Octahedral Hexapalladium Pseudo- Pd(μ-CO)(PEt) with 80 Electron-Deficient Cluster Valence Electrons (CVEs) and a Comparison with Octahedral Hexapalladium Pseudo- Pd(μ-CO)(PMe) with 82 CVEs: Computational Analysis and Resulting Implications.

The elusive octahedral hexapalladium Pd(μ-CO)(PEt) () was obtained by the reaction of Pd(CO)(PEt) with TlCo(CO) in tetrahydrofuran under N at 55 °C. Its pseudo- octahedral structure, established from a CCD X-ray diffractometry study at 100 K, has the highest ideal symmetry of any of the characterized octahedral-based CO/PR-ligated homopalladium Pd clusters ( = 6, 7, 8, 10). Each Pd atom in is coordinated to a PEt ligand, and each nonadjacent triangular Pd face is capped by a triply bridging μ-CO ligand.

Isolation and Structural Characterization of a Mackay 55-Metal-Atom Two-Shell Icosahedron of Pseudo-Ih Symmetry, Pd55L12(μ3-CO)20 (L = PR3, R = Isopropyl): Comparative Analysis with Interior Two-Shell Icosahedral Geometries in Capped Three-Shell Pd145, Pt-Centered Four-Shell Pd-Pt M165, and Four-Shell Au133 Nanoclusters.

We present the first successful isolation and crystallographic characterization of a Mackay 55-metal-atom two-shell icosahedron, Pd55L12(μ3-CO)20 (L = PPr(i)3) (1). Its two-shell icosahedron of pseudo-Ih symmetry (without isopropyl substituents) enables a structural/bonding comparison with interior 55-metal-atom two-shell icosahedral geometries observed within the multi-shell capped 145-metal-atom three-shell Pd145(CO)72(PEt3)30 and 165-metal-atom four-shell Pt-centered (μ12-Pt)Pd164-xPtx(CO)72(PPh3)20 (x ≈ 7) nanoclusters, and within the recently reported four-shell Au133(SC6H4-p-Bu(t))52 nanocluster. DFT calculations carried out on a Pd55(CO)20(PH3)12 model analogue, with triisopropyl phosphine substituents replaced by H atoms, revealed a positive +0.

Nanosized {Pd4(μ4-C)}Pd32(CO)28(PMe3)14 Containing Tetrahedrally Deformed Pd4 Cage with Encapsulated Carbide Atom: Formal Substitution of Geometrically Analogous Interior Au4 Entity in Isostructural Au4Pd32(CO)28(PMe3)14 by Electronically Equivalent Pd4(μ4-C) and Computational/Catalytic Implications.

This first homopalladium carbido cluster, {Pd4(μ4-C)}Pd32(CO)28(PMe3)14 (1), was isolated (3-7% yields) from an ultimately simplified procedure-the reaction of CHCl3 under N2 with either Pd8(CO)8(PMe3)7 or Pd10(CO)12(PMe3)6 at room temperature. Charge-coupled device (CCD) X-ray diffraction data at 100 K for 1·2.5 C6H14 (1a) and 1·3 CHCl3 (1b) produced closely related molecular parameters for 1.

Acid/base-controlled AuI/Au0 reductive transformations of the monogold [(μ14-Au)Pd22(CO)20(PEt3)8]+ monocation into three different neutral digold nanoclusters: Au2Pd21(CO)20(PEt3)10, Au2Pd28(CO)26(PEt3)10, and new five-layer hexagonal close-packed (μ12-Au)2Pd42(CO)30(PEt3)12 with a trigonal-bipyramidal AuPd3Au kernel.

The monogold [(μ(14)-Au)Pd(22)(CO)(20)(PEt(3))(8)](+) nanocation (2, with a [(CF(3)CO(2))(2)H](-) counterion) is shown to be a versatile precursor for the generation of three different neutral Au-Pd nanoclusters with double gold content in their distinctly dissimilar bimetallic architectures. These carbon monoxide (CO)-induced conversions are based on the reduction of Au(I) to Au(0) that is controlled by the reaction medium. Under basic and acidic conditions, the known Au(2)Pd(21)(CO)(20)(PEt(3))(10) (3; >90% yield) and Au(2)Pd(28)(CO)(26)(PEt(3))(10) (4; ∼40% yield), respectively, were obtained, whereas neutral conditions gave rise to the new (μ(12)-Au)(2)Pd(42)(CO)(30)(PEt(3))(12) (1; ∼10-20% yield; all yields based on gold).

Ion exchange of protons by coinage metals to give gold and silver encapsulation within a pseudo-D2d distorted face-capped Pd14 cubic kernel: [(μ14-M)Pd22(CO)20(PEt3)8]+ (M = Au, Ag).

