Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
2004-8-5
pubmed:abstractText
Spectroscopic and photophysical properties of safranine O (Sf) were investigated in binary water/solvent mixtures. It was found that these properties are strongly solvent-dependent. A blue shift is observed for both the ground-state absorption and the triplet-triplet main absorption band when the solvent polarity augments. At the same time a red shift of the fluorescence emission band takes place. These facts are interpreted in terms of higher dipole moment of the dye molecule in the S(1) state as compared with the S(0) state, while a decrease in the dipole moment of the triplet state T(n) with respect to the triplet state T(1) occurs. The Stokes' shift and the fluorescence lifetime shows a linear correlation with the E(T)(30) parameter, while a non-linear behavior is observed when a correlation with models of a continuous dielectric solvent is attempted. These results suggest the operation of strong specific interactions of Sf with solvent molecules, most likely hydrogen bonding. From fluorescence lifetime and quantum yield determinations, as well as intersystem-crossing quantum yields, the solvent dependence of the photophysical kinetic parameters were obtained. The radiative fluorescence rate constant can be adequately reproduced by calculations based on the UV-Vis absorption and emission spectra, as given by the Strickler-Berg equation.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
1386-1425
pubmed:author
pubmed:issnType
Print
pubmed:volume
60
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2433-9
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed:year
2004
pubmed:articleTitle
Photophysical properties of safranine O in protic solvents.
pubmed:affiliation
Departamento de Química, Universidad Nacional de Río Cuarto, 5800 Río Cuarto, Argentina.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't