Artigos de revistas sobre o tema "Électrocatalyseur à base de palladium"
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Sodeoka, Mikiko, e Yoshitaka Hamashima. "Acid-base catalysis using chiral palladium complexes". Pure and Applied Chemistry 78, n.º 2 (1 de janeiro de 2006): 477–94. http://dx.doi.org/10.1351/pac200678020477.
Texto completo da fonteNagle, Lorraine C., e L. D. Burke. "Anomalous electrochemical behaviour of palladium in base". Journal of Solid State Electrochemistry 14, n.º 8 (2 de dezembro de 2009): 1465–79. http://dx.doi.org/10.1007/s10008-009-0975-2.
Texto completo da fonteVila, J. M., M. T. Pereira, A. Suárez, E. Gayoso, M. Gayoso, J. Selbin e A. Sen. "Cyclometallation, Palladium(II) Complexes with Schiff Base Ligands". Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 16, n.º 4 (janeiro de 1986): 499–511. http://dx.doi.org/10.1080/00945718608055924.
Texto completo da fonteWang, Xiaoping, Nancy Kariuki, Suhas Niyogi, Matt C. Smith, Deborah J. Myers, Timo Hofmann, Yufeng Zhang, Marcus Bär e Clemens Heske. "Bimetallic Palladium-Base Metal Nanoparticle Oxygen Reduction Electrocatalysts". ECS Transactions 16, n.º 2 (18 de dezembro de 2019): 109–19. http://dx.doi.org/10.1149/1.2981848.
Texto completo da fonteR., Dileep, e Badekai Ramachandra Bhat. "Palladium-Schiff base-triphenylphosphine catalyzed oxidation of alcohols". Applied Organometallic Chemistry 24, n.º 9 (26 de agosto de 2010): 663–66. http://dx.doi.org/10.1002/aoc.1683.
Texto completo da fonteKumar, Rajnish, e Ganesan Mani. "Exhibition of the Brønsted acid–base character of a Schiff base in palladium(ii) complex formation: lithium complexation, fluxional properties and catalysis of Suzuki reactions in water". Dalton Transactions 44, n.º 15 (2015): 6896–908. http://dx.doi.org/10.1039/c5dt00438a.
Texto completo da fonteMitin, Anton V., Alexander N. Kashin e Irina P. Beletskaya. "Role of base in palladium-catalyzed arylation of carbanions". Journal of Organometallic Chemistry 689, n.º 6 (março de 2004): 1085–90. http://dx.doi.org/10.1016/j.jorganchem.2003.12.039.
Texto completo da fonteLe Bras, Jean, e Jacques Muzart. "Base-free palladium-mediated cycloalkenylations of olefinic enolic systems". Tetrahedron 71, n.º 48 (dezembro de 2015): 9035–59. http://dx.doi.org/10.1016/j.tet.2015.09.060.
Texto completo da fonteBurke, L. D., e J. K. Casey. "The electrocatalytic behaviour of palladium in acid and base". Journal of Applied Electrochemistry 23, n.º 6 (junho de 1993): 573–82. http://dx.doi.org/10.1007/bf00721948.
Texto completo da fontePankajakshan, Sreekumar, e Teck-Peng Loh. "Base-Free Palladium-Catalyzed Sonogashira Coupling Using Organogold Complexes". Chemistry - An Asian Journal 6, n.º 9 (30 de junho de 2011): 2291–95. http://dx.doi.org/10.1002/asia.201100263.
Texto completo da fonteChen, Bo, e Xiao-Feng Wu. "Palladium-Catalyzed Carbonylative Synthesis of Benzogerminones". Synlett 30, n.º 13 (3 de julho de 2019): 1592–96. http://dx.doi.org/10.1055/s-0037-1611880.
Texto completo da fonteChe Soh, Siti Kamilah, e Mustaffa Shamsuddin. "Tetradentate N2O2Chelated Palladium(II) Complexes: Synthesis, Characterization, and Catalytic Activity towards Mizoroki-Heck Reaction of Aryl Bromides". Journal of Chemistry 2013 (2013): 1–8. http://dx.doi.org/10.1155/2013/632315.
Texto completo da fonteHong, Seok Jun, Jae Woong Choi, Gil Ho Hwang, Won Kyu Han, Joon Shik Park e Sung Goon Kang. "Effect of the Palladium Mid-Layer on the Cyclic Oxidation of Platinum Aluminide Bond Coating". Materials Science Forum 510-511 (março de 2006): 1058–61. http://dx.doi.org/10.4028/www.scientific.net/msf.510-511.1058.
