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Journal of Cluster Science

, Volume 16, Issue 3, pp 429–454 | Cite as

Synthesis and Stereochemical/Electrochemical Analyses of Cuboctahedral-Based Pd23(CO) x (PR3)10 Clusters (x=20 with R3=Bu n 3, Me2Ph; x=20, 21, 22 with R3=Et3): Geometrically Analogous Pd23(PEt3)10 Fragments with Variable Carbonyl Ligations and Resulting Implications

  • Evgueni G. Mednikov
  • Jatuporn Wittayakun
  • Lawrence F. Dahl
Article

Abstract

This research was an outgrowth of previous reactions with [Pd13Ni13(CO)34]4− which produced a tetragonal crystal form of Pd23(CO)20(PEt3)10 (1) that has the same cuboctahedral-based Pd23 framework with an identical number of PEt3 ligands but two fewer CO ligands than the monoclinic crystal form of Pd23(CO)22(PEt3)10 (3) originally reported from reactions with Pd10(CO)12(PEt3)6. A subsequent investigation presented herein to establish whether the carbonyl capacity is influenced by the nature of the phosphine ligands has led to syntheses of Pd23(CO) x (PR3)10 [R3=Et3 (1), Bu n 3 (4), and Me2Ph (5)] with 20 CO ligands (x=20) from corresponding Pd10(CO)12(PR3)6 precursors either by deligation with Pd(OAc)2, CF3CO2H, Ni(1,5-COD)2, [NMe4]2[Ni6(CO)12], or HCO2H or by spontaneous enlargement; yields varied from 15 to 79%. Although attempts to obtain the original Pd23(CO)22(PEt3)10 (3) were unsuccessful, a highly significant outcome was the isolation (one time) of another monoclinic crystal form possessing the triethylphosphine Pd23(CO) x (PEt3)10 cluster with 21 COs (2). Both the compositions and atomic arrangements for each of five Pd23 clusters [1a (solvated); 1b (unsolvated); 2, 4, and 5] were unambiguously established from low-temperature single-crystal CCD X-ray crystallographic determinations in accordance with their nearly identical IR carbonyl frequencies. Solution 31P{1H} NMR spectra of 1 and 4 at room temperature displayed three distinct signals with expected integral ratios of 2/4/4 that are consistent with the solid-state structures of Pd23(CO)20(PR3)10 [R3=Et3 (1), Bu n 3 (4)] remaining intact in solution. The metal-core geometries of all of these Pd23(CO) x (PR3)10 clusters, including the thermodynamically stable ones with 20 CO ligands and the kinetic products with additional CO ligands (x=21, 22), are essentially the same. The common Pd23 core may be best described as possessing a centered hexacapped cuboctahedral Pd19 kernel (alternatively denoted as a centered ν2 Pd19 octahedron) with four edge-connected exopolyhedral wingtip Pd(exo) atoms that reduce the pseudo metal-core symmetry from Oh to D2h. The 10 PR3 ligands are linked to the six tetracapped Pd(cap) and four edge-capped wingtip Pd(exo) atoms; the latter four Pd(exo) atoms are each composed of four trigonal-planar Pd(μ2-CO)2(PR3) units. These crystallographic results provide compelling geometrical evidence for a heretofore unknown stereochemical example involving variable carbonyl ligation (x=20, 21, 22) of a close-packed nanosized Pd n (CO) x (PR3) y cluster (in this case with identical PEt3 ligands) without significant changes being induced in either the overall metal-core architecture or steric dispositions of the same number of PR3 ligands. These experimental findings have particular relevance to the long-standing Muetterties cluster/surface science analogy in showing that the different number (as well as different modes) of carbonyl ligations observed in these large metal carbonyl clusters are directly related to pressure-induced dissociative/nondissociative migratory coverages in CO chemisorptions on metal surfaces. The observed expanded capacity of CO coordination on the same Pd23 polyhedron without notable changes in geometry is no doubt a consequence of its virtually nanosized metal-core architecture; distances between outermost centrosymmetrically related pairs of Pd(cap) and Pd(exo) atoms in the Pd23 framework are 0.8 and 0.9 nm, respectively. An electrochemical (CV) study revealed that 1 undergoes one quasi-reversible two-electron reduction to 1 2− (E1/2=−0.91 V) and two consecutive quasi-reversible one-electron oxidations to 1/1 + at E1/2=0.08 V and 1 +/1 2+ at E1/2=0.32 V (THF; Ag/AgCl as reference electrode). A stereochemical/electronic analysis with the isostructural Au2Pd21(CO)20(PEt3)10 analogue (9) and resulting implications are given.

KEYWORDS

Palladium clusters X-ray crystallographic stereochemical electrochemical analyses variable ligation 

Notes

ACKNOWLEDGMENTS

This research was supported by the National Science Foundation. The CCD area detector system was purchased, in part, from NSF Grant, CHE-9310428. The Bruker AC-300 NMR spectrometer was purchased, in part, by funds from NSF CHE-9208963 and NIH SIO RR 08389-01. We thank Dr. Sergei Ivanov (Los Alamos National Laboratory) for crystallographic assistance at the initial stage of this work and Dr. Ilia Guzei (UW–Madison) for helpful crystallographic advice. The authors are also grateful to Dr. Carlo Mealli (Istituto di Chimica dei Composti Organometallici, Firenze, Italy) for providing a preprint of the manuscript “Formation and Characterization of the Hexanuclear Platinum Cluster [Pt6(μ-PBu t 2)4(CO)6](CF3SO3)2 through Structural, Electrochemical, and Computational Analyses” which in particular contains some electrochemical information relevant to this work [15]. Drawings were prepared with Crystal Maker, Interactive Crystallography. David C. Palmer (P.O. Box 183 Bicester, Oxfordshire, UK OXG TBS).

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Copyright information

© Springer Science+Business Media, Inc. 2005

Authors and Affiliations

  1. 1.Department of ChemistryUniversity of Wisconsin–MadisonMadisonUSA

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