Gotowe bibliografie tematyczne / Charge transfer in biology

Gotowa bibliografia na temat „Charge transfer in biology”

Autor: Grafiati
Data publikacji: 4 czerwca 2021
Data aktualizacji: 19 lutego 2022

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Artykuły w czasopismach na temat "Charge transfer in biology"

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Wahadoszamen, Md, Tjaart P. J. Krüger, Anjue Mane Ara, Rienk van Grondelle i Michal Gwizdala. "Charge transfer states in phycobilisomes". Biochimica et Biophysica Acta (BBA) - Bioenergetics 1861, nr 7 (lipiec 2020): 148187. http://dx.doi.org/10.1016/j.bbabio.2020.148187.

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Kozma, Balázs, Romain Berraud-Pache, Attila Tajti i Péter G. Szalay. "Potential energy surfaces of charge transfer states". Molecular Physics 118, nr 19-20 (16.06.2020): e1776903. http://dx.doi.org/10.1080/00268976.2020.1776903.

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Pepi, Lauren E., Zachary J. Sasiene, Praneeth M. Mendis, Glen P. Jackson i I. Jonathan Amster. "Structural Characterization of Sulfated Glycosaminoglycans Using Charge-Transfer Dissociation". Journal of the American Society for Mass Spectrometry 31, nr 10 (21.08.2020): 2143–53. http://dx.doi.org/10.1021/jasms.0c00252.

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Torrens, Francisco, i Gloria Castellano. "Topological Charge-Transfer Indices: From Small Molecules to Proteins". Current Proteomics 6, nr 4 (1.12.2009): 204–13. http://dx.doi.org/10.2174/157016409789973770.

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Kornyshev, Alexei, Marshall Newton, Jens Ulstrup i Brett Sanderson. "Molecular charge transfer in condensed media – from physics and chemistry to biology and nanoengineering". Chemical Physics 319, nr 1-3 (grudzień 2005): 1–3. http://dx.doi.org/10.1016/j.chemphys.2005.09.014.

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Rigin, Sergei, Georgii Bogdanov, Marina Fonari i Tatiana V. Timofeeva. "Computational analysis of charge-transfer crystalline complexes". Acta Crystallographica Section A Foundations and Advances 74, a1 (20.07.2018): a310. http://dx.doi.org/10.1107/s0108767318096903.

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Bacchus-Montabonel, Marie-Christine. "Charge Transfer in Ionic and Molecular Systems". International Journal of Molecular Sciences 3, nr 3 (28.03.2002): 114. http://dx.doi.org/10.3390/i3030114.

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Bacchus-Montabonel, Marie-Christine, Ezinvi Baloïtcha, Michèle Desouter-Lecomte i Nathalie Vaeck. "Rate Coefficient Determination in Charge Transfer Reactions". International Journal of Molecular Sciences 3, nr 3 (28.03.2002): 176–89. http://dx.doi.org/10.3390/i3030176.

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Li, Xiaojuan, Cheng Lin, Liang Han, Catherine E. Costello i Peter B. O’Connor. "Charge remote fragmentation in electron capture and electron transfer dissociation". Journal of the American Society for Mass Spectrometry 21, nr 4 (kwiecień 2010): 646–56. http://dx.doi.org/10.1016/j.jasms.2010.01.001.

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Craven, Galen T., i Abraham Nitzan. "Electron transfer across a thermal gradient". Proceedings of the National Academy of Sciences 113, nr 34 (22.07.2016): 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 multidimensional transition state theory, the traditional Arrhenius picture of activation energy as a single point on a free energy surface is replaced with a bithermal property that is derived from statistical weighting over all configurations where the reactant and product states are equienergetic. The flow of energy associated with the electron transfer process is also examined, leading to relations between the rate of heat exchange among the donor and acceptor sites as functions of the temperature difference and the electronic driving bias. In particular, we find that an open electron transfer channel contributes to enhanced heat transport between sites even when they are in electronic equilibrium. The presented results provide a unified theory for charge transport and the associated heat conduction between sites at different temperatures.
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Rozprawy doktorskie na temat "Charge transfer in biology"

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Zhang, Houyu. "Theories of long-range charge transfer in DNA and quantum dissipation /". View Abstract or Full-Text, 2002. http://library.ust.hk/cgi/db/thesis.pl?CHEM%202002%20ZHANG.

