کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1336208 | 1500223 | 2016 | 10 صفحه PDF | دانلود رایگان |
The reactions of [Pt(styrene)(PMe3)2] with 2 equiv. of alkyl or aryl isocyanate affored five-membered platinacycles, cis-[Pt{–N(R)C(O)N(R)C(O)–}(PMe3)2] (R = CH2C6H5, p-ClC6H4, p-OMeC6H4). These complexes are the first examples of platinacycles containing an isocyanate dimer unit. When the five-membered bis(phosphine) platinacycles or palladacycles were treated with 2 equiv. of elemental sulfur, 16-membered cyclic products as an assembly of four platinacycles or palladacycles, [M(PR3){–N(R)C(O)N(R)C(O)–}]4, were readily obtained. These cyclic tetramers were cleaved using tert-butyl isocyanide (CN–tbutyl, 4 equiv.), affording the corresponding monomeric complexes, [M(PR3)(CN–tbutyl){–N(R)C(O)N(R)C(O)–}] (M = Pt, Pd). An unusual cyclotrimerization of organic isocyanates catalyzed by zerovalent Pt complexes or five-membered platinacycles was observed. In addition, the direct cyclotrimerization of alkyl or aryl isocyanates using dialkyl Pt(II) or Pd(II) complexes was investigated. The cross cyclotrimerization of an aryl isocyanate and its derivative using a zerovalent Pd complex was also investigated.
Upon treatment with sulfur, bis(phosphine) mononuclear Pd(II) and Pt(II) complexes containing an isocyanate dimer unit are converted to new macrocyclic complexes with four metallacycles.Figure optionsDownload as PowerPoint slide
Journal: Polyhedron - Volume 117, 15 October 2016, Pages 283–292