Abstract: The present invention relates to (2-arylpropyl)silanes represented by the formula (III) and a process for the preparation of the formula (III) by the Friedel-Crafts alkylation of various substituted aromatic compounds represented by the formula (I) with allylchlorosilanes as represented by the formula (II) in the presence of Lewis acid catalysts such as aluminum chloride. ##STR1## In the formulas (I) and (III), R and R' represent independently hydrogen, alkyl (C.sub.1 -C.sub.4), phenoxy, fluoro, chloro, bromo, mercapto, mercaptomethyl and Ar represents phenyl ring, naphthalene ring, or biphenyl ring. X.sup.1, X.sup.2, and X.sup.3 represent hydrogen or chloro group; and wherein formula (III) according to the present invention specifically excludes the compounds of the general formula (III) in which X.sup.1, X.sup.2 and X.sup.3 are all chloro group, and R is hydrogen and R' is hydrogen, chloro or bromo, and X.sup.1 is hydrogen and X.sup.2 and X.sup.3 are all chloro, and R and R' are all hydrogen.

Abstract: The novel compounds of 1-aryl-1-[.alpha.-(triazolyl]alkyl]-1-silacycloalkanes of the following formula I and their preparation are provided. The compounds of the present invention are useful in controlling fungal diseases of living plants. ##STR1## wherein R.sub.1 can be 4- or 2,4-substituted phenyl such as 4-fluorophenyl, 4-chlorophenyl, 4-ethoxyphenyl, 4-methoxyphenyl, 4-trifluoromethylphenyl, biphenyl, 2,4-difluorophenyl, and 2,4-dichlorophenyl and R.sub.2 can be hydrogen or methyl and n is 4 or 5.

Abstract: The present invention relates to novel cyclic or linear 2-(aryl)propylalkylpolysiloxane type silicone fluids as represented by the formula I and their preparation methods by hydrolyzing mixtures of 2-(aryl)propylalkyldichlorosilane and diorganodichlorosilane as represented by the formula II and formula III respectively. ##STR1## wherein, X.sub.1 and X.sub.2 represent independently hydrogen or alkyl(C.sub.1 -C.sub.3), phenyl, phenoxy, fluoro, chloro, bromo, mercapto, mercaptomethyl group; R.sup.2 and R.sup.3 represent independently methyl or phenyl group; R.sup.1 in the formula I is same as CH.sub.2 CH.sub.2 R in formula II or cyclohexyl wherein R is C.sub.n H.sub.2n+2 (n=1-16), chloromethylene, cyanomethylene, phenyl, or cyano group; M represents H or SiMe.sub.3 group wherein Me is methyl group and when M is hydrogen, the silanol groups at the both ends of the molecule easily undergo dehydration and cyclize to form the cyclic silicone fluids; n and m can be 2-200 and the ratio n/m can be 1:0.01-1:100.

Abstract: The present invention relates to novel cyclic or linear allylpolysiloxane type silicone fluids having allylalkylsiloxy and diorganosiloxy groups as represented by the formula I and their preparation methods by hydrolyzing mixtures of allyldichlorosilane and diorganodichlorosilane as represented by the formula II and formula III respectively. ##STR1## wherein R is selected from the group consisting of hydrogen alkyl(C.sub.3 -C.sub.20), chloroalkyl, cyanoalkyl, fluoroalkyl, and phenylalkyl group; R.sup.x and R.sup.2 represent independentlhydrogen, methyl or phenyl group; M represents H or SiMe.sub.3 group wherein Me is methyl group and when M is hydrogen, the silanol groups at the both ends of the molecule easily undergo dehydration and cyclize to form the cyclic silicone fluids as represented by the following formula I'; the mixing ratio (x/y) of the compounds as represented in formula I and formula HI respectively can be 1:0.01-1:100; CH.sub.2 CH.sub.2 R.sup.3 of formula II equals to R of formula I or I'.

