ZA200806370B - Transition metal catalysts - Google Patents

Transition metal catalysts

Info

Publication number
ZA200806370B
ZA200806370B ZA200806370A ZA200806370A ZA200806370B ZA 200806370 B ZA200806370 B ZA 200806370B ZA 200806370 A ZA200806370 A ZA 200806370A ZA 200806370 A ZA200806370 A ZA 200806370A ZA 200806370 B ZA200806370 B ZA 200806370B
Authority
ZA
South Africa
Prior art keywords
transition metal
metal catalysts
catalysts
transition
metal
Prior art date
Application number
ZA200806370A
Other languages
English (en)
Inventor
Spitzmesser Stefan Klaus
Elowe Paul Richard
John E Bercaw
Original Assignee
Ineos Europe Ltd
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 Ineos Europe Ltd filed Critical Ineos Europe Ltd
Publication of ZA200806370B publication Critical patent/ZA200806370B/xx

Links

Classifications

    • 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
    • B01J31/1845Catalysts 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 phosphorus
    • B01J31/1875Phosphinites (R2P(OR), their isomeric phosphine oxides (R3P=O) and RO-substitution derivatives thereof)
    • B01J31/188Amide derivatives thereof
    • 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
    • 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
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/02Compositional aspects of complexes used, e.g. polynuclearity
    • B01J2531/0238Complexes comprising multidentate ligands, i.e. more than 2 ionic or coordinative bonds from the central metal to the ligand, the latter having at least two donor atoms, e.g. N, O, S, P
    • B01J2531/0241Rigid ligands, e.g. extended sp2-carbon frameworks or geminal di- or trisubstitution
    • B01J2531/0247Tripodal ligands, e.g. comprising the tris(pyrazolyl)borate skeleton, "tpz", neutral analogues thereof by CH/BH exchange or anionic analogues of the latter by exchange of one of the pyrazolyl groups for an anionic complexing group such as carboxylate or -R-Cp
    • 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
    • B01J2531/60Complexes comprising metals of Group VI (VIA or VIB) as the central metal
    • B01J2531/62Chromium
    • 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
    • Y02P20/582Recycling of unreacted starting or intermediate materials

Landscapes

  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
ZA200806370A 2006-02-03 2008-07-22 Transition metal catalysts ZA200806370B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP06250599 2006-02-03

Publications (1)

Publication Number Publication Date
ZA200806370B true ZA200806370B (en) 2009-10-28

Family

ID=37521239

Family Applications (1)

Application Number Title Priority Date Filing Date
ZA200806370A ZA200806370B (en) 2006-02-03 2008-07-22 Transition metal catalysts

Country Status (7)

Country Link
US (1) US8067654B2 (xx)
EP (1) EP1991353A1 (xx)
CN (2) CN101415494A (xx)
BR (1) BRPI0707407A2 (xx)
CA (1) CA2637703A1 (xx)
WO (1) WO2007088329A1 (xx)
ZA (1) ZA200806370B (xx)

