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    • 2. 发明授权
    • Process for the manufacturing of acrylic organopolysiloxanes
    • 制备丙烯酸有机聚硅氧烷的方法
    • US5292849A
    • 1994-03-08
    • US997485
    • 1992-12-28
    • Kazutoshi FujiokaTakafumi SakamotoMasatoshi Arai
    • Kazutoshi FujiokaTakafumi SakamotoMasatoshi Arai
    • C07F7/18C08F290/00C08F299/08C08G77/20C08G77/38C08G77/06
    • C08G77/20
    • This invention enables the selective and easy manufacturing of acrylic organopolysiloxanes which are cured by the irradiation of UV light, by the reaction of the hydroxyl group containing organosilicon compounds (A) of formula (1): ##STR1## wherein each R.sup.1 independently is a substituted or an unsubstituted monovalent hydrocarbon group, and n designates integers from 1 to 10,000 with the acrylic group containing silane compounds (B) of formula (2): ##STR2## wherein each R.sup.2 and R.sup.3 independently is a substituted or an unsubstituted monovalent hydrocarbon group, R.sup.4 is either a hydrogen atom or a methyl group, and each of a and b is an integer from 1 to 3, in the presence of a divalent tin compound of formula (3):SnX.sub.2wherein each X independently is a halogen atom, alkoxy group, or a residue of a carboxyl group, in order to produce the acrylic organopolysiloxanes of formula (4): ##STR3## wherein R.sup.1 through R.sup.4, n, a and b are described as above.
    • 本发明能够通过含羟基的式(1)的有机硅化合物(A):(*化学结构*)(1)的反应,使紫外光的照射固化的丙烯酸有机聚硅氧烷的选择性和容易制造,其中 每个R 1独立地是取代或未取代的单价烃基,n表示1至10,000的整数,其中丙烯酸基含有式(2)的硅烷化合物(B):(*化学结构*)(2)其中每个R 2和 R3独立地为取代或未取代的单价烃基,R4为氢原子或甲基,a和b各自为1〜3的整数,在式(3)的二价锡化合物的存在下, :其中每个X独立地是卤素原子,烷氧基或羧基的残基,以便制备式(4)的丙烯酸有机聚硅氧烷:(*化学结构*)(4)其中R1至R4,n ,a和b是描述 如上所述。
    • 3. 发明授权
    • Acrylic-functional organopolysiloxane and method for the preparation
thereof
    • 丙烯酸官能的有机聚硅氧烷及其制备方法
    • US5391677A
    • 1995-02-21
    • US105164
    • 1993-08-12
    • Masatoshi AraiTakafumi SakamotoKazutoshi Fujioka
    • Masatoshi AraiTakafumi SakamotoKazutoshi Fujioka
    • C07F7/08C08G77/20C08G77/40
    • C07F7/0859C07F7/0852C08G77/20
    • A novel acrylic-functional organopolysiloxane is proposed which has a plural number of silicon-bonded (meth)acryloxyalkyl groups at each molecular chain end along with one or more of silicon-bonded alkoxy groups. The organopolysiloxane exhibits high curability by the irradiation with ultraviolet light or dual curability either by the ultraviolet irradiation or by the dealcoholation condensation reaction in a moisture-containing atmosphere. The acrylic-functional organopolysiloxane is prepared by the dealcoholation condensation reaction between a starting organopolysiloxane having a plural number of silicon-bonded alkoxy groups at each molecular chain end and a (meth)acryloxyalkyl dimethyl silanol compound in the presence of a specific condensation catalyst which is a divalent tin compound such as tin (II) dioctoate promoting the dealcoholation condensation but suppressing the silanol condensation reaction between the moleculaes of the (meth)acryloxyalkyl dimethyl silanol compound.
