JPS6247298B2 - - Google Patents

Info

Publication number: JPS6247298B2
Authority: JP; Japan
Prior art keywords: electron beam; image; sensitive; secondary amine; composition
Prior art date: 1980-01-16
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

JP55004045A

Other languages

English (en)

Japanese (ja)

Other versions

JPS56101146A (en

Inventor

Hideo Komizu

Koichi Pponda

Masami Kawasaki

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.)

National Institute of Advanced Industrial Science and Technology AIST

Original Assignee

Agency of Industrial Science and Technology

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.)

1980-01-16

Filing date

1980-01-16

Publication date

1987-10-07

1980-01-16 Application filed by Agency of Industrial Science and Technology filed Critical Agency of Industrial Science and Technology

1980-01-16 Priority to JP404580A priority Critical patent/JPS56101146A/ja

1981-08-13 Publication of JPS56101146A publication Critical patent/JPS56101146A/ja

1987-10-07 Publication of JPS6247298B2 publication Critical patent/JPS6247298B2/ja

Status Granted legal-status Critical Current

Links

238000010894 electron beam technology Methods 0.000 claims description 25
239000000203 mixture Substances 0.000 claims description 22
150000001875 compounds Chemical class 0.000 claims description 18
-1 aromatic secondary amine Chemical class 0.000 claims description 11
229920000620 organic polymer Polymers 0.000 claims description 8
VZIRCHXYMBFNFD-HNQUOIGGSA-N 3-(2-Furanyl)-2-propenal Chemical compound O=C\C=C\C1=CC=CO1 VZIRCHXYMBFNFD-HNQUOIGGSA-N 0.000 claims description 7
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 8
HJUGFYREWKUQJT-UHFFFAOYSA-N tetrabromomethane Chemical compound BrC(Br)(Br)Br HJUGFYREWKUQJT-UHFFFAOYSA-N 0.000 description 8
238000000034 method Methods 0.000 description 7
LBUJPTNKIBCYBY-UHFFFAOYSA-N 1,2,3,4-tetrahydroquinoline Chemical class C1=CC=C2CCCNC2=C1 LBUJPTNKIBCYBY-UHFFFAOYSA-N 0.000 description 5
VHHHONWQHHHLTI-UHFFFAOYSA-N hexachloroethane Chemical compound ClC(Cl)(Cl)C(Cl)(Cl)Cl VHHHONWQHHHLTI-UHFFFAOYSA-N 0.000 description 5
239000000758 substrate Substances 0.000 description 5
AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methylaniline Chemical compound CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 description 4
238000010521 absorption reaction Methods 0.000 description 4
239000000463 material Substances 0.000 description 4
239000011259 mixed solution Substances 0.000 description 4
239000002904 solvent Substances 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000011521 glass Substances 0.000 description 3
238000002156 mixing Methods 0.000 description 3
229920003229 poly(methyl methacrylate) Polymers 0.000 description 3
239000004926 polymethyl methacrylate Substances 0.000 description 3
230000003595 spectral effect Effects 0.000 description 3
125000001424 substituent group Chemical group 0.000 description 3
239000008096 xylene Substances 0.000 description 3
IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
HYBBIBNJHNGZAN-UHFFFAOYSA-N Furaldehyde Natural products O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 2
PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
238000004040 coloring Methods 0.000 description 2
OKJPEAGHQZHRQV-UHFFFAOYSA-N iodoform Chemical compound IC(I)I OKJPEAGHQZHRQV-UHFFFAOYSA-N 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
239000000243 solution Substances 0.000 description 2
229940126062 Compound A Drugs 0.000 description 1
NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
230000001133 acceleration Effects 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
150000004982 aromatic amines Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
125000004093 cyano group Chemical group *C#N 0.000 description 1
230000018044 dehydration Effects 0.000 description 1
238000006297 dehydration reaction Methods 0.000 description 1
239000003814 drug Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
230000005611 electricity Effects 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
150000002476 indolines Chemical class 0.000 description 1
230000001678 irradiating effect Effects 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000002075 main ingredient Substances 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
239000000123 paper Substances 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
150000003336 secondary aromatic amines Chemical class 0.000 description 1
GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical class [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 description 1

