کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1325783 | 977401 | 2006 | 8 صفحه PDF | دانلود رایگان |

A series of bis-phosphine monoxide (BPMO) palladium(II) and platinum(II) cationic complexes of the type [M(BPMO-κ2-P,O)2][X]2 (M = Pd, Pt; BPMO = Ph2P–(CH2)n–P(O)Ph2 with n = 1 (dppmO), 2 (dppeO), 3 (dpppO); X = BF4, TfO) were prepared from the corresponding chlorides [MCl2(BPMO-κ1-P)2] upon treatment with 2 equiv. of AgX in wet acetone/CH2Cl2 or MeOH solutions. They were characterized by 1H and 31P{1H} NMR spectroscopies and, in the case of the complex [Pt(dppeO-κ2-P,O)2][BF4]2, also by X-ray crystallography. These complexes were tested as catalysts in some Diels–Alder and oxidation reactions with different substrates. In the latter reaction Pt(II) complexes showed moderate activity, while for the former one, both classes of complexes were active in the C–C coupling, in particular the Pt(II) species showed interesting high endo/exo diasteroselectivity depending on the counteranion.
A series of bis-phosphine monoxide Pd(II) and Pt(II) dicationic complexes were prepared and tested as catalysts in some Diels–Alder and oxidation reactions with different substrates. In the C–C coupling, the Pt(II) species showed interesting high endo/exo diasteroselectivity depending on the counteranion.Figure optionsDownload as PowerPoint slide
Journal: Journal of Organometallic Chemistry - Volume 691, Issue 17, 15 August 2006, Pages 3659–3666