NZ528582A - A novel catalytic formulation and its preparation - Google Patents

A novel catalytic formulation and its preparation

Info

Publication number
NZ528582A
NZ528582A NZ528582A NZ52858201A NZ528582A NZ 528582 A NZ528582 A NZ 528582A NZ 528582 A NZ528582 A NZ 528582A NZ 52858201 A NZ52858201 A NZ 52858201A NZ 528582 A NZ528582 A NZ 528582A
Authority
NZ
New Zealand
Prior art keywords
metal
catalytically active
compound
composite material
formula
Prior art date
Application number
NZ528582A
Inventor
Raghunath Vitthal Chaudhari
Avinash Narendra Mahajan
Original Assignee
Council Scient Ind Res
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 Council Scient Ind Res filed Critical Council Scient Ind Res
Priority to NZ528582A priority Critical patent/NZ528582A/en
Priority claimed from PCT/IN2001/000083 external-priority patent/WO2002078842A1/en
Publication of NZ528582A publication Critical patent/NZ528582A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/49Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide
    • C07C45/50Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide by oxo-reactions
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J37/00Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/02Impregnation, coating or precipitation
    • B01J37/03Precipitation; Co-precipitation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J27/00Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/14Phosphorus; Compounds thereof
    • B01J27/186Phosphorus; Compounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J27/188Phosphorus; Compounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium with chromium, molybdenum, tungsten or polonium
    • 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
    • B01J31/1616Coordination complexes, e.g. organometallic complexes, immobilised on an inorganic support, e.g. ship-in-a-bottle type catalysts
    • 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
    • B01J31/1805Catalysts 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
    • 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
    • B01J31/1805Catalysts 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
    • B01J31/181Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine
    • B01J31/1825Ligands comprising condensed ring systems, e.g. acridine, carbazole
    • B01J31/183Ligands comprising condensed ring systems, e.g. acridine, carbazole with more than one complexing nitrogen atom, e.g. phenanthroline
    • 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
    • B01J31/24Phosphines, 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
    • 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
    • B01J31/24Phosphines, 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
    • B01J31/2404Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
    • 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
    • B01J31/24Phosphines, 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
    • B01J31/2404Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
    • B01J31/2409Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring with more than one complexing phosphine-P atom
    • 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
    • B01J2231/30Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
    • B01J2231/32Addition reactions to C=C or C-C triple bonds
    • B01J2231/321Hydroformylation, metalformylation, carbonylation or hydroaminomethylation
    • 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
    • B01J2231/30Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
    • B01J2231/34Other additions, e.g. Monsanto-type carbonylations, addition to 1,2-C=X or 1,2-C-X triplebonds, additions to 1,4-C=C-C=X or 1,4-C=-C-X triple bonds with X, e.g. O, S, NH/N
    • B01J2231/3411,2-additions, e.g. aldol or Knoevenagel condensations
    • 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
    • B01J2231/40Substitution reactions at carbon centres, e.g. C-C or C-X, i.e. carbon-hetero atom, cross-coupling, C-H activation or ring-opening reactions
    • B01J2231/42Catalytic cross-coupling, i.e. connection of previously not connected C-atoms or C- and X-atoms without rearrangement
    • B01J2231/4205C-C cross-coupling, e.g. metal catalyzed or Friedel-Crafts type
    • B01J2231/4211Suzuki-type, i.e. RY + R'B(OR)2, in which R, R' are optionally substituted alkyl, alkenyl, aryl, acyl and Y is the leaving group
    • 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
    • B01J2231/40Substitution reactions at carbon centres, e.g. C-C or C-X, i.e. carbon-hetero atom, cross-coupling, C-H activation or ring-opening reactions
    • B01J2231/42Catalytic cross-coupling, i.e. connection of previously not connected C-atoms or C- and X-atoms without rearrangement
    • B01J2231/4205C-C cross-coupling, e.g. metal catalyzed or Friedel-Crafts type
    • B01J2231/4261Heck-type, i.e. RY + C=C, in which R is aryl
    • 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
    • B01J2231/50Redistribution or isomerisation reactions of C-C, C=C or C-C triple bonds
    • B01J2231/52Isomerisation reactions
    • 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
    • B01J2231/60Reduction reactions, e.g. hydrogenation
    • B01J2231/64Reductions in general of organic substrates, e.g. hydride reductions or hydrogenations
    • B01J2231/641Hydrogenation of organic substrates, i.e. H2 or H-transfer hydrogenations, e.g. Fischer-Tropsch processes
    • 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
    • B01J2531/025Ligands with a porphyrin ring system or analogues thereof, e.g. phthalocyanines, corroles
    • 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
    • B01J2531/70Complexes comprising metals of Group VII (VIIB) as the central metal
    • B01J2531/72Manganese
    • 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
    • B01J2531/80Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82Metals of the platinum group
    • B01J2531/821Ruthenium
    • 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
    • B01J2531/80Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82Metals of the platinum group
    • B01J2531/822Rhodium
    • 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
    • B01J2531/80Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82Metals of the platinum group
    • B01J2531/824Palladium
    • 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
    • B01J2531/80Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82Metals of the platinum group
    • B01J2531/827Iridium
    • 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
    • B01J2531/80Complexes comprising metals of Group VIII as the central metal
    • B01J2531/84Metals of the iron group
    • B01J2531/847Nickel
    • 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
    • B01J31/40Regeneration or reactivation
    • B01J31/4015Regeneration or reactivation of catalysts containing metals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/12Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/14The ring being saturated
    • 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
    • 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
    • Y02P20/584Recycling of catalysts