Classifications

- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/675—Compositions containing polyhalogenated compounds as photosensitive substances

Landscapes

Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Thermal Transfer Or Thermal Recording In General (AREA)
Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)

JP404580A 1980-01-16 1980-01-16 Electron beam-sensitive image-forming composition Granted JPS56101146A (en)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP404580A JPS56101146A (en)	1980-01-16	1980-01-16	Electron beam-sensitive image-forming composition

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP404580A JPS56101146A (en)	1980-01-16	1980-01-16	Electron beam-sensitive image-forming composition

Publications (2)

Publication Number	Publication Date
JPS56101146A JPS56101146A (en)	1981-08-13
JPS6247298B2 true JPS6247298B2 (de)	1987-10-07

Family

ID=11573949

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP404580A Granted JPS56101146A (en)	1980-01-16	1980-01-16	Electron beam-sensitive image-forming composition

Country Status (1)

Country	Link
JP (1)	JPS56101146A (de)

1980
- 1980-01-16 JP JP404580A patent/JPS56101146A/ja active Granted

Also Published As

Publication number	Publication date
JPS56101146A (en)	1981-08-13

Publication	Publication Date	Title
US3284205A (en)	1966-11-08	Benzotriazole and heterocyclic ketimide activators for leuco compounds
US4904555A (en)	1990-02-27	Photosensitive composition for making repeatably tonable layers
US3813245A (en)	1974-05-28	Photochromic composition containing polyhalogenated compound,spiropyran compound and sensitizer and the use thereof
DE1917543C3 (de)	1974-01-24	Lichtempfindliches Gemisch
EP0272298B1 (de)	1990-10-03	Irreversible photochrome markierungen
US3980480A (en)	1976-09-14	Photographic recording and reproduction of information photochromic composition containing polyhalogenated hydrocarbon, spiropyran compound and heterocyclic mercapto compound and the use thereof
US3916069A (en)	1975-10-28	Reduced styryl/cyanine dye
US3042516A (en)	1962-07-03	Print-out compositions for photographic purposes and process of using same
US4482489A (en)	1984-11-13	Light-sensitive diazonium trifluoromethane sulfonates
US3884697A (en)	1975-05-20	Photographic process utilizing spiropyran compound dispersed in nitrocellulose films with high nitrogen content
US3846131A (en)	1974-11-05	Recording material containing a polyhalogenated hydrocarbon photoactivator and a dye forming combination of an indolizine derivative and an aldehyde and the use thereof
US4066459A (en)	1978-01-03	Free radical photosensitive compositions with improved sensitivity and shelf life stability
US3974147A (en)	1976-08-10	Reduced styryl dyes
US4308341A (en)	1981-12-29	Non-silver imaging compositions having improved speeds and processing temperatures
JPS6247298B2 (de)	1987-10-07
JPS6123543B2 (de)	1986-06-06
US3773515A (en)	1973-11-20	Light-sensitive material containing a polyhalogenated hydrocarbon, an n-vinylcarbazole, and a furfurylidene compound as an image enhancer and stabilizer
US3799779A (en)	1974-03-26	Light-desensitizable imaging sheet
US3272635A (en)	1966-09-13	Compositions containing leuco xanthene dyes and suitable activators
JPS648812B2 (de)	1989-02-15
JPS6250382A (ja)	1987-03-05	フオトクロミツク材料
JPH01161253A (ja)	1989-06-23	レーザー光用電子写真感光体
JPH04212969A (ja)	1992-08-04	電子写真平版印刷版材料
GB1312746A (en)	1973-04-04	Recording materials for electron beam images
US4316984A (en)	1982-02-23	Thermolabile acutance dyes