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Tridentate Lewis-acids based on triphenylsilane
被引:23
|作者:
Tomaschautzky, Janek
[1
]
Neumann, Beate
[1
]
Stammler, Hans-Georg
[1
]
Mix, Andreas
[1
]
Mitzel, Norbert W.
[1
]
机构:
[1] Univ Bielefeld, CM2, Inorgan & Struct Chem, Fak Chem, Univ Str 25, D-33615 Bielefeld, Germany
关键词:
SOLID-STATE STRUCTURES;
2 SILICON ATOMS;
MOLECULAR-STRUCTURE;
DYNAMIC-BEHAVIOR;
COMPLEXATION;
FLUORIDE;
HYDROGALLATION;
BRIDGE;
HOST;
TIN;
D O I:
10.1039/c6dt04293g
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
Several derivatives of the propeller-shaped ortho-substituted triphenylsilanes, carrying metal-or silicon-based acceptor groups, are reported. They were synthesized starting from tris(2-bromophenyl) fluorosilane, tris(2-vinylphenyl) fluorosilane and tris(2-ethynylphenyl) fluorosilane to generate a scope of Lewis-acidic molecules with different cavities. An improved synthetic protocol for donor-free tris(2-lithiophenyl) silanes is described. First attempts in host-guest chemistry to probe the binding between a threefold alane-functionalised ortho-substituted triphenylsilane and a tridentate Lewis-basic guest molecule are presented. The synthesis and a first molecular structure determination in the crystalline state of a bisma-silatriptycene is reported.
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页码:1645 / 1659
页数:15
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