Loading…
Synthesis, characterization, crystal structure and electrochemical behavior of a nickel(II) complex of 5,6-dihydro-2H-pyran-3-aldehyde thiosemicarbazone
A new Ni^sup II^ complex of 5,6-dihydro-2H-pyran-3-aldehyde thiosemicarbazone (HDPTSC) has been synthesized and characterized by microanalyses, magnetic susceptibility, molar conductance measurements and by spectral methods (i.r., u.v.-vis., ^sup 1^H-n.m.r.). The structure of [Ni(DPTSC)^sub 2^] · B...
Saved in:
Published in: | Transition metal chemistry (Weinheim) 2005-03, Vol.30 (2), p.121-127 |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | A new Ni^sup II^ complex of 5,6-dihydro-2H-pyran-3-aldehyde thiosemicarbazone (HDPTSC) has been synthesized and characterized by microanalyses, magnetic susceptibility, molar conductance measurements and by spectral methods (i.r., u.v.-vis., ^sup 1^H-n.m.r.). The structure of [Ni(DPTSC)^sub 2^] · B DMF has been solved using X-ray diffraction and found to be highly symmetrical with a trans -arrangement of the two bidentate ligands. The thiosemicarbazone coordinates as an anionic ligand via the thiosemicarbazone moiety's azomethine nitrogen and thiolate sulfur [on loss of the N2 hydrogen]. The electrochemical behavior of the ligand and its Ni^sup II^ complex, determined by cyclic voltammetry, shows that the redox process of the ligand was highly irreversible, whereas the redox process of the Ni^sup II^ complex was observed as a one electron transfer process in a quasi-reversible and diffusion-controlled reaction.[PUBLICATION ABSTRACT] |
---|---|
ISSN: | 0340-4285 1572-901X |
DOI: | 10.1007/s11243-004-1565-x |