JPWO2022181563A5 - - Google Patents

Info

Publication number

JPWO2022181563A5

JPWO2022181563A5 JP2023502408A JP2023502408A JPWO2022181563A5 JP WO2022181563 A5 JPWO2022181563 A5 JP WO2022181563A5 JP 2023502408 A JP2023502408 A JP 2023502408A JP 2023502408 A JP2023502408 A JP 2023502408A JP WO2022181563 A5 JPWO2022181563 A5 JP WO2022181563A5

Authority

JP

Japan

Prior art keywords

group

liquid composition

photocurable liquid

formula

composition according

Prior art date

2022-02-21

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

Links

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• 239000007788 liquid Substances 0.000 claims description 34
• 239000000178 monomer Substances 0.000 claims description 24
• -1 nitrogen-containing compound Chemical class 0.000 claims description 22
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 10
• 125000004432 carbon atom Chemical group C* 0.000 claims description 8
• 229910044991 metal oxide Inorganic materials 0.000 claims description 8
• 150000004706 metal oxides Chemical class 0.000 claims description 8
• 239000002105 nanoparticle Substances 0.000 claims description 8
• 150000001875 compounds Chemical class 0.000 claims description 6
• 150000002466 imines Chemical class 0.000 claims description 6
• 125000000962 organic group Chemical group 0.000 claims description 6
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
• 125000000217 alkyl group Chemical group 0.000 claims description 4
• 125000002947 alkylene group Chemical group 0.000 claims description 4
• 239000003999 initiator Substances 0.000 claims description 4
• 238000000465 moulding Methods 0.000 claims description 3
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
• NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 2
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
• 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 claims description 2
• 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 2
• 125000005843 halogen group Chemical group 0.000 claims description 2
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
• 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
• 229910052717 sulfur Inorganic materials 0.000 claims description 2
• 239000011593 sulfur Substances 0.000 claims description 2
• 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 claims description 2
• 125000003118 aryl group Chemical group 0.000 claims 4
• 150000007824 aliphatic compounds Chemical class 0.000 claims 1
• 238000004519 manufacturing process Methods 0.000 claims 1
• 125000001424 substituent group Chemical group 0.000 claims 1
• 238000000034 method Methods 0.000 description 8
• 238000000576 coating method Methods 0.000 description 4
• 239000011248 coating agent Substances 0.000 description 3
• 230000004807 localization Effects 0.000 description 2
• 230000000694 effects Effects 0.000 description 1
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
• 230000001771 impaired effect Effects 0.000 description 1
• 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
• 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
• 239000012528 membrane Substances 0.000 description 1
• 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
• 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
• 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
• 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
• 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
• 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
• 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
• 239000004014 plasticizer Substances 0.000 description 1
• 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
• 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
• 239000002904 solvent Substances 0.000 description 1
• 239000000758 substrate Substances 0.000 description 1
• 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
• 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1