2937282B2 (en) | Third-order nonlinear optical material | |
| Choi et al. | Synthesis and second-order nonlinear optical properties of polymethacrylates containing organic salt dye chromophore | |
| JPS62448A (en) | Quinodimethane compound | |
| JPH04297470A (en) | Reticualted epoxy resin having nonlinear optical characteristics | |
| Xiong et al. | Functionalized picolinium quinodimethane chromophores for electro-optics: synthesis, aggregation behavior, and nonlinear optical properties | |
| JP3039832B2 (en) | Nonlinear optical material | |
| Smith et al. | The second and third order non-linear optical properties of liquid crystalline polymers | |
| US4938896A (en) | High performance nonlinear optical media | |
| US4983325A (en) | High performance nonlinear optical media | |
| JP2988574B2 (en) | Wavelength selection method for optical signal processor | |
| JPH04277724A (en) | Organic nonlinear optical materials | |
| JPH06250244A (en) | Cubic nonlinear optical material | |
| Ray et al. | Second harmonic generation in poled molecularly doped polymer films: Push-pull butadienes in poly (methyl methacrylate) and polystyrene | |
| Teshome et al. | Optimizing the second-order nonlinear optical response in some indoline-based chromophores at the molecular and macroscopic levels | |
| JPS63163827A (en) | Organic nonlinear optical material | |
| JP2614301B2 (en) | Nonlinear optical device | |
| JPH0256525A (en) | Optical nonlinear material and production thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| S111 | Request for change of ownership or part of ownership |
Free format text: JAPANESE INTERMEDIATE CODE: R313115 |
|
| R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
| LAPS | Cancellation because of no payment of annual fees |