Relevant bibliographies by topics / Rhenium compounds

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Rhenium compounds'

Author: Grafiati
Published: 4 June 2021
Last updated: 31 January 2023

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Journal articles on the topic "Rhenium compounds"

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Voronkova, Y. S., and N. I. Shtemenko. "Вплив кластерних сполук ренію з органічними лігандами на активність глюкозооксидази." Visnyk of Dnipropetrovsk University. Biology, medicine 2, no. 1 (March 21, 2011): 18–23. http://dx.doi.org/10.15421/021103.

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Influence of cluster rhenium compounds with different ligands on the activity of glucoseoxidase was studied. Ability of the rhenium compounds to influence on the enzyme’s activity was ascertained. Itis depended on the compound structure and the time of incubation: activity of the glucoseoxidase changed by 4–24 %. The cluster compound with GABA ligand reduced the enzymatic activity, but compounds with hydrophobic ligands increased the activity of glucoseoxidase. Different mechanisms of the cluster rhenium compound–enzyme interactions are suspected.
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Suponko, J. V., and N. I. Shtemenko. "Вплив нанопрепаратів кластерних сполук ренію на активність ферментів печінки в моделі пухлинного росту." Visnyk of Dnipropetrovsk University. Biology, medicine 1, no. 2 (June 10, 2010): 76–80. http://dx.doi.org/10.15421/021030.

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Enzymes’ level in rat’s hepatocytes under Guerin's carcinoma T8 development as well as after injection of rhenium compounds and cis-platin has been studied. It has been determined that the decrease of enzymatic activity to the level of the animals of control group was observed at the simultaneous injection of cis-platin and cluster rhenium compounds in nanoliposomal and water-soluble forms. That confirms possible hepatoprotective properties of the rhenium compounds. It has been shown that hepatoprotective properties of rhenium cluster compounds mostly don’t depend on the form of their injection and are detected regardless of anticancer properties. Rhenium-platinum system with β-alanine ligand in aqueous solution, has been found. Its injection is accompanied by the hepatoprotective effect.
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Golichenko, Alexander, and Alexander Shtemenko. "HYDROLYSIS OF RHENIUM(III) CLUSTER COMPOUNDS." Ukrainian Chemistry Journal 85, no. 3 (June 7, 2019): 27–34. http://dx.doi.org/10.33609/0041-6045.85.3.2019.27-34.

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Study of hydrolysis of cis-tetrachlorodi-m-carboxylates of dirhenium (III) was carried out due to the electronic adsorption and IR spectroscopy and pHmeter. As a result, itwas shown that the hydrolysis is a multistage process which can be attributed to the reactions of the pseudo-first order. It is also shown that the electronic absorption spectroscopy (EAS) is a reliable method of investigation to study the hydrolysis of rhenium (III) complex compounds. This conclusion is based on the fact that in the systems with halide and carboxylic ligands, each of the five structural types can be clearly identified by the EAS in the region of both d–d* electron transition and charge transfer transition of L*Hal ®Re type. It is shown that with the increase in the length of the alkyl group and in its branching, the hydrolysis rate decreases, as a result of a change in the positive inductive effect of these groups and, consequently, an increase in the strengthening of quadruple Re–Re bond. In addition, with the help of the EAS, a transition of the chloride ligands to OHgroups can be observed. As a result of the study, a hydrolysis route, which initially leds to the gradual replacement of the chloride ligands of a complex compound with OH groups, and subsequently to the conversion of Re(III) compounds into the derivative of Re(IV) was proposed. The dependence of resistance to hydrolysis on the structure of the complex compound, the temperature and pH was determined. It allowed to predict the stability of the investigated compounds while their usage as biologically active substances and reagents in the synthesis of new compounds. The obtained results allow us to presence of anticancer, cytostabilizing and other biological activities is the coordination of Re(III) complex compounds with the components of biomolecules (proteins, DNA).
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Golichenko, Alexander, and Alexander Shtemenko. "HYDROLYSIS OF RHENIUM(III) CLUSTER COMPOUNDS." Ukrainian Chemistry Journal 85, no. 3 (June 7, 2019): 27–34. http://dx.doi.org/10.33609/6045.85.3.2019.27-34.

