Literatura académica sobre el tema "Carbon(0) complexes"
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Artículos de revistas sobre el tema "Carbon(0) complexes"
Klein, Hans-Friedrich, Goetz Lull, Birgit Rodenhäuser, Gerhard Cordier y Helmut Paulus. "Monoolefincobalt(0)-Komplexe / Monoolefincobalt(0) Complexes". Zeitschrift für Naturforschung B 43, n.º 10 (1 de octubre de 1988): 1256–62. http://dx.doi.org/10.1515/znb-1988-1008.
Texto completoZhao, Lili, Chaoqun Chai, Wolfgang Petz y Gernot Frenking. "Carbones and Carbon Atom as Ligands in Transition Metal Complexes". Molecules 25, n.º 21 (26 de octubre de 2020): 4943. http://dx.doi.org/10.3390/molecules25214943.
Texto completoFrenking, Gernot y Ralf Tonner. "Divalent carbon(0) compounds". Pure and Applied Chemistry 81, n.º 4 (1 de enero de 2009): 597–614. http://dx.doi.org/10.1351/pac-con-08-11-03.
Texto completoMour, İzzet A., Saim Ozkar y Cornelius G. Kreiter. "Synthesis and Spectroscopic Studies of Pentacarbonylfumaronitrile-chromium(0), -molybdenum(0), and -tungsten(0)". Zeitschrift für Naturforschung B 49, n.º 8 (1 de agosto de 1994): 1059–62. http://dx.doi.org/10.1515/znb-1994-0808.
Texto completoBohanna, Cristina, Miguel A. Esteruelas, Fernando J. Lahoz, Enrique Onate, Luis A. Oro y Eduardo Sola. "Synthesis of Butadiene-Osmium(0) and -Ruthenium(0) Complexes by Reductive Carbon-Carbon Coupling of Two Alkenyl Fragments". Organometallics 14, n.º 10 (octubre de 1995): 4825–31. http://dx.doi.org/10.1021/om00010a051.
Texto completoMorkan, İ. Amour y A. Uztetik-Morkan. "Photochemical Synthesis and Identification of Tetracarbonyl-bis(olefin)metal(0) Complexes of Group VI B Elements". Zeitschrift für Naturforschung B 55, n.º 12 (1 de diciembre de 2000): 1153–56. http://dx.doi.org/10.1515/znb-2000-1208.
Texto completoMour, İzzet A. y Saim Özkar. "Synthesis and Spectroscopic Study of Pentacarbonyl(η2-tetracyanoethylene) Metal(0) Complexes of the Group 6 B Elements". Zeitschrift für Naturforschung B 49, n.º 5 (1 de mayo de 1994): 717–20. http://dx.doi.org/10.1515/znb-1994-0525.
Texto completoAlcock, Nathaniel W., Graham A. Pike, Christopher J. Richards y Susan E. Thomas. "Generation of homochiral quaternary carbon centres from (vinylketenimine)tricarbonyliron(0) complexes". Tetrahedron: Asymmetry 1, n.º 8 (enero de 1990): 531–34. http://dx.doi.org/10.1016/s0957-4166(00)80542-x.
Texto completoRaubenheimer, Helgard G., Simon Lotz, Gert J. Kruger, Antonie van A. Lombard y Joey C. Viljoen. "Reactions of deprotonated sulphur-donor complexes of pentacarbonylchromium(0) with carbon disulphide or carbon diselenide". Journal of Organometallic Chemistry 336, n.º 3 (diciembre de 1987): 349–60. http://dx.doi.org/10.1016/0022-328x(87)85194-x.
Texto completoPAGANELLI, S., U. MATTEOLI, A. SCRIVANTI y C. BOTTEGHI. "ChemInform Abstract: Pt(0) Complexes as Catalyst Precursors for Homogeneous Carbon-Carbon and Carbon-Oxygen Double Bond Hydrogenation." ChemInform 22, n.º 6 (23 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199106053.
Texto completoTesis sobre el tema "Carbon(0) complexes"
Gigou, Thomas. "Vers des complexes de carbone(0) à l'aide de la chimie de l'iode hypervalent : Nouveaux ylures d’iodonium nucléophiles stabilisés par une sulfone". Electronic Thesis or Diss., Bordeaux, 2023. http://www.theses.fr/2023BORD0501.