Heart of gold (or silver): The pseudo-D2d distorted MPd14 cubic kernel of [(μ14-M)Pd22(CO)20(PEt3)8](+) cations, with M = Au (1), Ag (2), has an encapsulated M atom (see picture; yellow) coordinated to eight cubic corner (black) and six face-capping Pd atoms (gray). Compounds 1 and 2 were obtained (28-60 % yields) from two-step/one-pot reactions of a Pd10 precursor with CF3CO2 H followed by coinage-metal ion exchange of protons.

How innocent is thallium(I)? Corrected formulations of [Tl2Pd14(CO)9(PMe3)11][PF6]2 and [TlPd9(CO)9(PPh3)6][PF6] clusters previously reported as corresponding Au2Pd14 and AuPd9 clusters.

Two previously reported cationic clusters, Au(2)Pd(14) (1-Me) and AuPd(9) (2-Ph), obtained by similar reactions of CO/PR(3)-ligated Pd(0) clusters with in the presence of TlPF(6) are shown to be [Tl(2)Pd(14)(CO)(9)(PMe(3))(11)](2+) (1a-Me) and [TlPd(9)(CO)(9)(PPh(3))(6)](+) (2a-Ph), respectively. These clusters ([PF(6)](-) counterion) were prepared without the presence of gold by reactions of either Pd(10)(CO)(12)(PMe(3))(6) or Pd(10)(CO)(12)(PPh(3))(6) with TlPF(6) and characterized crystallographically and spectroscopically.

CO-induced formation of an interpenetrating bicuboctahedral Au2Pd18 kernel in nanosized Au2Pd28(CO)26(PEt3)10: formal replacement of an interior (μ12-Pd)2 fragment in the corresponding known isostructural homopalladium Pd30(CO)26(PEt3)10 with nonisovalent (μ12-Au)2 and resulting experimental/theoretical implications.

Initially isolated from Pd(10)(CO)(12)(PEt(3))(6) (5) and Au(SMe(2))Cl precursors in a two-step carbon monoxide (CO)-involved procedure, the nanosized interpenetrating bicuboctahedral gold (Au)-palladium (Pd) Au(2)Pd(28)(CO)(26)(PEt(3))(10) (1) was then directly obtained in 25-30% yield from the CO-induced reaction of the CO-stable Au-centered cuboctahedral Au(2)Pd(21)(CO)(20)(PEt(3))(10) (3) with the structurally analogous CO-unstable Pd(23)(CO)(20)(PEt(3))(10) (4). Our hypothesis that this latter synthesis is initiated by the reaction of 3 with coordinatively unsaturated homopalladium species resulting from CO-induced fragmentation of 4 was subsequently substantiated by the alternatively designed synthesis of 1 (∼25% yield) from the CO-induced reaction of 3 with the structurally dissimilar CO-unstable Pd(38)(CO)(28)(PEt(3))(12) (6). The composition of 1, unambiguously established from a 100 K CCD X-ray diffractometry study, is in accordance with single-crystal X-ray Au-Pd field-emission microanalysis.

Syntheses, structures and properties of primarily nanosized homo/heterometallic palladium CO/PR3-ligated clusters.

Syntheses, properties and structures of nanosized palladium CO/PR(3)-ligated homo- and heterometallic clusters containing up to 165 metal atoms are the focus of this review. The work discussed is primarily that of the authors and their coworkers. We propose that the unparalleled variety of structural types and the distinctive reactivities of neutral Pd(n)(CO)(x)(PR(3))(y) clusters composed of zerovalent Pd atoms are a consequence of relatively weak Pd-L(ligand) and Pd(0)-Pd(0) interactions that result from the stable 5s(0)4d(10) closed-shell electron configuration of atomic Pd in its ground state.

Nanosized Pd37(CO)28{P(p-Tolyl)3}12 containing geometrically unprecedented central 23-atom interpenetrating tri-icosahedral palladium kernel of double icosahedral units: its postulated metal-core evolution and resulting stereochemical implications.

Pd37(CO)28{P(p-Tolyl)3}12 (1) was obtained in approximately 50% yield by the short-time thermolysis of Pd10(CO)12{P(p-Tolyl)3}6 in THF solution followed by crystallization via layering with hexane under N2. The low-temperature (100 K) CCD X-ray diffraction study of 1 revealed an unusual non-spheroidal Pd37-atom polyhedron, which may be readily envisioned to originate via the initial formation of a heretofore non-isolated central Pd23 kernel composed of three interpenetrating trigonal-planar double icosahedra (DI) that are oriented along the three bonding edges of its interior Pd3 triangle. This central Pd23 kernel is augmented by face condensations with two additional phosphorus-free and 12 tri(p-C6H4Me)phosphine-ligated Pd atoms, which lower the pseudo-symmetry of the resulting 37-atom metal core from D(3h) to C2.

Nanosized (mu12-Pt)Pd164-xPtx(CO)72(PPh3)20 (x approximately 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 approximately 60) containing capped three-shell Pd145 core.

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).