The syntheses, structures and nonlinear optical and related properties of salts with julolidinyl electron donor groups

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• 作者：Benjamin J. Coe ; Simon P. Foxon ; Elizabeth C. Harper ; James A. Harris ; Madeleine Helliwell ; James Raftery ; Inge Asselberghs ; Koen Clays ; Edith Franz ; Bruce S. Brunschwig ; Anthony G. Fitch
• 关键词：Organic synthesis ; Nonlinear optics ; Julolidinyl dyes ; Hyper-Rayleigh scattering ; Stark spectroscopy
• 刊名：Dyes and Pigments
• 出版年：2009
• 出版时间：August 2009
• 年：2009
• 卷：82
• 期：2
• 页码：171-186
• 全文大小：727 K

文摘

Twelve, dipolar cations with 2,3,6,7-tetrahydro-1H,5H-pyrido[3,2,1-ij]quinolin-9-yl (julolidinyl, Jd) electron donor groups and N-methyl/arylpyridinium, N-methylquinolinium or N-methylbenzothiazolium acceptor groups were synthesised. The chromophores were characterised as their PF₆⁻ salts using various techniques including electronic absorption spectroscopy and cyclic voltammetry; single crystal X-ray structures were determined for a large number of salts, all of which form nonpolar materials. A broad correlation between the electron acceptor strength and the degree of bond length alternation is evident. A key focus of this work is detailed comparisons of the Jd-containing chromophores with their previously studied 4-(dimethylamino)phenyl (Dap) analogues. Molecular, quadratic, nonlinear optical responses were determined using femtosecond hyper-Rayleigh scattering at both 1300 and 800 nm, as well as using Stark (electroabsorption) spectroscopic studies of intense, visible π → π^* intramolecular charge-transfer bands. Substantial red shifts in the latter transitions are observed on replacing Dap with Jd which indicate that the latter acts as a more effective π-electron donor. With few exceptions, both hyper-Rayleigh scattering and Stark data generally show that using Jd instead of Dap increases the static first hyperpolarizability β₀, in accord with expectations based on the two-state model. β₀ values as high as 6 times larger than that of the chromophore in the technologically important material E-4′-(dimethylamino)-N-methyl-4-stilbazolium tosylate are observed.