NO982240L - Process for oxidizing organic substrates in the presence of metal complexes of tetra-, penta- and hexacoridinated ligands, as well as oxidation catalysts containing these - Google Patents

Process for oxidizing organic substrates in the presence of metal complexes of tetra-, penta- and hexacoridinated ligands, as well as oxidation catalysts containing these

Info

Publication number
NO982240L
NO982240L NO982240A NO982240A NO982240L NO 982240 L NO982240 L NO 982240L NO 982240 A NO982240 A NO 982240A NO 982240 A NO982240 A NO 982240A NO 982240 L NO982240 L NO 982240L
Authority
NO
Norway
Prior art keywords
metal complex
hexacoridinated
penta
ligands
tetra
Prior art date
Application number
NO982240A
Other languages
Norwegian (no)
Other versions
NO982240D0 (en
Inventor
Laurent Fraisse
Jean-Jacques Girerd
Fruduric Perie
Alain Rabion
David Tetard
Jean-Baptiste Verlhac
Alexander Nivorozhkin
Original Assignee
Elf Aquitaine
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 Elf Aquitaine filed Critical Elf Aquitaine
Publication of NO982240D0 publication Critical patent/NO982240D0/en
Publication of NO982240L publication Critical patent/NO982240L/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C409/00Peroxy compounds
    • C07C409/16Peroxy compounds the —O—O— group being bound between two carbon atoms not further substituted by oxygen atoms, i.e. peroxides
    • C07C409/18Peroxy compounds the —O—O— group being bound between two carbon atoms not further substituted by oxygen atoms, i.e. peroxides at least one of the carbon atoms belonging to a ring other than a six-membered aromatic 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
    • B01J31/18Catalysts 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
    • B01J31/1815Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine with more than one complexing nitrogen atom, e.g. bipyridyl, 2-aminopyridine
    • 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
    • B01J31/1815Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine with more than one complexing nitrogen atom, e.g. bipyridyl, 2-aminopyridine
    • B01J31/182Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine with more than one complexing nitrogen atom, e.g. bipyridyl, 2-aminopyridine comprising aliphatic or saturated rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B41/00Formation or introduction of functional groups containing oxygen
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/48Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxidation reactions with formation of hydroxy groups
    • C07C29/50Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxidation reactions with formation of hydroxy groups with molecular oxygen only
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C407/00Preparation of peroxy compounds
    • 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
    • C07C45/27Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/28Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of CHx-moieties
    • 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
    • C07C45/27Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/29Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of hydroxy groups
    • 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
    • C07C45/27Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/29Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of hydroxy groups
    • C07C45/294Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of hydroxy groups with hydrogen peroxide
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/385Saturated compounds containing a keto group being part of a ring
    • C07C49/417Saturated compounds containing a keto group being part of a ring polycyclic
    • C07C49/423Saturated compounds containing a keto group being part of a ring polycyclic a keto group being part of a condensed ring system
    • C07C49/453Saturated compounds containing a keto group being part of a ring polycyclic a keto group being part of a condensed ring system having three rings
    • 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
    • B01J2231/70Oxidation reactions, e.g. epoxidation, (di)hydroxylation, dehydrogenation and analogues
    • 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
    • B01J2531/84Metals of the iron group
    • B01J2531/842Iron
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00Systems containing at least three condensed rings
    • C07C2603/56Ring systems containing bridged rings
    • C07C2603/58Ring systems containing bridged rings containing three rings
    • C07C2603/70Ring systems containing bridged rings containing three rings containing only six-membered rings
    • C07C2603/74Adamantanes

