The anionic lanthanide(iii) complexes of the macrocyclic ligand 1,4,7,10-tetraazacyclododecane-N,N',N'',-N'''-tetramethylenephosphonate (DOTP) are present in aqueous solution as a racemic mixture of two enantiomeric forms interconverting slowly on the NMR time scale. The metal chelates form diastero
1H and 13C NMR study of paramagnetic chiral macrocyclic lanthanide complexes
✍ Scribed by Jerzy Lisowski
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 129 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
The chiral macrocyclic complexes obtained in a template condensation of (R,R)-1,2-diaminocyclohexane and 2,6-diformylpyridine, Ln \ La(III), Ce(III), Eu(III) and Yb(III), were studied by 1H [LnL](NO 3 ) 3 , and 13C NMR spectroscopy. The signal assignment was based on COSY, NOESY and HMQC measurements and the isotropic shifts of the paramagnetic complexes were analysed. The spectra of the investigated compounds in methanolÈchloroform solution indicate a helical conformation of the ligand. The chiral D 2 -symmetrical, complexes are able to form diastereoisomeric adducts with D-and L-aminoacids that can be distin-[LnL](NO 3 ) 3 guished by 1H NMR spectroscopy.
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