Weak attractive interactions between closed shell metal ions have been increasingly studied in the last few years and are generally designated as metallophilic interactions. They are best evidenced in the solid state where structural data obtained by X-ray diffraction provide precise information about the distance between the metals involved. The strength of such metal-metal interactions has been compared to that of hydrogen bonding (ca. 7-11 kcal mol(-1)) and is clearly sufficient to bring about novel bonding and structural features and confer interesting physical properties such as luminescence, polychromism, magnetism or one-dimensional electrical conductivity. The Cu(I)-Cu(I), Ag(I)-Ag(I) and Au(I)-Au(I) interactions have been increasingly observed and the latter have certainly been the most studied. Early qualitative analyses of the aurophilic attraction focused on Au-Au bonding originating from 6s, 6p and 5d orbital mixing. Numerous theoretical studies on metallophilic interactions continue to be carried out at various levels of sophistication which take into account relativistic and correlation effects to describe these van der Waals-type interactions. In this critical review, we would like to focus on the synthesis and structures of heterometallic clusters of the transition metals in which intra- rather than intermolecular d(10)-d(10) interactions are at work, in order to limit the role of packing effects. We wish to provide the reader with a comparative overview of the metal core structures resulting from or favoring metallophilic interactions but do not intend to provide a comprehensive coverage of the literature. We will first examine heterometallic clusters displaying homometallic and then heterometallic d(10)-d(10) interactions. Although the focus of this review is on d(10)-d(10) interactions involving metals from the group 11, we shall also briefly examine for comparison some complexes displaying intramolecular d(10)-d(10) interactions involving metals from other groups (188 references).
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Dalton Trans
December 2020
Departamento de Química, Universidade Federal de Santa Catarina, Campus Universitário Trindade, CP 476, Florianópolis, SC 88040-900, Brazil.
The synthesis and characterization of heteromultimetallic complexes has been one of the biggest challenges faced by inorganic chemists in the last few years. Here, the physical nature behind the relative stability of tri-heteronuclear complexes, involving the [M(PR3)]+ (M = Au(i), Ag(i) and Cu(i); and R = Ph and H) cation bridged by the [Fe(CO)4]2- anion, at the relativistic DFT-D3 level of theory is presented. Although the synthetic route to afford the [Fe(CO)4(AuPPh3)2] complex has been known for a long time, information about its copper and silver counterparts is scarce.
View Article and Find Full Text PDFDalton Trans
March 2018
Anorganische Chemie und Strukturchemie, Centrum für molekulare Materialien, CM2, Fakultät für Chemie, Universität Bielefeld, Universitätsstraße 25, 33615 Bielefeld, Germany.
Neutral, homoleptic gold(i) dithiocarboxylate complexes with different-sized Me, iPr, Mes, Tip, Mes* and Dmp substituents at the dithiocarboxylate unit were synthesized by reacting the corresponding dithiocarboxylic acid with potassium dicyanoaurate(i). They were characterized by IR spectroscopy and elemental analyses and their structures were determined by single crystal X-ray diffraction. The dinuclear complexes with an intramolecular d10-d10 type aurophilic interaction aggregate through additional intermolecular aurophilic interactions in different binding motifs.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
June 2017
Department of Chemistry, University of North Texas, Denton, TX 76203;
Outer-shell s/p orbital mixing with d orbitals and symmetry reduction upon cupriphication of cyclic trinuclear trigonal-planar gold(I) complexes are found to sensitize ground-state Cu(I)-Au(I) covalent bonds and near-unity phosphorescence quantum yields. Heterobimetallic AuCu {[Au(μ-C,N-EtIm)Cu(µ-3,5-(CF)Pz)], (4a)}, AuCu {[Au(μ-C,N-BzIm)Cu(µ-3,5-(CF)Pz)], (1) and [Au(μ-C,N-MeIm)Cu(µ-3,5-(CF)Pz)], (3a)}, AuCu {[Au(μ-C,N-MeIm)Cu(µ-3,5-(CF)Pz)], (3b) and [Au(μ-C,N-EtIm)Cu(µ-3,5-(CF)Pz)], (4b)} and stacked Au/Cu {[Au(μ-C,N-BzIm)][Cu(µ-3,5-(CF)Pz)], (2)} form upon reacting Au {[Au(μ-C,N-(N-R)Im)] ((N-R)Im = imidazolate; R = benzyl/methyl/ethyl = BzIm/MeIm/EtIm)} with Cu {[Cu(μ-3,5-(CF)Pz)] (3,5-(CF)Pz = 3,5-bis(trifluoromethyl)pyrazolate)}. The crystal structures of 1 and 3a reveal stair-step infinite chains whereby adjacent dimer-of-trimer units are noncovalently packed via two Au(I)⋯Cu(I) metallophilic interactions, whereas 4a exhibits a hexanuclear cluster structure wherein two monomer-of-trimer units are linked by a genuine d-d polar-covalent bond with ligand-unassisted Cu(I)-Au(I) distances of 2.
View Article and Find Full Text PDFInorg Chem
September 2013
Dipartimento di Chimica Industriale "Toso Montanari", Università di Bologna, Viale Risorgimento 4, 40136 Bologna, Italy.
The Ni6C(CO)9(AuPPh3)4 bimetallic carbide carbonyl cluster was obtained from the reaction of [Ni9C(CO)17](2-) with Au(PPh3)Cl. It contains a rare carbon-centered (distorted) Ni6C octahedral core decorated by four Au(PPh3) fragments. These are μ3-bonded to four contiguous Ni3-triangular faces and display weak intramolecular Au···Au d(10)-d(10) interactions.
View Article and Find Full Text PDFJ Phys Chem A
August 2012
Departamento de Ciencias Quimicas, Universidad Andres Bello, Republica 275, Santiago, Chile.
The interesting case of long intramolecular d(10)-d(10) contacts has been studied through [Ag(4)L(2)](2+) and [Au(4)L(2)](2+) (L = 3,5-bis((N-methylimidazolyl)methyl)pyrazole) systems, showing interesting features gained by analysis of the electronic structure and the overall shielding tensor in the molecular domain, in terms of its components. The long intramolecular closed-shell separations are attributed to the population of the bonding, nonbonding, and antibonding combinations of the ns atomic shells in the [M(4)](4+) core, contrasting with that observed in systems with shorter d(10)-d(10) distances. This point allows to concludeb that separations shorter then the sum of the van der Waals radii (3.
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