Literatura científica selecionada sobre o tema "Double electron transfer (DET)"
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Artigos de revistas sobre o assunto "Double electron transfer (DET)"
Mukerjee, Sanjeev, Benjamin William Kaufold, Sijia Dong, Parisa Nematollahi, Bernardo Barbiellini e Dirk Lamoen. "(Invited) Plasmonic Enhancement of Electrochemical Reactions Using LSPR Phenomenon". ECS Meeting Abstracts MA2023-01, n.º 30 (28 de agosto de 2023): 1798. http://dx.doi.org/10.1149/ma2023-01301798mtgabs.
Texto completo da fonteChen, Ling, Yue Lu, Manman Duanmu, Xin Zhao, Shenglu Song, Liyue Duan, Zhipeng Ma, Ailing Song e Guangjie Shao. "Stably Improving the Catalytic Activity of Oxygen Evolution Reactions via Two-Dimensional Graphene Oxide-Incorporated NiFe-Layered Double Hydroxides". Catalysts 14, n.º 4 (19 de abril de 2024): 278. http://dx.doi.org/10.3390/catal14040278.
Texto completo da fonteWu, Hsing-Ju, e Cheng-Chung Chang. "Fabrication of Double Emission Enhancement Fluorescent Nanoparticles with Combined PET and AIEE Effects". Molecules 25, n.º 23 (4 de dezembro de 2020): 5732. http://dx.doi.org/10.3390/molecules25235732.
Texto completo da fonteWang, Ze, Qianyu Zhou, Yanni Zhu, Yangfan Du, Weichun Yang, Yuanfu Chen, Yong Li e Shifeng Wang. "NiFeMn-Layered Double Hydroxides Linked by Graphene as High-Performance Electrocatalysts for Oxygen Evolution Reaction". Nanomaterials 12, n.º 13 (27 de junho de 2022): 2200. http://dx.doi.org/10.3390/nano12132200.
Texto completo da fonteChen, Zhuo, Qiang Qu, Xinsheng Li, Katam Srinivas, Yuanfu Chen e Mingqiang Zhu. "Room-Temperature Synthesis of Carbon-Nanotube-Interconnected Amorphous NiFe-Layered Double Hydroxides for Boosting Oxygen Evolution Reaction". Molecules 28, n.º 21 (27 de outubro de 2023): 7289. http://dx.doi.org/10.3390/molecules28217289.
Texto completo da fonteZhang, Zhichao, Jiahao Guo, Yuhan Sun, Qianwei Wang, Mengyang Li, Feng Cao e Shuang Han. "Sulfur-Doped Nickel–Iron LDH@Cu Core–Shell Nanoarrays on Copper Mesh as High-Performance Electrocatalysts for Oxygen Evolution Reaction". Journal of Composites Science 7, n.º 12 (23 de novembro de 2023): 486. http://dx.doi.org/10.3390/jcs7120486.
Texto completo da fonteWiedemeier, Allison M. D., Jan E. Judy-March, Charles H. Hocart, Geoffrey O. Wasteneys, Richard E. Williamson e Tobias I. Baskin. "Mutant alleles of Arabidopsis RADIALLY SWOLLEN 4 and 7 reduce growth anisotropy without altering the transverse orientation of cortical microtubules or cellulose microfibrils". Development 129, n.º 20 (15 de outubro de 2002): 4821–30. http://dx.doi.org/10.1242/dev.129.20.4821.
Texto completo da fonteSolangi, Muhammad Yameen, Abdul Hanan Samo, Abdul Jaleel Laghari, Umair Aftab, Muhammad Ishaque Abro e Muhammad Imran Irfan. "MnO2@Co3O4 nanocomposite based electrocatalyst for effective oxygen evolution reaction". Sukkur IBA Journal of Emerging Technologies 5, n.º 1 (30 de junho de 2022): 32–40. http://dx.doi.org/10.30537/sjet.v5i1.958.
