Biaryl-bridged Schiff base complexes of zirconium alkyls: synthesis structure and stability
UNSPECIFIED (2003) Biaryl-bridged Schiff base complexes of zirconium alkyls: synthesis structure and stability. In: 224th ACS National Meeting, BOSTON, MASSACHUSETTS, AUG, 2002. Published in: JOURNAL OF ORGANOMETALLIC CHEMISTRY, 683 (1). pp. 103-113.Full text not available from this repository.
Official URL: http://dx.doi.org/10.1016/S0022-328X(03)00455-8
Three substituted salicylaldirnine derivatives H2L1-3 of 2,2'-diamino-6,6'-dimethylbiphenyl give, under appropriate conditions, isolable alkyls of zirconium [ZrL1-3R2] (R = CH2Ph, CH2Bu'). Two molecular structures confirm their cis-alpha geometry (C-2-symmetric with cis alkyl ligands). They decompose via 1,2-migratory insertion of an alkyl group to imine, followed in some instances by a second similar reaction. The dimeric molecular structure of one such doubly-inserted product is presented. The kinetics of decomposition by this process are studied briefly, and it is noted that the rate increases with increased steric demand of the salicylaidimine unit. (C) 2003 Elsevier B.V. All rights reserved.
|Item Type:||Conference Item (UNSPECIFIED)|
|Subjects:||Q Science > QD Chemistry|
|Journal or Publication Title:||JOURNAL OF ORGANOMETALLIC CHEMISTRY|
|Publisher:||ELSEVIER SCIENCE SA|
|Date:||7 October 2003|
|Number of Pages:||11|
|Page Range:||pp. 103-113|
|Title of Event:||224th ACS National Meeting|
|Location of Event:||BOSTON, MASSACHUSETTS|
|Date(s) of Event:||AUG, 2002|
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