Department of Chemistry
The University
Sheffield S3 7HF, UK
tel: +44 (0)114 222 9304
fax: +44 (0)114 222 9303
I was educated at Poole Grammar School in Dorset before going to the Univeristy of Bristol where I spent six years (BSc, Bristol (1975); PhD, Bristol (1978, with Professor Selby Knox and Professor Gordon Stone). I then spent two years as a SRC-NATO Postdoctoral Fellow at The University of California, Berkeley, USA (1978-80) in the laboratories of Professor Peter Vollhardt before taking up a position in Sheffield back in the UK, where I am a senior lecturer in chemistry. I was the RSC Sir Edward Frankland Fellow for 1986 and 1987 and the Royal Society of Chemistry HE award winner for 1998.
If you are writing concerning WebElements, Chemdex, or other InterNet services please address correspondence to: webelements@sheffield.ac.uk - otherwise please adress all personal and other correspondence to: m.winter@sheffield.ac.uk. Please DO NOT use this second second address for WebElements and Chemdex correspondence. Both addresses are, however, spammed to pretty well to death and mail to these accounts is largely devoured by automatic viscious spam eaters.
I've written three shorts text books, all in the Oxford University Press chemistry primer series.
organometallic, reaction mechanisms, migration reactions, carbenes, carbynes, vinylidenes, World Wide Web (WWW), cricket.
Migration reactions are an important fundamental class of reactions in organometallic chemistry. Our current main research thrust concerns migrations of hydride and alkyl groups to metal coordinated carbene (see Scheme 1) in processes which result in new alkyl ligands. To date, most of our work has involved molybdenum (see Scheme 2 for an example), tungsten, iron, and ruthenium.


Such reactions are models for some important C--H and C--C bond formation processes but surprisingly little is known about these rearrangements. We are particularly concerned to discover the the mechanisms by which they proceed. These migrations are the reverse of α-elimination reactions and we now find that some of the above products α-eliminate under photochemical excitation to regenerate the initial carbene starting materials.
Many of the compounds are somewhat air-sensitive. The work has a large synthetic component but research workers use mass spectrometry, IR spectroscopy, and NMR spectroscopy extensively for characterization and monitoring. We also make great use of the Department X-ray crystallographic service.
A recent interest concerns applications of the 'World Wide Web' (WWW) for chemistry. This is an international hypertext networked information system that show great promise for information movement in chemistry.
Cyclopropanation in the reaction of [M(CO)3Tp]- [M = Mo, W; Tp = hydridotris(pyrazolyl)borato] with I(CH2)3I and the insertion of isocyanide into metal-acyl bonds", H. Adams, R.J. Cubbon, M.J. Sarsfield and M.J. Winter, J. Chem., Soc., Chem. Commun., 1999, 491-492.
"Syntheses of neutral iron, ruthenium, and manganese half-sandwich vinylidene complexes. Crystal structure of Fe(SnPh3)(CO)(=C=CHPh)(η-C5H5)", H. Adams, S.G. Broughton, C. Sumner, S.J. Walters, and M.J. Winter, J. Chem., Soc., Chem. Commun., 1999, 1231-1232.
"Methyl to alkylidene migration within trans-WMe(=CHPh)(CO)2(η-C5H5)", J. E Muir, A. Haynes, and M.J. Winter, J. Chem., Soc., Chem. Commun., 1996, 1765-1766.
"Syntheses of acyloxy carbene complexes M(SnPh3)(CO)n{=C(OCOR)Ph}(η-C5H5) (M = Mo,W, n = 2, R = Me; M = Fe, Ru, n = 1, R = Me, Ph, But ) and X-ray crystal structures of Fe(SnPh3)(CO){=C(OCOR)Ph}η-C5H5) (R = Me, Ph)", H. Adams, C.A. Maloney, J.E. Muir, S.J. Walters and M.J. Winter, J. Chem., Soc., Chem. Commun., 1995, 1511-1512.
Page author: Mark Winter [last update- December 2005]