Organic polyalkyleneoxy silicates

Polyoxyalkylene silicates of general formula [R-O-(CH2CHR1-O)m- 1 -(CH2CH2O)n]4- r -Si(R2)r wherein R is an alkyl group of 1 to 28 carbon atoms or an aryl group of 6 to 14 carbon atoms which may be substituted by one to three alkyl groups containing 1 to 18 carbon atoms, R1 is a methyl or ethyl grou...

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Hauptverfasser: LEARY ROBERT E, JR. LESLIE G. NUNN, SCHENCK LESLIE M
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creator LEARY ROBERT E
JR. LESLIE G. NUNN
SCHENCK LESLIE M
description Polyoxyalkylene silicates of general formula [R-O-(CH2CHR1-O)m- 1 -(CH2CH2O)n]4- r -Si(R2)r wherein R is an alkyl group of 1 to 28 carbon atoms or an aryl group of 6 to 14 carbon atoms which may be substituted by one to three alkyl groups containing 1 to 18 carbon atoms, R1 is a methyl or ethyl group, each R2 represents an alkoxy group of 1 to 27 carbon atoms, or an aryloxy group of 6 to 14 carbon atoms, either of which may be substituted by halogen, an alkyl radical of 1 to 27 carbon atoms or a polyalkyloneoxy chain of 5 to 35 units, r is 0-3, and m and n are each 1 to 150 (see Division C3) may be used as lubricants and hydraulic fluids.ALSO:The invention comprises polyoxyalkylene silicates of general formula [R-O-(CH2CHR1-O)m- 1 -(CH2CH2O)n]4- r -Si(R2)r wherein R is an alkyl group of 1 to 28 carbon atoms, or an aryl group of 6 to 14 carbon atoms which may be substituted by one to three alkyl groups containing 1 to 18 carbon atoms, R1 is a methyl or ethyl group, each R2 represents an alkoxy group of 1 to 27 carbon atoms, or an aryloxy group of 6 to 14 carbon atoms, either of which may be substituted by a halogen atom, an alkyl radical of 1 to 27 carbon atoms or a polyalkyloneoxy chain of 5 to 35 units, r is 0-3, and m and n are each 1 to 150. Many R, R1 and R2 groups are specified. These compounds are prepared by the ester-exchange of an alkyl- or aryl-polyalkyleneoxyalkanol and a tetra-substituted silicate at 170-250 DEG C.; a list of suitable tetra-substituted silicate-starting materials is given. Typical examples describe the preparation of (II) [C9H19.C6H4. O(CH2CH2O)6]4Si and (III) C6H5O(CH2CH2O)120. Si-(OC6H5)3 in (XIV) the product of (III) is further transesterified with other polyethyleneoxymonoethers to yield products containing several different polyalkyleneoxy groups. Uses.-In lubricating and functional liquid formulations, catalysts, drugs, hydraulics, refrigeration, cosmetics, detergents, cleaning products, paints, plastics, greases, textile processing, modifying surface properties of leather, wood and paper, enamels, coatings, biocidal formulations, defoamers, corrosion inhibitors, and refractory binders.
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NUNN ; SCHENCK LESLIE M</creatorcontrib><description>Polyoxyalkylene silicates of general formula [R-O-(CH2CHR1-O)m- 1 -(CH2CH2O)n]4- r -Si(R2)r wherein R is an alkyl group of 1 to 28 carbon atoms or an aryl group of 6 to 14 carbon atoms which may be substituted by one to three alkyl groups containing 1 to 18 carbon atoms, R1 is a methyl or ethyl group, each R2 represents an alkoxy group of 1 to 27 carbon atoms, or an aryloxy group of 6 to 14 carbon atoms, either of which may be substituted by halogen, an alkyl radical of 1 to 27 carbon atoms or a polyalkyloneoxy chain of 5 to 35 units, r is 0-3, and m and n are each 1 to 150 (see Division C3) may be used as lubricants and hydraulic fluids.ALSO:The invention comprises polyoxyalkylene silicates of general formula [R-O-(CH2CHR1-O)m- 1 -(CH2CH2O)n]4- r -Si(R2)r wherein R is an alkyl group of 1 to 28 carbon atoms, or an aryl group of 6 to 14 carbon atoms which may be substituted by one to three alkyl groups containing 1 to 18 carbon atoms, R1 is a methyl or ethyl group, each R2 represents an alkoxy group of 1 to 27 carbon atoms, or an aryloxy group of 6 to 14 carbon atoms, either of which may be substituted by a halogen atom, an alkyl radical of 1 to 27 carbon atoms or a polyalkyloneoxy chain of 5 to 35 units, r is 0-3, and m and n are each 1 to 150. Many R, R1 and R2 groups are specified. These compounds are prepared by the ester-exchange of an alkyl- or aryl-polyalkyleneoxyalkanol and a tetra-substituted silicate at 170-250 DEG C.; a list of suitable tetra-substituted silicate-starting materials is given. Typical examples describe the preparation of (II) [C9H19.C6H4. O(CH2CH2O)6]4Si and (III) C6H5O(CH2CH2O)120. Si-(OC6H5)3 in (XIV) the product of (III) is further transesterified with other polyethyleneoxymonoethers to yield products containing several different polyalkyleneoxy groups. Uses.