CN105555402B - 复分解催化剂及使用该催化剂的反应 - Google Patents
复分解催化剂及使用该催化剂的反应 Download PDFInfo
- Publication number
- CN105555402B CN105555402B CN201480024618.XA CN201480024618A CN105555402B CN 105555402 B CN105555402 B CN 105555402B CN 201480024618 A CN201480024618 A CN 201480024618A CN 105555402 B CN105555402 B CN 105555402B
- Authority
- CN
- China
- Prior art keywords
- phenyl
- alkyl
- optionally substituted
- group
- compound
- 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.)
- Active
Links
Classifications
-
- 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)
-
- 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
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/12—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
- B01J31/14—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides of aluminium or boron
- B01J31/143—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides of aluminium or boron of aluminium
-
- 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
- B01J31/18—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 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
- B01J31/18—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
- B01J31/181—Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine
-
- 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
- B01J31/2204—Organic complexes the ligands containing oxygen or sulfur as complexing atoms
- B01J31/2208—Oxygen, e.g. acetylacetonates
-
- 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
- B01J31/2204—Organic complexes the ligands containing oxygen or sulfur as complexing atoms
- B01J31/2208—Oxygen, e.g. acetylacetonates
- B01J31/2226—Anionic ligands, i.e. the overall ligand carries at least one formal negative charge
-
- 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
- B01J31/2204—Organic complexes the ligands containing oxygen or sulfur as complexing atoms
- B01J31/2208—Oxygen, e.g. acetylacetonates
- B01J31/2226—Anionic ligands, i.e. the overall ligand carries at least one formal negative charge
- B01J31/223—At least two oxygen atoms present in one at least bidentate or bridging ligand
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/28—Preparation of carboxylic acid esters by modifying the hydroxylic moiety of the ester, such modification not being an introduction of an ester group
- C07C67/293—Preparation of carboxylic acid esters by modifying the hydroxylic moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
- C07C67/333—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
- C07C67/343—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
- C07C67/347—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by addition to unsaturated carbon-to-carbon bonds
-
- 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
- C07F11/00—Compounds containing elements of Groups 6 or 16 of the Periodic Table
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/02—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes
- C08G61/04—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms
- C08G61/06—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms prepared by ring-opening of carbocyclic compounds
- C08G61/08—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms prepared by ring-opening of carbocyclic compounds of carbocyclic compounds containing one or more carbon-to-carbon double bonds in 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
- 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
- B01J2231/543—Metathesis reactions, e.g. olefin metathesis alkene metathesis
-
- 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
- B01J2531/02—Compositional aspects of complexes used, e.g. polynuclearity
- B01J2531/0261—Complexes comprising ligands with non-tetrahedral chirality
