Investigation of new push-pull pyridine-1-oxide derivatives as 1D NLO chromophores with vanishing dipole moment

被引:3
作者
Bourgogne, C
Masson, P
Nicoud, JF
Brasselet, S
Zyss, J
机构
[1] Inst Phys & Chim Mat Strasbourg, Grp Mat Organ, F-67037 Strasbourg, France
[2] Ecole Normale Super, LPQM, F-94235 Cachan, France
关键词
non-linear optics; organic materials; hyperpolarizability; vanishing dipole moment; N-oxide derivatives; hyper-Rayleigh scattering; molecular modeling;
D O I
10.1016/S0379-6779(01)00453-2
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The non-linear optical properties of new one-dimensional (ID) hyperpolarizable chromophores bearing a pyridine-1-oxide donor group and a 4-nitrophenyl acceptor group, linked by C=C or N=N double bonds have been studied. These molecules present a true intramolecular donor/acceptor charge transfer (ICT) leading to high beta hyperpolarizability, but unlike the classical ICT chromophores exhibit a vanishing dipole moment mu. Such a property can lead to a better control of the non-centrosymmetric alignment of the hyperpolarizable chromophores in the solid state, as observed previously in 3-methyl-4-nitropyridine-1-oxide crystals (POM). Due to the lack of dipole moment beta cannot be measured by EFISHG. In this paper, the synthesis, modeling of mu and beta, and hyper-Rayleigh scattering (HRS) hyperpolarizability measurements of 4 ' -nitro-4-stilbazole-N-oxide and its azo analogue, as two representative chromophores in this series, are reported. The values are compared with these of the polar analogue 4-methoxy-4 ' -nitrostilbene (MONS). Hartree-Fock calculations confirm their vanishing dipole moment and give beta -values in good accordance with those obtained experimentally by HRS. Longer 1D chromophores in this series are currently under investigation. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:213 / 216
页数:4
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