本文从分子工程和材料工程的角度介绍了有机吡啶盐及其衍生物在非线性光学中的应用.有机吡啶盐分子由于独特的化学结构,除了具有较大的分子超极化率外,其分子设计上的灵活性和功能上的多样性,使其在非线性光学材料领域占有重要的一席之地,同时该类体系多种多样的组装形式也极大地丰富了非线性光学材料的种类.
参考文献
| [1] | Davydov B L;Derkacheva L D;Duna V V et al.[J].Soviet Physics JETP,1970,12:16. |
| [2] | Oudar J L;Chemla D S .[J].Journal of Chemical Physics,1977,66:2664. |
| [3] | Chemla D S;Oudar J L;Jrphagnon J .[J].Physical Review B,1975,12:4543. |
| [4] | Marder S R;Beratan D N;Cheng L T .[J].Science,1991,252:103. |
| [5] | Pierce B;Zyss J;Joffre M .[J].Proceedings of SPIE,1993,2025:2. |
| [6] | Meerholz K;Volodin B L;Sandalphon et al.[J].Nature,1994,371:497. |
| [7] | Marder S R;Perry J W .[J].Science,1994,263:1706. |
| [8] | Ahlheim M;Barzoukas M;Bedworth P V et al.[J].Science,1996,271:335. |
| [9] | Albota M;Beljonne D;Bredas J L et al.[J].Science,1998,281:1653. |
| [10] | Marder S R;Beratan D N;Cheng L T.[J].Science,1991:252:406. |
| [11] | Stiegman A E;Graham E;Perry K J et al.[J].Journal of the American Chemical Society,1991,113:7661. |
| [12] | 钱鹰,孙岳明,刘举正,吴建跃,李富铭.具有电子给-受体结构的二茂铁衍生物的分子二阶非线性极化率[J].化学学报,1998(04):340-346. |
| [13] | Duan X M;Okada S;Nakanishi H et al.[J].Proceedings of SPIE,1994,2143:41. |
| [14] | Moylan G R;Twieg R J;Lee V Y et al.[J].Journal of the American Chemical Society,1993,115:12599. |
| [15] | Katz H E;Dirk C W;Singer K D et al.[J].Proceedings of SPIE,1987,824:86. |
| [16] | Duan X M;Okada S;Oikawa H et al.[J].Molecular Crystals and Liquid Crystals,1995,267:89. |
| [17] | Meredith G R.In Nonlinear Optical Properties of Organic and Polymeric Materiala[A].Washington DC,1983:30. |
| [18] | Seth R Marder;Joseph W Perry;Christopher P Yakymyshyn .[J].Chemistry of Materials,1994,6:1137. |
| [19] | Marder Seth R;Tiemann Bruce G;Perry Joseph W.Materials for Nonlinear Optics[A].Washington DC,1991:187. |
| [20] | Marder Seth R;Perry J W;Tiemann B G et al.[J].Organometallics,1991,10:1896. |
| [21] | Marder S R;Perry J W;schaefer W P .[J].Science,1989,245:626. |
| [22] | Shuji Okada;Atsushi Masaki;Hiro Matsuda et al.[J].Japanese Journal of Applied Physics,1990,29:1112. |
| [23] | Pan F;Knopfle G;Bosshard Ch et al.[J].Applied Physics Letters,1996,69:13. |
| [24] | 友清.[J].激光与光电子学进展,1995(09):9. |
| [25] | Follonfer S;Bosshard Ch;Pan F et al.[J].Optics Letters,1996,21:1655. |
| [26] | Burrows PE.;Sapochak LS.;Schwartz J.;Fenter P.;Buma T. Ban VS.;Forrest JL.;Forrest SR. .ORGANIC VAPOR PHASE DEPOSITION - A NEW METHOD FOR THE GROWTH OF ORGANIC THIN FILMS WITH LARGE OPTICAL NON-LINEARITIES[J].Journal of Crystal Growth,1995(1/2):91-98. |
| [27] | Forrest S R;Burrows P E;Stroustrup A et al.[J].Applied Physics Letters,1996,68:1326. |
| [28] | Burland D M;Miller R D;Walsh C A .[J].Chemical Reviews,1994,94:31. |
| [29] | Ye C;Marks T J;Yang J et al.[J].Macromolecules,1987,20:2322. |
| [30] | Choi D H;Kim H M;Wijekoon W M K P et al.[J].Chemistry of Materials,1992,4:1253. |
| [31] | Moon KJ.;Lee KS.;Zieba J.;Prasad PN.;Shim HK. .SYNTHESIS, CHARACTERIZATION, AND SECOND-ORDER OPTICAL NONLINEARITY OF A POLYURETHANE STRUCTURE FUNCTIONALIZED WITH A HEMICYANINE DYE[J].Macromolecules,1996(3):861-867. |
