Orientation phenomena in chromophore DR1-containing polymer films and their non-linear optical response

被引:6
作者
Moencke, Doris [1 ]
Mountrichas, Grigoris [1 ]
Pispas, Stergios [1 ]
Kamitsos, Efstratios I. [1 ]
机构
[1] Natl Hellen Res Fdn, Inst Theoret & Phys Chem, GR-11635 Athens, Greece
来源
MATERIALS SCIENCE AND ENGINEERING B-ADVANCED FUNCTIONAL SOLID-STATE MATERIALS | 2011年 / 176卷 / 06期
关键词
Infrared spectroscopy; Nuclear magnetic resonance; Nonlinear optical effects; Polymers; Thin films; Electric field effect; AZO-DYES; SPECTRA; PHOTOISOMERIZATION; DISPERSE-RED-1; METHACRYLATE); SPECTROSCOPY; RAMAN; NMR;
D O I
10.1016/j.mseb.2011.01.002
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The effectiveness of chromophore alignment in polymer films following corona poling can be assessed by the generated second harmonic signal. Optimization of the stability and strength of this nonlinear optical response may improve with a better understanding of the underlying principal order phenomena. Structural analysis by vibrational, optical, and (1)H NMR spectroscopy reveals side chain tacticity, aggregation effects, and changes in orientation as a function of temperature. Co-polymers with the functionalized chromophore Disperse Red 1 methacrylate (MDR1) were prepared for three different methacrylate types. High side chain polarity and short side chain length increase generally chromophore aggregation in films, whereas the very long poly-ether side chains in PMEO based co-polymers are wrapped separately around the DR1 entities. Side chain tacticity depends on space requirements, but also on the capacity of side groups to form OH-bridges. Side chain tacticity might present an additional parameter for the assessment of chromophore aggregation and poling induced alignments. Stepwise heating of co-polymer films causes an increase in the number of random over ordered side chain arrangements. Cross-linking by anhydride formation is observed after heating the methacrylic acid based co-polymer. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:515 / 520
页数:6
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