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1. WO1999006146 - SUPPORTED DIOLS AND SUPPORTED BIS(PHOSPHORUS) LIGANDS

Publication Number WO/1999/006146
Publication Date 11.02.1999
International Application No. PCT/US1998/015199
International Filing Date 23.07.1998
Chapter 2 Demand Filed 18.12.1998
IPC
B01J 31/02 2006.1
BPERFORMING OPERATIONS; TRANSPORTING
01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
31Catalysts comprising hydrides, coordination complexes or organic compounds
02containing organic compounds or metal hydrides
B01J 31/16 2006.1
BPERFORMING OPERATIONS; TRANSPORTING
01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
31Catalysts comprising hydrides, coordination complexes or organic compounds
16containing coordination complexes
B01J 31/18 2006.1
BPERFORMING OPERATIONS; TRANSPORTING
01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
31Catalysts comprising hydrides, coordination complexes or organic compounds
16containing coordination complexes
18containing nitrogen, phosphorus, arsenic or antimony
C07C 5/03 2006.1
CCHEMISTRY; METALLURGY
07ORGANIC CHEMISTRY
CACYCLIC OR CARBOCYCLIC COMPOUNDS
5Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
02by hydrogenation
03of non-aromatic carbon-to-carbon double bonds
C07C 253/10 2006.1
CCHEMISTRY; METALLURGY
07ORGANIC CHEMISTRY
CACYCLIC OR CARBOCYCLIC COMPOUNDS
253Preparation of carboxylic acid nitriles
08by addition of hydrogen cyanide or salts thereof to unsaturated compounds
10to compounds containing carbon-to-carbon double bonds
C07C 255/04 2006.1
CCHEMISTRY; METALLURGY
07ORGANIC CHEMISTRY
CACYCLIC OR CARBOCYCLIC COMPOUNDS
255Carboxylic acid nitriles
01having cyano groups bound to acyclic carbon atoms
02of an acyclic and saturated carbon skeleton
04containing two cyano groups bound to the carbon skeleton
CPC
B01J 2231/32
BPERFORMING OPERATIONS; TRANSPORTING
01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
2231Catalytic reactions performed with catalysts classified in B01J31/00
30Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
32Addition reactions to C=C or C-C triple bonds
B01J 2231/321
BPERFORMING OPERATIONS; TRANSPORTING
01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
2231Catalytic reactions performed with catalysts classified in B01J31/00
30Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
32Addition reactions to C=C or C-C triple bonds
321Hydroformylation, metalformylation, carbonylation or hydroaminomethylation
B01J 2231/323
BPERFORMING OPERATIONS; TRANSPORTING
01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
2231Catalytic reactions performed with catalysts classified in B01J31/00
30Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
32Addition reactions to C=C or C-C triple bonds
323Hydrometalation, e.g. bor-, alumin-, silyl-, zirconation or analoguous reactions like carbometalation, hydrocarbation
B01J 2231/641
BPERFORMING OPERATIONS; TRANSPORTING
01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
2231Catalytic reactions performed with catalysts classified in B01J31/00
60Reduction reactions, e.g. hydrogenation
64Reductions in general of organic substrates, e.g. hydride reductions or hydrogenations
641Hydrogenation of organic substrates, i.e. H2 or H-transfer hydrogenations, e.g. Fischer-Tropsch processes
B01J 2231/645
BPERFORMING OPERATIONS; TRANSPORTING
01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
2231Catalytic reactions performed with catalysts classified in B01J31/00
60Reduction reactions, e.g. hydrogenation
64Reductions in general of organic substrates, e.g. hydride reductions or hydrogenations
641Hydrogenation of organic substrates, i.e. H2 or H-transfer hydrogenations, e.g. Fischer-Tropsch processes
645of C=C or C-C triple bonds
B01J 2531/821
BPERFORMING OPERATIONS; TRANSPORTING
01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
2531Additional information regarding catalytic systems classified in B01J31/00
80Complexes comprising metals of Group VIII as the central metal
82Metals of the platinum group
821Ruthenium
Applicants
  • E.I. DU PONT DE NEMOURS AND COMPANY [US]/[US]
Inventors
  • DRULINER, Joseph, D.
  • MOLOY, Kenneth, Gene
  • WANG, Manxue
Agents
  • SIEGELL, Barbara, C.
Priority Data
60/054,00329.07.1997US
Publication Language English (en)
Filing Language English (EN)
Designated States
Title
(EN) SUPPORTED DIOLS AND SUPPORTED BIS(PHOSPHORUS) LIGANDS
(FR) DIOLS SUR SUPPORT ET LIGANDS BIS(PHOSPHORE) SUR SUPPORT
Abstract
(EN) Supported bis(phosphorus) ligands are disclosed for use in a variety of catalytic processes, including the hydrocyanation of unsaturated organic compounds. Catalysts are formed when the ligands are combined with a catalytically active metal (e.g., nickel). Furthermore, supported diols are disclosed, said diols being based on a binaphthal, 2-naphthal or 2,4-dimethylphenol structure.
(FR) L'invention concerne des ligands bis(phosphore) sur support, utiles dans divers processus catalytiques, notamment dans la cyanhydratation de composés organiques insaturés. On forme des catalyseurs en combinant des ligands à un métal actif sur le plan catalytique (par exemple du nickel). En outre, l'invention concerne des diols sur support, à base d'une structure binaphtol, 2-naphtol ou 2,4-diméthylphenol.
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