Abstract: The present invention relates to allylakylsilanes represented by the general formula (III) and their preparation methods by reacting allylsilanes represented by the formula I with olefin compounds represented by the formula II in the presence of hydrosilation catalysts such as chloroplatinic acid, platinum on silica, tributyl amine and Pd, Rh, Ni metals. ##STR1## wherein X represents independently chloro or alkoxy (C.sub.1-C.sub.4) and R is selected from the group consisting of Ph, CH.sub.2 Cl, C.sub.n H.sub.2n CH.sub.3 (n=0-15), Si(Me).sub.m Cl.sub.3-m (m=0-3), CF.sub.3, CH.sub.2 CF.sub.3, CN, CH.sub.2 CN, ##STR2## CH.sub.2 Si(Me).sub.m CL.sub.3-m (m=0-3), Si(Me).sub.m (OR.sup.1).sub.3-m (m=0-3), CH.sub.2 Si(Me).sub.m (OR.sup.1).sub.3-m (m=0-3), (wherein Me is methyl and R.sup.1 is methoxy or ethoxy group), Ph-CH.sub.2 Cl, and cyclohexenyl group.

Abstract: The present invention relates to novel 2-(aryl)hydrogenpolysiloxane type silicone fluids as represented by the formula I and their preparation methods by hydrolyzing mixtures of 2-(aryl)hydrogendichlorosilane and diorganodichlorosilane as represented by the formula II and formula III respectively. ##STR1## wherein X.sup.1 and X.sup.2 represent independent hydrogen or alkyl (C.sub.1 -C.sub.3), phenyl, phenoxy, fluoro, chloro, bromo, mercapto, mercaptomethyl group; R.sup.1 and R.sup.2 represent independently methyl or phenyl group; M represents H or SiMe.sub.3 group wherein Me represents methyl and when M is hydrogen, the silanol groups at the both ends of the molecule easily undergo dehydration so that they can cyclize to form the cyclic silicone fluids. The mixing ratio (x/y) of the compounds as represented in formula II and formula III respectively can be 1:0.01-1:100.

Abstract: The present invention relates to a process for preparing (2-arylpropyl)alkylsilanes represented by the formula III by reacting (2-arylpropyl)silanes represented by the formula I with olefin compounds represented by the formula II in the presence of hydrosilation catalysts such as chloroplatanic acid, platinum on silica, tributylamine and Pd, Rh, Ni metals. ##STR1## Olefin compounds(cyclohexene or CH.sub.2 =CH--R.sup.3) (II) ##STR2## In the formulas (I) and (III), R.sup.1 and R.sup.2 represent independently hydrogen, alkyl(C.sub.1 -C.sub.4), fluoro, chloro or bromo; and Ar represents phenyl ring, naphthalene ring, or biphenyl ring. X represents hydrogen or chloro group. In the formula (III), R represents --(CH.sub.2 CH.sub.2)--R.sup.3, sec-butyl, or cyclohexyl wherein R.sup.3 =Ph, CH.sub.2 Cl, C.sub.n H.sub.2n CH.sub.3 (n=0-15), CH.sub.2 Si(Me).sub.m Cl.sub.3-m (m=O-3), (CH.sub.2).sub.2 Si(Me).sub.m (OMe).sub.3-m (m=O-3), (CH.sub.2).sub.3 Si(Me).sub.m (OMe).sub.3-m (m=O-3), Si(Me).sub.m Cl.sub.3-m (m=0-3), CF.

Abstract: Alkenylchlorosilane of formula I and a direct synthesis thereof are disclosed, wherein silicon metal is reacted with mixed gas comprising alkenyl chloride of formula II and hydrogen chloride or alkyl chloride of formula III in the presence of copper catalyst at a temperature range from 220.degree. C. to 350.degree. C. ##STR1## In formula I, R.sub.1 represents hydrogen, methyl, SiHCl.sub.2, SiCl.sub.3 or CH.sub.2 SiCl.sub.3 and R.sub.2 represents hydrogen or chlorine. ##STR2## In formula II, R.sub.3 represents hydrogen or chlorine and R.sub.2 represents hydrogen, methyl or CH.sub.2 Cl.Cl--R.sub.5 (III)In formula III, R.sub.5 represents hydrogen, C.sub.1 -C.sub.4 alkyl or CH.sub.2 CH.sub.2 Cl.