Texto completoBis ylides are divalent carbonated s pecies on which a central carbon atom bears two negative charges, both stabilized by two α, positively charged heteroatoms. Selectively transferring the central carbon atom, using both ylides simultaneously is of great interest for synthetic chemists. Such atomic carbon sources are scarce, as most of the bis ylides developed until now were too tightly bind to his ligands. With this in mind, this thesis ambitions to develop bis ylides and other reactive species containing an iodonium ligand, an extremely labile fragment which could allowed an efficient liberation of the central carbon atom. The first chapter is dedicated to the state of the art of “carbon(0)” compounds and their application as atomic carbon sources, as well as the structure and reactivity of hypervalent iodine compounds. The second chapter is about releasing bis ylides by cleaving a covalent bond, either a P C bond from a phosphine oxide stabilized mixt phospho iodonium ylide, or a Si C bond from a silane stabilized mixt phospho iodonium ylide. A third chapter explains our attempts to obtain bis ylides precursor by direct iodination of nucleophilic phosphonium or sulfoxonium ylides. The last chapter is dedicated to our attempt to develop an iodonium yldiide, in which only one of the two negative charges borne by the central carbon is next to a positively charged heteroatom, the other being stabilized by a sulfonyl mesomeric and inductive effects. The results of those attempts allowed us to describe the reactivity of a new nucleophilic, mono stabilized iodonium ylide towards aldehydes
Rochon, Alexandra. "Cycloaddition Reactions of Ni(0) Difluorocarbene Complexes: Investigating the Formation of Various Perfluorometallacycles". Thesis, Université d'Ottawa / University of Ottawa, 2019. http://hdl.handle.net/10393/39026.
Texto completoLevell, Tamzyn J. "Substituted Fischer carbene complexes of molybdenum(0)". Diss., University of Pretoria, 2014. http://hdl.handle.net/2263/46250.
Texto completoDissertation (MSc)--University of Pretoria, 2014.
tm2015
Chemistry
MSc
Unrestricted
Fraser, Roan. "Fischer and N-heterocyclic carbene complexes of chromium(0)". Diss., University of Pretoria, 2012. http://hdl.handle.net/2263/31504.
Texto completoDissertation (MSc)--University of Pretoria, 2012.
Chemistry
MSc
Unrestricted
Pretorius, René. "Fischer and N-heterocyclic carbene complexes of tungsten(0)". Diss., University of Pretoria, 2012. http://hdl.handle.net/2263/31515.
Texto completoDissertation (MSc)--University of Pretoria, 2012.
Chemistry
MSc
Unrestricted
Boussouf, Karim. "Etude systématique des complexes Znq+Imn (où q = 0, 1, 2; n = 1 – 4)". Thesis, Paris Est, 2016. http://www.theses.fr/2016PESC1094/document.
Texto completoThe main goal of this work is to examine the capabilities of M05-2X, M05-2X+D3, PBE0, PBE0+D3, PBE, PBE+D3 and M11 functionals with and without inclusion of D3 dispersion correction for the accurate description of medium sized organometallic compounds and therefore their use for the determination of study of the equilibrium structure, the stability, the spectroscopy and the chemical bonding (covalent, charge transfer and van der Waals) of Znq+Im (q = 0,1,2) complexes. This is done through close comparisons of the results obtained by the M05-2X, M05-2X+D3, PBE0, PBE0+D3, PBE, PBE+D3, M11 functionals with and without inclusion of D3 dispersion correction and those from the standard ((R)MP2 and (R)CCSD(T)) and explicitly correlated ab initio methods (R)CCSD(T)-F12 and (R)MP2-F12. Therefore, we definitely establish that M05-2X+D3 and PBE0+D3 in connection with the 6-311++G(d,p) basis set are the methods of choice for the accurate description of medium sized organometallic compounds. This is illustrated through a systematic study of Zn+qIm of (q=0, 1, 2) complexes which play crucial roles in chemical, biological and industrial domains. Through these comparisons, we show that the results obtained at the M05-2X, M05-2X+D3, PBE0, PBE0+D3, PBE, PBE+D3, M11 levels are in good agreement with those explicitly correlated (R)MP2-F12 and (R)CCSD(T)-F12 methods. Through these comparisons, our study establishes the ability and reliability of M05-2X(+D3) functional for the accurate description of covalent and noncovalent interactions between Znq+ and Im since it leads to close agreement with the large ab initio techniques. PBE0 and M11 may be used also for that purposes. Then, we used high performance M05-2X and PBE0 functionals with and without inclusion of D3 dispersion correction in connection along with the 6-311++G(d,p) basis set to study the equilibrium structure, the stability, the spectroscopy and the chemical bonding (covalent, charge transfer and van der Waals) of Znq+Imn (q = 0, 1, 2, n = 1−4) complexes. This work, at the microscopic level, is useful for understanding the structural and bonding occurring in naturally zinc-binding sites and to figure out the behavior of much more complex biological systems. This should help for designing new zinc-binding proteins and more generally new metal sites in known proteins or ZIFs. The structural backbone of ZIFs is constructed from tetrahedral units formed by one bivalent metal ion (M2+ = Zn2+/Co2+) and four imidazolate anions. Such compounds present a well-established structural topology with a large structural diversity. They exhibit a high porosity which is potentially used for gas storage and separation techniques.Such quantities at the microscopic level are needed to deduce the macroscopic and thermochemical properties of these compounds with good accuracy after incorporation into dynamical simulations
Ansell, Melvyn B. "Novel (N-heterocyclic carbene)-palladium(0) complexes as catalysts in element-element bond additions to unsaturated moieties". Thesis, University of Sussex, 2017. http://sro.sussex.ac.uk/id/eprint/68072/.