- B01J2531/0266—Axially chiral or atropisomeric ligands, e.g. bulky biaryls such as donor-substituted binaphthalenes, e.g. "BINAP" or "BINOL"
-
- 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
- B01J2531/02—Compositional aspects of complexes used, e.g. polynuclearity
- B01J2531/0286—Complexes comprising ligands or other components characterized by their function
- B01J2531/0288—Sterically demanding or shielding ligands
-
- 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
- B01J2531/60—Complexes comprising metals of Group VI (VIA or VIB) as the central metal
- B01J2531/64—Molybdenum
-
- 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
- B01J2531/60—Complexes comprising metals of Group VI (VIA or VIB) as the central metal
- B01J2531/66—Tungsten
-
- 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
-
- 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
-
- 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
- B01J2540/225—Non-coordinating groups comprising halogens comprising fluorine, e.g. trifluoroacetate comprising perfluoroalkyl groups or moieties
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- C07C2531/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- C07C2531/12—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
-
- 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
- C07C2531/22—Organic complexes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
- C07C2601/10—Systems containing only non-condensed rings with a five-membered ring the ring being unsaturated
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/40—Polymerisation processes
- C08G2261/41—Organometallic coupling reactions
- C08G2261/418—Ring opening metathesis polymerisation [ROMP]
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361781120P | 2013-03-14 | 2013-03-14 | |
| EP13001297.4 | 2013-03-14 | ||
| US61/781120 | 2013-03-14 | ||
| EP13001297 | 2013-03-14 | ||
| PCT/EP2014/000671 WO2014139679A2 (en) | 2013-03-14 | 2014-03-13 | Metathesis catalysts and reactions using the catalysts |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN105555402A CN105555402A (zh) | 2016-05-04 |
| CN105555402B true CN105555402B (zh) | 2019-03-22 |
Family
ID=47912849
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201480024618.XA Active CN105555402B (zh) | 2013-03-14 | 2014-03-13 | 复分解催化剂及使用该催化剂的反应 |
Country Status (7)
| Country | Link |
|---|---|
| US (3) | US10343153B2 (cg-RX-API-DMAC7.html) |
| EP (2) | EP3662996A3 (cg-RX-API-DMAC7.html) |
| JP (2) | JP6636804B2 (cg-RX-API-DMAC7.html) |
| CN (1) | CN105555402B (cg-RX-API-DMAC7.html) |
| BR (1) | BR112015023269B8 (cg-RX-API-DMAC7.html) |
| CA (1) | CA2905209C (cg-RX-API-DMAC7.html) |
| WO (1) | WO2014139679A2 (cg-RX-API-DMAC7.html) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8362311B2 (en) | 2009-09-30 | 2013-01-29 | Massachusetts Institute Of Technology | Highly Z-selective olefins metathesis |
| JP6636804B2 (ja) | 2013-03-14 | 2020-01-29 | フェルビオ フェルアイニクテ ビオエネルギー アクチェンゲゼルシャフト | メタセシス触媒及び触媒を用いた反応 |
| US20140330018A1 (en) * | 2013-05-01 | 2014-11-06 | Massachusetts Institute Of Technology | Metathesis catalysts and methods thereof |
| EP3019510B1 (en) | 2013-07-12 | 2020-12-02 | Verbio Vereinigte BioEnergie AG | Use of immobilized molybden- und tungsten-containing catalysts in olefin cross metathesis |
| US10427146B2 (en) | 2013-10-01 | 2019-10-01 | Ximo Ag | Immobilized metathesis tungsten oxo alkylidene catalysts and use thereof in olefin metathesis |
| US9850268B2 (en) * | 2014-11-05 | 2017-12-26 | Trustees Of Boston College | Metathesis catalysts and methods thereof |
| JP6583289B2 (ja) * | 2014-12-26 | 2019-10-02 | Agc株式会社 | 含塩素含フッ素オレフィンの製造方法 |
| WO2016104518A1 (ja) * | 2014-12-26 | 2016-06-30 | 旭硝子株式会社 | オレフィンの製造方法 |