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Study of hydrolysis of cis-tetrachlorodi-m-carboxylates of dirhenium (III) was carried out due to the electronic adsorption and IR spectroscopy and pHmeter. As a result, itwas shown that the hydrolysis is a multistage process which can be attributed to the reactions of the pseudo-first order. It is also shown that the electronic absorption spectroscopy (EAS) is a reliable method of investigation to study the hydrolysis of rhenium (III) complex compounds. This conclusion is based on the fact that in the systems with halide and carboxylic ligands, each of the five structural types can be clearly identified by the EAS in the region of both d–d* electron transition and charge transfer transition of L*Hal ®Re type. It is shown that with the increase in the length of the alkyl group and in its branching, the hydrolysis rate decreases, as a result of a change in the positive inductive effect of these groups and, consequently, an increase in the strengthening of quadruple Re–Re bond. In addition, with the help of the EAS, a transition of the chloride ligands to OHgroups can be observed. As a result of the study, a hydrolysis route, which initially leds to the gradual replacement of the chloride ligands of a complex compound with OH groups, and subsequently to the conversion of Re(III) compounds into the derivative of Re(IV) was proposed. The dependence of resistance to hydrolysis on the structure of the complex compound, the temperature and pH was determined. It allowed to predict the stability of the investigated compounds while their usage as biologically active substances and reagents in the synthesis of new compounds. The obtained results allow us to presence of anticancer, cytostabilizing and other biological activities is the coordination of Re(III) complex compounds with the components of biomolecules (proteins, DNA).
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Kononova, G. S., S. V. Antonuk, and N. I. Shtemenko. "Вплив реній-платинової системи у вигляді наноліпосом на проліферативну активність ракових клітин." Visnyk of Dnipropetrovsk University. Biology, medicine 2, no. 1 (March 30, 2011): 59–67. http://dx.doi.org/10.15421/021110.

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Decrease of proliferative activity of the cells of Guerin’s carcinoma T8 in the different conditions of administration of the Rhenium-Platinum anti-tumour system as nanolyposomes is shown. The Rhenium-Platinum anti-tumour system influenced on the morphological indices of tumour tissue. The cluster rhenium compounds reduced the indices of pathological mitoses 3.0–3.6 times in comparison with a control group. The amount of PCNA-positive cells under the Rhenium-Platinum system treatment went down by 82.5–84.5 %. The anti-tumour system led to the predominance of apoptotic cell death over the necrotic one. The most effective agent was the compound with cis-adamantan organic ligand cis-Re2(C10H15COO)2Cl4·2DMSO introducted on the 9th day.
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Brink, Alice, and John R. Helliwell. "Formation of a highly dense tetra-rhenium cluster in a protein crystal and its implications in medical imaging." IUCrJ 6, no. 4 (June 13, 2019): 695–702. http://dx.doi.org/10.1107/s2052252519006651.

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The fact that a protein crystal can serve as a chemical reaction vessel is intrinsically fascinating. That it can produce an electron-dense tetranuclear rhenium cluster compound from a rhenium tricarbonyl tribromo starting compound adds to the fascination. Such a cluster has been synthesized previously in vitro, where it formed under basic conditions. Therefore, its synthesis in a protein crystal grown at pH 4.5 is even more unexpected. The X-ray crystal structures presented here are for the protein hen egg-white lysozyme incubated with a rhenium tricarbonyl tribromo compound for periods of one and two years. These reveal a completed, very well resolved, tetra-rhenium cluster after two years and an intermediate state, where the carbonyl ligands to the rhenium cluster are not yet clearly resolved, after one year. A dense tetranuclear rhenium cluster, and its technetium form, offer enhanced contrast in medical imaging. Stimulated by these crystallography results, the unusual formation of such a species directly in an in vivo situation has been considered. It offers a new option for medical imaging compounds, particularly when considering the application of the pre-formed tetranuclear cluster, suggesting that it may be suitable for medical diagnosis because of its stability, preference of formation and biological compatibility.
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Kuninobu, Yoichiro, Yuta Nishina, Atsushi Kawata, Makoto Shouho, and Kazuhiko Takai. "Rhenium-catalyzed synthesis of indene derivatives via C-H bond activation." Pure and Applied Chemistry 80, no. 5 (January 1, 2008): 1149–54. http://dx.doi.org/10.1351/pac200880051149.

