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Journal articles on the topic 'Electron charge transfer'

Author: Grafiati

Published: 4 June 2021

Last updated: 7 February 2022

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1

Fujitsuka, Mamoru, and Tetsuro Majima. "Charge transfer in DNA." Pure and Applied Chemistry 85, no. 7 (2013): 1367–77. http://dx.doi.org/10.1351/pac-con-12-09-09.

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In the past few decades, charge transfer in DNA has attracted considerable attention from researchers in a wide variety of fields ranging from bioscience and physical chemistry to nanotechnology. Charge transfer in DNA has been investigated using various techniques. Among them, time-resolved spectroscopic methods have provided information on charge-transfer dynamics in DNA, an important basis for therapy applications, nanomaterials, and so on. In charge transfer in DNA, holes and excess electrons act as positive and negative charge carriers, respectively. Hole-transfer (HT) dynamics have been

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2

Hess, B., H. L. Lin, J. E. Niu, and W. H. E. Schwarz. "Electron Density Distributions and Atomic Charges." Zeitschrift für Naturforschung A 48, no. 1-2 (1993): 180–92. http://dx.doi.org/10.1515/zna-1993-1-237.

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Abstract Accurate electron densities and X-ray form factors of Li, Be, F and their ions have been calculated. Electron correlation, crystal fields and ionic charge transfer change the form factors by up to a few percent, mainly in the range of sin θ/ λ < 1/3 Â -1 . Although electron correlation and crystal fields are small perturbations, their effects on the density and form factor are not additive. Densities or form factors of atomic and ionic systems are very similar; [Li0F0] and [Li+F-] procrystals differ by an effective charge transfer of not more than 0.4 e. Charge transfer and charge

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3

Zhu, Yimei, and J. Tafto. "Direct imaging of charge transfer." Proceedings, annual meeting, Electron Microscopy Society of America 54 (August 11, 1996): 680–81. http://dx.doi.org/10.1017/s0424820100165860.

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The electron holes confined to the CuO2-plane are the charge carriers in high-temperature superconductors, and thus, the distribution of charge plays a key role in determining their superconducting properties. While it has been known for a long time that in principle, electron diffraction at low angles is very sensitive to charge transfer, we, for the first time, show that under a proper TEM imaging condition, it is possible to directly image charge in crystals with a large unit cell. We apply this new way of studying charge distribution to the technologically important Bi2Sr2Ca1Cu2O8+δ superc

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4

Li, Sheng-Yong, Zuo-Bang Sun та Cui-Hua Zhao. "Charge-Transfer Emitting Triarylborane π-Electron Systems". Inorganic Chemistry 56, № 15 (2017): 8705–17. http://dx.doi.org/10.1021/acs.inorgchem.6b02847.

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5

Selenius, Elli, Sami Malola, Mikael Kuisma, and Hannu Häkkinen. "Charge Transfer Plasmons in Dimeric Electron Clusters." Journal of Physical Chemistry C 124, no. 23 (2020): 12645–54. http://dx.doi.org/10.1021/acs.jpcc.0c02889.

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6

Yoon, Kyung Byung. "Electron- and charge-transfer reactions within zeolites." Chemical Reviews 93, no. 1 (1993): 321–39. http://dx.doi.org/10.1021/cr00017a015.

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7

Bush, N., K. Stefanov, D. Hall, D. Jordan, and A. Holland. "Simulations of charge transfer in Electron Multiplying Charge Coupled Devices." Journal of Instrumentation 9, no. 12 (2014): C12042. http://dx.doi.org/10.1088/1748-0221/9/12/c12042.

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8

Matyushov, Dmitry V. "Non-Ergodic Electron Transfer in Mixed-Valence Charge-Transfer Complexes." Journal of Physical Chemistry Letters 3, no. 12 (2012): 1644–48. http://dx.doi.org/10.1021/jz300630t.

