Synthesis, spectroscopic characterization and biological studies of organotin derivatives of 2-(2,6-dichlorophenyl)aminophenylacetic acid

Article abstract of DOI:10.1080/00945710009351864

Infrared, multinuclear NMR, mass and Moessbauer spectral techniques have been used to characterize new organotin compounds of 2-(2,6-dichlorophenyl)aminophenylacetic acid anion with the general formulae R₃SnL, R₂SnL₂ and R

Full text of DOI:10.1080/00945710009351864

This article was downloaded by: [The UC Irvine Libraries]
On: 04 November 2014, At: 16:34
Publisher: Taylor & Francis
Informa Ltd Registered in England and Wales Registered Number: 1072954
Registered office: Mortimer House, 37-41 Mortimer Street, London W1T 3JH,
UK
Synthesis and Reactivity in
Inorganic and Metal-Organic
Chemistry
Publication details, including instructions for
authors and subscription information:
http://www.tandfonline.com/loi/lsrt19
Synthesis, Spectroscopic
Characterization and
Biological Studies of Organotin
Derivatives of 2- (2,6-
dichlorophenyl)aminophenylacetica
Moazzam Hussain Bhatti a , Saqib Ali a , Hajra
Masood a , Muhammad Mazhar a & Sajid Iqbal
Qureshi a
a Department of Chemistry , Quaid-I-Azam
University , 45320, Islamabad, Pakistan
Published online: 23 Apr 2008.
To cite this article: Moazzam Hussain Bhatti , Saqib Ali , Hajra Masood ,
Muhammad Mazhar & Sajid Iqbal Qureshi (2000) Synthesis, Spectroscopic
Characterization and Biological Studies of Organotin Derivatives of 2- (2,6-
dichlorophenyl)aminophenylaceticacid, Synthesis and Reactivity in Inorganic and
Metal-Organic Chemistry, 30:9, 1715-1729, DOI: 10.1080/00945710009351864
To link to this article: http://dx.doi.org/10.1080/00945710009351864
PLEASE SCROLL DOWN FOR ARTICLE
Taylor & Francis makes every effort to ensure the accuracy of all the
information (the “Content”) contained in the publications on our platform.
However, Taylor & Francis, our agents, and our licensors make no
representations or warranties whatsoever as to the accuracy, completeness,
or suitability for any purpose of the Content. Any opinions and views

expressed in this publication are the opinions and views of the authors, and
are not the views of or endorsed by Taylor & Francis. The accuracy of the
Content should not be relied upon and should be independently verified with
primary sources of information. Taylor and Francis shall not be liable for any
losses, actions, claims, proceedings, demands, costs, expenses, damages,
and other liabilities whatsoever or howsoever caused arising directly or
indirectly in connection with, in relation to or arising out of the use of the
Content.
This article may be used for research, teaching, and private study purposes.
Any substantial or systematic reproduction, redistribution, reselling, loan,
sub-licensing, systematic supply, or distribution in any form to anyone is
expressly forbidden. Terms & Conditions of access and use can be found at
http://www.tandfonline.com/page/terms-and-conditions