Branched Polyorganosiloxanes And Related Curable Compositions, Methods, Uses, and Devices
US-2017130108-A1 · May 11, 2017 · US
US9944758B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9944758-B2 |
| Application number | US-201414766769-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 10, 2014 |
| Priority date | Feb 11, 2013 |
| Publication date | Apr 17, 2018 |
| Grant date | Apr 17, 2018 |
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A hydrosilylation process is used to prepare a clustered functional polyorganosiloxane. The clustered functional polyorganosiloxane comprises a reaction product of a reaction of a) a polyorganosiloxane having an average, per molecule, of at least 2 aliphatically unsaturated organic groups; b) a polyorganohydrogensiloxane having an average of 4 to 15 silicon atoms per molecule; and c) a reactive species having, per molecule at least 1 aliphatically unsaturated organic group and 1 or more radical curable groups selected from an acrylate group and a methacrylate group; in the presence of d) a hydrosilylation catalyst, and e) an isomer reducing agent. The weight percent of silicon bonded hydrogen atoms in component b) divided by the weight percent of aliphatically unsaturated organic groups in component a) (the SiH b /Vi a ratio) ranges from 4/1 to 20/1. The resulting clustered functional polyorganosiloxane is useful in a curable silicone composition for electronics applications.
Opening claim text (preview).
The invention claimed is: 1. A clustered functional polyorganosiloxane comprising a reaction product of a reaction of: a) a polyorganosiloxane having an average, per molecule, of at least 2 aliphatically unsaturated organic groups, b) a polyorganohydrogensiloxane having an average of 4 to 15 silicon atoms per molecule; and c) a reactive species having, per molecule, at least one aliphatically unsaturated organic group and one or more radical curable groups comprising acrylate groups, methacrylate groups, or combinations thereof; in the presence of d) a hydrosilylation catalyst and e) an isomer reducing agent; with the proviso that a weight percent of silicon bonded hydrogen atoms in component b)/weight percent of aliphatically unsaturated organic groups in component a) (the SiHb/Via ratio) ranges from 4/1 to 20/1 and the reaction product prepared by the process has more than one curable group at each molecular terminal of the polyorganosiloxane of component a); wherein the isomer reducing agent e) is added in an amount based on the total weight of the clustered functional polyorganosiloxane to produce at least a 10% reduction in the beta-addition of SiH groups of the polyorganosiloxane to the aliphatically unsaturated group of the reactive species c) in the clustered functional polyorganosiloxane reaction product as compared to a clustered functional polyorganosiloxane formed as the reaction product of components a), b) and c) in the presence of d) but in the absence of the isomer reducing agent e); wherein the isomer reducing agent e) comprises one or more carboxylic silyl esters or 2,6-Di-tert-butyl-4-(dimethylaminomethyl)phenol; and wherein the isomer reducing agent e) is added in an amount of 0.001 to 1 weight percent, based on the total weight of the clustered functional polyorganosilxoane. 2. The clustered functional polyorganosiloxane as set forth in claim 1 wherein the isomer reducing agent e) comprises one or more carboxylic silyl esters. 3. The clustered functional polyorganosiloxane as set forth in claim 1 wherein the isomer reducing agent e) comprises 2,6-Di-tert-butyl-4-(dimethylaminomethyl)phenol. 4. A curable silicone composition comprising: (I) a clustered functional polyorganosiloxane comprising a reaction product of a reaction of: a) a polyorganosiloxane having an average, per molecule, of at least 2 aliphatically unsaturated organic groups, b) a polyorganohydrogensiloxane having an average of 4 to 15 silicon atoms per molecule, and c) a reactive species having, per molecule at least one aliphatically unsaturated organic group and one or more radical curable groups comprising acrylate groups, methacrylate groups or combination thereof, in the presence of d) a hydrosilylation catalyst and e) an isomer reducing agent; with the proviso that a weight percent of silicon bonded hydrogen atoms in component b)/weight percent of aliphatically unsaturated organic groups in component a) (the SiHb/Via ratio) Page 3 of 11 wherein the isomer reducing agent e) is added in an amount based on the total weight of the clustered functional polyorganosiloxane to produce at least a 10% reduction in the beta-addition of SiH groups of the polyorganosiloxane a) to the aliphatically unsaturated group of the reactive species c) as compared to a clustered functional polyorganosiloxane formed in the absence of the isomer reducing agent e); and (II) a curing agent; and an iron oxide pigment. 