AU2007350983A1 - Hydrogen splitting composition - Google Patents

Hydrogen splitting composition Download PDF

Info

Publication number
AU2007350983A1
AU2007350983A1 AU2007350983A AU2007350983A AU2007350983A1 AU 2007350983 A1 AU2007350983 A1 AU 2007350983A1 AU 2007350983 A AU2007350983 A AU 2007350983A AU 2007350983 A AU2007350983 A AU 2007350983A AU 2007350983 A1 AU2007350983 A1 AU 2007350983A1
Authority
AU
Australia
Prior art keywords
aryl
alkyl
compound
cycloalkyl
forms
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.)
Abandoned
Application number
AU2007350983A
Other languages
English (en)
Other versions
AU2007350983A8 (en
Inventor
Preston A. Chase
Douglas W. Stephan
Gregory C. Welch
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.)
Stephan Consulting Corp
Original Assignee
Stephan Consulting 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 Stephan Consulting Corp filed Critical Stephan Consulting Corp
Publication of AU2007350983A1 publication Critical patent/AU2007350983A1/en
Publication of AU2007350983A8 publication Critical patent/AU2007350983A8/en
Abandoned legal-status Critical Current

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
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0272—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing elements other than those covered by B01J31/0201 - B01J31/0255
    • 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
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/28—Phosphorus compounds with one or more P—C bonds
    • C07F9/50—Organo-phosphines
    • 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
    • B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/14—Phosphorus; Compounds thereof
    • B01J27/16—Phosphorus; Compounds thereof containing oxygen, i.e. acids, anhydrides and their derivates with N, S, B or halogens without carriers or on carriers based on C, Si, Al or Zr; also salts of Si, Al and Zr
    • B01J27/18—Phosphorus; Compounds thereof containing oxygen, i.e. acids, anhydrides and their derivates with N, S, B or halogens without carriers or on carriers based on C, Si, Al or Zr; also salts of Si, Al and Zr with metals other than Al or Zr
    • 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
    • B01J31/0234—Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
    • B01J31/0255—Phosphorus containing compounds
    • B01J31/0267—Phosphines or phosphonium compounds, i.e. phosphorus bonded to at least one carbon atom, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, the other atoms bonded to phosphorus being either carbon or hydrogen
    • 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
    • B01J31/0272—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing elements other than those covered by B01J31/0201 - B01J31/0255
    • B01J31/0275—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing elements other than those covered by B01J31/0201 - B01J31/0255 also containing elements or functional groups covered by B01J31/0201 - B01J31/0269
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B31/00—Reduction in general
    • 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
    • C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
    • C07F5/02—Boron compounds
    • 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
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/28—Phosphorus compounds with one or more P—C bonds
    • C07F9/50—Organo-phosphines
    • C07F9/5022—Aromatic phosphines (P-C aromatic linkage)

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Molecular Biology (AREA)
  • General Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Hydrogen, Water And Hydrids (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
AU2007350983A 2006-11-14 2007-11-14 Hydrogen splitting composition Abandoned AU2007350983A1 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US86568406P 2006-11-14 2006-11-14
US60/865,684 2006-11-14
US89655707P 2007-03-23 2007-03-23
US60/896,557 2007-03-23
PCT/IB2007/004577 WO2008125911A2 (en) 2006-11-14 2007-11-14 Hydrogen splitting composition

Publications (2)

Publication Number Publication Date
AU2007350983A1 true AU2007350983A1 (en) 2008-10-23
AU2007350983A8 AU2007350983A8 (en) 2009-06-25

Family

ID=39864421

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2007350983A Abandoned AU2007350983A1 (en) 2006-11-14 2007-11-14 Hydrogen splitting composition

Country Status (10)

