Mechanisms and rates of proton transfer to coordinated carboxydithioates: studies on [Ni(S2CR){PhP(CH2CH2PPh2)2}]+ (R = Me, Et, Bun or Ph)
Author:
Affiliation:
1. School of Chemistry
2. Newcastle University
3. Newcastle upon Tyne
4. UK
5. Department of Chemistry
Abstract
Kinetics of protonation of [Ni(S2CR)(PhP{CH2CH2PPh2}2)]+ (R = Me, Et, Bun or Ph) with HCl reveals hydrogen-bonded precursor and subsequent chelate opening.
Publisher
Royal Society of Chemistry (RSC)
Subject
Inorganic Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2015/DT/C4DT03543G
Reference29 articles.
1. Protonation of Unsaturated Hydrocarbon Ligands: Regioselectivity, Stereoselectivity, and Product Specificity
2. Proton Transfer, Acid-Base Catalysis, and Enzymatic Hydrolysis. Part I: ELEMENTARY PROCESSES
3. Rates of Mercapto Proton Exchange for 2-Mercaptoethanol in Aqueous Solution1a,b
4. Kinetics of Proton Transfer from Benzoylnitromethane and 1,2-Diphenyl-2-nitroethanone to Various Bases. Resonance, Inductive, Solvation, Steric, and Transition State Hydrogen-Bonding Effects on Intrinsic Rate Constants
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2. Synthesis, protonation and x-ray crystal structures of [Ni(SC6H3Me2-2,6){triphos}]BPh4 and [Ni(SC6H4R-2){triphos}]BPh4 {R = Me, MeO Or Cl; triphos = PhP(Ph2PCH2CH2)2}: Unusual structure when R = Cl;THE 7TH INTERNATIONAL CONFERENCE ON APPLIED SCIENCE AND TECHNOLOGY (ICAST 2019);2019
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