A hexanuclear gold carbonyl cluster.

A molecular wire incorporating a robust hexanuclear platinum cluster.

Reaction of [Pt(6)(CO)(4)(P(t)Bu(2))(4)Cl(2)] with excess HS(CH(2))(4)SH in Et(2)NH gave highly stable [Pt(6)(CO)(4)(P(t)Bu(2))(4){S(CH(2))(4)SH}(2)], which adsorbs unchanged onto gold surfaces. This permitted the fabrication and electrical characterisation of gold|molecule|gold junctions involving a well-defined metal carbonyl cluster compound.

A hexanuclear gold carbonyl cluster† †Dedicated to Prof. Dr Pablo Espinet on the occasion of his 65th birthday. Abbreviations are defined prior to the Acknowledgements section. As defined in ref. 1, “clusters are molecular units which may contain small or large numbers of similar atoms where there are several short internuclear distances between atom pairs.” This definition is fully compatible with that originally given by F. A. Cotton (ref. 2). ‡ ‡Electronic supplementary information (ESI) available: Experimental procedures, comments on the X-ray structure determinations and 3D Hirschfeld surfaces for the ions constituting the crystal of 4. CCDC 1049919–1049921. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c5sc01578b Click here for additional data file. Click here for additional data file.

Alkynyl-functionalized gold NHC complexes and their coinage metal clusters.

Phenylpropynyl-functionalized imidazolium salts, as well as their gold complexes, were prepared in excellent yields affording suitable starting materials for metal cluster synthesis. The reactions of these gold complexes with coinage metal phenylacetylides [M(CCPh)](x) (M = Cu, Ag) resulted in the formation of novel heterometallic hexanuclear clusters which exhibit mixed metallophillic interact...

The maximum number of carbonyl groups around an Ru6C polyhedral cluster: hexanuclear ruthenium carbonyl carbides.

Octahedral, trigonal prismatic, and capped square pyramidal structures have been optimized for the Ru(6)C(CO)(n) clusters (15 ≤ n ≤ 20) using density functional theory. The experimentally known very stable Ru(6)C(CO)(17) is predicted to have an octahedral structure in accord with experiment as well as the Wade-Mingos rules. The stability of Ru(6)C(CO)(17) is indicated by its high carbonyl disso...

Enantiopure Radical Cation Salt Based on Tetramethyl-Bis(ethylenedithio)-Tetrathiafulvalene and Hexanuclear Rhenium Cluster

Electrocrystallization of the (S,S,S,S) enantiomer of tetramethyl-bis(ethylenedithio)tetrathiafulvalene donor 1 in the presence of the dianionic hexanuclear rhenium (III) cluster [Re6S6Cl8]2 ́ affords a crystalline radical cation salt formulated as [(S)-1]2 ̈Re6S6Cl8, in which the methyl substituents of the donors adopt an unprecedented all-axial conformation. A complex set of intermolecular TTF ̈...