Country Link
US (2) US8299284B2 (enExample)
EP (1) EP2091957A4 (enExample)
JP (1) JP2010509393A (enExample)
KR (1) KR20090078835A (enExample)
CN (1) CN102066390A (enExample)
AU (1) AU2007350983A1 (enExample)
CA (1) CA2669545C (enExample)
MX (1) MX2009005127A (enExample)
SG (1) SG176482A1 (enExample)
WO (1) WO2008125911A2 (enExample)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2894146A1 (en) * 2012-12-07 2014-06-12 University Of Central Florida Research Foundation, Inc. Heterogeneous metal-free catalyst
EP2928600B1 (en) 2012-12-07 2024-02-21 University of Central Florida Research Foundation, Inc. Heterogeneously catalyzed chemical reduction of carbon dioxide
GB2522858A (en) * 2014-02-05 2015-08-12 Imp Innovations Ltd Fuel cell and battery
WO2016097734A1 (en) * 2014-12-16 2016-06-23 Isis Innovation Limited Solid-phase catalysts comprising supported frustrated lewis pairs
JP6563029B2 (ja) 2015-04-13 2019-08-21 ガーマー インク．Ｇａｒｍｏｒ， Ｉｎｃ． コンクリート又はアスファルトなどのホスト中の酸化グラファイト強化繊維
US10988488B2 (en) 2015-04-23 2021-04-27 UNIVERSITé LAVAL Process for the functionalization of sp2-H carbons using frustrated lewis pair catalysts
CA3006603A1 (en) * 2015-12-15 2017-06-22 Universite Laval Precatalysts and process for the metal-free functionalization of sp2 carbons using the same
US10821429B2 (en) 2015-12-15 2020-11-03 UNIVERSITé LAVAL Precatalysts and process for the metal-free functionalization of SP2 carbons using the same
JP7079696B2 (ja) * 2018-08-29 2022-06-02 株式会社日本触媒 ホウ素化合物、およびそれを用いた水素化物、重合体ならびに付加体の製造方法
WO2020247338A1 (en) 2019-06-04 2020-12-10 Dow Silicones Corporation BRIDGED FRUSTRATED LEWIS PAIRS AS THERMAL TRIGGER FOR REACTIONS BETWEEN Si-H AND EPOXIDE
CN113950514B (zh) 2019-06-04 2023-01-24 美国陶氏有机硅公司 甲硅烷基氢化物与α-β不饱和酯之间的热引发酸催化反应
KR20220016899A (ko) 2019-06-04 2022-02-10 다우 실리콘즈 코포레이션 실릴 수소화물과 실록산의 열적으로 개시된 산 촉매화된 반응
EP3980426B1 (en) 2019-06-04 2023-04-19 Dow Silicones Corporation Bridged frustrated lewis pairs as thermal trigger for reactions between si-h and si-o-si
US12104019B2 (en) 2019-06-04 2024-10-01 Dow Silicones Corporation Bridged frustrated Lewis pairs as thermal trigger for reactions between Si—H and alpha-beta unsaturated esters
US12116459B2 (en) 2019-06-04 2024-10-15 Dow Silicones Corporation Thermally initiated acid catalyzed reaction between silyl hydride and silyl ether and/or silanol
KR20220016902A (ko) 2019-06-04 2022-02-10 다우 실리콘즈 코포레이션 Si-H와 Si-OR의 반응을 위한 열 트리거로서의 가교된 불완전 루이스 쌍
WO2021146093A1 (en) * 2020-01-14 2021-07-22 University Of Vermont And State Agricultural College Methods of preparing primary phosphine products using lewis acid catalysts

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4522932A (en) * 1982-09-27 1985-06-11 Exxon Research & Engineering Co. Phosphine and phosphonium compounds and catalysts
WO1999006449A1 (en) * 1997-08-01 1999-02-11 The Dow Chemical Company Zwitterionic catalyst activator
US6395847B2 (en) 1999-11-19 2002-05-28 Exxonmobil Chemical Patents Inc. Supported organometallic catalysts and their use in olefin polymerization
GB0314220D0 (en) 2003-06-19 2003-07-23 Univ Durham Bifunctional catalyst

