Conclusions
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1.
Potentiometric titration was used to determine the stability constants of homoligand complexes of cupric ions with 1,2-diamines and their N-methyl and N-benzyl derivatives.
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2.
Enantioselectivity was observed in the formation of complexes of cupric ions with N2-benzyl-2-aminomethylpyrrolidine: the optically active complex is more stable than the meso form by 2 kJ/mole.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 7, pp. 1537–1539, July, 1988.
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Kurganov, A.A., Ulanovskii, I.L., Ponomareva, T.M. et al. First case of enantioselectivity in square planar copper(II) complexes with 1,2-diamines. Russ Chem Bull 37, 1357–1360 (1988). https://doi.org/10.1007/BF00962739
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DOI: https://doi.org/10.1007/BF00962739