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Donor transfer

Values of CP measured in the presence of added PMMA (for example) will depend on how the PMMA was prepared and its molecular weight (i.e. on the concentration of unsaturated ends). PMMA formed by radical polymerization in the presence of a good H-donor transfer agent (or by anionic polymerization) would have only saturated chain ends. These PMMA chains should have a different transfer constant to those formed by normal radical polymerization where termination occurs by a mixture of combination and disproportionation. This could account for some of the variation in the values of CP for this polymer... [Pg.322]

First entry on each line is the tag. Square brackets enclose the probe donor + transfer enzyme (where applicable) or reaction. Probe organic fluorophores, nanoparticles (can be QDs as in methods 2, 3, 8, 9) or a bridging/recognition moiety. If desired, the latter can serve in a second orthogonal reaction ( piggyback strategy). See text. Biotin readout probes linked to avidin, streptavidin, anti-biotin 7[101] ... [Pg.502]

The authors suggest that the photoexdted electron donor transfers an electron to the sulfonyl group of the tosylamine to provide an anion-radical that undergoes a heterolytic S — N bond cleavage to produce the deblocked amine after protonation as well as tosylsulfonic and sulfuric add. The function of the reducing agent is to reduce spedes such as the dimethoxybenzene cation-radical and the sulfonyl radical. [Pg.86]

The compression towards the active site revealed in Fig. 24 is what causes the donor-acceptor distances for the hydride and proton transfers to reach their minimum. When they reach their minimum, interactions across the donor, transferring atom, and acceptor are initiated. The events that occur next are critical for... [Pg.345]

As expected, the inferred value for rF turned out to be larger than the value based upon the spectral overlap integral because that analysis ignores donor-donor transfer prior to donor-acceptor transfer. The current theory takes proper account of this fact. [Pg.125]

FRET is the process by which one fluorophore, "the donor," transfers energy to a second fluorophore, "the acceptor." When both chromophores are fluorescent, FRET occurs. In the case of FRET between fluorophores, the emission spectrum of the donor fluorophore must overlap with the absorption spectrum of the acceptor. In this case, the emission from the donor excites the acceptor causing it to emit light (fluoresce). The efficiency of FRET depends on the distance between the two fluorophores, the spectral overlap, and the relative orientations between the donor emission dipole and the acceptor absorption dipole. [Pg.2]

Fig. 11. Schematic representation of transfer processes observed within an inhomogeneously broadened line using pulsed TRFLN. Experimental traces illustrate the dynamics observed within the P state of Pr iLaF, as a function of time. Information on the microscopic interactions producing the transfer are carried in the manner in which the background develops. TRFLN has proven very useful in the study of like-ion or donor-donor transfer. Data from Huber et al. (1977). Fig. 11. Schematic representation of transfer processes observed within an inhomogeneously broadened line using pulsed TRFLN. Experimental traces illustrate the dynamics observed within the P state of Pr iLaF, as a function of time. Information on the microscopic interactions producing the transfer are carried in the manner in which the background develops. TRFLN has proven very useful in the study of like-ion or donor-donor transfer. Data from Huber et al. (1977).
Conventional spectroscopic methods have been more than adequate to demonstrate the existence of donor to acceptor transfer and have allowed the extraction of the donor to acceptor transfer rates in a variety of lanthanide doped solids. In order to accomplish this extraction, a model is assumed to fit an observed decay. Implicit in this assumption is an estimate of the relative magnitude of the donor to donor transfer rate relative to the donor to acceptor rate. The former cannot be easily measured directly using broad band sources. [Pg.472]


See other pages where Donor transfer is mentioned: [Pg.144]    [Pg.190]    [Pg.248]    [Pg.16]    [Pg.14]    [Pg.215]    [Pg.265]    [Pg.150]    [Pg.291]    [Pg.1418]    [Pg.440]    [Pg.39]    [Pg.43]    [Pg.81]    [Pg.109]    [Pg.117]    [Pg.413]    [Pg.633]    [Pg.735]    [Pg.124]    [Pg.913]    [Pg.64]    [Pg.114]    [Pg.198]    [Pg.248]    [Pg.6]    [Pg.117]    [Pg.429]    [Pg.63]    [Pg.543]    [Pg.201]    [Pg.400]    [Pg.472]    [Pg.811]   


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Acetyl group, donor transfer

Anions as Electron Donors in Charge-Transfer Salts

Charge transfer and other donor---acceptor PLC complexes

Charge transfer complexes, biological electron donor-acceptor

Charge transfer dithiolene-donor complexes

Charge transfer donor-acceptor sites, molecular

Charge transfer transitions, donor-acceptor

Charge-transfer absorption band different electron donors

Charge-transfer absorption band donor

Charge-transfer donor-acceptor complexes

Charge-transfer interactions electron-donor-acceptor

Cyclohexadiene, 1,4-, hydrogen donor transfer hydrogenolysis

Donor back electron transfer

Donor charge transfer absorption

Donor charge transfer fluorescence

Donor charge-transfer assemblies

Donor contact charge transfer

Donor electron transfer

Donor energy transfer

Donor-Acceptor energy transfer

Donor-acceptor arrangements intramolecular charge transfer

Donor-acceptor charge transfer

Donor-acceptor complex Charge-transfer complexes

Donor-acceptor complexes photoinduced electron transfer

Donor-acceptor distance, electron-transfer

Donor-acceptor distance, electron-transfer coupling

Donor-acceptor distances, energy-transfer studies

Donor-acceptor pairs charge-transfer process

Donor-acceptor transfer

Donor-acceptor transfer compounds

Donor-acceptor transfer compounds photochemistry

Electron Transfer in Hydrogen-Bonded Donor-Acceptor Supramolecules

Electron donor pairs, charge transfer systems

Electron donor-acceptor transfer compounds

Electron donors charge transfer interactions

Electron donors intramolecular charge transfer

Electron transfer dithiolene-donor complexes

Electron transfer donor acceptor complexes

Electron transfer donor radical cations

Electron transfer donor-acceptor pairing

Electron transfer donor-acceptor separation

Electron transfer from donor to monomer

Electron transfer in donor-bridge-acceptor supermolecules

Electron-transfer donor-acceptor salts

Energy Transfer Within Noncovalently Linked Donor-Acceptor Complex

Energy transfer donor-acceptor distance

Energy transfer processes, donor-acceptor interaction

Energy transfer, from donor to acceptor

Exciplexes, Electron Donor-Acceptor Complexes, and Related Charge-transfer Phenomena

Excitation energy transfer donor-bridge-acceptor system

Forster resonance energy transfer donor

Intramolecular charge transfer alternating donor-acceptor

Nonlinear optical response of charge-transfer excitons at donor-acceptor interface

Photoinduced Electron Transfer in Donor-Acceptor Systems

Photoinduced electron transfer donor-acceptor compounds

Primary donor-to-carotenoid triplet energy transfer

Pyridinium salts, charge-transfer donors

Recognition Based on Cation Control of Photoinduced Electron Transfer in Nonconjugated Donor-Acceptor Systems

Resonance energy transfer donor lifetimes

Single-Step Electron Transfer Process in Acceptor-DNA-Donor Systems

Transfer hydrogenation ammonium formate hydrogen donor

Transfer hydrogenation hydrogen donors

Tunneling charge transfer bands of donor-acceptor pairs attached to proteins

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