Size scaling of intramolecular charge transfer driven optical properties of substituted polyenes and polyynes

被引:22
|
作者
Lee, JY
Mhin, BJ
Mukamel, S
Kim, KS
机构
[1] Chonnam Natl Univ, Dept Chem, Kwangju 500757, South Korea
[2] PaiChai Univ, Dept Chem, Taejon 302735, South Korea
[3] Univ Rochester, Dept Chem, Rochester, NY 14627 USA
[4] Univ Rochester, Dept Phys & Astron, Rochester, NY 14627 USA
[5] Pohang Univ Sci & Technol, Natl Creat Res Initiat Ctr Superfunct Mat, Pohang 790784, South Korea
[6] Pohang Univ Sci & Technol, Dept Chem, Div Mol & Life Sci, Pohang 790784, South Korea
来源
JOURNAL OF CHEMICAL PHYSICS | 2003年 / 119卷 / 14期
关键词
D O I
10.1063/1.1607917
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
The origin of dramatic variation in optical polarizabilities of push-pull conjugated chains with respect to the conjugation length is discussed. Ab initio calculations of intramolecular charge transfer (ICT)-driven dipole moment (mu(CT)), polarizability (alpha(CT)), and first hyperpolarizability (beta(CT)) show that the values of alpha(CT)/mu(CT) and beta(CT)/mu(CT) change linearly and quadratically with respect to the conjugation length, respectively. The maximum ICT-driven coherence sizes of alpha(CT) and beta(CT) are consistent with the time-dependent densities to the first (rho((1))) and second (rho((2))) orders of the electric field obtained from the collective electronic oscillators method. (C) 2003 American Institute of Physics.
引用
收藏
页码:7519 / 7524
页数:6
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