Статті в журналах з теми "Metal-arene compounds"
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Harris, Ronald L. "Bis(arene)metal compounds." Journal of Organometallic Chemistry 299, no. 1 (January 1986): 105–10. http://dx.doi.org/10.1016/0022-328x(86)84037-2.
Повний текст джерелаPekachaki, Henrik Margharian, Saeed Taghvaei-Ganjali, Fereshteh Motiee, and Mandana Saber-Tehrani. "APPLICATION OF CALIXARENE DERIVATIVES AS TACKIFIER RESIN IN RUBBER COMPOUNDS FOR TIRE APPLICATIONS." Rubber Chemistry and Technology 92, no. 3 (July 1, 2019): 467–80. http://dx.doi.org/10.5254/rct.19.81510.
Повний текст джерелаHansen, Valerie M., Jonathan L. Male, and Roland K. Pomeroy. "Arene–manganese and arene–rhenium compounds of formula (arene)M(CO)2(SiCl3)." Canadian Journal of Chemistry 75, no. 5 (May 1, 1997): 531–35. http://dx.doi.org/10.1139/v97-062.
Повний текст джерелаWang, Jie, Hongyu Guan, Chunhua Ge, Ping Fan, Xijuan Xing, and Yunshan Shang. "Azocalix[4]arene with three distal ethyl ester residues as a highly selective chromogenic sensor for Ca2+ ions." Heterocyclic Communications 24, no. 3 (June 27, 2018): 147–50. http://dx.doi.org/10.1515/hc-2017-0239.
Повний текст джерелаZhi, Sanjun, Hongjun Yao, and Wei Zhang. "Difunctionalization of Dienes, Enynes and Related Compounds via Sequential Radical Addition and Cyclization Reactions." Molecules 28, no. 3 (January 23, 2023): 1145. http://dx.doi.org/10.3390/molecules28031145.
Повний текст джерелаSchneider, Jörg J., та Dirk Wolf. "Mechanistische Untersuchungen zum reversiblen Gleichgewicht von metallorganischen Tripeldecker- und Sandwichkomplexen des Typs [Bis{(η5-CpR)Co}-μ-{η4:η4-aren}] und [(η5-CpR)Co(η6-aren)] / Mechanistic Studies towards the Reversible Equilibrium between Metal Organic Triple Decker and Sandwich Complexes [Bis{(η5 -CpR)Co}-μ-{η4 :η4-arene}] and [{(η5-CpR)Co(η6-arene)]". Zeitschrift für Naturforschung B 53, № 11 (1 листопада 1998): 1267–72. http://dx.doi.org/10.1515/znb-1998-1105.
Повний текст джерелаKüppers, Luca, та Walter Frank. "Investigation of mesitylene-solvated group 13 mixed-metal halides: syntheses and crystal structures of bis(1,3,5-trimethylbenzene)gallium(I) tetrachlorido- and tetrabromidoaluminate(III) and (1,3,5-trimethylbenzene)gallium(I) tetraiodidoaluminate(III). Variation of the gallium-π-arene bond strength". Zeitschrift für Naturforschung B 74, № 10 (25 жовтня 2019): 773–82. http://dx.doi.org/10.1515/znb-2019-0139.
Повний текст джерелаPreda, Ana-Maria, Małgorzata Krasowska, Lydia Wrobel, Philipp Kitschke, Phil C. Andrews, Jonathan G. MacLellan, Lutz Mertens та ін. "Evaluation of dispersion type metal···π arene interaction in arylbismuth compounds – an experimental and theoretical study". Beilstein Journal of Organic Chemistry 14 (15 серпня 2018): 2125–45. http://dx.doi.org/10.3762/bjoc.14.187.
Повний текст джерелаHanif, Muhammad, Patricia Schaaf, Wolfgang Kandioller, Michaela Hejl, Michael A. Jakupec, Alexander Roller, Bernhard K. Keppler та Christian G. Hartinger. "Influence of the Arene Ligand and the Leaving Group on the Anticancer Activity of (Thio)maltol Ruthenium(II)–(η6-Arene) Complexes". Australian Journal of Chemistry 63, № 11 (2010): 1521. http://dx.doi.org/10.1071/ch10232.