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Thesis (Ph. D.)--Hong Kong University of Science and Technology, 2002.
Includes bibliographical references (leaves 169-170). Also available in electronic version. Access restricted to campus users.
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Bjorklund, Chad Christopher. "The effects of nucleosome core particle packaging on DNA charge transport". Online access for everyone, 2006. http://www.dissertations.wsu.edu/Dissertations/Fall2006/c_bjorklund_120606.pdf.

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Amstutz, Michael D. "Development of a charge-shifting polyion-mediated intramammary gene transfer system for production of recombinant proteins in milk /". The Ohio State University, 1997. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487943610785448.

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Güler, Gözde. "Part 1 controlling barriers to charge transfer in DNA : Part 2 : DNA-directed assembly of conducting oligomers /". Atlanta, Ga. : Georgia Institute of Technology, 2008. http://hdl.handle.net/1853/26621.

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Thesis (Ph. D.)--Chemistry and Biochemistry, Georgia Institute of Technology, 2009.
Committee Chair: Schuster, Gary; Committee Member: Barry, Bridgette; Committee Member: Collard, David; Committee Member: Tolbert, Laren; Committee Member: Wartell, Roger. Part of the SMARTech Electronic Thesis and Dissertation Collection.
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Roberts, Lezah Wilette. "Effect of Netropsin on One-electron Oxidation of DNA". Diss., Georgia Institute of Technology, 2005. http://hdl.handle.net/1853/7228.

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One electron oxidation of DNA has been studied extensively over the years. When a charge is injected into a DNA duplex, it migrates through the DNA until it reaches a trap. Upon further reactions, damage occurs in this area and strand cleavage can occur. Many works have been performed to see what can affect this damage to DNA. Netropsin is a minor groove binder that can bind to tracts of four to five A:T base pairs. It has been used in the studies within to determine if it can protect DNA against oxidative damage, caused by one-electron oxidation, when it is bound within the minor groove of the DNA. By using a naphthacenedione derivative as a photosensitizer, several DNA duplexes containing netropsin binding sites as well as those without binding sites, were irradiated at 420 nm, analyzed, and visualized to determine its effect on oxidative damage. It has been determined netropsin creates a quenching sphere of an average of 5.8 * 108 Šwhether bound to the DNA or not. Herein we will show netropsin protects DNA against oxidative damage whether it is free in solutions or bound within the minor groove of a DNA duplex.
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Güler, Gözde. "Part 1: Controlling barriers to charge transfer in DNA Part 2: DNA-directed assembly of conducting oligomers". Diss., Georgia Institute of Technology, 2008. http://hdl.handle.net/1853/26621.

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A series of anthraquinone-linked DNA oligonucleotides was prepared and the efficiency of long-distance radical cation migration was measured. In one set of oligonucleotides, two GG steps are separated by either a TATA or an ATAT bridge. In these two compounds, the efficiency of radical cation migration from GG to GG differs by more than an order of magnitude. Replacement of the thymines in the TATA or ATAT bridges with 3-methyl-2-pyridone (t, a thymine analog) results in the much more efficient radical cation migration across the bridge in both cases. This is attributed to a decrease in the oxidation potential of t to a value below that of A. In contrast, replacement of the thymines in the TATA or ATAT bridges with difluorotoluene (f, a thymine analog with high oxidation potential) does not measurably affect radical cation migration. These findings are readily accommodated by the phonon-assisted polaron-hopping mechanism for long-distance charge transfer in duplex DNA and indicate that DNA in solution behaves as a polaronic semiconductor. Oligomers containing thiophene-pyrrole-thiphene (SNS) monomers were covalently linked to the nucleobases of DNA. Treatment of these oligomers with horseradish peroxidase and hydrogen peroxide lead to the formation of conducting oligomers conjoined to the DNA. The DNA template aligns the oligomers along one strand of the duplex and limits the intermolecular reaction of monomers. This method enables utilization of the unique self-recognizing properties and programmability of DNA to create tailored oligomers.
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Ghosh, Avik Kumar. "Charge migration and one-electron oxidation at adenine and thymidine containing DNA strands and role of guanine N1 imino proton in long range charge migration through DNA". Diss., Available online, Georgia Institute of Technology, 2007, 2007. http://etd.gatech.edu/theses/available/etd-05132007-000502/.

