Amphiphilic azo-dyes (RED-PEGM).: Part 2:: Charge transfer complexes, preparation of Langmuir-Blodgett films and optical properties

被引:33
作者
Rivera, Ernesto
Carreon-Castro, Maria del Pilar
Rodriguez, Lorena
Cedillo, Gerardo
Fomine, Serguei
Morales-Saavedra, Omar G.
机构
[1] Univ Nacl Autonoma Mexico, Inst Invest Mat, Mexico City 04510, DF, Mexico
[2] Univ Nacl Autonoma Mexico, Inst Ciencias Nucl, Mexico City 04510, DF, Mexico
[3] Univ Nacl Autonoma Mexico, Ctr Ciencias Aplicadas & Desarrollo Tecnol, Mexico City 04510, DF, Mexico
关键词
charge transfer; azobenzene; poly(ethylene glycol); Langmuir-Blodgett films; optical properties;
D O I
10.1016/j.dyepig.2006.02.023
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Optical properties of three amphiphilic azo-dyes bearing end-capped oligo(ethylene glycol) segments: N-methyl-N-{4-[(E)-(4-nitrophenyl)diazenyl] phenyl)-N-(3, 6,9-trioxadecas-1-yl)amine (RED-PEGM-3),N-methyl-N-(4-[(E)-(4-nitrophenyl)diazenyl] phenyl)-N-(3, 6,9, 12, 15, 18, 21, 24-octaoxapentaeicos-1-yl)amine (RED-PEGM-8) and N-methyl-N-(4-[(E)-(4-nitrophenyl)diazenyl] phenyl}-N-(3, 6, 9, 12, 15, 18, 21, 24, 27, 30)-decaoxauntricontas-1-yl)amine (RED-PEGM-10) were studied in Z-type LB films by absorption spectroscopy. RED-PEGM-8 and RED-PEGM-10 formed intramolecular charge transfer complexes in aqueous solution due to coiling of the end-capped poly(ethylene glycol) side-chain around the azobenzene groups. This was detected by H-1 NMR, 2D NOESY spectroscopy and the optimised geometties of the complexes were estimated by DFT calculations. The formation and optical properties of CT complexes are discussed with respect to the poly(ethylene glycol) segments length. Z-type Langmuir-Blodgett (LB) films of RED-PEGM-8 exhibited chi((2)) non-linear optical properties (NLO) like second harmonic generation (SHG) depending on the number of deposited layers. The chi((2))(31) and chi((2))(33) NLO-coefficients were evaluated to be approximately 2.7 and 12.5 pm V-1, respectively for a single RED-PEGM-8 layer sample. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:396 / 403
页数:8
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