| [32] | Lee KS.;Woo HY.;Moon KJ.;Shim HK.;Jeong MY.;Lim TK.;Choi SW. .Second-order nonlinear optical properties and relaxation dynamics of aligned cross-linked polyurethanes with hemicyanine-type chromophores[J].Journal of the Optical Society of America, B. Optical Physics,1998(1):393-400. |
| [33] | Xu X;Wu B;Dalton L R et al.[J].Macromolecules,1992,25:6714. |
| [34] | Boogers J A F;Klaase P Th A;de Vlieger J J et al.[J].Macromolecules,1994,27:197. |
| [35] | Dentan V;Blaochard D M;Palacin S et al.[J].Thin Solid Pilms,1992,210:221. |
| [36] | Ashwell G J;Hargresves R C;Beldwin C E et al.[J].Nature,1992,357:393. |
| [37] | Zhou DJ.;Huang CH.;Ashwell GJ. .IMPROVED SECOND HARMONIC GENERATION FROM LANGMUIR-BLODGETT MONOLAYERS OF AN IONICALLY COMBINED BIS-CHROMOPHORE ZINC COMPLEX[J].Chemistry Letters,1997(1):7-8. |
| [38] | Steinhoff R;Chi L F;Marowaky G .[J].Journal of the Optical Society of America B:Optical Physics,1989,6:843. |
| [39] | Lupo D;Prass W;Scheunemann U et al.[J].Journal of the Optical Society of America B:Optical Physics,1988,6:300. |
| [40] | Li D Q;Ratner M A;Marks T J et al.[J].Journal of the American Chemical Society,1990,112:7389. |
| [41] | Lin W B;Yitachaik S;Lin W P et al.[J].Angewandte Chemie International Edition,1995,34:1497. |
| [42] | Lin WB;Lin WP;Wong GK;Marks TJ .SUPRAMOLECULAR APPROACHES TO SECOND-ORDER NONLINEAR OPTICAL MATERIALS - SELF-ASSEMBLY AND MICROSTRUCTURAL CHARACTERIZATION OF INTRINSICALLY ACENTRIC [(AMINOPHENYL)AZO]PYRIDINIUM SUPERLATTICES[J].Journal of the American Chemical Society,1996(34):8034-8042. |
| [43] | Lacroix P G;Clement R;Nakatani K et al.[J].Science,1994,263:658. |
| [44] | Kim O K;Choi L S;Zhang H Y et al.[J].Journal of the American Chemical Society,1996,118:12220. |
| [45] | Kim O K;Choi L S .[J].LANGMUIR,1994,10:2842. |
| [46] | Ruland G;Gvishi R;Prasad PN .MULTIPHASIC NANOSTRUCTURED COMPOSITE - MULTI-DYE TUNABLE SOLID STATE LASER[J].Journal of the American Chemical Society,1996(12):2985-2991. |
| [47] | He G S;Bhawallker J D;Zhao C F et al.[J].Applied Physics Letters,1995,67:2433. |
| [48] | Denk W;Strickler J H;Webb W W .[J].Science,1990,246:73. |
| [49] | Parhenopoules D A;Rentzepis P M .[J].Science,1989,245:843. |
| [50] | Bhawalker J D;He G S;Prasad P N .[J].Reports on Progress in Physics,1996,59:1041. |
| [51] | Sakaguchi H;Nalcommora H;Nagaraura T.[J].Chemistry Letters,1989:1715. |
| [52] | 市场消息[J].光学学报,1997(12):1692. |
| [53] | Dhenaut C;Ledoux I;Samuel I D W et al.[J].NATURE,1995,374:339. |
| [54] | Peng Zh H;Yu L P .[J].Journal of the American Chemical Society,1996,118:3777. |
| [55] | Peng Zh H;Gharavi A R;Yu L P .[J].Applied Physics Letters,1996,67:4002. |
| [56] | Bryce M R;Petty M C .[J].NATURE,1995,374:771. |
| [57] | Richard J;Vandevyver M;Lesieur P et al.[J].Journal of Chemical Physics,1987,86:2428. |
| [58] | Merz A;Reimeier S .[J].Angewandte Chemie International Edition,1989,28:507. |
| [59] | Jager W F;Kudasheva D;Neckers D C .[J].Macromolecules,1996,29:7353. |
上一张
下一张
上一张
下一张
计量
- 下载量()
- 访问量()
文章评分
- 您的评分：
-
10%
-
20%
-
30%
-
40%
-
50%