Acid- and radical-generating agent and method for generating acid and radical
US-2016342084-A1 · Nov 24, 2016 · US
US10774062B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10774062-B2 |
| Application number | US-201716072794-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 25, 2017 |
| Priority date | Jan 26, 2016 |
| Publication date | Sep 15, 2020 |
| Grant date | Sep 15, 2020 |
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Step 2: this is a step in which in the presence of the compound (A) and (E) compound having a carbonyl group generating a radical by photoirradiation and a group generating a base by being decarboxylated by photoirradiation, the compound (A) and the compound (E) are irradiated with light to create alkaline conditions in a reaction system by decarboxylating the carboxyl group of the compound (A) and generating a base from the compound (E), and radicals are generated from the compound (A) and the compound (E) to generate a crosslinked product containing a constitutional unit derived from the silane compound (D) from the silane compound (D) and, if necessary, from (F) compound having two or more polymerizable unsaturated groups.
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The invention claimed is: 1. A photocuring method comprising a step 1 and a step 2 performed after the step 1; wherein in the step 1, in the presence of (A) compound having a carbonyl group generating a radical by photoirradiation and a carboxyl group decarboxylated by photoirradiation, (B) silane coupling agent having a mercapto group or a (meth)acryl group is reacted with (C) water under acidic conditions to obtain (D) silane compound having a mercapto group or a (meth)acryl group and at least one silanol group, and in the step 2, in the presence of the compound (A) and (E) compound having a carbonyl group generating a radical by photoirradiation and a group generating a base by being decarboxylated by photoirradiation, the compound (A) and the compound (E) are irradiated with light to create alkaline conditions in a reaction system by decarboxylating the carboxyl group of the compound (A) and generating a base from the compound (E), and radicals are generated from the compound (A) and the compound (E) to generate a crosslinked product containing a constitutional unit derived from the silane compound (D) from the silane compound (D) and, from (F) compound having two or more polymerizable unsaturated groups. 2. The photocuring method according to claim 1 , wherein the step 1 is performed at a pH in a range of 3 to 5. 3. The photocuring method according to claim 1 , wherein the step 2 is performed at a pH in a range of 8 to 14. 4. The photocuring method according to claim 1 , wherein the silane coupling agent (B) is (B′) silane coupling agent having a mercapto group, the silane compound (D) is (D′) silane compound having a mercapto group and at least one silanol group, and the crosslinked product obtained using the compound (F) further contains a constitutional unit derived from the compound (F). 5. The photocuring method according to claim 1 , wherein the silane coupling agent (B) is (B″) silane coupling agent having a (meth)acryl group, the silane compound (D) is (D″) silane compound having a (meth)acryl group and at least one silanol group, and the crosslinked product is obtained by reacting the silane compounds (D″) with each other. 6. The photocuring method according to claim 1 , wherein the compound (A) and compound (E) are (A/E) compound having a carbonyl group generating a radical by photoirradiation, a carboxyl group decarboxylated by photoirradiation, and a group generating a base by being decarboxylated by photoirradiation. 7. The photocuring method according to claim 1 , wherein the compound (A) and the compound (E) are decomposed by light having the same wavelength. 8. The photocuring method according to claim 1 , wherein the compound (A) is a compound represented by a general formula [1]; wherein R 1 to R 8 each independently represent a hydrogen atom, an alkyl group having 1 to 12 carbon atoms, an aryl group having 6 to 14 carbon atoms, an arylalkyl group having 7 to 15 carbon atoms, an alkoxy group having 1 to 12 carbon atoms, a halogen atom, a nitro group, a group represented by a general formula [2], or a group represented by a general formula [3], R 9 and R 10 each independently represent a hydrogen atom, an alkyl group having 1 to 12 carbon atoms, an aryl group having 6 to 14 carbon atoms, an arylalkyl group having 7 to 15 carbon atoms, an alkoxy group having 1 to 12 carbon atoms, a halogen atom, or a nitro group; or represent a state where R 9 and R 10 are bonded to each other through an oxygen atom, a sulfur atom, or a carbonyl group, provided that at least one of the groups represented by R 1 to R 8 is the group represented by the general formula [2]; wherein R 11 and R 12 each independently represent a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, or a hydroxyalkyl group having 1 to 6 carbon atoms; wherein Z 1 + represents an amidinium cation, a guanidium cation, a biguanidinium cation, or a phosphazenium cation, and R 13 and R 14 each independently represent a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, or a hydroxyalkyl group having 1 to 6 carbon atoms. 9. The photocuring method according to claim 1 , wherein the compound (A) is a compound represented by any of general formulae [1-A] to [1-C]; wherein R 2a , R 4a , R 5a , and R 7a each independently represent a hydrogen atom, an alkyl group having 1 to 12 carbon atoms, an aryl group having 6 to 14 carbon atoms, an arylalkyl group having 7 to 15 carbon atoms, an alkoxy group having 1 to 12 carbon atoms, a halogen atom, a nitro group, a group represented by a general formula [2], or a group represented by a general formula [3], R 1a , R 3a , R 6a , R 8a , R 9a , and R 10a each independently represent a hydrogen atom, an alkyl group having 1 to 12 carbon atoms, an aryl group having 6 to 14 carbon atoms, an arylalkyl group having 7 to 15 carbon atoms, an alkoxy group having 1 to 12 carbon atoms, a halogen atom, or a nitro group, provided that at least one of groups represented by R 2a , R 4a , R 5a , and R 7a is the group represented by the general formula [2]; wherein R 11 and R 12 each independently represent a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, or a hydroxyalkyl group having 1 to 6 carbon atoms; wherein Z 1 + represents an amidinium cation, a guanidium cation, a biguanidinium cation, or a phosphazenium cation, and R 13 and R 14 each independently represent a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, or a hydroxyalkyl group having 1 to 6 carbon atoms; wherein R 2b , R 4b , R 5b and R 7b each independently represent a hydrogen atom, an alkyl group having 1 to 12 carbon atoms, an aryl group having 6 to 14 carbon atoms, an arylalkyl group having 7 to 15 carbon atoms, an alkoxy group having 1 to 12 carbon atoms, a halogen atom, a nitro group, the group represented by the general formula [2], or the group represented by the general formula [3], R 1b , R 3b , R 6b , and R 8b each independently represent a hydrogen atom, and an alkyl group having 1 to 12 carbon atoms, an aryl group having 6 to 14 carbon atoms, an arylalkyl group having 7 to 15 carbon atoms, an alkoxy group having 1 to 12 carbon atoms, a halogen atom, or a nitro group, Y 1 represents an oxygen atom or a sulfur atom, provided that at least one of the groups represented by R 2b , R 4b , R 5b , and R 7b is the group represented by the general formula [2]; wherein R 1c to R 8c each independently represent a hydrogen atom, an alkyl group having 1 to 12 carbon atoms, an aryl group having 6 to 14 carbon atoms, an arylalkyl group having 7 to 15 carbon atoms, an alkoxy group having 1 to 12 carbon atoms, a halogen atom, a nitro group, the group represented by the general formula [2], or the group represented by the general formula [3], provided that at least one of the groups represented by R 1c to R 8c is the group represented by the general formula [2].
Photosensitive materials (G03F7/12, G03F7/14 take precedence) · CPC title
Oxygen atoms, e.g. xanthones · CPC title
containing six membered aromatic rings · CPC title
from polysiloxanes · CPC title
from mercapto compounds and unsaturated compounds · CPC title
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