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Anthony W. Addison

Researcher at Drexel University

Publications -  163
Citations -  13356

Anthony W. Addison is an academic researcher from Drexel University. The author has contributed to research in topics: Copper & Ligand. The author has an hindex of 39, co-authored 157 publications receiving 12428 citations. Previous affiliations of Anthony W. Addison include University of Washington & University of British Columbia.

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Synthesis, structure, and spectroscopic properties of copper(II) compounds containing nitrogen–sulphur donor ligands; the crystal and molecular structure of aqua[1,7-bis(N-methylbenzimidazol-2′-yl)-2,6-dithiaheptane]copper(II) perchlorate

TL;DR: In this article, the linear quadridentate N2S2 donor ligand 1,7-bis(N-methylbenzimidazol-2′-yl)-2,6-dithiaheptane (bmdhp) forms mono-and di-hydrate 1 : 1 copper(II) complexes which are significantly more stable toward autoreduction than those of the non-methylated analogue.
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Conversion constants for redox potentials measured versus different reference electrodes in acetonitrile solutions at 25°C

TL;DR: In this paper, a critical review of conversion constants amongst various reference electrodes reported in the literature reveals that in most cases the comparisons of redox potential values are far from accurate, and therefore, caution should be exercised when one is comparing the redox properties of complexes measured in CH 3 CN solutions versus different reference electrodes.
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Spectroscopic and redox studies of some copper(II) complexes with biomimetic donor atoms: implications for protein copper centres

TL;DR: The tetrahedral CuIIS4 center generated by γ-irradiation of single crystals of a thioacetamide complex of CuI has a low value of |A∥| as discussed by the authors, indicating that most type I copper in proteins is tetrahedrally, rather than tetragonally, coordinated.
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Synthesis of some imidazole- and pyrazole- derived chelating agents

TL;DR: In this article, condensation of o-phenylenediamines with carboxylic acids and reaction of bifunctional alkyl halides with bifunctionsal nucleophiles are described.
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Iridium dihydroxybipyridine complexes show that ligand deprotonation dramatically speeds rates of catalytic water oxidation.

TL;DR: Mechanistic studies show that the rate law is first-order in an iridium precatalyst, and dynamic light scattering studies indicate that catalysis appears to be homogeneous, and a higher pH facilitates oxidation of precatalysts 2 and 3 and their salt analogues 5 and 6.