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Relevant bibliographies by topics / Donor-Acceptor pairs

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Academic literature on the topic 'Donor-Acceptor pairs'

Author: Grafiati

Published: 22 February 2025

Last updated: 31 July 2025

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Journal articles on the topic "Donor-Acceptor pairs"

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Forkel, D., N. Achtziger, A. Baurichter, et al. "Acceptor-donor pairs in germanium." Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms 63, no. 1-2 (1992): 217–20. http://dx.doi.org/10.1016/0168-583x(92)95198-z.

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Zhong, Cheng, Jinwei Zhou, and Charles L. Braun. "Electron-transfer absorption of sterically bulky donor–acceptor pairs: electron donor–acceptor complexes or random pairs?" Journal of Photochemistry and Photobiology A: Chemistry 161, no. 1 (2003): 1–9. http://dx.doi.org/10.1016/s1010-6030(03)00233-8.

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Lee, Jungho, Sang Myeon Lee, Shanshan Chen, et al. "Organic Photovoltaics with Multiple Donor–Acceptor Pairs." Advanced Materials 31, no. 20 (2018): 1804762. http://dx.doi.org/10.1002/adma.201804762.

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Yamamoto, S., J. Pirillo, Y. Hijikata, Z. Zhang, and K. Awaga. "Nanopore-induced host–guest charge transfer phenomena in a metal–organic framework." Chemical Science 9, no. 13 (2018): 3282–89. http://dx.doi.org/10.1039/c7sc05390h.

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Using the “crystal sponge” approach, weak organic electron donor molecules were impregnated and evenly distributed in a crystal of a metal–organic framework (MOF), with the self-assembly of the donor–acceptor pairs with electron acceptor ligands. The nanopores of the MOF confined them and induced a charge transfer phenomenon, which would not occur between donor and acceptor molecules in a bulk scale.

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Cheng, K. H., T. Wiedmer, and P. J. Sims. "Fluorescence resonance energy transfer study of the associative state of membrane-bound complexes of complement proteins C5b-8." Journal of Immunology 135, no. 1 (1985): 459–64. http://dx.doi.org/10.4049/jimmunol.135.1.459.

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Abstract Human complement protein C8 was labeled with the fluorescent chromophores fluorescein-5-isothiocyanate (FITC), 3-(4-isothiocyanatophenyl)-7-diethylamine-4-methyl coumarin (IPM), eosin-5-isothiocyanate (EOS), or Texas Red (sulforhodamine-101-sulfonyl chloride; TR) with only minor reduction in the specific hemolytic activity of the protein. The distribution of C5b-8 complexes bound to sheep erythrocyte membranes was investigated by monitoring fluorescence resonance energy transfer (RET) between the following RET donor/acceptor pairs of labeled C8: FITC-C8/EOS-C8, IPM-C8/EOS-C8, and FITC

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Sheng, Yinghong, and Jerzy Leszczynski. "Theoretical Study of the Substituent and Solvent Effects on the Molecular Structures, Absorption and Emission Spectra of Open-Form Spiropyrans." Collection of Czechoslovak Chemical Communications 69, no. 1 (2004): 47–62. http://dx.doi.org/10.1135/cccc20040047.

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The effects of substituents and solvents on the molecular structures, excitation energies and emission energies of a series of donor-acceptor substituted spiropyrans were investigated using the density functional methods. Different donor-acceptor pairs lead to alternations of the molecular structures. A relationship between the strengths of donor-acceptor pairs and the structural parameter BLA (bond length alternation) was examined and discussed. The impact on geometrical parameters induced by the solvents is more significant than that caused by the substituents, as indicated by the larger BLA

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Harvey, Pierre D., Mikhail A. Filatov, and Roger Guilard. "Bis- and trisporphyrin bio-inspired models for bacterial antennas and photosystems." Journal of Porphyrins and Phthalocyanines 15, no. 11n12 (2011): 1150–71. http://dx.doi.org/10.1142/s1088424611004221.