| KR102483724B1 (ko) * | 2015-03-09 | 2022-12-30 | 니폰 제온 가부시키가이샤 | 수지 성형체, 수지 필름, 및 사출 성형품 |
| JP7186502B2 (ja) * | 2015-03-09 | 2022-12-09 | 日本ゼオン株式会社 | 樹脂成形体の製造方法、樹脂フィルムの製造方法、及び射出成形品の製造方法 |
| PL3377465T3 (pl) | 2015-11-18 | 2024-02-12 | Provivi, Inc. | Wytwarzanie pochodnych olefin tłuszczowych przez metatezę olefin |
| BR112018010108A2 (pt) | 2015-11-18 | 2018-11-21 | Provivi Inc | micro-organismos para a produção de ferormônios de inseto e compostos relacionados |
| EP3394074B1 (en) | 2015-12-23 | 2019-10-09 | XiMo AG | Immobilized metal alkylidene catalysts and use thereof in olefin metathesis |
| GB201604110D0 (en) * | 2016-03-10 | 2016-04-20 | Givaudan Sa | Preparation of macrocyclic lactones |
| US11214818B2 (en) | 2016-06-06 | 2022-01-04 | Provivi, Inc. | Semi-biosynthetic production of fatty alcohols and fatty aldehydes |
| US11020730B2 (en) | 2016-07-15 | 2021-06-01 | Massachusetts Institute Of Technology | Halogen-containing metathesis catalysts and methods thereof |
| WO2018150379A2 (en) | 2017-02-17 | 2018-08-23 | Provivi, Inc. | Synthesis of pheromones and related materials via olefin metathesis |
| CN110914442B (zh) | 2017-05-17 | 2025-02-18 | 普罗维维股份有限公司 | 用于产生昆虫信息素及相关化合物的微生物 |
| WO2019060749A1 (en) | 2017-09-22 | 2019-03-28 | Trustees Of Boston College | PROCESS FOR THE PREPARATION OF TRISUBSTITUTED ETHYLENE COMPOUNDS |
| US11702436B2 (en) | 2018-03-22 | 2023-07-18 | Verbio Vereinigte Bioenergie Ag | Tetraphenylphenoxy tungsten oxo alkylidene complexes and methods of making same and use thereof |
| WO2020239859A1 (en) | 2019-05-27 | 2020-12-03 | Verbio Vereinigte Bioenergie Ag | Tungsten imido alkylidene o-bitet and o-binol complexes and use thereof in olefin metathesis reactions |
| US10995049B2 (en) | 2019-07-19 | 2021-05-04 | California Institute Of Technology | Total synthesis of prostaglandin J natural products and their intermediates |
| WO2021188337A1 (en) | 2020-03-19 | 2021-09-23 | Exxonmobil Chemical Patents Inc. | Pentavalent dimeric group 6 transition metal complexes and methods for use thereof |
| JP2023528012A (ja) * | 2020-05-27 | 2023-07-03 | フェルビオ フェルアイニクテ ビオエネルギー アクチェンゲゼルシャフト | 空気中で安定なイミドアルキリデン錯体及びオレフィンメタセシス反応におけるその使用 |
| CN113980097B (zh) * | 2021-12-29 | 2022-03-29 | 浙江湃肽生物有限公司南京分公司 | 棕榈酰三肽-5的纯化方法 |
| CN114230702B (zh) * | 2022-01-17 | 2023-10-13 | 万华化学集团股份有限公司 | 一种萘氧基骨架的烯烃聚合催化剂、制备方法与应用 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20110015430A1 (en) * | 2009-07-15 | 2011-01-20 | Massachusetts Institute Of Technology | Catalysts and processes for the formation of terminal olefins by ethenolysis |
| CN102781888A (zh) * | 2009-09-30 | 2012-11-14 | 麻省理工学院 | 高度z-选择性烯烃复分解 |
| EP2703081A1 (en) * | 2012-09-04 | 2014-03-05 | XiMo AG | Molybdenum and tungsten complexes as olefin metathesis catalysts and reactions using the catalysts |
Family Cites Families (56)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1037866A (en) * | 1962-05-28 | 1966-08-03 | Ethyl Corp | Improved process for preparing alpha olefins of high vinyl olefin content |
| BE755794A (fr) * | 1969-09-08 | 1971-03-08 | Polymer Corp | Procede de purification d'hydrocarbures olefiniques |
| US3689584A (en) * | 1970-08-24 | 1972-09-05 | Ethyl Corp | A chemical process of separating olefins from aluminum alkyls by forming complexes of the aluminum alkyls which are insoluble in the olefins |
| US3696161A (en) * | 1970-09-30 | 1972-10-03 | Ethyl Corp | A chemical process of separating hydrocarbyl aluminum from olefins by the use of 2:1 complexes of aluminum alkyls and an alkali metal salt |
| DE2845974A1 (de) * | 1978-10-21 | 1980-04-30 | Basf Ag | Verfahren zur herstellung von carbonsaeureestern vicinaler glykole |
| IN160358B (cg-RX-API-DMAC7.html) | 1983-01-10 | 1987-07-11 | Thiokol Corp | |
