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On the molecular optical nonlinearity of halogen-bond-forming azobenzenes

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Details

Original languageEnglish
Pages (from-to)28810-28817
Number of pages8
JournalPhysical Chemistry Chemical Physics
Volume20
Issue number45
DOIs
Publication statusPublished - 2018
Publication typeA1 Journal article-refereed

Abstract

We study hyper-Rayleigh scattering and computed molecular hyperpolarizability in a series of azobenzene chromophores in chloroform and dimethylformamide as solvents. The chromophores form halogen or hydrogen bonds of varying strength with dimethylformamide molecules, differently from what is expected for chloroform. We show that hyperpolarizability is unaffected or sligthly lower with the azobenzene forming the strongest halogen bond. Solid supramolecular polymers with the same chromophores have previously demonstrated clearly higher second-order nonlinear responses when a halogen-bond-accepting polymer is used, the larger increase being associated with the stronger halogen bond. The present study proves that the higher optical nonlinearity in polymers lies in the better ordering of the chromophores instead of changes in molecular hyperpolarizability, highlighting the unique properties of halogen bonding in supramolecular chemistry.

Publication forum classification

Field of science, Statistics Finland