Texto completo da fonteKhanna, P. K., e Deepti Kulkarni. "Reduction of PdCl2 by Emeraldine Base; Synthesis of Palladium Nanoparticles". Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry 38, n.º 7 (5 de setembro de 2008): 629–33. http://dx.doi.org/10.1080/15533170802293402.
Texto completo da fonteTyulyaeva, E. Yu, O. V. Kosareva, M. E. Klyueva e T. N. Lomova. "Acid-base and coordination properties of some palladium(II)porphyrins". Russian Journal of Inorganic Chemistry 53, n.º 9 (setembro de 2008): 1405–10. http://dx.doi.org/10.1134/s0036023608090106.
Texto completo da fonteCuevas, JoséV, e Gabriel García-Herbosa. "Base-catalyzed dehydrogenation of palladium(II) amino to imino complexes". Inorganic Chemistry Communications 1, n.º 10 (outubro de 1998): 372–74. http://dx.doi.org/10.1016/s1387-7003(98)00095-1.
Texto completo da fonteCima, M., e L. Brewer. "The generalized lewis acid-base titration of palladium and niobium". Metallurgical Transactions B 19, n.º 6 (dezembro de 1988): 893–917. http://dx.doi.org/10.1007/bf02651413.
Texto completo da fonteBurke, L. D., e J. K. Casey. "An Examination of the Electrochemical Behavior of Palladium in Base". Journal of The Electrochemical Society 140, n.º 5 (1 de maio de 1993): 1292–98. http://dx.doi.org/10.1149/1.2220973.
Texto completo da fonteKeith, Jason M., e William A. Goddard. "Chelating Base Effects in Palladium-Mediated Activation of Molecular Oxygen". Organometallics 31, n.º 2 (11 de janeiro de 2012): 545–52. http://dx.doi.org/10.1021/om200809u.
Texto completo da fonteCoombs, Robin R., Melissa K. Ringer, Johanna M. Blacquiere, Joshua C. Smith, J. Scott Neilsen, Yoon-Seo Uh, J. Bryson Gilbert et al. "Palladium(II) Schiff base complexes derived from sulfanilamides and aminobenzothiazoles". Transition Metal Chemistry 30, n.º 4 (maio de 2005): 411–18. http://dx.doi.org/10.1007/s11243-004-7625-4.
Texto completo da fonteNoor, Asif, Daniel L. Maloney, James E. M. Lewis, Warrick K. C. Lo e James D. Crowley. "Acid-Base Driven Ligand Exchange with Palladium(II) “Click” Complexes". Asian Journal of Organic Chemistry 4, n.º 3 (24 de outubro de 2014): 208–11. http://dx.doi.org/10.1002/ajoc.201402197.
Texto completo da fonteDileep R., Dileep R., e Badekai Ramachandra Bhat. "ChemInform Abstract: Palladium -Schiff Base - Triphenylphosphine Catalyzed Oxidation of Alcohols." ChemInform 42, n.º 3 (23 de dezembro de 2010): no. http://dx.doi.org/10.1002/chin.201103036.
Texto completo da fonteYamamoto, Yutaro, Hiroshi Matsubara, Hideki Yorimitsu e Atsuhiro Osuka. "Base-Free Palladium-Catalyzed Borylation of Aryl Chlorides with Diborons". ChemCatChem 8, n.º 14 (27 de junho de 2016): 2317–20. http://dx.doi.org/10.1002/cctc.201600456.
Texto completo da fonteSathya, M., e G. Venkatachalam. "Synthesis, Spectral and Catalytic Properties of Palladium(II) Complexes Containing Hydrazone Schiff Base Ligands". Asian Journal of Chemistry 34, n.º 11 (2022): 2922–28. http://dx.doi.org/10.14233/ajchem.2022.23979.
Texto completo da fonteTardiff, Bennett J., Joshua C. Smith, Stephen J. Duffy, Christopher M. Vogels, Andreas Decken e Stephen A. Westcott. "Synthesis, characterization, and reactivity of Pd(II) salicylaldimine complexes derived from aminophenols". Canadian Journal of Chemistry 85, n.º 5 (1 de maio de 2007): 392–99. http://dx.doi.org/10.1139/v07-036.
Texto completo da fonteParunov, Vitaliy Anatol’evich, M. A. Kareva, S. D. Tykochinskiy e I. Yu Lebedenko. "THE DEVELOPMENT OF A NEW METAL ALLOY BASED ON PALLADIUM WITHIN THE FRAMEWORK OF PRACTICAL IMPLEMENTATION OF THE CONCEPT OF DEVELOPMENT OF THE DOMESTIC DENTAL MATERIALS SCIENCE". Russian Journal of Dentistry 21, n.º 3 (15 de junho de 2017): 126–28. http://dx.doi.org/10.18821/1728-2802-2017-21-3-126-128.