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Epoxy Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

Disclosed is a solid catalyst comprising a solid support having deposited thereon a catalytically active composite material that is practically insoluble in a variety of liquid media, wherein the insoluble catalytically active composite material is formed by precipitating an anionically charged catalytically active entity, selected from metal complexes quaternary compounds, metal oxo anions, polyoxometallates and combinations thereof, with a group II A metal cation selected from Ca2+, Sr2+ and Ba2+, where the metal complex has the formula (M)x(L)y(L*)z, wherein: M is a catalytic metal atom or ion of a coordination complex of a transition metal from group IIIB, IVB, VB, VIB, VIIB, IB or IIB, x is from 1-60, L is aliphatic, aromatic or heterocyclic compound, Y is at least 1, L* is a radical selected from an organic anion, inorganic anion and coordinating compound, z is from 0-7, and the quaternary compound has the formula [(Y+)(R*)I][Z-], wherein: I is 4 for Y+ is N+, P+ or As+, and I is 3 for Y+ is S+, and R* is alkyl, aryl, arylalkyl, alkylaryl, alkoxy, aryloxy, or cycloalkyl.
NZ528582A 2001-03-30 2001-03-30 A novel catalytic formulation and its preparation NZ528582A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
NZ528582A NZ528582A (en) 2001-03-30 2001-03-30 A novel catalytic formulation and its preparation

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
PCT/IN2001/000083 WO2002078842A1 (en) 2001-03-30 2001-03-30 A novel catalytic formulation and its preparation
NZ528582A NZ528582A (en) 2001-03-30 2001-03-30 A novel catalytic formulation and its preparation

Publications (1)

Publication Number Publication Date
NZ528582A true NZ528582A (en) 2006-03-31

Family

ID=29415767

Family Applications (1)

Application Number Title Priority Date Filing Date
NZ528582A NZ528582A (en) 2001-03-30 2001-03-30 A novel catalytic formulation and its preparation

Country Status (7)

