GB1236616A - Metal catalytised reactions - Google Patents

Metal catalytised reactions

Info

Publication number
GB1236616A
GB1236616A GB45772/68A GB4577268A GB1236616A GB 1236616 A GB1236616 A GB 1236616A GB 45772/68 A GB45772/68 A GB 45772/68A GB 4577268 A GB4577268 A GB 4577268A GB 1236616 A GB1236616 A GB 1236616A
Authority
GB
United Kingdom
Prior art keywords
metal
resin
catalyst
reactions
reacting
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB45772/68A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ExxonMobil Oil Corp
Original Assignee
Mobil Oil Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Mobil Oil Corp filed Critical Mobil Oil Corp
Publication of GB1236616A publication Critical patent/GB1236616A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/49Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide
    • C07C45/50Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide by oxo-reactions
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/06Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing polymers
    • B01J31/08Ion-exchange resins
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/165Polymer immobilised coordination complexes, e.g. organometallic complexes
    • B01J31/1658Polymer immobilised coordination complexes, e.g. organometallic complexes immobilised by covalent linkages, i.e. pendant complexes with optional linking groups, e.g. on Wang or Merrifield resins
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/18Catalysts 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
    • B01J31/1805Catalysts 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/40Regeneration or reactivation
    • B01J31/4015Regeneration or reactivation of catalysts containing metals
    • B01J31/4023Regeneration or reactivation of catalysts containing metals containing iron group metals, noble metals or copper
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/27Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/32Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
    • C07C45/33Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties
    • C07C45/34Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties in unsaturated compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/20Olefin oligomerisation or telomerisation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/30Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
    • B01J2231/32Addition reactions to C=C or C-C triple bonds
    • B01J2231/321Hydroformylation, metalformylation, carbonylation or hydroaminomethylation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/50Redistribution or isomerisation reactions of C-C, C=C or C-C triple bonds
    • B01J2231/52Isomerisation reactions
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/60Reduction reactions, e.g. hydrogenation
    • B01J2231/64Reductions in general of organic substrates, e.g. hydride reductions or hydrogenations
    • B01J2231/641Hydrogenation of organic substrates, i.e. H2 or H-transfer hydrogenations, e.g. Fischer-Tropsch processes
    • B01J2231/645Hydrogenation of organic substrates, i.e. H2 or H-transfer hydrogenations, e.g. Fischer-Tropsch processes of C=C or C-C triple bonds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/70Oxidation reactions, e.g. epoxidation, (di)hydroxylation, dehydrogenation and analogues
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82Metals of the platinum group
    • B01J2531/824Palladium
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/584Recycling of catalysts

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

1,236,616. Resin-metal catalysts. MOBIL OIL CORP. 26 Sept., 1968 [2 Oct., 1967], No. 45772/68. Heading B1E. Catalysts having an unusual degree of selectivity for hydrogenation and other reactions are prepared by reacting an ion-exchange resin in particulate form with a solution of a metal compound to form a resin-metal complex in which the metal moiety is chemically bonded to the resin, e.g. by ionic or coordinate bonds, and reacting the complex with a reducing agent to reduce the metal to a state of lower valency. The metal may be Cu, Ag, Au, Zn, Cd, Hg, Sc, Y, La, Ac, Ti, Zr, Hf, V, Nb, Ta, Cr, Mo, W, Mn, Re, Fe, Co, Ni, Ru, Rh, Pd, Pt, Os and Ir and is preferably reduced to zero-valent state. After the reduction of the metal the catalyst may be treated with a regenerating agent to regenerate the functional groups of the catalyst. These catalyst can be used in reactions involving hydrogenation, carbonylation, or formylation of unsaturated compounds.
GB45772/68A 1967-10-02 1968-09-26 Metal catalytised reactions Expired GB1236616A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US67201167A 1967-10-02 1967-10-02

Publications (1)

Publication Number Publication Date
GB1236616A true GB1236616A (en) 1971-06-23

Family

ID=24696791

Family Applications (1)

Application Number Title Priority Date Filing Date
GB45772/68A Expired GB1236616A (en) 1967-10-02 1968-09-26 Metal catalytised reactions

Country Status (7)

Country Link
JP (1) JPS4810441B1 (en)
BE (1) BE721687A (en)
CH (1) CH507740A (en)
DE (1) DE1800380A1 (en)
FR (1) FR1583594A (en)
GB (1) GB1236616A (en)
NL (1) NL6814000A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1593668A1 (en) * 2003-02-14 2005-11-09 Wako Pure Chemical Industries, Ltd. Method for producing hydroxylamine compound using platinum catalyst fixed on ion exchange resin
EP2230012A1 (en) 2009-03-13 2010-09-22 Industrial Technology Research Institute Catalyst for catalyzing hydrogen releasing reaction and manufacturing method thereof
US8466242B2 (en) 2011-02-28 2013-06-18 Midori Renewables, Inc. Polymeric acid catalysts and uses thereof
US9238845B2 (en) 2012-08-24 2016-01-19 Midori Usa, Inc. Methods of producing sugars from biomass feedstocks
CN114471568A (en) * 2022-01-14 2022-05-13 西安建筑科技大学 Monoatomic cobalt catalyst and gram-level preparation method and application thereof

