UNSPECIFIED (1999) Crystallographic characterization of stepwise changes in ligand conformations as their internal topology changes and two novel cross-bridged tetraazamacrocyclic Copper(II) complexes. INORGANIC CHEMISTRY, 38 (20). pp. 4435-4446. ISSN 0020-1669

Full text not available from this repository.

Abstract

The parallel syntheses of two new cross-bridged tetraazamacrocyclic complexes whose ligands are derived from 1,4,8,1 1-tetraazacyclotetradecane (cyclam = 14N4) and rac-1,4,8,1 1-tetraaza-5,5,7,12,12,14-hexamethylcyclotetradecane (tetB = 14N4Me(6)) have been characterized through the crystal structure determination of every stepwise intermediate ligand in the multistep ligand syntheses. These structures show that although the final ligand skeletons are nearly identical, the immediate precursors differ greatly because of the six additional methyl groups of the 14N4Me(6) macrocycle. The inversion from one diastereomer to another of the tetracycle derived from mc-14N4Me(6) has been chemically induced through the successive addition of methyl groups to the reactive tertiary nitrogens, and the novel heterocycles produced have been crystallographically characterized with one showing a conformation not previously known for these systems. The structures of the two copper(rr) complexes have significant geometrical differences, and accordingly, their electrochemical and spectroscopic properties are compared. The complexes exhibit remarkable kinetic stability under harsh conditions.

Item Type:	Journal Article
Subjects:	Q Science > QD Chemistry
Journal or Publication Title:	INORGANIC CHEMISTRY
Publisher:	AMER CHEMICAL SOC
ISSN:	0020-1669
Date:	4 October 1999
Volume:	38
Number:	20
Number of Pages:	12
Page Range:	pp. 4435-4446
Publication Status:	Published
URI:	http://wrap.warwick.ac.uk/id/eprint/14120

Data sourced from Thomson Reuters' Web of Knowledge

Request changes to a record

Actions (login required)

View Item