Highly substituted pyrazolylborate ligands TpR,Me were used to limit the coordination number of zinc towards cysteine‐ and histidine‐derived coligands. Monodentate thiolate attachment (→ 1a–f) was achieved with N‐ and C‐protected cysteine, monodentate carboxylate attachment (→ 3) with N‐protected histidine. C‐protected cysteine was found to form a five‐membered N,S‐chelate ring (2). While imidazole coordination with N‐ and C‐protected histidine could not be achieved, cationic pyrazolylborate‐zinc‐coligand complexes [TpZn–L]+ (4a, b) were obtained for L = 2‐methylimidazole. The new complexes were characterized by their spectra and three structure determinations.
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Ruf et al. (1996) studied this question.
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