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9

Miller, John B., and James R. Salvador. "Photoinduced Electron-Transfer Substitution Reactions via Unusual Charge-Transfer Intermediates." Journal of Organic Chemistry 67, no. 2 (2002): 435–42. http://dx.doi.org/10.1021/jo015896k.

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10

Jarzęba, Włodzimierz. "Ultrafast electron transfer in arene - Br atom charge transfer complexes." Journal of Molecular Liquids 68, no. 1 (1996): 1–11. http://dx.doi.org/10.1016/0167-7322(95)00921-3.

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11

Li, Xiaojuan, Cheng Lin, Liang Han, Catherine E. Costello, and Peter B. O’Connor. "Charge remote fragmentation in electron capture and electron transfer dissociation." Journal of the American Society for Mass Spectrometry 21, no. 4 (2010): 646–56. http://dx.doi.org/10.1016/j.jasms.2010.01.001.

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12

Jiwan, J. L. Habib, and J. Ph Soumillion. "Photoinduced Charge Separation in Rigid Bichromophoric Compounds and Charge Transfer State Electron Transfer Reactivity." Journal of Physical Chemistry 99, no. 39 (1995): 14223–30. http://dx.doi.org/10.1021/j100039a007.

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13

Cupellini, Lorenzo, Paweł Wityk, Benedetta Mennucci, and Janusz Rak. "Photoinduced electron transfer in 5-bromouracil labeled DNA. A contrathermodynamic mechanism revisited by electron transfer theories." Physical Chemistry Chemical Physics 21, no. 8 (2019): 4387–93. http://dx.doi.org/10.1039/c8cp07700b.

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14

Fialko, Nadezhda, Maxim Olshevets, and Victor Lakhno. "Charge Transfer in Dimer with Dissipation." EPJ Web of Conferences 224 (2019): 03006. http://dx.doi.org/10.1051/epjconf/201922403006.

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The study of the charge transfer processes in biomacromolecules such as DNA is essential for the development of nanobioelectronics, design and construction of DNA-based nanowires, memory devices, logical elements, etc. Mathematical and computer modeling of charge transfer in biopolymer chains is an important part of these investigations. Some properties of charge transfer can be demonstrated by modeling of two-site chain. Based on the semi-classical Holstein model we consider a system of two sites and charged particle (electron or hole) in which the oscillations of the first site are not relat

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15

Mavroyannis, Constantine. "Charge transfer electron–exciton complexes in single crystals." Canadian Journal of Chemistry 63, no. 7 (1985): 1345–48. http://dx.doi.org/10.1139/v85-229.

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We have considered the excitation spectrum arising from the coherent electron–exciton pairing in crystals at low temperatures. For the pairing processes, three different types of excitons have been considered: Frenkel excitons (tightly bound), Wannier–Mott excitons (loosely bound), and excitons of the intermediate binding. Expressions for the gap functions and transition temperatures at which metal-to-nonmetal phase transitions occur have been derived and discussed for each type of pairing. In the electron pairing with the intermediate exciton, the dispersion relations which determine the exci

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16

Schlag, E. W., and R. D. Levine. "Ionization, charge separation, charge recombination, and electron transfer in large systems." Journal of Physical Chemistry 96, no. 26 (1992): 10608–16. http://dx.doi.org/10.1021/j100205a010.

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17

Tran-Thi, T. H., A. M. Koulkes-Pujo, J. C. Mialocq, and G. Folcher. "Influence of Viscous Media on Charge Transfer Reactions." Laser Chemistry 5, no. 6 (1986): 351–66. http://dx.doi.org/10.1155/lc.5.351.