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Thesis (Ph. D.)--Chemistry and Biochemistry, Georgia Institute of Technology, 2008.
Wartell, Roger, Committee Member ; Bunz, Uwe, Committee Member ; Doyle, Donald, Committee Member ; Fahrni, Christoph, Committee Member ; Schuster, Gary, Committee Chair.
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Das, Prolay. "Long-Range Charge Transfer in Plasmid DNA Condensates and DNA-Directed Assembly of Conducting Polymers". Diss., Georgia Institute of Technology, 2007. http://hdl.handle.net/1853/19856.

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Long-distance radical cation transport was studied in DNA condensates where linearized pUC19 plasmid was ligated to an oligomer and transformed into DNA condensates with spermidine. DNA condensates were detected by Dynamic Light Scattering and observed by Transmission Electron Microscopy. Introduction of charge into the condensates causes long-distance charge migration, which is detected by reaction at the remote guanines. The efficiency of charge migration in the condensate is significantly less than it is for the corresponding oligomer in solution. This result is attributed to a lower mobility for the migrating radical cation in the condensate, caused by inhibited formation of charge-transfer-effective states. Radical cation transport was also studied in DNA condensates made from an oligomer sandwiched between two linearized plasmids by double ligation. Unlike the single ligated plasmid condensates, the efficiency of charge migration in the double ligated plasmid-condensates is high, indicative of local structural and conformational transformation of the DNA duplexes. Organic monomer units having extended ð-conjugation as part of a long conducting polymer was synthesized and characterized. The monomer units were covalently attached to particular positions in DNA oligonucleotides by either the convertible nucleotide approach or by phosphoramidite chemistry. Successful attachment of the monomer units to DNA were confirmed by mass spectral analysis. The DNA-conjoined monomer units can self assemble in the presence of complementary sequences which act as templates that can control polymer formation and structure. By this method the para-direction of the polymer formation can be enforced and may be used to generate materials having nonrecurring, irregular structures.
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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 mechanical principles behind efficient electron transfer and ultimately copying Nature and construct similar efficient devices. Two main approaches towards a better understanding of the mechanisms involved have been taken. The more biological disciplines isolate, cultivate and alternate reaction centres whereas synthetic chemists prefer to construct well-defined models that mimic certain aspects of the reaction centres. Such a synthetic approach is described in the 'Synthesis of Advanced 'Special Pair' Models for the Photosynthetic Reaction Centre'. The aspect to be mimicked is the 'special pair'. One or two porphyrins in a well-defined spatial disposition (kinked or non-kinked in respect to each other) were to act as electron donor in rigid bichromophoric and trichromophoric systems. A tetracyanonaphthoquinodimethane (TCNQ) unit was employed as the electron acceptor in the series of dyads synthesised. The TCNQ acceptor was replaced by a naphthoquinone (NQ) primary acceptor covalently linked to a TCNQ secondary electron acceptor in the series of triads. Rigid norbornylogous bridges held the chromophores in place and Diels-Alder methodology as well as condensation reactions were applied to link donor, bridge and acceptor components. Despite larger interchromophoric separation than in the natural 'special pair', the two porphyrin chromophores of the series of 'special pair' dyads show some interaction and thereby prove the success of our approach towards 'special pair' mimics. Strong fluorescence quenching in the porphyrin-TCNQ dyads indicates the sought after electron transfer process. A number of synthetic problems experienced and overcome in the synthesis of the series of triads led to discovery of a one-step 'bis-ketonisation' from an olefin under Sharpless bis-hydroxylation conditions with N-methylmorpholine-N-oxide. High pressure was applied to circumvent a lack of reactivity in the condensation reaction used to attach the porphyrin moieties (one or two) to the donor backbone. For the linkage of donor, bridge and acceptor component, a procedure was developed and successfully applied to give the giant mono-porphyrin-NQ-TCNQ trichromophore. In a similar manner 'special pair' trichromophoric systems should be available as part of future work.
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Umeweni, Chiko. "Synthesis of Internally Linked Carbazole DNA Oligomers: A Potential Monitor for Charge Transfer in DNA Studies". Thesis, Available online, Georgia Institute of Technology, 2005, 2005. http://etd.gatech.edu/theses/available/etd-07052005-161648/.