Texto completo da fonteJaksic, Ljiljana, e Radmila Dzudovic. "Coulometric-potentiometric determination of pKA of several organic bases in propylene carbonate". Journal of the Serbian Chemical Society 73, n.º 6 (2008): 655–59. http://dx.doi.org/10.2298/jsc0806655j.
Texto completo da fonteVeltri, Lucia, Bartolo Gabriele, Raffaella Mancuso, Patrizio Russo, Giuseppe Grasso, Corrado Cuocci e Roberto Romeo. "Palladium-Catalyzed Carbonylative Synthesis of Functionalized Benzimidazopyrimidinones". Synthesis 50, n.º 02 (23 de novembro de 2017): 267–77. http://dx.doi.org/10.1055/s-0036-1591835.
Texto completo da fonteRen, Li, Austin C. Chen, Andreas Decken e Cathleen M. Crudden. "Chiral bidentate N-heterocyclic carbene complexes of Rh and Pd". Canadian Journal of Chemistry 82, n.º 12 (1 de dezembro de 2004): 1781–87. http://dx.doi.org/10.1139/v04-165.
Texto completo da fonteCeledón, Salvador, Thierry Roisnel, Vania Artigas, Mauricio Fuentealba, David Carrillo, Isabelle Ledoux-Rak, Jean-René Hamon e Carolina Manzur. "Palladium(ii) complexes of tetradentate donor–acceptor Schiff base ligands: synthesis and spectral, structural, thermal and NLO properties". New Journal of Chemistry 44, n.º 22 (2020): 9190–201. http://dx.doi.org/10.1039/d0nj01982h.
Texto completo da fonteM. Sathya e G. Venkatachalam. "Synthesis, Structural Characterization and Catalytic Activities of Palladium(II) Schiff base Complexes Containing Tetradentate N2O2 & N2S2 Donor Ligands". International Journal For Multidisciplinary Research 04, n.º 04 (2022): 417–28. http://dx.doi.org/10.36948/ijfmr.2022.v04i04.045.
Texto completo da fonteAlia, Shaun M., e Yushan Yan. "Palladium Coated Copper Nanowires as a Hydrogen Oxidation Electrocatalyst in Base". Journal of The Electrochemical Society 162, n.º 8 (2015): F849—F853. http://dx.doi.org/10.1149/2.0211508jes.
Texto completo da fonteKhanna, P. K., e Deepti Kulkarni. "Reduction of PdCl2 by Emeraldine Base; Synthesis of Palladium Nano-Particles". Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry 38, n.º 5 (5 de agosto de 2008): 459–63. http://dx.doi.org/10.1080/15533170802255443.
Texto completo da fonteHu, Yanhe, Jing Liu, Zhixin Lü, Xiancai Luo, Heng Zhang, Yu Lan e Aiwen Lei. "Base-Induced Mechanistic Variation in Palladium-Catalyzed Carbonylation of Aryl Iodides". Journal of the American Chemical Society 132, n.º 9 (10 de março de 2010): 3153–58. http://dx.doi.org/10.1021/ja909962f.
Texto completo da fonteStrelow, Franz W. E., e André Victor. "Improved separation of palladium from base metals by cation-exchange chromatography". Analytica Chimica Acta 248, n.º 2 (agosto de 1991): 535–40. http://dx.doi.org/10.1016/s0003-2670(00)84672-3.
Texto completo da fonteHisatsune, Kunihiro, Masayuki Hasaka, Bambang Irawan Sosrosoedirdjo e Koichi Udoh. "Age-hardening behavior in a palladium-base dental porcelain-fused alloy". Materials Characterization 25, n.º 2 (setembro de 1990): 177–84. http://dx.doi.org/10.1016/1044-5803(90)90008-8.
Texto completo da fonteKumagai, N., A. Kawashima, K. Asami e K. Hashimoto. "Anodic characteristics of amorphorous palladium-base alloys in sodium chloride solutions". Journal of Applied Electrochemistry 16, n.º 4 (julho de 1986): 565–74. http://dx.doi.org/10.1007/bf01006851.
Texto completo da fonteAlexander, S., V. Udayakumar e V. Gayathri. "Hydrogenation of olefins by polymer-bound palladium(II) Schiff base catalyst". Journal of Molecular Catalysis A: Chemical 314, n.º 1-2 (dezembro de 2009): 21–27. http://dx.doi.org/10.1016/j.molcata.2009.08.012.
