385
and physical properties. Journal of Polymer Science Part A: Polymer Chemistry, 39(14),
2414–2425. https://doi.org/10.1002/pola.1218.
Andrianov, K. A., Abhazova, I. I., Khananashvili, L. M., Bogratishvili, G. D., Dogsopulc, T. P., &
Chagelishvili, V. A. (1971b). Zhurn. Obshch. Khim. 41, 606.
Andrianov, K. A., Gavrikova, L. A., & Rodionova, E. F. (1971a). Vysokomol. Soed., 13A, 937–940.
Andrianov, K. A., Kochetkova, A. S., & Khananashvili, L. M. (1968a). Copolymerization of methylvinylsiloxane oligomers with methylhydridosiloxanes. Zhurnal Obshchei Khimii, 38(1),
175–178.
Andrianov, K. A., Nogaideli, A. J., Khananashvili, L. M., & Nakaidze, L. D. (1968b). Izv. Akad.
Nauk SSSR, 2146.
Andrianov, K. A., Astakhin, V. V., Pyzhov, V. K. (1962). Izv. Akad. Nauk SSSR, Otd. Khim.
Nauk, 2243.
Antić, V. V., AntiĆ, M. P., Govedarica, M. N., & Dvornić, P. R. (2007). Kinetics and mechanism of
the formation of poly[(1,1,3,3-tetramethyldisiloxanyl)ethylene] and poly(methyldecylsiloxane)
by hydrosilylation. Journal of Polymer Science Part A: Polymer Chemistry, 45(11), 2246–2258.
https://doi.org/10.1002/pola.21992.
Aranguren, M. I., & Macosko, C. W. (1988). Modulus of polybutadiene networks made by
hydrosilation crosslinking. Macromolecules, 21(8), 2484–2491. https://doi.org/10.1021/
ma00186a030.
Arkles, B. (1983). Look what you can make out of silicones. ChemTech, 13(9), 542–555. Available
in: https://www.researchgate.net/publication/272480980
Ba, C.-Y., Shen, Z.-R., Gu, H.-W., Guo, G.-Q., Xie, P., Zhang, R.-B., Zhu, C.-F., Wan, L.-J., Li,
F.-Y., & Huang, C. H. (2003). A triphenylene-containing side chain liquid crystalline ladderlike polysiloxane and its highly ordered superstructure. Liquid Crystals, 30(3), 391–397.
https://doi.org/10.1080/0267829031000089924.
Babonneau, F., & Maquet, J. (2000). Nuclear magnetic resonance techniques for the structural
characterization of siloxane–oxide hybrid materials. Polyhedron, 19(3), 315–322. https://doi.
org/10.1016/S0277-5387(99)00361-7.
Babonneau, F., Soraru, G. D., D’andrea, G., Dire, S., & Bois, L. (1992). Silicon oxycarbide glasses
from sol-gel precursors. MRS Online Proceedings Library Archive, 271, 789–794. https://doi.
org/10.1557/proc-271-789.
Bachari, A., Bélorgey, G., Hélary, G., & Sauvet, G. (1995). Synthesis and characterization of
multiblock copolymers poly[poly(L-lactide)-block-polydimethylsiloxane]. Macromolecular
Chemistry and Physics, 196(1), 411–428. https://doi.org/10.1002/macp.1995.021960130.
Bachrach, A., & Zilkha, A. (1984). Attachment of drugs to polydimethylsiloxanes. European
Polymer Journal, 20(5), 493–500. https://doi.org/10.1016/0014-3057(84)90032-6.
Barr, K. J., Berk, S. C., & Buchwald, S. L. (1994). Titanocene-catalyzed reduction of esters using
polymethylhydrosiloxane as the stoichiometric reductant. The Journal of Organic Chemistry,
59(15), 4323–4326. https://doi.org/10.1021/jo00094a056.
Bassindale, A. R., & Gentle, T. E. (1993). Siloxane and hydrocarbon octopus molecules with silsesquioxane cores. Journal of Materials Chemistry, 3(12), 1319–1325. https://doi.org/10.1039/
jm9930301319.
Baum, K., Baum, J. C., & Ho, T. (1998). Side-loop polymers based on the hydrosilylation of
polybutadiene. Journal of the American Chemical Society, 120(13), 2993–2996. https://doi.
org/10.1021/ja973666a.
Baumann, T. F., Jones, T. V., Wilson, T., Saab, A. P., & Maxwell, R. S. (2009). Synthesis and
characterization of novel PDMS nanocomposites using POSS derivatives as cross-linking
filler. Journal of Polymer Science Part A: Polymer Chemistry, 47(10), 2589–2596. https://doi.
org/10.1002/pola.23344.
Bażant, V., Rathouský, B., & Chvalovský V. (1965) Encyclopedia “Organosilicon compounds”,
vol. 1, Chemistry of Organosilicon Compounds, Publ. House of the Czechoslov. Acad. of
Sci., Prague.
Belot, V., Corriu, R., Leclercq, D., Mutin, P. H., & Vioux, A. (1991). Thermal reactivity of hydrogenosilsesquioxane gels. Chemistry of Materials, 3(1), 127–131. https://doi.org/10.1021/
cm00013a029.