Texto completo da fonteAdachi, Taiki, Yuki Kitazumi, Osamu Shirai e Kenji Kano. "Direct Electron Transfer-Type Bioelectrocatalysis of Redox Enzymes at Nanostructured Electrodes". Catalysts 10, n.º 2 (15 de fevereiro de 2020): 236. http://dx.doi.org/10.3390/catal10020236.
Texto completo da fonteSchachinger, Franziska, Hucheng Chang, Stefan Scheiblbrandner e Roland Ludwig. "Amperometric Biosensors Based on Direct Electron Transfer Enzymes". Molecules 26, n.º 15 (27 de julho de 2021): 4525. http://dx.doi.org/10.3390/molecules26154525.
Texto completo da fonteTeses / dissertações sobre o assunto "Double electron transfer (DET)"
Fall, Arona. "Donneurs d’électrons organiques : développement d’un nouveau système catalytique photoredox". Electronic Thesis or Diss., Aix-Marseille, 2021. http://www.theses.fr/2021AIXM0607.
Texto completo da fonteDuring this last decade, the reactivity of enamine-based organic electron donor (OED) has been widely explored in electron transfer processes. With exceptionally negative redox potentials, OEDs spontaneously promote single (SET) or double electron transfer (DET) to an organic substrate, to form radical or anionic intermediates. However, the use of stoichiometric amount of OEDs limits their competitivity compared to their organometallic and organic catalysts. This thesis project consisted in developing a new catalytic system with OEDs. Different strategies were envisaged. In a first method a catalytic amount of OED would initiate the electron transfer to reduce the substrate. The oxidation of the generated radical intermediate would allow the regeneration of OED. Unfortunately, this strategy was unsuccessful. The second strategy would consist in regenerating the OED from its air-stable oxidized form OED2+ and a sacrificial electron donor (tertiary amine, sodium dithionite or Rongalite®) under photoactivation. Several optimizing steps allowed the development of a new efficient catalytic photoredox system with the oxidized form as photocatalyst and Rongalite® as sacrificial electron donor. This new photoredox catalytic system was applied to the reduction of various functionals groups (sulfone, aryl halide and triflate) by single electron transfer (SET) and double electron transfer (DET). The reactivity of the photocatalytic system was also explored in radical addition reactions
Eggers, Paul Kahu Chemistry Faculty of Science UNSW. "Probing the electrochemical double layer: an examination of how the physical and electrical structure affects heterogeneous electron transfer". Publisher:University of New South Wales. Chemistry, 2008. http://handle.unsw.edu.au/1959.4/41285.
Texto completo da fonteBellamy, Michael Bruce. "A double strand DNA break model of photon and electron relative biological effectiveness". Diss., Georgia Institute of Technology, 2013. http://hdl.handle.net/1853/47711.
Texto completo da fonteAbhijit, Saha. "Chemical Biology Approaches for the Molecular Recognition of DNA Double Helix". 京都大学 (Kyoto University), 2015. http://hdl.handle.net/2433/199116.
Texto completo da fonteLy, Danith. "Mechanism of electron transfer in double-stranded DNA and PNA-DNA hybrids, and the development of a fluorescence probe for DNA and RNA detection". Diss., Georgia Institute of Technology, 1998. http://hdl.handle.net/1853/30485.
Texto completo da fonteĐorđe, Ilić. "Analiza problema višeplodnih trudnoća nastalih vantelesnom oplodnjom". Phd thesis, Univerzitet u Novom Sadu, Medicinski fakultet u Novom Sadu, 2015. http://www.cris.uns.ac.rs/record.jsf?recordId=90376&source=NDLTD&language=en.
