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Quinine fluorescence quenching at low ionic strength
Author(s) -
Bigger S. W.,
Watkins P. J.,
Verity B.
Publication year - 2000
Publication title -
international journal of chemical kinetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.341
H-Index - 68
eISSN - 1097-4601
pISSN - 0538-8066
DOI - 10.1002/1097-4601(2000)32:8<473::aid-kin4>3.0.co;2-9
Subject(s) - chemistry , ionic strength , quenching (fluorescence) , bromide , chloride , ion , ionic bonding , dication , analytical chemistry (journal) , inorganic chemistry , fluorescence , aqueous solution , chromatography , organic chemistry , physics , quantum mechanics
The effect of ionic activity on the quenching of the quinine dication fluorescence by chloride and bromide ions is examined in solutions of sufficiently low ionic strength to enable ionic activities to be taken into account by means of the Debye‐Hückel equation. An equation for the dependence of the Stern‐Volmer constant on the ionic strength is derived in a novel way and an iterative, linear least‐squares computer program is described from which the optimized values of the ionic size parameter for chloride ( a Cl −= 4.56 ± 0.07 Å) and bromide ( a Br −= 4.98 ± 0.23 Å) quenching were obtained. The ratio of these parameters ( a Br −/ a Cl −= 1.09 ± 0.07) is found to be similar to the ratio of the ionic radii of the two species, r Br −/ r Cl −= 1.08. The experimental results suggest that the quenching of quinine fluorescence by bromide ions is about 28% faster than that observed for chloride ions. The results are consistent with the notion that the quenching process is a dynamic one involving the formation of an activated complex whose rate of deactivation is dependent on the ionic strength of the medium. © 2000 John Wiley & Sons, Inc. Int J Chem Kinet 32: 473–477, 2000