JP2013529826A5 - - Google Patents

Info

Publication number

JP2013529826A5

JP2013529826A5 JP2013516787A JP2013516787A JP2013529826A5 JP 2013529826 A5 JP2013529826 A5 JP 2013529826A5 JP 2013516787 A JP2013516787 A JP 2013516787A JP 2013516787 A JP2013516787 A JP 2013516787A JP 2013529826 A5 JP2013529826 A5 JP 2013529826A5

Authority

JP

Japan

Prior art keywords

substituted

liquid composition

curable liquid

formula

layer

Prior art date

2011-06-24

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
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• 238000000034 method Methods 0.000 claims 15
• 239000000758 substrate Substances 0.000 claims 12
• 239000007788 liquid Substances 0.000 claims 10
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 6
• 125000000217 alkyl group Chemical group 0.000 claims 6
• 229910052739 hydrogen Inorganic materials 0.000 claims 6
• 239000001257 hydrogen Substances 0.000 claims 6
• NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 4
• LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 3
• 125000003118 aryl group Chemical group 0.000 claims 2
• 125000004432 carbon atom Chemical group C* 0.000 claims 2
• 150000001875 compounds Chemical class 0.000 claims 2
• 125000000392 cycloalkenyl group Chemical group 0.000 claims 2
• 125000000753 cycloalkyl group Chemical group 0.000 claims 2
• 238000012682 free radical photopolymerization Methods 0.000 claims 2
• 125000001183 hydrocarbyl group Chemical group 0.000 claims 2
• 239000003999 initiator Substances 0.000 claims 2
• 239000002184 metal Substances 0.000 claims 2
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
• -1 n- butyl Chemical group 0.000 claims 2
• DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 claims 1
• NQIJAAURIDJBPB-UHFFFAOYSA-N 2-cyclopentyloxyethoxycyclopentane Chemical compound C1CCCC1OCCOC1CCCC1 NQIJAAURIDJBPB-UHFFFAOYSA-N 0.000 claims 1
• 125000002947 alkylene group Chemical group 0.000 claims 1
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
• 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 1
• 238000013500 data storage Methods 0.000 claims 1
• 230000001678 irradiating effect Effects 0.000 claims 1
• 125000001624 naphthyl group Chemical group 0.000 claims 1
• 230000003287 optical effect Effects 0.000 claims 1
• 238000000059 patterning Methods 0.000 claims 1
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
• 229920000642 polymer Polymers 0.000 claims 1
• 230000001568 sexual effect Effects 0.000 claims 1