Повний текст джерелаProfilet, Robert D., Arlene P. Rothwell, and Ian P. Rothwell. "Surface-supported group 5 metal organometallic compounds for catalytic arene hydrogenation." Journal of the Chemical Society, Chemical Communications, no. 1 (1993): 42. http://dx.doi.org/10.1039/c39930000042.
Повний текст джерелаKniazeva, Mariia V., Alexander S. Ovsyannikov, Daut R. Islamov, Aida I. Samigullina, Aidar T. Gubaidullin, Svetlana E. Solovieva, Igor S. Antipin, and Sylvie Ferlay. "Formation of Unsymmetrical Trinuclear Metallamacrocycles Based on Two Different Cone Calix[4]arene Macrocyclic Rings." Crystals 10, no. 5 (May 1, 2020): 364. http://dx.doi.org/10.3390/cryst10050364.
Повний текст джерелаOhto, Keisuke, Nako Fuchiwaki, Hiroaki Furugou, Shintaro Morisada, Hidetaka Kawakita, Marco Wenzel, and Jan J. Weigand. "Comparative Extraction of Aluminum Group Metals Using Acetic Acid Derivatives with Three Different-Sized Frameworks for Coordination." Separations 8, no. 11 (November 8, 2021): 211. http://dx.doi.org/10.3390/separations8110211.
Повний текст джерелаBush, Benjamin F., Vincent M. Lynch, and J. J. Lagowski. "Transition-metal organometallic compounds. 8. Arene exchange reactions of bis(naphthalene)chromium." Organometallics 6, no. 6 (June 1987): 1267–75. http://dx.doi.org/10.1021/om00149a024.
Повний текст джерелаCasagrande, Jr., Osvaldo L., Elton L. S. Gomes, Jairton Dupont, Robert Burrow та Alan J. Lough. "Heterometallic metal carbonyl compounds derived from (η6-arene)tricarbonylchromium bearing propargyl units". Journal of the Chemical Society, Dalton Transactions, № 10 (2001): 1634–38. http://dx.doi.org/10.1039/b009591p.
Повний текст джерелаSchwamm, Ryan J., Christopher M. Fitchett та Martyn P. Coles. "Intramolecular Metal⋅⋅⋅π‐Arene Interactions in Neutral and Cationic Main Group Compounds". Chemistry – An Asian Journal 14, № 8 (16 січня 2019): 1204–11. http://dx.doi.org/10.1002/asia.201801729.
Повний текст джерелаBahojb Noruzi, Ehsan, Behrouz Shaabani, Silvano Geremia, Neal Hickey, Patrizia Nitti, and Hossein Samadi Kafil. "Synthesis, Crystal Structure, and Biological Activity of a Multidentate Calix[4]arene Ligand Doubly Functionalized by 2-Hydroxybenzeledene-Thiosemicarbazone." Molecules 25, no. 2 (January 16, 2020): 370. http://dx.doi.org/10.3390/molecules25020370.
Повний текст джерелаTabaza, Taha A., Omar T. Tabaza, and Amjad Al-Sakarneh. "CVD Technology for Preparing Chromium Oxide Coatings, Study of the Kinetics of Growth of Coatings." Key Engineering Materials 765 (March 2018): 193–98. http://dx.doi.org/10.4028/www.scientific.net/kem.765.193.
Повний текст джерелаPROFILET, R. D., A. P. ROTHWELL, and I. P. ROTHWELL. "ChemInform Abstract: Surface-Supported Group 5 Metal Organometallic Compounds for Catalytic Arene Hydrogenation." ChemInform 24, no. 17 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199317093.
Повний текст джерелаHarvey, Pierre D., Jonathan Gagnon, Réjean Provencher, Bing Xu, and Timothy M. Swager. "Tungsten and molybdenum oxo complexes of tetrakis(phenyldiazenyl)calix[4]arene substituted derivatives: EHMO calculations, spectroscopic characterization, and perturbations of the photophysical properties by neutral guest molecules." Canadian Journal of Chemistry 74, no. 11 (November 1, 1996): 2279–88. http://dx.doi.org/10.1139/v96-256.
