Lin et al., 2013 - Google Patents
Boryl-mediated reversible H2 activation at cobalt: catalytic hydrogenation, dehydrogenation, and transfer hydrogenationLin et al., 2013
View PDF- Document ID
- 2984964611120172323
- Author
- Lin T
- Peters J
- Publication year
- Publication venue
- Journal of the American Chemical Society
External Links
Snippet
We describe the synthesis of a cobalt (I)–N2 complex (2) supported by a meridional bis- phosphino-boryl (PBP) ligand. Complex 2 undergoes a clean reaction with 2 equiv of dihydrogen to afford a dihydridoboratocobalt dihydride (3). The ability of boron to switch …
- 238000006356 dehydrogenation reaction 0 title abstract description 59
Classifications
-
- 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
- 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
-
- 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
- C07F5/02—Boron compounds
- C07F5/025—Boronic and borinic acid 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
- C07F17/00—Metallocenes
- C07F17/02—Metallocenes of metals of Groups 8, 9 or 10 of the Periodic System
-
- 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
-
- 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
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Lin et al. | Boryl-mediated reversible H2 activation at cobalt: catalytic hydrogenation, dehydrogenation, and transfer hydrogenation | |
Wang et al. | Divalent silicon-assisted activation of dihydrogen in a bis (N-heterocyclic silylene) xanthene nickel (0) complex for efficient catalytic hydrogenation of olefins | |
Burford et al. | β-Elimination-immune PCcarbeneP iridium complexes via double C–H activation: ligand–metal cooperation in hydrogen activation | |
Obligacion et al. | Cobalt catalyzed Z-selective hydroboration of terminal alkynes and elucidation of the origin of selectivity | |
Saper et al. | Mechanistic investigations of the hydrogenolysis of diaryl ethers catalyzed by nickel complexes of N-heterocyclic carbene ligands | |
Nakajima et al. | Hydroboration of Alkynes Catalyzed by Pyrrolide-Based PNP Pincer–Iron Complexes | |
Brzozowska et al. | Highly chemo-and stereoselective transfer semihydrogenation of alkynes catalyzed by a stable, well-defined manganese (II) complex | |
Cammarota et al. | Tuning nickel with Lewis acidic group 13 metalloligands for catalytic olefin hydrogenation | |
Ibrahim et al. | Insights into a chemoselective cobalt catalyst for the hydroboration of alkenes and nitriles | |
Goldfogel et al. | Intermolecular hydroamination of 1, 3-dienes catalyzed by bis (phosphine) carbodicarbene–rhodium complexes | |
Segawa et al. | Syntheses of PBP pincer iridium complexes: A supporting boryl ligand | |
Wu et al. | Synthesis and reactivity of silyl iron, cobalt, and nickel complexes bearing a [PSiP]-pincer ligand via Si–H bond activation | |
Chakraborty et al. | Selective hydrogenation of nitriles to secondary imines catalyzed by an iron pincer complex | |
Zhao et al. | DFT studies on the mechanism of the diboration of aldehydes catalyzed by copper (I) boryl complexes | |
Semproni et al. | Four-coordinate cobalt pincer complexes: electronic structure studies and ligand modification by homolytic and heterolytic pathways | |
Johnson et al. | Catching the first oligomerization event in the catalytic formation of polyaminoboranes: H3B· NMeHBH2· NMeH2 bound to iridium | |
Obligacion et al. | Cobalt-catalyzed C–H borylation | |
Chen et al. | Iron-catalyzed, Markovnikov-selective hydroboration of styrenes | |
Bart et al. | Low-valent α-diimine iron complexes for catalytic olefin hydrogenation | |
Bézier et al. | Applications of PC (sp3) P iridium complexes in transfer dehydrogenation of alkanes | |
Park et al. | Ruthenium catalyzed hydrohydroxyalkylation of isoprene with heteroaromatic secondary alcohols: isolation and reversible formation of the putative metallacycle intermediate | |
Venkanna et al. | Synthesis, characterization, and catalytic activity of nickel (II) alkyl complexes supported by pyrrole–diphosphine ligands | |
Zeng et al. | Insights into Dehydrogenative Coupling of Alcohols and Amines Catalyzed by a (PNN)–Ru (II) Hydride Complex: Unusual Metal–Ligand Cooperation | |
Haller et al. | Activation of an Alkyl C− H Bond Geminal to an Agostic Interaction: An Unusual Mode of Base-Induced C− H Activation | |
Kosog et al. | Uranium (III)-mediated C–C-coupling of terminal alkynes: Formation of dinuclear uranium (IV) vinyl complexes |