Journal
EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
Volume -, Issue 20, Pages 2994-3002Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejic.200900296
Keywords
N,P ligands; Silver; Metal-metal interactions; Coordination modes
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Funding
- National Science Foundation Major Research Instrumentation Program [CHE-0321214]
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A series of new bridging phosphane and phosphonite structures forming three- and six-membered rings with the metal centers were synthesized and characterized. The resulting compounds of phenylbis(pyrid-2-ylmethyl)phosphane (1) with the silver(I) salts of trifluoroacetate (tfa(-)), tetrafluoroborate (BF4-), and trifluoromethanesulfonate (OTf-), and copper tetrakis(acetonitrile) hexafluorophosphate (PF6-) shows the flexibility of the ligand by displaying different coordination modes associated with the electronic and structural characteristics of the corresponding anion. Accordingly, ligand 1 in these complexes displays two different binding modes. With Agtfa and AgBF4 compounds 3 and 4 are obtained where the ligand chelates to two silver atoms that exhibit normal Ag-Ag contacts in the range of 2.9 angstrom. When AgOTf or Cu(NCCH3)(4)PF6 are used, one molecule of 1 bridges the metal centers through a phosphorus atom while another is terminally bound. This induces short M-M distances of 2.6871 and 2.568 angstrom for 5 and 6, respectively. Similarly, the coordination behavior of the heterofunctional bis(pyrid-2-ylmethyl) phenylphosphonite ligand (2) is reported with Cu(NCCH3)(4)PF6 (7) and AgBF4 (8) to form two novel discrete molecules. In these complexes 2 coordinates through the P and N atoms, with the difference that in 7 the O atom of one of the carbinol arms is also bound to the Cu. Elemental analysis, variable-temperature multinuclear NMR spectroscopy, single-crystal X-ray diffraction, and low-temperature luminescence studies were carried out to fully characterize the compounds. ((C) Wiley-VCH Veflag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
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