Texto completo da fonteIntroduction: Multiple pregnancies occur in 1.5% of all pregnancies after spontaneous conception and in more than 20 % of all pregnancies concieved after assisted reproductive technologies in Europe, with large variations between countries. In our setting, the rate of multiple pregnancies after the ART is well above 30%. The occurrence of hypertensive syndrome in pregnancy, gestational diabetes, operative delivery, premature birth, low birth weight, neurological and developmental impairment in children, and almost all the other complications for the mother and fetus, as well as the entire burden of the health system are several times higher in multiple pregnancies compared with singleton pregnancies. Incidence of forementioned complications rises with number of fetuses. On the other hand, children from in vitro fertilization procedures make up 4.5% of all live births in some countries, which together with the fact that infertility affects aproximately 16-18% of couples in our country gives an extra dimension to this phenomenon and makes it not just medical but wider social problem. Perinatal outcomes of pregnancies after assisted reproductive technologies (ART) are greatly compromised by the high rate of multiple pregnancies, which are now considered to be a complication rather than success of ART procedures. ART Singleton pregnancies have, in larger studies, show discretely lower perinatal outcomes compared with those conceived spontaneously, while for the multiple pregnancies, this correlation is not clearly expressed and documented. There remains dilemma whether multiplicity itself or the way of conception (ART vs. non ART) constitutes a major problem in the observed differences regarding perinatal outcome of ART pregnancies. Objective: To compare the perinatal outcomes of multiple pregnancies conceived by In vitro fertilization (IVF) and spontaneously and perinatal outcomes of IVF conceived singleton and multiple pregnancies. Additional aim of this thesis is to point out the complexity of this problem and offer possible solutions. Materials and Methods: Design of a study was a combination of retrospective and prospective observational longitudinal cohort study. Analysis included pregnancies which had delivery at the Department of Gynecology and Obstetrics, Clinical Center of Vojvodina in the period from 1.01.2008. to 31.12.2010. The study analyzed and compared the perinatal outcomes in 174 spontaneous conceived multiple pregnancies, 163 multiple pregnancies resulting from IVF procedures, and 155 singleton pregnancies conceived by IVF procedure. Analyzed parameters were newborns birth weight, gestational age at delivery, the value of the Apgar score, occurrence of hypertensive syndrome in pregnancy, gestational diabetes, as well as numerous parameters of perinatal outcome. Taken by trained clinicians and were entered into a specially designed database, the results were statistically analyzed in JMP ver 9.0 software (SAS publisher) using ANOVA analysis to test the statistical significance between the mean values of continuous variables, while the statistical significance of the difference in frequency of categorical variables was assessed by Pearsons χ2 test. Results: ART singleton pregnancies had an average mothers age of 33.5 years, the average gestational age at birth of 38.26 gestational weeks (gw), preterm delivery rate of 12.9%, average birth weight 3258 g, Apgar score (AS) in the first minute 8.35, and in the fifth minute 9.2, cesarean section rate 65.81%, Gestational diabetes (GDM) in 7.1% pregnancies, anemia occurred in 41.94% of pregnancies, while preeclampsia was observed in 4.52% of all pregnancies. All relevant parameters of perinatal outcome were significantly (p<0.0001) superior to both ART and non-ART twin pregnancies. ART twin pregnancy showed the average mothers age of 32.9 years, the average gestational age at birth of 35.6 gw, the preterm delivery rate 58.27%, the average body weight newborns 2374 g, AS in the first minute of 7.45, and in the fifth minute of 8.65, the cesarean section rate of 83.7%, GDM in 15.11% of all pregnancies, anemia occurred in 78.42% and preeclampsia in 12.23% of pregnancies, while the non-ART twin pregnancy showed an average mothers age of 28.8 years, the average gestational age at birth of 36.08 gw, the preterm delivery rate of 49.71%, the average body weight of 2433 g, AS in the first minute of 7.75 in the fifth minute 8.75, the caesarian section rate of 58.33%, GDM-a occurred in 7.02%, anemia in 67.84% and preeclampsia in 11.11% of pregnancies. Except for maternal age and the caesarean section rate, which were significantly higher in ART twin pregnancies (p<0.0001), as well as small increase in proportion of amniotic fluid volume disorders (p = 0.033), almost all other parameters of perinatal outcome of were comparable in these groups. Discussion and Conclusion: The study showed that the course and outcome of multiple pregnancies conceived spontaneous and after IVF procedures are equivalent in almost all parameters with similar average body weight and gestational age at birth, and that all these parameters of multiple pregnancies regardless of the conception mode are equally worse compared with singleton pregnancies from IVF procedures. With the exception of multiplicity as a risk factor children from in vitro fertilization procedures are generally healthy. Multiplicity itself and not the mode of conception presented a problem, which is rightly considered the major complication of IVF today. Additional analysis of the experiences of other health system indicates that only a broad and comprehensive implementation of strategy to return only one embryo (SET–single embryo transfer) can lead to a reduction of the rate of multiple pregnancies after IVF procedures, and the accompanying complications, without compromising IVF success. The experience of other health systems indicate that a successful implementation of SET is only possible with the involvement of the whole society, along with a number of legislative measures in the field of monitoring, control and reimbursement of assisted reproduction procedures. The scope and funding of an IVF procedures (with more free attempts for infertile couples, reimbursed by public health) with mandatory use of SET, and good cryopreservation programs are, based on examples in other countries who had successfully dealt with his problem, is the key in reducing the problem of multiple pregnancies after IVF procedures.
