Silyl (meth)acrylate compound containing a siloxy group having a bulky substituent and its production method
A silyl (meth)acrylate compound containing a siloxy group having a bulky substituent is provided. The compound is represented by the following general formula (1): wherein R 1 and R 2 are independently a C 3-10 monovalent branched hydrocarbon group having a hydrocarbon group at α or β position or a monovalent C 3-10 cyclic hydrocarbon group; R 3 , R 4 , and R 5 are independently an unsubstituted or substituted C 1-20 hydrocarbon group or a siloxy group represented by the following general formula (2): —OSiR 7 R 8 R 9 (2) wherein R 7 , R 8 , and R 9 are independently an unsubstituted or substituted C 1-20 hydrocarbon group; and R 6 is hydrogen atom or methyl group. This compound is hydrolyzed at a reduced speed, and use of a polymer obtained by copolymerization with an alkyl methacrylate is capable of suppressing attachment of marine organisms to the ship with no or reduced biocide, and this polymer is useful for a hydrolytic self-polishing paint.
1. A silyl (meth)acrylate compound containing a siloxy group having a bulky substituent represented by the following general formula (1):
wherein R 1 and R 2 are independently a monovalent branched hydrocarbon group containing 3 to 10 carbon atoms having a hydrocarbon group at α or β position or a monovalent cyclic hydrocarbon group containing 3 to 10 carbon atoms; R 3 , R 4 , and R 5 are independently an unsubstituted or substituted hydrocarbon group containing 1 to 20 carbon atoms or a siloxy group represented by the following general formula (2):
—OSiR 7 R 8 R 9 (2)
wherein R 7 , R 8 , and R 9 are independently an unsubstituted or substituted hydrocarbon group containing 1 to 20 carbon atoms; and R 6 is hydrogen atom or methyl group.
2. A silyl (meth)acrylate compound containing a siloxy group according to claim 1 wherein R 1 and R 2 in the general formula (1) are independently isopropyl group or sec-butyl group.
3. A silyl (meth)acrylate compound containing a siloxy group according to claim 1 wherein R 3 , R 4 , and R 5 in the general formula (1) are independently methyl group or trimethylsiloxy group.
4. A method for producing the silyl (meth)acrylate compound containing a siloxy group of claim 1 comprising the step of reacting a chlorosilane compound containing a siloxy group having a bulky substituent represented by the following general formula (3):
wherein R 1 and R 2 are independently a monovalent branched hydrocarbon group containing 3 to 10 carbon atoms having a hydrocarbon group at α or β position or a monovalent cyclic hydrocarbon group containing 3 to 10 carbon atoms, and R 3 , R 4 , and R 5 are independently an unsubstituted or substituted hydrocarbon group containing 1 to 20 carbon atoms or a siloxy group represented by the following general formula (2):
—OSiR 7 R 8 R 9 (2)
wherein R 7 , R 8 , and R 9 are independently an unsubstituted or substituted hydrocarbon group containing 1 to 20 carbon atoms with acrylic acid or methacrylic acid in the presence of a basic compound.
5. A method for producing a silyl (meth)acrylate compound containing a siloxy group according to claim 4 wherein a phase transfer catalyst is used.
6. A method for producing a silyl (meth)acrylate compound containing a siloxy group according to claim 4 wherein 0.5 to 2.0 mole of the chlorosilane compound of the general formula (3) is reacted per mole of the acrylic acid or methacrylic acid, and the reaction is conducted at temperature of −20° C. to 200° C.