JPS6361198B2 - - Google Patents
Info
- Publication number
- JPS6361198B2 JPS6361198B2 JP56180634A JP18063481A JPS6361198B2 JP S6361198 B2 JPS6361198 B2 JP S6361198B2 JP 56180634 A JP56180634 A JP 56180634A JP 18063481 A JP18063481 A JP 18063481A JP S6361198 B2 JPS6361198 B2 JP S6361198B2
- Authority
- JP
- Japan
- Prior art keywords
- hydroxyphenyl
- carbon atoms
- electron
- group
- sulfone
- 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
Links
- 150000001875 compounds Chemical class 0.000 claims description 20
- 125000004432 carbon atom Chemical group C* 0.000 claims description 17
- 239000000463 material Substances 0.000 claims description 13
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 3
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 3
- 125000005129 aryl carbonyl group Chemical group 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000004391 aryl sulfonyl group Chemical group 0.000 claims description 2
- 150000003457 sulfones Chemical class 0.000 description 30
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
- -1 4-hydroxydiphenoxide Chemical compound 0.000 description 10
- 230000015572 biosynthetic process Effects 0.000 description 9
- KZTYYGOKRVBIMI-UHFFFAOYSA-N diphenyl sulfone Chemical compound C=1C=CC=CC=1S(=O)(=O)C1=CC=CC=C1 KZTYYGOKRVBIMI-UHFFFAOYSA-N 0.000 description 9
- 239000000975 dye Substances 0.000 description 9
- 238000003786 synthesis reaction Methods 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 7
- 238000000576 coating method Methods 0.000 description 7
- 150000002989 phenols Chemical class 0.000 description 6
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 6
- 239000004372 Polyvinyl alcohol Substances 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 5
- 239000006185 dispersion Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 229920002451 polyvinyl alcohol Polymers 0.000 description 5
- 230000018109 developmental process Effects 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 125000001424 substituent group Chemical group 0.000 description 4
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical compound C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 3
- 239000005995 Aluminium silicate Substances 0.000 description 3
- 235000012211 aluminium silicate Nutrition 0.000 description 3
- 238000004040 coloring Methods 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000012188 paraffin wax Substances 0.000 description 3
- 229910000027 potassium carbonate Inorganic materials 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 2
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 150000001350 alkyl halides Chemical class 0.000 description 2
- IMHDGJOMLMDPJN-UHFFFAOYSA-N biphenyl-2,2'-diol Chemical group OC1=CC=CC=C1C1=CC=CC=C1O IMHDGJOMLMDPJN-UHFFFAOYSA-N 0.000 description 2
- YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical compound C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical class C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 150000003951 lactams Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052751 metal Chemical class 0.000 description 2
- 239000002184 metal Chemical class 0.000 description 2
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229940043267 rhodamine b Drugs 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 150000004897 thiazines Chemical class 0.000 description 2
- 125000001834 xanthenyl group Chemical class C1=CC=CC=2OC3=CC=CC=C3C(C12)* 0.000 description 2
- LIZLYZVAYZQVPG-UHFFFAOYSA-N (3-bromo-2-fluorophenyl)methanol Chemical compound OCC1=CC=CC(Br)=C1F LIZLYZVAYZQVPG-UHFFFAOYSA-N 0.000 description 1
- VMKOFRJSULQZRM-UHFFFAOYSA-N 1-bromooctane Chemical compound CCCCCCCCBr VMKOFRJSULQZRM-UHFFFAOYSA-N 0.000 description 1
