Structures of [(amino)phenylsilyl]lithiums and related compounds in solution and in the solid state

Citation
A. Kawachi et K. Tamao, Structures of [(amino)phenylsilyl]lithiums and related compounds in solution and in the solid state, J AM CHEM S, 122(9), 2000, pp. 1919-1926
Citations number
88
Categorie Soggetti
Chemistry & Analysis",Chemistry
Journal title
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
ISSN journal
00027863 → ACNP
Volume
122
Issue
9
Year of publication
2000
Pages
1919 - 1926
Database
ISI
SICI code
0002-7863(20000308)122:9<1919:SO[ARC>2.0.ZU;2-B
Abstract
The solution structures of [bis (diethylamino)phenylsilyl] lithium (1), [(d iethylamino)diphenylsilyl] Lithium (2), and [(diethylamino)phenylmethylsily l] lithium (3) were investigated by C-13, Si-29, Li-7, and N-15 NMR spectro scopic experiments. The Si-29-Li-7(6) coupling can be observed in each spec ies at low temperature. The coupling patterns indicate that these three spe cies exist as monomers in THF. Using a N-15-enrichment technique, the Si-29 -N-15 couplings in 1 and 2 are observed. Next, the solid-state structures o f [(diphenylamino)diphenylsilyl] lithium ((Ph2N)Ph2Si-X; X = Li) (4) and it s fluoro (X = Fl (16), stannyl (X SnMe3) (17), and hydro (X H) (18) derivat ives were revealed by crystallographic studies as well as by solid-state 29 Si NMR experiments. In the solid state, 4 exists as a monomer solvated with three THF molecules arising from the reaction solvent. The electropositive substituent X, such as lithium, causes the elongation of the Si-C and Si-N bonds, reduction of the sum of the C-Si-N (or C) angles, and a downfield s hift of the 29Si resonances.