5. The composition as set forth in claim 4 , where the composition is radiation curable, and the curing agent (II) comprises a radical initiator. 6. The composition as set forth in claim 4 , wherein the composition is thermal curable wherein the curing agent (II) comprises a thermal radical initiator, or wherein the composition is curable at room temperature wherein the curing agent (II) comprises an organoborane, or wherein the composition is curable via a redox reaction. 7. A process for producing a clustered functional polyorganosiloxane comprising: 1) concurrently reacting components comprising a) a polyorganosiloxane having an average, per molecule, of at least 2 aliphatically unsaturated organic groups, b) a polyorganohydrogensiloxane having an average of 4 to 15 silicon atoms per molecule, c) a reactive species having, per molecule at least one aliphatically unsaturated organic group and one or more radical curable groups comprising acrylate groups, methacrylate groups, or combinations thereof; in the presence of d) a hydrosilylation catalyst and e) an isomer reducing agent; with the proviso that a weight percent of silicon bonded hydrogen atoms in component b)/weight percent of aliphatically unsaturated organic groups in component a) (the SiH b /Vi a ratio) ranges from 4/1 to 20/1 and the reaction product prepared by the process has more than one curable group at each molecular terminal of the polyorganosiloxane of component a), wherein the isomer reducing agent e) is added in an amount based on the total weight of the clustered functional polyorganosiloxane to produce at least a 10% reduction in the beta-addition of SiH groups of the polyorganosiloxane a) to the aliphatically unsaturated group of the reactive species c) as compared to a clustered functional polyorganosiloxane formed in the absence of the isomer reducing agent e); wherein the isomer reducing agent e) comprises one or more carboxylic silyl esters or 2,6-Di-tert-butyl-4-(dimethylaminomethyl)phenol, and wherein the isomer reducing agent e) is added in an amount of 0.001 to 1 weight percent, based on the total weight of the clustered functional polyorganosilxoane. 8. A process for producing a clustered functional polyorganosiloxane comprising: 1) concurrently reacting components comprising a) a polyorganosiloxane having an average, per molecule, of at least 2 aliphatically unsaturated organic groups, and b) a polyorganohydrogensiloxane having an average, per molecule, of 4 to 15 silicon atoms and at least 4 silicon bonded hydrogen atoms per aliphatically unsaturated organic group in component a) (the SiH b /Vi a ratio), where component b) is present in an amount sufficient to provide 1 molecule of component b) per each aliphatically unsaturated organic group of component a), in the presence of d) a hydrosilylation catalyst to form a product; and thereafter 2) reacting the product of step 1) with a component comprising: c) a reactive species having, per molecule at least one aliphatically unsaturated organic group and 1 or more radical curable groups comprising acrylate groups, methacrylate groups or combinations thereof, in the presence of e) an isomer reducing agent; with the proviso that a weight percent of silicon bonded hydrogen atoms in component b)/weight percent of aliphatically unsaturated organic groups in component a) ranges from 4/1 to 20/1 and the reaction product prepared by the process has more than one curable group at each molecular terminal of the polyorganosiloxane a), wherein the isomer reducing agent e) is added in an amount based on the total weight of the clustered functional polyorganosiloxane to produce at least a 10% reduction in the beta-addition of SiH groups of the polyorganosiloxane a) to the aliphatically unsaturated group of the reactive species c) as compared to a clustered functional polyorganosiloxane formed in the absence of the isomer reducing agent e); wherein the isomer reducing agent e) comprises one or more carboxylic silyl esters or 2,6-Di-tert-butyl-4-(dimethylaminomethyl)phenol and wherein the isomer reducing agent e) is added in an amount of 0.001 to 1 weight percent, based on the total weight of the clustered functional polyorganosilxoane. 9. The process of claim 7 further comprising step 3) adding a catalyst inhibitor and optionally step 4)
containing silicon bound to hydrogen · CPC title
containing silicon bound to oxygen-containing groups (C08L83/12 takes precedence) · CPC title
Preparatory processes · CPC title
containing silicon bound to unsaturated aliphatic groups · CPC title
of metals · CPC title
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