JPS643176A - Phenoxazine compound and transfer agent for thermally sensitive recording - Google Patents

Phenoxazine compound and transfer agent for thermally sensitive recording

Info

Publication number
JPS643176A
JPS643176A JP62156637A JP15663787A JPS643176A JP S643176 A JPS643176 A JP S643176A JP 62156637 A JP62156637 A JP 62156637A JP 15663787 A JP15663787 A JP 15663787A JP S643176 A JPS643176 A JP S643176A
Authority
JP
Japan
Prior art keywords
compound
formula
thermally sensitive
alkyl
phenoxazine
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
JP62156637A
Other languages
Japanese (ja)
Other versions
JPH013176A (en
Inventor
Mitsutoshi Anzai
Akira Utsunomiya
Masahiko Yamaguchi
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.)
Hodogaya Chemical Co Ltd
Original Assignee
Hodogaya Chemical Co 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 Hodogaya Chemical Co Ltd filed Critical Hodogaya Chemical Co Ltd
Priority to JP62-156637A priority Critical patent/JPH013176A/en
Priority claimed from JP62-156637A external-priority patent/JPH013176A/en
Publication of JPS643176A publication Critical patent/JPS643176A/en
Publication of JPH013176A publication Critical patent/JPH013176A/en
Pending legal-status Critical Current

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/382—Contact thermal transfer or sublimation processes
    • B41M5/385—Contact thermal transfer or sublimation processes characterised by the transferable dyes or pigments
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
    • B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
    • B41M5/382—Contact thermal transfer or sublimation processes
    • B41M5/385—Contact thermal transfer or sublimation processes characterised by the transferable dyes or pigments
    • B41M5/39—Dyes containing one or more carbon-to-nitrogen double bonds, e.g. azomethine

Landscapes

  • Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Thermal Transfer Or Thermal Recording In General (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

NEW MATERIAL:A phenoxazine compound of formula I (R<1>, R<2> are 1-4C alkyl; R<3> is 1-4C alkyl, aryl; Y is halogen, alkoxy, 1-8C alkyl which may be substituted with an dialkylamino group, aryl, aralkyl). EXAMPLE:10-Mehtoxycarbonyl-3,7-bis(diethylamino)phenoxazine. USE:It is used as a thermally sensitive transfer recording substance. It has high sublimation color-developing speed and develops cyan color of high brightness, deepness and good light resistance. Further, the thermally sensitive transfer recording substance shown high stability and causes no reduction in sublimation color-developing sensitivity, even after long-term storage. PREPARATION:For example, a phenoxazonium chloride of formula II is dissolved in water with heat as subjected to alkaline reduction in the presence of a solvent immiscible with water, then the product is allowed to react with a compound of formula III to give the compound of formula I.
JP62-156637A 1987-06-25 Phenoxazine compound and transfer material for thermal recording Pending JPH013176A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62-156637A JPH013176A (en) 1987-06-25 Phenoxazine compound and transfer material for thermal recording

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62-156637A JPH013176A (en) 1987-06-25 Phenoxazine compound and transfer material for thermal recording

Publications (2)

Publication Number Publication Date
JPS643176A true JPS643176A (en) 1989-01-06
JPH013176A JPH013176A (en) 1989-01-06

Family

ID=

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1086984A2 (en) * 1999-09-24 2001-03-28 Ciba SC Holding AG Compounds for mass colouration of polymers

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1086984A2 (en) * 1999-09-24 2001-03-28 Ciba SC Holding AG Compounds for mass colouration of polymers
EP1086984A3 (en) * 1999-09-24 2003-10-22 Ciba SC Holding AG Compounds for mass colouration of polymers

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