Добірка наукової літератури з теми "Phosphene"
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Статті в журналах з теми "Phosphene"
Kvašňák, E., M. Orendáčová, and J. Vránová. "Phosphene Attributes Depend on Frequency and Intensity of Retinal tACS." Physiological Research 71, no. 4 (August 31, 2022): 561–71. http://dx.doi.org/10.33549/physiolres.934887.
Повний текст джерелаIndahlastari, Aprinda, Aditya K. Kasinadhuni, Christopher Saar, Kevin Castellano, Bakir Mousa, Munish Chauhan, Thomas H. Mareci, and Rosalind J. Sadleir. "Methods to Compare Predicted and Observed Phosphene Experience in tACS Subjects." Neural Plasticity 2018 (December 6, 2018): 1–10. http://dx.doi.org/10.1155/2018/8525706.
Повний текст джерелаEt.al, Manami, K. "Investigation of Electrical Interference towards Phosphene-Based Walking Support System." Turkish Journal of Computer and Mathematics Education (TURCOMAT) 12, no. 3 (April 10, 2021): 2178–83. http://dx.doi.org/10.17762/turcomat.v12i3.1164.
Повний текст джерелаMassumi, Brian. "Purple phosphene." Angelaki 4, no. 3 (December 1999): 219–20. http://dx.doi.org/10.1080/09697259908572072.
Повний текст джерелаKanamaru, Manami, Phan Xuan Tan, and Eiji Kamioka. "Simulation-Based Designing of Suitable Stimulation Factors for Presenting Two Phosphenes Simultaneously to Lower Side of Field of View." Bioengineering 9, no. 12 (December 2, 2022): 752. http://dx.doi.org/10.3390/bioengineering9120752.
Повний текст джерелаAvraham, David, and Yitzhak Yitzhaky. "Effects of Depth-Based Object Isolation in Simulated Retinal Prosthetic Vision." Symmetry 13, no. 10 (September 22, 2021): 1763. http://dx.doi.org/10.3390/sym13101763.
Повний текст джерелаSteidley, K. David. "The radiation phosphene." Vision Research 30, no. 8 (January 1990): 1139–43. http://dx.doi.org/10.1016/0042-6989(90)90171-g.
Повний текст джерелаNissi, Janita, and Ilkka Laakso. "Magneto- and electrophosphene thresholds in the retina: a dosimetry modeling study." Physics in Medicine & Biology 67, no. 1 (January 7, 2022): 015001. http://dx.doi.org/10.1088/1361-6560/ac46df.
Повний текст джерелаKanamaru, Manami, Phan Xuan Tan, and Eiji Kamioka. "Simulation-Based Clarification of Appropriate Factors for Presenting Phosphene in Two Directions Avoiding Electrical Interference." Bioengineering 8, no. 8 (August 5, 2021): 111. http://dx.doi.org/10.3390/bioengineering8080111.
Повний текст джерелаNiketeghad, Soroush, Abirami Muralidharan, Uday Patel, Jessy Dorn, Robert Greenberg, and Nader Pouratian. "150 Effect of Stimulation Parameters on Visual Percepts Elicited by Stimulation of a Visual Cortical Prosthesis for the Blind." Neurosurgery 64, CN_suppl_1 (August 24, 2017): 236. http://dx.doi.org/10.1093/neuros/nyx417.150.
Повний текст джерелаДисертації з теми "Phosphene"
Deerenberg, Sirik. "Stereogenic phosphorus containing phosphine-phosphite ligands in asymmetric catalysis." [S.l. : Amsterdam : s.n.] ; Universiteit van Amsterdam [Host], 2000. http://dare.uva.nl/document/57171.
Повний текст джерелаPassays, Johan. "Nouveaux ligands mixtes de type phosphore / carbène N-hétérocyclique : synthèse et applications en catalyse asymétrique." Thesis, Rouen, INSA, 2011. http://www.theses.fr/2011ISAM0008.
