TW308600B

TW308600B -

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Publication number: TW308600B
Authority: TW; Taiwan
Prior art keywords: cns; ministry; page; please read; economic affairs
Prior art date: 1994-10-10

Application number

TW084110269A

Other languages

English (en)

Chinese (zh)

Original Assignee

Ciba Sc Holding Ag

Priority date

1994-10-10

Filing date

1995-10-02

Publication date

1997-06-21

1995-10-02 Application filed by Ciba Sc Holding Ag filed Critical Ciba Sc Holding Ag

1997-06-21 Application granted granted Critical

1997-06-21 Publication of TW308600B publication Critical patent/TW308600B/zh

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-1 silver halide Chemical class 0.000 claims description 370
150000001875 compounds Chemical class 0.000 claims description 221
239000010410 layer Substances 0.000 claims description 180
238000011049 filling Methods 0.000 claims description 174
239000000203 mixture Substances 0.000 claims description 136
125000000217 alkyl group Chemical group 0.000 claims description 113
238000000034 method Methods 0.000 claims description 76
239000006096 absorbing agent Substances 0.000 claims description 71
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 62
239000004332 silver Substances 0.000 claims description 61
229910052709 silver Inorganic materials 0.000 claims description 61
239000000126 substance Substances 0.000 claims description 55
229910052739 hydrogen Inorganic materials 0.000 claims description 54
239000001257 hydrogen Substances 0.000 claims description 51
239000000839 emulsion Substances 0.000 claims description 49
238000000576 coating method Methods 0.000 claims description 43
229920001577 copolymer Polymers 0.000 claims description 43
239000000123 paper Substances 0.000 claims description 39
239000011248 coating agent Substances 0.000 claims description 38
239000003381 stabilizer Substances 0.000 claims description 36
150000001412 amines Chemical class 0.000 claims description 33
239000000463 material Substances 0.000 claims description 31
125000003545 alkoxy group Chemical group 0.000 claims description 29
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 27
229910052760 oxygen Inorganic materials 0.000 claims description 26
239000000853 adhesive Substances 0.000 claims description 25
230000001070 adhesive effect Effects 0.000 claims description 25
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 24
239000001301 oxygen Substances 0.000 claims description 24
229910052736 halogen Inorganic materials 0.000 claims description 22
150000002367 halogens Chemical class 0.000 claims description 21
238000007639 printing Methods 0.000 claims description 21
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QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 19
125000000753 cycloalkyl group Chemical group 0.000 claims description 16
239000000654 additive Substances 0.000 claims description 14
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239000004611 light stabiliser Substances 0.000 claims description 13
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YHCGGLXPGFJNCO-UHFFFAOYSA-N 2-(2H-benzotriazol-4-yl)phenol Chemical compound OC1=CC=CC=C1C1=CC=CC2=C1N=NN2 YHCGGLXPGFJNCO-UHFFFAOYSA-N 0.000 claims description 4
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PCTMTFRHKVHKIS-BMFZQQSSSA-N (1s,3r,4e,6e,8e,10e,12e,14e,16e,18s,19r,20r,21s,25r,27r,30r,31r,33s,35r,37s,38r)-3-[(2r,3s,4s,5s,6r)-4-amino-3,5-dihydroxy-6-methyloxan-2-yl]oxy-19,25,27,30,31,33,35,37-octahydroxy-18,20,21-trimethyl-23-oxo-22,39-dioxabicyclo[33.3.1]nonatriaconta-4,6,8,10 Chemical compound C1C=C2C[C@@H](OS(O)(=O)=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2.O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/C=C/C=C/C=C/[C@H](C)[C@@H](O)[C@@H](C)[C@H](C)OC(=O)C[C@H](O)C[C@H](O)CC[C@@H](O)[C@H](O)C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 PCTMTFRHKVHKIS-BMFZQQSSSA-N 0.000 claims 3
HTTGVORJOBRXRJ-UHFFFAOYSA-N 2-(triazin-4-yl)phenol Chemical compound OC1=CC=CC=C1C1=CC=NN=N1 HTTGVORJOBRXRJ-UHFFFAOYSA-N 0.000 claims 1
101100298295 Drosophila melanogaster flfl gene Proteins 0.000 claims 1
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims 1
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125000003118 aryl group Chemical group 0.000 description 29
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CIWBQSYVNNPZIQ-PKWREOPISA-N dexamethasone dipropionate Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@@H](C)[C@@](C(=O)COC(=O)CC)(OC(=O)CC)[C@@]1(C)C[C@@H]2O CIWBQSYVNNPZIQ-PKWREOPISA-N 0.000 description 22
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 20
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238000002360 preparation method Methods 0.000 description 19
FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical class C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 description 18
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ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 10
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JMTMSDXUXJISAY-UHFFFAOYSA-N 2H-benzotriazol-4-ol Chemical compound OC1=CC=CC2=C1N=NN2 JMTMSDXUXJISAY-UHFFFAOYSA-N 0.000 description 7
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JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 5
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NPZTUJOABDZTLV-UHFFFAOYSA-N hydroxybenzotriazole Substances O=C1C=CC=C2NNN=C12 NPZTUJOABDZTLV-UHFFFAOYSA-N 0.000 description 5
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125000001841 imino group Chemical group [H]N=* 0.000 description 5
REOJLIXKJWXUGB-UHFFFAOYSA-N mofebutazone Chemical group O=C1C(CCCC)C(=O)NN1C1=CC=CC=C1 REOJLIXKJWXUGB-UHFFFAOYSA-N 0.000 description 5
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