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Alkoxy silanes

Oxazolidines 90Egg Silanes, alkoxy 75Har, 82Zic, 83Lie... [Pg.364]

MS polymers, silane-alkoxy-modified prepolymers of poly(propylene glycol), one-pack systems. Uses Many surfaces no primer necessary. [Pg.18]

Each of these silanes consist of two functionahties the moistuie-ieactive functionahty (usually alkoxy), and the organic functionahty. It is beheved that this... [Pg.310]

Alkyl, aryl, alkoxy and halogen subsituted silanes are referred to by prefixing silane by the specific group present. The following are typical examples ... [Pg.816]

Orthosilicates are derivatives of orthosilicic acid Si(OH)4. The most common is tetraethyl orthosilicate Si(OC2H04, often called TEOS, an acronym that also fits the alternative way of naming such a compound, tetraethoxysilane. Thus orthosilicates are actually a sub-set of the larger class of XRSi(OR )3 silanes, where the XR group is also an alkoxy group. The XR and OR groups do not have to be the... [Pg.409]

Two-part room temperature condensation cure. Silicone can be formulated into two-part systems [3,12,14,33] that prevent the reactive groups from coming into contact before they are needed. The reactions in these systems are based on the condensation of a silanol group with an alkoxy silane group, catalyzed by organo-tin compounds (Scheme 9). [Pg.684]

This excellent method of oxidative cleavage (/) of carbon-silicon bonds requires that the silane carry an electronegative substituent (2), such as alkoxy or fluoro. Either hydrogen peroxide or mcpba may be used as oxidant, and the alcohol is produced with retention of configuration (3). Fluoride ion is normally a mandatory additive in what is believed to be a fluoride ion-assisted rearrangement of a silyl peroxide, as shown below ... [Pg.123]


See other pages where Alkoxy silanes is mentioned: [Pg.411]    [Pg.87]    [Pg.228]    [Pg.240]    [Pg.255]    [Pg.361]    [Pg.194]    [Pg.247]    [Pg.278]    [Pg.163]    [Pg.411]    [Pg.87]    [Pg.228]    [Pg.240]    [Pg.255]    [Pg.361]    [Pg.194]    [Pg.247]    [Pg.278]    [Pg.163]    [Pg.1009]    [Pg.410]    [Pg.21]    [Pg.42]    [Pg.72]    [Pg.73]    [Pg.74]    [Pg.495]    [Pg.45]    [Pg.403]    [Pg.409]    [Pg.416]    [Pg.421]    [Pg.684]    [Pg.690]    [Pg.160]    [Pg.593]    [Pg.136]    [Pg.217]    [Pg.22]    [Pg.83]    [Pg.131]    [Pg.170]    [Pg.171]    [Pg.802]   
See also in sourсe #XX -- [ Pg.431 ]

See also in sourсe #XX -- [ Pg.83 ]

See also in sourсe #XX -- [ Pg.431 ]

See also in sourсe #XX -- [ Pg.371 ]




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Aldehydes, p-alkoxy reaction with enol silanes

Alkoxy silanes hydrolysis

Alkoxy silanes, reactivity

Alkyl alkoxy silane

Enol silanes reaction with chiral a-alkoxy aldehydes

Preparation of alkoxy(aroxy)silanes

Silanes, alkoxy derivates

Trifunctional alkoxy silanes

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