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Chiral organotin complexes stabilized by C,N-chelating oxazolinyl-o-carboranes

Authors
Lee, Jong-DaeKim, Hyo-SukHan, Won-SikKang, Sang Ook
Issue Date
1-2월-2010
Publisher
ELSEVIER SCIENCE SA
Keywords
Organotin complexes; Chiral oxazoline; o-Carborane backbone; Intramolecular coordination
Citation
JOURNAL OF ORGANOMETALLIC CHEMISTRY, v.695, no.3, pp.463 - 468
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF ORGANOMETALLIC CHEMISTRY
Volume
695
Number
3
Start Page
463
End Page
468
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/117013
DOI
10.1016/j.jorganchem.2009.10.030
ISSN
0022-328X
Abstract
A series of chiral organotin halides containing 2-(4-R)-oxazolinyl-o-carboranes (R = i-propyl 1, t-butyl 2; Cab(Oxa)) was prepared from o-carborane with a chiral oxazoline auxiliary. X-ray structural analysis of the representative chiral organotin halide, [2-(4-i-propyl)-oxazolinyl-o-carboranyl]SnMe(2)Br (4), revealed the formation of a stable penta-coordinated tin center due to a N -> Sn interaction. Similar O -> Sn assisted intramolecular penta-coordinated tin complexes (9 and 10) were prepared from methoxy-o-carborane ligands, MeOCH(Z)-o-carborane (Z = H 7, Ph 8; Cab(OMe)), respectively, and a rigid o-carboranyl backbone provided the basic skeleton for the facile formation of organotin complexes. (C) 2009 Elsevier B.V. All rights reserved.
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