Viñas et al., 1998 - Google Patents
exo-nido-Monothio-and exo-nido-Monophosphinorhodacarboranes: Synthesis, Reactivity, and Catalytic Properties in Alkene HydrogenationViñas et al., 1998
- Document ID
- 10737171276683274608
- Author
- Viñas C
- Flores M
- Núñez R
- Teixidor F
- Kivekäs R
- Sillanpää R
- Publication year
- Publication venue
- Organometallics
External Links
Snippet
Reaction of Cs [7-SR-8-R '-7, 8-C2B9H10](R= Ph, R '= Me; R, R '= Ph; R= Et, R '= Me) with [RhCl (PPh3) 3] in toluene− ethanol (8: 1) affords [Rh (7-SR-8-R '-7, 8-C2B9H10)(PPh3) 2]. Reaction of tetraalkylammonium salts of [7-PR2-8-R '-7, 8-C2B9H10]-(R= Ph, R '= H; R= Ph …
- 238000005984 hydrogenation reaction 0 title abstract description 31
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System compounds of the platinum group
- C07F15/0073—Rhodium compounds
- C07F15/008—Rhodium compounds without a metal-carbon linkage
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F17/00—Metallocenes
- C07F17/02—Metallocenes of metals of Groups 8, 9 or 10 of the Periodic System
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System compounds of the platinum group
- C07F15/0086—Platinum compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
- C07F9/02—Phosphorus compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/22—Organic complexes
- B01J31/2282—Unsaturated compounds used as ligands
- B01J31/2295—Cyclic compounds, e.g. cyclopentadienyls
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
- B01J31/1805—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing nitrogen
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/82—Metals of the platinum group
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/60—Reduction reactions, e.g. hydrogenation
- B01J2231/64—Reductions in general of organic substrates, e.g. hydride reductions or hydrogenations
- B01J2231/641—Hydrogenation of organic substrates, i.e. H2 or H-transfer hydrogenations, e.g. Fischer-Tropsch processes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/24—Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
- B01J31/2404—Cyclic ligands, including non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
- B01J31/2409—Cyclic ligands, including non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring with more than one complexing phosphine-P atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic System
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Teixidor et al. | Exo-nido-Cyclooctadienerhodacarboranes: Synthesis, reactivity, and catalytic properties in alkene hydrogenation | |
Goldberg et al. | The importance of steric factors in iridium pincer complexes | |
Lesueur et al. | A bidentate bisphosphine functioning in intramolecular aliphatic metalation and as an NMR spectroscopic probe for the metal coordination environment | |
Bhattacharyya et al. | Palladium (II) and platinum (II) complexes of the heterodifunctional ligand Ph2PNHP (O) Ph2 | |
Yu et al. | New Rhodium (I) carbene complexes from carbene transfer reactions | |
Viñas et al. | exo-nido-Monothio-and exo-nido-Monophosphinorhodacarboranes: Synthesis, Reactivity, and Catalytic Properties in Alkene Hydrogenation | |
Cohen et al. | The Methylene-Transfer Reaction: Synthetic and Mechanistic Aspects of a Unique C− C Coupling and C− C Bond Activation Sequence | |
Venkateswaran et al. | Ruthenium (II) complexes containing bis (2-(diphenylphosphino) phenyl) ether and their catalytic activity in hydrogenation reactions | |
Smoleński et al. | New rhodium (III) and ruthenium (II) water-soluble complexes with 3, 5-diaza-1-methyl-1-azonia-7-phosphatricyclo [3.3. 1.13, 7] decane | |
Viñas et al. | Modulation of agostic B− H⇀ Ru bonds in exo-Monophosphino-7, 8-Dicarba-nido-undecaborate derivatives | |
Alonso et al. | Reactivity of a secondary phosphine Platinum (II) complex with [Pt (norbornene) 3] and PPh3. Synthesis of new single phosphido-bridged derivatives of Platinum (I) and phosphido-bridged Platinum (II) hydrides | |
Nemeh et al. | Iridium Chemistry of 1, 6-Bis ((tert-butylphosphino) methyl)-1, 3, 5-cycloheptatriene | |
Alvarez et al. | M− P versus MM Bonds as Protonation Sites in the Organophosphide-Bridged Complexes [M2Cp2 (μ-PR2)(μ-PR ‘2)(CO) 2],(M= Mo, W; R, R ‘= Ph, Et, Cy) | |
Schlaf et al. | Synthesis and Structure of the Chiral Dihydrogen Complex trans-[Ru (η2-H2) H (R, R ‘-Me-DuPHOS) 2] PF6 and the Dinitrogen Complex trans-[Ru (N2) H (R, R ‘-Me-DuPHOS) 2] PF6 (R, R ‘-Me-DuPHOS= 1, 2-Bis ((2 R, 5 R)-2, 5-dimethylphospholano) benzene) | |
Esteruelas et al. | Synthesis and reactivity of osmium complexes containing a cyclopentadienyl ligand with a pendant phosphine donor group | |
Rankin et al. | Exploring the Influence of Ancillary Ligand Charge and Geometry on the Properties of New Coordinatively Unsaturated Cp*(κ2-P, N) Ru+ Complexes: Linkage Isomerism, Double C− H Bond Activation, and Reversible α-Hydride Elimination | |
Deeming et al. | Trinuclear Clusters of Ruthenium-Containing Bridging and Ortho-Metalated 2, 2 ‘-Bis (diphenylphosphino)-1, 1 ‘-binaphthyl (BINAP): X-ray Structures of (R)-BINAP and [Ru3 (μ-OH) 2 (CO) 8 {μ-(R)-BINAP}] | |
Burns et al. | Polyazolyl Chelate Chemistry. 6.1 Bidentate Coordination of HB (pz) 3 (pz= Pyrazol-1-yl) to Ruthenium and Osmium: Crystal Structure of [RuH (CO)(PPh3) 2 {κ2-HB (pz) 3}] | |
Zhuravel et al. | Synthesis and structure of dinuclear palladium (II) complexes with bridging hydrido and phosphido ligands | |
Jia et al. | Dioxygen Complexes from the Reactions of [Cp* RuH2 (PP)]+(PP= dppm, dppe) with Air | |
Schnabel et al. | Polyhydride (Fluoroalkyl) phosphine Complexes of Iridium. Synthesis, Dynamics, and Reactivity Properties of (dfepe) 2Ir2 (μ-H) 3 (H) | |
Núñez et al. | Formation of new η5-rhodium (III) complexes from η5-Rh (I) rhodacarborane-containing charge-compensated ligands | |
Leung et al. | Organometallic compounds of ruthenium containing an anionic oxygen tripod ligand | |
Andrieu et al. | Synthesis of new phosphino amino alcohol ligands via ortho-alkyllithiation reactions. Versatile coordination behavior toward copper (I) and palladium (II) | |
Teixidor et al. | Influence of S-Aryl Groups in the Coordination and Reactivity of (n ido-Thiocarborane) ruthenium Complexes |