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Rhenium complex, [ReBr(CO)3(thf)]2-catalyzed reactions between aromatic imines and either acetylenes or α,β-unsaturated carbonyl compounds gave indene derivatives in good to excellent yields. These reactions proceed via C-H bond activation, insertion of acetylenes or α,β-unsaturated carbonyl compounds, intramolecular nucleophilic cyclization, and reductive elimination. Indene derivatives were also obtained from aromatic ketones and α,β-unsaturated carbonyl compounds in the presence of catalytic amounts of the rhenium complex and p-anisidine. Sequential ruthenium-catalyzed hydroamination of aromatic acetylenes with anilines, and rhenium-catalyzed reactions of the formed aromatic ketimines with α,β-unsaturated carbonyl compounds also provided indene derivatives.
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KUSAMA, Hiroyuki, and Koichi NARASAKA. "Rhenium Compounds in Organic Synthesis." Journal of Synthetic Organic Chemistry, Japan 54, no. 8 (1996): 644–53. http://dx.doi.org/10.5059/yukigoseikyokaishi.54.644.

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Adams, Richard D., and William C. Pearl. "Rhenium−Bismuth Carbonyl Cluster Compounds." Inorganic Chemistry 48, no. 19 (October 5, 2009): 9519–25. http://dx.doi.org/10.1021/ic901176x.

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Feller, J., H. Oppermann, M. Binnewies, and E. Milke. "Zum Chemischen Transport von Rhenium und Rheniumoxiden/On the Chemical Transport of Rhenium and Rhenium Oxides." Zeitschrift für Naturforschung B 53, no. 2 (February 1, 1998): 184–90. http://dx.doi.org/10.1515/znb-1998-0210.

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Abstract Synthesis and single crystal growth by chemical transport reactions of rhenium and rhenium oxides is reported. Several transport agents like the mercury halides HgCl2, HgBr2, HgI2, tellurium tetrachloride and iodine have been employed the transport of the rhenium compounds. Mass spectrometric experiments gave informations about the composition of the gas phase. The transport reactions were traced by calculations based on the knowledge of the gas phase species and their thermodynamical data.
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Dissertations / Theses on the topic "Rhenium compounds"

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DuMez, Darin David. "Synthesis and selective oxidations of rhenium hydrotris(1-pyrazolyl) borate compounds /." Thesis, Connect to this title online; UW restricted, 1997. http://hdl.handle.net/1773/8674.

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薛文梅 and Wenmei Xue. "Syntheses, photophysical and photochemical properties of Rhenium(V) and Rhenium(VI) Benzylidyne complexes." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1997. http://hub.hku.hk/bib/B31237927.

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Xue, Wenmei. "Syntheses, photophysical and photochemical properties of Rhenium(V) and Rhenium(VI) Benzylidyne complexes /." Hong Kong : University of Hong Kong, 1997. http://sunzi.lib.hku.hk/hkuto/record.jsp?B19667255.

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Leblond, Nicolas. "Technetium(VII) and rhenium(VII) oxofluorides and the role of noble-gas fluorides in their syntheses /." *McMaster only, 1998.

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Schoultz, Xandri. "Isocyanide complexes of rhenium." Thesis, Nelson Mandela Metropolitan University, 2013. http://hdl.handle.net/10948/d1021069.

