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{{Short description|Organic compounds of the form R3–Si–OH}} In [[organosilicon chemistry]], '''organosilanols''' are a group of [[chemical compound]]s der ...

...le=ru:Кремнийорганические соединения|language=ru|trans-title=Organosilicon Compounds|location=Moscow|publisher=State scientific and technical publishing house o ...

...ion]], and C-C, C-N, and C-Si bond formation via [[cross-coupling]] with [[organosilicon]] reagents.<ref name="hiyamalabwebsite-research">[http://www.chem.chuo-u.ac ...yl halide|aryl]], [[alkenyl halide|alkenyl]] or [[alkyl halides]] and an [[organosilicon]] compound to form a C-C bond. ...

In [[organosilicon chemistry]], '''polysilazanes''' are [[polymer]]s in which [[silicon]] and ...of [[silazane]] chemistry. In the 1960s, the first attempts to transform [[organosilicon]] polymers into quasi-ceramic materials were described.<ref>P. G. Chantrell ...

...rd University Press, 2005, pp. 201–214 {{ISBN|0195131193}}.</ref> Although organosilicon polymers can be considered structural derivatives of polysilicon hydrides, [[Category:Inorganic silicon compounds]] ...

The functional groups on the thiol and alkene compounds can affect the reactivity of the radical species and their respective rate ...and acyl thiyl radicals has been used to access alicyclic and heteorcyclic compounds, ''via'' anti-Markovnikov thiol-ene reactions on 1,6-dienes, under photoche ...

A '''silsesquioxane''' is an [[organosilicon compound]] with the [[chemical formula]] [RSiO_3/2]_n ...combination of partially-condensed tetrasilanolphenyl POSS with [[Terbium compounds|terbium acetate]] and/or [[Europium(III) acetate|europium acetate]] (at dif ...

...and didecyldimethylammonium chloride). These last two are membrane-active compounds; against S. aureus the first forms a single monolayer coverage of the S. au ...ings systems take advantage of this by including photocatalytically active compounds in their formulations (i.e. titanium dioxide) that cause the coating to “fl ...