Kelley, Shana O. "Electron transfer through the DNA double helix: spectroscopic and electrochemical studies". Thesis, 1999. https://thesis.library.caltech.edu/4085/1/Kelley_so_1999.pdf.
Texto completo da fonteYu, Wei-Shan, e 游偉盛. "Excited-State Double Proton Transfer on 3-Substituted-7-Azaindole Analogues and Photoinduced Electron Transfer of New Type Donor-Bridge-Acceptor Molecules". Thesis, 2002. http://ndltd.ncl.edu.tw/handle/84410813424643570922.
Texto completo da fonte國立中正大學
化學研究所
90
Abstract Unlike 7-azaindole consisting of the tetrameric configuration, 3-methyl-7-azaindole (3MAI) exists solely as intact double hydrogen-bonded dimeric forms in a single crystal. Both steady state and time-resolved measurements down to 8.0 K reveal remarkable deuterium isotope effects on the rate of excited-state double proton transfer (ESDPT) in the N(1)-deuterated 3MAI (3MAI-d) single crystal. The rates of ESDPT for the 3MAI-d dimer resolved at < 150 K are mainly governed by the proton tunneling mechanism. At < 12 K, the nearly temperature-independent ESDPT dynamics lead us to qualitatively deduce a barrier height of ~ 1.73 kcal/mol for the 3MAI-d dimer. The results provide an ideal model to investigate the intrinsic ESDPT dynamics for 7-azaindole analogues in which the structural information is well documented. The mechanism of excited-state double proton transfer (ESDPT) reaction of 7-azaindoles in pure water has been solved through design and syntheses of 3-Cyano-7-azaindole (3CAI) and its derivatives. Dual emission consisting of normal (lmax = 350 nm) and tautomer band (lmax = 475 nm) was resolved for 3CAI in pure water. Dynamical studies clearly revealed that the entire rise time of the tautomer emission of 850 ps is identical with the decay time (tf = 855 ps) of the normal emission. Remarkable deuterium isotope effect was observed in D2O where the rise time of 3.50 ns of the tautomer emission correlates well with the lifetime (3.45 ns) of the normal emission. The results lead us to conclude that dynamics of ESDPT with a rate of 850 ps-1 in water (or 3.50 ns-1 in D2O) originate from the entire ground-state solvated species, resolving a long-standing controversy regarding the mechanism of water catalyzed ESDPT in 7-azaindoles. We have demonstrated a new class of donor-{saturated hydrocarbon bridge}-acceptor (D-B-A) dyads based on a systematic approach to evaluate the corresponding photoinduced electron transfer process. Among these dyads heptacyclo[6.6.0.02,6.03,13.04,11.05,9.010,14]tetradecane (HCTD) was used as a unique spacer, which possesses a geometry of high symmetry (D2d), rigidity and linearity so that electron transfer processes can be examined between donor and acceptor substituents aligned along a straight line across the s-framework. In certain cases, via synthetic routes, the relative orientation of p-orbitals between donor and acceptor was adjusted to either a coplanar (0º) or perpendicular (90º) dihedral angle with respect to each other so that a comparative study could be made by tuning their relative electron coupling properties. The results in combination with theoretical approaches render valuable information on the spectroscopy and dynamics of excited-state electron transfer as functions of donor/acceptor electronic states, orientation as well as solvent properties.