Повний текст джерелаMokhtari, Bahram, and Kobra Pourabdollah. "Extraction of s-block metals by nano-baskets of calix[4]crown-3." Canadian Journal of Chemistry 90, no. 6 (June 2012): 560–66. http://dx.doi.org/10.1139/v2012-020.
Повний текст джерелаSaloutin, Victor I., Yulia S. Kudyakova, Marina V. Goryaeva, Yanina V. Burgart, and Oleg N. Chupakhin. "Polyfluoroalkylated 2-ethoxymethylene- 3-oxo esters: synthesis and chemical properties overview." Pure and Applied Chemistry 89, no. 8 (July 26, 2017): 1209–22. http://dx.doi.org/10.1515/pac-2016-1015.
Повний текст джерелаShahnavaz, Zohreh, Lia Zaharani, Mohd Rafie Johan, and Nader Ghaffari Khaligh. "A Green Alternative for Aryl Iodide Preparation from Aromatic Amines." Current Organic Synthesis 17, no. 2 (May 8, 2020): 131–35. http://dx.doi.org/10.2174/1570179417666200203121437.
Повний текст джерелаFerguson, George, Alan J. Lough, Anna Notti, Sebastiano Pappalardo, Melchiorre F. Parisi та Giuseppe Resnati. "Synthesis and ESI-MS Alkali Metal Ion Binding Selectivities of Cone, Partial Cone, and 1,3-Alternate 1,3-Bis(α-picolyloxy)-p-tert-butylcalix[4]arene Crown-6 and 1,1'-Binaphthalene-2,2'-diyl Crown-6 Conformers". Collection of Czechoslovak Chemical Communications 69, № 5 (2004): 1109–25. http://dx.doi.org/10.1135/cccc20041109.
Повний текст джерелаMartins, Felipe Terra, Angélica Faleiros da Silva Maia, Fernando Machado dos Santos, Meiry Edivirges Alvarenga, Leandro Ribeiro, Leonardo da Silva Neto, and Ângelo de Fátima. "Guest-driven unusual conformations in two calix[6]arene solvates and a new calix[8]arene." Zeitschrift für Kristallographie - Crystalline Materials 233, no. 8 (July 26, 2018): 565–78. http://dx.doi.org/10.1515/zkri-2017-2110.
Повний текст джерелаTu, Chuqiao, Kazimierz Surowiec, and Richard A. Bartsch. "Efficient divalent metal cation extractions with di-ionizable calix[4]arene-1,2-crown-4 compounds." Tetrahedron 63, no. 19 (May 2007): 4184–89. http://dx.doi.org/10.1016/j.tet.2007.02.105.
Повний текст джерелаSurowiec, Malgorzata, Radu Custelcean, Kazimierz Surowiec, and Richard A. Bartsch. "Alkali metal cation complexation by 1,3-alternate, mono-ionisable calix[4]arene-benzocrown-6 compounds." Supramolecular Chemistry 27, no. 1-2 (April 23, 2014): 59–64. http://dx.doi.org/10.1080/10610278.2014.904869.
Повний текст джерелаOktavia, Rizka, and Sumardi Sumardi. "Kemampuan Bacillus sp. Sebagai Bioremediasi Bahan Pencemar." Jurnal Bioterdidik: Wahana Ekspresi Ilmiah 10, no. 2 (September 30, 2022): 110–25. http://dx.doi.org/10.23960/jbt.v10i2.23919.
Повний текст джерелаWeber, Jaques, E. Peter Kundig, Annick Goursot та Edouard Penigault. "The electronic structures of bis(η6-benzene)- and bis(η6-naphthalene)chromium(0)". Canadian Journal of Chemistry 63, № 7 (1 липня 1985): 1734–40. http://dx.doi.org/10.1139/v85-291.
Повний текст джерелаElsegood, Mark, Lynne Horsburgh, Carl Redshaw, Oliver Rowe, and Simon Teat. "Pillared 2-D MOFs Based on a Lower-Rim Acid-Appended Calix[4]arene." Acta Crystallographica Section A Foundations and Advances 70, a1 (August 5, 2014): C1226. http://dx.doi.org/10.1107/s2053273314087737.
Повний текст джерелаMotswainyana, William M., and Peter A. Ajibade. "Anticancer Activities of Mononuclear Ruthenium(II) Coordination Complexes." Advances in Chemistry 2015 (February 19, 2015): 1–21. http://dx.doi.org/10.1155/2015/859730.
