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Functionalized silsesquioxanes synthesis organic functional groups

Figure 3.9 Co-condensation method (direct synthesis) employing TEOS and a terminal organotrialk-oxysilane (top) or TEOS and an organo-bridged silsesquioxane (bottom) as mixed precursors for the organic modification of mesoporous pure silica phases. R = organic functional group. Figure 3.9 Co-condensation method (direct synthesis) employing TEOS and a terminal organotrialk-oxysilane (top) or TEOS and an organo-bridged silsesquioxane (bottom) as mixed precursors for the organic modification of mesoporous pure silica phases. R = organic functional group.
See other pages where Functionalized silsesquioxanes synthesis organic functional groups is mentioned: [Pg.672]    [Pg.228]    [Pg.140]    [Pg.325]    [Pg.824]    [Pg.134]    [Pg.6]    [Pg.12]    [Pg.410]    [Pg.659]    [Pg.672]    [Pg.673]    [Pg.675]    [Pg.533]    [Pg.535]    [Pg.536]    [Pg.255]    [Pg.1308]    [Pg.1316]    [Pg.159]    [Pg.4]   
See also in sourсe #XX -- [ Pg.144 ]

See also in sourсe #XX -- [ Pg.144 ]



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Functional synthesis

Functionalized synthesis

Functions synthesis

Group syntheses

Organ function

Organic functional groups

Organic functionalization

Organic groups

Organization functional

Silsesquioxane

Silsesquioxane synthesis

Silsesquioxanes

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