Landscapes

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

Abstract

Selektiv oksidasjonsprosess for organiske substrater ved å bringe substratene i berøring med et oksidasjons- middel utvalgt, fra hydroperoksd der og/eller hyd^ogen- peroksid i nærvær av en katalysator som inneholder et metallkompleks av minst en multikoordinerende nitroge- nert ligand, kjennetegnet ved at det molare metallkom- pleks/peroksid-forhold ligger mellom l og 10"10, idet temperaturen er lavere enn 120°C, og tnetallkomplekset har den generelle formel: [LxMyXj"Yq, hvor M betyr et mangan- eller jernatom i oksidert tilstand, X er en bro mellom metaller, Y er et motion, x og y er > l, O < u < 3, z er ladningen av metallkcmplekset, q = z/ladningen av Y, og L er en ligand med formel: RjA^N- (CH2)r-NAr2R2, hvor A^ og Ar3 er rettkjedede C^- til C6- karbonkjeder, forbundet med en nitrogenert hetero- cyklus, Rt og R2 er hydrogen eller en C^-Cs-alkylkjede som valgfritt kan være forbundet med en nitrogenert heterocyklus, og 2 < r <. 4.Selective oxidation process for organic substrates by contacting the substrates with an oxidizing agent selected, from hydroperoxide there and / or hydrogen peroxide in the presence of a catalyst containing a metal complex of at least one multi-coordinating nitrogenous ligand, characterized in that the molar metal complex / peroxide ratio is between 1 and 10 "10, the temperature being lower than 120 ° C, and the metal complex having the general formula: [LxMyXj" Y X is a bridge between metals, Y is a motion, x and y are> l, O <u <3, z is the charge of the metal complex, q = z / the charge of Y, and L is a ligand of the formula: R - (CH 2) r -NaR 2 R 2, where A 1 and Ar 3 are straight chain C 1 - to C 6 carbon chains linked by a nitrogenated hetero cycle, R t and R 2 are hydrogen or a C 1 a nitrogenized heterocycle, and 2 <r <. 4.

NO982240A 1995-11-16 1998-05-15 Process for oxidizing organic substrates in the presence of metal complexes of tetra-, penta- and hexacoridinated ligands, as well as oxidation catalysts containing these NO982240L (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR9513580A FR2741340B1 (en) 1995-11-16 1995-11-16 PROCESS FOR OXIDIZING ORGANIC SUBSTRATES IN THE PRESENCE OF METAL COMPLEXES OF TETRA-, PENTA- AND HEXACOORDINANTS AND OXIDATION CATALYSTS CONTAINING THEM
PCT/FR1996/001804 WO1997018035A1 (en) 1995-11-16 1996-11-15 Oxidation process of organic substrates in the presence of metal complexes of tetra-, penta- and hexacoordinating ligands, and oxidation catalysts containing them

Publications (2)

Publication Number Publication Date
NO982240D0 NO982240D0 (en) 1998-05-15
NO982240L true NO982240L (en) 1998-07-16

Family

ID=9484620

Family Applications (1)

Application Number Title Priority Date Filing Date
NO982240A NO982240L (en) 1995-11-16 1998-05-15 Process for oxidizing organic substrates in the presence of metal complexes of tetra-, penta- and hexacoridinated ligands, as well as oxidation catalysts containing these

Country Status (7)

Country Link
EP (1) EP0914205A1 (en)
JP (1) JP2000500151A (en)
AU (1) AU7628996A (en)
CA (1) CA2235764A1 (en)
FR (1) FR2741340B1 (en)
NO (1) NO982240L (en)
WO (1) WO1997018035A1 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE69817832T2 (en) * 1998-11-10 2004-10-07 Unilever Nv Bleaching and oxidation catalyst
ES2223108T3 (en) * 1998-11-10 2005-02-16 Unilever N.V. DETERGENT WHITENING COMPOSITIONS.
US6573409B1 (en) 1999-07-02 2003-06-03 The Nutrasweet Company Process for the preparation of 3,3-dimethylbutanal
JP2005194244A (en) * 2004-01-09 2005-07-21 Shigenobu Yano Zinc ion fluorescence sensor
WO2013183591A1 (en) * 2012-06-06 2013-12-12 保土谷化学工業株式会社 Method for producing adamantanetriol