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This review presents the synthetic aspects and photophysical properties of trimeric systems constructed with a first unit consisting of a cofacial porphyrin and then of another porphyrin attached as a side arm. Two scenarios are dealt with. The first one is the case where the three chromophores are different, called donor 1–donor 2–acceptor, specifically where the cofacial fragment is composed of donor 1 and donor 2, and the side arm is the acceptor. They are considered as models for the apo-proteins used in the LH II (light harvesting device) in the purple photosynthetic bacteria. The second

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POY, Cecília Dominical, and Marinônio Lopes CORNÉLIO. "Electron migration in DNA matrix: an electron transfer reaction." Eclética Química 23 (1998): 99–109. http://dx.doi.org/10.1590/s0100-46701998000100009.

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This paper brings an active and provocative area of current research. It describes the investigation of electron transfer (ET) chemistry in general and ET reactions results in DNA in particular. Two DNA intercalating molecules were used: Ethidium Bromide as the donor (D) and Methyl-Viologen as the acceptor (A), the former intercalated between DNA bases and the latter in its surface. Using the Perrin model and fluorescence quenching measurements the distance of electron migration, herein considered to be the linear spacing between donor and acceptor molecule along the DNA molecule, was obtained

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Poy, Cecília Dominical, and Marinônio Lopes Cornélio. "Electron migration in DNA matrix: an electron transfer reaction." Ecletica Quimica 23, no. 1 (1998): 99–109. http://dx.doi.org/10.26850/1678-4618eqj.v23.1.1998.p99-109.

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This paper brings an active and provocative area of current research. It describes the investigation of electron transfer (ET) chemistry in general and ET reactions results in DNA in particular. Two DNA intercalating molecules were used: Ethidium Bromide as the donor (D) and Methyl-Viologen as the acceptor (A), the former intercalated between DNA bases and the latter in its surface. Using the Perrin model and fluorescence quenching measurements the distance of electron migration, herein considered to be the linear spacing between donor and acceptor molecule along the DNA molecule, was obtained

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10

Lu, Xin. "Single photon emitters originating from donor–acceptor pairs." Journal of Semiconductors 44, no. 1 (2023): 010401. http://dx.doi.org/10.1088/1674-4926/44/1/010401.

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Dissertations / Theses on the topic "Donor-Acceptor pairs"

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Tautz, Raphael Verfasser], and Jochen [Akademischer Betreuer] [Feldmann. "Charge separation in organic photovoltaics : enhanced formation of weakly bound polaron pairs in donor-acceptor-copolymers / Raphael Tautz. Betreuer: Jochen Feldmann." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2013. http://d-nb.info/1031380655/34.

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Nguyen, Thi Huyen Trang. "Optical and spin properties of 3D methylammonium lead iodine single crystals." Electronic Thesis or Diss., université Paris-Saclay, 2025. http://www.theses.fr/2025UPAST002.

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Les pérovskites halogénées (PHs) sont apparues comme une nouvelle classe de matériaux semiconducteurs très prometteurs pour des applications en photovoltaïque et optoélectronique. Ces matériaux présentent des propriétés remarquables telles qu'un long temps de vie et une importante longueur de diffusion des porteurs de charge malgré une densité de défauts élevée. Cependant, l'origine physique de la tolérance aux défauts des PHs est encore très débattue. Une meilleure compréhension de la nature et de l'impact des défauts est encore nécessaire pour optimiser les dispositifs. De plus, de part nota

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Mecker, Christoph J. Chemistry Faculty of Science UNSW. "The synthesis of advanced " special pair " models for the photosynthetic reaction centre." Awarded by:University of New South Wales. School of Chemistry, 2000. http://handle.unsw.edu.au/1959.4/17835.

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Multi-step photoinduced electron transfer takes place over a large distance in the photosynthetic reaction centres (PRCs). Electron donor in this life-spending event is the photo-excited 'special pair', a unit of two electronically coupled porphyrinoid chromophores. Bacteriopheophytin and two quinone molecules function as electron acceptors and contribute to the charge separation with almost unit quantum efficiency. The natural photosynthetic reaction centre is the most sophisticated molecular electronic device to date and interest is high in increasing our understanding of the basic quantum

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Delices, Annette. "Organized Organic Dye / Hole Transporting Materials for TiO2- and ZnO- based Solid-State Dye-Sensitized Solar Cells (s-DSSCs)." Electronic Thesis or Diss., Sorbonne Paris Cité, 2017. https://theses.md.univ-paris-diderot.fr/DELICES_Annette_2_va_20170929.pdf.

