Method for the preparation of organopolysiloxanes having (meth)acrylate functions
US-2019135983-A1 · May 9, 2019 · US
US12442039B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12442039-B2 |
| Application number | US-202318400702-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 29, 2023 |
| Priority date | Jul 20, 2018 |
| Publication date | Oct 14, 2025 |
| Grant date | Oct 14, 2025 |
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An example of a resin composition includes a free radical curable resin matrix including an acrylate and a siloxane, and a free radical photoinitiator. When cured, the resin composition has low or no autofluorescence when exposed to blue excitation wavelengths ranging from about 380 nm to about 480 nm or green excitation wavelengths ranging from about 510 nm to about 560 nm.
Opening claim text (preview).
What is claimed is: 1. A resin composition, consisting of: a free radical curable resin matrix including an acrylate and a siloxane; a free radical photoinitiator selected from the group consisting of 2,2-dimethoxy-2-phenylacetophenone, a blend of diphenyl(2,4,6-trimethylbenzoyl) phosphine oxide and 2-hydroxy-2-methylpropiophenone, phenylbis(2,4,6-trimethylbenzoyl) phosphine oxide, ethyl(2,4,6-trimethylbenzoyl)phenylphosphinate, and combinations thereof; and a solvent; wherein, when cured, the resin composition has low or no autofluorescence when exposed to blue excitation wavelengths ranging from about 380 nm to about 480 nm or green excitation wavelengths ranging from about 510 nm to about 560 nm, and wherein the free radical curable resin matrix is an acryloxypropyl methylsiloxane homopolymer having a structure: wherein m is 30 to 200. 2. The resin composition as defined in claim 1 , wherein the cured resin composition has low autofluorescence, and wherein the low autofluorescence corresponds with: a grey value of less than 25,000 when the cured resin composition is exposed to the blue excitation wavelengths; or a grey value of less than 5,000 when the cured resin composition is exposed to the blue excitation wavelengths; or with a grey value of less than 10,000 when the cured resin composition is exposed to the green excitation wavelengths; or a grey value of less than 2,500 when the cured resin composition is exposed to the green excitation wavelengths. 3. The resin composition as defined in claim 1 wherein a weight % ratio of the free radical curable resin matrix to the free radical photoinitiator ranges from about 99.8:0.2 to about 90:10. 4. A resin composition, consisting of: a free radical curable resin matrix including an acrylate and a siloxane; a free radical photoinitiator selected from the group consisting of 2,2-dimethoxy-2-phenylacetophenone, a blend of diphenyl(2,4,6-trimethylbenzoyl) phosphine oxide and 2-hydroxy-2-methylpropiophenone, phenylbis(2,4,6-trimethylbenzoyl) phosphine oxide, ethyl(2,4,6-trimethylbenzoyl)phenylphosphinate, and combinations thereof; a dark quencher selected from the group consisting of an azo dye, 4-dimethylaminobenzene-4′-carboxylic acid, dabcyl azide, dabsyl azide, disperse red 19, a black dye-based quencher, and combinations thereof; and a solvent, and wherein the free radical curable resin matrix is an acryloxypropyl methylsiloxane homopolymer having a structure: wherein m is 30 to 200. 5. A resin composition, consisting of: a free radical curable resin matrix including an acrylate and a siloxane, and being selected from the group consisting of 1,3-bis(3-methacryloxypropyl)tetramethyldisiloxane, methacryloxypropyl-terminated polydimethylsiloxane, tetramethyl tetrakis [3-acryloxypropyl]cyclotetrasiloxane, acryloxypropyl methylsiloxane homopolymer, and combinations thereof; a free radical photoinitiator selected from the group consisting of 2,2-dimethoxy-2-phenylacetophenone, a blend of diphenyl(2,4,6-trimethylbenzoyl) phosphine oxide and 2-hydroxy-2-methylpropiophenone, phenylbis(2,4,6-trimethylbenzoyl) phosphine oxide, ethyl(2,4,6-trimethylbenzoyl)phenylphosphinate, and combinations thereof; and a solvent; wherein, when cured, the resin composition has low or no autofluorescence when exposed to blue excitation wavelengths ranging from about 380 nm to about 480 nm or green excitation wavelengths ranging from about 510 nm to about 560 nm; and wherein the solvent is selected from the group consisting of propylene glycol monomethyl ether acetate, toluene, dimethyl sulfoxide, and tetrahydrofuran.
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