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Książki na temat "Charge transfer in biology"

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Kuznetsov, A. M. Charge transfer in physics, chemistry and biology: Physical mechanisms of elementary processes and an introduction to the theory. Amsterdam: Gordon and Breach Publishers, 1995.

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1941-, Ulstrup Jens, red. Electron transfer in chemistry and biology: An introduction to the theory. Chichester: Wiley, 1999.

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Charge transfer in physics, chemistry, and biology: Physical mechanisms of elementary processes and an introduction to the theory. Luxembourg: Gordon and Breach Publishers, 1995.

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Stephen, Bone. Bioelectronics. Chichester: Wiley, 1992.

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Misra, Ramprasad, i S. P. Bhattacharyya. Intramolecular Charge Transfer. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2018. http://dx.doi.org/10.1002/9783527801916.

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Horváth, Ottó. Charge transfer photochemistry of coordinationcompounds. New York: VCH, 1993.

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Horvath, Otto. Charge transfer photochemistry of coordination compounds. New York City, NY, USA: VCH, 1993.

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Kagakkai, Nihon, red. Denshi idō: Electron transfer. Tōkyō-to Bunkyō-ku: Kyōritsu Shuppan, 2013.

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Schuster, G. B., red. Longe-Range Charge Transfer in DNA I. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/b84245.

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Schuster, G. B., red. Long-Range Charge Transfer in DNA II. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/b14032.

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Części książek na temat "Charge transfer in biology"

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Kasha, Michael. "Energy Transfer, Charge Transfer, and Proton Transfer in Molecular Composite Systems". W Physical and Chemical Mechanisms in Molecular Radiation Biology, 231–55. Boston, MA: Springer US, 1991. http://dx.doi.org/10.1007/978-1-4684-7627-9_8.

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Bacchus-Montabonel, M. C. "Charge Transfer Rate Constants in Ion-Atom and Ion-Molecule Processes". W Advances in Quantum Methods and Applications in Chemistry, Physics, and Biology, 119–29. Cham: Springer International Publishing, 2013. http://dx.doi.org/10.1007/978-3-319-01529-3_6.

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Nadig, Gautham, Laura C. Van Zant, Steve L. Dixon i Kenneth M. Merz. "Charge Transfer Interactions in Biology: A New View of the Protein-Water Interface". W ACS Symposium Series, 439–47. Washington, DC: American Chemical Society, 1999. http://dx.doi.org/10.1021/bk-1999-0721.ch034.

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Collins, Tammy R. L., i Tao-shih Hsieh. "Monitoring the Topoisomerase II DNA Gate Conformational Change with Fluorescence Resonance Energy Transfer". W Methods in Molecular Biology, 59–70. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60761-340-4_6.

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Longo, Dario Livio, Pietro Irrera, Lorena Consolino, Phillip Zhe Sun i Michael T. McMahon. "Renal pH Imaging Using Chemical Exchange Saturation Transfer (CEST) MRI: Basic Concept". W Methods in Molecular Biology, 241–56. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-0978-1_14.

