KR0177180B1 - 승화형 열전사 기록용 색소 - Google Patents
승화형 열전사 기록용 색소 Download PDFInfo
- Publication number
- KR0177180B1 KR0177180B1 KR1019920023206A KR920023206A KR0177180B1 KR 0177180 B1 KR0177180 B1 KR 0177180B1 KR 1019920023206 A KR1019920023206 A KR 1019920023206A KR 920023206 A KR920023206 A KR 920023206A KR 0177180 B1 KR0177180 B1 KR 0177180B1
- Authority
- KR
- South Korea
- Prior art keywords
- group
- thermal transfer
- carbon atoms
- atom
- dye
- Prior art date
Links
- 238000000859 sublimation Methods 0.000 title claims abstract description 16
- 230000008022 sublimation Effects 0.000 title claims abstract description 16
- 239000000049 pigment Substances 0.000 title 1
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 21
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 11
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 11
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 9
- 125000003277 amino group Chemical group 0.000 claims abstract description 9
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 8
- 125000004430 oxygen atom Chemical group O* 0.000 claims abstract description 8
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 6
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims abstract description 6
- 125000004122 cyclic group Chemical group 0.000 claims abstract description 6
- 125000004663 dialkyl amino group Chemical group 0.000 claims abstract description 6
- 125000005843 halogen group Chemical group 0.000 claims abstract description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 6
- 125000005265 dialkylamine group Chemical group 0.000 claims abstract description 5
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical group CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims abstract description 3
- 125000003368 amide group Chemical group 0.000 claims abstract description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims abstract 2
- 238000000034 method Methods 0.000 claims description 9
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 239000000975 dye Substances 0.000 description 26
- 150000001875 compounds Chemical class 0.000 description 14
- 239000010410 layer Substances 0.000 description 14
- 239000000463 material Substances 0.000 description 14
- 239000000203 mixture Substances 0.000 description 14
- 239000000758 substrate Substances 0.000 description 12
- 230000035945 sensitivity Effects 0.000 description 7
- -1 polyethylene terephthalate Polymers 0.000 description 6
- 239000011230 binding agent Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 229920001477 hydrophilic polymer Polymers 0.000 description 3
- 229920002647 polyamide Polymers 0.000 description 3
- 229920000515 polycarbonate Polymers 0.000 description 3
- 239000004417 polycarbonate Substances 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 229920002301 cellulose acetate Polymers 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 229920002545 silicone oil Polymers 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- UHKAJLSKXBADFT-UHFFFAOYSA-N 1,3-indandione Chemical compound C1=CC=C2C(=O)CC(=O)C2=C1 UHKAJLSKXBADFT-UHFFFAOYSA-N 0.000 description 1
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- BMTAFVWTTFSTOG-UHFFFAOYSA-N Butylate Chemical compound CCSC(=O)N(CC(C)C)CC(C)C BMTAFVWTTFSTOG-UHFFFAOYSA-N 0.000 description 1
- 229920008347 Cellulose acetate propionate Polymers 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 1
- BZWDXWRDMRLVSA-UHFFFAOYSA-N NC1=C(C=C(C=2C(C3=CC=CC=C3C(C12)=O)=O)N)OC1=C(C=CC=C1)Cl Chemical compound NC1=C(C=C(C=2C(C3=CC=CC=C3C(C12)=O)=O)N)OC1=C(C=CC=C1)Cl BZWDXWRDMRLVSA-UHFFFAOYSA-N 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- ZMZINYUKVRMNTG-UHFFFAOYSA-N acetic acid;formic acid Chemical compound OC=O.CC(O)=O ZMZINYUKVRMNTG-UHFFFAOYSA-N 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 230000008033 biological extinction Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical class OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 229940071826 hydroxyethyl cellulose Drugs 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 125000005429 oxyalkyl group Chemical group 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920006380 polyphenylene oxide Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000012463 white pigment Substances 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
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
Landscapes
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
Abstract
Description
Claims (5)
- 하기 일반식(I)로 표시되는 승화형 열전사 기록용 색소.[상기식중 R1, R2는 각각 수소원자, 탄소수 1∽4의 직쇄 또는 분지형 알킬기, 알콕시기, 디알킬아미노기, 카르보닐기, 시아노기, 또는 할로겐 원자를 나타낸다. Z가 산소원자일 경우 X, Y는 비공유전자쌍을 표시하며, 탄소원자일 경우는 X, Y는 시아노기, 아미드기, 메틸 또는 에틸 카르복실레이트기를 나타낸다. D는 히드록시기, 탄소수 1∽4의 직쇄 또는 분지형의 모노 또는 디알킬아민기, 산소원자를 포함한 탄소수 3∽4로 이루어진 고리아민기, 탄소수 4∽5로 이루어진 고리아민기, 또는를 나타낸다.(A는 수소원자 또는 탄소수 1∽4의 알킬기를 나타내고, C와 B는 각각 디알킬아미노기, 시아노기, 할로겐원자, 아미노기, 수소원자, 히드록시기, 알콕시기, 카르보닐기, 탄소수 1∽4의 알킬기, 히드록시알킬기, 또는 니트로기를 나타낸다.)]