Lin, Yan-Duo, e 林彥多. "Intramolecular Electron Transfer Induced C-N Bond Cleavage and Exciplex Formation of the double bond Constrained Aminostilbenes Derivatives". Thesis, 2008. http://ndltd.ncl.edu.tw/handle/30731139014850662384.
Texto completo da fonte國立中央大學
化學研究所
96
This thesis is aimed to study the relationship between the photoinduced intramolecular electron transfer processes and the excited-state C-N bond cleavage reaction as well as intramolecular exciplex formation of a series of amine-bridge-stilbene derivatives. The fluorescence spectra of DPhI, MPhI and DEtI show dual fluorescence in polar solvents, but DCEtI and DPyI display only the locally-excited (LE) fluorescence in both nonpolar and polar solvents. Compounds DPhI and MPhI in nonpolar and polar solvents and DPyI and DPyCI in CH3CN undergo the C-N bond cleavage, leading to the formation of HI and CI of higher fluorescence quantum yields (Φf). However, such a C-N bond fragmentation reaction was not observed for DEtI in either nonpolar or polar solvents. The Φf and the quantum yields of the C-N bond cleavage reaction (Φfra) for DPyI and DPyCI increase as increasing the solvent polarity. In contrast, an opposite solvent dependence of Φfra was observed for DPhI and MPhI because the intramolecular electron transfer and back electron transfer processes locate in the Marcus normal and inverted region, respectively, and the value of ΦBET increases more than that of ΦICT with increasing the solvent polarity. Compounds DPyI2 and DPyI3 display only the LE fluorescence in both nonpolar and polar solvents, but the fluorescence quantum yields decrease and the fluorescence life times increase with increasing the solvent polarity. This indicates the presence of electron donor and acceptor interactions. Compounds DPhI2 and DPhI3 show dual fluorescence in moderate and highly polar solvents, and the long-wavelength emission band results from intramolecular exciplexes. When compared with the one-mothylene-bridged compounds, compounds DPyI2, DPyI3, DPhI2 and DPhI3 do not undergo the cleavage of C-N bond in both nonpolar and polar solvents.
Arabi, Alya A. "Density Functional Theory: Dispersion Interactions & Biological Applications". 2012. http://hdl.handle.net/10222/15525.
Texto completo da fonteLivros sobre o assunto "Double electron transfer (DET)"
Canada. Bill: An act to remove doubts as to the title of Leonidas Burwell to certain lands in the Township of Bayham. Quebec: Printed for the Contractors by Hunter, Rose & Lemieux, 2001.
Encontre o texto completo da fonteLaunay, Jean-Pierre, e Michel Verdaguer. The moving electron: electrical properties. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198814597.003.0003.
Texto completo da fonteStafström, Sven, e Mikael Unge. Disorder-induced electron localization in molecular-based materials. Editado por A. V. Narlikar e Y. Y. Fu. Oxford University Press, 2017. http://dx.doi.org/10.1093/oxfordhb/9780199533046.013.25.
Texto completo da fonteEland, John H. D., e Raimund Feifel. Diatomic molecules. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198788980.003.0003.
Texto completo da fonteShi, Z. J., e Z. N. Gu. New phenomena in the nanospace of single-wall carbon nanotubes. Editado por A. V. Narlikar e Y. Y. Fu. Oxford University Press, 2017. http://dx.doi.org/10.1093/oxfordhb/9780199533053.013.12.
Texto completo da fonteCapítulos de livros sobre o assunto "Double electron transfer (DET)"
Rejou-Michel, Agnes, M. Ahsan Habib e John O’M Bockris. "Electron Transfer at Biological Interfaces". In Electrical Double Layers in Biology, 167–83. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-8145-7_12.
