Manipulation of electronic structure via supporting ligands: a charge disproportionate model within the linear metal framework of asymmetric nickel string [Ni(7)(phdptrany)(4)Cl](PF(6)).

This paper describes the synthesis and physical properties of an uniquely asymmetric heptanickel string complex exhibiting a charge disproportionate model along the linear nickel framework.

Further investigations of linear trirhodium complexes: experimental and theoretical studies of [Rh3(dpa)4Cl2] and [Rh3(dpa)4Cl2](BF4) [dpa = bis(2-pyridyl)amido anion].

The linear trirhodium compound, Rh3(dpa)4Cl2 (1), and its one-electron oxidation product, [Rh3(dpa)4Cl2]BF4 (2), have been synthesized and studied extensively. The magnetic measurement for compound 1 shows that it possesses one unpaired electron that is assigned to occupy the sigma(nb) orbital (2A2) by DFT calculations. Upon oxidation, a beta-spin electron of 1 is removed, that causes compound 2 to exhibit a triplet ground state.

Supramolecular assembly of gold(I) complexes of diphosphines and N,N'-bis-4-methylpyridyl oxalamide.

We report herein the supramolecular assembly and spectroscopic and luminescent properties of gold(I) complexes of diphosphines (dppm [bis(diphenylphosphino)methane], dppp [1,3-bis(diphenylphosphino)propane], and dpppn [1,5-bis(diphenylphosphino)pentane]) and N,N'-bis-4-methylpyridyl oxalamide (L). The dppm and dppp cases form the rectangular structures, [dppm(Au(2))L](2)(ClO(4))(4) and [dppp(Au(2))L](2)(ClO(4))(4), with four gold(I) ions at the corners, as well as two L and two dppm or dppp ligands as edges, featuring 38- and 42-membered rings for the former and the latter, respectively. Remarkably, the packing of the dppp complexes shows interesting one-dimensional rectangular channels in the solid state, most likely due to intermolecular pi.