Chemically amplified positive resist composition and resist pattern forming process
US-12164231-B2 · Dec 10, 2024 · US
US11142592B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11142592-B2 |
| Application number | US-201716329987-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 4, 2017 |
| Priority date | Sep 7, 2016 |
| Publication date | Oct 12, 2021 |
| Grant date | Oct 12, 2021 |
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Polymerizable compositions are described which contain, as photoinitiator, at least one acyltin compound according to the general formula (I):
Opening claim text (preview).
The invention claimed is: 1. A polymerizable composition, comprising, (a) 0.001 to 5 wt.-% of at least one acyltin compound according to the general formula (I), as photoinitiator, (b) 10 to 99.999 wt.-% radically polymerizable binder, (c) 0 to 85 wt.-% filler and (d) 0 to 70 wt.-% additive(s), in each case relative to the total mass of the composition, in which the variables of formula (I) have the following meanings: R 1 , R 2 , R 3 independently of each other are in each case a group of the formula (II) an aromatic C 6-30 radical, which can be substituted by one or more cyclic, branched or linear C 1-20 -alkyl, C 1-20 -alkenyl, C 1-20 -alkoxy, C 1-20 -alkylthio or C 1-20 -alkenoxy radicals, wherein the named substituents themselves can be interrupted one or more times by —O —, —S — or —NR 9 - and/or can be substituted by one or more radically polymerizable groups and/or radicals R 10 , a cyclic, branched or linear C 1-20 -alkyl, C 1-20 -alkenyl, C 1-20 -alkoxy, C 1-20 -alkylthio, C 1-20 -alkenoxy or C 1-20 -acyloxy radical, which can be interrupted one or more times by —O—, —S — or —NR 9 - and/or can be substituted by one or more radically polymerizable groups and/or radicals R 10 , or a benzoyloxy radical, —H, trimethylsilyl, —OH, halogen or —CN, wherein R 1 and R 2 , taken together, can also represent a double-bonded oxygen or sulfur atom or, together with the Sn atom to which they are bonded, can form an aliphatic saturated or unsaturated ring which in addition to the Sn atom contains 2 to 6 carbon atoms and optionally one or more oxygen atoms, wherein one or more carbon atoms can be substituted by a double-bonded oxygen atom and/or the ring can be fused with an aromatic ring, R 4 , R 5 , R 6 , R 7 , R 8 independently of each other are in each case —H, a cyclic, branched or linear C 1-20 -alkyl, C 1-20 -alkenyl, C 1-20 -alkyloxy or C 1-20 -alkenoxy radical, which can be interrupted one or more times by —O—, —S — or —NR 9 - and/or can be substituted by one or more radically polymerizable groups and/or radicals R 10 , or —OR 9 , halogen, —SR 9 , —N(R 9 ) 2 , —CF 3 , —CN, —NO 2 , —COOR 9 or —CONHR 9 , R 9 is —H or a cyclic, branched or linear C 1-20 -alkyl or C 1-20 -alkenyl radical and R 10 is —OH, —C x F 2x+1 with x=1 to 20 or —[Si(CH 3 ) 2 ] y —CH 3 with y=1 to 20. 2. The polymerizable composition according to claim 1 , in which, in each case independently of each other, R 1 , R 2 , R 3 independently of each other are in each case a group of the formula (II), an aromatic C 6-15 radical, which can be substituted by one or more branched or linear C 1-12 -alkyl or C 1-12 -alkoxy radicals, wherein the named substituents themselves can be interrupted one or more times by —O— and/or can be substituted by one or more radically polymerizable groups and/or —OH, or a branched or linear C 1-12 -alkyl, C 1-12 -alkenyl, C 1-12 -alkoxy, C 1-12 -alkylthio or C 1-12 -acyloxy radical, which can be interrupted one or more times by —O— and/or can be substituted by one or more radically polymerizable groups and/or —OH, or a benzoyloxy radical, trimethylsilyl, —OH, halogen or —CN, wherein R 1 and R 2 , taken together, can also represent a double-bonded oxygen or sulfur atom or, together with the Sn atom to which they are bonded, can form an aliphatic saturated or unsaturated ring which in addition to the Sn atom contains 2 to 6 carbon atoms and optionally one or more oxygen atoms, wherein one or more carbon atoms can be substituted by a