Solid-state photodimerization reactions of racemic and homochiral phenylalanine sulfonamidecinnamic acids

Zhiqing Yan; Andrew J. Bolokowicz; Teage K. Collett; Sarah A. Reeb; Joshua D. Wiseman; Kraig A. Wheeler

doi:10.1039/C2CE26307F

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Solid-state photodimerization reactions of racemic and homochiral phenylalanine sulfonamidecinnamic acids†

Zhiqing Yan,^a Andrew J. Bolokowicz,^a Teage K. Collett,^a Sarah A. Reeb,^a Joshua D. Wiseman^a and Kraig A. Wheeler*^a

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^a Department of Chemistry, Eastern Illinois University, Charleston, Illinois, USA
E-mail: kawheeler@eiu.edu
Tel: +(1) 217 581 3119

Abstract

Racemic and enantiopure phenylalanine sulfonamides preferentially crystallize to give supramolecular dimers with favorable olefin⋯olefin spacing (3.77–4.01 Å) for programmed solid-state [2 + 2] photodimerizations.

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DOI: https://doi.org/10.1039/C2CE26307F
Article type: Communication
Submitted: 15 Aug 2012
Accepted: 01 Sep 2012
First published: 03 Sep 2012

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CrystEngComm, 2013,15, 27-30

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Solid-state photodimerization reactions of racemic and homochiral phenylalanine sulfonamidecinnamic acids

Z. Yan, A. J. Bolokowicz, T. K. Collett, S. A. Reeb, J. D. Wiseman and K. A. Wheeler, CrystEngComm, 2013, 15, 27 DOI: 10.1039/C2CE26307F

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CrystEngComm

Solid-state photodimerization reactions of racemic and homochiral phenylalanine sulfonamidecinnamic acids†

Abstract

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Solid-state photodimerization reactions of racemic and homochiral phenylalanine sulfonamidecinnamic acids

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