409
of Polymer Science Part A: Polymer Chemistry, 44(10), 3261–3270. https://doi.org/10.1002/
pola.21439.
Siliniakova, I. B., Budkevitsch, G. B., & Nejmark, I. J. (1964). Doklady Akademii Nauk SSSR,
154, 692–694.
Siliniakova, I. B., Budkevitsch, G. B., & Nejmark, I. J. (1965). Koloid Zhurn., 27, 758–764.
Skrodzki, M., Witomska, S., & Pawluć, P. (2018a). Sodium triethylborohydride as a catalyst for the
dehydrogenative silylation of terminal alkynes with hydrosilanes. Dalton Transactions, 47(17),
5948–5951. https://doi.org/10.1039/c8dt00684a.
Skrodzki, M., Zaranek, M., Witomska, S., & Pawluc, P. (2018b). Direct dehydrogenative coupling
of alcohols with hydrosilanes promoted by sodium tri(sec-butyl) borohydride. Catalysts, 8(12),
618. https://doi.org/10.3390/catal8120618.
Śledzińska, I., Sołtysiak, J., & Stańczyk, W. (1994). Liquid crystal oligo(cyclosiloxanes). Journal of
Inorganic and Organometallic Polymers, 4(2), 199–204. https://doi.org/10.1007/bf01036543.
Soh, M. S., Yap, A. U., & Sellinger, A. (2007). Methacrylate and epoxy functionalized nanocomposites based on silsesquioxane cores for use in dental applications. European Polymer
Journal, 43(2), 315–327. https://doi.org/10.1016/j.eurpolymj.2006.11.020.
Sokołow, N. N. (1961). Metody syntezy poliorganosiloksanów. Warsaw: PWN.
Sommer, L. H., Ulland, L. A., & Parker, G. A. (1972). Stereochemistry of asymmetric silicon. XX. Hydroxylation and carbene insertion reactions of R 3 SiH. Journal of the American
Chemical Society, 94(10), 3469–3471. https://doi.org/10.1021/ja00765a036.
Song, Y. S., Yoo, B. R., Lee, G. H., & Jung, I. N. (1999). Lewis acid-catalyzed regio-and stereoselective hydrosilylation of alkenes with trialkylsilanes. Organometallics, 18(16), 3109–3115.
https://doi.org/10.1021/om990220p.
Sorarù, G. D., D’Andrea, G., Campostrini, R., & Babonneau, F. (1995b). Characterization of
methyl-substituted silica gels with Si-H functionalities. Journal of Materials Chemistry, 5(9),
1363–1374. https://doi.org/10.1039/jm9950501363.
Sorarù, G. D., D’andrea, G., Campostrini, R., Babonneau, F., & Mariotto, G. (1995a). Structural
characterization and high-temperature behavior of silicon oxycarbide glasses prepared from
sol-gel precursors containing Si-H bonds. Journal of the American Ceramic Society, 78(2),
379–387. https://doi.org/10.1111/j.1151-2916.1995.tb08811.x.
Soucek, M. D., Dworak, D. P., & Chakraborty, R. (2007). A new class of silicone resins for coatings. Journal of Coatings Technology and Research, 4(3), 263–274. https://doi.org/10.1007/
s11998-007-9044-x.
Speier, J. L., Webster, J. A., & Barnes, G. H. (1957). The addition of silicon hydrides to olefinic
double bonds. Part II. The use of group VIII metal catalysts. Journal of the American Chemical
Society, 79(4), 974–979. https://doi.org/10.1021/ja01561a054.
Stein, J., Grade, H., Williams, E. A., Codella, P. J., & Smith, J. F. (1993). Network structure and
properties of platinum-catalyzed addition cure release coatings. Journal of Applied Polymer
Science, 47(12), 2257–2267. https://doi.org/10.1002/app.1993.070471219.
Stiubianu, G., Racles, C., Cazacu, M., & Simionescu, B. C. (2010). Silicone-modified cellulose.
Crosslinking of cellulose acetate with poly[dimethyl(methyl-H) siloxane] by Pt-catalyzed
dehydrogenative coupling. Journal of Materials Science, 45(15), 4141–4150. https://doi.
org/10.1007/s10853-010-4503-7.
Stober, M. R., Musolf, M. C., & Speier, J. L. (1965). The addition of silicon hydrides to olefinic double bonds. XI. Exchange of methyl and trimethylsiloxy groups in bistrimethylsiloxymethylsilane. The Journal of Organic Chemistry, 30(5), 1651–1652. https://doi.org/10.1021/
jo01016a506.
Stochmal, E., Strzezik, J., & Krowiak, A. (2016). Preparation and characterization of polysiloxane
networks containing metallic platinum particles. Journal of Applied Polymer Science, 133(10).
https://doi.org/10.1002/app.43096.
Stock, A., & Somieski, K. (1919). Siliciumwasserstoffe, VII.: Über das Prosiloxan, SiH 2 (O).
Berichte der deutschen chemischen Gesellschaft (A and B Series), 52(9), 1851–1860. https://
doi.org/10.1002/cber.19190520909.
