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Enantiopure dinuclear silver(I) double helicates were prepared in simple one-pot reactions from commercially available starting materials and the pure complexes isolated as the hexafluorophosphate salts. The (R),(+) and (S),(−) enantiomers of 1,1′-binaphthalene-2,2′-diamine were used as spacer groups and reacted with pyridine-2-carbaldehyde to form chiral didentate imine ligands. These chiral ligands predetermine the chirality of the helicates: the R spacer gives a P helicate and the S spacer an M helicate. The dinuclear double helical structures are confirmed by single crystal X-ray analysis and their persistence in solution is supported by inter-strand NOE data. Enantiopure copper(I) dinuclear species were also prepared by similar one-pot procedures and analysed by 1H NMR, mass spectrometry and circular dichroism.
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Hamblin et al. (2001) studied this question.
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