Convenient preparation of (η4-alkadiene)dichloroplatinum(II) complexes from [PtCl6]2− anions and their reduction to platinum(0) alkene complexes under phase-transfer catalysis conditions

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Title: Convenient preparation of (η4-alkadiene)dichloroplatinum(II) complexes from [PtCl6]2− anions and their reduction to platinum(0) alkene complexes under phase-transfer catalysis conditions
Authors: Dell’Amico, Daniela Belli belli@dcci.unipi.it, Labella, Luca1, Marchetti, Fabio1, Samaritani, Simona1
Source: Journal of Organometallic Chemistry. Apr2011, Vol. 696 Issue 7, p1349-1354. 6p.
Subjects: Platinum, Metal complexes, Metal ions, Chemical reduction, Alkenes, Phase-transfer catalysis, Potassium compounds, X-ray diffraction, Solid solutions
Abstract: Abstract: Convenient one-pot reduction-complexation reactions of hexachloroplatinato(IV) anions to (η4-alkadiene)dichloroplatinum(II) complexes (η4-alkadiene=COD, DAE, DCPD, NBD) under suitable phase-transfer catalysis conditions are reported. Reduction to zerovalent platinum alkene complexes has been obtained in the presence of an excess of alkene, potassium formate and 18-crown-6 as phase-transfer catalyst (alkene=COD, NB, dba). The crystal and molecular structure of [Pt1.03(dba)3]·CH2Cl2 has been studied by X-ray diffraction methods: it can be described as a solid solution of Pt(dba)3 and Pt2(dba)3, the mononuclear complex being largely prevailing. [Copyright &y& Elsevier]
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Database: Engineering Source
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Abstract:Abstract: Convenient one-pot reduction-complexation reactions of hexachloroplatinato(IV) anions to (η4-alkadiene)dichloroplatinum(II) complexes (η4-alkadiene=COD, DAE, DCPD, NBD) under suitable phase-transfer catalysis conditions are reported. Reduction to zerovalent platinum alkene complexes has been obtained in the presence of an excess of alkene, potassium formate and 18-crown-6 as phase-transfer catalyst (alkene=COD, NB, dba). The crystal and molecular structure of [Pt1.03(dba)3]·CH2Cl2 has been studied by X-ray diffraction methods: it can be described as a solid solution of Pt(dba)3 and Pt2(dba)3, the mononuclear complex being largely prevailing. [Copyright &y& Elsevier]
ISSN:0022328X
DOI:10.1016/j.jorganchem.2010.12.043