WO2006018161A3 - Am zentralatom substituierte, immobilisierbare ruthenium(ii)-katalysatoren, verfahren zu deren herstellung und verwendung - Google Patents
Am zentralatom substituierte, immobilisierbare ruthenium(ii)-katalysatoren, verfahren zu deren herstellung und verwendung Download PDFInfo
- Publication number
- WO2006018161A3 WO2006018161A3 PCT/EP2005/008526 EP2005008526W WO2006018161A3 WO 2006018161 A3 WO2006018161 A3 WO 2006018161A3 EP 2005008526 W EP2005008526 W EP 2005008526W WO 2006018161 A3 WO2006018161 A3 WO 2006018161A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- catalysts
- metathesis
- ruthenium
- production
- immobilizable
- Prior art date
Links
- 239000003054 catalyst Substances 0.000 title abstract 6
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 title abstract 3
- 238000004519 manufacturing process Methods 0.000 title abstract 3
- 238000000034 method Methods 0.000 title abstract 3
- 229910052707 ruthenium Inorganic materials 0.000 title abstract 3
- 238000007152 ring opening metathesis polymerisation reaction Methods 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 3
- 238000010535 acyclic diene metathesis reaction Methods 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 2
- 238000005686 cross metathesis reaction Methods 0.000 abstract 2
- 238000006798 ring closing metathesis reaction Methods 0.000 abstract 2
- 150000001336 alkenes Chemical class 0.000 abstract 1
- 150000001450 anions Chemical class 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 239000000969 carrier Substances 0.000 abstract 1
- 238000005859 coupling reaction Methods 0.000 abstract 1
- 238000007037 hydroformylation reaction Methods 0.000 abstract 1
- 238000005984 hydrogenation reaction Methods 0.000 abstract 1
- 229910052809 inorganic oxide Inorganic materials 0.000 abstract 1
- 238000006317 isomerization reaction Methods 0.000 abstract 1
- 238000005649 metathesis reaction Methods 0.000 abstract 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 abstract 1
- 238000006884 silylation reaction Methods 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C6/00—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions
- C07C6/02—Metathesis reactions at an unsaturated carbon-to-carbon bond
- C07C6/04—Metathesis reactions at an unsaturated carbon-to-carbon bond at a carbon-to-carbon double bond
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR 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
- B01J31/1608—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes the ligands containing silicon
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR 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
- B01J31/1616—Coordination complexes, e.g. organometallic complexes, immobilised on an inorganic support, e.g. ship-in-a-bottle type catalysts
- B01J31/1625—Coordination complexes, e.g. organometallic complexes, immobilised on an inorganic support, e.g. ship-in-a-bottle type catalysts immobilised by covalent linkages, i.e. pendant complexes with optional linking groups
- B01J31/1633—Coordination complexes, e.g. organometallic complexes, immobilised on an inorganic support, e.g. ship-in-a-bottle type catalysts immobilised by covalent linkages, i.e. pendant complexes with optional linking groups covalent linkages via silicon containing groups
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR 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
- B01J31/2265—Carbenes or carbynes, i.e.(image)
- B01J31/2269—Heterocyclic carbenes
- B01J31/2273—Heterocyclic carbenes with only nitrogen as heteroatomic ring members, e.g. 1,3-diarylimidazoline-2-ylidenes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR 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 e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
- B01J31/2404—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/0201—Impregnation
- B01J37/0209—Impregnation involving a reaction between the support and a fluid
-
- 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 Table
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
- C07F15/0046—Ruthenium compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/30—Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
- B01J2231/32—Addition reactions to C=C or C-C triple bonds
- B01J2231/321—Hydroformylation, metalformylation, carbonylation or hydroaminomethylation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/30—Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
- B01J2231/32—Addition reactions to C=C or C-C triple bonds
- B01J2231/323—Hydrometalation, e.g. bor-, alumin-, silyl-, zirconation or analoguous reactions like carbometalation, hydrocarbation
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/50—Redistribution or isomerisation reactions of C-C, C=C or C-C triple bonds
- B01J2231/52—Isomerisation reactions
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/50—Redistribution or isomerisation reactions of C-C, C=C or C-C triple bonds
- B01J2231/54—Metathesis reactions, e.g. olefin metathesis
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR 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
- B01J2531/821—Ruthenium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2540/00—Compositional aspects of coordination complexes or ligands in catalyst systems