Country Link
JP (1) JP2005502446A (en)
KR (1) KR100756070B1 (en)
CN (1) CN100371074C (en)
AU (1) AU2001258725B8 (en)
CA (1) CA2442288C (en)
GB (1) GB2389324B (en)
NZ (1) NZ528582A (en)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060258875A1 (en) * 2005-05-10 2006-11-16 Clementine Reyes Methods for manufacturing supported nanocatalysts and methods for using supported nanocatalysts
DE102009051462B4 (en) 2009-10-30 2015-02-05 Clariant International Ag Process for producing a composite material, composite material and its use
JP6028980B2 (en) * 2013-03-07 2016-11-24 国立研究開発法人産業技術総合研究所 Process for producing aromatic olefins
CN106854159B (en) * 2015-12-09 2019-01-04 中国科学院大连化学物理研究所 A kind of phenylacetylene carbonyl compound at unsaturated aromatic ester method
WO2020085170A1 (en) * 2018-10-25 2020-04-30 学校法人早稲田大学 Method and apparatus for producing catalyst-adhered body, and method and apparatus for producing fibrous carbon nanostructure
EP4086227A4 (en) * 2020-02-28 2024-01-03 Murata Manufacturing Co., Ltd. Metal double salt liquid dispersion, method for producing metal double salt liquid dispersion, metal oxide nanoparticle liquid dispersion, and method for producing metal oxide nanoparticle liquid dispersion
CN111841658A (en) * 2020-08-14 2020-10-30 上海组波智能仪器科技有限公司 Porous plastic heterogeneous catalyst carrier and preparation method and application thereof
CN112522701B (en) * 2020-11-26 2022-10-21 太仓史密斯理查森精密制造有限公司 Defoaming type surface treatment process for chaplet
CN113231097B (en) * 2021-05-11 2023-02-03 山东科技大学 Thermal cracking catalyst and preparation method thereof
CN113410474B (en) * 2021-06-21 2024-04-02 澳门大学 SiNC catalyst and preparation method and application thereof
CN113477275B (en) * 2021-07-08 2023-06-02 青岛科技大学 Preparation method of nitrogen-rich ionic liquid polymer and application of nitrogen-rich ionic liquid polymer in catalytic hydrogenation reaction
CN113651855B (en) * 2021-08-19 2023-08-22 东北师范大学 Novel crystalline porous framework material, and preparation method and application thereof
CN116328832A (en) * 2021-12-24 2023-06-27 中国石油化工股份有限公司 Organic polymer carrier, main catalyst, ethylene polymerization catalyst composition and application thereof
CN114738603B (en) * 2022-04-21 2024-02-23 中机数控科技(福建)有限公司 Hydrogen purity detection equipment for hydrogen storage of metal hydride and use method
CN115282967A (en) * 2022-08-31 2022-11-04 青岛理工大学 Application and method of palygorskite-loaded bimetallic oxide in degradation of organic wastewater
CN115805102B (en) * 2022-11-25 2024-04-05 中科合成油技术股份有限公司 Heterogeneous catalyst for preparing high-carbon aldehyde by hydroformylation of medium-long chain alpha-olefin and preparation method thereof
CN117229248B (en) * 2023-08-21 2024-07-02 浙江晟格生物科技有限公司 Method for preparing and purifying vitronectin by using solid alkali

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05270806A (en) * 1992-03-25 1993-10-19 Mitsubishi Gas Chem Co Inc Production of hydrogen peroxide
DE69406828T2 (en) * 1993-03-26 1998-04-09 Nippon Oil Co Ltd Solid acid catalyst for the conversion of paraffins and methods for paraffin conversion using the same
US5750457A (en) * 1993-03-26 1998-05-12 Nippon Oil Company, Ltd. Solid acid catalyst for paraffin conversion and process for paraffin conversion using the same
US5536858A (en) * 1994-02-12 1996-07-16 Hoffmann-La Roche Inc. Tetrasulfonated diphosphine compounds and metal complexes thereof for asymmetric catalytic reactions
FR2766818B1 (en) * 1997-08-01 1999-09-10 Rhodia Chimie Sa METHOD OF HOUSEHOLD OXIDATION OF SUBSTITUTED HYDROCARBON DERIVATIVES AND HETEROPOLYACID COMPOSITIONS USEFUL AS HOUSEHOLD OXIDATION CATALYSTS