Texto completo da fonteSaha, Abhijit. "Examining Cooperative Binding of Sox2 on DC5 Regulatory Element Upon Complex Formation with Pax6 Through Excess Electron Transfer Assay". In Molecular Recognition of DNA Double Helix, 81–100. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-8746-2_5.
Texto completo da fonteLin, Shiquan, Xiangyu Chen e Zhong Lin Wang. "Electron transfer in liquid–solid contact electrification and double-layer formation". In Reference Module in Chemistry, Molecular Sciences and Chemical Engineering. Elsevier, 2023. http://dx.doi.org/10.1016/b978-0-323-85669-0.00142-2.
Texto completo da fonteIan, Fleming. "Group transfer reactions". In Pericyclic Reactions. Oxford University Press, 2015. http://dx.doi.org/10.1093/hesc/9780199680900.003.0006.
Texto completo da fonteLan, Wen-Jie, Henry White e Shengli Chen. "Electrical Double-Layer Effects on Electron Transfer and Ion Transport at the Nanoscale". In Nanoelectrochemistry, 29–70. CRC Press, 2015. http://dx.doi.org/10.1201/b18066-4.
Texto completo da fonteFuke, K., A. Nakajima e K. Kaya. "Dynamics of double proton transfer reaction in the excited state of hydrogen bonded dimers as studied in a supersonic jet". In Dynamics and Mechanisms of Photoinduced Electron Transfer and Related Phenomena, 167–73. Elsevier, 1992. http://dx.doi.org/10.1016/b978-0-444-89191-4.50019-7.
Texto completo da fonteMULVANEY, P. C., F. GRIESER e D. MEISEL. "ELECTRICAL DOUBLE LAYER EFFECTS ON ELECTRON TRANSFER REACTIONS AT COLLOIDAL METAL OXIDE-AQUEOUS SOLUTION INTERFACES". In Radiation Research: A Twentieth-century Perspective, 81. Elsevier, 1991. http://dx.doi.org/10.1016/b978-0-12-168561-4.50423-6.
Texto completo da fonteMulvaney, Paul, Franz Grieser e Dan Meisel. "ELECTRICAL DOUBLE-LAYER EFFECTS ON ELECTRON TRANSFER REACTIONS AT COLLOIDAL METAL OXIDE - AQUEOUS SOLUTION INTERFACES". In Congress Proceedings, 127–32. Elsevier, 1992. http://dx.doi.org/10.1016/b978-0-12-168562-1.50027-6.
Texto completo da fonteCorrea, Núria, Rita Vassena, Jesús Cerquides e Josep Lluís Arcos. "Limits of Conventional Machine Learning Methods to Predict Pregnancy and Multiple Pregnancy After Embryo Transfer". In Frontiers in Artificial Intelligence and Applications. IOS Press, 2021. http://dx.doi.org/10.3233/faia210141.
Texto completo da fonteCorrea, Núria, Rita Vassena, Jesús Cerquides e Josep Lluís Arcos. "Limits of Conventional Machine Learning Methods to Predict Pregnancy and Multiple Pregnancy After Embryo Transfer". In Frontiers in Artificial Intelligence and Applications. IOS Press, 2021. http://dx.doi.org/10.3233/faia210141.
Texto completo da fonteTrabalhos de conferências sobre o assunto "Double electron transfer (DET)"
Zaharakis, K. E., R. R. Haar, J. A. Tanis, M. W. Clark e V. L. Plano. "Search for resonant electron transfer and double excitation in Kr34+ + H2 collisions". In 6th International conference on the physics of highly charged ions. AIP, 1993. http://dx.doi.org/10.1063/1.43718.
Texto completo da fonteQiu, H., R. Qiu, C. Liu e H. Zhou. "InGaZnO/SnO2 Double Electron Transfer Layer Perovskite Solar Cells". In 2018 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2018. http://dx.doi.org/10.7567/ssdm.2018.f-3-04.