| US4637197A (en) | 1984-10-15 | 1987-01-20 | Epoxy Technology, Inc. | Method and compositions for removal of moisture |
| JPH0428714A (ja) | 1990-05-23 | 1992-01-31 | Nippon Zeon Co Ltd | 高重合活性ジシクロペンタジエンの製造法およびその重合法 |
| US5210365A (en) | 1990-08-27 | 1993-05-11 | Shell Oil Company | Olefin disproportionation catalyst and process |
| US5194534A (en) | 1991-09-24 | 1993-03-16 | Hercules Incorporated | Tungsten-imido catalysts for ring-opening metathesis polymerization of cycloolefins |
| EP0864595B1 (en) | 1997-03-13 | 2001-08-16 | Borealis Technology Oy | Supported catalysts for the ringopening metathesis polymerization of cycloolefins |
| DE19744102A1 (de) * | 1997-10-06 | 1999-04-15 | Targor Gmbh | Katalysatorsystem |
| US6121473A (en) | 1998-02-19 | 2000-09-19 | Massachusetts Institute Of Technology | Asymmetric ring-closing metathesis reactions |
| JP2004500364A (ja) * | 1999-12-21 | 2004-01-08 | サゾル テクノロジー(プロプライアタリー)リミティド | 短鎖オレフィンを長鎖オレフィンに変換するための転換方法 |
| US7411108B2 (en) * | 2000-06-30 | 2008-08-12 | Chevron Phillips Chemical Company Lp | Process for the removal of conjugated olefins from a monoolefin stream |
| US6720468B2 (en) * | 2000-06-30 | 2004-04-13 | Chevron Phillips Chemical Company Lp | Process for the removal of conjugated olefins from a monoolefin stream |
| US20050124839A1 (en) | 2001-06-13 | 2005-06-09 | Gartside Robert J. | Catalyst and process for the metathesis of ethylene and butene to produce propylene |
| EP1501784B1 (en) | 2002-04-29 | 2019-03-13 | Dow Global Technologies LLC | Integrated chemical processes for industrial utilization of seed oils |
| WO2005049672A1 (en) * | 2003-11-14 | 2005-06-02 | Exxonmobil Chemical Patents Inc. | Transparent and translucent crosslinked propylenebased elastomers, and their production and use |
| US7813511B2 (en) | 2005-07-01 | 2010-10-12 | Cisco Technology, Inc. | Facilitating mobility for a mobile station |
| US7932397B2 (en) | 2006-11-22 | 2011-04-26 | Massachusetts Institute Of Technology | Olefin metathesis catalysts and related methods |
| US8642824B2 (en) * | 2007-08-09 | 2014-02-04 | Elevance Renewable Sciences, Inc. | Chemical methods for treating a metathesis feedstock |
| US9284515B2 (en) | 2007-08-09 | 2016-03-15 | Elevance Renewable Sciences, Inc. | Thermal methods for treating a metathesis feedstock |
| MX2010001615A (es) | 2007-08-09 | 2010-04-22 | Elevance Renewable Sciences | Metodos termicos para tratar un material de alimentacion para la metatesis. |
| WO2009094201A2 (en) | 2008-01-25 | 2009-07-30 | Trustees Of Boston College | Catalysts for metathesis reactons including enantioselective olefin metathesis, and related methods |
| JP5483940B2 (ja) | 2009-07-13 | 2014-05-07 | ユニ・チャーム株式会社 | 吸収体及び吸収性物品 |
| US9222056B2 (en) | 2009-10-12 | 2015-12-29 | Elevance Renewable Sciences, Inc. | Methods of refining natural oils, and methods of producing fuel compositions |
| US8735640B2 (en) | 2009-10-12 | 2014-05-27 | Elevance Renewable Sciences, Inc. | Methods of refining and producing fuel and specialty chemicals from natural oil feedstocks |
| JP6224896B2 (ja) | 2009-10-12 | 2017-11-01 | エレバンス・リニューアブル・サイエンシズ,インコーポレーテッド | 天然油供給原料から燃料を精製および製造する方法 |
| US9051519B2 (en) * | 2009-10-12 | 2015-06-09 | Elevance Renewable Sciences, Inc. | Diene-selective hydrogenation of metathesis derived olefins and unsaturated esters |
| JP5557536B2 (ja) | 2010-01-26 | 2014-07-23 | シンポ株式会社 | 油脂回収フィルター |
| EP2534140B1 (en) * | 2010-02-08 | 2018-04-11 | Trustees of Boston College | Efficient methods for z- or cis-selective cross-metathesis |
| US8704029B2 (en) | 2010-03-30 | 2014-04-22 | Uop Llc | Conversion of butylene to propylene under olefin metathesis conditions |
