Publication | Closed Access
Photophysical Primary Processes in Solutions of p‐Substituted Dialkylanilines
94
Citations
23
References
1979
Year
Dual FluorescenceOrganic Charge-transfer CompoundBiochemistryPhotochemistryNatural SciencesMechanistic PhotochemistryPolar SolutionsMolecular SwitchOrganic ChemistryChemistryPhotophysical Primary ProcessesMolecular ChemistryPhotophysical PropertyFirst Case
Abstract The variation of the acceptor substituent in p‐substituted dimethylanilines leads to a reversal of the 1 L b and 1 L a type excited states. By fluorescence and fluorescence polarization measurements it is shown to occur between p‐dimethylaminobenzonitrile (DMABN) and p‐di‐methylaminoacetophenone. — As a consequence, the two components of dual fluorescence emitted by these molecules in polar solutions originate from different hypersurfaces in the first case but from the same in the second case. The fluorescence of p‐dimethylaminobenzoic acid ethyl ester in nonpolar solutions is assigned to arise from S 2 .
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