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Approach to the conformational behaviour of tetraazamacrocycles in the solution state. NMR and molecular modelling studies

✍ Scribed by R. Boetzel; S. Failla; P. Finocchiaro; G. Hägele


Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
537 KB
Volume
33
Category
Article
ISSN
0749-1581

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✦ Synopsis


Abstract

The differences in complexation behaviour of two diastereomeric tetraazamacrocycles, meso (1) and racemic (2) 5,5,7,12,12,14‐hexamethyl‐1,4,8,11‐tetraazacyclotetradecane, are explained by different conformations in solution, 1 being one stable conformer of almost rigid structure while 2 shows higher conformational flexibility to avoid steric strain. The methods used were ^1^H and ^13^C NMR and molecular modelling.


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