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Reactivity of C,N-Chelated Stannylene with Azobenzene
被引:22
|作者:
Padelkova, Zdenka
[1
]
Nechaev, Mikhail S.
[2
]
Lycka, Antonin
[3
]
Holubova, Jana
[1
]
Zevaco, Thomas A.
[4
]
Ruzicka, Ales
[1
]
机构:
[1] Univ Pardubice, Fac Chem Technol, Dept Gen & Inorgan Chem, Pardubice 53210, Czech Republic
[2] Moscow MV Lomonosov State Univ, Dept Chem, Moscow 119992, Russia
[3] Res Inst Organ Synth VUOS, Pardubice 53218 20, Czech Republic
[4] Forschungszentrum Karlsruhe, Bereich Chem Phys Verfahren, Inst Tech Chem, D-76344 Eggenstein Leopoldshafen, Germany
关键词:
Stannylene;
Azobenzene;
C-H activation;
N ligands;
MOLECULAR-STRUCTURE;
CRYSTAL-STRUCTURE;
UNSATURATED MOLECULES;
ALKYNES;
ANALOGS;
TIN;
COMPLEXES;
GERMANIUM;
COMPOUND;
HALIDES;
D O I:
10.1002/ejic.200900181
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
The reactivity of a C,N-chelated stannylene L2Sn [L=2-(Me2NCH2)C6H4] with azobenzene yielded two different products. In the case of reaction in diethyl ether at room temperature, the cyclic complex L2Sn-N(Ph)-N(Ph)-SnL2 was isolated. The second compound, isolated from the reaction in boiling THF, is the product of C-H activation and orthometallation of azobenzene, the cyclic [2-(SnL2)-C6H4]-N-N-[C6H4-2-(SnL2)]. Byproducts in the second reaction are the free ligand (LH) and the cyclic complex L2Sn-(L)Sn-Sn(L)(2)-O(H). ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
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页码:2058 / 2061
页数:4
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