alexa Abstract | Synthesis, characterization and potentiometric study on stability of N-[2-hydroxy-1-napthalydene]-2-methylanilline complexes with transition elements

Journal of Chemical and Pharmaceutical Research
Open Access

OMICS International organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations

700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)

Original Articles Open Access


Organic ligand N-[2-hydroxy-1-napthalydene]-2-methylanilline (3) was obtained by the condensation of 2-hydroxy- 1-napthalydene (1)with 2-methylanilline (2). Formation of Schiff base (3) confirmed by TLC, M.P., IR and C,H,N analysis. Further formation of complexes of transition elements like Mn(II), CO(II), Ni(II), Cu(II) and Zn(II) with organic ligand N-[2-hydroxy-1-napthalydene]-2-methylanilline was studied by the potentiometric technique at 27±0.10C in 60%(v/v) Dioxane - water medium at 0.1M (NaClO4) ionic strength. The stability constants of N-[2- hydroxy-1-napthalydene]-2-methylanilline with transition elements were evaluated and Order of stability constant found as Cu >Co > Zn >Ni > Mn.

To read the full article Peer-reviewed Article PDF image

Author(s): Shivaji Jadhava Megha Raia Farooque Basheer Ansarib and R K Pardeshic


Schiff base, Transition elements, Potentiometric technique and Stability constant, potentiometric study

Peer Reviewed Journals
Make the best use of Scientific Research and information from our 700 + peer reviewed, Open Access Journals
International Conferences 2017-18
Meet Inspiring Speakers and Experts at our 3000+ Global Annual Meetings

Contact Us

© 2008-2017 OMICS International - Open Access Publisher. Best viewed in Mozilla Firefox | Google Chrome | Above IE 7.0 version