Повний текст джерелаA straightforward method for the preparation of new bidentate ligands containing aphosphine or a phosphite and a carbene function was developed. Different phosphorus-imidazolium compounds were prepared according to this method. First, diphenylphosphine-NHC ligands featuring a stereogenic center a to the phosphine were synthesized from b-hydroxyesters. This strategy was then extended to the preparation of phosphite-imidazoliumand dialkylphosphine-imidazolium compounds. Complexation of these phosphorus-NHCligands with different metals like Ir or Rh was performed in order to study there catalytic properties in asymmetric hydrogenation
Phung, Quang Linh. "Synthèse de ligands chiraux de type phosphine-phosphite et phosphine-carbène N-hétérocyclique pour la catalyse asymétrique." Rouen, 2005. http://www.theses.fr/2005ROUES033.
Повний текст джерелаCatalytic asymmetric synthesis using organometallic reagents has become one of the most active areas of research in modern organic synthesis. To achieve the highest levels of reactivity and selectivity in catalytic enantioselective reactions, several reactions parameters must be optimized. Among them, the selection and design of the chiral ligand is perhaps the most crucial step. We have developed two families of bidentate ligands : phosphine-phosphite and phosphine N-heterocyclic carbene. These two series of ligands have a chiral center to the α-position next to the phosphine moiety. This stereogenic α-position could be of great importance since the phosphorus atom is directly associated with the transition metal in the asymmetric reaction. Phosphine-phosphite ligands were tested in the Rh-catayzed asymmetric hydrogenation (ee up to 84%) and hydroformylation (no asymmetric induction). Phosphine N-heterocyclic carbene ligands were tested in the Ir-catalyzed asymmetric hydrogenation and hydrosilylation (no asymmetric induction), and with promising results in the Suzuki-Miyaura cross-coupling reaction
Klüpfel, Bernd. "P-chirale funktionelle Phosphane durch Hydrophosphinierung mit kationischen Phosphan-Eisenkomplexen." [S.l. : s.n.], 2002. http://deposit.ddb.de/cgi-bin/dokserv?idn=966083458.
Повний текст джерелаJavierre, Guilhem. "Understand the inversion mechanism of P-stereogenic compound using kinetic studies and in silico modeling." Thesis, Ecole centrale de Marseille, 2018. http://www.theses.fr/2018ECDM0001/document.
Повний текст джерелаThis thesis is about the racemization of alkyl hydrogeno-phenylphosphinate, a molecule centered on a stereogenic phosphorus atom. We have synthetized compounds of interest, and studied their kinetic of racemization with chiral HPLC and phosphorus NMR. The first theoretical study (SMD//M06-2X/6-31++G**) about the enantiomerization of alkyl phosphinate after an SN2 with an alcohol have shown that the most favored mechanism was a syn-addition of the alcohol onto the double bond P=O on the opposite side of the alkoxy group. Kinetic studies with ethyl phosphinate in ethanol under reflux have shown an inversion barrier around 135 kJ.mol-1, in excellent agreement with this model (136 kJ.mol-1). The addition of a basic compound during kinetic measurements has shown a decreasing of the barrier to 121.5 kJ.mol-1, showing a catalytic effect. Kinetic and theoretical models have suggested that the mechanism would go through an activation of the alcohol by the basic compound which would facilitate its addition. The first tests about the nature of the alkyl group of phosphinate and alcohol have shown a general dependency of the barrier with the hindrance, but some DFT models, especially with adamantyl, have been in disagreement with this hypothesis
Alcaraz, Gilles. "Espèces déficientes en électrons et cycles tendus alpha-phosphorés." Toulouse 3, 1995. http://www.theses.fr/1995TOU30126.
Повний текст джерелаSchmidt, Anette. "Phosphide und Phosphate des Cobalts Kristallisation, Thermodynamik, Strukturen und Farben /." [S.l. : s.n.], 2002. http://deposit.ddb.de/cgi-bin/dokserv?idn=965185273.
Повний текст джерелаHarrison, Mark Anthony. "EXPOSURE TO PHOSPHINE GAS DURING APPLICATION OF MAGNESIUM PHOSPHIDE IN STORED PRODUCT WAREHOUSES." VCU Scholars Compass, 1990. http://scholarscompass.vcu.edu/etd/4909.
Повний текст джерелаTohme, Ayham. "Synthèse et étude de phosphines organométalliques électrocommutables pour la catalyse." Thesis, Rennes 1, 2014. http://www.theses.fr/2014REN1S012/document.
