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Copper(I) Complex Mediated Nitric Oxide Reductive Coupling: Ligand Hydrogen Bonding Derived Proton Transfer Promotes N2O(g) Release
Author(s) -
Gayan B. Wijeratne,
Mayukh Bhadra,
Maxime A. Siegler,
Kenneth D. Karlin
Publication year - 2019
Publication title -
journal of the american chemical society (print)
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.9b07286
Subject(s) - chemistry , hydrogen bond , methanol , ligand (biochemistry) , proton , copper , chelation , nitric oxide , bond cleavage , coupling (piping) , hydrogen , photochemistry , inorganic chemistry , stereochemistry , crystallography , molecule , catalysis , organic chemistry , receptor , mechanical engineering , biochemistry , physics , quantum mechanics , engineering
A cuprous chelate bearing a secondary sphere hydrogen bonding functionality, [(PV-tmpa)Cu I ] + , transforms • NO (g) to N 2 O (g) in high-yields in methanol. Ligand derived proton transfer facilitates N-O bond cleavage of a putative hyponitrite intermediate releasing N 2 O (g) , underscoring the crucial balance between H-bonding capabilities and acidities in (bio)chemical • NO (g) coupling systems.

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