Structural modulation of the dipolar-octupolar contributions to the NLO response in subphthalocyanines

被引:100
作者
Claessens, CG
González-Rodríguez, D
Torres, T [1 ]
Martín, G
Agulló-López, F
Ledoux, I
Zyss, J
Ferro, VR
de la Vega, JMG
机构
[1] Univ Autonoma Madrid, Dept Quim Fis Aplicada C 14, E-28049 Madrid, Spain
[2] Univ Autonoma Madrid, Dept Quim Organ C 1, E-28049 Madrid, Spain
[3] Univ Autonoma Madrid, Dept Fis Mat C 4, E-28049 Madrid, Spain
[4] Ecole Normale Super, Lab Photon Qunat & Mol, F-94235 Cachan, France
关键词
D O I
10.1021/jp045322u
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
ySecond order nonlinear optical properties of a series of trinitrosubphthalocyanine (SubPc) isomers were studied experimentally by electric field induced second harmonic (EFISH) generation and hyper Rayleigh scattering (HRS). These experimental values were compared to the ones obtained theoretically employing both sum over states (SOS) and finite field (FF) methods. From these studies, it was shown that the dipolar contributions to the beta tensor are very much dependent on the substitution pattern at the periphery of the subphthalocyanine macrocycle, whereas the octupolar contributions remain mostly unchanged. Consequently, it was deduced that SubPc is extremely well Suited for the decoupling of octupolar and dipolar contribution to the NLO response.
引用
收藏
页码:3800 / 3806
页数:7
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