1993
DOI: 10.1016/s0040-4039(00)60358-1
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Polyfunctional carbosilanes and organosilicon compounds. Synthesis via grignard reactions

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Cited by 53 publications
(33 citation statements)
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“…Obviously, it is a very attractive route to synthesize the HBPCS from non‐corrosive alkoxysilanes, such as (chloromethyl)alkoxysilanes . But the ceramic yield of the reported precursor prepared from (chloromethyl)trimethoxysilane (ClCH 2 Si(OMe) 3 ) is very low …”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…Obviously, it is a very attractive route to synthesize the HBPCS from non‐corrosive alkoxysilanes, such as (chloromethyl)alkoxysilanes . But the ceramic yield of the reported precursor prepared from (chloromethyl)trimethoxysilane (ClCH 2 Si(OMe) 3 ) is very low …”
Section: Introductionmentioning
confidence: 99%
“…13,14 But the ceramic yield of the reported precursor prepared from (chloromethyl)trimethoxysilane (ClCH 2 Si(OMe) 3 ) is very low. 15,16 To increase the ceramic yield, olefinic side chain groups, vinyl, ethynyl or allyl, which could sufficiently promote crosslinking reactions at lower temperature and the ceramic yield, were introduced into the HBPCS backbone. 17,18 For example, by incorporation of allyl chloride or HC ≡ CMgBr into the starting materials, PCSs with approximate formulas [SiH 1.2 (CH 3 ) 0.71 (CH 2 CH = CH 2 ) 0.09 CH 2 ] n and [SiH 1.35 (CH 3 ) 0.37 (C ≡ CH) 0.28 CH 2 ] n respectively were synthesized.…”
Section: Introductionmentioning
confidence: 99%
“…[13][14][15][16] They permit the trialkoxysilylation by reaction of the organolithium reagent with ClSi(OR) 3 (where R ¼ Me, Et, OiPr). [13][14][15][16] They permit the trialkoxysilylation by reaction of the organolithium reagent with ClSi(OR) 3 (where R ¼ Me, Et, OiPr).…”
Section: Methods Permitting the Introduction Of Si(or) 3 Groupsmentioning
confidence: 99%
“…Note that this reaction permits also the preparation of functional systems which may undergo successive reactions, since it is possible to 14 and p-MgBrC 6 H 4 Si (OiPr) 3 (II) 17 have been obtained by metallation of molecules bearing Si (OiPr) 3 groups. These reagents allow the introduction of groups containing the Si(OR) 3 function.…”
Section: Methods Permitting the Introduction Of Si(or) 3 Groupsmentioning
confidence: 99%
“…Recently, a novel ring‐shaped precursor was introduced, that is, 1,3,5‐tris[diethoxysila]cyclohexane [{(EtO) 2 SiCH 2 } 3 ],33, 34 in which each silicon atom has two organic substituents compared to one in all previous systems. This arrangement allows for a higher degree of organic functionalization in the walls.…”
mentioning
confidence: 99%