- DXYZIGZCEVJFIX-UHFFFAOYSA-N 2'-(dibenzylamino)-6'-(diethylamino)spiro[2-benzofuran-3,9'-xanthene]-1-one Chemical compound C=1C(N(CC)CC)=CC=C(C2(C3=CC=CC=C3C(=O)O2)C2=C3)C=1OC2=CC=C3N(CC=1C=CC=CC=1)CC1=CC=CC=C1 DXYZIGZCEVJFIX-UHFFFAOYSA-N 0.000 description 1
- YMTYZTXUZLQUSF-UHFFFAOYSA-N 3,3'-Dimethylbisphenol A Chemical compound C1=C(O)C(C)=CC(C(C)(C)C=2C=C(C)C(O)=CC=2)=C1 YMTYZTXUZLQUSF-UHFFFAOYSA-N 0.000 description 1
- ABJAMKKUHBSXDS-UHFFFAOYSA-N 3,3-bis(6-amino-1,4-dimethylcyclohexa-2,4-dien-1-yl)-2-benzofuran-1-one Chemical compound C1=CC(C)=CC(N)C1(C)C1(C2(C)C(C=C(C)C=C2)N)C2=CC=CC=C2C(=O)O1 ABJAMKKUHBSXDS-UHFFFAOYSA-N 0.000 description 1
- FFXPOZNUNSROLU-UHFFFAOYSA-N 3-[4-(dimethylamino)phenyl]-3-(1,3-dimethyl-2h-indol-3-yl)-2-benzofuran-1-one Chemical compound C1=CC(N(C)C)=CC=C1C1(C2(C)C3=CC=CC=C3N(C)C2)C2=CC=CC=C2C(=O)O1 FFXPOZNUNSROLU-UHFFFAOYSA-N 0.000 description 1
- ZKUWHPNJONEJEE-UHFFFAOYSA-N 3-[4-(dimethylamino)phenyl]-3-(2-methyl-1h-indol-3-yl)-2-benzofuran-1-one Chemical compound C1=CC(N(C)C)=CC=C1C1(C=2C3=CC=CC=C3NC=2C)C2=CC=CC=C2C(=O)O1 ZKUWHPNJONEJEE-UHFFFAOYSA-N 0.000 description 1
- QHPQWRBYOIRBIT-UHFFFAOYSA-N 4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C=C1 QHPQWRBYOIRBIT-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- IPAJDLMMTVZVPP-UHFFFAOYSA-N Crystal violet lactone Chemical compound C1=CC(N(C)C)=CC=C1C1(C=2C=CC(=CC=2)N(C)C)C2=CC=C(N(C)C)C=C2C(=O)O1 IPAJDLMMTVZVPP-UHFFFAOYSA-N 0.000 description 1
- ZKURGBYDCVNWKH-UHFFFAOYSA-N [3,7-bis(dimethylamino)phenothiazin-10-yl]-phenylmethanone Chemical compound C12=CC=C(N(C)C)C=C2SC2=CC(N(C)C)=CC=C2N1C(=O)C1=CC=CC=C1 ZKURGBYDCVNWKH-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 150000001502 aryl halides Chemical class 0.000 description 1
- 125000004104 aryloxy group Chemical group 0.000 description 1
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 1
- 229940073608 benzyl chloride Drugs 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical compound C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- JSGBYRDSFDPXFC-UHFFFAOYSA-N n-[5-[(fluoroamino)methyl]-2-methylcyclohexyl]aniline Chemical compound CC1CCC(CNF)CC1NC1=CC=CC=C1 JSGBYRDSFDPXFC-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229920003169 water-soluble polymer Polymers 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
- B41M5/30—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used using chemical colour formers
- B41M5/333—Colour developing components therefor, e.g. acidic compounds
- B41M5/3333—Non-macromolecular compounds
- B41M5/3335—Compounds containing phenolic or carboxylic acid groups or metal salts thereof
- B41M5/3336—Sulfur compounds, e.g. sulfones, sulfides, sulfonamides
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
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Claims (1)
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Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56180634A JPS5882788A (ja) | 1981-11-11 | 1981-11-11 | æç±èšé²ææ |
GB08231698A GB2112156B (en) | 1981-11-11 | 1982-11-05 | Heat-sensitive recording materials |
US06/440,659 US4446209A (en) | 1981-11-11 | 1982-11-10 | Heat-sensitive recording materials |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56180634A JPS5882788A (ja) | 1981-11-11 | 1981-11-11 | æç±èšé²ææ |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5882788A JPS5882788A (ja) | 1983-05-18 |
JPS6361198B2 true JPS6361198B2 (ja) | 1988-11-28 |
Family
ID=16086621
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56180634A Granted JPS5882788A (ja) | 1981-11-11 | 1981-11-11 | æç±èšé²ææ |
Country Status (3)
Country | Link |
---|---|
US (1) | US4446209A (ja) |
JP (1) | JPS5882788A (ja) |
GB (1) | GB2112156B (ja) |
