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Issue 12, 2011
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Facile structure and property tuning through alteration of ring structures in conformationally locked phenyltetraene nonlinear optical chromophores

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Abstract

A series of phenyltetraene-based nonlinear optical (NLO) chromophores 1a–c with the same donor and acceptor groups, but different tetraene bridges that are partly connected by various sizes of aliphatic rings, have been synthesized and systematically investigated. The interposed conjugated tetraene segments in three chromophores studied are based on isophorone, (1S)-(−)-verbenone, and 3,4,4-trimethyl-2-cyclopentenone, respectively. This kind of structural alteration has significant effect on the intrinsic electronic structures and physical properties of these highly polarizable chromophores as revealed by a variety of characterization techniques. The introduction of the verbenone- and trimethylcyclopentenone-based tetraene bridges could significantly improve the glass-forming ability of chromophores 1b and 1c in comparison with the highly crystalline characteristics of isophorone-based chromophores 1a. More importantly, chromophores 1a–c exhibited distinct optical features in absorption band shape, solvatochromic behavior, as well as energy band gap from the UV-vis-NIR absorption measurements. Quantum mechanical calculations using density functional theory (DFT) were also used to evaluate second-order NLO properties of these chromophores. The electro-optic (EO) coefficients of 1a–c in poled polymers with the 10 wt% chromophore content showed an apparent decrease from 78 pm V−1 for 1a to 42 pm V−1 for 1c. This decrease is attributed to the gradual decrease of the molecular hyperpolarizability (β) of the chromophores which is associated with the progressive cyanine-like electronic structure from the isophorone-based 1a to the cyclopentenone-based 1cchromophore.

Graphical abstract: Facile structure and property tuning through alteration of ring structures in conformationally locked phenyltetraene nonlinear optical chromophores

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Publication details

The article was received on 29 Aug 2010, accepted on 21 Dec 2010 and first published on 01 Feb 2011


Article type: Paper
DOI: 10.1039/C0JM02855J
J. Mater. Chem., 2011,21, 4437-4444

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    Facile structure and property tuning through alteration of ring structures in conformationally locked phenyltetraene nonlinear optical chromophores

    X. Zhou, J. Davies, S. Huang, J. Luo, Z. Shi, B. Polishak, Y. Cheng, T. Kim, L. Johnson and A. Jen, J. Mater. Chem., 2011, 21, 4437
    DOI: 10.1039/C0JM02855J

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