Sivagnanam, Usha ; Palaniandavar, Mallayan (1994) Influence of chelate-ring size and number of sulfur-donor atoms on spectra and redox behaviour of copper(II) bis(benzimidazolyl) tetra- and penta-thloether complexes Journal of the Chemical Society, Dalton Transactions (15). pp. 2277-2283. ISSN 0300-9246
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Official URL: http://pubs.rsc.org/en/Content/ArticleLanding/1994...
Related URL: http://dx.doi.org/10.1039/DT9940002277
Abstract
The linear quadridentate R(CH2)mSCH2CH2S(CH2)nSCH2CH2S(CH2)mR, where m= 1, n= 2 (L1), or 3 (L2), m= 2 n= 2 (L3) or 3 (L4), and the pentadentate RCH2(SCH2CH2)4SCH2R (L5)(R = benzimidazol-2-yl) compounds formed 1:1 copper(II) perchlorate complexes. Some of the quadridentate compounds also formed complexes of the type CuLX2(X = Cl-, NO3- or BF4-). All the complexes exhibited an absorption band around 30 000 cm-1 originating from a S(σ )→ CuII charge-transfer transition. In solution the ClO4- and BF4- salts of [CuL1]2+ exhibit only one ligand-field band (14 800 cm-1) while the other complexes show two bands (≈ 11 000, 15 000-16 000 cm-1). The polycrystalline EPR spectra of the former complexes are axial while those of the other complexes are rhombic. The cryogenic solution EPR spectra of the former complexes differ from those of the other complexes by exhibiting comparatively low gII values and well resolved nitrogen superhyperfine structures. All these spectral features suggest a unique 'folded' geometry for the [CuL1]2+ complex. Among the tetrathioether complexes, the CuII-CuI redox potential increases with increase in the number of six-membered chelate rings, implying an increase in preference for the copper(I) over the copper(II) state. For copper(II) complexes of bis(benzimidazolyl) thioether ligands with all-five-membered chelate rings the potential increases with increase in the number of thioether donors.
Item Type: | Article |
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Source: | Copyright of this article belongs to Royal Society of Chemistry. |
ID Code: | 31022 |
Deposited On: | 27 Dec 2010 06:54 |
Last Modified: | 05 Mar 2011 06:26 |
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