Published in
Royal Society of Chemistry, Dalton Transactions, 26(44), p. 11977-11983, 2015
DOI: 10.1039/c5dt01716e
Links
Tools
Mechanism of proton transfer to coordinated thiolates: encapsulation of acid stabilizes precursor intermediate
Journal article published in 2015 by
Ahmed Alwaaly,
William Clegg 
,
Ross W. Harrington,
Athinoula L. Petrou,
Richard A. Henderson
,
Ross W. Harrington,
Athinoula L. Petrou,
Richard A. Henderson
This paper was not found in any repository, but could be made available legally by the author.
Full text: Unavailable
Published version:
archiving forbidden
Data provided by 
Abstract
Hydrogen bonded intermediate in protonation of [Ni(thiolate)(triphos)]+ by 2,6-lutidinium is stabilized by encapsulation of the acid by phenyl groups of triphos.