- B01J2540/20—Non-coordinating groups comprising halogens
- B01J2540/22—Non-coordinating groups comprising halogens comprising fluorine, e.g. trifluoroacetate
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- C07C2531/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
Abstract
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102004039277A DE102004039277A1 (de) | 2004-08-13 | 2004-08-13 | Am Zentralatom substituierte, immoblisierbare Ruthenium(II)-Katalysatoren, Verfahren zu deren Herstellung und Verwendung |
DE102004039277.3 | 2004-08-13 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2006018161A2 WO2006018161A2 (de) | 2006-02-23 |
WO2006018161A3 true WO2006018161A3 (de) | 2006-07-13 |
Family
ID=35721351
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2005/008526 WO2006018161A2 (de) | 2004-08-13 | 2005-08-05 | Am zentralatom substituierte, immobilisierbare ruthenium(ii)-katalysatoren, verfahren zu deren herstellung und verwendung |
Country Status (2)
Country | Link |
---|---|
DE (1) | DE102004039277A1 (de) |
WO (1) | WO2006018161A2 (de) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2904243B1 (fr) * | 2006-07-31 | 2008-10-31 | Inst Francais Du Petrole | Catalyseur a base d'un support hybride organique - inorganique et son utilisation en hydroraffinage et hydroconversion |
WO2008031889A2 (de) * | 2006-09-15 | 2008-03-20 | Basf Se | Pnicogenhaltige pseudochelatliganden |
EP2082804B1 (de) * | 2008-01-25 | 2012-10-03 | Universite Claude Bernard Lyon 1 | Organisch-anorganische Hybridmaterialien mit stabilisiertem Carben |
US20120289617A1 (en) * | 2011-05-10 | 2012-11-15 | Saudi Arabian Oil Company | Hybrid Catalyst for Olefin Metathesis |
CN102351907B (zh) * | 2011-08-22 | 2014-07-09 | 浙江大学 | 一种合成金属氮杂环卡宾配合物的方法 |
US9828347B2 (en) | 2014-10-09 | 2017-11-28 | The United States Of America As Represented By The Secretary Of The Air Force | Backfunctionalized imidazolinium salts and NHC carbene-metal complexes |
US11094997B2 (en) | 2017-05-29 | 2021-08-17 | Sumitomo Chemical Company, Limited | Nonaqueous electrolyte secondary battery |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003062253A1 (en) * | 2002-01-22 | 2003-07-31 | Universiteit Gent | Metal complexes for use in metathesis |
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2004
- 2004-08-13 DE DE102004039277A patent/DE102004039277A1/de not_active Withdrawn
-
2005
- 2005-08-05 WO PCT/EP2005/008526 patent/WO2006018161A2/de active Application Filing
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003062253A1 (en) * | 2002-01-22 | 2003-07-31 | Universiteit Gent | Metal complexes for use in metathesis |
Non-Patent Citations (10)
Title |
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ASTRUC D: "The metathesis reactions: from a historical perspective to recent developments", NEW JOURNAL OF CHEMISTRY, vol. 29, no. 1, 21 December 2004 (2004-12-21), XP002372866 * |
BUCHMEISER M R ET AL: "Ring-opening metathesis polymerization for the preparation of surface-grafted polymer supports", MACROMOLECULES, ACS, WASHINGTON, DC, US, vol. 33, 2000, pages 32 - 39, XP002324916, ISSN: 0024-9297 * |
BUCHMEISER M R: "Recent advances in the synthesis of supported metathesis catalysts", NEW JOURNAL OF CHEMISTRY, vol. 28, no. 5, 8 April 2004 (2004-04-08), pages 549 - 557, XP002372864 * |
CLERCQ B D ET AL: "Immobilization of multifunctional Schiff base containing ruthenium complexes on MCM-41", APPLIED CATALYSIS A: GENERAL, ELSEVIER SCIENCE, AMSTERDAM, NL, vol. 247, no. 2, 25 July 2003 (2003-07-25), pages 345 - 364, XP004440496, ISSN: 0926-860X * |
DROZDZAK ET AL: "Ruthenium complexes bearing bidentate Schiff base ligands as efficient catalysts for organic and polymer syntheses", COORDINATION CHEMISTRY REVIEWS, ELSEVIER SCIENCE, AMSTERDAM, NL, vol. 249, no. 24, 6 June 2005 (2005-06-06), pages 3055 - 3074, XP005174429, ISSN: 0010-8545 * |
FUERSTNER A: "OLEFIN METATHESIS AND BEYOND", ANGEWANDTE CHEMIE. INTERNATIONAL EDITION, WILEY VCH VERLAG, WEINHEIM, DE, vol. 39, 2000, pages 3012 - 3043, XP002957487, ISSN: 1433-7851 * |
GESSLER S ET AL: "Synthesis and metathesis reactions of a phosphine-free dihydroimidazole carbene ruthenium complex", TETRAHEDRON LETTERS, ELSEVIER, AMSTERDAM, NL, vol. 41, no. 51, 16 December 2000 (2000-12-16), pages 9973 - 9976, XP004225200, ISSN: 0040-4039 * |
HARRITY ET AL: "Chromenes through Metal-Catalyzed Reactions of Styrenyl Ethers. Mechanism and Utility in Synthesis", JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, AMERICAN CHEMICAL SOCIETY, WASHINGTON, DC, US, vol. 120, 18 March 1998 (1998-03-18), pages 2343 - 2351, XP002083201, ISSN: 0002-7863 * |
KINGSBURY J S ET AL: "A RECYCLABLE RU-BASED METATHESIS CATALYST", JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, AMERICAN CHEMICAL SOCIETY, WASHINGTON, DC, US, vol. 121, no. 4, 3 February 1999 (1999-02-03), pages 791 - 799, XP002906691, ISSN: 0002-7863 * |
KRAUSE J O ET AL: "Monolith- and Silica-Supported Carboxylate-Based Grubbs-Herrmann-Type Metathesis Catalysts", ADVANCED SYNTHESIS & CATALYSIS, vol. 345, no. 8, 7 August 2003 (2003-08-07), pages 996 - 1004, XP002372865 * |
Also Published As
Publication number | Publication date |
---|---|
DE102004039277A1 (de) | 2006-02-23 |
WO2006018161A2 (de) | 2006-02-23 |
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