Oxidative oligomerisation of 2-naphthol by cis-bis(glycinato)copper(II)

Citation
Jg. Handique et Jb. Baruah, Oxidative oligomerisation of 2-naphthol by cis-bis(glycinato)copper(II), J MOL CAT A, 166(2), 2001, pp. 225-231
Citations number
27
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
ISSN journal
13811169 → ACNP
Volume
166
Issue
2
Year of publication
2001
Pages
225 - 231
Database
ISI
SICI code
1381-1169(20010215)166:2<225:OOO2BC>2.0.ZU;2-S
Abstract
The reaction of 2-naphthol with tert-butylhydroperoxide by cis-bis(glycinat o)copper(II) oligomerises 2-naphthol. One of the isolated tetramer A contai ns a tert-butyloxy group. Similar reaction of 2-naphthol with hydrogen pero xide in the presence of cis-bis(glycinato) copper(II) oligomerises 2-naphth ol gives tetramer through hydroxylative oligomerisation. The oligomers are bound to ore-bridged copper cores to give B and C. These oligomers exhibit thermal sensing property. The oligomer (B) converts benzamide to benzoic ac id, as well as catalyses oxidation of aromatic aldehydes such as benzaldehy de to corresponding acids. (C) 2001 Elsevier Science B.V. All rights reserv ed.