Xing et al., 2020 - Google Patents
Reversible nickel-metallacycle formation with a phosphinimine-based pincer ligandXing et al., 2020
View PDF- Document ID
- 12497072392556219423
- Author
- Xing X
- Zhang S
- Thierer L
- Gau M
- Carroll P
- Tomson N
- Publication year
- Publication venue
- Dalton Transactions
External Links
Snippet
Pincer ligands have a remarkable ability to impart control over small molecule activation chemistry and catalytic activity; therefore, the design of new pincer ligands and the exploration of their reactivity profiles continues to be a frontier in synthetic inorganic …
- 230000027455 binding 0 title abstract description 57
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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6581—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and nitrogen atoms with or without oxygen or sulfur atoms, as ring hetero atoms
-
- 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
-
- 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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic System
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C-Si linkages
-
- 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
- C07F15/002—Osmium 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
- 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
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic System
- C07F5/02—Boron 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
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
- C07F15/04—Nickel compounds
- C07F15/045—Nickel 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
- C07F1/00—Compounds containing elements of Groups 1 or 11 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
- C07F13/00—Compounds containing elements of Groups 7 or 17 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
- C07F3/00—Compounds containing elements of Groups 2 or 12 of the Periodic System
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Stephan | Zirconium–phosphorus chemistry: Strategies in syntheses, reactivity, catalysis, and utility | |
Kira | An isolable dialkylsilylene and its derivatives. A step toward comprehension of heavy unsaturated bonds | |
Hofmann et al. | Bis (di-t-butylphosphino) methane complexes of rhodium: homogeneous alkyne hydrosilylation by catalyst-dependent alkyne insertion into Rh Si or Rh H bonds. Molecular structures of the dimer [(dtbpm) RhCl] 2 and of the silyl complex (dtbpm) Rh [Si (OEt) 3](PMe3) | |
Trifonov et al. | Reduction of Azobenzene by Naphthaleneytterbium: A Tetranuclear Ytterbium (iii) Complex Combining 1, 2‐Diphenylhydrazido (2−) and Phenylimido Ligands | |
Otsuka et al. | Univalent palladium complexes | |
Wong et al. | Hydrido complexes of ruthenium with carborane ligands | |
Findlater et al. | Synthesis and structure of two new (guanidinate) boron dichlorides and their attempted conversion to boron (i) derivatives | |
Xing et al. | Reversible nickel-metallacycle formation with a phosphinimine-based pincer ligand | |
Schaub et al. | A diazabutadiene stabilized nickel (0) cyclooctadiene complex: Synthesis, characterization and the reaction with diphenylacetylene | |
Vaughan et al. | Synthesis and characterization of zinc complexes and reactivity with primary phosphines | |
Wilson et al. | Reactions of ruthenium (II) tris (pyrazolyl) borate and tris (pyrazolyl) methane complexes with diphenylvinylphosphine and 3, 4-dimethyl-1-phenylphosphole | |
Hoidn et al. | Reaction of a 2, 4, 6-triphenylphosphinine ferrate anion with electrophiles: a new route to phosphacyclohexadienyl complexes | |
Youngs et al. | Formation of a chelating. sigma.-allyl by the intramolecular activation of a cyclopropylphosphine. Synthesis and crystal structure of [PdCl (P (tert-Bu) 2CH: C (CH3) CH2)] 2 | |
Poli et al. | Reactions of CpMoCl2L2 (Cp=. eta. 5-C5H5; L= PMe3, PMe2Ph) with methyllithium. Preparation and structure of a molybdenum (II) compound containing an ortho-metalated PMe2Ph ligand: CpMo (o-C6H4PMe2)(PMe2Ph) 2 | |
Duraczyńska et al. | Diphenylvinylphosphine (DPVP) complexes containing the (η 5-MeC 5 H 4) Ru (ii) moiety: synthesis, characterization and reactions | |
Szajek et al. | Stereodynamics and Reactivity of the Indenyliridium (I) Complex (. eta. 5-C9H7) Ir (. eta. 2-C8H14)(CO). Comparison with the Cyclopentadienyl Analog (. eta. 5-C5H5) Ir (. eta. 2-C8H14)(CO) | |
Carmichael et al. | Synthesis, structure and dynamics of methoxynaphthalene-substituted phospha-ruthenocenes and-ferrocenes | |
Klitzke et al. | Zinc (II) complexes based on sterically hindered hydrotris (pyrazolyl) borate ligands: Synthesis, reactivity and solid-state structures | |
Brandt et al. | The Proton Catalyzed Transformation of a Cobaltacyclopentadiene into a η4‐Cyclobutadiene Complex | |
Gafoor et al. | Synthesis, characterization and structure of the ethylene-bridged dimer [Cp (CO) 2RuCH2CH2RU (CO) 2Cp] and comparison of its reactivity with that of [Cp (CO) 2RuCH2CH3] and [CpCO) 2Ru (CH2) 5Ru (CO) 2Cp]: models for Fischer-Tropsch surface intermediates | |
Hamura et al. | “Bidentate” and “tridentate” sulfonamide ligands for titanium complexes: crystal structures and solution dynamics elucidating an η 2 or η 3-coordination mode | |
Kim | Alkene Transformations Catalyzed by β-Dialdiminate Cobalt Complexes | |
Barrow et al. | Enhanced substitutional lability of [Fe (CO) 2 {P (OPh) 3} 2 (η 2-PhCCPh)]: facile insertion of CO and organoisocyanides into iron–alkyne bonds | |
Phan | Synthesis and Reactivity of Aluminum (III) Complexes Supported by Non-Innocent Bis (enol) amine and Di (imino) pyridine Ligands | |
Meloni et al. | Exploring the reductive CO 2 fixation with amines and hydrosilanes using readily available Cu (ii) NHC–phenolate catalyst precursors |