Please use this identifier to cite or link to this item: https://doi.org/10.1071/CH09263
DC FieldValue
dc.titleDiphenoxo-bridged copper(II) complexes of reduced schiff base ligands as functional models for catechol oxidase
dc.contributor.authorSreenivasulu, B.
dc.date.accessioned2014-06-23T05:54:55Z
dc.date.available2014-06-23T05:54:55Z
dc.date.issued2009
dc.identifier.citationSreenivasulu, B. (2009). Diphenoxo-bridged copper(II) complexes of reduced schiff base ligands as functional models for catechol oxidase. Australian Journal of Chemistry 62 (9) : 968-979. ScholarBank@NUS Repository. https://doi.org/10.1071/CH09263
dc.identifier.issn00049425
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/77428
dc.description.abstractThe design and development of synthetic analogues for the active dicopper(ii) sites of catechol oxidase, with the help of binucleating ligands in particular, is an attractive strategy to generate relevant information on structurefunction relationships. Dicopper(ii) complexes of different yet closely related series of reduced Schiff base ligands (N-(2-hydroxybenzyl)-amino acids; N-(2-hydroxybenzyl)-amino amides, N-(2-hydroxybenzyl)-aminomethane or ethanesulfonic acids, and N-(2-hydroxy-5-substituted-benzyl)-cyclopentane or hexanecarboxylic acids) derived from various substituted salicylaldehydes and natural or unnatural amino acids or amides explored as functional models for the Type 3 copper enzyme catecholase oxidase are reviewed in the present paper. The catalytic activity of different series of dicopper(ii) complexes to oxidize the model substrate 3,5-di-tert-butylcatechol to the corresponding 3,5-di-tert-butylquinone is discussed with respect to the various ligand properties such as the length and chelating ability of the amino acid side-arm of the ligands, conformation of the ligand, nature of the donor groups on the amino acid backbone and role of different para-substituents. This article provides a short review summarizing the trend observed in the catecholase activity of different series of dicopper(ii) complexes investigated in our laboratory. © CSIRO 2009.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1071/CH09263
dc.sourceScopus
dc.typeConference Paper
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1071/CH09263
dc.description.sourcetitleAustralian Journal of Chemistry
dc.description.volume62
dc.description.issue9
dc.description.page968-979
dc.description.codenAJCHA
dc.identifier.isiut000269853200004
Appears in Collections:Staff Publications

Show simple item record
Files in This Item:
There are no files associated with this item.

SCOPUSTM   
Citations

16
checked on Sep 21, 2019

WEB OF SCIENCETM
Citations

17
checked on Sep 13, 2019

Page view(s)

61
checked on Sep 8, 2019

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.