-In lubricating and functional liquid formulations, catalysts, drugs, hydraulics, refrigeration, cosmetics, detergents, cleaning products, paints, plastics, greases, textile processing, modifying surface properties of leather, wood and paper, enamels, coatings, biocidal formulations, defoamers, corrosion inhibitors, and refractory binders.</description><language>eng</language><subject>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM ; CHEMISTRY ; COMPOSITIONS BASED THEREON ; MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS ; METALLURGY ; ORGANIC CHEMISTRY ; ORGANIC MACROMOLECULAR COMPOUNDS ; THEIR PREPARATION OR CHEMICAL WORKING-UP</subject><creationdate>1967</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19670307&amp;DB=EPODOC&amp;CC=US&amp;NR=3308149A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76516</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19670307&amp;DB=EPODOC&amp;CC=US&amp;NR=3308149A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>LEARY ROBERT E</creatorcontrib><creatorcontrib>JR. LESLIE G. NUNN</creatorcontrib><creatorcontrib>SCHENCK LESLIE M</creatorcontrib><title>Organic polyalkyleneoxy silicates</title><description>Polyoxyalkylene silicates of general formula [R-O-(CH2CHR1-O)m- 1 -(CH2CH2O)n]4- r -Si(R2)r wherein R is an alkyl group of 1 to 28 carbon atoms or an aryl group of 6 to 14 carbon atoms which may be substituted by one to three alkyl groups containing 1 to 18 carbon atoms, R1 is a methyl or ethyl group, each R2 represents an alkoxy group of 1 to 27 carbon atoms, or an aryloxy group of 6 to 14 carbon atoms, either of which may be substituted by halogen, an alkyl radical of 1 to 27 carbon atoms or a polyalkyloneoxy chain of 5 to 35 units, r is 0-3, and m and n are each 1 to 150 (see Division C3) may be used as lubricants and hydraulic fluids.ALSO:The invention comprises polyoxyalkylene silicates of general formula [R-O-(CH2CHR1-O)m- 1 -(CH2CH2O)n]4- r -Si(R2)r wherein R is an alkyl group of 1 to 28 carbon atoms, or an aryl group of 6 to 14 carbon atoms which may be substituted by one to three alkyl groups containing 1 to 18 carbon atoms, R1 is a methyl or ethyl group, each R2 represents an alkoxy group of 1 to 27 carbon atoms, or an aryloxy group of 6 to 14 carbon atoms, either of which may be substituted by a halogen atom, an alkyl radical of 1 to 27 carbon atoms or a polyalkyloneoxy chain of 5 to 35 units, r is 0-3, and m and n are each 1 to 150. Many R, R1 and R2 groups are specified. These compounds are prepared by the ester-exchange of an alkyl- or aryl-polyalkyleneoxyalkanol and a tetra-substituted silicate at 170-250 DEG C.; a list of suitable tetra-substituted silicate-starting materials is given. Typical examples describe the preparation of (II) [C9H19.C6H4. O(CH2CH2O)6]4Si and (III) C6H5O(CH2CH2O)120. Si-(OC6H5)3 in (XIV) the product of (III) is further transesterified with other polyethyleneoxymonoethers to yield products containing several different polyalkyleneoxy groups. Uses.-In lubricating and functional liquid formulations, catalysts, drugs, hydraulics, refrigeration, cosmetics, detergents, cleaning products, paints, plastics, greases, textile processing, modifying surface properties of leather, wood and paper, enamels, coatings, biocidal formulations, defoamers, corrosion inhibitors, and refractory binders.