Macrocyclic ligand design. Structure–function relationships involving the interaction of pyridinyl-containing, oxygen–nitrogen donor macrocycles with selected transition and post transition metal ions on progressive N-benzylation of their secondary amines-Reference-Cited by-同舟云学术

Macrocyclic ligand design. Structure–function relationships involving the interaction of pyridinyl-containing, oxygen–nitrogen donor macrocycles with selected transition and post transition metal ions on progressive N-benzylation of their secondary amines

Published:2004 Issue:21 Volume: Page:3715-3726
ISSN:1477-9226
Container-title:Dalton Trans.
language:en
Short-container-title:Dalton Trans.

Author:

Price Jason R.,Fainerman-Melnikova Marina,Fenton Ronald R.,Gloe Karsten,Lindoy Leonard F.,Rambusch Torsten,Skelton Brian W.,Turner Peter,White Allan H.,Wichmann Kathrin

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2004/DT/B412437E

Reference44 articles.

1. Macrocyclic ligand design. X-Ray, DFT and solution studies of the effect of N-methylation and N-benzylation of 1,4,10,13-tetraoxa-7,16-diazacyclooctadecane on its affinity for selected transition and post-transition metal ions

2. The Effect of Alkylation of N- and O-Donor Atoms on Their Strength of Coordination to Silver(I)

3. Metal ion recognition. The interaction of cobalt(ii), nickel(ii), copper(ii), zinc(ii), cadmium(ii), silver(i) and lead(ii) with N-benzylated macrocycles incorporating O2N2-, O3N2- and O2N3-donor sets

4. Metal ion recognition via ‘selective detuning’. The interaction of selected transition and post-transition metal ions with a mono-N-benzylated O2N3-donor macrocycle and its xylyl-bridged ring analogue

5. Metal ion recognition. Interaction of a series of successively N-benzylated derivatives of 1,4,8,11-tetraazacyclotetradecane (cyclam) with selected transition and post-transition metal ions

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