- 제1항에 있어서, 상기의 일반식(I)의 Z기는 산소원자인 것을 특징으로 하는 승화형 열전사 기록용 색소.
- 제1항에 있어서, 상기의 일반식(I)의 Z기는 탄소원자이고, X와 Y는 시아노기인 것을 특징으로 하는 승화형 열전사 기록용 색소.
- 제1항에 있어서, 상기한 일반식(I)의 D기는 디알킬아민기인 것을 특징으로 하는 승화형 열전사 기록용 색소.
- 제1항에 있어서, 상기한 일반식(I)의 D기가,일때, A기가 수소원자이고, B 또는 C기가 벤젠핵의 오르토(ortho) 또는 파라(para) 위치에 치환된 것을 특징으로 하는 승화형 열전사 기록용 색소.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1019920023206A KR0177180B1 (ko) | 1992-12-03 | 1992-12-03 | 승화형 열전사 기록용 색소 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1019920023206A KR0177180B1 (ko) | 1992-12-03 | 1992-12-03 | 승화형 열전사 기록용 색소 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR940013873A KR940013873A (ko) | 1994-07-16 |
KR0177180B1 true KR0177180B1 (ko) | 1999-04-01 |
Family
ID=19344643
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019920023206A KR0177180B1 (ko) | 1992-12-03 | 1992-12-03 | 승화형 열전사 기록용 색소 |
Country Status (1)
Country | Link |
---|---|
KR (1) | KR0177180B1 (ko) |
-
1992
- 1992-12-03 KR KR1019920023206A patent/KR0177180B1/ko not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
KR940013873A (ko) | 1994-07-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0307713B1 (en) | Blue-green dye donor element for thermal dye transfer | |
EP0227096A2 (en) | Cyan dye-donor element used in thermal dye transfer | |
EP0279467A2 (en) | Heat transfer sheet | |
JPH01165486A (ja) | 染料の熱転写に用いる無彩黒色染料供与素子 | |
JPH023450A (ja) | 熱転写用アリーリデン ピラゾロン染料供与素子 | |
KR970007419B1 (ko) | 승화형 열전사 기록용 색소 | |
JPH02252582A (ja) | 熱染料昇華転写用染料供与体材料 | |
US5929218A (en) | Pyridone-based yellow monoazo dye for use in thermal transfer and ink compositions comprising same | |
KR0177180B1 (ko) | 승화형 열전사 기록용 색소 | |
KR950008183B1 (ko) | 승화형 열전사 기록용 색소 | |
JPH0444918B2 (ko) | ||
KR950008184B1 (ko) | 승화형 열전사 기록용 색소 | |
EP0393252B1 (en) | Novel cyan dyes for use in thermal dye sublimation transfer | |
KR100201923B1 (ko) | 승화형 열전사 기록용 색소 | |
JPS62191191A (ja) | 感熱式ダイトランスフア−に用いられるシアン色素供与素子 | |
KR0177835B1 (ko) | 승화형 열전사 기록용 색소 | |
KR0177834B1 (ko) | 승화형 열전사 기록용 색소 | |
KR0177833B1 (ko) | 승화형 열전사 기록용 색소 | |
JPS61148269A (ja) | インドアニリン系化合物及び感熱転写記録用色素 | |
KR0180885B1 (ko) | 인도아닐린계 염료, 이를 함유한 잉크조성물 및 전사시트 | |
KR100199563B1 (ko) | 승화형 열전사 기록 용색소 | |
US5356854A (en) | Dye and dye carrier ink ribbon for thermal dye transfer hard copy | |
JPH047317B2 (ko) | ||
JP2956802B2 (ja) | キノリンメチン染料 | |
JPH0422713B2 (ko) |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PA0109 | Patent application |
Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 19921203 |
|
PG1501 | Laying open of application | ||
A201 | Request for examination | ||
PA0201 | Request for examination |
Patent event code: PA02012R01D Patent event date: 19961217 Comment text: Request for Examination of Application Patent event code: PA02011R01I Patent event date: 19921203 Comment text: Patent Application |
|
E701 | Decision to grant or registration of patent right | ||
PE0701 | Decision of registration |
Patent event code: PE07011S01D Comment text: Decision to Grant Registration Patent event date: 19981029 |
|
GRNT | Written decision to grant | ||
PR0701 | Registration of establishment |
Comment text: Registration of Establishment Patent event date: 19981117 Patent event code: PR07011E01D |
|
PR1002 | Payment of registration fee |
Payment date: 19981117 End annual number: 3 Start annual number: 1 |
|
PG1601 | Publication of registration | ||
PR1001 | Payment of annual fee |
Payment date: 20011107 Start annual number: 4 End annual number: 4 |
|
FPAY | Annual fee payment |
Payment date: 20021025 Year of fee payment: 5 |
|
PR1001 | Payment of annual fee |
Payment date: 20021025 Start annual number: 5 End annual number: 5 |
|
LAPS | Lapse due to unpaid annual fee | ||
PC1903 | Unpaid annual fee |
Termination category: Default of registration fee Termination date: 20040810 |