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Bis-Triethoxysilyl ethane

According to equation 2, disilatranylalkanes can be obtained from THEA and the corresponding bis(triethoxysilyl)alkanes (equation 3)45. For example, heating (up to 220 °C) of l,2-bis(triethoxysilyl)ethane (n = 2) with THEA in the... [Pg.1450]

The hydrosilylation of 1-hexene (28) with triethoxysilane (29) in the presence of a poly-y-mercaptopropylsiloxane platinum complex leads to hexyltriethoxysilane (30) (equation 16), whereas the hydrosilylation of acetylene (31) can afford both the mono- and disilylated product, i.e. vinyltriethoxysilane (32) and l,2-bis(triethoxysilyl)ethane (33) respectively (equation 17)34. [Pg.661]

Chemicals. Tetramethylorthosilicate (TMOS), methyltrimethoxysilane (MTMOS), phenyltrimethoxysilane (PTMOS), l,2-bis(triethoxysilyl)ethane (BTSE), and... [Pg.357]

Bis (triethoxysilyl) ethane CAS 16068-37-4 EINECS/ELINCS 240-212-2 Synonyms 1,2-Bis (triethoxysilyl) ethane Hexaethoxydisilethylene... [Pg.533]

Hexaethoxydisilethylene. See Bis (triethoxysilyl) ethane Hexaethylene glycol. See PEG-6 Hexafluoroepoxypropane Hexafluoro-1,2-epoxypropane. See 1,2-Epoxy-1,1,2,3,3,3-hexafluoropropane Hexafluoroethane... [Pg.2001]

Bis (triethoxysilyl) ethane Cl3-15 amine p-Carboxyethyl acrylate 4-Chlorophenol Copolyvidone... [Pg.4790]

Chromium sulfate (ic) crosslinking agent Acrylic acid/acrylamide copolymer Allylglycidyl ether alcohol resin Allyl isocyanate Aluminum acetylacetonate N-2-Aminoethyl-3-aminopropyl trimethoxysilane Ammonium persulfate t-Amyl peroxyacetate Bis (triethoxysilyl) ethane Chromic acetylacetonate Cobalt acetate (ous). [Pg.5038]

Bis (triethoxysilyl) ethane SIB1817.0 240-263-0 Dithiothreitol 240-273-5 Eltesol PT 45 Eltesol PT 93 Hartotrope KTS 44 Hartotrope KTS 50 Naxonate 4KT Naxonate 5KT... [Pg.6923]

Wahab, M.A., Kim, I.I., and Ha, C.S. (2004) Hybrid periodic mesoporous organosilica materials prepared from l,2-bis(triethoxysilyl)ethane and (3-cyanopropyl)triethoxysilane. Microporous Mesoporous Mater., 69, 19-27. [Pg.218]

At nearly the same time as the report of PMO synthesized by CTAB, PMOs with large pores of 6.0-7.4 nm in diameter were synthesized using a triblock copolymer as template. Caber and coworkers [67] reported a PMO that was synthesized by the acid-catalyzed hydrolysis and condensation of bis-(triethoxysilyl)ethane (BTSE) using the triblock copolymer Pluronic P123 as the SDA. Another report deals with... [Pg.96]

The BTEE-PMO (BTEE, l,2-bis(triethoxysilyl)ethane) functionalized with a bulky N-heterocyclic carbene was prepared by Hao et al. They were used as catalysts for the Suzuki coupling reaction. These materials also exhibited enhanced activity and selectivity [81]. The PdL (silylated carbapalladacycle precursor)-PMO was applied to the Suzuki reaction of p-bromobenzoic acid and phenylboronic add [65]. The results showed high catalyst activity with short reaction times compared to PdL-Si02 (synthesized by co-condensation of precursors and SiOj) due to the benefidal influence by increased porosity and regular distribution of the active site. [Pg.104]

See other pages where Bis-Triethoxysilyl ethane is mentioned: [Pg.176]    [Pg.586]    [Pg.804]    [Pg.89]    [Pg.89]    [Pg.527]    [Pg.202]    [Pg.500]    [Pg.533]    [Pg.3906]    [Pg.6440]    [Pg.7089]    [Pg.539]    [Pg.464]    [Pg.687]    [Pg.689]    [Pg.186]    [Pg.357]    [Pg.143]    [Pg.354]    [Pg.1059]    [Pg.254]   
See also in sourсe #XX -- [ Pg.539 ]



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