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This study investigates the synthesis of rhenium(III)-isocyanide complexes with potentially bidentate ligands, as well as the reactivity of isocyanide ligands toward rhenium(I) and (V). The crystal structures of all the complexes have been determined by X-ray diffraction methods. The coordination behaviour of trans-[ReIIICl3(t-BuNC)(PPh3)2] with aniline and its derivatives were investigated. The isocyanide-containing rhenium(V) complexes [ReCl3(t-BuNC)(L)(PPh3)] were isolated, with the ligands H2L (aniline, o-phenylenediamine and anthranilic acid). In all these complexes the dianionic ligands L are coordinated monodentately as the imide. However, with 2-aminophenol the complexes [ReVCl2(t-BuNC)(L)(PPh3)2](ReO4) and [ReIIICl2(t-BuNC)(ibq)(PPh3)2] (ibq- = 2-iminobenzoquinonate) were identified as the products. [ReCl2(t-BuNC)(L)(PPh3)2](ReO4) is the product of a disproportionation reaction from Re(III) to Re(VII) and Re(V). All the above complexes show a distorted octahedral geometry around the rhenium. The products of the reaction of the Re(I) complex [Re(CO)5Cl] with isocyanides (tert-butyl- and cyclohexylisocyanide) are reported. Rhenium(I) tricarbonyl complexes of the form [Re(CO)3(CNR)2Cl] were isolated and they were characterized structurally and spectroscopically. The tricarbonyls are coordinated in the typical facial-fashion, whereas the isocyanides are coordinated cis to each other. The reaction of [Re(CO)3(t-BuNC)2Cl] with H2O led to the formation of the rhenium(I) complex [Re(CO)3(t-BuNC)2(OH2)] in which the aquo ligand can readily be substituted by a more complex ligand. The reaction of the rhenium(V) complexes cis-[ReO2I(PPh3)2] and mer-[ReOCl3(SMe2)(OPPh3)] with isocyanides were studied. The seven-coordinate trigonal prismatic, square faced monocapped rhenium(III) complex [ReI3(t-BuNC)3(PPh3)] was surprisingly isolated upon reacting cis-[ReO2I(PPh3)2] with tert-butyl isocyanide. The dimeric complex (μ-O)[ReOCl2(CNC6H11)2]2 was obtained from the reaction of mer-[ReOCl3(SMe2)(OPPh3)] with cyclohexyl isocyanide.
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Wong, A. C. C. "Cluster alkyls and related compounds of rhenium." Thesis, Imperial College London, 1988. http://hdl.handle.net/10044/1/47311.

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Mukiza, Janvier. "Synthesis and characterisation of oxorhenium(V) and tricarbonylrhenium(I) complexes with biologically active N, O and N, S-Donor ligands." Thesis, Nelson Mandela Metropolitan University, 2013. http://hdl.handle.net/10948/d1020769.

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This study investigated the synthesis of rhenium(I) and rhenium(V) complexes with a variety of multidentate NS, NSO, NO and SO-donor ligands. It also investigated the synthesis of dinuclear dihalogeno- and trihalogeno-bridged rhenium(I) complexes based on the fac-[Re(CO)3]+ core. The reactions of hydrated folic acid with [Re(CO)5X] (X = Cl, Br) were studied, and the complexes [Re(CO)3(H2O)3]+[Re2(μ-X)3CO)6]−.5H2O [X= Br (1), Cl(2)] were isolated. The reaction of orotic acid potassium salt [Re(CO)5Br] was performed, and the complex [Re2(μ-Br)2(CO)8] was isolated. The reaction of bis(piperidin-1- yl)methanone with [Re(CO)5Cl] followed by recrystallisation of the resulting precipitate in dichloromethane/acetontrile resulted in the complex [Re2(μ- Cl)2(CO)6(MeCN)2]. The X-ray crystal structures