Head-to-tail photodimerization of a thiophene in a co-crystal and a rare adipic acid dimer in the presence of a heterosynthon

Kristin Hutchins, Joseph C. Sumrak, Dale C. Swenson, Leonard R. Macgillivray

Research output: Contribution to journalArticle

Abstract

A saturated dicarboxylic acid is employed to achieve a photoreactive hydrogen-bonded assembly based on a thiophene that reacts to generate a head-to-tail photoproduct. A co-crystal that exhibits both a homo- and heterosynthon in the same co-crystal based on adipic acid and the thiophene is also presented. © the Partner Organisations 2014.
Original languageEnglish
Pages (from-to)5762-5764
JournalCrystEngComm
StatePublished - Jul 14 2014

Fingerprint Dive into the research topics of 'Head-to-tail photodimerization of a thiophene in a co-crystal and a rare adipic acid dimer in the presence of a heterosynthon'. Together they form a unique fingerprint.

  • Cite this