Repozytorium

Zinc(II) complexes with asymmetric 3,5-substituted 1H-pyrazoles.

Autorzy

Sergey O. Malinkin

Larysa V. Penkova

Yurii S. Moroz

Matti Haukka

Anna Maciąg

Elżbieta Gumienna-Kontecka

Vadim A. Pavlenko

Svetlana V. Pavlova

Ebbe Nordlander

Igor O. Fritsky

Rok wydania

2012

Czasopismo

European Journal of Inorganic Chemistry

Strony

1639-1649

DOI

10.1002/ejic.201101090

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

Two new pyrazolate‐based ligands, N′‐[1‐(3‐acetyl‐4‐methyl‐1H‐pyrazol‐5‐yl)ethylidene]‐2‐(hydroxyimino)propanehydrazide (L1) and 5‐[(E)‐1‐(2‐{(E)‐2‐(hydroxyimino}propanoyl}hydrazono)ethyl]‐4‐methyl‐1H‐pyrazole‐3‐carboxylic acid (L2), were synthesized and studied for zinc(II) complexation. A set of pH‐dependent UV/Vis measurements has been performed to determine the complex formation properties of L2. According to the calculations, in solution, L2 forms variously protonated mononuclear (ZnII/L2 = 1:1) and dinuclear (ZnII/L2 = 2:1) complexes. The reaction of the deprotonated ligands with hydrated ZnII salts and slow diffusion of ammonia into the reaction mixtures gave mononuclear [Zn(L1‐2H)(NH3)2]·DMF (1) and trinuclear μ‐pyrazolato‐bridged [Zn3(L2‐3H)2(NH3)5]·4H2O (3). In both complexes, the zinc ions are in the same distorted trigonal‐bipyramidal environment, coordinated to two nitrogen atoms of the ammonia and one oxygen and two nitrogen atoms of the pyrazolate and hydrazide groups. The molecular structures of all of the ligands and complexes have been elucidated by X‐ray crystallography.

Słowa kluczowe

N, O ligands, Zinc, structure elucidation

Adres publiczny

https://doi.org/10.1002/ejic.201101090

Strona internetowa wydawcy

onlinelibrary.wiley.com

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