double-bonded oxygen atom and/or the ring can be fused with an aromatic six-membered, ring, R 4 , R 5 , R 8 independently of each other are in each case —H, a branched or linear C 1-12 -alkyl, C 1-12 -alkenyl, C 1-12 -alkyloxy or C 1-12 -alkenoxy radical, which can be interrupted one or more times by —O— and/or can be substituted by one or more radically polymerizable groups and/or —OH, or —OR 9 , halogen, —SR 9 , —N(R 9 ) 2 , —CF 3 , —CN or —NO 2 , R 6 ,R 7 independently of each other are in each case —H or —F or a branched or linear C 1-12 -alkyl, C 1-12 -alkenyl, C 1-12 -alkyloxy or C 1-12 -alkenoxy radical, which can be interrupted one or more times by —O— and/or can be substituted by one or more radically polymerizable groups and/or —OH, and R 9 is —H or methyl. 3. The polymerizable composition according to claim 1 , in which, in each case independently of each other, R 1 , R 2 , R 3 independently of each other are in each case a group of the formula (II), phenyl, trimethylphenyl, a branched or linear C 1-8 -alkyl, C 1-12 -alkylthio or C 1-12 -acyloxy radical, a benzoyloxy, vinyl or methacryloyl radical, trimethylsilyl, —OH, —Cl or —CN, wherein R 1 and R 2 , taken together, can also represent a double-bonded oxygen or sulfur atom or, together with the Sn atom to which they are bonded, can form a dioxastannepin ring, wherein one or two carbon atoms of the dioxastannepin ring can be substituted by a double-bonded oxygen atom and/or the ring can be fused with a benzene ring, R 4 , R 5 , R 8 independently of each other are in each case —H, a branched or linear C 1-8 -alkyl radical, which can be interrupted by 1 to 3 O atoms and/or can be substituted by vinyl, or —OR 9 , halogen, —SR 9 , —N(R 9 ) 2 , —CF 3 , —CN or —NO 2 , R 6 , R 7 independently of each other are in each case —H, —F or a branched or linear C 1-8 -alkyl radical, which can be interrupted by 1 to 3 O atoms and/or can be substituted by vinyl, and R 9 is —H or methyl. 4. The polymerizable composition according to claim 1 , in which, in each case independently of each other, R 1 , R 2 , R 3 independently of each other are in each case a group of the formula (II), phenyl, a linear C 1 -C 8 -alkyl radical or trimethylsilyl, R 4 , R 5 , R 8 independently of each other are in each case —H, methyl, —OR 9 or —F, R 6 , R 7 independently of each other are in each case —H or —F and R 9 is —H or methyl. 5. The polymerizable composition according to claim 1 , comprising at least one radically polymerizable monomer and/or prepolymer as the at least one polymerizable binder. 6. The polymerizable composition according to claim 5 , comprising at least one mono- or multifunctional (meth)acrylate or a mixture thereof as the at least one polymerizable binder. 7. The polymerizable composition according to claim 1 for use as dental material. 8. The polymerizable composition according to claim 7 for intraoral use as cement, filling composite or veneering material. 9. The polymerizable composition according to claim 1 for use as dental cement, comprising (a) 0.001 to 5 wt.-% acyltin compound(s) of the general formula (I), (b) 10 to 50 wt.-% radically polymerizable binder, (c) 40 to 70 wt.-% filler and (d) 0 to 5 wt.-% additive(s). 10. The polymerizable composition according to claim 1 for use as dental composite, comprising (a) 0.001 to 5 wt.-% acyltin compound(s) of the general formula (I), (b) 10 to 40 wt.-% radically polymerizable binder, (c) 50 to 85 wt.-% filler and (d) 0 to 5 wt.-% additive(s). 11. The polymerizable composition according to claim 1 for use as dental coating material, comprising (a) 0.001 to 5 wt.-% acyltin compound(s) of the general formula (I), (b) 10 to 99.989 wt.-% radically polymerizable binder, (c) 0 to 20 wt.-% nanoparticulate filler, (d) 0.01 to 2 wt.-% additive(s) and (e) 0 to 70 wt.-% solvent. 12.
with sensitising agents · CPC title
Organo-tin compounds · CPC title
Compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds · CPC title
Nanostructured additives · CPC title
Photochemical radical initiators · CPC title
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