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US4058546A Expired / Lapsed US ⏱️ 0.0 years remaining

Alkoxysilane double cluster compounds with silicone bridges and their preparation and use

Assignee: Olin Corp
•
Filing: 1977-04-28
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Granted: 1977-11-15
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Expires: 1997-04-28
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Abstract

Abstract Novel alkoxysilane cluster compounds are described having the formula: <IMAGE> wherein n is an integer from 0 to 300; R is hydrogen, alkyl, alkenyl, aryl, aralkyl or -OSi(OR')3; each R' is independently selected from alkyl, alkenyl, aryl or aralkyl with the proviso that at least a majority of R' radicals are sterically hindered alkyl groups having at least 3 carbon atoms; and R'' and R''' are independently selected from hydrogen, alkyl, alkenyl, aryl, aralkyl, hydroalkyl, and halo or cyano substituted alkyl, alkenyl, aryl, aralkyl, and hydroalkyl. The preparation and use of these alkoxysilane cluster compounds also are described.

Inventors

  • 👤 Karl O. Knollmueller

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-06 15:25
CPC Classifications
C; C10; C10M; C10M107/00; C10M107/50; C07; C07F; C07F7/00; C07F7/02; C07F7/08; C07F7/18; C07F7/1804; C08; C08G; C08G77/00; C08G77/04; C10M3/00; 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; C10M2229/02; C10M2229/04; C10M2229/041; C10M2229/042; C10M2229/043; C10M2229/044; C10M2229/05; C10M2229/051; C10M2229/052; C10N; C10N2020/00; C10N2020/01; C10N2030/00; C10N2030/08; C10N2040/00; C10N2040/08; C10N2040/12; C10N2040/13