Also Published As

Publication number Publication date
JP2010509393A (ja) 2010-03-25
KR20090078835A (ko) 2009-07-20
EP2091957A4 (en) 2012-03-21
US20100048949A1 (en) 2010-02-25
WO2008125911A3 (en) 2011-03-03
CA2669545A1 (en) 2008-10-23
CN102066390A (zh) 2011-05-18
CA2669545C (en) 2016-01-05
WO2008125911A2 (en) 2008-10-23
AU2007350983A8 (en) 2009-06-25
US8642812B2 (en) 2014-02-04
MX2009005127A (es) 2009-07-03
WO2008125911A8 (en) 2009-04-23
US20130018207A1 (en) 2013-01-17
US8299284B2 (en) 2012-10-30
EP2091957A2 (en) 2009-08-26
SG176482A1 (en) 2011-12-29

Similar Documents

Publication Publication Date Title
AU2007350983A1 (en) Hydrogen splitting composition
CA2845017C (en) Hydrogenation and dehydrogenation catalyst, and methods of making and using the same
Schrock et al. Recent advances in the syntheses and applications of molybdenum and tungsten alkylidene and alkylidyne catalysts for the metathesis of alkenes and alkynes
Dagorne et al. Synthesis, characterization, and applications of group 13 cationic compounds
US7148356B2 (en) Process for the catalytic synthesis of biaryls and polymers from aryl compounds
Huang et al. Ruthenium (II) complexes with N-heterocyclic carbene–phosphine ligands for the N-alkylation of amines with alcohols
Dagorne et al. Synthesis and structure of neutral and cationic aluminum complexes incorporating bis (oxazolinato) ligands
CN112010898B (zh) 一种制备二芳基甲基取代膦酸酯的新方法
Stelmach et al. Tin-catalyzed hydrophosphination of alkenes
Sun et al. Iron‐Catalyzed Stereoconvergent 1, 4‐Hydrosilylation of Conjugated Dienes
CN110156832A (zh) 双缩醛基苯基膦、它们的制备方法及在偶联反应中的用途
Samanta et al. Redox-enabled cooperative catalysis by activating secondary alcohols using low-valent Zn complexes
Lachguar et al. Catalytic H/D exchange of (hetero) arenes with early–late polyhydride heterobimetallic complexes: impact of transition metal pairs
EP4293002A1 (en) Method for producing alkenyl phosphorus compound
Fandos et al. A new titanium building block for early–late heterometallic complexes; preparation of a new tetrameric metallomacrocycle by self assembly
Sato et al. Synthesis and reactivities of the indenyl-ruthenium cluster [(η5-C9H7) Ru (μ-SEt)] 3: indenyl effect in the trinuclear ruthenium cluster
Li et al. Photoredox/Ni-Catalytic Synthesis of cis-Vinyl Iodides from Acetylene
CA3060028A1 (en) Transition metal isonitrile catalysts
Aydemir et al. Cationic and neutral ruthenium (II) complexes containing both arene or Cp* and functionalized aminophosphines. Application to hydrogenation of aromatic ketones
CN109369514A (zh) 一种六元碳环衍生物的合成方法
Yang et al. Additive-controlled selective hydrosilylation of aryl alkenes catalyzed by bis (silylene) pincer nickel (II) chloride
Aydemir et al. New active ruthenium (II) complexes based N3, N3′-bis (diphenylphosphino)-2, 2′-bipyridine-3, 3′-diamine and P, P′-diphenylphosphinous acid-P, P′-[2, 2′-bipyridine]-3, 3′-diyl ester ligands for transfer hydrogenation of aromatic ketones by propan-2-ol
RU2478641C2 (ru) Способ получения 1-фтор-2,3-диалкилбороциклопент-2-енов
Coles Vanadium, niobium and tantalum
Tseng Structure and Reactivity Studies of Bis (pyridylimino) isoindolate Transition Metal Complexes.

Legal Events

Date Code Title Description
TH Corrigenda

Free format text: IN VOL 23, NO 20, PAGE(S) 8298 UNDER THE HEADING PCT APPLICATIONS THAT HAVE ENTERED THE NATIONAL PHASE - NAME INDEX UNDER THE NAME PRESTON A. CHASE; DOUGLAS W. STEPHEN; GREGORY C. WELCH, APPLICANT NO. 2007350983, UNDER INID (71) CORRECT THE APPLICANT NAME TO DOUGLAS W. STEPHAN

MK4 Application lapsed section 142(2)(d) - no continuation fee paid for the application