Повний текст джерелаDuring this work, we have synthesized and characterized new metalloligands bearing redox-active organometallic end-groups. Switching the redox state of the latter should modify the electronic properties of the studied metalloligands. Once these are complexed to a metal, this should induce a change of the metal’s electronic density, which results ideally in a change of its catalytic activity. First, we studied triarylphosphine ligands bearing one or three organoiron end-groups. Four of these metalloligands were fully characterized in both their reduced and oxidized states, and their electronic parameters were evaluated using two different experimental methods. Later on, corresponding Pd(II) complexes were also synthesized and their catalytic preformances were tested. In the second part of this work, organometallic Fe(II) alkynyldiarylphosphine derivatives were synthesized. Upon oxidation, the resulting species was found to be unstable, leading to the formation of dicationic bis-acetylide Fe(II) complexes, that were isolated and characterized. The dimerization process was inhibited either by sequestration of the electronic lone pair of the phosphorus atom, or by controlling the steric hindrance around that center. Finally, corresponding precatalysts were synthesized and, upon the oxidation of the metalloligands, they were found to be fairly stable compounds. Some of these complexes were also tested in a catalytic transformation
Mocanu, Olivia. "Phosphole and phosphepine-based π-systems : synthesis, reactivity and physical properties". Thesis, Rennes 1, 2017. http://www.theses.fr/2017REN1S166.
Повний текст джерелаThis manuscript describes the synthesis and characterisation of new heterocyclic π-conjugated systems built around the phosphorus atom. Firstly, an introduction to the phosphole chemistry (synthesis methods and integration into π-conjugated systems) is presented. The chapter I describes the synthesis and physico-chemical properties of pyrene functionalised either by a phosphole or silole ring. The synthesis of these new structures was achieved by using a transition-metal catalysis. Two types of regioisomers were synthesised in order to study the effect of the heteroatom (P or Si) on the optical and electrochemical properties together with the impact on the solid-state organisation. The chapter II describes the synthesis and the physical properties of the first phosphole-based Ir(III) ortho-metallated complexes. The presence of two stereogenic centres in the complex induced diastereoselectivity issues that could be solved by carefully choosing the reaction conditions. Furthermore, it was demonstrated that the nature of the ligands can tune the optical and the redox properties. The chapter III describes the use of P-containing seven-membered rings (phosphepines) for the development of new π-conjugated systems. Two original π-systems have been synthesised and studied: (i) phosphepine based PAH and (ii) dithieno-phosphepines. The optical and redox properties have been investigated and discussed in the manuscript
Книги з теми "Phosphene"
executive, Health and safety. Fumigation using phosphine. London: H.M.S.O., 1986.
Знайти повний текст джерелаDavis, B. E. Recovery of phosphate from Florida phosphate slimes. Pittsburgh, Pa: U.S. Dept. of the Interior, Bureau of Mines, 1987.
Знайти повний текст джерелаRazzaque, Mohammed S., ed. Phosphate Metabolism. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-91623-7.
Повний текст джерелаGriffith, Edward J. Phosphate Fibers. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-1045-5.
Повний текст джерелаBergeron, Pierre. Phosphènes célestes. Longueuil, Québec: Productions Imagie, 2009.
Знайти повний текст джерелаInternational Program on Chemical Safety., International Labour Organisation, World Health Organization, United Nations Environment Programme, and WHO Task Group on Environmental Health Criteria For Tricresyl Phosphate., eds. Tricresyl phosphate. Geneva: World Health Organization, 1990.
Знайти повний текст джерелаGriffith, Edward J. Phosphate Fibers. Boston, MA: Springer US, 1995.
Знайти повний текст джерелаPhosphate fibers. New York: Plenum Press, 1995.
Знайти повний текст джерелаGreat Britain. Ministry of Agriculture Fisheries and Food., ed. Phosphate fertilisers. Alnwick: Great Britain, 1987.
Знайти повний текст джерелаN, Nikonov G., та Arbuzov Boris Aleksandrovich 1903-, ред. Funkt͡s︡ionalʹnozameshchennye fosfiny i ikh proizvodnye. Moskva: "Nauka", 1986.
