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US3965136A Expired / Lapsed US ⏱️ 0.0 years remaining

Alkoxysilane cluster compounds and their preparation

Assignee: Olin Corp
•
Filing: 1975-09-24
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Granted: 1976-06-22
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Expires: 1995-09-24
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Abstract

Abstract Novel alkoxysilane cluster compounds are described having the formula RSi[Osi(OR')3]3 wherein R is hydrogen, an alkyl, alkenyl, aryl or aralkyl group and each R' is independently selected from the same group as R with the proviso that at least a majority of R' radicals are sterically hindered alkyl groups having at least 3 carbon atoms. The preparation of these novel alkoxysilane cluster compounds is also described.

Inventors

  • 👤 Karl O. Knollmueller

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-31 08:00
CPC Classifications
C; C10; C10M; C10M3/00; C07; C07F; C07F7/00; C07F7/02; C07F7/025; C07F7/08; C07F7/18; C07F7/1804; C10M2203/00; C10M2203/06; C10M2207/00; C10M2207/02; C10M2207/021; C10M2207/022; C10M2207/023; C10M2207/10; C10M2207/18; C10M2207/20; C10M2209/00; C10M2209/10; C10M2209/103; C10M2209/104; C10M2215/00; C10M2215/02; C10M2215/04; C10M2215/042; C10M2215/06; C10M2215/064; C10M2215/065; C10M2215/22; C10M2215/221; C10M2215/225; C10M2215/226; C10M2215/24; C10M2215/26; C10M2215/30; C10M2219/00; C10M2219/10; C10M2219/104; C10M2219/108; C10M2229/00; C10M2229/04; C10M2229/041; C10M2229/042; C10M2229/043; C10M2229/044; C10M2229/045; C10M2229/046; C10M2229/047; C10M2229/048; C10N; C10N2020/00; C10N2020/01; C10N2030/00; C10N2030/08; C10N2040/00; C10N2040/08; C10N2040/12; C10N2040/13

