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Noncovalent Interactions of π Systems with Sulfur: The Atomic Chameleon of Molecular Recognition
Authors:Prof. William B. Motherwell  Dr. Rafael B. Moreno  Dr. Ilias Pavlakos  Josephine R. T. Arendorf  Dr. Tanzeel Arif  Dr. Graham J. Tizzard  Prof. Simon J. Coles  Dr. Abil E. Aliev
Affiliation:1. Department of Chemistry, University College London, London, UK;2. School of Chemistry, University of Southampton, Southampton, UK
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.
Keywords:conformational analysis  molecular balances  NMR spectroscopy  noncovalent interactions  π  -interactions
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