%0 Journal Article
%@ 1521-3757
%A Aliev, AE
%A Pavlakos, I
%A Arif, T
%A Aliev, AE
%A Motherwell, WB
%A Tizzard, GJ
%A Coles, SJ
%D 2015
%F discovery:1466630
%I Wiley
%J Angewandte Chemie International Edition
%N 28
%P 8169-8174
%T Noncovalent Lone Pair⋅⋅⋅(No-π!)-Heteroarene Interactions: The Janus-Faced Hydroxy Group
%U https://discovery.ucl.ac.uk/id/eprint/1466630/
%V 54
%X A comparative study by NMR using designed top pan molecular balances demonstrates that the noncovalent interaction of a hydroxyl group with π-deficient pyrazine and quinoxaline units involves a lone pair•••heteroarene interaction which is much stronger and essentially solvent independent when measured relative to the classical π-facial hydrogen bond to a benzene ring. Alkyl fluorides also prefer the heteroarene rings over the benzene ring. The attractive interaction between a quinoxaline and a terminal alkyne is also stronger than the intramolecular hydrogen bond to an arene.
%Z This is the peer reviewed version of the following article: Aliev, AE; Pavlakos, I; Arif, T; Aliev, AE; Motherwell, WB; Tizzard, GJ; Coles, SJ; (2015) Noncovalent Lone Pair⋅⋅⋅(No-π!)-Heteroarene Interactions: The Janus-Faced Hydroxy Group. Angewandte Chemie International Edition , 54 (28) pp. 8169-8174. 10.1002/anie.201502103, which has been published in final form at http://dx.doi.org10.1002/anie.201502103. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.