| US8993470B2 (en) | 2010-04-03 | 2015-03-31 | Studiengesellschaft Kohle Mbh | Catalysts for the alkyne metathesis |
| US8722950B2 (en) * | 2010-04-26 | 2014-05-13 | Saudi Basic Industries Corporation | Process for producing propylene and aromatics from butenes by metathesis and aromatization |
| US8935891B2 (en) | 2011-06-09 | 2015-01-20 | Uop Llc | Olefin metathesis catalyst containing tungsten fluorine bonds |
| DE102011012629A1 (de) | 2011-02-28 | 2012-08-30 | Studiengesellschaft Kohle Mbh | Metallkomplexe des Molybdäns und Wolframs und ihre Verwendung als Präkatalysatoren für die Olefinmetathese |
| JP2013014562A (ja) | 2011-07-06 | 2013-01-24 | Nippon Zeon Co Ltd | タングステン錯体、メタセシス反応用触媒および環状オレフィン開環重合体の製造方法 |
| EP2864447B3 (en) | 2012-06-20 | 2019-07-17 | Elevance Renewable Sciences, Inc. | Natural oil metathesis compositions |
| EP2690838A1 (en) | 2012-07-23 | 2014-01-29 | Alcatel Lucent | Authentification system preserving secret data confidentiality |
| KR102202927B1 (ko) | 2013-03-14 | 2021-01-14 | 윌마르 트레이딩 피티이 엘티디 | 처리된 복분해 기질 물질 및 이의 제조 및 사용 방법 |
| WO2014150470A1 (en) | 2013-03-14 | 2014-09-25 | Elevance Renewable Sciences, Inc. | Methods for treating a metathesis feedstock with metal alkoxides |
| JP6636804B2 (ja) | 2013-03-14 | 2020-01-29 | フェルビオ フェルアイニクテ ビオエネルギー アクチェンゲゼルシャフト | メタセシス触媒及び触媒を用いた反応 |
| EP3019510B1 (en) | 2013-07-12 | 2020-12-02 | Verbio Vereinigte BioEnergie AG | Use of immobilized molybden- und tungsten-containing catalysts in olefin cross metathesis |
| WO2015003815A1 (en) | 2013-07-12 | 2015-01-15 | Ximo Ag | Immobilized metathesis tungsten catalysts and use thereof in olefin metathesis |
| US10427146B2 (en) | 2013-10-01 | 2019-10-01 | Ximo Ag | Immobilized metathesis tungsten oxo alkylidene catalysts and use thereof in olefin metathesis |
| WO2015108874A1 (en) | 2014-01-16 | 2015-07-23 | Elevance Renewable Sciences, Inc. | Olefinic ester compositions and their use in oil- and gas-related applications |
| US9328055B2 (en) | 2014-03-19 | 2016-05-03 | Elevance Renewable Sciences, Inc. | Systems and methods of refining natural oil feedstocks and derivatives thereof |
| GB201406591D0 (en) | 2014-04-11 | 2014-05-28 | Ximo Ag | Compounds |
| DE102014105885A1 (de) | 2014-04-25 | 2015-10-29 | Universität Stuttgart | N-Heterozyklische Carbenkomplexe von Metallimidoalkylidenen und Metalloxoalkylidenen und deren Verwendung |
| EP3233274A1 (en) | 2014-12-17 | 2017-10-25 | ETH Zürich | Activation of supported olefin metathesis catalysts by organic reductants |
| US20170011038A1 (en) | 2015-07-06 | 2017-01-12 | David Revelle | System and method for multiple factor sorting and user interface thereof |
| PL3377465T3 (pl) | 2015-11-18 | 2024-02-12 | Provivi, Inc. | Wytwarzanie pochodnych olefin tłuszczowych przez metatezę olefin |
| DE102016122096A1 (de) | 2016-11-17 | 2018-05-17 | Universität Stuttgart | Latente Katalysatoren zur vernetzenden Polymerisation von Dicyclopentadien (DCPD) |
| DE102017101431A1 (de) | 2017-01-25 | 2018-07-26 | Universität Stuttgart | Molybdän- und Wolfram-Alkylidin-N-heterozyklische Carben-Komplexe |
| WO2018150379A2 (en) | 2017-02-17 | 2018-08-23 | Provivi, Inc. | Synthesis of pheromones and related materials via olefin metathesis |
-
2014
- 2014-03-13 JP JP2015561980A patent/JP6636804B2/ja active Active
- 2014-03-13 EP EP19210969.2A patent/EP3662996A3/en not_active Withdrawn
- 2014-03-13 BR BR112015023269A patent/BR112015023269B8/pt active IP Right Grant
- 2014-03-13 US US14/209,313 patent/US10343153B2/en active Active
- 2014-03-13 EP EP14710501.9A patent/EP2969204A2/en not_active Withdrawn
- 2014-03-13 WO PCT/EP2014/000671 patent/WO2014139679A2/en not_active Ceased
- 2014-03-13 CN CN201480024618.XA patent/CN105555402B/zh active Active
