Effect of the orientation of donor and acceptor on the probability of energy transfer involving electronic transitions of mixed polarization

Biochemistry ◽  
1978 ◽  
Vol 17 (23) ◽  
pp. 5064-5070 ◽  
Author(s):  
Elisha Haas ◽  
Ephraim Katchalski-Katzir ◽  
Izchak Z. Steinberg
Keyword(s):  
Energy Transfer ◽  
Electronic Transitions ◽  
Donor And Acceptor

Control of Förster energy transfer in the vicinity of metallic surfaces and hyperbolic metamaterials

2015 ◽  
Vol 178 ◽  
pp. 395-412 ◽  
Author(s):  
T. U. Tumkur ◽  
J. K. Kitur ◽  
C. E. Bonner ◽  
A. N. Poddubny ◽  
E. E. Narimanov ◽  
...  
Keyword(s):  
Energy Transfer ◽  
Spontaneous Emission ◽  
Practical Importance ◽  
Index Of Refraction ◽  
Metallic Surfaces ◽  
Dielectric Media ◽  
Plasmonic Structures ◽  
Donor And Acceptor ◽  
Förster Energy Transfer ◽  
Photonic States

Optical cavities, plasmonic structures, photonic band crystals and interfaces, as well as, generally speaking, any photonic media with homogeneous or spatially inhomogeneous dielectric permittivity (including metamaterials) have local densities of photonic states, which are different from that in vacuum. These modified density of states environments are known to control both the rate and the angular distribution of spontaneous emission. In the present study, we question whether the proximity to metallic and metamaterial surfaces can affect other physical phenomena of fundamental and practical importance. We show that the same substrates and the same nonlocal dielectric environments that boost spontaneous emission, also inhibit Förster energy transfer between donor and acceptor molecules doped into a thin polymeric film. This finding correlates with the fact that in dielectric media, the rate of spontaneous emission is proportional to the index of refractionn, while the rate of the donor–acceptor energy transfer (in solid solutions with a random distribution of acceptors) is proportional ton−1.5. This heuristic correspondence suggests that other classical and quantum phenomena, which in regular dielectric media depend onn, can also be controlled with custom-tailored metamaterials, plasmonic structures, and cavities.

scholarly journals Horizontal versus vertical charge and energy transfer in hybrid assemblies of semiconductor nanoparticles

2012 ◽  
Vol 3 ◽  
pp. 629-636 ◽  
Author(s):  
Gilad Gotesman ◽  
Rahamim Guliamov ◽  
Ron Naaman
Keyword(s):  
Energy Transfer ◽  
Charge Transfer ◽  
Horizontal Plane ◽  
Quartz Substrate ◽  
Vertical Direction ◽  
Time Resolved ◽  
Transfer Processes ◽  
Donor And Acceptor ◽  
Hybrid Assemblies ◽  
Time Resolved Photoluminescence

We studied the photoluminescence and time-resolved photoluminescence from self-assembled bilayers of donor and acceptor nanoparticles (NPs) adsorbed on a quartz substrate through organic linkers. Charge and energy transfer processes within the assemblies were investigated as a function of the length of the dithiolated linker (DT) between the donors and acceptors. We found an unusual linker-length-dependency in the emission of the donors. This dependency may be explained by charge and energy transfer processes in the vertical direction (from the donors to the acceptors) that depend strongly on charge transfer processes occurring in the horizontal plane (within the monolayer of the acceptor), namely, parallel to the substrate.

scholarly journals Distribution of a Glycosylphosphatidylinositol-anchored Protein at the Apical Surface of MDCK Cells Examined at a Resolution of <100 Å Using Imaging Fluorescence Resonance Energy Transfer

1998 ◽  
Vol 142 (1) ◽  
pp. 69-84 ◽  
Author(s):  
A.K. Kenworthy ◽  
M. Edidin
Keyword(s):  
Energy Transfer ◽  
Lipid Rafts ◽  
Fluorescence Resonance Energy Transfer ◽  
Mdck Cells ◽  
Resonance Energy Transfer ◽  
Resonance Energy ◽  
Membrane Microdomains ◽  
Apical Surface ◽  
Donor And Acceptor ◽  
Fluorescence Resonance

Membrane microdomains (“lipid rafts”) enriched in glycosylphosphatidylinositol (GPI)-anchored proteins, glycosphingolipids, and cholesterol have been implicated in events ranging from membrane trafficking to signal transduction. Although there is biochemical evidence for such membrane microdomains, they have not been visualized by light or electron microscopy. To probe for microdomains enriched in GPI- anchored proteins in intact cell membranes, we used a novel form of digital microscopy, imaging fluorescence resonance energy transfer (FRET), which extends the resolution of fluorescence microscopy to the molecular level (&lt;100 Å). We detected significant energy transfer between donor- and acceptor-labeled antibodies against the GPI-anchored protein 5′ nucleotidase (5′ NT) at the apical membrane of MDCK cells. The efficiency of energy transfer correlated strongly with the surface density of the acceptor-labeled antibody. The FRET data conformed to theoretical predictions for two-dimensional FRET between randomly distributed molecules and were inconsistent with a model in which 5′ NT is constitutively clustered. Though we cannot completely exclude the possibility that some 5′ NT is in clusters, the data imply that most 5′ NT molecules are randomly distributed across the apical surface of MDCK cells. These findings constrain current models for lipid rafts and the membrane organization of GPI-anchored proteins.

