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Relevant bibliographies by topics / Perrhenates

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Academic literature on the topic 'Perrhenates'

Author: Grafiati

Published: 4 June 2021

Last updated: 16 February 2022

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Journal articles on the topic "Perrhenates"

1

Leszczyńska-Sejda, Katarzyna, Grzegorz Benke, Joanna Malarz, et al. "Rhenium(VII) Compounds as Inorganic Precursors for the Synthesis of Organic Reaction Catalysts." Molecules 24, no. 8 (2019): 1451. http://dx.doi.org/10.3390/molecules24081451.

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Rhenium is an element that exhibits a broad range of oxidation states. Synthesis paths of selected rhenium compounds in its seventh oxidation state, which are common precursors for organic reaction catalysts, were presented in this paper. Production technologies for copper perrhenate, aluminum perrhenate as well as the ammonia complex of cobalt perrhenate, are thoroughly described. An ion exchange method, based on Al or Cu metal ion sorption and subsequent elution by aqueous perrhenic acid solutions, was used to obtain perrhenates. The produced solutions were neutralized to afford the targeted

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Baer, Sebastian A., Alexander Pöthig, Salem M. Bawaked, Hubert Schmidbaur, and Florian Kraus. "Bis(triphenylphosphine)gold(I) Perrhenate." Zeitschrift für Naturforschung B 68, no. 11 (2013): 1173–79. http://dx.doi.org/10.5560/znb.2013-3223.

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Bis(triphenylphosphine)gold(I) perrhenate [Ph3PAuPPh3]+ReO4 - has been prepared in high yield from Ph3PAuCl, Ph3P and AgReO4 in a mixed solvent. The compound is stable in air and decomposes at 235 °C. In the crystal structure, the two independent perrhenate anions are not approaching the gold centers of the two independent cations, but weak interionic interactions are entertained via π-π stacking of phenyl groups and C-H···O contacts. As three-blade chiral rotors, the Ph3P ligands of the cations are in a staggered conformation at the gold atoms with only slightly bent P-Au-P axes. IR and NMR d

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Reich, Robert M., Mirza Cokoja, Iulius I. E. Markovits, et al. "Influence of substituents on cation–anion contacts in imidazolium perrhenates." Dalton Transactions 44, no. 18 (2015): 8669–77. http://dx.doi.org/10.1039/c5dt00735f.

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Karimova, Oxana V., and Peter C. Burns. "Structural Units in Three Uranyl Perrhenates." Inorganic Chemistry 46, no. 24 (2007): 10108–13. http://dx.doi.org/10.1021/ic701128b.

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John, Gordon H., Iain May, Mark J. Sarsfield, David Collison, and Madeleine Helliwell. "Dimeric uranyl complexes with bridging perrhenates." Dalton Transactions, no. 16 (2007): 1603. http://dx.doi.org/10.1039/b614481k.

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LIU, Linlin, Shu LI, and Yang LIU. "ANTI--FRICTION BEHAVIORS OF SEVERAL SYNTHESIZED PERRHENATES." ACTA METALLURGICA SINICA 2010, no. 2 (2010): 233–38. http://dx.doi.org/10.3724/sp.j.1037.2009.00426.

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Schriewer-P�ttgen, Marietta S., and Wolfgang Jeitschko. "The crystal structures of two Mercury Perrhenates." Zeitschrift f�r anorganische und allgemeine Chemie 620, no. 11 (1994): 1855–60. http://dx.doi.org/10.1002/zaac.19946201104.

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Chay, Clarissa, Maxim Avdeev, Helen E. A. Brand, Sean Injac, Thomas A. Whittle, and Brendan J. Kennedy. "Crystal structures and phase transition behaviour in the 5d transition metal oxides AReO4 (A = Ag, Na, K, Rb, Cs and Tl)." Dalton Transactions 48, no. 47 (2019): 17524–32. http://dx.doi.org/10.1039/c9dt04021h.

