Solvent-Responsive Radical Dimers

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2020-07-16
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Peterson, Joshua
Winter, Arthur
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Winter, Arthur
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Chemistry

The Department of Chemistry seeks to provide students with a foundation in the fundamentals and application of chemical theories and processes of the lab. Thus prepared they me pursue careers as teachers, industry supervisors, or research chemists in a variety of domains (governmental, academic, etc).

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The Department of Chemistry was founded in 1880.

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Abstract

An air- and thermally stable aryl dicyanomethyl radical is reported that switches between two dimeric forms—a σ dimer and a π dimer—by changing the solvent. The two dimer forms exhibit unique optical properties leading to solvatochromic behavior. The solvent-responsive behavior of these radicals can be explained by the higher polarizability of the pimer than the σ dimer that leads to pimer stabilization in polar solvents.

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This document is the unedited Author’s version of a Submitted Work that was subsequently accepted for publication in Organic Letters, copyright © American Chemical Society after peer review. To access the final edited and published work see DOI: 10.1021/acs.orglett.0c02152. Posted with permission.

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Wed Jan 01 00:00:00 UTC 2020
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