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Functionalized N-heterocyclic carbene iridium complexes: Synthesis, structure and addition polymerization of norbornene
被引:49
|作者:
Xiao, Xu-Qiong
[1
]
Jin, Guo-Xin
[1
]
机构:
[1] Fudan Univ, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China
基金:
美国国家科学基金会;
关键词:
iridium;
carbene;
half-sandwich complexes;
addition polymerization;
norbornene;
D O I:
10.1016/j.jorganchem.2008.08.019
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
Picolyl, pyridine, and methyl functionalized N-heterocyclic carbene iridium complexes [Cp*Ir(C<boolean AND>N)Cl]Cl (4, C<boolean AND>N = 3-Methyl-1-picolyimidazol-2-ylidene), [Cp*Ir(C<boolean AND>N)Cl][Cp*IrCl3] (5), [Cp*Ir(C-N)Cl]Cl (6, C-N = 3-Methyl-1-pyridylimidazol-2-ylidene) and [Cp*Ir(L)Cl-2] (7, L = 1,3-dimethylimidazol-2-ylidene) have been synthesized by transmetallation from Ag(I) carbene species, and characterized by H-1 NMR, C-13 NMR spectra and elemental analyses. The molecular structures of 5-7 have been confirmed by X-ray single-crystal analyses. The iridium carbene complexes 4 and 6 show moderate catalytic activities (3.03 x 10(5) g PNB (mol Ir) (1)h (1) and 1.70 x 10(6) g PNB (mol Ir) (1) h (1)) for the addition polymerization of norbornene in the presence of methylaluminoxane (MAO) as co-catalyst. The produced polynorbornene have been characterized by IR, H-1 NMR and C-13 NMR spectra, showing it follows the vinyl-addition-type of polymerization.
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页码:3363 / 3368
页数:6
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