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The structures of the six perrhenates (AReO<sub>4</sub> A = Ag, Na, K, Rb, Cs and Tl) at RT and the phase transitions associated with change in the orientation of the ReO<sub>4</sub><sup>−</sup> tetrahedra seen for A = Rb, Cs and Tl are described.

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Szabo, A. J., and R. J. C. Brown. "NQR Spin-Lattice Relaxation of Re in Perrhenates." Zeitschrift für Naturforschung A 49, no. 1-2 (1994): 302–10. http://dx.doi.org/10.1515/zna-1994-1-245.

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AbstractThe temperature dependence of the spin-lattice relaxation time T1 for the Re NQR in KReO4 , NH4ReO4 and ND4ReO4 has been measured between 77 K and 323 K. The relaxation is electric quadrupolar in all cases, and because of the large quadrupole moment of Re, T1 is short. In KReO4 T1 follows a T2 dependence. In NH4ReO4 , T1 decreases more rapidly than T-2 above about 100 K; between 170 K and 250 K T1 is smaller than 100 (is and could not be measured, but above 250 K, T1 increases to about 140 μs, and the measured data near room temperature lie close to the T-2 extrapolation from the T1 va

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10

Gazzoli, D., M. Valigi, B. Vielhaber, and H. Knözinger. "Raman and optical spectra of magnesia-supported perrhenates." Journal of the Less Common Metals 134, no. 1 (1987): 67–77. http://dx.doi.org/10.1016/0022-5088(87)90443-7.

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Dissertations / Theses on the topic "Perrhenates"

1

Grupe, Sven. "Perrhenate mit dreiwertigen Metallen." [S.l. : s.n.], 2002. http://deposit.ddb.de/cgi-bin/dokserv?idn=967442435.

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2

Morris, Daniel S. "Redox chemistry of perrhenate and other anions." Thesis, University of Edinburgh, 2017. http://hdl.handle.net/1842/31480.

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This thesis discusses reduction and oxidation reactions catalysed by the perrhenate anion and oxidation reactions catalysed by other oxo-anions i.e. sulfate and nitrate. Chapter one introduces catalytic hydrosilylation, hydroboration, deoxydehydration and alkene epoxidation and some of their applications, with a focus on high oxidation state complexes. Chapter two describes the synthesis of a salt of perrhenate [N(hexyl)4][ReO4] which is highly soluble in organic solvents. The use of this salt as a catalyst for both the hydrosilylation and hydroboration of carbonyl compounds and carbon dioxide

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3

Wells, Debra J. "Extraction of the perrhenate and pertechnetate anions from aqueous solutions using inorganic anion exchangers." Thesis, University of Reading, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.306851.

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Breitenstein, Jacques. "Etude par spectroscopie raman de conducteurs organiques unidimensionnels, (tmtsf) 2x." Paris 7, 1988. http://www.theses.fr/1988PA077179.

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Trois sels de bechgaard (tmtsf)::(2)x (ou x=pf::(6), clo::(4) et reo::(4)) sont etudies dans des conditions de double resonance raman. Determination des modes de vibration donnant des termes importants dans ces conditions de double resonance. Mise en evidence de l'existence des modes rendus actifs grace a un forty couplage avec des transferts dynamiques de charge intermoleculaires ou intramoleculaires. Les informations importantes concernant ce couplage de modes internes - transferts de charge sont obtenues lors de l'etude de la transition metal - isolant et de la mise en ordre a 2k::(f) des a

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5

Grupe, Sven [Verfasser]. "Perrhenate mit dreiwertigen Metallen / vorgelegt von Sven Grupe." 2002. http://d-nb.info/967442435/34.

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Book chapters on the topic "Perrhenates"

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Thompson, Richard J., Tung-Ch'Ing Wang, Jacob Kleinberg, George M. Adams, and Burl E. Bryant. "Ammonium Perrhenate." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132395.ch44.

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Schmidt, Max, Hubert Schmidbaur, Sherman Thomas, and Doyle Britton. "Trimethylsilyl Perrhenate." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132401.ch40.