Повний текст джерелаSahnoun, Riadh, and Claude Mijoule. "Density Functional Study of Metal−Arene Compounds: Mono(benzene)chromium, Bis(benzene)chromium and Their Cations." Journal of Physical Chemistry A 105, no. 25 (June 2001): 6176–81. http://dx.doi.org/10.1021/jp0034271.
Повний текст джерелаWard, James P., Jonathan M. White, and Charles G. Young. "Synthesis, characterization and metal ion complexation and extraction capabilities of calix[4]arene Schiff base compounds." Tetrahedron 69, no. 41 (October 2013): 8824–30. http://dx.doi.org/10.1016/j.tet.2013.05.120.
Повний текст джерелаCiardelli, Francesco, and Paolo Pertici. "Structure and Reactivity of Aromatic Polymers/Ruthenium Catalysts." Zeitschrift für Naturforschung B 40, no. 2 (February 1, 1985): 133–40. http://dx.doi.org/10.1515/znb-1985-0201.
Повний текст джерелаCay, Seydahmet, Serkan Sayin, and Mehmet Soner Engin. "Calix[4]arene Embedded Polyamide Supported Liquid Membrane for Separation of Heavy Metals from Aqueous Solutions." Turkish Journal of Agriculture - Food Science and Technology 8, no. 2 (February 27, 2020): 387. http://dx.doi.org/10.24925/turjaf.v8i2.387-391.3064.
Повний текст джерелаYang, Fafu, Yanhua Wang, Hongyu Guo, Jianwei Xie, and Zhiqiang Liu. "Novel lariat calix[4]-1,3-aza-crowns with two branched chains — The excellent phase transfer catalysts for nucleophilic substitution reaction." Canadian Journal of Chemistry 88, no. 7 (July 2010): 622–27. http://dx.doi.org/10.1139/v10-061.
Повний текст джерелаАлександров, В., V. Aleksandrov, М. Морщилов, and M. Morshchilov. "Formation of wear resistant coatings on aluminum alloys by chromium deposition from gas-phase organometallic compounds." Science intensive technologies in mechanical engineering 1, no. 2 (February 28, 2016): 34–38. http://dx.doi.org/10.12737/17807.
Повний текст джерелаKemp, Samuel A., Timothy J. Prior, Huguette Savoie, Ross W. Boyle, and Benjamin S. Murray. "The Application of Reversible Intramolecular Sulfonamide Ligation to Modulate Reactivity in Organometallic Ruthenium(II) Diamine Complexes." Molecules 25, no. 2 (January 7, 2020): 244. http://dx.doi.org/10.3390/molecules25020244.
Повний текст джерелаIbrahim, Mohamed, Fahad A. Al-Zahrani, Francisco J. Diaz, Tareq Al-Attas, Hasan Zahir, Syed A. Ali, Mohammed Abdul Bari Siddiqui, and Mohammad M. Hossain. "Experimental Investigation of Metal-Based Calixarenes as Dispersed Catalyst Precursors for Heavy Oil Hydrocracking." Catalysts 12, no. 10 (October 17, 2022): 1255. http://dx.doi.org/10.3390/catal12101255.
Повний текст джерелаOkumura, Mikiko, and David Sarlah. "Arenophile-Mediated Photochemical Dearomatization of Nonactivated Arenes." CHIMIA International Journal for Chemistry 74, no. 7 (August 12, 2020): 577–83. http://dx.doi.org/10.2533/chimia.2020.577.
Повний текст джерелаLu, Bing-Bing, Xue Han, Cheng-Jie Feng, Duo Wang, and Fei Ye. "Two Co(II)-Based MOFs Constructed from Resorcin[4]Arene Ligand: Syntheses, Structures, and Heterogeneous Catalyst for Conversion of CO2." Crystals 11, no. 6 (May 21, 2021): 574. http://dx.doi.org/10.3390/cryst11060574.
Повний текст джерелаPadnya, Pavel, Ksenia Shibaeva, Maxim Arsenyev, Svetlana Baryshnikova, Olga Terenteva, Igor Shiabiev, Artur Khannanov, et al. "Catechol-Containing Schiff Bases on Thiacalixarene: Synthesis, Copper (II) Recognition, and Formation of Organic-Inorganic Copper-Based Materials." Molecules 26, no. 8 (April 17, 2021): 2334. http://dx.doi.org/10.3390/molecules26082334.
Повний текст джерелаSchmidbaur, Hubert, Theodore Zafiropoulos, Wolfgang Bublak, Paul Burkert, and Frank H. Köhler. "High Resolution and Solid State NMR Investigations of Subvalent Gallium Compounds." Zeitschrift für Naturforschung A 41, no. 1-2 (February 1, 1986): 315–18. http://dx.doi.org/10.1515/zna-1986-1-258.
Повний текст джерелаWard, James, Li Li, Fiona Regan, Mary Deasy, and Fintan Kelleher. "Bis(spirolactam) 1,3-double-armed calix[4]arene compounds and their application as extractants for the determination of heavy metal ions." Journal of Inclusion Phenomena and Macrocyclic Chemistry 83, no. 3-4 (October 15, 2015): 377–86. http://dx.doi.org/10.1007/s10847-015-0574-z.
Повний текст джерелаZaki, Mehvash, Suboot Hairat, and Elham S. Aazam. "Scope of organometallic compounds based on transition metal-arene systems as anticancer agents: starting from the classical paradigm to targeting multiple strategies." RSC Advances 9, no. 6 (2019): 3239–78. http://dx.doi.org/10.1039/c8ra07926a.
Повний текст джерелаDanil de Namor, Angela F., and Samir Chahine. "Solvation Effect of Guest, Supramolecular Host, and Host−Guest Compounds on the Thermodynamic Selectivity of Calix(4)arene Derivatives and Soft Metal Cations." Journal of Physical Chemistry B 109, no. 38 (September 2005): 18096–102. http://dx.doi.org/10.1021/jp053134d.
Повний текст джерелаOtsuka, Hideyuki, Yoshio Suzuki, Atsushi Ikeda, Koji Araki, and Seiji Shinkai. "Guest inclusion properties of calix[6]arene-based unimolecular cage compounds. On their high Cs+ and Ag+ selectivity and very slow metal exchange rates." Tetrahedron 54, no. 3-4 (January 1998): 423–46. http://dx.doi.org/10.1016/s0040-4020(97)10261-7.
Повний текст джерелаMendoza-Ferri, Maria G., Christian G. Hartinger, Alexey A. Nazarov, Rene E. Eichinger, Michael A. Jakupec, Kay Severin, and Bernhard K. Keppler. "Influence of the Arene Ligand, the Number and Type of Metal Centers, and the Leaving Group on thein VitroAntitumor Activity of Polynuclear Organometallic Compounds." Organometallics 28, no. 21 (November 9, 2009): 6260–65. http://dx.doi.org/10.1021/om900715j.
Повний текст джерелаSivkov, Danil, Olga Petrova, Alena Mingaleva, Anatoly Ob’edkov, Boris Kaverin, Sergey Gusev, Ilya Vilkov, et al. "The Structure and Chemical Composition of the Cr and Fe Pyrolytic Coatings on the MWCNTs’ Surface According to NEXAFS and XPS Spectroscopy." Nanomaterials 10, no. 2 (February 21, 2020): 374. http://dx.doi.org/10.3390/nano10020374.
Повний текст джерелаTu, Chuqiao, Dazhan Liu, Kazimierz Surowiec, David W. Purkiss, and Richard A. Bartsch. "Di-ionizable p-tert-butylcalix[4]arene-1,2-crown-5 and -crown-6 compounds in the cone conformation: synthesis and alkaline earth metal cation extraction." Organic & Biomolecular Chemistry 4, no. 15 (2006): 2938. http://dx.doi.org/10.1039/b604218j.
Повний текст джерелаUmemoto, Teruo, Lloyd M. Garrick, and Norimichi Saito. "Discovery of practical production processes for arylsulfur pentafluorides and their higher homologues, bis- and tris(sulfur pentafluorides): Beginning of a new era of “super-trifluoromethyl” arene chemistry and its industry." Beilstein Journal of Organic Chemistry 8 (March 29, 2012): 461–71. http://dx.doi.org/10.3762/bjoc.8.53.
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