- 2014-03-13 CA CA2905209A patent/CA2905209C/en active Active
- 2014-03-13 US US14/774,404 patent/US9919299B2/en active Active
-
2018
- 2018-07-12 JP JP2018132278A patent/JP2018193379A/ja not_active Withdrawn
-
2019
- 2019-06-12 US US16/439,512 patent/US11285466B2/en active Active
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20110015430A1 (en) * | 2009-07-15 | 2011-01-20 | Massachusetts Institute Of Technology | Catalysts and processes for the formation of terminal olefins by ethenolysis |
| CN102781888A (zh) * | 2009-09-30 | 2012-11-14 | 麻省理工学院 | 高度z-选择性烯烃复分解 |
| EP2703081A1 (en) * | 2012-09-04 | 2014-03-05 | XiMo AG | Molybdenum and tungsten complexes as olefin metathesis catalysts and reactions using the catalysts |
Also Published As
| Publication number | Publication date |
|---|---|
| US20160030936A1 (en) | 2016-02-04 |
| BR112015023269B8 (pt) | 2022-08-16 |
| JP6636804B2 (ja) | 2020-01-29 |
| CA2905209A1 (en) | 2014-09-18 |
| CN105555402A (zh) | 2016-05-04 |
| CA2905209C (en) | 2021-11-09 |
| US9919299B2 (en) | 2018-03-20 |
| EP3662996A2 (en) | 2020-06-10 |
| WO2014139679A3 (en) | 2015-02-19 |
| BR112015023269A2 (pt) | 2017-07-18 |
| US20140309466A1 (en) | 2014-10-16 |
| WO2014139679A2 (en) | 2014-09-18 |
| JP2018193379A (ja) | 2018-12-06 |
| JP2016510070A (ja) | 2016-04-04 |
| EP2969204A2 (en) | 2016-01-20 |
| US11285466B2 (en) | 2022-03-29 |
| WO2014139679A8 (en) | 2014-12-11 |
| BR112015023269B1 (pt) | 2021-05-04 |
| US10343153B2 (en) | 2019-07-09 |
| US20190366318A1 (en) | 2019-12-05 |
| EP3662996A3 (en) | 2020-12-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN105555402B (zh) | 复分解催化剂及使用该催化剂的反应 | |
| CN102781888B (zh) | 高度z-选择性烯烃复分解 | |
| US9328132B2 (en) | Ruthenium complexes, their use in the metathesis reactions, and a process for carrying out the metathesis reaction | |
| EP3019510B1 (en) | Use of immobilized molybden- und tungsten-containing catalysts in olefin cross metathesis | |
| Dash et al. | Diverse catalytic activity of the cationic actinide complex [(Et2N) 3U][BPh4] in the dimerization and hydrosilylation of terminal alkynes. Characterization of the first f-element alkyne π-complex [(Et2N) 2U (C CtBu)(η2-HC CtBu)][BPh4] | |
| Neves et al. | Heterogeneous oxidation catalysts formed in situ from molybdenum tetracarbonyl complexes and tert-butyl hydroperoxide | |
| JP6617264B2 (ja) | 単核鉄錯体およびそれを使用した有機合成反応 | |
| JPH11315087A (ja) | 酸化レニウムの有機誘導体 | |
| Hsu et al. | Chiral Bis (oxazoline) Ligand‐Supported Alkyl Aluminum Cations | |
| WO2014128717A2 (en) | A process for dehydrogenating alkane to alkadiene | |
| EP3394074B1 (en) | Immobilized metal alkylidene catalysts and use thereof in olefin metathesis | |
| Tkach et al. | Palladium carboxylate/boron trifluoride etherate catalyst system for the selective dimerization of styrene | |
| CN110156837A (zh) | 用于烷氧羰基化的丙基桥联的二膦配体 | |
| Kroke et al. | Silicon compounds with strong intramolecular steric interactions. 58. Reactions of a disilene and a silylene with cyclopentadiene, furan, and thiophene:[2+ 4]-Cycloadditions versus chalcogen abstraction | |
| Tekavec | The development of nickel catalyzed [2+ 2+ 2] cycloadditions and cycloisomerizations |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant | ||
| TR01 | Transfer of patent right | ||
| TR01 | Transfer of patent right |
Effective date of registration: 20190920 Address after: leipzig germany Patentee after: Welbio Joint Bioenergy Co.Ltd. Address before: Luzern, Switzerland Patentee before: XIMO AG |
|
| CP02 | Change in the address of a patent holder | ||
| CP02 | Change in the address of a patent holder |
Address after: Zerbich, Germany Patentee after: Welbio Joint Bioenergy Co.Ltd. Address before: leipzig germany Patentee before: Welbio Joint Bioenergy Co.Ltd. |