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En raison des problèmes d'instabilité à moyen termes des cellules solaires à colorant (DSSC), l'électrolyte liquide à base d'iodure a été remplacé par plusieurs types de matériaux solides transport de trous (HTM) pour obtenir des DSSCs à l'état solide (s-DSSCs). Parmi ces matériaux, l’utilisation des polymères conducteurs(PC) a attiré une attention considérable en raison de leur bonne stabilité, de leur haute conductivité et de la facilité de leur dépôt sur le semi-conducteur mésoporeux TiO2. Dans ce travail de thèse, plusieurs s-DSSCs basées sur des PC utilisés comme HTM ont été développés da

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Faulmann, Christophe. "Conducteurs derives de metaux de transition : complexes moleculaires, polymeres, oxydes de cuivre." Toulouse 3, 1988. http://www.theses.fr/1988TOU30160.

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Mecker, Christoph J. "The synthesis of advanced "special pair" models for the photosynthetic reaction centre /." 2000. http://www.library.unsw.edu.au/~thesis/adt-NUN/public/adt-NUN20011128.150754/index.html.

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Book chapters on the topic "Donor-Acceptor pairs"

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Gutowski, J., K. Sebald, and T. Voss. "ZnSe: donor acceptor pairs." In New Data and Updates for III-V, II-VI and I-VII Compounds. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-92140-0_341.

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Gutowski, J., K. Sebald, and T. Voss. "ZnTe: donor-acceptor-pairs." In New Data and Updates for III-V, II-VI and I-VII Compounds. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-92140-0_361.

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Gutowski, J., K. Sebald, and T. Voss. "Cd1–xZnxTe: donor acceptor pairs." In New Data and Updates for III-V, II-VI and I-VII Compounds. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-92140-0_246.

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Gutowski, J., K. Sebald, and T. Voss. "CdTe: donor-acceptor pairs, free-to-bound transitions." In New Data and Updates for III-V, II-VI and I-VII Compounds. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-92140-0_235.

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Gutowski, J., K. Sebald, and T. Voss. "ZnSe: donor-acceptor pairs, free-to-bound transitions." In New Data and Updates for III-V, II-VI and I-VII Compounds. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-92140-0_342.

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Mikhailova, Valentina A., Sergey V. Feskov, Vladimir N. Ionkin, Vladislav V. Yudanov, and Anatoly I. Ivanov. "Nonequilibrium Ultrafast Charge Transfer Reactions in Photoexcited Donor-Acceptor Pairs." In Chemistry for Sustainable Development. Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-90-481-8650-1_19.

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7

Pispisa, B., A. Palleschi, M. Venanzi, and G. Zanotti. "Conformational features of sequential peptides probed by fluorescent donor-acceptor pairs." In Peptides. Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0683-2_272.

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Ivanov, I. G., Anne Henry, and Erik Janzén. "Donor-Acceptor Pair Luminescence of Phosphorus-Aluminum and Nitrogen-Aluminum Pairs in 4H SiC." In Silicon Carbide and Related Materials 2005. Trans Tech Publications Ltd., 2006. http://dx.doi.org/10.4028/0-87849-425-1.601.

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Zehe, A., E. Reynoso, and A. Ramírez. "Quenching of Luminescence Emission due to a Transient Bonding State of Donor-Acceptor Pairs at High Excitation Levels in GaAlAs Crystals Doped to Compensation." In Materials Science Forum. Trans Tech Publications Ltd., 2005. http://dx.doi.org/10.4028/0-87849-962-8.457.

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Dischler, Bernhard. "Donor–Acceptor Pair Transitions in Diamond." In Handbook of Spectral Lines in Diamond. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-22215-3_10.

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Conference papers on the topic "Donor-Acceptor pairs"

1

Khoussa, Khoukha, Patrick Leveque, and Larbi Boubchir. "On the use of Machine Learning to Discover Novel Donor-Acceptor Pairs For Organic Photovoltaic Devices." In 2024 IEEE International Conference on Big Data (BigData). IEEE, 2024. https://doi.org/10.1109/bigdata62323.2024.10825948.

