Synthesis and spectral characterization of diorganodiaminosilanes [(ArNH)(2)SiPhMe] (Ar=2,6-(Pr2C6H3)-Pr-i; 2,4,6-Me3C6H2) and lithium silylamide [(2,6-Et2C6H3NLi)(2,6-Et2C6H3NH)SiPh2]
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Title |
Synthesis and spectral characterization of diorganodiaminosilanes [(ArNH)(2)SiPhMe] (Ar=2,6-(Pr2C6H3)-Pr-i; 2,4,6-Me3C6H2) and lithium silylamide [(2,6-Et2C6H3NLi)(2,6-Et2C6H3NH)SiPh2]
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Creator |
PALANISAMI, N
MURUGAVEL, R |
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Subject |
precursors
bulky aminosilanes half-sandwich lithium nmr spectroscopy x-ray diffraction |
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Description |
Aminosilanes bearing bulky substituents on nitrogen centers, [(ArNH)(2)SiPhMe] (Ar = 2,6-(Pr2C6H3)-Pr-i (1), 2,4,6-Me3C6H2 (2)) and half-sandwich lithium silylamide [(2,6-Et2C6H3NLi)(2,6-Et2C6H3NH)SiPh2] (3) have been prepared and characterized by elemental analysis, IR, EI mass and NMR (H-1 and Si-29) spectroscopic studies. The solid state structures of 2 and 3 have been determined by single crystal X-ray diffraction studies. The molecule 2 has a C-1 symmetry due to the steric crowding, and the two N-H protons are approximately trans to each other. The amido nitrogen atoms in 2 show significant deviation from trigonal-planar geometry, and as a result, the observed Si-N bonds are marginally longer than those observed in aminosilanes with planar nitrogen atoms. The molecule 3 exists as discrete dimer with an inversion center. The Li ion in 3 forms intramolecular pi-complex with the neighboring aryl (2,6-Et2C6H3) group, to form a half-sandwich lithium silylamide. (c) 2006
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Publisher |
ELSEVIER SCIENCE SA
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Date |
2011-07-28T22:48:47Z
2011-12-26T12:47:40Z 2011-12-27T05:38:09Z 2011-07-28T22:48:47Z 2011-12-26T12:47:40Z 2011-12-27T05:38:09Z 2006 |
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Type |
Article
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Identifier |
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 691(15), 3260-3266
0022-328X http://dx.doi.org/10.1016/j.jorganchem.2006.03.039 http://dspace.library.iitb.ac.in/xmlui/handle/10054/7517 http://hdl.handle.net/10054/7517 |
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Language |
en
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