Texto completoDesjardins, Sylvie Yolande. "N-0 Chelated Nickel(II) Complexes as Catalysts for Ethene Oligomerisation, Polymerisation and Ethene/Carbon Monoxide Co-Polymerisation". Thesis, 1997. https://eprints.utas.edu.au/19946/1/whole_DesjardinsSylvieYolande1997_thesis.pdf.
Texto completoJhou, Yang Ming y 周晏銘. "Synthesis of Palladium Metal Complexes Containing N-heterocyclic Carbene as Catalysts for C-C Coupling Reactions, and Study of Oxidative Addition by Pd(0) Complex". Thesis, 2011. http://ndltd.ncl.edu.tw/handle/31478569479309711823.
Texto completo國立彰化師範大學
化學系
99
The goal of this study is to design a series of active metal complexes for catalyzing various organic chemstry. During the last two decades, stable carbenes, especially N-heterocyclic carbene (NHCs), have been widely used as ligands for transition-metal complexes. Among their most appealing features is their strong -donor ability which can be superior to that of very basic phosphine. The monodentate palladium (0) and bidentate palladium (II) N-heterocyclic carbene complexes which bear amide functionalities have been successfully synthesized and were prepared from the amide-imidazolium salt. The series of palladium (0) complexes included two types of unsaturated N-heterocyclic carbene ligand precursors bearing amide moieties. Besides, the palladium (II) complexes contained bis-bidentate trans-configured isomer and chelating bidentate trans/cis isomers with pyridine-type ligand. All complexes are characterized by NMR analysis and their structural properties are determined by single-crystal X-ray crystallography. Through the study, it can be seen that the hereby palladium (0) complexes obtaining N-heterocyclic carbene and amide moieties with high electron donating property have a most salient advantage, which is able to catalyze with high efficiency in Suzuki-Miyaura、Mizoroki-Heck and direct arylation aryl-indolyl C-C coupling reactions. We also demonstrated using pentafluoroiodobenzene that the palladium (0) complex which contained a steric bulky mesityl functionality and a monodentate amide methyl-blocked moiety can proceed through oxidative addition pathway. This pathway leads to many interesting products and it is difficult to understand the mechanism and carry out the isolation. In this thesis, we resolve the problem by a preparative method such that a very interesting complex was successfully obtained and structurally characterized. Finally, the catalytic results show that the active palladim (0) complexes can deliver higher activities in the C-C coupling reactions under Suzuki、Heck and direct arylation reaction conditions.
Shen, Jiun-Shian y 沈俊賢. "Synthesis of Palladium (0) Complexes Containing Phosphine and N-heterocyclic Carbene Ligands for-Application in C-C Cross Coupling Reactions and Synthesis of-Self-Assembly Material for Application in Hydrothermal Synthesis". Thesis, 2012. http://ndltd.ncl.edu.tw/handle/18703033005423025555.