Знайти повний текст джерелаЧастини книг з теми "Phosphene"
Stronks, H. Christiaan, and Gislin Dagnelie. "Phosphene Mapping Techniques for Visual Prostheses." In Visual Prosthetics, 367–83. Boston, MA: Springer US, 2011. http://dx.doi.org/10.1007/978-1-4419-0754-7_19.
Повний текст джерелаEvreinova, Tatiana G., Grigori Evreinov, and Roope Raisamo. "Camera Based Target Acquisition Augmented with Phosphene Sensations." In Lecture Notes in Computer Science, 282–89. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-14100-3_42.
Повний текст джерелаBhalla, Ashish. "Phosphate and Phosphine." In Critical Care Toxicology, 1875–85. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-17900-1_84.
Повний текст джерелаBhalla, Ashish. "Phosphine and Metal Phosphide." In Critical Care Toxicology, 1–11. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-20790-2_84-1.
Повний текст джерелаChen, Hao, and Luwu He. "Catalytic activity for hydrogen evolution reaction in phosphene nanoribbons: A first-principles study." In Advances in Applied Chemistry and Industrial Catalysis, 292–97. London: CRC Press, 2022. http://dx.doi.org/10.1201/9781003308553-45.
Повний текст джерелаFehervari, Tamas, Masaru Matsuoka, Hirotsugu Okuno, and Tetsuya Yagi. "Real-Time Simulation of Phosphene Images Evoked by Electrical Stimulation of the Visual Cortex." In Neural Information Processing. Theory and Algorithms, 171–78. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-17537-4_22.
Повний текст джерелаLoubser, Christa, Simon Lotz, and John E. Ellis. "Tricarbonyl Phosphine, Phosphite, and Arsine Derivatives of Cobalt(I)." In Inorganic Syntheses, 174–82. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132609.ch42.
Повний текст джерелаPasek, Matthew A. "Phosphine." In Encyclopedia of Astrobiology, 1229. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-11274-4_1186.
Повний текст джерелаPerkins, Michael W., Benjamin Wong, Dorian Olivera, and Alfred Sciuto. "Phosphine." In Hamilton & Hardy's Industrial Toxicology, 1295–300. Hoboken, New Jersey: John Wiley & Sons, Inc., 2015. http://dx.doi.org/10.1002/9781118834015.ch118.
Повний текст джерелаPasek, Matthew A. "Phosphine." In Encyclopedia of Astrobiology, 1858–59. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-44185-5_1186.
Повний текст джерелаТези доповідей конференцій з теми "Phosphene"
Feely, Grace, and Young-A. Lee. "Phosphene." In Pivoting for the Pandemic. Iowa State University Digital Press, 2020. http://dx.doi.org/10.31274/itaa.11778.
Повний текст джерелаNanduri, D., M. S. Humayun, R. J. Greenberg, M. J. McMahon, and J. D. Weiland. "Retinal prosthesis phosphene shape analysis." In 2008 30th Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 2008. http://dx.doi.org/10.1109/iembs.2008.4649524.
Повний текст джерелаZhao, Ying, Kun Yang, Bo Pang, Yongji Wang, and Qiushi Ren. "Simulated phosphene model for visual prosthesis." In 2012 5th International Conference on Biomedical Engineering and Informatics (BMEI). IEEE, 2012. http://dx.doi.org/10.1109/bmei.2012.6512915.
Повний текст джерелаDagnelie, Gislin, and Jacob V. Vogelstein. "Phosphene Mapping Procedures for Prosthetic Vision." In Vision Science and its Applications. Washington, D.C.: OSA, 1999. http://dx.doi.org/10.1364/vsia.1999.mb3.
Повний текст джерелаBollen, Caroline J. M., Richard J. A. van Wezel, Marcel A. J. van Gerven, and Yağmur Güçlütürk. "Emotion Recognition with Simulated Phosphene Vision." In the 2nd Workshop. New York, New York, USA: ACM Press, 2019. http://dx.doi.org/10.1145/3347319.3356836.
Повний текст джерелаSavage, Craig O., and Mark E. Halpern. "Phosphene brightness modelling for voltage driven waveforms." In 2011 Seventh International Conference on Intelligent Sensors, Sensor Networks and Information Processing (ISSNIP). IEEE, 2011. http://dx.doi.org/10.1109/issnip.2011.6146575.
