激发态
手性(物理)
化学
发光
基态
光化学
轴手性
圆极化
螺旋度
圆二色性
原子物理学
结晶学
物理
光学
有机化学
微带线
手征对称破缺
量子力学
对映选择合成
粒子物理学
Nambu–Jona Lasinio模型
夸克
催化作用
作者
Richard A. van Delden,Nina P. M. Huck,Jacob J. Piet,John M. Warman,Stefan C. J. Meskers,Harry P. J. M. Dekkers,Ben L. Feringa
摘要
The photochemical control of ground- and excited-state chirality of (M)-cis-(1) and (P)-trans-(2)-2-nitro-7-(dimethylamino)-9-(2',3'-dihydro-1'H-naphtho[2,1-b]-thiopyran-1'-ylidene)-9H-thioxanthene is described. It is shown that while ground state chirality can be controlled photochemically by irradiation with light of different wavelengths, the excited state chirality can be tuned either photochemically in a similar way or by appropriate choice of solvent. In benzene solution, circularly polarized luminescence of the two isomers with opposite ground-state helicity, (M)-cis-1 and (P)-trans-2, revealed corresponding excited states of opposite helicity. On the contrary, in n-hexane solution, circularly polarized luminescence was identical for the two forms indicating identical excited state chirality. Circularly polarized luminescence (CPL), steady-state and time-dependent fluorescence, and time-resolved microwave conductivity (TRMC) measurements in both n-hexane and benzene are reported, which provide an explanation for the remarkable solvent dependence of excited-state chirality.
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