Effect of hydrogen bonding and solvent polarity on the fluorescence quenching and dipole moment of 2-methoxypyridin-3-yl-3-boronic acid (Record no. 8518)

MARC details
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fixed length control field a
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20190315103055.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 190313b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 8040
Author Melavanki, Raveendra
245 ## - TITLE STATEMENT
Title Effect of hydrogen bonding and solvent polarity on the fluorescence quenching and dipole moment of 2-methoxypyridin-3-yl-3-boronic acid
250 ## - EDITION STATEMENT
Volume, Issue number Vol. 56(12), December
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. New Delhi
Name of publisher, distributor, etc. NISCAIR
Year 2018
300 ## - PHYSICAL DESCRIPTION
Pagination 989-996
520 ## - SUMMARY, ETC.
Summary, etc. Two photophysical properties namely, fluorescence quenching and dipole moment (both ground state and excited state) of 2-methoxypyridin-3-yl-3-boronic acid (2MPBA) have been investigated in alcohol environment using steady state fluorescence technique at 300 K. In quenching studies, a rare but not unusual observation; negative Stern-Volmer (S-V) deviation has been noticed. It has been explained using the concept of solute’s conformational changes in the ground state due to inter-molecular and intra-molecular hydrogen bonding in alcohol environment. The spectroscopic data has been processed using Lehrer equation and thereby Stern-Volmer constant (KSV) has been evaluated. It has been found to be above 100 for most of the solvents used. The data related to dipole moment has been examined using different solvent polarity functions. Theoretical calculation of dipole moment in the ground state has been done using Gaussian software. The general solute–solvent interactions and hydrogen bond interactions have been found to be operative. An appreciable red shift of about 25 nm in the emission spectra has been identified with the rise in solvent polarity and decrease in molar mass of alcohols. It confirms the π→π* transition as well as the possibility of intra-molecular charge transfer (ICT) character in the emitting singlet state of 2MPBA.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4639
Topical term or geographic name entry element PHARMACEUTICS
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 8041
Co-Author Geethanjali, H. S.
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 8042
Co-Author Thipperudrappa, J.
773 0# - HOST ITEM ENTRY
Place, publisher, and date of publication New Delhi CSIR-NISCAIR
International Standard Serial Number 0019-5596
Title Indian journal of pure & applied physics (IJPAP)
856 ## - ELECTRONIC LOCATION AND ACCESS
URL http://nopr.niscair.res.in/handle/123456789/45461
Link text Click here
942 ## - ADDED ENTRY ELEMENTS (KOHA)
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    Dewey Decimal Classification     School of Pharmacy School of Pharmacy Archieval Section 30/03/2019   2018464 19/06/2019 30/03/2019 Articles Abstract Database
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