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3026504A1 (en) * 1980-07-12 1982-02-04 EC Erdölchemie GmbH, 5000 Köln METHOD FOR PRODUCING ALKYLTERT.-ALKYLETHERS
DE3036481A1 (en) * 1980-09-27 1982-05-19 EC Erdölchemie GmbH, 5000 Köln METHOD FOR THE SIMULTANEOUS PRODUCTION OF C 4-OLIGOMERS AND ALKYL-TERT.-BUTYL ETHERS
FR2556238B1 (en) * 1983-12-12 1987-10-23 Commissariat Energie Atomique MATERIAL COMPRISING MICROAGGREGATES OF INORGANIC OR ORGANOMETALLIC COMPOUNDS, IN PARTICULAR FOR USE IN HETEROGENEOUS CATALYSIS AND METHOD FOR THE PRODUCTION THEREOF
DE3626581A1 (en) * 1986-08-06 1988-02-11 Bayer Ag CATALYST RESIN AND METHOD FOR THE PRODUCTION THEREOF

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1593668A1 (en) * 2003-02-14 2005-11-09 Wako Pure Chemical Industries, Ltd. Method for producing hydroxylamine compound using platinum catalyst fixed on ion exchange resin
EP1593668A4 (en) * 2003-02-14 2007-07-11 Wako Pure Chem Ind Ltd Method for producing hydroxylamine compound using platinum catalyst fixed on ion exchange resin
EP2230012A1 (en) 2009-03-13 2010-09-22 Industrial Technology Research Institute Catalyst for catalyzing hydrogen releasing reaction and manufacturing method thereof
US8466242B2 (en) 2011-02-28 2013-06-18 Midori Renewables, Inc. Polymeric acid catalysts and uses thereof
US8476388B2 (en) 2011-02-28 2013-07-02 Midori Renewables, Inc. Polymeric acid catalysts and uses thereof
US9079171B2 (en) 2011-02-28 2015-07-14 Midori Usa, Inc. Polymeric acid catalysts and uses thereof
US9205418B2 (en) 2011-02-28 2015-12-08 Midori Usa, Inc. Polymeric acid catalysts and uses thereof
US10131721B2 (en) 2011-02-28 2018-11-20 Cadena Bio, Inc. Polymeric acid catalysts and uses thereof
US10787527B2 (en) 2011-02-28 2020-09-29 Cadena Bio, Inc. Polymeric acid catalysts and uses thereof
US9238845B2 (en) 2012-08-24 2016-01-19 Midori Usa, Inc. Methods of producing sugars from biomass feedstocks
CN114471568A (en) * 2022-01-14 2022-05-13 西安建筑科技大学 Monoatomic cobalt catalyst and gram-level preparation method and application thereof

Also Published As

Publication number Publication date
NL6814000A (en) 1969-04-08
DE1800380B2 (en) 1978-03-09
JPS4810441B1 (en) 1973-04-03
CH507740A (en) 1971-05-31
BE721687A (en) 1969-04-01
DE1800380A1 (en) 1969-05-08
FR1583594A (en) 1969-11-14

Similar Documents

Publication Publication Date Title
GB1236616A (en) Metal catalytised reactions
CA2139356A1 (en) Transition Metal Olefin Polymerization Catalysts
GB988941A (en) Process for the preparation of aldehydes and/or alcohols
WO2002000339A3 (en) Ligands and catalyst systems thereof for ethylene oligomerisation to linear alpha olefins
US3907705A (en) Catalyst for hydrogenation of organic compounds
GB1456369A (en) Catalyst preparation
KR100251076B1 (en) Process of preparation of alcohol through hydrofication of carbonylic compounds
CA1194502A (en) Process for hydroxylating olefins using a supported osmium catalyst
Tang et al. Heterogenization of homogeneous catalysts—The immobilization of transition metal complexes on ion-exchange resins
GB1517662A (en) Photochemical preparation of catalysts for addition reactions of olefines
GB1531958A (en) Catalyst regeneration
GB1185453A (en) Multiphase Catalysis.
ES8102842A1 (en) Hydroformylation catalyst system and processes
Dobson et al. Carboxylato complexes of the platinum group metals
GB1238703A (en)
US3794598A (en) Catalyst preparation method
GB1307962A (en) Regeneration of nickel-aluminum catalysts
Tsuji et al. Organic Syntheses by Means of Noble Metal Compounds. XIX. The Hydroformylation Reaction Catalyzed by Metallic Palladium.
NL167944C (en) PROCESS FOR THE CATALYTIC HYDROGENATION OF OLEFINES ALKYN COMPOUNDS IN PRESENCE OF A TITANIC DICYCLOPENTADIENYL CARBONYL COMPOUND AND FORMED CATALYST FOR THIS HYDROGENATION.
GB1318881A (en) Hydroformylation process
BRUCE et al. NEW ORGANOMETALLIC CHEMISTRY OF COPPER
CH437264A (en) Process for the preparation of monooxation products of the cyclic di- and trimers of butadiene- (1,3)
GB1335285A (en) Method for reactivating deactivated catalysts containing pla tinum and lead
ES8506561A1 (en) Process for upgrading synthesis gas and catalysts therefor.
Levin THE EFFECTS OF METAL OXIDE PROMOTION ON THE ADSORPTIVE AND CATALYTIC PROPERTIES OF RHODIUM.