ISSN:
0021-8383
Keywords:
Chemistry
;
Organic Chemistry
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Chemistry and Pharmacology
Notes:
Deactivation Behaviour of Arenes and Heteroarenes. XXXVI. The Solvent and Temperature Dependence of Deactivation Behaviour of 9, 9′-Bis(acridizinium-yl) at High ConcentrationAt room temperature the geometrical structure of the fluoresceing singlet state of 9, 9′-bis(acridizinium-yl) is determined by the solvent. In solvents of the type A (water, methanol, acetonitril) a plain S1-state emits, in the case of the solvent type B (ethanol, propanol-(2)) the S1-state is twisted. Both excited states have different emission spectroscopical properties.At high concentration (c ≥ 10-4 mol l-1) in the case of the solvent type B a new emission band is observed, and the monomer emission is quenched. This new band is interpreted as a fluorescence from a molecular associate in the excited state. The intensity of this associate band is increasing with decreasing temperature. It is shown that this band is the result of molecular association in the ground state. From the photochemical irradiation it follows that only in the case of the solvent type B a photocycloaddition is possible. The plain S1-state does not react.
Additional Material:
3 Ill.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1002/prac.19833250207
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