In situ reversible electrochemical switching of the molecular first hyperpolarizability

被引:101
作者
Asselberghs, I
Clays, K
Persoons, A
McDonagh, AM
Ward, MD
McCleverty, JA
机构
[1] Katholieke Univ Leuven, Dept Chem, Ctr Res Mol Electr & Photon, B-3001 Heverlee, Belgium
[2] Univ Bristol, Sch Chem, Bristol BS8 1TH, Avon, England
基金
英国工程与自然科学研究理事会;
关键词
D O I
10.1016/S0009-2614(02)01890-0
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In situ reversible electrochemical switching of the molecular second-order nonlinear optical (NLO) polarizability, or first hyperpolarizability, has been implemented in a specially designed cell. The redox-switchable NLO chromophore is based on the octamethylferrocene/octamethylferrocenium redox system as electron-donor (D) group, in conjunction with nitrothiophene as the electron-acceptor (A) group and ethenyl as the pi-conjugation bridge. This D-pi-A chromophore has been shown to exhibit reversible redox switching of its linear and nonlinear optical properties. The importance and potential of this electrochemical switching of the first hyperpolarizability is discussed in the context of current and future applications of second-order NLO effects. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:408 / 411
页数:4
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