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AbstractMagnetic Resonance Imaging (MRI) has been actively explored in the last several decades for assessing renal function by providing several physiological information, including glomerular filtration rate, renal plasma flow, tissue oxygenation and water diffusion. Within MRI, the developing field of chemical exchange saturation transfer (CEST) has potential to provide further functional information for diagnosing kidney diseases. Both endogenous produced molecules as well as exogenously administered CEST agents have been exploited for providing functional information related to kidney diseases in preclinical studies. In particular, CEST MRI has been exploited for assessing the acid-base homeostasis in the kidney and for monitoring pH changes in several disease models. This review summarizes several CEST MRI procedures for assessing kidney functionality and pH, for monitoring renal pH changes in different kidney injury models and for evaluating renal allograft rejection.This chapter is based upon work from the COST Action PARENCHIMA, a community-driven network funded by the European Cooperation in Science and Technology (COST) program of the European Union, which aims to improve the reproducibility and standardization of renal MRI biomarkers. This introduction chapter is complemented by two separate chapters describing the experimental procedure and data analysis.
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Kim, Hahnsung, Yin Wu, Daisy Villano, Dario Livio Longo, Michael T. McMahon i Phillip Zhe Sun. "Analysis Protocol for the Quantification of Renal pH Using Chemical Exchange Saturation Transfer (CEST) MRI". W Methods in Molecular Biology, 667–88. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-0978-1_40.

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AbstractThe kidney plays a major role in maintaining body pH homeostasis. Renal pH, in particular, changes immediately following injuries such as intoxication and ischemia, making pH an early biomarker for kidney injury before the symptom onset and complementary to well-established laboratory tests. Because of this, it is imperative to develop minimally invasive renal pH imaging exams and test pH as a new diagnostic biomarker in animal models of kidney injury before clinical translation. Briefly, iodinated contrast agents approved by the US Food and Drug Administration (FDA) for computed tomography (CT) have demonstrated promise as novel chemical exchange saturation transfer (CEST) MRI agents for pH-sensitive imaging. The generalized ratiometric iopamidol CEST MRI analysis enables concentration-independent pH measurement, which simplifies in vivo renal pH mapping. This chapter describes quantitative CEST MRI analysis for preclinical renal pH mapping, and their application in rodents, including normal conditions and acute kidney injury.This publication is based upon work from the COST Action PARENCHIMA, a community-driven network funded by the European Cooperation in Science and Technology (COST) program of the European Union, which aims to improve the reproducibility and standardization of renal MRI biomarkers. This analysis protocol chapter is complemented by two separate chapters describing the basic concepts and experimental procedure.
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Gooch, Jan W. "Charge-Transfer". W Encyclopedic Dictionary of Polymers, 136. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_2223.

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Stebbings, R. F. "Charge Transfer". W Advances in Chemical Physics, 195–246. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470143568.ch6.

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Charnley, Steven B. "Charge Transfer". W Encyclopedia of Astrobiology, 1–2. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-27833-4_264-3.

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Charnley, Steven B. "Charge Transfer". W Encyclopedia of Astrobiology, 427–28. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-44185-5_264.

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Streszczenia konferencji na temat "Charge transfer in biology"

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Fialko, N. S., i V. D. Lakhno. "Simulation of charge transfer in GA...AGGG nucleotide chains". W Mathematical Biology and Bioinformatics. Pushchino: IMPB RAS - Branch of KIAM RAS, 2020. http://dx.doi.org/10.17537/icmbb20.7.

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Zaytsev, A. Y., M. M. Olshevets, N. S. Fialko, V. V. Yakovlev i V. D. Lakhno. "Artificial Normalization in the Modeling of Charge Transfer in Molecular Chains". W Mathematical Biology and Bioinformatics. Pushchino: IMPB RAS - Branch of KIAM RAS, 2020. http://dx.doi.org/10.17537/icmbb20.8.

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Fialko, N. S., i V. D. Lakhno. "Modeling of charge transfer in heterogeneous oligonucleotides at a biologically significant temperature". W Mathematical Biology and Bioinformatics. Pushchino: IMPB RAS - Branch of KIAM RAS, 2018. http://dx.doi.org/10.17537/icmbb18.64.

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Fialko, N. S., i V. D. Lakhno. "Modeling of charge transfer in «donor–homogeneous brige–acceptor» chains at T = 300 K". W Mathematical Biology and Bioinformatics. Pushchino: IMPB RAS - Branch of KIAM RAS, 2018. http://dx.doi.org/10.17537/icmbb18.58.

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Korshunova, A. N., i V. D. Lakhno. "Various regimes of charge transfer in a Holstein chain in a constant electric field depending on its intensity and the initial charge distribution". W Mathematical Biology and Bioinformatics. Pushchino: IMPB RAS - Branch of KIAM RAS, 2018. http://dx.doi.org/10.17537/icmbb18.89.