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Gryczynski, Ignacy, Zygmunt Gryczynski, Wieslaw M. Wiczk, Jozef Kusba, and Joseph R. Lakowicz. "Effect of molecular ordering on distance distributions of flexible donor-acceptor pairs." In OE/LASE '92, edited by Joseph R. Lakowicz. SPIE, 1992. http://dx.doi.org/10.1117/12.58257.

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Oleshko, Vladimir, and Svetlana Vilchinskaya. "Spectral-kinetic characteristics Of donor-acceptor pairs in ZnSe and CdS crystals." In 2012 7th International Forum on Strategic Technology (IFOST). IEEE, 2012. http://dx.doi.org/10.1109/ifost.2012.6357557.

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Maliwal, Badri P., Jozef Kusba, and Joseph R. Lakowicz. "Dimensionality of energy transfer between intercalated and surface-bound donor-acceptor pairs in DNA." In OE/LASE '92, edited by Joseph R. Lakowicz. SPIE, 1992. http://dx.doi.org/10.1117/12.58253.

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Sensfuss, Steffi, Maher Al-Ibrahim, Alexander Konkin, et al. "Characterization of potential donor acceptor pairs for polymer solar cells by ESR, optical, and electrochemical investigations." In Optical Science and Technology, SPIE's 48th Annual Meeting, edited by Zakya H. Kafafi and Paul A. Lane. SPIE, 2004. http://dx.doi.org/10.1117/12.505628.

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Wiczk, Wieslaw M., Peggy S. Eis, Mayer N. Fishman, Michael L. Johnson, and Joseph R. Lakowicz. "Global analysis of distance distribution data for donor-acceptor pairs with different Förster distances." In OE/LASE '90, 14-19 Jan., Los Angeles, CA, edited by Joseph R. Lakowicz. SPIE, 1990. http://dx.doi.org/10.1117/12.17757.

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Roy, Sayan, Zixuan Hu, Sabre Kais, and Peter Bermel. "Tailoring Donor-Acceptor Pairs of Tungsten-based Transition Metal Di-Chalcogenides (TMDCs) for Improved Photovoltaic Current Generation." In 2019 IEEE 46th Photovoltaic Specialists Conference (PVSC). IEEE, 2019. http://dx.doi.org/10.1109/pvsc40753.2019.8981337.

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Akin, Onur, Tuncay Ozel, and Hilmi Volkan Demir. "Cascading plasmonic and nonradiative energy transfer interactions by plasmon-coupling only donor or only acceptor quantum dots of the energy transfer pairs." In 2010 23rd Annual Meeting of the IEEE Photonics Society (Formerly LEOS Annual Meeting). IEEE, 2010. http://dx.doi.org/10.1109/photonics.2010.5699021.

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Hormann, A., E. J. C. Olson, P. F. Barbara, et al. "Time Resolved Electron Transfer Studies Between Metallointercalators in DNA." In International Conference on Ultrafast Phenomena. Optica Publishing Group, 1996. http://dx.doi.org/10.1364/up.1996.sab.6.

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This paper reports the first ultrafast studies on the rates of DNA-mediated forward and reverse electron transfer between photoexcited [M(phen)2dppz]2+ (M=Ru or Os, phen =1,10-phenanthroline, dppz = dipyrido[3,2:a-2′,3′:c]-phenazine) and various electron acceptors in order to ultimately determine the distance dependence of electron transfer kinetics with DNA as an environment.1,2 Previously Barton, Turro, and coworkers have presented evidence that electron transfer in DNA can occur rapidly over an extraordinarily large distance3 with a more shallow distance dependence than that for other media

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Sun, J. W., G. Zoulis, J. C. Lorenzzi, et al. "Splitting of close N-Al donor-acceptor-pair spectra in 3C-SiC." In 2010 WIDE BANDGAP CUBIC SEMICONDUCTORS: FROM GROWTH TO DEVICES: Proceedings of the E-MRS Symposium∗ F∗. AIP, 2010. http://dx.doi.org/10.1063/1.3518273.

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