show that all these complexes display a distorted octahedral geometry around the central rhenium atoms. The reactions of aroylhydrazone-based ligands such as 3-((pyridin- 2yl)methyleneamino)-2,3-dihydro-2-pyridin-2yl)quinazolin-4-(1H)-one (Hppq) and N-(di(pyridin-2-yl)methylene)benzohydrazide (Hdpmb) with [Re(CO)5Cl] were studied and led to the formation of the complexes [Re(CO)3Cl(Hdpmb)] and [Re(CO)3Cl(Hppq)]. The Hdpmb and Hppq coordinated to the fac-[Re(CO)3]+ core as neutral bidentate chalates via the pyridinic nitrogens (for Hdpmb) and via imino and pyridinic nitrogens for Hppq. The X-ray crystal structures show that the geometry around the rhenium in both complexes is a distorted octahedral. The treatment of the dithizone (H2dz) ligand with rhenium(V) precursors containing a triphenylphosphine group (PPh3) led to the decomposition of dithizone. The decomposition product reacted with the triphenylphosphine group and generated a new ligand triphenylphosphazeno-N-phenylmethanethiohydrazide (H2L). The reaction of trans-[ReOX3(PPh3)2] (X = Cl, Br) with dithizone (H2dz) led to the complex [ReO(dz)2][ReO(HL)2]. The reaction of trans-[ReOI2(OEt)(PPh3)2] with H2dz led to the same product. The reaction of cis-[ReO2I(PPh3)2] with H2dz in methanol led to [ReO(dz)2][ReO(HL)2](MeOH)2 in which methanol bonded to HLvia hydrogen bonds. The H2dz was doubly deprotonated and coordinated to the [ReO]3+ moiety via a thiolate sulfur and deprotonated hydrazinic nitrogen to yield [ReO(dz)2]−, while the H2L was singly deprotonated and coordinated to [ReO]3+ moiety via the neutral sulfur atom and deprotonated hydrazinic nitrogen to yield [ReO(HL)2]+. The X-ray crystal structure show that in both [ReO(HL)2]+ and [ReO(dz)2]−, the rhenium atoms are five-coordinated and adopt a distorted squarebased pyramidal geometry. The reaction of thiosemicarbazones such as salcylidene-4- phenylthiosemicarbazide (H3salpt) with cis-[ReO2I(PPh3)2] was investigated and led to the complex [ReO(Hsalpt)(H2salpt)]. The X-ray study reveals that Hsalpt is present as a tridentate chelate coordinating via the thiolate sulfur, imino nitrogen and phenolic oxygen, while H2salpt coordinates as a bidentate chelate via the thiolate sulfur and imino nitrogen atoms. The geometry around rhenium is distorted octahedral. The coordination mode of the benzoylthiourea derivatives 4-tert-butyl-N- (diphenylcarbamothioyl)benzamide (Htpb) and N-(diethylcarbamothioyl)benzamide (Heb) to the [Re2O3]4+ and fac-[Re(CO)3]+ cores were investigated. The reaction of [Re(CO)5Cl] in presence of sodium acetate with Htpb led to the dimeric complex [Re(CO)3(tpb)]2 in which the tpb coordinated to the fac-[Re(CO)3]+ core via the ketonic oxygen and bridging thiolate sulfur. The same reaction with Heb led to the monomeric complex [Re(CO)3(eb)(Heb)], in which the eb coordinates to the fac-[Re(CO)3]+core via thiolate sulfur and ketonic oxygen with Heb binding via the neutral sulfur atom. The reaction of Heb with cis-[ReO2I(PPh3)2] at room temperature with excess of sodium acetate led to the dimeric complex (μ-O)[ReO(eb)2]2 in which Heb is present as a monoanionic (deprotonated) bidentate with coordination through the thiolate sulfur and ketonic oxygen.
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Tse, Chui-wan. "Rhenium containing hyperbranched polymers for photonic applications." Click to view the E-thesis via HKUTO, 2007. http://sunzi.lib.hku.hk/hkuto/record/B38574512.