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Stephan, Holger, Karsten Gloe, Werner Kraus, et al. "Binding and Extraction of Pertechnetate and Perrhenate by Azacages." In Fundamentals and Applications of Anion Separations. Springer US, 2004. http://dx.doi.org/10.1007/978-1-4419-8973-4_10.

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Hudson, Michael J., and Debra J. Tyler. "Extraction of the Perrhenate Anion Using Goethite Surface-Modified with Hydrophobic Quaternary Amines." In Recent Developments in Ion Exchange. Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0777-5_28.

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5

Schmidbaur, H. "Trimethylsilyl Perrhenate—A Nonionic Reagent Soluble in Organic Solvents for the Preparation of Perrhenates." In Efficient Methods for Preparing Silicon Compounds. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-12-803530-6.00005-6.

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Kühn, F. E., C. C. Romäo, and W. A. Herrmann. "From Silver(I) Perrhenate." In Compounds of Groups 7-3 (Mn..., Cr..., V..., Ti..., Sc..., La..., Ac...). Georg Thieme Verlag KG, 2003. http://dx.doi.org/10.1055/sos-sd-002-00192.

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Conference papers on the topic "Perrhenates"

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Wang, Junhai, Lixiu Zhang, and Ke Zhang. "Primary Exploration on Tribological Behavior of Perrhenates as Lubricating Oil Additive in a Wide Temperature Range." In 2016 7th International Conference on Mechatronics, Control and Materials (ICMCM 2016). Atlantis Press, 2016. http://dx.doi.org/10.2991/icmcm-16.2016.21.

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2

Wang, Xiaoxia, Qinglan Zhao, Jirun Luo, Xianheng Liao, Yun Li, and Qi Zhang. "An ammonium perrhenate impregnated Ni sponge oxide cathode." In 2013 14th International Vacuum Electronics Conference (IVEC). IEEE, 2013. http://dx.doi.org/10.1109/ivec.2013.6570912.

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3

Wang, Xiaoxia, Shikai Qi, Yanwen Liu, et al. "Emission uniformity of the ammonium perrhenate impregnated Ni sponge oxide cathode." In 2014 IEEE International Vacuum Electronics Conference (IVEC). IEEE, 2014. http://dx.doi.org/10.1109/ivec.2014.6857528.

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4

Wang, Xiaoxia, Xiaoqian Chen, Shuai Zhang, Yun Li, and Qi Zhang. "The work function of the Ammonium Perrhenate Impregnated W Matrix Ba-W Cathode." In 2019 International Vacuum Electronics Conference (IVEC). IEEE, 2019. http://dx.doi.org/10.1109/ivec.2019.8745291.

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Wang, Xiaoxia, Mingwei Hu, Shikai Qi, et al. "Preparation and performance of the ammonium perrhenate impregnated W matrix Ba-W cathode." In 2015 IEEE International Vacuum Electronics Conference (IVEC). IEEE, 2015. http://dx.doi.org/10.1109/ivec.2015.7223933.

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Xiaoxia Wang, Mingwei Hu, Shikai Qi, Jirun Luo, and Qinglan Zhao. "Evaporation and lifetime of the ammonium perrhenate impregnated W matrix Ba-W cathode." In 2016 IEEE International Vacuum Electronics Conference (IVEC). IEEE, 2016. http://dx.doi.org/10.1109/ivec.2016.7561927.

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Reports on the topic "Perrhenates"

1

B.E. Anderson, U. Becker, K.B. Helean, and R.C. Ewing. Perrhenate and Pertechnetate Behavior on Iron and Sulfur-Bearing Compounds. Yucca Mountain Project, Las Vegas, Nevada, 2006. http://dx.doi.org/10.2172/894740.

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2

Duffey, C., W. King, and L. Hamm. DETERMINATION OF PERRHENATE ADSORPTION KINETICS FROM HANFORD WASTE SIMULANTS USING SUPERLING 639 RESIN. Office of Scientific and Technical Information (OSTI), 2002. http://dx.doi.org/10.2172/1050235.

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