JP2011021151A5 - - Google Patents

Info

Publication number

JP2011021151A5

JP2011021151A5 JP2009169104A JP2009169104A JP2011021151A5 JP 2011021151 A5 JP2011021151 A5 JP 2011021151A5 JP 2009169104 A JP2009169104 A JP 2009169104A JP 2009169104 A JP2009169104 A JP 2009169104A JP 2011021151 A5 JP2011021151 A5 JP 2011021151A5

Authority

JP

Japan

Prior art keywords

meth

acrylic copolymer

group

ethylenically unsaturated

unsaturated monomer

Prior art date

2009-07-17

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.)

Granted

Links

• Espacenet
• Global Dossier
• Discuss

• 239000000178 monomer Substances 0.000 claims description 14
• -1 thiol compound Chemical class 0.000 claims description 7
• 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims description 6
• NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 2
• 229920006243 acrylic copolymer Polymers 0.000 claims 14
• 229920005989 resin Polymers 0.000 claims 10
• 239000011347 resin Substances 0.000 claims 10
• 238000004519 manufacturing process Methods 0.000 claims 9
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 5
• 125000002723 alicyclic group Chemical group 0.000 claims 5
• 125000001931 aliphatic group Chemical group 0.000 claims 5
• 125000004432 carbon atom Chemical group C* 0.000 claims 5
• 125000004122 cyclic group Chemical group 0.000 claims 5
• 229910052739 hydrogen Inorganic materials 0.000 claims 5
• 239000001257 hydrogen Substances 0.000 claims 5
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
• 239000000203 mixture Substances 0.000 claims 5
• 239000003795 chemical substances by application Substances 0.000 claims 4
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 3
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
• IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims 3
• 239000011248 coating agent Substances 0.000 claims 2
• MPIAGWXWVAHQBB-UHFFFAOYSA-N [3-prop-2-enoyloxy-2-[[3-prop-2-enoyloxy-2,2-bis(prop-2-enoyloxymethyl)propoxy]methyl]-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(COC(=O)C=C)(COC(=O)C=C)COCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C MPIAGWXWVAHQBB-UHFFFAOYSA-N 0.000 claims 1
• 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 claims 1
• 229920006026 co-polymeric resin Polymers 0.000 claims 1
• 238000000576 coating method Methods 0.000 claims 1
• 150000001875 compounds Chemical class 0.000 claims 1
• 230000009477 glass transition Effects 0.000 claims 1
• 239000003999 initiator Substances 0.000 claims 1
• 230000001678 irradiating effect Effects 0.000 claims 1
• 238000010526 radical polymerization reaction Methods 0.000 claims 1
• 125000003396 thiol group Chemical group [H]S* 0.000 claims 1
• 0 C*CC(C)(C)CC(*)(CC(C)(*)*)[N+]([O-])O**(*)N(N)O[N+]([N+](*)[N-])[O-] Chemical compound C*CC(C)(C)CC(*)(CC(C)(*)*)[N+]([O-])O**(*)N(N)O[N+]([N+](*)[N-])[O-] 0.000 description 2
• RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 2
• FYYIUODUDSPAJQ-UHFFFAOYSA-N 7-oxabicyclo[4.1.0]heptan-4-ylmethyl 2-methylprop-2-enoate Chemical compound C1C(COC(=O)C(=C)C)CCC2OC21 FYYIUODUDSPAJQ-UHFFFAOYSA-N 0.000 description 1
• DPTGFYXXFXSRIR-UHFFFAOYSA-N 7-oxabicyclo[4.1.0]heptan-4-ylmethyl prop-2-enoate Chemical compound C1C(COC(=O)C=C)CCC2OC21 DPTGFYXXFXSRIR-UHFFFAOYSA-N 0.000 description 1
• VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
• 230000011987 methylation Effects 0.000 description 1
• 238000007069 methylation reaction Methods 0.000 description 1