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Dinuclear palladium(0) and platinum(0) complexes with p-benzoquinone and norbornene ligands
被引:33
作者:
Yamamoto, Y
[1
]
Ohno, T
[1
]
Itoh, K
[1
]
机构:
[1] Nagoya Univ, Grad Sch Engn, Dept Mol Design & Engn, Chikusa Ku, Nagoya, Aichi 4648603, Japan
关键词:
D O I:
10.1021/om030029m
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
Palladium(0) and platinum(0) precursor complexes, Pd-2(dba)(3) and Pt(dba)(2), reacted with p-benzoquinone (bq) and norbornene (nbe) to afford new dinuclear complexes possessing p-benzoquinone as a bridging ligand and norbornene as a monodentate ligand, Pd-2(bq)(2)(nbe)(2) and Pt-2(bq)(2)(nbe)(2), respectively. The solid-state structure of the obtained complexes presented the short metal-metal distances similar to predecessors possessing the significant d(10)-d(10) bonding interaction. The formations of the previously reported mononuclear p-benzoquinone and p-naphthoquinone complexes using 1,5-cyclooctadiene in place of norbornene were also unambiguously confirmed by the single-crystal X-ray diffraction studies. The present dinuclear palladium complex proved to be an efficient catalyst precursor for the linear cotrimerization of 1-octene and dimethyl acetylenedicarboxylate. On the other hand, the platinum analogue catalyzed the hydrosilylation of styrene under mild reaction conditions.
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页码:2267 / 2272
页数:6
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