Motherwell, WB;
Moreno, RB;
Pavlakos, I;
Arendorf, JRT;
Arif, T;
Tizzard, GJ;
Coles, SJ;
(2018)
Noncovalent Interactions of pi Systems with Sulfur: The Atomic Chameleon of Molecular Recognition.
[Rapid communication].
Angewandte Chemie International Edition
, 57
(5)
pp. 1193-1198.
10.1002/anie.201708485.
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Abstract
The relative strength of noncovalent interactions between a thioether sulfur atom and various π systems in designed top pan molecular balances was determined by NMR spectroscopy. Compared to its oxygen counterpart, the sulfur atom displays a remarkable ability to interact with almost equal facility over the entire range of π systems studied, with the simple alkene emerging as the most powerful partner. With the exception of the O⋅⋅⋅heteroarene interaction, all noncovalent interactions of sulfur with π systems are favoured over oxygen.
Type: | Article |
---|---|
Title: | Noncovalent Interactions of pi Systems with Sulfur: The Atomic Chameleon of Molecular Recognition |
Open access status: | An open access version is available from UCL Discovery |
DOI: | 10.1002/anie.201708485 |
Publisher version: | http://dx.doi.org/10.1002/anie.201708485 |
Language: | English |
Additional information: | This version is the author accepted manuscript. For information on re-use, please refer to the publisher’s terms and conditions. |
Keywords: | Science & Technology, Physical Sciences, Chemistry, Multidisciplinary, Chemistry, conformational analysis, molecular balances, NMR spectroscopy, noncovalent interactions, pi-interactions, Aromatic interactions, arene interactions, lone-pair, dispersion, chemistry, rings, accuracy, balances, design, forces |
UCL classification: | UCL UCL > Provost and Vice Provost Offices > UCL BEAMS UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Maths and Physical Sciences UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Maths and Physical Sciences > Dept of Chemistry |
URI: | https://discovery-pp.ucl.ac.uk/id/eprint/10044525 |
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