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The influence of viscous H2O-Dextran media on two charge transfer reactions has been investigated using laser photolysis coupled with pico and nanosecond time resolved absorption spectroscopy.In the first case, a charge-transfer reaction from a solute (potassium ferrocyanide) to the solvent was studied and the electron solvation dynamics was followed. A solvation time delay, depending on the polymer concentration, is observed which indicates that electrons remain quasi-free for longer periods in these media.In the second case, the quenching process of the triplet state of an excited metallo po

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18

Decker, Frank, and Jörg Eichler. "Consistent treatment of electron screening in charge transfer." Physical Review A 39, no. 3 (1989): 1530–33. http://dx.doi.org/10.1103/physreva.39.1530.

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19

Campbell, E. E. B., I. V. Hertel, and S. E. Nielsen. "Electron translation factors in orienting charge transfer collisions." Journal of Physics B: Atomic, Molecular and Optical Physics 24, no. 17 (1991): 3825–36. http://dx.doi.org/10.1088/0953-4075/24/17/018.

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20

Tergiman, Y. S., and M. C. Bacchus-Montabonel. "Double-electron capture processes in charge transfer reactions." International Journal of Quantum Chemistry 99, no. 5 (2004): 628–33. http://dx.doi.org/10.1002/qua.10843.

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21

Nellist, Peter, Gerardo Martinez, Timothy Pennycook, et al. "Imaging charge transfer in crystals using electron ptychography." Acta Crystallographica Section A Foundations and Advances 73, a2 (2017): C121. http://dx.doi.org/10.1107/s2053273317094517.

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22

Telo, João P., Stephen F. Nelsen, and Yi Zhao. "Electron Transfer within Charge-Localized Dinitroaromatic Radical Anions." Journal of Physical Chemistry A 113, no. 27 (2009): 7730–36. http://dx.doi.org/10.1021/jp9017508.

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23

Wang, Ye-Fei, Zhang-Yu Yu, Jian Wu, and Cheng-Bu Liu. "Electron Delocalization and Charge Transfer in Polypeptide Chains." Journal of Physical Chemistry A 113, no. 39 (2009): 10521–26. http://dx.doi.org/10.1021/jp9020036.

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24

Viggiano, A. A., Thomas M. Miller, Amy E. Stevens Miller, Robert A. Morris, Jane M. Van Doren, and John F. Paulson. "SF4: electron affinity determination by charge-transfer reactions." International Journal of Mass Spectrometry and Ion Processes 109 (November 1991): 327–38. http://dx.doi.org/10.1016/0168-1176(91)85112-y.

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25

Kang, E. T. "Charge transfer interactions in polyphenylacetylene-electron acceptor systems." European Polymer Journal 21, no. 11 (1985): 919–24. http://dx.doi.org/10.1016/0014-3057(85)90176-4.

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26

Verma, Sandeep, Sunil Aute, Amitava Das, and Hirendra N. Ghosh. "Proton-Coupled Electron Transfer in a Hydrogen-Bonded Charge-Transfer Complex." Journal of Physical Chemistry B 120, no. 41 (2016): 10780–85. http://dx.doi.org/10.1021/acs.jpcb.6b06032.

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27

Zhang, Wenyan, Chao Kong, Wei Gao, and Gongxuan Lu. "Intrinsic magnetic characteristics-dependent charge transfer and visible photo-catalytic H2 evolution reaction (HER) properties of a Fe3O4@PPy@Pt catalyst." Chemical Communications 52, no. 14 (2016): 3038–41. http://dx.doi.org/10.1039/c5cc09017b.

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The electron transfer and visible-light-driven hydrogen evolution of a ternary nano-architecture could be regulated effectively by electro-magnetic interaction between the magnetic catalysts and photo-generated electrons.

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28

Ashokkumar, P., V. Thiagarajan, S. Vasanthi, and P. Ramamurthy. "Triple fluorescence of acridinedione: Locally excited, photoinduced electron transfer promoted charge transfer and anion induced charge transfer states." Journal of Photochemistry and Photobiology A: Chemistry 208, no. 2-3 (2009): 117–24. http://dx.doi.org/10.1016/j.jphotochem.2009.09.004.