14 Hydrosilyl-Functional Polysiloxanes: Synthesis Reactions and Applications
and physical properties. Journal of Polymer Science Part A: Polymer Chemistry, 39(14),
2414–2425. https://doi.org/10.1002/pola.1218.
Andrianov, K. A., Abhazova, I. I., Khananashvili, L. M., Bogratishvili, G. D., Dogsopulc, T. P., &
Chagelishvili, V. A. (1971b). Zhurn. Obshch. Khim. 41, 606.
Andrianov, K. A., Gavrikova, L. A., & Rodionova, E. F. (1971a). Vysokomol. Soed., 13A, 937–940.
Andrianov, K. A., Kochetkova, A. S., & Khananashvili, L. M. (1968a). Copolymerization of methylvinylsiloxane oligomers with methylhydridosiloxanes. Zhurnal Obshchei Khimii, 38(1),
175–178.
Andrianov, K. A., Nogaideli, A. J., Khananashvili, L. M., & Nakaidze, L. D. (1968b). Izv. Akad.
Nauk SSSR, 2146.
Andrianov, K. A., Astakhin, V. V., Pyzhov, V. K. (1962). Izv. Akad. Nauk SSSR, Otd. Khim.
Nauk, 2243.
Antić, V. V., AntiĆ, M. P., Govedarica, M. N., & Dvornić, P. R. (2007). Kinetics and mechanism of
the formation of poly[(1,1,3,3-tetramethyldisiloxanyl)ethylene] and poly(methyldecylsiloxane)
by hydrosilylation. Journal of Polymer Science Part A: Polymer Chemistry, 45(11), 2246–2258.
https://doi.org/10.1002/pola.21992.
Aranguren, M. I., & Macosko, C. W. (1988). Modulus of polybutadiene networks made by
hydrosilation crosslinking. Macromolecules, 21(8), 2484–2491. https://doi.org/10.1021/
ma00186a030.
Arkles, B. (1983). Look what you can make out of silicones. ChemTech, 13(9), 542–555. Available
in: https://www.researchgate.net/publication/272480980
Ba, C.-Y., Shen, Z.-R., Gu, H.-W., Guo, G.-Q., Xie, P., Zhang, R.-B., Zhu, C.-F., Wan, L.-J., Li,
F.-Y., & Huang, C. H. (2003). A triphenylene-containing side chain liquid crystalline ladderlike polysiloxane and its highly ordered superstructure. Liquid Crystals, 30(3), 391–397.
https://doi.org/10.1080/0267829031000089924.
Babonneau, F., & Maquet, J. (2000). Nuclear magnetic resonance techniques for the structural
characterization of siloxane–oxide hybrid materials. Polyhedron, 19(3), 315–322. https://doi.
org/10.1016/S0277-5387(99)00361-7.
Babonneau, F., Soraru, G. D., D’andrea, G., Dire, S., & Bois, L. (1992). Silicon oxycarbide glasses
from sol-gel precursors. MRS Online Proceedings Library Archive, 271, 789–794. https://doi.
org/10.1557/proc-271-789.
Bachari, A., Bélorgey, G., Hélary, G., & Sauvet, G. (1995). Synthesis and characterization of
multiblock copolymers poly[poly(L-lactide)-block-polydimethylsiloxane]. Macromolecular
Chemistry and Physics, 196(1), 411–428. https://doi.org/10.1002/macp.1995.021960130.
Bachrach, A., & Zilkha, A. (1984). Attachment of drugs to polydimethylsiloxanes. European
Polymer Journal, 20(5), 493–500. https://doi.org/10.1016/0014-3057(84)90032-6.
Barr, K. J., Berk, S. C., & Buchwald, S. L. (1994). Titanocene-catalyzed reduction of esters using
polymethylhydrosiloxane as the stoichiometric reductant. The Journal of Organic Chemistry,
59(15), 4323–4326. https://doi.org/10.1021/jo00094a056.
Bassindale, A. R., & Gentle, T. E. (1993). Siloxane and hydrocarbon octopus molecules with silsesquioxane cores. Journal of Materials Chemistry, 3(12), 1319–1325. https://doi.org/10.1039/
jm9930301319.
Baum, K., Baum, J. C., & Ho, T. (1998). Side-loop polymers based on the hydrosilylation of
polybutadiene. Journal of the American Chemical Society, 120(13), 2993–2996. https://doi.
org/10.1021/ja973666a.
Baumann, T. F., Jones, T. V., Wilson, T., Saab, A. P., & Maxwell, R. S. (2009). Synthesis and
characterization of novel PDMS nanocomposites using POSS derivatives as cross-linking
filler. Journal of Polymer Science Part A: Polymer Chemistry, 47(10), 2589–2596. https://doi.
org/10.1002/pola.23344.
Bażant, V., Rathouský, B., & Chvalovský V. (1965) Encyclopedia “Organosilicon compounds”,
vol. 1, Chemistry of Organosilicon Compounds, Publ. House of the Czechoslov. Acad. of
Sci., Prague.
Belot, V., Corriu, R., Leclercq, D., Mutin, P. H., & Vioux, A. (1991). Thermal reactivity of hydrogenosilsesquioxane gels. Chemistry of Materials, 3(1), 127–131. https://doi.org/10.1021/
cm00013a029.
14 Hydrosilyl-Functional Polysiloxanes: Synthesis Reactions and Applications