Data di Pubblicazione:
2006
Citazione:
Synthesis of New Enantiomerically Pure Macrocycles Containing Phenanthroline Subunits / F. Colombo, R. Annunziata, L. Raimondi, M. Benaglia. - In: CHIRALITY. - ISSN 0899-0042. - 2006:18(2006), pp. 446-456. [10.1002/chir.20283]
Abstract:
New enantiomerically pure macrocycles have been prepared by combining 1,10-phenanthroline 2,9-dicarboxylic acid and two -amino-acids linked through spacers. Different diamine linkers have been employed in order to modify the dimensions and the properties of the macrocycles whose structures have been studied by 1H and 13C NMR spectroscopy. The ability of the (L)-valine containing macrocycles to bind metal ions and phenolic molecules has been investigated by 1H NMR experiments and Molecular Mechanics calculations.
Tipologia IRIS:
01 - Articolo su periodico
Keywords:
Asymmetric catalysis; Chiral macrocycles; Molecular modeling; Molecular recognition; Phenanthroline
Elenco autori:
F. Colombo, R. Annunziata, L. Raimondi, M. Benaglia
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