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29

Lou, Zhigang, Shuyan Liang, Jiabei Yuan, et al. "Contrasting Electron and Hole Transfer Dynamics from CH(NH2)2PbI3 Perovskite Quantum Dots to Charge Transport Layers." Applied Sciences 10, no. 16 (2020): 5553. http://dx.doi.org/10.3390/app10165553.

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In this work, the ultrafast transient absorption spectroscopy (TAs) was utilized to first investigate the charge transfer from the emerging FAPbI3 (FA = CH(NH2)2) perovskite quantum dots (PQDs) to charge transport layers. Specifically, we compared the TAs in pure FAPbI3 PQDs, PQDs grown with both electron and hole transfer layers (ETL and HTL), and PQDs with only ETL or HTL. The TA signals induced by photoexcited electrons decay much faster in PQDs samples with the ETL (~20 ps) compared to the pure FAPbI3 PQDs (>1 ns). These results reveal that electrons can effectively transport between co

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30

D'Alessandro, Deanna M., and F. Richard Keene. "Stereochemical effects on intervalence charge transfer." Pure and Applied Chemistry 80, no. 1 (2008): 1–16. http://dx.doi.org/10.1351/pac200880010001.

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Recent work has revealed the first observation of stereochemical effects on intervalence charge transfer (IVCT) in di- and trinuclear mixed-valence complexes. The differential IVCT characteristics of the diastereoisomers of polypyridyl complexes of ruthenium and osmium offer a new and intimate probe of the fundamental factors that govern the extent of electronic delocalization and the barrier to electron transfer. These findings challenge prior assertions that the inherent stereochemical identity of such complexes would have no influence on the intramolecular electron-transfer properties of po

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31

Imato, Keiichi, Ryota Yamanaka, Hidekazu Nakajima, and Naoya Takeda. "Fluorescent supramolecular mechanophores based on charge-transfer interactions." Chemical Communications 56, no. 57 (2020): 7937–40. http://dx.doi.org/10.1039/d0cc03126g.

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Supramolecular mechanofluorophores based on charge-transfer interactions between fluorescent electron-rich pyrene and electron-deficient naphthalene diimide(s) are newly developed and show turn-on fluorescence upon application of mechanical forces.

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32

Jennings, James R., and Qing Wang. "Charge Transport and Interfacial Charge Transfer in Dye-Sensitized Nanoporous Semiconductor Electrode Systems." Key Engineering Materials 451 (November 2010): 97–121. http://dx.doi.org/10.4028/www.scientific.net/kem.451.97.

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General characteristics of dye-sensitized nanoporous semiconductor electrode systems are summarized, with a particular emphasis on dye-sensitized solar cells. Properties of these electrode systems which distinguish them from conventional bulk semiconductor electrodes are highlighted. Current understanding of electron transport in dye-sensitized solar cells, in terms of the diffusion and multiple trapping models, is reviewed. Alternative transport and recombination theories are also briefly reviewed. Electron transfer at the semiconductor/electrolyte interface in dye-sensitized solar cells is r

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33

HABIB JIWAN, J. L., and J. PH SOUMILLION. "ChemInform Abstract: Photoinduced Charge Separation in Rigid Bichromophoric Compounds and Charge Transfer State Electron Transfer Reactivity." ChemInform 27, no. 5 (2010): no. http://dx.doi.org/10.1002/chin.199605029.

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34

Nagamura, T., H. Kawai, T. Ichihara, and H. Sakaguchi. "Photoinduced electron transfer and charge resonance band in ion-pair charge-transfer complexes of styrylpyridinium tetraphenylborate." Synthetic Metals 71, no. 1-3 (1995): 2069–70. http://dx.doi.org/10.1016/0379-6779(94)03170-b.

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35

Kato, Yuki, Ryo Nagao, and Takumi Noguchi. "Redox potential of the terminal quinone electron acceptor QB in photosystem II reveals the mechanism of electron transfer regulation." Proceedings of the National Academy of Sciences 113, no. 3 (2015): 620–25. http://dx.doi.org/10.1073/pnas.1520211113.

