Lifetime detection methods

Luminescence has been used in conjunction with flow cells to detect electro-generated intennediates downstream of the electrode. The teclmique lends itself especially to the investigation of photoelectrochemical processes, since it can yield mfonnation about excited states of reactive species and their lifetimes. It has become an attractive detection method for various organic and inorganic compounds, and highly sensitive assays for several clinically important analytes such as oxalate, NADH, amino acids and various aliphatic and cyclic amines have been developed. It has also found use in microelectrode fundamental studies in low-dielectric-constant organic solvents. 

Abstract The response signal of an immense number of fluorescence reporters with a broad variety of structures and properties can be realized through the observation in changes of a very limited number of fluorescence parameters. They are the variations in intensity, anisotropy (or polarization), lifetime, and the spectral changes that allow wavelength-ratiometric detection. Here, these detection methods are overviewed, and specific demands addressed to fluorescence emitters for optimization of their response are discussed. 

To be detected, the presence of target should provide significant change of % recorded within the time resolution of the method. Application of lifetime detection in sensing is based on several principles ... 

Implementation of time domain FLIM methods is comparatively straightforward in laser scanning microscopes (LSMs). Here, pointscanning is used so that single channel lifetime detection suffices. In principle, standard fluorescence lifetime detection equipment developed for spectroscopy can be used in combination with point-scanning systems and a pulsed laser. 

Laser flash photolysis methods have also been applied to the study of nitrenium ion trapping rates and hfetimes. This method relies on short laser pulses to create a high transient concentration of the nitrenium ion, and fast detection technology to characterize its spectrum and lifetime The most frequently used detection method is fast UV-vis spectroscopy. This method has the advantage of high sensitivity, but provides very little specific information about the structure of the species being detected. More recently, time-resolved infrared (TRIR) and Raman spectroscopies have been used in conjunction with flash photolysis methods. These provide very detailed structural information, but suffer from lower detection sensitivity. 

Despite the short lifetimes of most silylenes, improvements in flash photolysis techniques for their generation and time-resolved spectroscopic detection methods in the past decade have made possible direct kinetic measurements on the reactions of silylenes. The purpose of these kinetic studies has been to elucidate the mechanisms of silylene reactions. While considerable work remains to be done, transition state structures and activation barriers are emerging from these experiments, and aspects of silylene insertion and addition mechanisms have been revealed that were not uncovered by product studies and were, indeed, unexpected. 

Electronic Absorption and Luminescence (Volume 12) Absorption and Luminescence Probes Fluorescence Imaging Microscopy Fluorescence Lifetime Measurements, Applications of Indirect Detection Methods in Capillary Electrophoresis Surface Measurements using Absorption/Luminescence... 

In parallel to the development of the above methods for detecting spontaneous decompositions of ions with a longer lifetime than those fragmenting in the source, decomposition reactions induced by collisions in a cell where gas pressure is much higher than that in the analyzers were developed. The gas may be nitrogen, helium, etc. The collision cell is located either in the first FFR or second FFR and the respective detection methods are linked scan B/E or B /E) and MIKE. 

Phase shift fluorimetry, the other important method for measuring fluorescent lifetimes, also continues to be developed and improved. The effects of Inaccurate reference lifetimes on the interpretation of frequency domain fluorescence data can be removed or minimized by a least squares analysis method.The direct collection of multi-frequency data for obtaining fluorescence lifetimes can be achieved by the use of digital parallel acquisition in frequency domain fluorimetry. Frequency domain lifetime measurement has been used for on-line fluorescence lifetime detection of eluents in chromatography. An unusual use of frequency domain measurement which has been reported is for the examination of photon migration in living tissue. Photons in the... 

A second direct optical-detection method for selective population and depopulation is microwave-induced delayed phosphorescence in zero field (Bq = 0) [25]. Figure 7.26 shows the phosphorescence intensity from quinoline in a durene (tet-ramethyl benzene) host crystal at T= 1.35 K as a function of the time after the end of the UV excitation. The phosphorescing zero-field component here is Tz). Its lifetime is considerably shorter than those of the other two zero-field components, from which furthermore no phosphorescence is emitted. If the zero-field transition... 

With the advent of powerful lasers capable of generating short light pulses, a new era of research commenced [62-64]. Notably, the new light sources permit the measurement of lifetimes of excited states and the detection of short-lived intermediates such as free radicals and ions. The concomitant development of sophisticated detection methods has also brought about continuous progress during the... 

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