Kinetic studies show that azamacrocycles functionalised with pendent co-ordinating 2,2′-bipyridyl-yl-methyl arms co-ordinate to labile metal ions in two stages; the first stage is rapid and second-order, and involves formation of an intermediate with rate-determining co-ordination of the pendent bipyridyl arm, and the second stage is slower and first-order, involving chelation by the macrocyclic ring.
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McLaren et al. (1989) studied this question.