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Tse, Chui-wan, and 謝翠雲. "Rhenium containing hyperbranched polymers for photonic applications." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2007. http://hub.hku.hk/bib/B38574512.

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Lee, Sang Woo 1952. "Reduction Pathways in Cyclopentadienyl Rhenium Dicarbonyl Dibromide Deriviatives and Indenyl Rhenium Tricarbonyl: Synthesis, Structure, and Reactivity of Anionic Cyclopentadienyl Rhenium Complexes. Ring Attack vs. Metal-Halogen Exchange." Thesis, University of North Texas, 1989. https://digital.library.unt.edu/ark:/67531/metadc332212/.

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The reactions of diagonal and lateral Cp'Re(CO)2Br2 (where Cp' = n5-C5H5, n5-C5Me5) and (n5-CgH7)Re(CO)3 with reducing agents have been examined. Hydride reduction at -78 °C is observed to occur at the Cp ring in both CpRe(CO)2Br2 isomers, affording a thermally unstable [(n4 -C5Hg)Re(CO)2Br2]- complex. The product of hydride ring attack has been characterized by low-temperature IR and 1H NMR measurements in addition to 13C NOE and heteronuclear 2D NMR measurements. Reaction of lateral CpRe(CO)2Br2 with either MeLi or PhLi affords both Cp-ring attack and metalhalogen exchange, [CpRe(CO)2Br]- (1) while t-BuLi reacts exclusively via metal-halogen exchange. diag-CpRe(CO)2Br2 reacts with the above lithium reagents to yield the same metal-halogen exchange anion. Analogous reactions using diag- and lat-Cp*Re(CO)2Br2 (where Cp* = n5-CgMe5) afford only the corresponding rhenium metal-halogen exchange anion, [Cp*Re(CO)2Br] (2). The molecular structures of 1-[Li/15-Crown-5] and 2-PPP were established by X-ray crystallography. 1-[Li/15-Crown-5] crystallizes in the monoclinic space group P21 with a = 10.860(4) A, b = 13.116(5) A, c = 7.417(3) A, B = 105.26(3)0, V = 1018.7(3) A3 , and Z = 2. 2-PPP crystallizes in the orthorhombic space group Pbca with a = 20.646(5) A, b = 17.690(5) A, c = 17.553(3) A, and z = 8. Solution FT-IR studies of 2 in THF reveal the presence of only solvent-separated ion pairs when the gegencation is Li+, K+, or PPP+ from -70 °C to room temperature. 2-Na at room temperature displays a 39:61 mixture of carbonyl oxygen-sodium and solvent-separated ion pairs, respectively. These ion pairs reveals a reversible temperature-dependent equilibrium. The equilibrium constant has been determined by IR band shape analysis over the temperature range -70 °C to room temperature and values of AH and AS are reported. The reaction of the ring-attacked complex, diag-[(n4-C5H6)Re(CO)2Br2]- with PPh3, P(OPh)3, or Me3CNC leads to the formation of the CpRe(CO)2L. Treatment of [Cp'Re(CO)2Br]- with methyltriflate, TFA, and magic ethyl yields the corresponding diag-Cp'Re(CO)2Br(R) (R = CH3, H, C2H5) complexes based on in situ IR analysis. All of these functionalized complexes decomposed in solution over a period of days to give Cp'Re(CO)3 as the only isolable product (20-30 %). The reaction of the [Cp,Re(C0)2Br]- with Bu3SnH at 60 °C leads to the formation of diag-Cp'Re(CO)2(SnBu3)2, which was also synthesized independently by the deprotonation of diag-Cp'Re(CO)2H2 with Et3N in the presence of Bu3SnBr at room temperature. The reaction of Cp'Re(CO)2Br2 with Bu3SnH at room temperature was discovered to afford the dihydride in excellent yield and, thus represents an improved synthetic route for the synthesis of diag-Cp'Re(CO)2H2. The hydride reduction of (n5-CgH7)Re(CO)3 at room temperature leads to the immediate formation of [(n5-CgH7)Re(CO)2H]- complex, which has been characterized by IR analysis and 1H and 13C NMR spectroscopy.
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Books on the topic "Rhenium compounds"

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Untersuchungen zur Chemie von Rhenium-Nitrosyl-Komplexen. Konstanz: Hartung-Gorre, 1991.

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Banberry, Hilary J. The structures of rhenium compounds which act as models for technetium radiopharmaceuticals. Birmingham: University of Birmingham, 1989.

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Pateman, Jeffrey. Handbook of Filled Polytetrafluoroethylene Compounds: Technology, Manufacture, Processing, Properties and Applications. Elsevier Science & Technology Books, 2018.

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Ness, Stephanie L. Evidence for a stepwise mechanism in the cycloreversion of rhenium diolates. 1999.

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Striplin, Durwin R. Spectroscopic and magnetic investigations of Re(I)Cl(CO)₃(Ü,Üʹ-diimine) complexes and group (1B,8B) bimetallic complexes. 1994.

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Thornton, Nancy Byrnes. Chromophore-quencher-based luminescence probes for DNA. 1995.

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Albrecht, Reinhard. Re Rhenium - Organorhenium Compounds: Binuclear Compounds (Gmelin - Handbooks of Inorganic and Organometallic Chemistry , Part 7). 8th ed. Springer, 1997.

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Trace, Rhonda. A new synthetic methodology applied to the preparation of some novel, alkyl substituted, cyclic carbene complexes of ruthenium, tungsten, and rhenium. 1991.

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Element R-e Re. Rhenium, System-nr. 70, Erganzungsband 1-8 Re-organische Verbindungen / Organorhenium Compounds (Gmelin Handbook of Inorganic and Organometallic Chemistry). Springer, 1997.

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Book chapters on the topic "Rhenium compounds"

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Templeton, J. L. "Trimeric Rhenium Compounds." In Inorganic Reactions and Methods, 89–91. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145296.ch70.

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Macintyre, J. E. "Re Rhenium." In Dictionary of Organometallic Compounds, 284–90. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4615-6847-6_42.

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MacIntyre, Jane E. "Re Rhenium." In Dictionary of Organometallic Compounds, 196–206. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4899-6848-7_45.