Повний текст джерелаOkuno, H., T. Fehervari, M. Matsuoka, S. Kameda, and T. Yagi. "Portable phosphene image generator simulating cortical visual prosthesis." In 2012 IEEE Biomedical Circuits and Systems Conference (BioCAS 2012). IEEE, 2012. http://dx.doi.org/10.1109/biocas.2012.6418465.
Повний текст джерелаGranley, Jacob, and Michael Beyeler. "A Computational Model of Phosphene Appearance for Epiretinal Prostheses." In 2021 43rd Annual International Conference of the IEEE Engineering in Medicine & Biology Society (EMBC). IEEE, 2021. http://dx.doi.org/10.1109/embc46164.2021.9629663.
Повний текст джерелаPerez-Yus, Alejandro, Jesus Bermudez-Cameo, Jose J. Guerrero, and Gonzalo Lopez-Nicolas. "Depth and Motion Cues with Phosphene Patterns for Prosthetic Vision." In 2017 IEEE International Conference on Computer Vision Workshop (ICCVW). IEEE, 2017. http://dx.doi.org/10.1109/iccvw.2017.179.
Повний текст джерелаZhao, Ying, and Qiushi Ren. "Recognition of Chinese character formed by irregular simulated phosphene arrays." In 2012 11th International Conference on Signal Processing (ICSP 2012). IEEE, 2012. http://dx.doi.org/10.1109/icosp.2012.6492028.
Повний текст джерелаЗвіти організацій з теми "Phosphene"
Raghothama, Kashchandra G., Avner Silber, and Avraham Levy. Biotechnology approaches to enhance phosphorus acquisition of tomato plants. United States Department of Agriculture, January 2006. http://dx.doi.org/10.32747/2006.7586546.bard.
Повний текст джерелаCollings, R. K. Phosphate. Natural Resources Canada/CMSS/Information Management, 1991. http://dx.doi.org/10.4095/328633.
Повний текст джерелаChandler, F. W., and R. L. Christie. Stratiform phosphate. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1995. http://dx.doi.org/10.4095/207952.
Повний текст джерелаHay, M., and W. King. PHOSPHATE MANAGEMENT: FY2010 RESULTS OF PHOSPHATE PRECIPITATION TESTS. Office of Scientific and Technical Information (OSTI), April 2011. http://dx.doi.org/10.2172/1013047.
Повний текст джерелаGrasby, S. E., and J. M. Galloway. Rare-earth elements of Permian through Cretaceous strata of the Sverdrup Basin, Nunavut and Northwest Territories. Natural Resources Canada/CMSS/Information Management, 2022. http://dx.doi.org/10.4095/330202.
Повний текст джерелаLumetta, Gregg J., Jenifer C. Braley, Matthew K. Edwards, Odeta Qafoku, Andrew R. Felmy, Jennifer C. Carter, and Paul J. MacFarlan. Removing Phosphate from Hanford High-Phosphate Tank Wastes: FY 2010 Results. Office of Scientific and Technical Information (OSTI), September 2010. http://dx.doi.org/10.2172/992014.
Повний текст джерелаMailen, J. C., and O. K. Tallent. Separation of uranium and dibutyl phosphate contained in 30 vol % tributyl phosphate solvents. Office of Scientific and Technical Information (OSTI), July 1986. http://dx.doi.org/10.2172/5399500.
Повний текст джерелаBoyd, Bruce A., and Robert H. Neilson. Synthesis of (1,3-Disilylpropenyl)Phosphines. Fort Belvoir, VA: Defense Technical Information Center, January 1989. http://dx.doi.org/10.21236/ada204375.
Повний текст джерелаZhang, X., A. Linsebigler, U. Heiz, J. T. Yates, and Jr. Phosphine Chemistry on Mo(110) and Oxidized Mo(110). Fort Belvoir, VA: Defense Technical Information Center, January 1993. http://dx.doi.org/10.21236/ada266717.
Повний текст джерелаAnderson, M. A., W. A. Zeltner, and C. G. Jr Hill. Development of phosphate-based ceramic membranes. Office of Scientific and Technical Information (OSTI), November 1992. http://dx.doi.org/10.2172/7164518.
Повний текст джерела