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Ustinin, D. M. "Brownian dynamics simulation of intra-cellular charge transfer processes using Julia programming language for scientific computing". W Mathematical Biology and Bioinformatics. Pushchino: IMPB RAS - Branch of KIAM RAS, 2018. http://dx.doi.org/10.17537/icmbb18.93.

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Pyatkov, M. I., A. Y. Zaytsev, M. M. Olshevets i N. S. Fialko. "Implementation of partially automated calculations on hybrid supercomputers in the modelling of charge transfer in quasi-one-dimensional molecular chains". W Mathematical Biology and Bioinformatics. Pushchino: IMPB RAS - Branch of KIAM RAS, 2018. http://dx.doi.org/10.17537/icmbb18.66.

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Frost, Christopher M., Paul S. Cederna, David C. Martin, Bong Sup Shim i Melanie G. Urbanchek. "Decellular biological scaffold polymerized with PEDOT for improving peripheral nerve interface charge transfer". W 2014 36th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC). IEEE, 2014. http://dx.doi.org/10.1109/embc.2014.6943618.

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Elwassif, Maged M., Qingjun Kong, Maribel Vazquez i Marom Bikson. "Bio-Heat Transfer Model of Deep Brain Stimulation Induced Temperature changes". W Conference Proceedings. Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 2006. http://dx.doi.org/10.1109/iembs.2006.4398221.

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Elwassif, Maged M., Qingjun Kong, Maribel Vazquez i Marom Bikson. "Bio-Heat Transfer Model of Deep Brain Stimulation Induced Temperature changes". W Conference Proceedings. Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 2006. http://dx.doi.org/10.1109/iembs.2006.259425.

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Raporty organizacyjne na temat "Charge transfer in biology"

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Milinazzo, Jared Joseph. Energy Transfer of a Shaped Charge. Office of Scientific and Technical Information (OSTI), listopad 2016. http://dx.doi.org/10.2172/1334941.

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Brus, Louis. Graphene Charge Transfer, Spectroscopy, and Photochemical Reactions. Office of Scientific and Technical Information (OSTI), styczeń 2017. http://dx.doi.org/10.2172/1341618.

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Carroll, David L. Charge Transfer Nanocomposites: The Effects of Scale-Hierarchy. Fort Belvoir, VA: Defense Technical Information Center, grudzień 2006. http://dx.doi.org/10.21236/ada468765.

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Hervier, Antoine. Charge Transfer and Support Effects in Heterogeneous Catalysis. Office of Scientific and Technical Information (OSTI), grudzień 2011. http://dx.doi.org/10.2172/1076791.

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Last, Isidore, i Thomas F. George. Cooperative Absorption-Induced Charge Transfer in a Solid. Fort Belvoir, VA: Defense Technical Information Center, grudzień 1990. http://dx.doi.org/10.21236/ada229553.

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Baker, Lawrence Robert. Charge Transfer and Catalysis at the Metal Support Interface. Office of Scientific and Technical Information (OSTI), lipiec 2012. http://dx.doi.org/10.2172/1174166.

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Khalil, Munira. Correlating electronic and vibrational motions in charge transfer systems. Office of Scientific and Technical Information (OSTI), czerwiec 2014. http://dx.doi.org/10.2172/1168632.

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John F. Endicott. Photoinduced Charge and Energy Transfer Processes in Molecular Aggregates. Office of Scientific and Technical Information (OSTI), październik 2009. http://dx.doi.org/10.2172/966130.

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Edward C. Lim. INTRAMOLECULAR CHARGE AND ENERGY TRANSFER IN MULTICHROMOPHORIC AROMATIC SYSTEMS. Office of Scientific and Technical Information (OSTI), wrzesień 2008. http://dx.doi.org/10.2172/936771.

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Piotr Piotrowiak. Electronic and Nuclear Factors in Charge and Excitation Transfer. Office of Scientific and Technical Information (OSTI), wrzesień 2004. http://dx.doi.org/10.2172/832834.

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