Visible-Light-Triggered Molecular Photoswitch Based on Reversible E/Z Isomerization of a 1,2-Dicyanoethene Derivative

被引:67
作者
Guo, Xin [1 ]
Zhou, Jiawang [2 ]
Siegler, Maxime A. [2 ]
Bragg, Arthur E. [2 ]
Katz, Howard E. [1 ,2 ]
机构
[1] Johns Hopkins Univ, Dept Mat Sci & Engn, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Dept Chem, Baltimore, MD 21218 USA
关键词
1; 2-dicyanoethene; diarylethenes; molecular switches; photochromism; photoisomerization; IRREVERSIBLE PHOTOCHROMIC SYSTEMS; PHOTOISOMERIZATION; PHOTOCYCLIZATION; ROTATION;
D O I
10.1002/anie.201410945
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A designed bis(dithienyl) dicyanoethene-based, strictly E/Z photoswitch (4TCE) operates through state-selective (E and Z isomer) photoactivation with visible light. The E and Z isomers of 4TCE exhibit remarkably different spectroscopic characteristics, including a large separation (70nm) in their absorption maxima ((max)) and a 2.5-fold increase in molar extinction coefficient from cis to trans. The energetically stable trans form can be completely converted to the cis form within minutes when exposed to white light, whereas the reverse isomerization occurs readily upon irradiation by blue light (<480nm) or completely by thermal conversion at elevated temperatures. These features together with excellent thermal stability and photostability of both isomers make this new E/Z photoswitch a promising building block for photoswitchable materials that operate without the need for UV light.
引用
收藏
页码:4782 / 4786
页数:5
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