</description><subject>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM</subject><subject>CHEMISTRY</subject><subject>COMPOSITIONS BASED THEREON</subject><subject>MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><subject>ORGANIC MACROMOLECULAR COMPOUNDS</subject><subject>THEIR PREPARATION OR CHEMICAL WORKING-UP</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1967</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZFD0L0pPzMtMVijIz6lMzMmuzEnNS82vqFQozszJTE4sSS3mYWBNS8wpTuWF0twM8m6uIc4euqkF-fGpxQWJyUAdJfGhwcbGBhaGJpaOxoRVAAA2RSWn</recordid><startdate>19670307</startdate><enddate>19670307</enddate><creator>LEARY ROBERT E</creator><creator>JR. LESLIE G. NUNN</creator><creator>SCHENCK LESLIE M</creator><scope>EVB</scope></search><sort><creationdate>19670307</creationdate><title>Organic polyalkyleneoxy silicates</title><author>LEARY ROBERT E ; JR. LESLIE G. NUNN ; SCHENCK LESLIE M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_US3308149A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1967</creationdate><topic>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM</topic><topic>CHEMISTRY</topic><topic>COMPOSITIONS BASED THEREON</topic><topic>MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><topic>ORGANIC MACROMOLECULAR COMPOUNDS</topic><topic>THEIR PREPARATION OR CHEMICAL WORKING-UP</topic><toplevel>online_resources</toplevel><creatorcontrib>LEARY ROBERT E</creatorcontrib><creatorcontrib>JR. LESLIE G. NUNN</creatorcontrib><creatorcontrib>SCHENCK LESLIE M</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>LEARY ROBERT E</au><au>JR. LESLIE G. NUNN</au><au>SCHENCK LESLIE M</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Organic polyalkyleneoxy silicates</title><date>1967-03-07</date><risdate>1967</risdate><abstract>Polyoxyalkylene silicates of general formula [R-O-(CH2CHR1-O)m- 1 -(CH2CH2O)n]4- r -Si(R2)r wherein R is an alkyl group of 1 to 28 carbon atoms or an aryl group of 6 to 14 carbon atoms which may be substituted by one to three alkyl groups containing 1 to 18 carbon atoms, R1 is a methyl or ethyl group, each R2 represents an alkoxy group of 1 to 27 carbon atoms, or an aryloxy group of 6 to 14 carbon atoms, either of which may be substituted by halogen, an alkyl radical of 1 to 27 carbon atoms or a polyalkyloneoxy chain of 5 to 35 units, r is 0-3, and m and n are each 1 to 150 (see Division C3) may be used as lubricants and hydraulic fluids.ALSO:The invention comprises polyoxyalkylene silicates of general formula [R-O-(CH2CHR1-O)m- 1 -(CH2CH2O)n]4- r -Si(R2)r wherein R is an alkyl group of 1 to 28 carbon atoms, or an aryl group of 6 to 14 carbon atoms which may be substituted by one to three alkyl groups containing 1 to 18 carbon atoms, R1 is a methyl or ethyl group, each R2 represents an alkoxy group of 1 to 27 carbon atoms, or an aryloxy group of 6 to 14 carbon atoms, either of which may be substituted by a halogen atom, an alkyl radical of 1 to 27 carbon atoms or a polyalkyloneoxy chain of 5 to 35 units, r is 0-3, and m and n are each 1 to 150. Many R, R1 and R2 groups are specified. These compounds are prepared by the ester-exchange of an alkyl- or aryl-polyalkyleneoxyalkanol and a tetra-substituted silicate at 170-250 DEG C.; a list of suitable tetra-substituted silicate-starting materials is given. Typical examples describe the preparation of (II) [C9H19.C6H4. O(CH2CH2O)6]4Si and (III) C6H5O(CH2CH2O)120. Si-(OC6H5)3 in (XIV) the product of (III) is further transesterified with other polyethyleneoxymonoethers to yield products containing several different polyalkyleneoxy groups. Uses.-In lubricating and functional liquid formulations, catalysts, drugs, hydraulics, refrigeration, cosmetics, detergents, cleaning products, paints, plastics, greases, textile processing, modifying surface properties of leather, wood and paper, enamels, coatings, biocidal formulations, defoamers, corrosion inhibitors, and refractory binders.</abstract><oa>free_for_read</oa></addata></record>
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subjects ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM
CHEMISTRY
COMPOSITIONS BASED THEREON
MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
METALLURGY
ORGANIC CHEMISTRY
ORGANIC MACROMOLECULAR COMPOUNDS
THEIR PREPARATION OR CHEMICAL WORKING-UP
title Organic polyalkyleneoxy silicates
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