Faculty Research and Creative Activity
Document Type
Article
Publication Date
January 2011
Abstract
The supramolecular patterns of three polymorphs of a chiral sulfonamidecinnamic acid reveal components effectively organized into predetermined hydrogen-bonded dimers with favorable <3.8A ° olefin spacing for enantioselective single-crystal-to-single-crystal [2 + 2] photodimerization reactions.
Recommended Citation
Wheeler, Kraig A.; Wiseman, Joshua D.; and Grive, Rebecca C., "Enantiocontrolled solid-state photodimerizations via a chiral sulfonamidecinnamic acid" (2011). Faculty Research and Creative Activity. 12.
https://thekeep.eiu.edu/chemistry_fac/12
