Forster quenching

In long-range, or Forster, quenching, energy transfer occurs without collisions between molecules. Dipole-dipole coupling between the excited fluorophore and the quencher account for the transfer. The dependence of the degree of quenching on the quencher... 

The monomer and exclmer fluorescence decay profiles obtained from P2NMA and 2NMA-co-6.2% BDHM dissolved In benzene at room temperature are compared In Figures 4 (i) and (ii) respectively. The steady-state quenching Is accompanied by a significant decrease in both the monomer and excimer fluorescence decay times as well as a reduction of the risetime of the excimer fluorescence to one which is response-limited. The decay of the excimer fluorescence from the copolymer Is nonexponential but is fitted successfully by the Forster quenching function [5,13] given In equation (6). 

Self-assembly of functionalized carboxylate-core dendrons around Er +, Tb +, or Eu + ions leads to the formation of dendrimers [19]. Experiments carried out in toluene solution showed that UV excitation of the chromophoric groups contained in the branches caused the sensitized emission of the lanthanide ion, presumably by an energy transfer Forster mechanism. The much lower sensitization effect found for Eu + compared with Tb + was ascribed to a weaker spectral overlap, but it could be related to the fact that Eu + can quench the donor excited state by electron transfer [20]. 

The pioneering work Forster and Hoffmann [28] on the viscosity dependence of the fluorescence quantum yield of triphenylmethane dyes (TPM) has set the foundation for several reports in these dyes (Fig. 12). It was found that both an ability to twist around the carbocationic center and the donor-acceptor properties are important [66], Specifically, a strong intramolecular quenching is observed for 34 that is virtually absent (two orders of magnitude slower quenching rate) in the bridged... 

Energy transfer, as described by Forster [78], requires a long range dipole-dipole interaction between the donor and the acceptor fluorophore. This energy transfer is possible at distances between 2 and 10 nm. Contrary to what happens in collisional quenching, there is no need for physical contact between the two molecules. 

Forster resonance energy transfer (FRET) is a form of quenching. For a fluorophore (donor) to be quenched by another molecule (acceptor), three criteria must be met ... 

Some tryptophans do not exhibit phosphorescence because of quenching by specific sites from within the protein. The absence of phosphorescence could be due to quenching of either the singlet state or the triplet state. For example, in horse heart cytochrome c the tryptophan is adjacent to the heme, and its fluorescence is quenched by Forster transfer to the heme. Since the singlet state is populating the triplet state, the lack of observable phosphorescence is likely to be due to an unpopulated triplet state. Another example where the redox center of the protein interacts with the tryptophan excited states is found in azurin. The copper(II) quenches both the singlet and triplet states.(28)... 

Triplet decay in the [Mg, Fe " (H20)] and [Zn, Fe (H20)] hybrids monitored at 415 nm, the Fe " / P isosbestic point, or at 475 nm, where contributions from the charge-separated intermediate are minimal, remains exponential, but the decay rate is increased to kp = 55(5) s for M = Mg and kp = 138(7) s for M = Zn. Two quenching processes in addition to the intrinsic decay process (k ) can contribute to deactivation of MP when the iron containing-chain of the hybrid is oxidized to the Fe P state electron transfer quenching as in Eq. (1) (rate constant kj, and Forster energy transfer (rate constant kj. The triplet decay in oxidized hybrids thus is characterized by kp, the net rate of triplet disappearance (kp = k -I- ki -I- kj. The difference in triplet decay rate constants for the oxidized and reduced hybrids gives the quenching rate constant, k = kp — kj, = k, -I- k , which is thus an upper bound to k(. 

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