The transition-metal chemistry of amidinatosilylenes, -germylenes and -stannylenes

Selective metal-ligand interactions in hetero-metallic transition metal clusters

The possible role of metal carbonyl clusters in nanoscience and nanotechnologies

Coordinatively unsaturated tripalladium and triplatinum clusters : models for reactions on metal surfaces

Presented herein are the preparation and crystallographic/microanalytical/magnetic/spectroscopic characterization of the Pt-centered four-shell 165-atom Pd-Pt cluster, (mu(12)-Pt)Pd(164-x)Pt(x)(CO)(72)(PPh(3))(20) (x approximately 7), 1, that replaces the geometrically related capped three-shell icosahedral Pd(145) cluster, Pd(145)(CO)(x)(PEt(3))(30) (x approximately 60), 2, as the largest crystallographically determined discrete transition metal cluster with direct metal-metal bonding. A detailed comparison of their shell-growth patterns gives rise to important stereochemical implications concerning completely unexpected structural dissimilarities as well as similarities and provides new insight concerning possible synthetic approaches for generation of multi-shell metal clusters. 1 was reproducibly prepared in small yields (<10%) from the reaction of Pd(10)(CO)(12)(PPh(3))(6) with Pt(CO)(2)(PPh(3))(2). Its 165-atom metal-core geometry and 20 PPh(3) and 72 CO ligands were established from a low-temperature (100 K) CCD X-ray diffraction study. The well-determined crystal structure is attributed largely to 1 possessing cubic T(h) (2/m3) site symmetry, which is the highest crystallographic subgroup of the noncrystallographic pseudo-icosahedral I(h) (2/m35) symmetry. The "full" four-shell Pd-Pt anatomy of 1 consists of: (a) shell 1 with the centered (mu(12)-Pt) atom encapsulated by the 12-atom icosahedral Pt(x)Pd(12-x) cage, x = 1.2(3); (b) shell 2 with the 42-atom nu(2) icosahedral Pt(x)Pd(42-x) cage, x = 3.5(5); (c) shell 3 with the anti-Mackay 60-atom semi-regular rhombicosidodecahedral Pt(x)Pd(60-x) cage, x = 2.2(6); (d) shell 4 with the 50-atom nu(2) pentagonal dodecahedral Pd(50) cage. The total number of crystallographically estimated Pt atoms, 8 +/- 3, which was obtained from least-squares (Pt(x)/Pd(1-x))-occupancy analysis of the X-ray data that conclusively revealed the central atom to be pure Pt (occupancy factor, x = 1.00(3)), is fortuitously in agreement with that of 7.6(7) found from an X-ray Pt/Pd microanalysis (WDS spectrometer) on three crystals of 1. Our utilization of this site-occupancy (Pt(x)Pd(1-x))-analysis for shells 1-3 originated from the microanalytical results; otherwise, the presumed metal-core composition would have been (mu(12)-Pt)Pd(164). [Alternatively, the (mu(12)-Pt)M(164) core-geometry of 1 may be viewed as a pseudo-Ih Pt-centered six-shell successive nu(1) polyhedral system, each with radially equivalent vertex atoms: Pt@M(12)(icosahedron)@M(30)(icosidodecahedron)@M(12)(icosahedron)@M(60)(rhombicosidodecahedron)@M(30)(icosidodecahedron)@M(20)(pentagonal dodecahedron)]. Completely surprising structural dissimilarities between 1 and 2 are: (1) to date 1 is only reproducibly isolated as a heterometallic Pd-Pt cluster with a central Pt instead of Pd atom; (2) the 50 atoms comprising the outer fourth nu(2) pentagonal dodecahedral shell in 1 are less than the 60 atoms of the inner third shell in 1, in contradistinction to shell-by-shell growth processes in all other known shell-based structures; (3) the 10 fewer PR3 ligands in 1 necessitate larger bulky PPh(3) ligands to protect the Pd-Pt core-geometry; (4) the 72 CO ligands consist of six bridging COs within each of the 12 pentagons in shell 4 that are coordinated to intershell metal atoms. SQUID magnetometry measurements showed a single-crystal sample of 1 to be diamagnetic over the entire temperature range of 10-300 K.

Nanosized (μ12-Pt)Pd164-xPtx(CO)72(PPh3)20 (x ≈ 7) Containing Pt-Centered Four-Shell 165-Atom Pd−Pt Core with Unprecedented Intershell Bridging Carbonyl Ligands: Comparative Analysis of Icosahedral Shell-Growth Patterns with Geometrically Related Pd145(CO)x(PEt3)30 (x ≈ 60) Containing Capped Three-Shell Pd145 Core

Synthesis and structure of polynuclear carbonylphosphine clusters of palladium

A high-nuclear carbonylphosphine cluster of palladium, Pd23(CO)22(PEt3)10

Synthesis and x-ray structure of 10-vertex palladium carbonylphosphine cluster with minimal PBun3 content

The state of the chemistry of the cluster compounds of palladium and platinum is examined. The principal properties, structure, chemical reactions, and methods of synthesis of the phosphinepalladium and phosphineplatinum carbonyl clusters are described and the methods used to regulate the nuclearity of the clusters and their interconversions are discussed. The bibliography includes 69 references.

Phosphinepalladium and Phosphineplatinum Carbonyl Cluster Compounds

Synthesis and X-ray structure of a novel 12-nuclear cluster Pd12(CO)12(PBun3)6

E. G. Mednikov

Papers

Synthesis and structure of polynuclear carbonylphosphine clusters of palladium

A high-nuclear carbonylphosphine cluster of palladium, Pd23(CO)22(PEt3)10

Synthesis and x-ray structure of 10-vertex palladium carbonylphosphine cluster with minimal PBun3 content

Phosphinepalladium and Phosphineplatinum Carbonyl Cluster Compounds

Synthesis and X-ray structure of a novel 12-nuclear cluster Pd12(CO)12(PBun3)6