Please use this identifier to cite or link to this item:
http://localhost:8080/xmlui/handle/123456789/2104
Title: | THERMAL AND SPECTROSCOPIC STUDIES OF DIVALENT TRANSITION METAL HYDRAZINE COMPLEXES WITH 2- NAPHTHOXY ACETIC ACID |
Authors: | N, Aruna Devi S, Vairam |
Keywords: | Hydrazine complexes IR 1-Naphthoxy acetic acid Thermal analysis |
Issue Date: | 10-Nov-2012 |
Publisher: | Journal of Engineering, Computers and Applied Sciences |
Abstract: | Complexes of 1-Naphthoxy acetic acid of divalent transition ions, with neutral hydrazine were prepared and characterized by the spectroscopic methods, IR & UV- visible, magnetic measurements and simultaneous TG – DTA methods. They are sparingly soluble in water and ethanol, formulated as [M(N2H4)2{2- C10H7OCH2(COO)}2].4H2O where M = Co & Ni, [M(N2H4){2-C10H7OCH2 (COO)}2] . nH2O where M = Mn, Zn & Cd ; n = 0 or 1and [Cu(N2H4){2-C10H7OCH2 (COO)}2] at pH 6. IR spectra of the compounds show υN-N in 954 -983 cm-1 region corresponding to coordinated, neutral bridging N2H4 ion and the symmetric υCO and asymmetric υCO in 1363-1400 cm-1 and 1598 - 1623 cm-1 evidence the complex formation respectively. Naphthoate complexes show weight loss due to dehydration and dehydrazination from 50°C to 290 °C and a strong exothermic decomposition between 290°C and 750°C leading to the formation of corresponding metal oxides as end products. The UV-Visible spectra and magnetic moment values of the compounds reveal their geometry, probably distorted octahedral with CN 6 for Ni (II), Co (II), Zn (II) & Mn (II) and tetrahedral for Cd and square planar for Cu complex with CN 4 |
URI: | http://www.borjournals.com/ http://localhost:8080/xmlui/handle/123456789/2104 |
ISSN: | 2319-5606 |
Appears in Collections: | International Journals |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
THERMAL AND SPECTROSCOPIC STUDIES OF DIVALENT TRANSITION METAL HYDRAZINE COMPLEXES WITH 2- NAPHTHOXY ACETIC ACID.docx | 10.89 kB | Microsoft Word XML | View/Open |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.