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Fluorescence quenching internal

In general, the presence of heavy atoms as substituents of aromatic molecules (e.g. Br, I) results in fluorescence quenching (internal heavy atom effect) because of the increased probability of intersystem crossing. In fact, intersystem crossing is favored by spin-orbit coupling whose efficiency has a Z4 dependence (Z is the atomic number). Table 3.3 exemplifies this effect. [Pg.56]

Intersystem crossing (i.e. crossing from the first singlet excited state Si to the first triplet state Tj) is possible thanks to spin-orbit coupling. The efficiency of this coupling varies with the fourth power of the atomic number, which explains why intersystem crossing is favored by the presence of a heavy atom. Fluorescence quenching by internal heavy atom effect (see Chapter 3) or external heavy atom effect (see Chapter 4) can be explained in this way. [Pg.30]

Furthermore, the quenching of internal residues in proteins by ionic quenchers, although not strong, is quite detectable.(56) A double-quenching method was developed to separate fluorescence quenching parameters characteristic of solvent-exposed and buried fluorophores.(57) The method uses two types of quenchers simultaneously, one type penetrating and the other not penetrating into the protein matrix. [Pg.79]

F. Tanaka and N. Mataga, Fluorescence quenching dynamics of tryptophan in proteins. Effect of internal rotation under potential barrier, Biophys. J. 51, 487-495 (1987). [Pg.111]

Add 500 J,L of crystal violet solution to the reaction mixture, and analyze another 10,000 cells. Crystal violet quenches extracellular fluorescein fluorescence of attached, uningested particles (18). The histogram profile in the presence of crysta 1 violet represents the fluorescence of internalized particles (see Note 8). [Pg.287]

Fisher, M. and C. Cumming. Detection of trace concentrations of vapor phase nitroaro-matic explosives by fluorescence quenching of novel polymer materials, in Proceedings of 7th International Symposium on the Analysis and Detection of Explosives, Defense Evaluation and Research Agency, Edinburgh, Scotland, UK, June, 2001. [Pg.149]

Figure 4.2 Jablohski diagram for a molecule in the singlet ground state (S0). Abs, absorption F, fluorescence 1C, internal conversion ISC, intersystem crossing Ph, phosphorescence Q, quenching VR, vibrational relaxation... Figure 4.2 Jablohski diagram for a molecule in the singlet ground state (S0). Abs, absorption F, fluorescence 1C, internal conversion ISC, intersystem crossing Ph, phosphorescence Q, quenching VR, vibrational relaxation...
A decrease in internal factors (radiationless processes which transfer a molecule into the state S0) as well as from external factors (interactions of excited molecules with other molecules). In the latter case, we distinguish photophysical and photochemical mechanisms of quenching. In analytical chemistry we have, first of all, take the concentration of a fluorescent substance into account, because the so-called concentration quenching may set in at higher concentrations. This phenomenon commences at a certain threshold concentration (C0) and the yield is an exponential function of concentration ... [Pg.60]

In both the procedures, by varying to, the dimensions of the synthesised particles can be altered. The pictorial representations of the above protocols are illustrated in Fig. 6.2. As can be seen, the internal phenomenon of droplet fusion followed by fission takes place. The materials formed during fusion by reaction get distributed among the droplets upon fission. By probability, some droplets may remain empty which is more in dilute solution of the reactants. The occurrence of the process of fusion and fission has been established by the TRFQ (time-resolved fluorescence quenching method [ 18-20]). The internal dynamics of the disperse particles essentially guide the formation characteristics of nanoparticles. [Pg.183]


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Fluorescent quenching

Internal fluorescence

Quenching internal

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