том 116 издание 4 страницы 1345-1355

Origin of Strong Synergism in Weakly Perturbed Binary Solvent System: A Case Study of Primary Alcohols and Chlorinated Methanes

Тип публикацииJournal Article
Дата публикации2012-01-24
scimago Q1
wos Q3
БС2
SJR0.742
CiteScore5.3
Impact factor2.9
ISSN15206106, 15205207, 10895647
Materials Chemistry
Surfaces, Coatings and Films
Physical and Theoretical Chemistry
Краткое описание
A strong synergistic solvation was observed for the mixtures of hydrogen bond donating and accepting solvent pairs. The nature of the interactions between two solvent pairs was investigated with different dye molecules viz. coumarin 480, coumarin 153, 4-aminophthalimide, and p-nitroaniline. Coumarin 480 in differenet alcohols-CHCl(3) (alcohols: MeOH, EtOH, BuOH) binary mixture shows a strong synergism, which is explained in the backdrop of solvent-solvent interactions. Fluorescence quenching of C480 by 1,2-phenylenediamine in the binary solvent mixture exhibited the maximum deviation in quenching constant corresponding to ~0.45 mol fraction of MeOH in MeOH-CHCl(3) binary mixture and hence suggested the maximum extent of hydrogen-bonding interactions prevailing at this proportion of mixture. The solvation behavior of MeOH-CHCl(3) mixture shows strong probe dependence with no synergism observed in p-nitroaniline, which is ascribed to its higher ground state dipole moment (8.8 D) relative to C480 (6.3 D). Interestingly, the strong synergistic signature observed through spectrophotometric measurement of C480 in alcohol-CHCl(3) binary mixture is absent when studied by fluorescence measurement. The higher excited state dipole moment of coumarin 480 (13.1 D) is considered to be the driving force for the absence of synergism in the excited state. In such strongly perturbed systems (due to high dipole moment values) the dominant phenomenon is preferential solvation. Analysis of proton NMR of MeOH-CHCl(3) binary solvent mixture indicates the existence of MeOH-CHCl(3) clusters in the stoichiometric ratio of 1:2.15. Refractive index measurement also infers the existence of hydrogen bonded network structure between MeOH and CHCl(3). A modified Bosch solvent exchange model has been used to determine the feasibility of synergistic behavior and polarity parameter of the mixed solvent structure of MeOH-CHCl(3) binary solvent mixture.
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Gupta S. et al. Origin of Strong Synergism in Weakly Perturbed Binary Solvent System: A Case Study of Primary Alcohols and Chlorinated Methanes // Journal of Physical Chemistry B. 2012. Vol. 116. No. 4. pp. 1345-1355.
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Gupta S., Rafiq S., Kundu M., Sen P. R. Origin of Strong Synergism in Weakly Perturbed Binary Solvent System: A Case Study of Primary Alcohols and Chlorinated Methanes // Journal of Physical Chemistry B. 2012. Vol. 116. No. 4. pp. 1345-1355.
RIS |
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TY - JOUR
DO - 10.1021/jp207741h
UR - https://doi.org/10.1021/jp207741h
TI - Origin of Strong Synergism in Weakly Perturbed Binary Solvent System: A Case Study of Primary Alcohols and Chlorinated Methanes
T2 - Journal of Physical Chemistry B
AU - Gupta, Shradhey
AU - Rafiq, Shahnawaz
AU - Kundu, Mainak
AU - Sen, Pratik Ranjan
PY - 2012
DA - 2012/01/24
PB - American Chemical Society (ACS)
SP - 1345-1355
IS - 4
VL - 116
PMID - 22200245
SN - 1520-6106
SN - 1520-5207
SN - 1089-5647
ER -
BibTex |
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@article{2012_Gupta,
author = {Shradhey Gupta and Shahnawaz Rafiq and Mainak Kundu and Pratik Ranjan Sen},
title = {Origin of Strong Synergism in Weakly Perturbed Binary Solvent System: A Case Study of Primary Alcohols and Chlorinated Methanes},
journal = {Journal of Physical Chemistry B},
year = {2012},
volume = {116},
publisher = {American Chemical Society (ACS)},
month = {jan},
url = {https://doi.org/10.1021/jp207741h},
number = {4},
pages = {1345--1355},
doi = {10.1021/jp207741h}
}
MLA
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Gupta, Shradhey, et al. “Origin of Strong Synergism in Weakly Perturbed Binary Solvent System: A Case Study of Primary Alcohols and Chlorinated Methanes.” Journal of Physical Chemistry B, vol. 116, no. 4, Jan. 2012, pp. 1345-1355. https://doi.org/10.1021/jp207741h.