Fluorescent Signaling Based on Control of Excited State Dynamics. Biarylacetylene Fluorescent Chemosensors
- 23 January 2002
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 124 (7) , 1178-1179
- https://doi.org/10.1021/ja017309i
Abstract
We have previously reported that metal ion binding could restrict the excited state rotation of a biaryl chromophore, suppressing intersystem crossing and leading to increased emission. We have now applied the restriction of excited state dynamics to suppression of the other fundamental nonradiative decay pathway, internal conversion, in biarylacetylenes. This indicates that both nonradiative decay pathways are subject to conformational control, and that this signaling pathway should be generally accessible in simple flexible fluorophores.Keywords
This publication has 5 references indexed in Scilit:
- Dual-Signaling Fluorescent Chemosensors Based on Conformational Restriction and Induced Charge TransferAngewandte Chemie International Edition in English, 2001
- Fluorescent Chemosensors Based on Conformational Restriction of a Biaryl FluorophoreJournal of the American Chemical Society, 2001
- Structure and Dynamics of S2 and S1 Diphenylacetylene in Solution Studied by Picosecond Time-Resolved CARS SpectroscopyThe Journal of Physical Chemistry A, 1998
- The central CC bond stretch frequencies and structure of S2 and S1 diphenylacetylene in solution studied by picosecond time-resolved CARS spectroscopyChemical Physics Letters, 1997
- Kinetic study of ion exchange of phosphate ions for chloride in a hydrotalcite-like compound, Ni0.75Al0.25(OH)2Cl0.25.mH2O, using the pressure-jump techniqueThe Journal of Physical Chemistry, 1984