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Photosystem II (PSII) extracts electrons from water at a Mn4CaO5 cluster using light energy and then transfers them to two plastoquinones, the primary quinone electron acceptor QA and the secondary quinone electron acceptor QB. This forward electron transfer is an essential process in light energy conversion. Meanwhile, backward electron transfer is also significant in photoprotection of PSII proteins. Modulation of the redox potential (Em) gap of QA and QB mainly regulates the forward and backward electron transfers in PSII. However, the full scheme of electron transfer regulation remains unr

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36

Watson, R. E., M. Weinert, G. W. Fernando, and J. W. Davenport. "Charge transfer, charge tailing, cohesion and electron promotion in the transition metals." Physica B: Condensed Matter 172, no. 1-2 (1991): 289–98. http://dx.doi.org/10.1016/0921-4526(91)90443-i.

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37

Franz, W., P. Lamparter, and S. Steeb. "Electronic Structure of Al-Li Alloys by Means of Electron Microprobe." Zeitschrift für Naturforschung A 42, no. 12 (1987): 1385–90. http://dx.doi.org/10.1515/zna-1987-1203.

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By means of an electron microprobe the lithium-K-and aluminium-K-X-ray emission lines of Al-Li alloys were studied. The Li-line can be well described by the calculated emission line. The evaluation yields the transfer of electrons from the Li-s- to the Al-p-band during alloying. The charge transfer is enhanced by heat treatment. The dependence of the elastic modulus on the charge transfer is discussed.

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38

Holzwarth, Alfred R., Martin Katterle, Marc G. Müller, Ying-Zong Ma, and Valentin Prokhorenko. "Electron-transfer dyads suitable for novel self-assembled light-harvesting antenna/electron-transfer devices." Pure and Applied Chemistry 73, no. 3 (2001): 469–74. http://dx.doi.org/10.1351/pac200173030469.

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The synthesis and photophysical and photochemical characterization of four novel bacterio-chlorin-fullerene dyads with fullerene C60 coupled at various positions and by various bridges to the chlorin ring are described. All dyads undergo rapid charge separation in the sub-picosecond to picosecond time range as characterized by time-resolved fluorescence and transient absorption spectroscopy.

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39

Makita, Hiroki, and Gary Hastings. "Inverted-region electron transfer as a mechanism for enhancing photosynthetic solar energy conversion efficiency." Proceedings of the National Academy of Sciences 114, no. 35 (2017): 9267–72. http://dx.doi.org/10.1073/pnas.1704855114.

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In all photosynthetic organisms, light energy is used to drive electrons from a donor chlorophyll species via a series of acceptors across a biological membrane. These light-induced electron-transfer processes display a remarkably high quantum efficiency, indicating a near-complete inhibition of unproductive charge recombination reactions. It has been suggested that unproductive charge recombination could be inhibited if the reaction occurs in the so-called inverted region. However, inverted-region electron transfer has never been demonstrated in any native photosynthetic system. Here we demon

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40

Fodil, Hamzaoui, and Chouaih Abdelkader. "The electron charge density distribution in a non linear optical compound." Acta Crystallographica Section A Foundations and Advances 70, a1 (2014): C380. http://dx.doi.org/10.1107/s2053273314096193.

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The 4, 4 dimethyl amino-cyanobiphenyl crystal (DMACB) is characterized by its nonlinear optical properties. The intra molecular charge transfer of this molecule (figure-1) results mainly from the electronic transmission of the electro-acceptor (Cyano) and the electro-donor (Di-Methyl-Amino) groups [1]. An accurate electron charge density distribution around the molecule has been calculated from a high-resolution X-ray diffraction study. The data were collected at 123 K using graphite-monochromated Mo-Kα radiation. The crystal structure has been validated and deposited at the Cambridge Crystall

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41

Tamaki, S. "Charge distribution in liquid metals and alloys." Canadian Journal of Physics 65, no. 3 (1987): 286–308. http://dx.doi.org/10.1139/p87-037.