Texto completo da fonteLee, Ching-Sung, Wei-Chou Hsu, Yeong-Jia Chen, Jun-Chin Huang e Dung-Hai Huang. "Double-Transconductance-Plateau Characteristics in InGaAs/GaAs Real-Space Transfer High Electron Mobility Transistor". In 2005 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2005. http://dx.doi.org/10.7567/ssdm.2005.p6-5.
Texto completo da fonteNido, Masaaki, M. G. Alexander, Wolfgang W. Ruehle e Klaus Koehler. "Electron and hole tunneling transfer times in GaAs/Al0.35Ga0.65As asymmetric double quantum wells under electric field". In The Hague '90, 12-16 April, editado por Andre Antonetti. SPIE, 1990. http://dx.doi.org/10.1117/12.20335.
Texto completo da fonteDey, Amrita, Alexander F. Richter, Tushar Debnath, He Huang, Lakshminarayan Polavarapu e Jochen Feldmann. "Transfer of Direct to Indirect Bound Excitons by Electron Intervalley Scattering in Cs2AgBiBr6 Double Perovskite Nanocrystals". In Internet Conference for Quantum Dots. València: Fundació Scito, 2020. http://dx.doi.org/10.29363/nanoge.icqd.2020.021.
Texto completo da fonteAsayama, T., T. Fujita, H. Kiyama, A. Oiwa, S. Tarucha, Jisoon Ihm e Hyeonsik Cheong. "Angular momentum transfer between a circularly polarized photon and an electron spin in double quantum dots". In PHYSICS OF SEMICONDUCTORS: 30th International Conference on the Physics of Semiconductors. AIP, 2011. http://dx.doi.org/10.1063/1.3666720.
Texto completo da fonteTanuma, Hajime. "Electron transfer to individual magnetic substates of multi-charged ions". In CORRELATIONS,POLARIZATION,AND IONIZATION IN ATOMIC SYSTEMS:Proceedings of the International Symposium on(e,2e),Double Photoionization and Related Topics and the Eleventh International Symposium on Polarization and Correlation in Electronic and Atomic .... AIP, 2002. http://dx.doi.org/10.1063/1.1449348.
Texto completo da fonteNorris, T. B., N. Vodjdani, B. Vinter, C. Weisbuch e G. A. Mourou. "Time-Resolved Observation of Luminescence from a Charge-Transfer State in Double Quantum Wells". In Picosecond Electronics and Optoelectronics. Washington, D.C.: Optica Publishing Group, 1989. http://dx.doi.org/10.1364/peo.1989.trt106.
Texto completo da fonteHormann, A., E. J. C. Olson, P. F. Barbara, M. R. Arkin, E. D. A. Stemp, R. E. Holmlin e J. K. Barton. "Time Resolved Electron Transfer Studies Between Metallointercalators in DNA". In International Conference on Ultrafast Phenomena. Washington, D.C.: Optica Publishing Group, 1996. http://dx.doi.org/10.1364/up.1996.sab.6.
Texto completo da fonteNorris, T. B., N. Vodjdani, B. Vinter, C. Weisbuch e G. A. Mourou. "Time-Resolved Observation of Luminescence from a Charge-Transfer State in Double Quantum Wells". In Quantum Wells for Optics and Opto-Electronics. Washington, D.C.: Optica Publishing Group, 1989. http://dx.doi.org/10.1364/qwoe.1989.wd2.
Texto completo da fonteRelatórios de organizações sobre o assunto "Double electron transfer (DET)"
Tzfira, Tzvi, Michael Elbaum e Sharon Wolf. DNA transfer by Agrobacterium: a cooperative interaction of ssDNA, virulence proteins, and plant host factors. United States Department of Agriculture, dezembro de 2005. http://dx.doi.org/10.32747/2005.7695881.bard.
Texto completo da fonteStockman, Mark I., Leonid S. Muratov, Lakshmi N. Pandey e Thomas F. George. Light-Induced Electron Transfer Counter to an Electric Field Force in an Asymmetric Double Quantum Well. Fort Belvoir, VA: Defense Technical Information Center, janeiro de 1992. http://dx.doi.org/10.21236/ada244138.
Texto completo da fonte