    • 提出了一种新的丙烯酸官能的有机聚硅氧烷,其在每个分子链端具有多个硅键合的(甲基)丙烯酰氧基烷基以及一个或多个与硅键合的烷氧基。 有机聚硅氧烷通过紫外线照射或通过紫外线照射或通过在含水气氛中的脱醇缩合反应的双重固化性,显示出高的固化性。 丙烯酸官能的有机聚硅氧烷是通过在各分子链末端具有多个与硅键合的烷氧基的起始有机聚硅氧烷与(甲基)丙烯酰氧基烷基二甲基硅烷醇化合物在特定的缩合催化剂存在下的脱醇缩合反应来制备的, 二异辛基锡化合物如二辛酸锡(II),促进脱醇缩合,但抑制(甲基)丙烯酰氧基烷基二甲基硅烷醇化合物的分子之间的硅烷醇缩合反应。
    • 7. 发明授权
    • 2-trimethoxysilylpropionate
    • 2-三甲氧基甲硅烷基丙酸酯
    • US5286892A
    • 1994-02-15
    • US985868
    • 1992-12-04
    • Masatoshi AraiTakafumi SakamotoYoshifumi InoueKei Miyoshi
    • Masatoshi AraiTakafumi SakamotoYoshifumi InoueKei Miyoshi
    • C07F7/04C07F7/18C09K3/00C07F7/08
    • C07F7/045C07F7/1836
    • The present novel organosilicon compound is a 2-trimethoxysilylpropionate represented by the following formula ##STR1## wherein R represents a monovalent hydrocarbon group having 6 to 12 carbon atoms. This ester reacts efficiently with alcohols and silanols and is useful, for example, as a terminal alkoxysilylating agent for organopolysiloxanes such as industrially useful .alpha.,.omega.-dihydroxypolydimethylsiloxane, or as a surface treatment for silicas, or as a storage stabilizer that serves as a scavenger of an alcohol for alcohol elimination type RTV. Further, since the present organosilicon compound is a three-functional alkoxysilane having three methoxy groups in the molecule, it is useful as a curing agent for alcohol elimination type RTV.
    • 本发明的新型有机硅化合物是由下式(*化学结构*)表示的2-三甲氧基甲硅烷基丙酸酯,其中R表示碳原子数为6〜12的一价烃基。 该酯与醇和硅烷醇有效反应,并且可用作例如工业上有用的(α),(ω) - 二羟基聚二甲基硅氧烷的有机聚硅氧烷的末端烷氧基硅烷化剂,或作为二氧化硅的表面处理或作为储存稳定剂 作为酒精消除型RTV的酒精清除剂。 此外,由于本发明的有机硅化合物是分子中具有三个甲氧基的三官能烷氧基硅烷,因此可用作醇消除型RTV的固化剂。
    • 10. 发明授权
    • Fluorine-containing organosilicon compound and its manufacture
    • 含氟有机硅化合物及其制造方法
    • US5461173A
    • 1995-10-24
    • US364448
    • 1994-12-27
    • Shinichi SatoTakashi MatsudaTakafumi SakamotoMasatoshi Arai
    • Shinichi SatoTakashi MatsudaTakafumi SakamotoMasatoshi Arai
    • C07F7/08C07F7/10C07F7/18
    • C07F7/0859C07F7/0852
    • A fluorine-containing organosilicon compound represented by the following general formula (1): ##STR1## wherein Rf represents a perfluoroalkyl group, a perfluorooxyalkyl group, a perfluoroalkylene group, or a perfluorooxyalkylene group, A represents a bivalent organic group, R.sup.1 represents an unsubstituted or substituted monovalent hydrocarbon group, X represents a hydrolyzable group, Y is 1 in the case where the above group Rf represents a perfluoroalkyl group or a perfluorooxyalkyl group or Y is 2 in the case where the above group Rf represents a perfluoroalkylene group or a perfluorooxyalkylene group, m is an integer of 0 to 2, and n is an integer of 1 to 3, with m+n being 3 or less. Since this compound has an acryloyloxy group(s), the compound when irradiated with ultraviolet light can be easily cured within a short period of time, for example, within about 1 to 2 min in the presence of a photopolymerization initiator.
    • 由以下通式(1)表示的含氟有机硅化合物:其中Rf表示全氟烷基,全氟氧烷基,全氟亚烷基或全氟氧化烯基,A表示二价有机基团,R1 表示未取代或取代的一价烃基,X表示可水解基团,在上述基团Rf表示全氟烷基或全氟氧烷基或Y为2的情况下,Y为1的情况下,上述基团R f表示全氟亚烷基 或全氟氧化烯基,m为0〜2的整数,n为1〜3的整数,m + n为3以下。 由于该化合物具有丙烯酰氧基,因此在光聚合引发剂存在下,紫外线照射时的化合物可以在短时间内例如约1〜2分钟内容易地固化。