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Electron distribution in liquid metals and charge transfer in liquid alloys are qualitatively and quantitatively discussed in terms of the structure factors and the thermodynamic quantities obtained experimentally. The electron distribution around an ion in liquid metals has been derived from the difference in structure factors determined by X-ray and neutron-diffraction methods with the help of a theoretical calculation of the electron–electron correlation function. Charge transfer in liquid alloys is also estimated by using the partial structure factors in the long-wavelength limit and the T

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42

Craven, Galen T., and Abraham Nitzan. "Electron transfer across a thermal gradient." Proceedings of the National Academy of Sciences 113, no. 34 (2016): 9421–29. http://dx.doi.org/10.1073/pnas.1609141113.

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Charge transfer is a fundamental process that underlies a multitude of phenomena in chemistry and biology. Recent advances in observing and manipulating charge and heat transport at the nanoscale, and recently developed techniques for monitoring temperature at high temporal and spatial resolution, imply the need for considering electron transfer across thermal gradients. Here, a theory is developed for the rate of electron transfer and the associated heat transport between donor–acceptor pairs located at sites of different temperatures. To this end, through application of a generalized multidi

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43

Clark, Catherine D., and Morton Z. Hoffman. "Ion-Pairing Control of Excited-State Electron-Transfer Reactions. Quenching, Charge Recombination, and Back Electron Transfer." Journal of Physical Chemistry 100, no. 18 (1996): 7526–32. http://dx.doi.org/10.1021/jp953747y.

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44

Kako, Masahiro, and Yasuhiro Nakadaira. "Charge transfer complexes and electron transfer reaction of organosilicon and related compounds." Coordination Chemistry Reviews 176, no. 1 (1998): 87–112. http://dx.doi.org/10.1016/s0010-8545(98)00145-3.

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45

Bockman, T. M., and Jay K. Kochi. "Charge-transfer ion pairs. Structure and photoinduced electron transfer of carbonylmetalate salts." Journal of the American Chemical Society 111, no. 13 (1989): 4669–83. http://dx.doi.org/10.1021/ja00195a022.

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46

Ponnu, Aravindan, Jiha Sung, and Kenneth G. Spears. "Ultrafast Electron-Transfer and Solvent Adiabaticity Effects in Viologen Charge-Transfer Complexes." Journal of Physical Chemistry A 110, no. 45 (2006): 12372–84. http://dx.doi.org/10.1021/jp0617322.

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47

Wu, K., J. Chen, J. R. McBride, and T. Lian. "Efficient hot-electron transfer by a plasmon-induced interfacial charge-transfer transition." Science 349, no. 6248 (2015): 632–35. http://dx.doi.org/10.1126/science.aac5443.

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48

Kimura, Y., Y. Takebayashi, and N. Hirota. "Electron-Transfer Rate in the Charge Transfer Complex in the Supercritical Fluids." REVIEW OF HIGH PRESSURE SCIENCE AND TECHNOLOGY 7 (1998): 1230–32. http://dx.doi.org/10.4131/jshpreview.7.1230.

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49

Zhang, Jie, Jingwang Cui, and Xiaodong Yang. "Construction of stimuli-responsive materials based on charge transfer and electron transfer." SCIENTIA SINICA Chimica 50, no. 9 (2020): 1045–63. http://dx.doi.org/10.1360/ssc-2020-0079.

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50

Moran, Andrew M., Ponnu Aravindan, and Kenneth G. Spears. "Solvent Adiabaticity Effects on Ultrafast Electron Transfer in Viologen Charge Transfer Complexes." Journal of Physical Chemistry A 109, no. 9 (2005): 1795–801. http://dx.doi.org/10.1021/jp0466082.

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