The new low symmetry pyrazole-based tripodal tetraamineligands 2-(1H-pyrazol-1-yl)-N,N-bis(1H-pyrazol-1-ylmethyl)ethanamine (bmpz) and 2-(1H-pyrazol-1-yl)-N-[2-(1H-pyrazol-1-yl)ethyl]-N-(1H-pyrazol-1-ylmethyl)ethanamine (bepz) have been prepared and characterised, as have metal complexes containing these ligands. X-ray crystal structures of [Co(bmpz)Cl]2[CoCl4]·H2O, [Co(bmpz)MeCN](ClO4)2·0.13H2O, [Zn(bmpz)MeCN](ClO4)2·0.15H2O, [Zn(bepz)OH2](ClO4)2·0.5H2O and [(Co(bepz)Cl)2]Cl2·6H2O confirm coordination of the intact tripodal ligands to the metal ions through all four N atoms. However, attempts to make Cu2+ complexes containing bmpz and bepz gave, respectively, [Cu(7)Cl2]·0.2H2O and [Cu(8)Cl2] (7 = 1-(1H-pyrazol-1-yl)-N-(1H-pyrazol-1-ylmethyl)ethanamine, 8 = 2-(1H-pyrazol-1-yl)-N-[2-(1H-pyrazol-1-yl)ethyl]ethanamine), complexes containing the tridentate ligands7 and 8 which are formed by loss of a pyrazolylmethyl arm from the appropriate tripodal ligand. This decomposition reaction occurs in protic solvents both in the presence and absence of metal ions, and is ascribed to the presence of an aminal functionality in the tripodal ligands. A possible mechanism for the decomposition, based on NMR and ESMS data, is suggested.
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