JPS55118441A - Anthracene derivative and luminescent composition - Google Patents

Anthracene derivative and luminescent composition

Info

Publication number
JPS55118441A
JPS55118441A JP2506879A JP2506879A JPS55118441A JP S55118441 A JPS55118441 A JP S55118441A JP 2506879 A JP2506879 A JP 2506879A JP 2506879 A JP2506879 A JP 2506879A JP S55118441 A JPS55118441 A JP S55118441A
Authority
JP
Japan
Prior art keywords
anthracene
formula
dissolved
solvent
anthracene derivative
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.)
Pending
Application number
JP2506879A
Other languages
Japanese (ja)
Inventor
Toshiaki Harada
Toshiyuki Hiramatsu
Teizo Yamaji
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.)
Teijin Ltd
Original Assignee
Teijin 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 Teijin Ltd filed Critical Teijin Ltd
Priority to JP2506879A priority Critical patent/JPS55118441A/en
Publication of JPS55118441A publication Critical patent/JPS55118441A/en
Pending legal-status Critical Current

Links

Abstract

NEW MATERIAL:An anthracene derivative of formula I (X is formula II and a substitute in the rings A and B of the anthracene nucleus; R is is lower alkyl).
EXAMPLE: 1,5-Bis-(2-methoxycarbonylpropionyl)-anthracene.
USE: A chemiluminescent material, luminescent in the visible region when dissolved in a solvent in the presence of a salt and brought into contact with molecular oxygen. Useful as light sources for safety of cars and on the ocean, or outdoor lightings, and as oxygen sensors.
PREPARATION: Friedel-Crafts reaction through alminium chloride anhydride is applied to the synthesis. Anthracene is dissolved or decomposed in dry carbon tetrachloride as a solvent and anhydrous alminum chloride is added to the solution, and then the carboxylic acid anhydride corresponding to the resulting mixed compound is added dropwise, to obtain the compound of formula I.
COPYRIGHT: (C)1980,JPO&Japio
JP2506879A 1979-03-06 1979-03-06 Anthracene derivative and luminescent composition Pending JPS55118441A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2506879A JPS55118441A (en) 1979-03-06 1979-03-06 Anthracene derivative and luminescent composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2506879A JPS55118441A (en) 1979-03-06 1979-03-06 Anthracene derivative and luminescent composition

Publications (1)

Publication Number Publication Date
JPS55118441A true JPS55118441A (en) 1980-09-11

Family

ID=12155601

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2506879A Pending JPS55118441A (en) 1979-03-06 1979-03-06 Anthracene derivative and luminescent composition

Country Status (1)

Country Link
JP (1) JPS55118441A (en)

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