Texto completo國立彰化師範大學
化學系
100
Two series of potentially bidentate ligands bearing N-heterocycylic carbene and phosphine moieties were synthesized. For the phosphine moieties, two different substituents with different electronic and steric properties (PPh2 and PCy2) were employed. After successfully isolation of the ligand precusors, palladium(0) complexes bearing these ligands, 4a–i, were prepared. The complexes were characterized by 1H and 31P{NMR} spectroscopy, electron-spray mass spectrometry, elemental analysis as well as X-ray crystallography. Interestinly, the structures exhibit two different orientations for the coordinated maleic anhydride. Complex 4i shows a fluxional behavior in solution and the exchange process has been successfully investigated by theoretical computation. The catalytic properties of these new complexes were examined. Among them, 4a proved to be the most active in Mizoroki—Heck coupling reaction. The substrate scope was then investigated in detail. Palladium(0) complex was never employed as catalyst system in direct arylation raction. Herein, we showed that 4a is very promising in such non-traditional coupling reaction. Finally, we applied the technology of direct arylation to prepare a bitopic ligand, dipa, and successfully obtain some interesting cooridination polymers.
Libros sobre el tema "Carbon(0) complexes"
Chauvin, Remi y Yves Canac, eds. Transition Metal Complexes of Neutral eta1-Carbon Ligands. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-04722-0.
Texto completoFischer, H., ed. Inorganic Radicals, Metal Complexes and Nonconjugated Carbon Centered Radicals. Part 1. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-48466-0.
Texto completoBalestero, Gabriela Soares. Gênero, raça, classe e o direito: uma análise inclusiva. Editora Amplla, 2022. http://dx.doi.org/10.51859/amplla.grc1006-0.
Texto completoCapítulos de libros sobre el tema "Carbon(0) complexes"
Sakaki, Shigeyoshi y Yasuo Musashi. "Hydrogenation of Carbon Dioxide". En Catalysis by Metal Complexes, 79–105. Boston, MA: Springer US, 2002. http://dx.doi.org/10.1007/0-306-47718-1_4.
Texto completoGali, A., T. Hornos, Peter Deák, N. T. Son, Erik Janzén y W. J. Choyke. "Theoretical Investigations of Complexes of p-Type Dopants and Carbon Interstitial in SiC: Bistable, Negative-U Defects". En Materials Science Forum, 519–22. Stafa: Trans Tech Publications Ltd., 2005. http://dx.doi.org/10.4028/0-87849-963-6.519.
Texto completoSolà, Miquel, Miquel Duran y Maricel Torrent. "The Dötz Reaction: A Chromium Fischer Carbene-Mediated Benzannulation Reaction". En Catalysis by Metal Complexes, 269–87. Boston, MA: Springer US, 2002. http://dx.doi.org/10.1007/0-306-47718-1_11.
Texto completoYusop, Mohd Rafii, Yusuff Oladosu, Abdul Rahim Harun, Asfaliza Ramli, Ghazali Hussin, Mohd Razi Ismail y Norhani Abdullah. "Application of mutation techniques and genotype × environment interaction for grain yield in ion beam induced mutant rice lines tested in multiple locations in Malaysia." En Mutation breeding, genetic diversity and crop adaptation to climate change, 226–34. Wallingford: CABI, 2021. http://dx.doi.org/10.1079/9781789249095.0023.
Texto completoQuesnel, Benoît, Christophe Scheffer y Georges Beaudoin. "The Light Stable Isotope (Hydrogen, Boron, Carbon, Nitrogen, Oxygen, Silicon, Sulfur) Composition of Orogenic Gold Deposits". En Isotopes in Economic Geology, Metallogenesis and Exploration, 283–328. Cham: Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-27897-6_10.
Texto completo"Carbon-carbon bond formation". En Catalysis by Metal Complexes, 209–36. Dordrecht: Springer Netherlands, 2002. http://dx.doi.org/10.1007/0-306-47510-3_6.
Texto completoOstrowska, Sylwia y Steven P. Nolan. "Carbon-Carbon Bond Formation Via Metal Carbene Complexes". En Reference Module in Chemistry, Molecular Sciences and Chemical Engineering. Elsevier, 2022. http://dx.doi.org/10.1016/b978-0-32-390644-9.00091-3.
Texto completoSmith, Anthony K. "Nickel Carbon σ-Bonded Complexes". En Comprehensive Organometallic Chemistry II, 29–106. Elsevier, 1995. http://dx.doi.org/10.1016/b978-008046519-7.00077-0.
Texto completoCanty, Allan J. "Palladium Carbon σ-Bonded Complexes". En Comprehensive Organometallic Chemistry II, 225–90. Elsevier, 1995. http://dx.doi.org/10.1016/b978-008046519-7.00080-0.