Also Published As

Publication number Publication date
JP2005502446A (en) 2005-01-27
CA2442288A1 (en) 2002-10-10
AU2001258725B2 (en) 2008-04-03
KR100756070B1 (en) 2007-09-07
GB0322868D0 (en) 2003-10-29
AU2001258725B8 (en) 2008-05-01
GB2389324B (en) 2005-08-17
CN1538876A (en) 2004-10-20
CN100371074C (en) 2008-02-27
CA2442288C (en) 2007-12-11
GB2389324A (en) 2003-12-10
KR20040004573A (en) 2004-01-13

Similar Documents

Publication Publication Date Title
NZ528582A (en) A novel catalytic formulation and its preparation
HK1046689A1 (en) Substituted pyridino pentaazamacrocyle complexes having superoxide dismutase activity.
Casely et al. Bismuth coordination chemistry with allyl, alkoxide, aryloxide, and tetraphenylborate ligands and the {[2, 6-(Me2NCH2) 2C6H3] 2Bi}+ cation
AU9392898A (en) Weakly coordinating anions containing polyfluoroalkoxide ligands
CA2205509A1 (en) Microbicidal triazolyl derivatives
NO996038D0 (en) New Catalyst Systems for Copolymerization Reactions, Metallocene Amide Halides, Their Preparation and Use
HUP0302153A2 (en) Piperidine derivetives as modulators of chemokine receptor activity, process for producing them and pharmaceutical compositions containing them
PL334915A1 (en) Pyrrolidine derivatives exhibiting phospholipase a2 inhibiting activity
ATE165361T1 (en) DIPHOSPHINE LIGANDS
MX9603202A (en) Process for epoxidising prochiral olefins and a catalyst therefor and intermediates for making the catalyst.
AU2001239442A1 (en) Ruthenium-diphosphine complexes and their use as catalysts
HUT50345A (en) Process for production of cefem-derivatives and their intermediers
TR200002988T2 (en) Catalytic composition containing a titanium compound, an amine and a phosphorus compound, its preparation and use
CA2186731A1 (en) Trinuclear cationic platinum complexes having antitumour activity and pharmaceutical compositions containing them
Hilfiker et al. Tricationic Metal Complexes ([ML][NO3] 3, M= Ga, In) of N, N ‘, N ‘‘-Tris (2-pyridylmethyl)-cis-1, 3, 5-triaminocyclohexane: Preparation and Structure
Feng et al. Synthesis and characterization of cyclohexadienyl-based constrained geometry complexes
CA2354775A1 (en) Quaternary phosphonium salt catalysts in catalytic hydrolysis of alkylene oxides
Horáček et al. Reactions of Substituted Zirconocene− Bis (trimethylsilyl) ethyne Complexes with Terminal Alkynes
Lente et al. Syntheses and structures of rhenium (IV) and rhenium (V) complexes with ethanedithiolato ligands
Zheng et al. Reactions of the cationic zinc thiolate model complex [Zn (Tab) 4](PF6) 2 with N-donor ligands and cobalt dichloride
ATE337327T1 (en) SUBSTITUTED FERROCENYL DIPHOSPINE LIGANDS FOR HOMOGENEOUS HYDROGENIERING CATALYSTS
Aguilar-Calderon et al. Redox-Controlled and Reversible N–N Bond Forming and Splitting with an IronIV Terminal Imido Ligand
Reger et al. Synthesis and Solid-State Structure of [HB (3, 5-Me2pz) 3] GaFe (CO) 4: A Compound with a Short, Two-Electron Ga (I)→ Fe Dative Bond
Xiong et al. A Novel Dimeric Zinc Complex: Bis {μ-[(dimercaptomethylene) propanedinitrilato-S, S ‘]} tetrakis (4-methylpyridine) dizinc (II)− Chloroform
Shongwe et al. Unprecedented [V2O] 6+ Core of a centrosymmetric thiosemicarbazonato dimer: Spontaneous deoxygenation of oxovanadium (IV)

Legal Events

Date Code Title Description
PSEA Patent sealed
RENW Renewal (renewal fees accepted)
RENW Renewal (renewal fees accepted)