Sample Originator: Michael B. Hursthouse, Simon J. Coles, J. W. Steed, C. Jones, D. L. Coombs, R. J. Calder and Simon Aldridge.
C9H15Cl3N2SiSn
InChI=1/2C9H15N2Si.6ClH.2Sn/c2*1-8-6-5-7-9(10-8)11-12(2,3)4;;;;;;;;/h2*5-7H,1-4H3;6*1H;;/q2*-1;;;;;;;2*+4/p-6
Identification Number: | 10.5258/ecrystals/127 |
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Date Created: | 30 January 2001 |
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Deposited On: | 21 Jan 2008 15:29 |
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Deposited By: | A.N. Admin |
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Depositor Comments
The coordination chemistry of alkoxo and amido ligands bearing pendant nitrogen or sulfur donors has been developed to include examples of main group complexes. The structural implications of amido ligand coordination augmented by a tethered pyridyl base have been investigated for group 13 and 14 derivatives {[6-(Me3SiN)-2-Me-C5H3N]SnCl3 and [6-(Me3SiN)-2-Me-C5H3N]BBr2}. Furthermore, the scope, kinetics and mechanism of the synthesis of alkoxo and amido derivatives from trimethylsilyl substituted precursors have been investigated in depth. The methodology is found to be applicable to a range of ligand frameworks of varying flexibility, stabilised by one or two tether arms.
Data collection parameters
Chemical formula | C9 H15 Cl3 N2 Si Sn |
Crystal morphology | |
Crystal system | Triclinic |
Space group symbol | P-1 |
Cell length a | 9.2498(18) |
Cell length b | 9.7081(19) |
Cell length c | 17.738(4) |
Cell angle alpha | 93.62(3) |
Cell angle beta | 90.61(3) |
Cell angle gamma | 104.26(3) |
Data collection temperature | 150(2) |
Refinement results
Solution figure of merit | 0.0333 |
R Factor (Obs) | 0.0307 |
R Factor (All) | 0.0386 |
Weighted R Factor (Obs) | 0.0769 |
Weighted R Factor (All) | 0.0812 |
Citation: Hursthouse, Michael B. and Coles, Simon J. and Steed, J. W. and Jones, C. and Coombs, D. L. and Calder, R. J. and Aldridge, Simon (2001) University of Southampton, Crystal Structure Report Archive. (doi:10.5258/ecrystals/127)
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