CARBON-HALOGEN BOND-CLEAVAGE REACTION CATALYZED BY ORGANOYTTRIUM HYDRIDE (IN-SITU) AND LANTHANIDE ALKOXIDES

Citation
Ct. Qian et al., CARBON-HALOGEN BOND-CLEAVAGE REACTION CATALYZED BY ORGANOYTTRIUM HYDRIDE (IN-SITU) AND LANTHANIDE ALKOXIDES, Applied organometallic chemistry, 9(5-6), 1995, pp. 457-460
Citations number
21
Categorie Soggetti
Chemistry Applied","Chemistry Inorganic & Nuclear
ISSN journal
02682605
Volume
9
Issue
5-6
Year of publication
1995
Pages
457 - 460
Database
ISI
SICI code
0268-2605(1995)9:5-6<457:CBRCBO>2.0.ZU;2-M
Abstract
Organic halides can be ubiquitous long-lived contaminants to the envir onment. Dehalogenation of organic halides with sodium hydride (NaH) as reductant catalyzed by two varieties of lanthanides was reported in r espect of environmental remediation. The first catalyst is a dicyclope ntadienyl yttrium halide, and organoyttrium hydride was thought to be the reactive species. The second catalyst is a lanthanide isopropoxide which showed higher catalytic reactivity, and an aggregate is involve d in the suggested mechanism.