Texto completoChung Wai Mak, Thomas, Yu-San Cheung, Gong-Du Zhou y Ying-Xia Wang. "Structural Chemistry of Group 14 Elements". En Structural Chemistry across the Periodic Table, 129–208. Oxford University PressOxford, 2023. http://dx.doi.org/10.1093/oso/9780198872955.003.0004.
Texto completoActas de conferencias sobre el tema "Carbon(0) complexes"
Kalia, Karun y Amir Ameli. "Tensile Properties of 3D-Printed Polycarbonate/Carbon Nanotube Nanocomposites". En ASME 2018 Conference on Smart Materials, Adaptive Structures and Intelligent Systems. American Society of Mechanical Engineers, 2018. http://dx.doi.org/10.1115/smasis2018-8048.
Texto completoSYCHLA, JAKUB y K. T. TAN. "INVESTIGATING EFFECTS OF FIBER LAYERS IN 3D PRINTED CARBON FIBER REINFORCED POLYMER COMPOSITES". En Proceedings for the American Society for Composites-Thirty Seventh Technical Conference. Destech Publications, Inc., 2022. http://dx.doi.org/10.12783/asc37/36490.
Texto completoLiu, Zhenshun y Hongdong Zhen. "Research on Simplified Method of Transients Combining and Loading in Fatigue Crack Growth Analysis of Carbon Steel Nuclear Piping". En 2018 26th International Conference on Nuclear Engineering. American Society of Mechanical Engineers, 2018. http://dx.doi.org/10.1115/icone26-81640.
Texto completoSheikh-Ahmad, Jamal y Rahul Yadav. "Force Prediction in Milling of Carbon Fiber Reinforced Polymers". En ASME 2005 International Mechanical Engineering Congress and Exposition. ASMEDC, 2005. http://dx.doi.org/10.1115/imece2005-81909.
Texto completoMONDAL, ANIRBAN, KUNTAL MAITY, MRINAL C. SAHA y YINGTAO LIU. "DIRECT-INK-WRITING (DIW) OF HIGHER WEIGHT CONCENTRATION OF MILLED CARBON FIBER (MCF) REINFORCED EPOXY COMPOSITE". En Thirty-sixth Technical Conference. Destech Publications, Inc., 2021. http://dx.doi.org/10.12783/asc36/35760.
Texto completoPatterson, Albert E., Seymur Hasanov y Bhaskar Vajipeyajula. "Influence of Matrix Material on Impact Properties of Chopped Carbon Fiber-Thermoplastic Composites Made Using FDM/FFF". En 2022 International Additive Manufacturing Conference. American Society of Mechanical Engineers, 2022. http://dx.doi.org/10.1115/iam2022-88941.
Texto completoOsborne, Dustin T., Doug Biagini, Harold Holmes, Steven G. Fritz, Michael Jaczola y Michael E. Iden. "PR30C-LE Locomotive With DOC and Urea Based SCR: Field Trial and Emissions Testing After 1,500 and 3,000 Hours of Operation". En ASME 2012 Internal Combustion Engine Division Fall Technical Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/icef2012-92014.
Texto completoWolf, Mark E., Jonathan Geersen, Ruben Rojas y Shahab Saadipour. "Project Case Study: Online Sand Removal System for Water Tanks". En SPE Western Regional Meeting. SPE, 2022. http://dx.doi.org/10.2118/209278-ms.
Texto completoShen, Li y Jiu Hui Wu. "Theoretical and Experimental Study on Phononic Crystal Structures for Low-Frequency Noise Reduction in the Brake". En ASME 2013 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/imece2013-62423.
Texto completoDurocher, Antoine, Luming Fan, Benjamin Francolini, Marc Füri, Gilles Bourque, Jeffrey M. Bergthorson, Sean Yun y Patrizio Vena. "Characterization of a Novel AM Micromix Nozzle Burning Methane to Hydrogen". En ASME Turbo Expo 2023: Turbomachinery Technical Conference and Exposition. American Society of Mechanical Engineers, 2023. http://dx.doi.org/10.1115/gt2023-104117.
Texto completoInformes sobre el tema "Carbon(0) complexes"
Chefetz, Benny, Baoshan Xing, Leor Eshed-Williams, Tamara Polubesova y Jason Unrine. DOM affected behavior of manufactured nanoparticles in soil-plant system. United States Department of Agriculture, enero de 2016. http://dx.doi.org/10.32747/2016.7604286.bard.
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