JPS6331463B2 - - Google Patents

Info

Publication number
JPS6331463B2
JPS6331463B2 JP54130093A JP13009379A JPS6331463B2 JP S6331463 B2 JPS6331463 B2 JP S6331463B2 JP 54130093 A JP54130093 A JP 54130093A JP 13009379 A JP13009379 A JP 13009379A JP S6331463 B2 JPS6331463 B2 JP S6331463B2
Authority
JP
Japan
Prior art keywords
bis
oxamide
trifluoromethylsulfonyl
compound represented
above formula
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.)
Expired
Application number
JP54130093A
Other languages
English (en)
Japanese (ja)
Other versions
JPS5569560A (en
Inventor
Matsukei Roohatsuto Maikeru
Shon Tsuen Shin
Goodensu Mohan Aasaa
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.)
Wyeth Holdings LLC
Original Assignee
American Cyanamid Co
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 American Cyanamid Co filed Critical American Cyanamid Co
Publication of JPS5569560A publication Critical patent/JPS5569560A/ja
Publication of JPS6331463B2 publication Critical patent/JPS6331463B2/ja
Granted legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/72—Nitrogen atoms
    • C07D213/76—Nitrogen atoms to which a second hetero atom is attached
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00—Luminescent materials, e.g. electroluminescent or chemiluminescent
    • C09K11/06—Luminescent materials, e.g. electroluminescent or chemiluminescent containing organic luminescent materials
    • C09K11/07—Luminescent materials, e.g. electroluminescent or chemiluminescent containing organic luminescent materials having chemically-interreactive components, e.g. reactive chemiluminescent compositions

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pyridine Compounds (AREA)
  • Luminescent Compositions (AREA)
JP13009379A 1978-11-01 1979-10-11 Novel n*n**bis*trifluoromethylsulfonyl*oxamide and chemical luminescence composition containing it Granted JPS5569560A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US05/956,567 US4226738A (en) 1978-11-01 1978-11-01 N,N-Bis(trifluoromethylsulfonyl)oxamides and chemiluminescent compositions containing the same

Publications (2)

Publication Number Publication Date
JPS5569560A JPS5569560A (en) 1980-05-26
JPS6331463B2 true JPS6331463B2 (enExample) 1988-06-23

Family

ID=25498387

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13009379A Granted JPS5569560A (en) 1978-11-01 1979-10-11 Novel n*n**bis*trifluoromethylsulfonyl*oxamide and chemical luminescence composition containing it

Country Status (8)

Country Link
US (1) US4226738A (enExample)
EP (1) EP0010844B1 (enExample)
JP (1) JPS5569560A (enExample)
AU (1) AU527467B2 (enExample)
BR (1) BR7906975A (enExample)
CA (1) CA1118434A (enExample)
DE (1) DE2960939D1 (enExample)
MX (1) MX152747A (enExample)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4282357A (en) * 1978-11-01 1981-08-04 American Cyanamid Company Aqueous chemiluminescent systems
US4366079A (en) * 1981-02-26 1982-12-28 American Cyanamid Company Sulfonated rubrene and aqueous chemiluminescent compositions containing the same
US4407743A (en) * 1982-03-19 1983-10-04 American Cyanamid Company Novel N,N'-bis(trifluoromethylsulfonyl)oxamides and chemiluminescent compositions containing the same
ATE18757T1 (de) * 1982-10-25 1986-04-15 American Cyanamid Co 9,10-bis-(phenylaethinyl)-anthracene.
DE3565994D1 (en) * 1984-09-24 1988-12-08 American Cyanamid Co Use of water-soluble polymers in aqueous chemical light formulations
ZA857300B (en) * 1984-09-24 1986-05-28 American Cyanamid Co Use of water-soluble polymers in aqueous chemical light formulations
EP0548616A1 (en) * 1991-12-26 1993-06-30 American Cyanamid Company Aqueous chemiluminescent systems
GB0106714D0 (en) * 2001-03-17 2001-05-09 Stg Aerospace Ltd Escape chute
US7943388B2 (en) 2003-11-14 2011-05-17 3M Innovative Properties Company Acoustic sensors and methods
WO2005066121A2 (en) * 2003-12-30 2005-07-21 3M Innovative Properties Company Multifunctional amine capture agents
US7342082B2 (en) 2004-12-17 2008-03-11 3M Innovative Properties Company Soluble polymers as amine capture agents and methods
US7402678B2 (en) 2004-12-17 2008-07-22 3M Innovative Properties Company Multifunctional amine capture agents
US7495118B2 (en) * 2004-12-30 2009-02-24 3M Innovative Properties Company Compositions containing C4-swallow tail silanes
US7544755B2 (en) 2005-09-30 2009-06-09 3M Innovative Properties Company Crosslinked polymers with amine binding groups
US7544756B2 (en) 2005-09-30 2009-06-09 3M Innovative Properties Company Crosslinked polymers with amine binding groups
US7544754B2 (en) 2005-09-30 2009-06-09 3M Innovative Properties Company Crosslinked polymers with amine binding groups
US20080128666A1 (en) * 2005-12-13 2008-06-05 Crayola, Llc Chemiluminescent system