Texto completo da fonteAlperine, S., P. Steinmetz, P. Josso e A. Costantini. "High temperature-resistant palladium-modified aluminide coatings for nickel-base superalloys". Materials Science and Engineering: A 120-121 (dezembro de 1989): 367–72. http://dx.doi.org/10.1016/0921-5093(89)90789-2.
Texto completo da fontePankajakshan, Sreekumar, e Teck-Peng Loh. "ChemInform Abstract: Base-Free Palladium-Catalyzed Sonogashira Coupling Using Organogold Complexes." ChemInform 42, n.º 51 (24 de novembro de 2011): no. http://dx.doi.org/10.1002/chin.201151081.
Texto completo da fonteYamamoto, Yutaro, Keisuke Nogi, Hideki Yorimitsu e Atsuhiro Osuka. "Base-Free Palladium-Catalyzed Hydrodechlorination of Aryl Chlorides with Pinacol Borane". ChemistrySelect 2, n.º 4 (1 de fevereiro de 2017): 1723–27. http://dx.doi.org/10.1002/slct.201700189.
Texto completo da fonteGogoi, Ankur, Anindita Dewan, Geetika Borah e Utpal Bora. "A palladium salen complex: an efficient catalyst for the Sonogashira reaction at room temperature". New Journal of Chemistry 39, n.º 5 (2015): 3341–44. http://dx.doi.org/10.1039/c4nj01822b.
Texto completo da fonteGaube, Gregory, Nahiane Pipaon Fernandez e David C. Leitch. "An evaluation of palladium-based catalysts for the base-free borylation of alkenyl carboxylates". New Journal of Chemistry 45, n.º 43 (2021): 20095–98. http://dx.doi.org/10.1039/d1nj04008a.
Texto completo da fonteDing, Dong, Gang Liu, Guangyang Xu, Jian Li, Guoping Wang e Jiangtao Sun. "Palladium catalyzed N–H bond insertion and intramolecular cyclization cascade: the divergent synthesis of heterocyclics". Org. Biomol. Chem. 12, n.º 16 (2014): 2533–37. http://dx.doi.org/10.1039/c4ob00001c.
Texto completo da fonteStogniy, Marina Yu, Svetlana A. Erokhina, Kirill Yu Suponitsky, Vitaliy Yu Markov e Igor B. Sivaev. "Synthesis and crystal structures of nickel(ii) and palladium(ii) complexes with o-carboranyl amidine ligands". Dalton Transactions 50, n.º 14 (2021): 4967–75. http://dx.doi.org/10.1039/d1dt00373a.
Texto completo da fonteNing, Yuantao, Zhengfen Yang e Huaizhi Zhao. "Platinum Recovery by Palladium Alloy Catchment Gauzes in Nitric Acid Plants". Platinum Metals Review 40, n.º 2 (1 de abril de 1996): 80–87. http://dx.doi.org/10.1595/003214096x4028087.
Texto completo da fonteKratochvíl, Bohumil, Jan Ondráček, Jaroslav Maixner, Josef Macíček e Václav Haber. "Structure of a palladium(II) complex with a non-symmetrical tetradentate Schiff base, [Pd(C14H20N3O)]NCS". Collection of Czechoslovak Chemical Communications 56, n.º 9 (1991): 1900–1907. http://dx.doi.org/10.1135/cccc19911900.
Texto completo da fonteXu, Zhaotao, Jinting Ai e Mingzhong Cai. "An Efficient Heterogeneous Palladium(0)-Catalysed Cross-Coupling between 1-Bromoalkynes and Terminal Alkynes Leading to Unsymmetrical 1,3-Diynes". Journal of Chemical Research 42, n.º 3 (março de 2018): 133–37. http://dx.doi.org/10.3184/174751918x15208574638459.
Texto completo da fonteAmadio, Emanuele, Zoraida Freixa, Piet W. N. M. van Leeuwen e Luigi Toniolo. "Palladium catalyzed oxidative carbonylation of alcohols: effects of diphosphine ligands". Catalysis Science & Technology 5, n.º 5 (2015): 2856–64. http://dx.doi.org/10.1039/c4cy01588f.
Texto completo da fonteChuc, Le Thi Ngoc, Thi Anh Hong Nguyen e Duen-Ren Hou. "Acid–base-sensitive allylic oxidation of 2-allylbenzoic acids to form phthalides". Organic & Biomolecular Chemistry 18, n.º 14 (2020): 2758–68. http://dx.doi.org/10.1039/d0ob00303d.
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