Isotopomeric polymorphism in a "doubly-polymorphic" multi-component molecular crystal

Marc Schmidtmann, Derek S. Middlemiss, Chick C. Wilson

Research output: Contribution to journalArticlepeer-review

4 Citations (Scopus)
137 Downloads (Pure)

Abstract

The deuterated molecular complexes of isonicotinamide with oxalic acid crystallise in two polymorphs, which are found to be distinct from the two polymorphs of the hydrogenous complexes previously reported. This phenomenon is known as isotopomeric polymorphism, is rarely observed in molecular materials and in particular the presence of multiple polymorphic forms of each isotopic material observed here appears to be unprecedented. The four polymorphic forms are found to exhibit different degrees of hydron transfer. Unlike the hydrogenous forms, the deuterated polymorphs do not show short, strong hydrogen bonding between the acid and the pyridine base. Periodic electronic structure calculations establish an energy scale for the polymorphism in these isotopomeric polymorphs.

Original languageEnglish
Pages (from-to)5273-5279
Number of pages7
JournalCrystEngComm
Volume17
Issue number28
Early online date25 Mar 2015
DOIs
Publication statusPublished - 28 Jul 2015

Fingerprint

Dive into the research topics of 'Isotopomeric polymorphism in a "doubly-polymorphic" multi-component molecular crystal'. Together they form a unique fingerprint.

Cite this