Energy transfer in liquid and solid nanoobjects: application in luminescent analysis

2018 ◽  
Vol 4 (3) ◽  
Author(s):  
T. D. Smirnova ◽  
S. N. Shtykov ◽  
E. A. Zhelobitskaya
Keyword(s):  
Energy Transfer ◽  
Physical Phenomenon ◽  
Excitation Energy Transfer ◽  
Electronic Energy ◽  
Luminescence Spectroscopy ◽  
Electronic Excitation Energy Transfer ◽  
Electronic Excitation Energy ◽  
Protein Chemistry ◽  
Luminescent Analysis ◽  
Donor And Acceptor

Abstract Radiationless resonance electronic excitation energy transfer (ET) is a fundamental physical phenomenon in luminescence spectroscopy playing an important role in natural processes, especially in photosynthesis and biochemistry. Besides, it is widely used in photooptics, optoelectronics, and protein chemistry, coordination chemistry of transition metals and lanthanides as well as in luminescent analysis. ET involves the transfer of electronic energy from a donor (D) (molecules or particles) which is initially excited, to an acceptor (A) at the ground state to emit it later. Fluorescence or phosphorescence of the acceptor that occurs during ET is known as sensitized. There do many kinds of ET exist but in all cases along with other factors the rate and efficiency of ET in common solvents depends to a large extent on the distance between the donor and the acceptor. This dependency greatly limits the efficiency of ET and, correspondingly, does not allow the determination of analytes in highly diluted (10–9–10–15 M) solutions. To solve the problem of distance-effect, the effects of concentrating and bring close together the donor and acceptor in surfactant micelles (liquid nanosystems) or sorption on solid nanoparticles are used. Various approaches to promote the efficiency of ET for improvement determination selectivity and sensitivity using liquid and solid nanoobjects is reviewed and analyzed.

Un exemple d'isomérisation radicalaire en chaînes: la photoinduction de l'isomérisation cis–trans de la pentène-3 one-2

1977 ◽  
Vol 55 (22) ◽  
pp. 3915-3926 ◽  
Author(s):  
Armel Rioual ◽  
André Deflandre ◽  
Jacques Lemaire
Keyword(s):  
Energy Transfer ◽  
Quantum Yields ◽  
Unsaturated Ketone ◽  
Chain Process ◽  
Triplet Energy ◽  
Low Concentrations ◽  
Energy Transfers ◽  
Donor And Acceptor ◽  
A Chain ◽  
Triplet Energy Transfer

Mechanisms of the photosensitized cis–trans photoisomerization of 3-penten-2-one which do not imply only classical triplet–triplet energy transfer are proposed; they are based upon measurements of the variations of initial quantum yields of isomerization with the initial donor and acceptor concentrations, the wavelength of excitation, and the nature of the donor and of the solvent. Carbonyl donors (acetophenone, benzophenone, acetone) induce a radical isomerization by a chain process in reducing solvents; the example of acetophenone is specially interesting. In solvents in which the donor is not photoreduced (as benzene or CCl4) classical triplet–triplet energy transfers occur. Sensitization with aromatic donors (benzene, mesitylene) proceeds through triplet–triplet energy transfer at low concentrations of the acceptor. At higher concentrations of acceptor, an exciplex is formed between the ketone and the aromatic in its singlet excited state; this exciplex is deactivated by dissociation and by causing the isomerization of the α,β-unsaturated ketone.

Elektronenanregungsenergieiibergang zwischen ungleichartigen Molekiilen in Losung / Electronic Excitation Energy Transition among unlike Molecules in Solution

1977 ◽  
Vol 32 (2) ◽  
pp. 140-143 ◽  
Author(s):  
J. Kamiński ◽  
A. Kawski
Keyword(s):  
Energy Transfer ◽  
Excitation Energy ◽  
Excitation Energy Transfer ◽  
Energy Transition ◽  
Mutual Orientation ◽  
Resonance Excitation ◽  
Electronic Excitation Energy ◽  
Radiationless Energy Transfer ◽  
Donor And Acceptor ◽  
Acceptor Molecules

In studying the radiationless energy transfer between unlike molecules (heterotransfer) in fluid and rigid solutions the fluctuations of the concentration of the acceptor molecules, as well as the dependence of the probability of resonance excitation energy transfer on the mutual orientation of the transition moments of the interacting donor and acceptor molecules have been taken into account. With these and the assumptions of the shell model of a luminescent centre (A. Kawski and J. Kaminski, Z. Naturforsch. 29 a, 452 [1974]) one obtains the Förster expression for the quantum yield of the donor fluorescence quenched by foreign absorbing substances

Mikrokristallbildung und intermolekulare Triplett-Triplett-Energieiibertragung in festen transparenten Glasern bei 77 K. Das System N-Methylcarbazol/Naphthalin / Microcrystal Formation and Intermolecular Triplet-Triplet Energy Transfer in Rigid Transparent Glasses at 77 K. The System N-Methyl-earbazole / Naphthalene

1984 ◽  
Vol 39 (5) ◽  
pp. 507-508
Author(s):  
M. Zander
Keyword(s):  
Energy Transfer ◽  
Triplet Energy ◽  
Donor And Acceptor ◽  
Triplet Energy Transfer

The efficient intermolecular triplet-triplet energy transfer between N-methylcarbazole (donor) and naphthalene (acceptor) observed at 10-2 ᴍ concentration of donor and acceptor in a rigid transparent methylcyclohexane/n-pentane glass at 77 K is shown to occur in microcrystals of the donor containing small amounts of the acceptor

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