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Diran Herebian

Researcher at Max Planck Society

Publications -  7
Citations -  1034

Diran Herebian is an academic researcher from Max Planck Society. The author has contributed to research in topics: Palladium & Crystal structure. The author has an hindex of 7, co-authored 7 publications receiving 961 citations.

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Analysis and Interpretation of Metal-Radical Coupling in a Series of Square Planar Nickel Complexes: Correlated Ab Initio and Density Functional Investigation of [Ni(LISQ)2] (LISQ=3,5-di-tert-butyl-o-diiminobenzosemiquinonate(1-))

TL;DR: A detailed theoretical study of the interaction between a central low-spin d(8) nickel ion and two N,N-coordinating diiminobenzosemiquinonate(1-) ligands in a square planar arrangement reveals that the complex features essentially two strongly interacting ligand radicals which interact with each other via an efficient superexchange mechanism that is mediated by a back-bonding interaction to the central metal.
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Molecular and electronic structures of bis-(o-diiminobenzosemiquinonato)metal(II) complexes (Ni, Pd, Pt), their monocations and -anions, and of dimeric dications containing weak metal-metal bonds.

TL;DR: Cyclic voltammetry established that the complete electron-transfer series consisting of a dianion, monoanion, neutral complex, a mono- and a dication exists.
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Molecular and electronic structure of four- and five-coordinate cobalt complexes containing two o-phenylenediamine- or two o-aminophenol-type ligands at various oxidation levels: an experimental, density functional, and correlated ab initio study.

TL;DR: It is shown that the corresponding nickel complexes 8 and 9 contain a low-spin nickel(II) ion regardless of the oxidation level of the ligand, whereas for the corresponding cobalt complexes the situation is more complicated.
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Experimental Evidence for the Noninnocence of o-Aminothiophenolates: Coordination Chemistry of o-Iminothionebenzosemiquinonate(1-) π-Radicals with Ni(II), Pd(II), Pt(II)

TL;DR: Analysis of the geometric features of 120 published structures of complexes containing ligands of the o-aminothiophenolate type show that high precision X-ray crystallography allows to discern the differing protonation and oxidation levels of these ligands.