Claims Analysis

Total Claims: 24
Claim 1
Independent Claim 50 words
A compound of the formula: ##EQU8## wherein R is hydrogen, an alkyl, alkenyl, aryl or aralkyl, and each R' is independently selected from the same group as R with the proviso that at least a majority of R' radicals are sterically hindered alkyl groups having at least 3 carbon atoms.
Claim 2
Dependent Claim 50 words
A compound of the formula: ##EQU8## wherein R is hydrogen, an alkyl, alkenyl, aryl or aralkyl, and each R' is independently selected from the same group as R with the proviso that at least a majority of R' radicals are sterically hindered alkyl groups having at least 3 carbon atoms.
Claim 3
Dependent Claim 52 words
The compound of claim 1 wherein R is hydrogen, an alkyl or alkenyl having about 1 to about 18 carbon atoms or an aryl or aralkyl having about 6 to about 24 carbon atoms and wherein each R' is independently selected from the same group as R, subject to the above proviso.
Claim 4
Dependent Claim 25 words
The compound of claim 2 wherein a majority of the R' radicals are sterically hindered alkyl groups having about 3 to about 24 carbon atoms.
Claim 5
Dependent Claim 50 words
The compound of claim 1 wherein R is hydrogen, an alkyl having about 1 to about 8 carbon atoms or an aryl or aralkyl having about 6 to about 14 carbon atoms and wherein each R' is independently selected from the same group as R, subject to the above proviso.
Claim 6
Dependent Claim 25 words
The compound of claim 4 wherein a majority of the R' radicals are sterically hindered alkyl groups having about 4 to about 12 carbon atoms.
Claim 7
Dependent Claim 25 words
The compound of claim 1 wherein a majority of the R' radicals are sterically hindered alkyl groups having about 3 to about 24 carbon atoms.
Claim 8
Dependent Claim 25 words
The compound of claim 6 wherein a majority of the R' radicals are sterically hindered alkyl groups having about 4 to about 12 carbon atoms.
Claim 9
Dependent Claim 109 words
A method of preparing the compound of claim 1 comprising: reacting a trihalosilane of the formula: R--SiX.sub.3 wherein R is defined in claim 1 above and each X is a halogen selected from F, Cl, Br and I; with about 2.5 to about 10 moles of a trialkoxysilanol per mole of trihalosilane, said trialkoxysilanol having the formula: HOSi(OR').sub.3 wherein R' is defined in claim 1 above; in the presence of about 2.5 to about 10 moles of a hydrogen halide acceptor base compound, per mole of trihalosilane; said reaction being carried out at about -30°C to about the reflux temperature of the lowest boiling constituent in the reaction mixture.
Claim 10
Dependent Claim 14 words
The method of claim 8 wherein X is selected from Cl, Br and I.
Claim 11
Dependent Claim 72 words
The method of claim 8 wherein R is hydrogen, an alkyl or alkenyl having about 1 to about 18 carbon atoms or an aryl or aralkyl having about 6 to about 24 carbon atoms and wherein each R' is independently selected from the same group as R with the proviso that at least a majority of the R' radicals are sterically hindered alkyl groups having about 3 to about 24 carbon atoms.
Claim 12
Dependent Claim 50 words
The method of claim 10 wherein R is hydrogen, an alkyl having about 1 to about 8 carbon atoms or an aryl or aralkyl having about 6 to about 14 carbon atoms and wherein each R' is independently selected from the same group as R, subject to the above proviso.
Claim 13
Dependent Claim 30 words
The method of claim 10 wherein a majority of the R' radicals are sterically hindered alkyl groups having about 4 to about 12 carbon atoms and wherein X is Cl.
Claim 14
Dependent Claim 21 words
The method of claim 10 wherein about --3 to about 6 moles of the trialkoxysilanol is used per mole of trihalosilane.
Claim 15
Dependent Claim 25 words
The method of claim 13 wherein about 3 to about 6 moles of the hydrogen halide acceptor base compound is used per mole of trihalosilane.
Claim 16
Dependent Claim 15 words
The method of claim 14 wherein said reaction is carried out at 0°C to 100°C.
Claim 17
Dependent Claim 106 words
A method of preparing the compound of claim 1 comprising: reacting an alkoxysilanol having the formula: ##EQU9## wherein R and R' are defined in claim 1 above, with about 1 to about 20 moles of a halosilane per mole of alkoxysilanol, the halosilane having the formula: XSi(OR').sub.3 wherein R' is defined above and each X is selected from F, Cl, Br and I, in the presence of about 2.5 to about 10 moles of a hydrogen halide acceptor base compound per mole of alkoxysilanol, said reaction being carried out at about -30°C to about the reflux temperature of the lowest boiling constituent in the reaction mixture.
Claim 18
Dependent Claim 14 words
The method of claim 16 wherein X is selected from Cl, Br and I.
Claim 19
Dependent Claim 72 words
The method of claim 16 wherein R is hydrogen, an alkyl or aralkenyl having about 1 to about 18 carbon atoms or an aryl or aralkyl having about 6 to about 24 carbon atoms and wherein each R' is independently selected from the same group as R with the proviso that at least a majority of the R' radicals are sterically hindered alkyl groups having about 3 to about 24 carbon atoms.
Claim 20
Dependent Claim 50 words
The method of claim 18 wherein R is hydrogen, an alkyl having about 1 to about 8 carbon atoms or an aryl or aralkyl having about 6 to about 12 carbon atoms and wherein each R' is independently selected from the same group as R, subject to the above proviso.
Claim 21
Dependent Claim 25 words
The method of claim 18 wherein a majority of the R' radicals are sterically hindered alkyl groups having about 4 to about 12 carbon atoms.
Claim 22
Dependent Claim 21 words
The method of claim 18 wherein about 1 to about 6 moles of the halosilane is used per mole of alkoxysilanol.
Claim 23
Dependent Claim 25 words
The method of claim 21 wherein about 3 to about 6 moles of the hydrogen halide acceptor base compound is used per mole of trialkoxyhalosilane.
Claim 24
Dependent Claim 15 words
The method of claim 22 wherein said reaction is carried out at 0°C to 100°C.

References Cited (Backward Citations)

US2566364A Cited
US2711418A Cited
US3019191A Cited
US2995593A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1979-06-22 1979-12-22 1980-06-22 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1983-06-22 1983-12-22 1984-06-22 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1987-06-22 1987-12-22 1988-06-22 $7700.00 Window Closed / Lapsed

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