Spectroscopic Studies on the Molecular Complex of the Drug Atenolol with Iodine

Spectroscopic and spectrofluorimetric studies were made of the interaction between the drug atenolol and iodine. The interaction was found to proceed through the initial formation of a charge transfer (CT) complex as an intermediate species. The product of this interaction has been isolated and char...

Full description

Saved in:
Bibliographic Details
Published in:Journal of solution chemistry Vol. 38; no. 12; pp. 1558 - 1572
Main Authors: Pandeeswaran, M., Elango, K. P.
Format: Journal Article
Language:English
Published: Boston Springer US 01-12-2009
Springer
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Spectroscopic and spectrofluorimetric studies were made of the interaction between the drug atenolol and iodine. The interaction was found to proceed through the initial formation of a charge transfer (CT) complex as an intermediate species. The product of this interaction has been isolated and characterized using UV-Vis, FT-IR and Raman spectroscopic techniques. Formation of the triodide species was confirmed by its electronic and Raman spectra. Peaks appeared in Raman spectrum of the isolated product at 153, 102 and 85 cm −1 that are assigned to ν as (I-I), ν s (I-I) and respectively, which confirmed the presence of the ion. The stoichiometry of the complex was found to be 1:2. The rate of their reaction has been measured as a function of time and solvent. Pseudo-first-order rate constants for the reaction were measured at various temperatures and the thermodynamic activation parameters (Δ G # ,Δ S # and Δ H # ) were computed. Preliminary fluorescence quenching studies indicated that the interaction between atenolol and iodine is spontaneous and proceeds through a CT complex, and the quenching of fluorescence of atenolol by iodine increases as the extent of such complexation increases
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0095-9782
1572-8927
DOI:10.1007/s10953-009-9467-3