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Macintyre, J. E., F. M. Daniel, D. J. Cardin, S. A. Cotton, R. J. Cross, A. G. Davies, R. S. Edmundson, et al. "Re Rhenium." In Dictionary of Organometallic Compounds, 162–66. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4757-4966-3_46.

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Nagy, Zoltán. "Re—Rhenium." In Electrochemical Synthesis of Inorganic Compounds, 388–89. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4899-0545-1_54.

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Green, M. "Re Rhenium." In Organometallic Compounds of the Lanthanides, Actinides and Early Transition Metals, 140–55. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4899-7164-7_24.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nitrosyl rhenium complex." In Magnetic Properties of Paramagnetic Compounds, 34–35. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_13.

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Brignole, Alicia B., F. A. Cotton, Z. Dori, Z. Dori, Z. Dori, and G. Wilkinson. "Rhenium and Molybdenum Compounds Containing Quadruple Bonds." In Inorganic Syntheses, 81–89. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132449.ch15.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of rhenium(II) complex with phthalocyanine." In Magnetic Properties of Paramagnetic Compounds, 947–48. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_539.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of rhenium(II) isocyanide complex with diphenylphosphinoethane." In Magnetic Properties of Paramagnetic Compounds, 939. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_534.

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Conference papers on the topic "Rhenium compounds"

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Sriyani, Maula Eka, Eva Maria Widyasari, and M. Fajri Satria Rinjani. "Synthesis of non-radioactive rhenium complexes with quercetin compounds." In INTERNATIONAL CONFERENCE ON SCIENCE AND APPLIED SCIENCE (ICSAS) 2021. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0072408.

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Banerjee, Hirendra N., Deidre Vaughan, Jewe Medley, Gwyn Hyman, Christopher Krauss, Carl Parson, Santosh Mandal, et al. "Abstract 4485: Anticancer properties of novel rhenium compounds against human cancer cell lines." In Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.am2013-4485.

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Banerjee, Hirendra N., Sasha Hodge, William Kahan, Santosh Mandal, David Weber, Rena Lapidus, Fazlul Sarkar, and Somiranjan Ghosh. "Abstract 120: A study of in vitro and in vivo effects of a novel peptide and rhenium compounds on prostate cancer." In Proceedings: AACR Annual Meeting 2017; April 1-5, 2017; Washington, DC. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.am2017-120.

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Stevenson, Monet, Jameel Joyner, Khadija Dildar, Oladipo Adedeji, Krishnan Prabhakaran, Hirendra N. Banerjee, Santosh Mandal, and Fazlul Sarkar. "Abstract 4840: The role of miR-146a and novel Rhenium compounds on prostate cancer cell lines derived from African Americans and European American patients." In Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-4840.

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Banerjee, Hirendra N., Jameel Joyner, Alexis Barfield, B. Morris, D. Bell, William Kahan, Monet Stevenson, et al. "Abstract 4831: An investigation to study the role of novel rhenium compounds on onco miR's and oncogenes involved in epithelial mesenchymal transition of prostate cancer cell lines derived from African American and Caucasian patients." In Proceedings: AACR 107th Annual Meeting 2016; April 16-20, 2016; New Orleans, LA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.am2016-4831.

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Kon, Yoshihiro. "Selective monoallylation of anilines to form fine chemicals using allyl alcohol derived from glycerol." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/mjrr3569.

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Abstract:
Glycerol is an important starting material for the production of value-added chemicals such as electronic materials and pharmaceuticals. We herein present a selective allylation reaction using allyl alcohol which is given from glycerol. First, we show the rhenium catalyzed high-yielding synthesis of allyl alcohol from glycerol through deoxydehydration reaction. Next, the selective N-allyl aniline synthesis from allyl alcohol with aniline is performed. The well-dispersed tungsten oxide supported on zirconium oxide can catalyze the reaction to produce the corresponding mono-allyl compound over 97% selectivity using a flow reactor. The developed catalyst is applicable to the production of various N-monoallyl anilines without the formation of N,N-diallyl anilines.
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Reports on the topic "Rhenium compounds"

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Shan, Xiaopeng. Mechanistic Study of Oxygen Atom Transfer Catalyzed by Rhenium Compounds. Office of Scientific and Technical Information (OSTI), January 2003. http://dx.doi.org/10.2172/816442.

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