Triplet acceptors

Note. Both the rearrangement In t-ButanoI) and the double bond isomerization of (114) (In Benzene) are quenched in a diffusion-controlled process by suitable triplet acceptors e.g., naphthalene or 2,5-dimethylhexa-2,4-diene). The rearrangement (114) (118) -I- (120) is also observed on irradiation in... 

Porter and Wilkinson(56) measured the rates of quenching for a variety of triplet donors with triplet acceptors at room temperature in fluid solution by flash photolysis. The appearance of the triplet-triplet absorption spectrum of the acceptor and the simultaneous disappearance of the donor triplet-triplet absorption spectrum provided unequivocal evidence for the triplet-triplet energy transfer process. Table 6.5 provides some of the quenching rate constants reported in this classic paper. 

The most direct demonstration of triplet-triplet energy transfer between the aromatic amino acids is the ODMR study by Rousslang and Kwiram on the tryptophanyl-tyrosinate dipeptide.(57) Since the first excited singlet state of tyrosinate is at lower energy than that of tryptophan, it is possible to excite tyrosinate preferentially. The phosphorescence of this dipeptide, however, is characteristic of tryptophan, which is consistent with the observation that the triplet state of tyrosinate is at higher energy than that of tryptophan, making tryptophan the expected triplet acceptor. 

The reactive excited state in the photodimerization of thymine is probably the triplet state Tt the dimerization process can be quenched by triplet acceptor molecules such as ketones and quinones. 

Sometimes the fluorescence and phosphorescence spectra of a compound in solution overlap. They may be separated as follows. If a suitable triplet energy acceptor is added, this will quench the phosphorescence, leaving the fluorescence unaffected, while a suitable triplet donor will sensitize the phosphorescence in the absence of any fluorescence. Back-strom and Sandros have analyzed the total luminescence spectra of biacetyl, benzil, and anisil in this way, using pyrene as the triplet acceptor and benzophenone as triplet donor.3... 

Consider a photoreactive molecule M. If the triplet state of M is involved in any photochemical reaction, then addition of triplet acceptors to the reaction solution should quench triplet state reactions by the diffusion controlled process... 

The sequence of reactions (31)—(33), illustrated in Fig. 35a for triplet ET occurring from the locally excited triplet acceptor, constitutes a potentially efficient... 

The spin status of the ion pair is another crucial variable affecting the overall efficiency of the process. The forward electron transfer from (or to) a diamagnetic molecule is not affected by the spin status of the excited component. The back electron transfer, however, is forbidden within the triplet ion pairs (it would violate Pauli s exclusion principle). In situations like that the intersystem crossing will very often determine the efficiency of BET. In practice, the triplet state acceptors or donors lead to overall efficiencies that are higher than those observed with singlet state acceptors or donors [38,78,102,103,116]. An additional bonus is the fact that triplet states have longer lifetimes [2] and are efficiently ET-quenched with lower concentrations of the ground state component. Quinones and ketones are the most common triplet acceptors, while aromatic amines often serve as triplet donors. 

Both absorption and emissirm processes may be intramolecular, localized in a single molecule. On the other hand, they can also involve whole crystals that may act as absorbers and emitters. Such energy transfers can manifest themselves in different ways that include sensitized fluorescence or phosphorescence, concentration depolarization of fluorescence, photo-conduction, and formation of triplet acceptor molecules. 

S) and triplet acceptors/annihilators (A) and (b) the associated molecular energetic requirements. 

Energy transfer into a low energy triplet acceptor in which molecule the triplet energy is rapidly degraded to heat typical examples are Ni complexes (11.10). 

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