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Chelating Behaviour of Dihydrothieno[3,4, d] Pyridazine Derivatives with Some Lanthanide and Actinide Metals |
DUBLIN | CORE | METADATA ITEM | METADATA FOR THIS DOCUMENT |
1 | Title | Title of Document | Chelating Behaviour of Dihydrothieno[3,4, d] Pyridazine Derivatives with Some Lanthanide and Actinide Metals |
2 | Creator | Author's name, affiliation, country | NADIA AHMED ABDALLA Chemistry Department, Faculty of Science, Aswan University, Aswan-81528, Egypt |
3 | Subject | Dicipline(s) | Chemical Science |
3 | Subject | Keywords | Dihydrothieno Pyridazine, Complexes, IR, NMR, Mass Spectra, Thermal analysis |
4 | Description | Abstract | Coordination compound formed by the interaction of Dihydrothieno[3,4-d]pyridazine with La(III), Ce(III), Sm(III), Th(IV) and UO2(II) are prepared and characterized by elemental analysis, IR, 1H NMR Mass spectra and thermal analysis. The analysis data indicate that the ligand acts as bidentate on chelation, thermogravimetric analysis confirm the presence of coordinates water. The IR spectra indicate that coordination takes place through the nitrogen of amino group and C=O group of pyridazine ring. Antimicrobial activity of selected compounds against some bacterial strains was tested and confirm the antimicrobial activities of the ligand increase on coordination with the metal ion. |
5 | Publishers | Organizing agency, location | WWW Publications, India |
6 | Contributor | Sponsor(s) | - |
7 | Date | Date (YYYY-MM-DD) | - |
8 | Type | Status & genre | Peer-reviewed Article |
8 | Type | Type | |
9 | Formate | File Formate | PDF |
10 | Identifier | Uniform Resource Identifier | Click Here |
10 | Identifier | Digital Object Identifier | |
11 | Source | Journal/conference title; vol., no. (Year) | Chemical Science Transactions, Volume 4 , Number (4), (2015) |
12 | Lanuguage | English=en | en |
13 | Relation | Supp.files | |
14 | Coverage | | - |
15 | Copyright | Copyright and permissions | |
Chemical Science Transactions | Chem Sci Trans | CST | Online Chemistry Journal | Open Access
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