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX2010005266A (es) * 2007-11-28 2010-06-02 Linde Ag Composicion catalizadora y proceso para oligomerizacion de etileno.
CA2639882C (en) * 2008-09-29 2016-07-12 Nova Chemicals Corporation Tetramerization
MY156607A (en) 2009-02-16 2016-03-15 Sasol Tech Pty Ltd Oligomerisation of olefinic compounds in the presence of an activated oligomerisation catalyst
CA2777323C (en) 2009-10-16 2017-07-11 Sasol Technology (Proprietary) Limited Separation of components from a multi-component hydrocarbon stream which includes ethylene
CA2758126C (en) * 2011-11-08 2018-07-31 Nova Chemicals Corporation Ethylene oligomerization process with aluminoxane/organoboron as activators using a halogenated aromatic solvent
ES2750659T3 (es) 2012-05-09 2020-03-26 Sasol Tech Pty Ltd Tetramerización de etileno
SG11201406965UA (en) 2012-05-09 2014-11-27 Sasol Tech Pty Ltd Separation of components from a multi-component hydrocarbon stream
CN104284714B (zh) 2012-05-09 2016-06-29 沙索技术有限公司 用于使烃低聚以形成至少一种共聚单体产物的方法
ES2656088T3 (es) 2012-05-09 2018-02-23 Sasol Technology (Proprietary) Limited Tetramerización de etileno
KR101483248B1 (ko) 2012-11-15 2015-01-16 주식회사 엘지화학 리간드 화합물, 유기크롬 화합물, 에틸렌 올리고머화용 촉매계, 이의 제조 방법 및 이를 이용한 에틸렌 올리고머화 방법
CA2908559C (en) 2013-05-09 2021-08-17 Sasol Technology (Proprietary) Limited Oligomerisation of ethylene to mixtures of 1-hexene and 1-octene
KR20160006192A (ko) 2013-05-09 2016-01-18 사솔 테크날러지 (프로프라이어터리) 리미티드 에틸렌의 1-헥센 및 1-옥텐의 혼합물로의 올리고머화 방법
KR101657259B1 (ko) * 2013-11-19 2016-09-13 주식회사 엘지화학 리간드 화합물, 올레핀 올리고머화용 촉매계, 및 이를 이용한 올레핀 올리고머화 방법
KR101607214B1 (ko) * 2014-06-18 2016-03-29 주식회사 엘지화학 올레핀 올리고머의 제조 방법
WO2015194801A1 (ko) * 2014-06-18 2015-12-23 주식회사 엘지화학 올레핀 올리고머의 제조 방법
KR101757370B1 (ko) 2015-06-01 2017-07-12 주식회사 엘지화학 1-옥텐 조성물
KR101982789B1 (ko) 2015-12-04 2019-05-27 주식회사 엘지화학 리간드 화합물, 유기 크롬 화합물, 올레핀 올리고머화용 촉매 시스템, 및 이를 이용한 올레핀의 올리고머화 방법
CN105693448B (zh) * 2016-03-18 2018-06-19 浙江大学 一种乙烯齐聚的多釜串联工艺
US10414699B2 (en) 2016-05-27 2019-09-17 Chevron Phillips Chemical Company Lp Process improvements in selective ethylene oligomerizations
US10329212B2 (en) 2016-05-27 2019-06-25 Chevron Phillips Chemical Company Lp Reduced polymer formation for selective ethylene oligomerizations
US10414698B2 (en) 2016-05-27 2019-09-17 Chevron Phillips Chemical Company Lp Reduced polymer formation for selective ethylene oligomerizations
US10232339B2 (en) 2017-06-06 2019-03-19 Chevron Phillips Chemical Company Lp Fouling protection for an oligomerization reactor inlet
US10493442B2 (en) 2017-09-22 2019-12-03 Chevron Phillips Chemical Company Lp Fluorinated N2-phosphinyl amidine compounds, chromium salt complexes, catalyst systems, and their use to oligomerize ethylene
US10294171B2 (en) 2017-09-22 2019-05-21 Chevron Phillips Chemical Company Lp Carbonyl-containing perfluorohydrocarbyl-N2-phosphinyl amidine compounds, chromium salt complexes and their use to oligomerize ethylene
US10183960B1 (en) 2017-09-22 2019-01-22 Chevron Phillips Chemical Company Lp Perfluorohydrocarbyl-N2-phosphinyl amidine compounds, chromium salt complexes, catalyst systems, and their use to oligomerize ethylene
US10464862B2 (en) 2017-09-28 2019-11-05 Chevron Phillips Chemical Company Lp Oligomerization reactions using aluminoxanes
US11492305B1 (en) 2021-11-08 2022-11-08 Chevron Phillips Chemical Company, Lp Chromium phosphinyl hydroisoindole amidine complexes for tetramerization of ethylene
US11583843B1 (en) 2021-11-08 2023-02-21 Chevron Phillips Chemical Company, Lp Chromium phosphinyl isoindole amidine complexes for tetramerization of ethylene
US11505513B1 (en) 2021-11-08 2022-11-22 Chevron Phillips Chemical Company, Lp Chromium bicyclic phosphinyl amidine complexes for tetramerization of ethylene
US11623901B1 (en) 2022-08-31 2023-04-11 Saudi Arabian Oil Company Catalyst systems that include silyl ether moieties
US11639321B1 (en) 2022-08-31 2023-05-02 Saudi Arabian Oil Company Catalyst systems that include meta-alkoxy substituted n-aryl bis-diphosphinoamine ligands

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0016895D0 (en) * 2000-07-11 2000-08-30 Bp Chem Int Ltd Olefin oligomerisation
CA2510190C (en) * 2002-12-20 2011-10-11 Sasol Technology (Pty) Limited Trimerisation of olefins
US7525009B2 (en) * 2002-12-20 2009-04-28 Sasol Technology (Pty) Limited Trimerisation of olefins

Also Published As

Publication number Publication date
US8067654B2 (en) 2011-11-29
CA2637703A1 (en) 2007-08-09
EP1991353A1 (en) 2008-11-19
WO2007088329A1 (en) 2007-08-09
BRPI0707407A2 (pt) 2011-05-03
CN104353493A (zh) 2015-02-18
CN101415494A (zh) 2009-04-22
US20070185363A1 (en) 2007-08-09

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