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  • 1
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Materials Research 8 (1978), S. 313-326 
    ISSN: 0084-6600
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1435-1536
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 5 (1956), S. 817-822 
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary 1. The syntheses were effected of new polymeric substances, i. e., polyorganostannosiloxanes and poly organotitanosiloxanes, the chains of which contain not only siloxane links but also and links. 2. It was shown that and links in polyorganostanno- and polyorganotitanosiloxanes are broken down by strong sulfuric acid. 3. It was found that polyorganostanno- and polyorganotitanosiloxanes are soluble in organic solvents. The fractional compositions of these products were studied, and it was shown that they are cocondensation products.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 5 (1956), S. 713-717 
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary 1. An Investigation was made into methods for the introduction of a silicon-attached alkyl containing an ether or ester grouping into certain alkoxyalkyl(or aryl)silanes and acetoxyalkylsilanes. 2. By the reaction of sodium and ethyl bromoacetate with chlorodiethoxyethylsilane and with chlorodi-thoxyphenylsilane, the following organosilicon compounds were prepared for the first time: diethoxy(ethoxycarbonylmethyl)ethylsilane and diethoxy(ethoxycarbonylmethyl)phenylsilane. 3. Reaction between alkoxy(chloroalkyl)silsnes and sodium alkoxides yielded two new compounds: diethoxy(ethoxytrethyl)methylsilane and diethoxytmettnoxymethyl)methylsilane. 4. Reaction between chloro(chloroalkyl)silanes and potassium acetate yielded two new compounds containing an acetoxy group in a silicon-attached alkyl radical: diacetoxy(acetoxymethyl)methylsilane and triacetoxy(acetnxymethyl)silane.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 6 (1957), S. 317-322 
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary New polymers — polyorganoborosiloxanes, the molecular chain of which contains silicon-oxygen-boron linkages — were prepared by the heterofunctional condensation of alkyl- and aryl-dialkoxysilanes with boron triacetate and of alkyl- and aryl-diacetoxysilanes with tributyl borate.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary 1. The following compounds were synthesized for the first time: dibutoxy(methoxymethyl)methylsilane, triethoxy(methoxymethyl)silane, [acetyl(ethoxycarbonyl)methyl]diethoxymethylsilane, and (bisethoxycarbonylmethyl) diethoxyethylsilane. 2. It was shown that, in the hydrolysis of diethoxy(ethoxycarbonylmethyl)ethylsilane and diethoxy(ethoxycarbonylmethyl)phenylsilane in alkaline and acid media, elimination of the ethoxycarbonylmethyl group occurs. 3. It was shown that, in the hydrolysis of diethoxy(ethoxymethyl)rnethylsilane, hydrolysis of siliconattached ethoxy groups is accompanied by partial elimination of the ethoxymethyl group, the extent of the elimination being greater in an acid medium than in an alkaline medium. 4. In the hydrolysis of diacetoxy(acetoxymethyl)methylsilane, rupture of the silicon-carbon link in the grouping Si- CH2OCOCH3 does not occur to any appreciable extent either in alkaline or in acid media. 5. Alkaline hydrolysis of [acetyl(ethoxycarbonyl)methyl]diethoxymethylsilane does not result in rupture of the link between silicon and the carbon of the ester grouping.Such rupture does occur in acid hydrolysis.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 7 (1958), S. 41-46 
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary 1. In a study of the reactions of 1,1,1-triethylsilylamine and its N-alkyl derivatives (including the new compounds 1,1,1-triethyl-N-methylsilylamine and 1,1,1-triethyl-N,N-dimethylsilylamine) it was shown that treatment of these compounds with water causes the amino group to be replaced by hydroxyl and treatment with alcohols brings about replacement by alkoxyl. 2. The reaction of silylamines with aliphatic alcohols was applied in the synthesis of new compounds, namely alkoxytriethylsilanes (C2H5)3SiOR (R = propyl, isopropyl, butyl, isobutyl, isopentyl, and octyl). 3. It was shown that silylamines are of fairly good thermal stability and are not decomposed by long boiling.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary 1. By the cohydrolysis of ethoxytrimethylsilane with N-substituted (aminomethyl)diethoxymethylsilanes, liquid organosilicon polymers were obtained in which the terminal groups were trimethylsiloxy groups and there were 1, 2, and 3 intermediate organosilicon repeating units. 2. Activation energies for viscous flow were determined, and it was shown that, for a given degree of polymerization, the activation energy depends on the structure of the group introduced into the amino group. The investigated groups can be placed in the following order of diminishing activation energy for viscous flow: ClC6H4NH 〉 C6H5NH ≥ C6H5C2H5N 〉 (C2H5)2N.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 7 (1958), S. 874-875 
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Diethoxymethy][m-(trifluoromethyl)phenyl]silane and triethoxy[m-(trifluoromethyl)phenyl]silane were synthesized.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary 1. New organosilicon liquid linear polymers of structure $$(CH_3 )_3 SiO\left| {\begin{array}{*{20}c} - \\ { - - } \\ - \\ \end{array} } \right.\begin{array}{*{20}c} {CH_3 } \\ | \\ {Si} \\ {|CH_3 X} \\ \end{array} - O\left. {\begin{array}{*{20}c} - \\ { - - } \\ - \\ \end{array} } \right|_n Si(CH_3 )_3 ,$$ in which X=OCH3, OC2H5, and OCOCH3 and the degree of polymerization n had various values, were synthesized, and their principal properties were studied. 2. The temperature-dependence of the viscosities of the compounds obtained was investigated, and it was shown that the dependence is more marked in compounds containing acetoxy in the methyl side groups. 3. The activation energy for viscous flow of the compounds investigated in the temperature range 0°–100° depends on the nature of the polar group present. With respect to their effects on the intensity of intermolecular action in compounds of structure $$(CH_3 )_3 SiO\left| {\begin{array}{*{20}c} - \\ { - - } \\ - \\ \end{array} } \right.\begin{array}{*{20}c} {CH_3 } \\ | \\ {SiO} \\ {|CH_2 X} \\ \end{array} \left. {\begin{array}{*{20}c} - \\ { - - - } \\ - \\ \end{array} } \right|_n Si(CH_3 )_3 ,$$ the investigated groups may be arranged in the following order: $$ - NHC_6 H_5 〉 - OCOCH_3 〉 - Cl 〉 - {\rm O}C_2 H_5 〉 - {\rm O}CH_3 〉 - {\rm N}(C_2 H_5 )_2 〉 - {\rm H}.$$
    Type of Medium: Electronic Resource
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