Families Citing this family (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58132593A (ja) * | 1982-02-02 | 1983-08-06 | Ricoh Co Ltd | æç±èšé²ã·âã |
DE3243945A1 (de) * | 1982-11-27 | 1984-05-30 | Basf Ag, 6700 Ludwigshafen | Waermeempfindliches aufzeichnungsmaterial |
US4536779A (en) * | 1982-12-10 | 1985-08-20 | Ciba-Geigy Corporation | Heat-sensitive recording material |
WO1984002882A1 (en) * | 1983-01-17 | 1984-08-02 | Yoshitomi Pharmaceutical | Heat-sensitive recording paper |
JPS59165687A (ja) * | 1983-03-10 | 1984-09-18 | Ricoh Co Ltd | æç±èšé²ææ |
JPS6013852A (ja) * | 1983-07-04 | 1985-01-24 | Shin Nisso Kako Co Ltd | ãžããšãã«ã¹ã«ãã³èªå°äœããã³ãããå«æããçºè²æ§èšé²ææ |
JPS6054884A (ja) * | 1983-09-05 | 1985-03-29 | Fuji Photo Film Co Ltd | èšé²ææ |
JPS6153084A (ja) * | 1984-08-23 | 1986-03-15 | Jujo Paper Co Ltd | æç±èšé²çŽ |
US4761396A (en) * | 1986-02-12 | 1988-08-02 | Kanzaki Paper Manufacturing Co., Ltd. | Heat-sensitive recording material |
DE3727201C1 (de) * | 1986-08-14 | 1988-03-10 | Ricoh Kk | Faerbende Phthalid-Verbindungen und diese als faerbenden Bestandteil enthaltende Aufzeichnungsmaterialien |
JP2605713B2 (ja) * | 1987-04-16 | 1997-04-30 | åžçå°å·æ ªåŒäŒç€Ÿ | æç±èšé²æ |
EP0465665B1 (en) * | 1990-01-29 | 1995-04-12 | Yoshitomi Pharmaceutical Industries, Ltd. | Process for producing diphenyl sulfone compound |
JPH0684107B2 (ja) * | 1991-03-14 | 1994-10-26 | åå¯è£œè¬æ ªåŒäŒç€Ÿ | æç±èšé²çŽ |
JP2671285B2 (ja) * | 1992-03-18 | 1997-10-29 | æ¥æ¬è£œçŽæ ªåŒäŒç€Ÿ | æç±èšé²ã·ãŒã |
EP0567314A1 (en) * | 1992-04-24 | 1993-10-27 | Fuji Photo Film Co., Ltd. | Electron-accepting compounds and color recording materials containing them |
JP3451109B2 (ja) * | 1992-10-01 | 2003-09-29 | æ¥æ¬æ¹éæ ªåŒäŒç€Ÿ | ãã§ããã«ã¢ã«ã³ãŒã«èªå°äœåã³ãããçšããèšé²ææ |
US5622909A (en) * | 1994-05-17 | 1997-04-22 | Ricoh Company, Ltd. | Thermosensitive recording materials |
US5693374A (en) * | 1994-06-23 | 1997-12-02 | Fuji Photo Film Co., Ltd. | Alpha-resorcyclic acid ester derivatives and recording materials using the same |
CN1087286C (zh) * | 1995-10-31 | 2002-07-10 | æ¥æ¬æ¹èŸŸæ ªåŒäŒç€Ÿ | äºè¯ç 亀èåååç©å䜿çšäºè¯¥ååç©çè®°åœææ |
US6143060A (en) * | 1995-11-01 | 2000-11-07 | Nippon Soda Co., Ltd. | Triazine derivatives and recording materials prepared therefrom |
JP3169574B2 (ja) * | 1997-12-24 | 2001-05-28 | æ¥è¯ååŠæ ªåŒäŒç€Ÿ | ïŒâããããã·âïŒââãã³ãžã«ãªãã·ãžãã§ãã«ã¹ã«ãã³ã®è£œé æ¹æ³ |
JP2000273081A (ja) | 1999-03-23 | 2000-10-03 | Nippon Soda Co Ltd | ãžãã§ãã«ã¹ã«ãã³ååç©ã®å·¥æ¥ç補é æ¹æ³ |
AU4456601A (en) * | 2000-03-28 | 2001-10-08 | Nippon Soda Co., Ltd. | Oxa(thia)zolidine derivative and anti-inflammatory drug |
US6831201B2 (en) | 2001-01-22 | 2004-12-14 | Nippon Soda Co., Ltd. | Process for producing diphenyl sulfone compound |
JP4807690B2 (ja) * | 2001-09-10 | 2011-11-02 | å°è¥¿ååŠå·¥æ¥æ ªåŒäŒç€Ÿ | ãžãã§ãã«ã¹ã«ãã³ååç©ã®è£œé æ¹æ³ |
JP4942463B2 (ja) * | 2006-11-27 | 2012-05-30 | æ¥è¯ååŠæ ªåŒäŒç€Ÿ | ã¢ã«ãã«ãªãã·ããããã·ãžãã§ãã«ã¹ã«ãã³ã®è£œé æ¹æ³ |
JP6184325B2 (ja) * | 2011-10-31 | 2017-08-23 | æ¥æ¬è£œçŽæ ªåŒäŒç€Ÿ | ãã§ããŒã«ã¹ã«ãã³é žã¢ãªãŒã«ãšã¹ãã«ãé¡è²å€ããã³æç±èšé²ææ |
CN107709027B (zh) | 2015-06-16 | 2019-08-02 | æ¥æ¬å¶çºžæ ªåŒäŒç€Ÿ | çæè®°åœäœ |
WO2017069141A1 (ja) | 2015-10-23 | 2017-04-27 | æ¥æ¬è£œçŽæ ªåŒäŒç€Ÿ | æç±èšé²äœ |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6127486A (ja) * | 1984-07-17 | 1986-02-06 | å·åŽè£œéæ ªåŒäŒç€Ÿ | å転çåºåŒå ç±ç |
-
1981
- 1981-11-11 JP JP56180634A patent/JPS5882788A/ja active Granted
-
1982
- 1982-11-05 GB GB08231698A patent/GB2112156B/en not_active Expired
- 1982-11-10 US US06/440,659 patent/US4446209A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPS5882788A (ja) | 1983-05-18 |
US4446209A (en) | 1984-05-01 |
GB2112156B (en) | 1985-08-14 |
GB2112156A (en) | 1983-07-13 |
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