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Synthesis, spectral and electrochemical study of coordination molecules Cu4OX6L4: 4-cyanopyridine Cu4OBrnCl(6−n)(4-CNpy)4complexes

✍ Scribed by Gregor Ondrejovič; Adela Kotočová; Marian Koman; Peter Segľa


Book ID
111491350
Publisher
Versita
Year
2010
Tongue
English
Weight
502 KB
Volume
64
Category
Article
ISSN
0366-6352

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✦ Synopsis


Abstract

New 4-cyanopyridine halide and mixed-halide Cu4OBrnCl(6−n)(4-CNpy)4 complexes (4-CNpy = 4-cyanopyridine, n = 0–6) were synthesised, characterised, and studied by infrared spectra, electronic spectra, and cyclic voltammetry. Infrared spectra revealed donor-acceptor vibrational couplings of the Cu4O, Cu-Cl, and Cu-N stretching vibrations with the in-plane and out-of-plane pyridine ring vibrations. The infrared spectra, electronic spectra, and half-wave potentials correspond to a weak donor and a strong acceptor behaviour of the 4-cyanopyridine ligands and to π-back bonding, Cu(II)→pyridine rings. The results were compared with the related pyridine and 4-substituted pyridine complexes.


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## Abstract Gaussian analysis of bands between 500 cm−1 and 600 cm−1 attributed to the $$ \tilde \nu $$ as (Cu4O) stretching vibration of the tetrahedral Cu4O core in Cu4OBrnCl(6−n)(4-Mepy)4 (n = 0–6) complexes showed two bands, symmetry reduction of the T 2 mode of vibration towards the A 1 and E

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