Mechanism energy transfer

C3.3.4 DEDUCING ENERGY TRANSFER MECHANISMS FROM POPULATION AND VELOCITY DISTRIBUTIONS OF THE SCATTERED BATH MOLECULES ROTATIONAL STATE POPULATION DISTRIBUTIONS FOR VIBRATIONAL EXCITATION OF THE BATH... 

Cutler, M. W. (1995). Characterization and energy transfer mechanism of green-fluorescent protein from Aequorea victoria, Ph.D. Dissertation, Rutgers University, New Brunswick, NJ. 

The fluorescent lifetime of chlorophyll in vivo was first measured in 1957, independently by Brody and Rabinowitch (62) using pulse methods, and by Dmitrievskyand co-workers (63) using phase modulation methods. Because the measured quantum yield was lower than that predicted from the measured lifetime, it was concluded that much of the chlorophyll molecule was non-fluorescent, suggesting that energy transfer mechanisms were the means of moving absorbed energy to reactive parts of the molecule. 

A combination of two separate energy-transfer mechanisms were considered for <7"ub a conduction mechanism as in saturation boiling, and a sensible heat transport mechanism. 

Collisions with a Cl-—C-Cl angle of approximately n, with the CH3C1 dipole oriented, do not form the Cl—CH3C1 complex. Collisions oriented in this manner could yield complexes by T — V, but this is an unimportant energy transfer mechanism.38... 

The observed luminescence properties of the copolymer yarns can be easily explained if an energy transfer mechanism is assumed to be operating (Figure 7). Triplet-triplet energy transfer from the terephthalate units to the 4,4 -biphenyl -dicarboxyl ate units explains both the dual fluorescent/phospho-rescent emissions from the 4,4 -biphenyldicarboxyl ate units as well as the quenched phosphorescence from the terephthalate units. 

Chemiluminescence also occurs during electrolysis of mixtures of DPACI2 99 and rubrene or perylene In the case of rubrene the chemiluminescence matches the fluorescence of the latter at the reduction potential of rubrene radical anion formation ( — 1.4 V) at —1.9 V, the reduction potential of DPA radical anion, a mixed emission is observed consisting of rubrene and DPA fluorescence. Similar results were obtained with the dibromide 100 and DPA and/or rubrene. An energy-transfer mechanism from excited DPA to rubrene could not be detected under the reaction conditions (see also 154>). There seems to be no explanation yet as to why, in mixtures of halides like DPACI2 and aromatic hydrocarbons, electrogenerated chemiluminescence always stems from that hydrocarbon which is most easily reduced. A great number of aryl and alkyl halides is reported to exhibit this type of rather efficient chemiluminescence 155>. 

FIGURE 3.21 (a) Energy transfer mechanisms of phosphorescent dye as a sensitizer and (b) the EL external efficiency of the DCM2 doped devices. (From Baldo, M.A., Thompson, M.E., and Forrest, S.R., Nature, 403, 750, 2000. With permission.)... 

FIGURE 4.8 Energy diagram and proposed energy transfer mechanism in the blend system. (From He, G., Chang, S., Chen, F., Li, Y., and Yang, Y., Appl. Phys. Lett., 81, 1509, 2002. With permission.)... 

Kasha M (1963) Energy transfer mechanisms and the molecular exciton model for molecular aggregates. Radiat Res 20 55-71... 

Murphy CB, Zhang Y, Troxler T, Ferry V, Martin JJ, Jones WE Jr (2004) Probing Forster and Dexter energy-transfer mechanisms in fluorescent conjugated polymer chemosensors. J Phys Chem B 108 1537-1543... 

More convincing proof for a particle-enhanced energy transfer mechanism comes from a study of the concentration dependence of the transfer. Bulk Forster transfer leads to a linear dependence on acceptor concentration with constant donor-to-acceptor ratio. The resonance mechanism would be expected to saturate at (relatively) high concentrations and fall off linearly at very low concentrations. 

For electric multipolar interactions, the energy transfer mechanism can be classified into several types, according to the character of the involved transitions of the donor (D) and acceptor (A) centers. Electric dipole-dipole (d-d) interactions occur when the transitions in D and A are both of electric dipole character. These processes correspond, in general, to the longest range order and the transfer probability varies with l/R, where R is the separation between D and A. Other electric multipolar interactions are only relevant at shorter distances dipole-quadrupole (d-q) interaction varies as l/R, while quadrupole-quadrupole interaction varies as l/R °. 

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