Synthesis and electrochemistry of complexes containing the ferrocenyl-phosphine ligand PPh(CH2CH2-η5-C5H4)2Fe

被引:16
作者
Adams, JJ
Curnow, OJ
Huttner, G
Smail, SJ
Turnbull, MM
机构
[1] Univ Canterbury, Dept Chem, Christchurch 1, New Zealand
[2] Univ Heidelberg, Inst Anorgan Chem, D-69120 Heidelberg, Germany
关键词
ferrocene; phosphine; heterobimetallics; cyclopentadienyl; Group; 10; molybdenum;
D O I
10.1016/S0022-328X(98)01032-8
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Treatment of the tethered bis(2-cyclopentadienyl)phenylphosphine compound bis(2-cyclopentadienylethyl)phenylphosp (1) produces moderate yields (40-50%) of the ferrocene complex PPh(CH2CH2-eta5-C5H4)(2)Fe (2). Reaction of 2 with Me,NO in tetrahydrofuran gives the phosphine oxide O=PPh(CH2CH2-eta5-C5H4)(2)Fe (3) whereas treatment with the metal complexes trans-PdCl2(PhCN)(2), cis-PtCl(2()PhCN2), Fe-2(CO)(9), and Mo(CO)(5)(THF) give the corresponding di- or tri-metallic complexes trans -PdCl2[PPh(CH2CH2 eta5 -C5H4)(2)Fe](2) (4), cis-PtCl2[PPh(CH2CH2-(5)(eta)-C5H4)(2)Fe](2) (5), (OC)(4)FePPh(CH2CH2-(5)(eta)-C5H4)(2)Fe (7), and (OC)(5)MoPPh(CH2CH2 eta5-C5H4)(2)Fe (8), respectively, in which 2 is acting as a neutral two-electron-donor phosphine ligand. The electrochemistry of complexes 2, 3, 4, 5 and 7 have been investigated and complexes 3, 4 and 7 have been characterised further by X-ray crystallography. (C) 1999 Elsevier Science S.A. All rights reserved.
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页码:44 / 57
页数:14
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