Issue 10, 2002

Synthesis, crystal structures, and quadratic nonlinear optical properties in a series of push–pull boronate derivatives

Abstract

A series of eighteen new ‘push–pull’ molecules obtained by self-assembly of salicylideniminophenols and various phenylboronic acids is reported. Electric field-induced second-harmonic measurements of the nonlinear optical response reveal that the nature of the phenylboron moieties has a modest influence on the molecular hyperpolarizabilities (β). The crystal data available suggest the possibility of easy rotation of the phenyl substituents, with an energy barrier around 10 kcal mol−1, while a computational investigation conducted at the semi-empirical (INDO) level leads to a prediction of 30% β-modulation occuring upon the rotation.

Graphical abstract: Synthesis, crystal structures, and quadratic nonlinear optical properties in a series of push–pull boronate derivatives

Supplementary files

Article information

Article type
Paper
Submitted
31 May 2002
Accepted
23 Jul 2002
First published
30 Aug 2002

J. Mater. Chem., 2002,12, 2898-2903

Synthesis, crystal structures, and quadratic nonlinear optical properties in a series of push–pull boronate derivatives

H. Reyes, B. M. Muñoz, N. Farfán, R. Santillan, S. Rojas-Lima, P. G. Lacroix and K. Nakatani, J. Mater. Chem., 2002, 12, 2898 DOI: 10.1039/B205308J

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