Fluorescence lifetime measurements and biological imaging.
Fluorescence lifetime measurements and biological imaging.
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DOI:
10.1021/cr900343z
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发表时间:
2010-05-12
期刊:
影响因子:
62.1
通讯作者:
Achilefu, Samuel
中科院分区:
文献类型:
--
作者:
Berezin, Mikhail Y.;Achilefu, Samuel
When a molecule absorbs a photon of appropriate energy, a chain of photophysical events ensues, such as internal conversion or vibrational relaxation (loss of energy in the absence of light emission), fluorescence, intersystem crossing (from singlet state to a triplet state), and phosphorescence, as shown in the Jablonski diagram for organic molecules (Figure 1). Each of the processes occurs with a certain probability, characterized by decay rate constants (k). It can be shown that the average length of time τ for the set of molecules to decay from one state to another is reciprocally proportional to the rate of decay: τ) 1/k. This average length of time is called the mean lifetime or simply lifetime. It can also be shown that the lifetime of a photophysical process is the time required by a population of N electronically excited molecules to be reduced by a factor of e. Correspondingly, the fluorescence lifetime is the time required by a population of excited fluorophores to decrease exponentially to N/e via the loss of energy through fluorescence and other nonradiative processes. The lifetime of photophycal
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