Claims Analysis

Total Claims: 19
Claim 1
Independent Claim 84 words
A compound having the formula: ##STR10## wherein n is an integer from 0 to 300; R is hydrogen, alkyl, alkenyl, aryl, aralkyl or --OSi(OR') 3 ; each R' is independently selected from alkyl, alkenyl, aryl or aralkyl with the proviso that at least a majority of R' radicals are sterically hindered alkyl groups having at least 3 carbon atoms; and R" and '" are independently selected from hydrogen, alkyl, alkenyl, aryl, aralkyl, hydroalkyl, and halo or cyano substituted alkyl, alkenyl, aryl, aralkyl, and hydroalkyl.
Claim 2
Dependent Claim 84 words
A compound having the formula: ##STR10## wherein n is an integer from 0 to 300; R is hydrogen, alkyl, alkenyl, aryl, aralkyl or --OSi(OR') 3 ; each R' is independently selected from alkyl, alkenyl, aryl or aralkyl with the proviso that at least a majority of R' radicals are sterically hindered alkyl groups having at least 3 carbon atoms; and R" and '" are independently selected from hydrogen, alkyl, alkenyl, aryl, aralkyl, hydroalkyl, and halo or cyano substituted alkyl, alkenyl, aryl, aralkyl, and hydroalkyl.
Claim 3
Dependent Claim 27 words
The compound of claim 1 wherein at least a majority of the R' groups are sterically hindered alkyl groups having about 3 to about 24 carbon atoms.
Claim 4
Dependent Claim 22 words
The compound of claim 2 wherein the R' groups are sterically hindered alkyl groups having about 4 to about 12 carbon atoms.
Claim 5
Dependent Claim 14 words
The compound of claim 1 wherein n is an integer from 0 to 5.
Claim 6
Dependent Claim 15 words
The compound of claim 4 wherein n is an integer from 0 to 3 .
Claim 7
Dependent Claim 88 words
The compound of claim 1 wherein R is hydrogen, alkyl or alkenyl having about 1 to about 18 carbon atoms or aryl or aralkyl having about 6 to about 24 carbon atoms, and each R' is independently selected from alkyl or alkenyl having about 1 to about 24 carbon atoms or aryl or aralkyl having about 6 to about 24 carbon atoms, subject to the proviso that at least a majority of the R' groups are sterically hindered alkyl groups having about 3 to about 24 carbon atoms.
Claim 8
Dependent Claim 88 words
The compound of claim 6 wherein R is hydrogen, alkyl or alkenyl having about 1 to about 8 carbon atoms or aryl or aralkyl having about 6 to about 14 carbon atoms, and each R' is independently selected from alkyl or alkenyl having about 1 to about 12 carbon atoms or aryl or aralkyl having about 6 to about 14 carbon atoms, subject to the proviso that at least a majority of the R' groups are sterically hindered alkyl groups having about 4 to about 12 carbon atoms.
Claim 9
Dependent Claim 25 words
The compound of claim 1 wherein R" and R'" are independently selected from lower alkyl and alkenyl of about 1 to about 4 carbon atoms.
Claim 10
Dependent Claim 52 words
The compound of claim 7 wherein R" and R'" are independently selected from lower alkyl and alkenyl of about 1 to about 4 carbon atoms, and n is an integer from 0 to 5, and the R' groups are all sterically hindered alkyl groups of about 4 to about 12 carbon atoms.
Claim 11
Dependent Claim 32 words
The compound of claim 1 wherein R is methyl, R' is sec-butyl, R" and R'" are selected from hydrogen, methyl, ethenyl and phenyl, and n is an integer from 0 to 3.
Claim 12
Dependent Claim 95 words
A method of preparing the compound of claim 1 comprising: reacting a dihalo silicon bridging compound of the formula: ##STR11## wherein X is any halogen and n, R" and R'" are as defined above in claim 1, with an alkoxysilanol cluster compound, said alkoxysilanol cluster compound having the formula: ##STR12## wherein R and R' are as defined above in claim 1, in the presence of a hydrogen halide acceptor base compound, said reaction being conducted at a temperature ranging from about -30° C to about the relfux temperature of the lowest boiling reaction mixture ingredient.
Claim 13
Dependent Claim 32 words
The method of claim 11 wherein the alkoxysilanol cluster compound reactant is used in an amount ranging from about 1.8 to about 5 moles per mole of the dihalo silicon bridging compound.
Claim 14
Dependent Claim 33 words
The method of claim 12 wherein the halogen halide acceptor base compound is present in an amount ranging from about 2 to about 5 moles per mole of the dihalo silicon bridging compound.
Claim 15
Dependent Claim 56 words
The method of claim 13 wherein said reaction is conducted at an initial temperature range of about -10 to about 30 20° C for 0.5 to about 2 hours, during addition of reactants, followed by a reaction period of about 0.5 to about 12 hours at a temperature range of about 50 to about 100° C.
Claim 16
Dependent Claim 30 words
The method of claim 14 wherein said reaction is conducted in a solvent medium comprising about 0.5 to about 10 parts of solvent per part of total reactants by volume.
Claim 17
Dependent Claim 98 words
The method of claim 15 wherein X is Cl, n is an integer from 0 to 5, R is hydrogen, alkyl or alkenyl having about 1 to about 18 carbon atoms or aryl or aralkyl having about 6 to 24 carbon atoms and each R' is indepedently selected from alkyl or alkenyl of about 1 to about 24 carbon atoms or aryl or aralkyl of about 6 to about 24 carbon atoms subject to the proviso that at least a majority of the R' groups are sterically hindered alkyl groups having from 3 to about 24 carbon atoms.
Claim 18
Dependent Claim 97 words
The method of claim 16 wherein n is an integer from 0 to 3, R is hydrogen, alkyl or alkenyl having about 1 to about 8 carbon atoms or aryl or aralkyl having about 6 to about 14 carbon atoms, and each R' is independently selected from alkyl or alkenyl having about 1 to about 12 carbon atoms or aryl or aralkyl having about 6 to about 14 carbon atoms subject to the proviso that at least a majority of the R' groups are sterically hindered alkyl groups having from about 4 to about 12 carbon atoms.
Claim 19
Dependent Claim 35 words
The method of claim 17 wherein X is Cl, R is methyl, R' is sec-butyl, R" and R'" are selected from hydrogen, methyl, ethenyl and phenyl, and n is an integer from 0 to 3.

References Cited (Backward Citations)

US3308148A Cited
US3960913A Cited
US3965136A Cited
US3965135A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1980-11-14 1981-05-16 1981-11-15 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1984-11-14 1985-05-16 1985-11-15 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1988-11-14 1989-05-16 1989-11-15 $7700.00 Window Closed / Lapsed

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