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3399137A (en) * 1965-09-08 1968-08-27 American Cyanamid Co Generation of light by the reaction of anhydrides of oxalic acid with a peroxide in tpresence of a fluorescer
GB1163436A (en) * 1966-09-06 1969-09-04 American Cyanamid Co Chemiluminescence
DE1293741B (de) * 1967-01-04 1969-04-30 Bayer Ag Verfahren zur Herstellung von Sulfonyldicarbonylimiden
US3637845A (en) * 1969-04-14 1972-01-25 Minnesota Mining & Mfg Fluoroalkanesulfonamides
US3843549A (en) * 1969-07-24 1974-10-22 American Cyanamid Co Chemiluminescent compositions containing polycarbonyl compounds
DE2024909B2 (de) * 1970-05-22 1977-09-29 Bayer Ag, 5090 Leverkusen Verfahren zur herstellung von n-hydroxyalkyl-perfluoralkansulfonamiden und einige n,n-bis-(hydroxyalkyl)-perfluor-alkansulfonamide
US3855261A (en) * 1972-03-27 1974-12-17 Goodrich Co B F (hydrocarbonthio)oxamide vulcanization retarders
US4005141A (en) * 1972-07-03 1977-01-25 Minnesota Mining And Manufacturing Company Perfluoroalkylsulfonamidoaryl compounds
US4022828A (en) * 1974-03-25 1977-05-10 Universal Oil Products Company Vulcanization inhibiting compounds
US4053430A (en) * 1976-07-16 1977-10-11 American Cyanamid Company Aqueous chemiluminescent systems

Also Published As

Publication number Publication date
EP0010844A1 (en) 1980-05-14
AU5070079A (en) 1980-05-08
JPS5569560A (en) 1980-05-26
BR7906975A (pt) 1980-07-15
MX152747A (es) 1985-11-07
EP0010844B1 (en) 1981-10-07
AU527467B2 (en) 1983-03-03
CA1118434A (en) 1982-02-16
DE2960939D1 (en) 1981-12-17
US4226738A (en) 1980-10-07

Similar Documents

Publication Publication Date Title
JPS6331463B2 (enExample)
US3557233A (en) Aromatic hydrocarbons substituted by phenylethynyl groups
US3597362A (en) Generation of light by the reaction of esters of oxalic-type acids
US5597517A (en) Two-component chemiluminescent composition
US3888786A (en) Chlorinated bis(phenylethynyl)anthracenes as fluorescers in chemiluminescent systems
JP5164902B2 (ja) ９―アリール−１０―ヨードアントラセン誘導体の合成方法及び発光材料の合成方法
US5281367A (en) Two-component chemiluminescent composition
KR900003429B1 (ko) 비스(p-알킬페닐에티닐)안트라센
US3729426A (en) Chemiluminescent fluorescer comprising phenylethynyl substituted organic compounds
US4053430A (en) Aqueous chemiluminescent systems
EP0089487B1 (en) Novel n,n'-bis(trifluoromethylsulfonyl)oxamides and chemiluminescent compositions containing the same
Felouat et al. Excited-state intramolecular proton transfer (ESIPT) emitters based on a 2-(2′-hydroxybenzofuranyl) benzoxazole (HBBO) scaffold functionalised with oligo (ethylene glycol)(OEG) chains
US3970660A (en) Chemiluminescence
US3734862A (en) Novel polychloro-1,3-dioxolanes
US3978079A (en) Chemiluminescence
US3704309A (en) Method of preparation of substituted diaryl oxalates
US3749677A (en) Chemiluminescent reaction of substituted 2,2,3,3-tetrachloro-1,4-benzodioxane
US3697432A (en) Chemiluminescent reaction of chlorinated glycolide with hydrogen peroxide in the presence of a fluorescer
US3442814A (en) Generation of chemiluminescent light
US3711415A (en) Chemiluminescent reaction of substituted vinylene carbonates with hydrogen peroxide in the presence of a fluorescer
US3843549A (en) Chemiluminescent compositions containing polycarbonyl compounds
CN118702615B (zh) 一类苯并吲哚衍生物及其所制备的发光材料
KR910009942B1 (ko) 9,10-비스(페닐에티닐)안트라센 함유 형광 조성물
US3894050A (en) Chlorinated glycolide
US3914255A (en) Anhydride of anthracene derivative