Issue 26, 2014

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

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.

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

Supplementary files

Article information

Article type
Communication
Submitted
07 Mar 2014
Accepted
24 Apr 2014
First published
24 Apr 2014

CrystEngComm, 2014,16, 5762-5764

Author version available

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

K. M. Hutchins, J. C. Sumrak, D. C. Swenson and L. R. MacGillivray, CrystEngComm, 2014, 16, 5762 DOI: 10.1039/C4CE00481G

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements