Academic literature on the topic 'Cyclopentadienyl'

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Journal articles on the topic "Cyclopentadienyl"

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Schumann, Herbert, Susanne Stenz, Frank Girgsdies, and Stefan H. Mühle. "Bis[dicarbonyl(cyclopentadienyl)ruthenium(I)] Komplexe / Bis[dicarbonyl(cyclopentadienyl)ruthenium(I)] Complexes." Zeitschrift für Naturforschung B 57, no. 9 (2002): 1017–26. http://dx.doi.org/10.1515/znb-2002-0908.

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Ru3(CO)12 reacts with 1-tert-butyl-2,4-cyclopentadiene (1), 1-trimethylsilyl-2,4-cyclopentadiene (2), 1-tert-butyl-3-methyl-2,4-cyclopentadiene (3), 1,3-di(tert-butyl)-2,4-cyclopentadiene (4), 1-iso-propyl-2,3,4,5-tetramethyl-2,4-cyclopentadiene (5), 1-tert-butyl-2,3,4,5-tetramethyl- 2,4-cyclopentadiene (6), 1-phenyl-2,3,4,5-tetramethyl-2,4-cyclopentadiene (7), 2,5- diphenyl-2,4-cyclopentadiene (8), or 2,3,4,5-tetraphenyl-2,4-cyclopentadiene (9) with formation of the corresponding bis[dicarbonyl(cyclopentadienyl) ruthenium(I)] complexes [RuCp# (CO)2]2 1a to 9a. The 1H and 13C NMR spectra of the new compounds 3a and 5a to 9a as well as the single crystal X-ray structures of 1a, 4a, 5a, 7a, 8a, and 9a are reported and discussed
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Deacon, GB, and RH Newnham. "Organolanthanoids .VIII. Some Ligand-Exchange Reactions of Pentafluorophenyllanthanoids and Bis(Phenylethynyl)Ytterbium(II)." Australian Journal of Chemistry 38, no. 12 (1985): 1757. http://dx.doi.org/10.1071/ch9851757.

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The cyclopentadienyl - and indenyl-lanthanoids, (C5H5)2Yb( dme ) ( dme = 1,2- dimethoxyethane ), (C9H7)2Yb( thf )2 ( thf = tetrahydrofuran ), (C5H5)2Eu( thf )n (n = 0.5 or 1), (C9H7)2Eu( thf ), (C5H5)3Sm, (MeC5H4)3Sm, and (C9H7)3Sm( thf ) have been prepared by ligand exchange reactions of (C6F5)2Yb, (C6F5)2Eu, and a pentafluorophenylsamarium species with cyclopentadiene , methylcyclopentadiene , or indene. This synthetic method has particular significance for the indenyllanthanoids . An explosive product was obtained from (C6F5)2Yb and methylcyclopentadiene. Reactions of ( PhCC )2Yb with cyclopentadienes and indene have yielded (C5H5)2Yb( dme ), (MeC5H4)2Yb( dme ), and (C9H7)2Yb( thf )2, but (C5H5)2Yb did not undergo ligand exchange with phenylacetylene.
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Zamkova, I. V. "APPROACHES TO TOXICOLOGICAL AND HYGIENE ASSESSMENT OF UNSTABLE METAL-ORGANIC COMPOUNDS ON THE EXAMPLE OF MAGNESOCENE (CP2MG) (BIS (CYCLOPENTADIENYL) MAGNESIUM)." Toxicological Review, no. 1 (February 28, 2018): 38–40. http://dx.doi.org/10.36946/0869-7922-2018-1-38-40.

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Approaches to the evaluation of toxicity and hazard of unstable substance bis(cyclopentadienyl) magnesium MAGNESOCENE (Cp2Mg)) are presented . The toxicity of the substance is determined by its main transformation products -magnesium oxide, magnesium hydroxide and cyclopentadiene. Due to the instability of the substance (it exists only in an inert environment) it is not possible to conduct studies on its sensitizing effect ,its reprotoxic, teratogenic, mutagenic and carcinogenic action on the organism. Control of the unstable compound bis (cyclopentadienyl) magnesium in the air of the working area and human habitat should be based on its transformation products: magnesium oxide and cyclopentadiene.
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Rapakousiou, Amalia, Colette Belin, Lionel Salmon, Jaime Ruiz, and Didier Astruc. "Click Co sandwich-terminated dendrimers as polyhydride reservoirs and micellar templates." Chemical Communications 53, no. 46 (2017): 6267–70. http://dx.doi.org/10.1039/c7cc03311g.

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Dendrimers containing 9, 27 and 81 [Co<sup>I</sup>(η<sup>4</sup>-cyclopentadiene)(η<sup>5</sup>-cyclopentadienyl)] termini serve as polyhydride reservoirs reducing protons to dihydrogen and Au<sup>III</sup> to micellar capsules.
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Kreiter, Cornelius G., та Wolfgang Conrad. "Gehinderte Ligandbewegungen in Übergangsmetallkomplexen, XLIII [1]: Photoreaktionen von Hexacarbonyl-μ-η5:5-fulvalen-dimolybdän und -diwolfram mit konjugierten Cyclodienen / Hindered Ligand Movements in Transition Metal Complexes, XLIII [1]: Photoreactions of Hexacarbonyl-μ-η5:5-fulvalene-dimolybdenum and -ditungsten with Conjugated Cyclodienes". Zeitschrift für Naturforschung B 49, № 3 (1994): 383–88. http://dx.doi.org/10.1515/znb-1994-0317.

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Abstract Hexacarbonyl-μ-η5:5-fulvalene-dimolybdenum (1) reacts photochemically with 1,3-cyclopentadiene (a), and 1,3-cyclohexadiene (b) to yield the corresponding tetracarbonyl-η4-1,3-cyclodiene-μ-η5:5-fulvalene-dimolybdenum complexes 4a, 4b. With a also mixed valent tricarbonyl-η5-cyclopentadienyl-μ-η5:5-fulvalene-hydrido-dimolybdenum (3) is formed. Hexacarbonyl-μ-η5:5-fulvalene-ditungsten (2) yields with a only tricarbonyl-η5-cyclopentadienyl-μ-η5:5-fulvalene-hydrido-ditungsten (5). The η4-1,3-cyclodiene ligands in 4a, 4b are u-oriented towards fulvalene. The complexes 4a, 4b show hindered inversions with energy barriers of ΔG#273 = 59.9 ± 2 kJ/mol (4a) and ΔG#293, = 62.7 ± 2 kJ/mol (4b).
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Maryin, V., and P. V. Petrovskii. "Chiral cyclopentadiene-cyclopentadienyl complexes of cobalt." Journal of Organometallic Chemistry 441, no. 1 (1992): 125–41. http://dx.doi.org/10.1016/0022-328x(92)80197-6.

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Schumann, Herbert, Susanne Stenz, and Stefan H. Mühle. "Ruthenocene mit sterisch anspruchsvollen Cyclopentadienylliganden." Zeitschrift für Naturforschung B 58, no. 6 (2003): 514–20. http://dx.doi.org/10.1515/znb-2003-0605.

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1-tert-Butyl-2,4-cyclopentadiene (1), 1,3-di(tert-butyl)-2,4-cyclopentadiene (2), 1-ethyl-2,3,4,5- tetramethyl-2,4-cyclopentadiene (3), 1-iso-propyl-2,3,4,5-tetramethyl-2,4-cyclopentadiene (4), 1- tert-butyl-2,3,4,5-tetramethyl-2,4-cyclopentadiene (5), and 1-phenyl-2,3,4,5-tetramethyl-2,4-cyclopentadiene (6) react with n-butyl lithium followed by tributyltin chloride to give the corresponding tributyl(cyclopentadienyl)stannanes Bu3SnCp# 1a to 6a. The reactions of 1a to 6a with Ru(COD)Cl2 result in the formation of the corresponding ruthenocenes RuCp2# 1b to 6b. Ru(C5H3Ph2)2 (7b) is prepared from [Ru(p-cymol)Cl2]2 and Na[C5H3Ph2]. The 1H and 13C NMR spectra of the new stannanes 1a to 6a and the ruthenocenes 1b to 7b as well as the single crystal X-ray structure of 4b are reported and discussed.
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Čermák, Jan, Kateřina Auerová, Huong Thi Thu Nguyen, Vratislav Blechta, Pavel Vojtíšek, and Jaroslav Kvíčala. "Synthesis of Rhodium Complexes with Novel Perfluoroalkyl Substituted Cyclopentadienyl Ligands." Collection of Czechoslovak Chemical Communications 66, no. 2 (2001): 382–96. http://dx.doi.org/10.1135/cccc20010382.

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Mixtures of isomers of (perfluoroalkyl)tetramethylcyclopenta-1,3-dienes (CH3)4C5H(CF2)nCF3 (n = 3, 5, 7, 9) were synthesized as precursors of new cyclopentadienyl ligands for organotransition metal catalysis in fluorous biphase media and characterized by combination of GC-MS and 13C NMR spectroscopy. Rhodium(III) chloro complexes [Rh{(CH3)4C5(CF2)nCF3}Cl2]2 and rhodium(I) carbonyl complexes [Rh{(CH3)4C5(CF2)nCF3}(CO)2] were prepared from the cyclopentadienes and molecular structure of [Rh{(CH3)4C5(CF2)5CF3}Cl2]2 was determined by X-ray diffraction. The ligands are electronically close to the unsubstituted cyclopentadienyl as shown by values of carbonyl stretching frequencies in the carbonyl complexes. Neither carbonyl frequencies nor NMR chemical shifts of the complexes are substantially affected by the length of the perfluoroalkyl chain.
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Razuvaev, G. A., V. P. Mar'in, Yu A. Andrianov, L. I. Vyshinskaya, and A. S. Smirnov. "New derivatives of (?5-cyclopentadienyl) (?4-cyclopentadiene)cobalt." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 36, no. 2 (1987): 423. http://dx.doi.org/10.1007/bf00959407.

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e Silva, Máfircio L. A., Alberto F. Neto, Silvia A. Cardoso, Sérgio Albuquerque, and Joseph Miller. "Synthesis and “in Vitro” Trypanocidal Activity Evaluation of Some Organo-iron Compounds." Metal-Based Drugs 8, no. 6 (2002): 329–32. http://dx.doi.org/10.1155/mbd.2002.329.

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Eight organo-iron ferrocene derivatives and arenocenium salts were prepared and evaluated by “in vitro” assay against one strain of Trypanosoma cruzi (Y). Six of the eight organo-iron compounds assayed, piperazinium diferrocenoate 1, η6-(o-xylene)-η5-(cyclopentadienyl) Iron(II) hexafluorophosphate 3, η6 -(mesitylene)-η5 -(cyclopentadienyl) iron(II) hexafluorphosphate 5, η6 -(durene)-η5 -(cyclopentadienyl) iron(II) hexafluorphosphate 6, η6 -(ρ-chlorotoluene)-η5 -(cyclopentadienyl) Iron(II) hexafluorphosphate 7 and η6 -(chlorobenzene)-η5 -(cyclopentadienyl) iron(II) picrate 8 , were poorly active in the “in vitro” assays. Only two compounds 1,1'–(N-pyperidinocarbonyl) ferrocene 2(IC50=2.4 μg/mL) and η6-(o-xylene)-η5(cyclopentadienyl) iron(II) picrate 4(IC50=12.08 μg/mL), were more active. Thus, some of the compounds are promising to be used against Chagas' disease as a prophylactic agents.
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Dissertations / Theses on the topic "Cyclopentadienyl"

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Sams, David W. I. "Studies on complexes bearing phosphaallyl, chiral cyclopentadienyl, di- or tri- cyclopentadienyl ligands." Thesis, University of Bristol, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.238828.

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Roy, Karin. "Kinetische Untersuchungen zur Hochtemperaturpyrolyse und -oxidation von Cyclopentadien und Cyclopentadienyl mit Hilfe der Stosswellentechnik." [S.l. : s.n.], 1999. http://deposit.ddb.de/cgi-bin/dokserv?idn=958163359.

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Roy, Karin. "Kinetische Untersuchungen zur Hochtemperaturpyrolyse und -oxidation von Cyclopentadien und Cyclopentadienyl mit Hilfe der Stoßwellentechnik." [S.l.] : Universität Stuttgart , Fakultät Chemie, 1999. http://www.bsz-bw.de/cgi-bin/xvms.cgi?SWB8385926.

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Harrison, Stephen Anthony. "Novel chiral cyclopentadienyl metal complexes." Thesis, University of Southampton, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.442873.

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Veighy, Clifford Robert. "Novel cyclopentadienyl transition metal complexes." Thesis, University of Southampton, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.327366.

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Ling, Xiaolan. "Silylated-cyclopentadienyl derivatives of zirconium." Thesis, University of Sussex, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.368492.

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Mackey, Olivia Nicola Denise. "Cyclopentadienyl derivatives of Main Group Elements." Thesis, Queen's University Belfast, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.334507.

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Beaumont, Ian R. "The chemistry of cyclopentadienyl cobalt complexes." Thesis, University of Nottingham, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.291970.

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Kuma, Karl Earl Adjetey. "A study of palladium cyclopentadienyl complexes." Thesis, University of Salford, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.299126.

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Plews, M. J. "Cyclopentadienyl uranium, neptunium and plutonium chemistry." Thesis, University of Manchester, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.355913.

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Books on the topic "Cyclopentadienyl"

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Aachen, Rheinisch-Westfälische Technische Hochschule, ed. Zur Reaktivität von Bis(j-cyclopentadienyl)niobhydrid-Derivaten [Bis-eta-cyclopentadienyl-niobhydrid-Derivaten] gegenüber Acetylenen, Heteroalkenen und Heteroallenen. [s.n.], 1987.

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Stenz, Susanne. Ruthenium- und Rhodiumkomplexe mit sterisch anspruchsvollen Cyclopentadienyl-Liganden. [s.n.], 1999.

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Carmichael, Adrian John. Synthesis of cationic bis(cyclopentadienyl)tungsten(IV) complexes. typescript, 1996.

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Sun, Ning-Yu. Studies of pyrazolylborato and permethylated cyclopentadienyl ruthenium complexes. University of Salford, 1992.

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Obuzor, Gloria U. Synthesis of new cyclopentadienyl and indenyl transition metal complexes. UMIST, 1998.

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Lena, Jorge Carvalho De. Synthetis and study of bis([eta]5-cyclopentadienyl) (ene-1,2-dithiolato)titanium(IV)complexes. University of Manchester, 1994.

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Gutenberg-Universität, Johannes, ed. Anwendung von [beta]-[Cyclopentadienyl(dicarbonyl)eisen]-substituierten [alpha, beta]-ungesättigten Carbonylverbindungen in der organischen Synthese. [s.n.], 1999.

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Moran, Paul H. Photochemische Reaktionen von Cyclopentadienyl-bis(ethen)-rhodium-Verbindungen mit Alkinen sowie Röntgenstrukturanalyse von Pt-, Rh- und Ir-Komplexen. [s.n.], 1998.

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Gelson N. Manzoni de Oliveira. Beiträge zur Komplexbildung von 6,6-Dimethylfulven [Dimethylfulven] mit Rhodium sowie zur Synthese und Reaktivität von Cyclopentadienyl-nitrosyl-metall-Komplexen. [s.n.], 1986.

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Körnich, Jan. Dinukleare Bis(cyclopentadiendiyl)keton-Komplexe. [s.n.], 1998.

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Book chapters on the topic "Cyclopentadienyl"

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Agbossou, Francine, Edward J. O'Connor, Charles M. Garner, et al. "Cyclopentadienyl Rhenium Complexes." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132609.ch51.

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Hirota, E., K. Kuchitsu, T. Steimle, J. Vogt, and N. Vogt. "7 C5H5 2,4-Cyclopentadienyl." In Molecules Containing Three or Four Carbon Atoms and Molecules Containing Five or More Carbon Atoms. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-41504-3_138.

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Doherty, N. M., S. A. R. Knox, C. P. Casey, and G. T. Whiteker. "(η5-Cyclopentadienyl)Diruthenium Complexes." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132562.ch44.

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Doherty, N. M., S. A. R. Knox, M. J. Morris, C. P. Casey, and G. T. Whiteker. "Tetracarbonylbis(η5-Cyclopentadienyl)-Diruthenium." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132593.ch48.

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Wailes, P. C., H. Weigold, Jeffrey Schwartz, and Chu Jung. "(η5 -Cyclopentadienyl)Hydridozirconium Complexes." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132593.ch65.

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Jolly, William L., N. A. D. Carey, and H. C. Clark. "Bis(Cyclopentadienyl)Iron: (Ferrocene)." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132425.ch23.

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Jolly, William L., David J. Chazan, N. A. D. Carey, and H. C. Clark. "Bis(Cyclopentadienyl)Nickel: (Nickelocene )." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132425.ch24.

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Segal, John A., and William E. Silverthorn. "(η6-Benzene)(η5-Cyclopentadienyl)Molybdenum and (η6-Benzene) (η5-Cyclopentadienyl)-Molybdenum Derivatives." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132517.ch43.

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Lucas, C. R., J. A. Labinger, and J. Schwartz. "Bis(η-Cyclopentadienyl)Niobium Complexes." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132470.ch31.

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Floriani, Carlo, Vladimir Mange, E. Kent Barefield, and Michael W. Carris. "Vanadocene, Bis(η5-Cyclopentadienyl) Vanadium." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132593.ch67.

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Conference papers on the topic "Cyclopentadienyl"

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Miller, Terry A. "Laser spectroscopy of aromatic and organometallic radicals." In OSA Annual Meeting. Optica Publishing Group, 1992. http://dx.doi.org/10.1364/oam.1992.thi1.

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Laser induced fluorescence techniques can be used to obtain rotationally resolved electronic spectra of moderately large aromatic and organometallic radicals cooled to &lt;2 K in a supersonic free jet expansion. Aromatic organic radicals studied include cyclopentadienyl, benzyl, triphenyl methyl, and substituted derivatives thereof. Organometallic radicals studied include Cd and Zn monomethyl as well as group IIA and IIB derivatives of cyclopentadienyl, methylcyclopentadienyl, and pyrrolyl radicals.
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Krasnoukhov, V. S., D. P. Porfiriev, M. V. Zagidullin, and A. M. Mebel. "The study of indenyl + cyclopentadienyl reaction." In INTERNATIONAL CONFERENCE ON PHYSICS AND CHEMISTRY OF COMBUSTION AND PROCESSES IN EXTREME ENVIRONMENTS (COMPHYSCHEM’20-21) and VI INTERNATIONAL SUMMER SCHOOL “MODERN QUANTUM CHEMISTRY METHODS IN APPLICATIONS”. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0033816.

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Sharma, Ketan, David Nesbitt, John Stanton, and Terry Miller. "THE ROVIBRONIC SPECTRA OF THE CYCLOPENTADIENYL RADICAL." In 72nd International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2017. http://dx.doi.org/10.15278/isms.2017.mg04.

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OLEINIKOV, A. D., V. N. AZYAZOV, and A. M. MEBEL. "OXIDATION OF CYCLOPENTADIENYL RADICAL WITH MOLECULAR OXYGEN: A THEORETICAL STUDY." In NONEQUILIBRIUM PROCESSES. TORUS PRESS, 2018. http://dx.doi.org/10.30826/nepcap2018-1-28.

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Preto, Ana, Ana Rita Brás, Pedro Fernandes, Tiago Moreira, and Andreia Valente. "New ruthenium-cyclopentadienyl agents as a new strategy to fight colorectal cancer." In 7th International Electronic Conference on Medicinal Chemistry. MDPI, 2021. http://dx.doi.org/10.3390/ecmc2021-11457.

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Castan, H., S. Duenas, H. Garcia, et al. "Study of Atomic Layer Deposited Zirconium Oxide Thin Films by Using Mono-Cyclopentadienyl Based Precursors." In 2009 Spanish Conference on Electron Devices. CDE 09. IEEE, 2009. http://dx.doi.org/10.1109/sced.2009.4800416.

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Miller, Terry A. "Clusters containing open-shell molecules." In OSA Annual Meeting. Optica Publishing Group, 1992. http://dx.doi.org/10.1364/oam.1992.mee1.

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Bonding between atoms and molecules can span wide extremes. Long, weak van der Waals bonds, e.g., between closed-shell inert gas atoms, at least in principle can be characterized in terms of multipolar interactions between separated charge distributions. Short, strong chemical bonds, e.g., between open-shell radical species, must be described in terms of delo­calization of the initial electronic distributions. We have recently begun to experimentally characterize complexes formed between one open- and one closed-shell species. Systems studied include inert gases (and some metal atoms) bonded to a series of radicals including OH, CdCH3, cyclopentadienyl, and hexafluorobenzene cation radicals. These results will be discussed in terms of both the unusual bonding present and, in some cases, the evolution of simple complexes to the condensed phase limit.
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To, Tung T., Edwin J. Heilweil, Charles B. Duke, and Theodore J. Burkey. "Ultrafast Chelation Dynamics of Model Photoswitches: Cyclopentadienyl Manganese and Arene Chromium Tricarbonyl Derivatives with Pendant Sulfides." In International Conference on Ultrafast Phenomena. OSA, 2006. http://dx.doi.org/10.1364/up.2006.tuc6.

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Kondo, H., S. Sakurai, A. Sakai, M. Ogawa, and S. Zaima. "Metalorganic Chemical Vapor Deposition of High-Dielectric-Constant Praseodymium Oxide Films using a Liquid Cyclopentadienyl Precursor." In 2008 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2008. http://dx.doi.org/10.7567/ssdm.2008.a-9-4.

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Pilon, Adhan, Maria Helena Garcia, and Andreia Valente. "Iron-cyclopentadienyl compounds with nitrile-based ligands show strong activity against a broad panel of human cancer cell lines." In 6th International Electronic Conference on Medicinal Chemistry. MDPI, 2020. http://dx.doi.org/10.3390/ecmc2020-07428.

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Reports on the topic "Cyclopentadienyl"

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Weydert, Marc. Tris(Cyclopentadienyl)Uranium-t-Butyl: Synthesis, reactions, and mechanisms. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/10159968.

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Weydert, M. Tris(Cyclopentadienyl)Uranium-t-Butyl: Synthesis, reactions, and mechanisms. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/6566863.

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Rosen, R. K. Reaction of Tris(cyclopentadienyl)uranium compounds with amines, azides, and related ligands. Office of Scientific and Technical Information (OSTI), 1989. http://dx.doi.org/10.2172/7257519.

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Ackroyd, Nathan C., and John A. Katzenellenbogen. Cyclopentadienyl Rhenium (Technetium) Tricarbonyl Complexes Integrated in Estrogen Receptor Ligands for ER+ Tumor Imaging. Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada456153.

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Schrock, R. R. Chemistry of bimetallic linked cyclopentadienyl complexes: Progress report, 1 December 1986--30 November 1989. Office of Scientific and Technical Information (OSTI), 1986. http://dx.doi.org/10.2172/5924493.

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Ackroyd, Nathan C., and John A. Katzenellenbogen. Cyclopentadienyl Rhenium (Technetium) Tricarbonyl Complexes Integrated in Estrogen Receptor Ligands for ER+ Tumor Imaging. Defense Technical Information Center, 2006. http://dx.doi.org/10.21236/ada463303.

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Sofield, Chadwick Dean. Steric and electronic effects of 1,3-disubstituted cyclopentadienyl ligands on metallocene derivatives of Cerium, Titanium, Manganese, and Iron. Office of Scientific and Technical Information (OSTI), 2000. http://dx.doi.org/10.2172/764394.

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Manna, Kuntal. Transition metal complexes of oxazolinylboranes and cyclopentadienyl-bis(oxazolinyl)borates: Catalysts for asymmetric olefin hydroamination and acceptorless alcohol decarbonylation. Office of Scientific and Technical Information (OSTI), 2012. http://dx.doi.org/10.2172/1082975.

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Nazyrov, Marat, and Yulia Yarkaeva. Enantioselective voltammetric sensor system based on mesoporous carbon black Carbopack X and cyclopentadiene derivatives for determination of clopidogrel enantiomers. Peeref, 2023. http://dx.doi.org/10.54985/peeref.2307p5734071.

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