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4326084A (en) * 1979-10-11 1982-04-20 E. I. Du Pont De Nemours And Company Process for producing a mixture containing cyclohexanol and cyclohexanone from cyclohexane
US4459427A (en) * 1981-10-31 1984-07-10 The British Petroleum Company P.L.C. Process for the conversion of an alkane to a mixture of an alcohol and a ketone
FR2573087B1 (en) * 1984-11-09 1987-07-10 Inst Francais Du Petrole METHOD OF SOFTENING OIL CUTTINGS CARRIED OUT IN THE ABSENCE OF AN ALKALINE COMPOUND
US5990363A (en) * 1987-01-02 1999-11-23 Sun Company, Inc. Method for oxidizing alkanes using novel porphyrins synthesized from dipyrromethanes and aldehydes
FR2692499B1 (en) * 1992-06-22 1994-08-26 Atochem Elf Sa Process for delignification and bleaching of a lignocellulosic material.
US5329024A (en) * 1993-03-30 1994-07-12 National Starch And Chemical Investment Holding Corporation Epoxidation of olefins via certain manganese complexes

Also Published As

Publication number Publication date
JP2000500151A (en) 2000-01-11
NO982240D0 (en) 1998-05-15
FR2741340A1 (en) 1997-05-23
EP0914205A1 (en) 1999-05-12
FR2741340B1 (en) 1997-12-26
AU7628996A (en) 1997-06-05
CA2235764A1 (en) 1997-05-22
WO1997018035A1 (en) 1997-05-22

Similar Documents

Publication Publication Date Title
Summers et al. New mechanism for photosubstitution of organometallic complexes. Generation of substitutionally labile oxidation states by excited-state electron transfer in the presence of ligands
MY133771A (en) Polymerisation catalysts
Gould Redox chemistry of chromium (IV) complexes
Nicholls et al. Oxidation of sulphide by cytochrome aa3
NO982240L (en) Process for oxidizing organic substrates in the presence of metal complexes of tetra-, penta- and hexacoridinated ligands, as well as oxidation catalysts containing these
Kadish et al. Effect of the porphyrin macrocycle on the spectroscopic properties and catalytic activity of electroreduced nickel (II) porphyrins
Kroneck et al. The copper site in nitrous oxide reductase
Chen et al. [Ru2II (ttha)(H2O) 2] 2− is a rapid No scavenger (ttha6−= triethylenetetraminehexaacetate)
Nakajima et al. Control of the co-ordination mode of 1, 8-naphthyridine ligated to ruthenium (II) bipyridine complexes
Leung et al. Kinetics and mechanism of autoxidation of 2-mercaptoethanol catalyzed by cobalt (II)-4, 4', 4'', 4'''-tetrasulfophthalocyanine in aqueous solution
Wilkins Substitution processes in simple and complicated metal complexes
Shepherd et al. Ligand field factors in promoting S= 32 {FeNO} 7 nitrosyls
Collman et al. Electrocatalysis of nitrous oxide reduction: Comparison of several porphyrins and binary “face-to-face” porphyrins
KR850000381A (en) Synthesis of Acetaldehyde
NO20021078D0 (en) Guard bed containing lead compounds upstream of a layer of copper-containing catalyst to prevent chlorine and sulfur contamination contamination
DE69814837D1 (en) Process for the preparation of heteroaryl zinc halides
Kodaka et al. Carbon dioxide fixation forming oxazolidone coupled with a thiol/Fe 4 S 4 cluster redox system
Yamamura et al. A square-planar NiS4 unit with an aliphatic thiolato–thioether donor set: a carbon monoxide dehydrogenase model that binds CO
FR2371960A2 (en) CATALYST FOR THE REDUCTION OF CARBON OXIDE
Sandi-Urena et al. Diferric tris (carboxylato) complexes of binucleating Schiff base ligands
Emanuel et al. Mechanism of action of sulfur-containing complexes in oxidation processes
Martell Formation and degradation of cobalt dioxygen complexes
Paulson et al. The reaction of ruthenium (II) octaethylporphyrin and ruthenium (II) tetraphenylporphyrin complexes with carbon monoxide
Suzuki et al. The active site of bovine serum amine oxidase
Kovář et al. Studies on the interaction of glutamate dehydrogenase with aporheine