激发态
化学
溶剂化
基态
分子
荧光
荧光光谱法
光化学
单重态
化学物理
原子物理学
有机化学
物理
量子力学
作者
J. F. Ireland,P. A. H. Wyatt
出处
期刊:Advances in Physical Organic Chemistry
日期:1976-01-01
卷期号:: 131-221
被引量:275
标识
DOI:10.1016/s0065-3160(08)60331-7
摘要
This chapter discusses acid–base properties of electronically excited states of organic molecules. Excited state pK-values are most easily accessible through the use of the Forster cycle. To perform this calculation for a particular molecule, it is necessary to know the ground state equilibrium constant for the reaction in question and to have some measure of the energy difference between the lowest vibrational level of the ground and the excited state in both the B and BH+ forms. The effects of solvation on 0–0 energies are discussed. The changes in molecular fluorescence with acidity give information about the protolytic behavior of the excited singlet state of a compound. Two techniques, phase and pulse fluorometry, are used for the direct measurement of fluorescence decay rates. The excited state acid-base behavior of molecules has direct implications in the field of analytical fluorimetry and phosphorimetry.
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