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H/F isosteric substitution to attest different equi-energetic molecular conformations in crystals†‡
Amol G. Dikundwar,Ch. Venkateswarlu,R. N. Chandrakala,Srinivasan Chandrasekaran,Tayur N. Guru Row
CrystEngComm Pub Date : 05/10/2013 00:00:00 , DOI:10.1039/C3CE40697K
Abstract

The sequential replacement of aromatic H-atoms by F-atoms in 1,6-bis(phenylcarbonate) hexa-2,4-diyne allows access to its possible iso-energetic “syn”, “gauche” and “anti” conformations.

Graphical abstract: H/F isosteric substitution to attest different equi-energetic molecular conformations in crystals
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