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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Pandey, H N | - |
| dc.contributor.author | Mathur, Pavan | - |
| dc.date.accessioned | 2017-02-01T06:31:31Z | - |
| dc.date.available | 2017-02-01T06:31:31Z | - |
| dc.date.issued | 1995-03 | - |
| dc.identifier.issn | 0975-0975(Online); 0376-4710(Print) | - |
| dc.identifier.uri | http://nopr.niscair.res.in/handle/123456789/39979 | - |
| dc.description | 186-190 | en_US |
| dc.description.abstract | The tetradentate tripodal ligand N,N',N" tris(2-benzothiazolylmethyl)amine has been used to synthesize mononuclear copper(lI) complexes with exogenous ligands X (where X=OAc-, HCOO-, N ), imidazole, benzimidazole). The X-band EPR spectra, in forzen DMF, indicate the trend of g values which in general is gll > g > 2.0. The complex with azide as a exogenous ligand is trigonal bipyramidal in nature. The covalency parameter, ɑ2, has been evaluated and reflects the increasing trend of covalency in the order imidazole > benzimidazole > acetate > formate. The E1/2 values for the above complexes have been reported. The present series of complexes possess a distorted five coordinate site, and may have potential relevance to type 3 copper sites in rhus laccase and ascorbate oxidase. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | NISCAIR-CSIR, India | en_US |
| dc.rights | CC Attribution-Noncommercial-No Derivative Works 2.5 India | en_US |
| dc.source | IJC-A Vol.34A(03) [March 1995] | en_US |
| dc.title | Synthesis and characterization of copper(ll) complexes of tris(2-benzothiazolylmethyl)amine:A tripodal N4donor ligand | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-A Vol.34A(03) [March 1995] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCA 34A(3) 186-190.pdf | 1.21 MB | Adobe PDF | View/Open |
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), imidazole, benzimidazole). The X-band EPR spectra, in forzen DMF, indicate the trend of g values which in general is gll > g
> 2.0. The complex with azide as a exogenous ligand is trigonal bipyramidal in nature. The covalency parameter, ɑ2, has been evaluated and reflects the increasing trend of covalency in the order imidazole > benzimidazole > acetate > formate. The E1/2 values for the above complexes have been reported. The present series of complexes possess a distorted five coordinate site, and may have potential relevance to type 3 copper sites in rhus laccase and ascorbate oxidase.