𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Solvent dependence of pyranine fluorescence and UV-visible absorption spectra

✍ Scribed by Noga Barrash-Shiftan; Brina (Beth) Brauer; Ehud Pines


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
232 KB
Volume
11
Category
Article
ISSN
0894-3230

No coin nor oath required. For personal study only.

✦ Synopsis


Fluorescence and UV-visible absorption spectra of HPTS (8-hydroxy-1,3,6-pyrenetrisulphonic acid trisodium salt, pyranine) were measured in a variety of solvents. Fluorescence maxima (in kcal mol -1 ) can be correlated with the Kosower Z parameter (r = 0.901), the Dimroth-Reichardt E T (30) parameter (r = 0.900) and the Winstein Y parameter (r = 0.916) using one-parameter fits. Good correlations (r = 0.98) were obtained for HPTS fluorescence in ethanol-water mixtures using the Y, Y OTs and Z parameters. Fluorescence maxima of HPTS in aqueous sulphuric acid solutions gave an excellent correlation with Y OTs (r = 0.991). Multi-parameter correlations, indicating the significance of specific solvent interactions, were also studied. In addition, fluorescence maxima correlate well with maximum/minimum ratios obtained from UV-visible absorption experiments. Results can be applied in the use of HPTS as a molecular probe of solvent environments and for extension of the Y OTs scale in acidic solutions. HPTS is a unique molecular probe, not only because of its photoacidic properties and its widespread use as a pH-sensitive biosensor, but also because of its relative stability in acidic environments.


πŸ“œ SIMILAR VOLUMES


Substituent and solvent effects on UV-vi
✍ P. Lakshmi Praveen; D. P. Ojha πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons 🌐 English βš– 387 KB

A computational approach has been carried out on liquid crystalline disubstituted biphenylcyclohexanes (BCHs) of general formula R-C 6 H 10 -C 6 H 4 -C 6 H 4 -X with R: C 3 H 7 ; X: H (BCH30) and R: C 5 H 11 ; X: CN (BCH5CN) using the CNDO/S + CI and INDO/S + CI methods. These methods have been empl

UV-visible absorption, fluorescence, and
✍ Krzysztof Polewski; Wanda Maciejewska πŸ“‚ Article πŸ“… 1993 πŸ› Elsevier Science 🌐 English βš– 533 KB

An extensive spectroscopic study of the amylose-Rose Bengal complex in aqueous solution has been undertaken in order to explain the physical and chemical mechanism of the complexation phenomenon. UV-visible absorption, fluorescence, and optical rotatory measurements provided information on the compl

Solvent Shifts and Signal Enhancement in
✍ J.R. Bowser; P.F. Gavin; N.D. Danielson πŸ“‚ Article πŸ“… 1993 πŸ› Elsevier Science 🌐 English βš– 194 KB

Hexamethyldisiloxane [ \(\mathrm{HMDS},\left(\mathrm{Me}_{3} \mathrm{Si}_{2} \mathrm{O}\right.\) ] has been found to be a useful solvent modifier for analytical studies of certain herbicides which contain aromatic rings. This solvent causes large bathochromic shifts in the \(\pi \rightarrow \pi^{*}\

A Theoretical Study of the UV/Visible Ab
✍ Wen-Ge Han; Tiqing Liu; Fahmi Himo; Alexei Toutchkine; Donald Bashford; Klaus M. πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 311 KB πŸ‘ 1 views

## Abstract Using the density‐functional vertical self‐consistent reaction field (VSCRF) solvation model, incorporated with the conductor‐like screening model (COSMO) and the self‐consistent reaction field (SCRF) methods, we have studied the solvatochromic shifts of both the absorption and emission

He(I) photoelectron and uv/visible absor
✍ R.E. Ballard; Jimmy Jones; Elizabeth Sutherland; Chun Bae Lee πŸ“‚ Article πŸ“… 1983 πŸ› Elsevier Science 🌐 English βš– 540 KB

The Ht<I) photoelectron spectra ha%e been measured of tetra-N-butyhmmonium salts of N;. NOS snd SO< in ad+nitrile solution; there are peaks or shoulders for Nj at 6.9 cV (lQ\_', for NO; at 7.0 eV (6~1)~' and 5.6 cV (Ibz)-I. and for NO; at =S.O eV (la;)-' 3s N; + N-methylpyridiniuiuh and x9.0 eV. Als

Solvent effects on absorption and fluore
✍ Y. Richter; I.B. Berlman; I. Agranat πŸ“‚ Article πŸ“… 1977 πŸ› Elsevier Science 🌐 English βš– 406 KB

Three representative diphenyltriafulvenes, 4,4'-dicy.mo-1 ,2-diphenyltriafulvenc (I), hexaphenyltriapentafulvalene (II) and IO-(3,3diphenylcyclopropenyliden)-anthrone (III) have been investigated. On excitation. the dipole moment of I decreases and reverses sign, i.e., from a value of 7.9 D in the g