14 Hydrosilyl-Functional Polysiloxanes: Synthesis Reactions and Applications
of Polymer Science Part A: Polymer Chemistry, 44(10), 3261–3270. https://doi.org/10.1002/
pola.21439.
Siliniakova, I. B., Budkevitsch, G. B., & Nejmark, I. J. (1964). Doklady Akademii Nauk SSSR,
154, 692–694.
Siliniakova, I. B., Budkevitsch, G. B., & Nejmark, I. J. (1965). Koloid Zhurn., 27, 758–764.
Skrodzki, M., Witomska, S., & Pawluć, P. (2018a). Sodium triethylborohydride as a catalyst for the
dehydrogenative silylation of terminal alkynes with hydrosilanes. Dalton Transactions, 47(17),
5948–5951. https://doi.org/10.1039/c8dt00684a.
Skrodzki, M., Zaranek, M., Witomska, S., & Pawluc, P. (2018b). Direct dehydrogenative coupling
of alcohols with hydrosilanes promoted by sodium tri(sec-butyl) borohydride. Catalysts, 8(12),
618. https://doi.org/10.3390/catal8120618.
Śledzińska, I., Sołtysiak, J., & Stańczyk, W. (1994). Liquid crystal oligo(cyclosiloxanes). Journal of
Inorganic and Organometallic Polymers, 4(2), 199–204. https://doi.org/10.1007/bf01036543.
Soh, M. S., Yap, A. U., & Sellinger, A. (2007). Methacrylate and epoxy functionalized nanocomposites based on silsesquioxane cores for use in dental applications. European Polymer
Journal, 43(2), 315–327. https://doi.org/10.1016/j.eurpolymj.2006.11.020.
Sokołow, N. N. (1961). Metody syntezy poliorganosiloksanów. Warsaw: PWN.
Sommer, L. H., Ulland, L. A., & Parker, G. A. (1972). Stereochemistry of asymmetric silicon. XX. Hydroxylation and carbene insertion reactions of R 3 SiH. Journal of the American
Chemical Society, 94(10), 3469–3471. https://doi.org/10.1021/ja00765a036.
Song, Y. S., Yoo, B. R., Lee, G. H., & Jung, I. N. (1999). Lewis acid-catalyzed regio-and stereoselective hydrosilylation of alkenes with trialkylsilanes. Organometallics, 18(16), 3109–3115.
https://doi.org/10.1021/om990220p.
Sorarù, G. D., D’Andrea, G., Campostrini, R., & Babonneau, F. (1995b). Characterization of
methyl-substituted silica gels with Si-H functionalities. Journal of Materials Chemistry, 5(9),
1363–1374. https://doi.org/10.1039/jm9950501363.
Sorarù, G. D., D’andrea, G., Campostrini, R., Babonneau, F., & Mariotto, G. (1995a). Structural
characterization and high-temperature behavior of silicon oxycarbide glasses prepared from
sol-gel precursors containing Si-H bonds. Journal of the American Ceramic Society, 78(2),
379–387. https://doi.org/10.1111/j.1151-2916.1995.tb08811.x.
Soucek, M. D., Dworak, D. P., & Chakraborty, R. (2007). A new class of silicone resins for coatings. Journal of Coatings Technology and Research, 4(3), 263–274. https://doi.org/10.1007/
s11998-007-9044-x.
Speier, J. L., Webster, J. A., & Barnes, G. H. (1957). The addition of silicon hydrides to olefinic
double bonds. Part II. The use of group VIII metal catalysts. Journal of the American Chemical
Society, 79(4), 974–979. https://doi.org/10.1021/ja01561a054.
Stein, J., Grade, H., Williams, E. A., Codella, P. J., & Smith, J. F. (1993). Network structure and
properties of platinum-catalyzed addition cure release coatings. Journal of Applied Polymer
Science, 47(12), 2257–2267. https://doi.org/10.1002/app.1993.070471219.
Stiubianu, G., Racles, C., Cazacu, M., & Simionescu, B. C. (2010). Silicone-modified cellulose.
Crosslinking of cellulose acetate with poly[dimethyl(methyl-H) siloxane] by Pt-catalyzed
dehydrogenative coupling. Journal of Materials Science, 45(15), 4141–4150. https://doi.
org/10.1007/s10853-010-4503-7.
Stober, M. R., Musolf, M. C., & Speier, J. L. (1965). The addition of silicon hydrides to olefinic double bonds. XI. Exchange of methyl and trimethylsiloxy groups in bistrimethylsiloxymethylsilane. The Journal of Organic Chemistry, 30(5), 1651–1652. https://doi.org/10.1021/
jo01016a506.
Stochmal, E., Strzezik, J., & Krowiak, A. (2016). Preparation and characterization of polysiloxane
networks containing metallic platinum particles. Journal of Applied Polymer Science, 133(10).
https://doi.org/10.1002/app.43096.
Stock, A., & Somieski, K. (1919). Siliciumwasserstoffe, VII.: Über das Prosiloxan, SiH 2 (O).
Berichte der deutschen chemischen Gesellschaft (A and B Series), 52(9), 1851–1860. https://
doi.org/10.1002/cber.19190520909.
14 Hydrosilyl-Functional Polysiloxanes: Synthesis Reactions and Applications