279
IARC. (1999). Surgical implants and other foreign bodies. World Heal. Organ. – Int. Agency Res.
Cancer, 74.
Igarashi, M., Matsumoto, T., Kobayashi, T., & Sato, K. (2014). Hydrosilylation of allyl derivatives with T, D and M type hydrosilanes. Journal of Organometallic Chemistry, 749, 421–427.
https://doi.org/10.1016/j.jorganchem.2013.10.014.
Ishiwari, F., Okabe, G., Ogiwara, H., Kajitani, T., Tokita, M., Takata, M., & Fukushima, T. (2018).
Terminal functionalization with a triptycene motif that dramatically changes the structural
and physical properties of an amorphous polymer. Journal of the American Chemical Society,
140(41), 13497–13502. https://doi.org/10.1021/jacs.8b09242.
Iwakiri, N., Nishikawa, T., Kaneko, Y., & Kadokawa, J. I. (2009). Synthesis of amphiphilic polysiloxanes and their properties for formation of nano-aggregates. Colloid & Polymer Science,
287(5), 577–582. https://doi.org/10.1007/s00396-009-2005-4.
Ji, Y., Huang, Y. Y., Tajbakhsh, A. R., & Terentjev, E. M. (2009). Polysiloxane surfactants for the
dispersion of carbon nanotubes in nonpolar organic solvents. Langmuir, 25(20), 12325–12331.
https://doi.org/10.1021/la901622c.
Jia, H., Bai, X., Li, N., Yu, L., & Zheng, L. (2011). Siloxane surfactant induced self-assembly of
gold nanoparticles and their application to SERS. CrystEngComm, 13(20), 6179–6184. https://
doi.org/10.1039/c1ce05715d.
Jiang, H., Chensha, L., & Xuenzhen, H. (2013). Actuators based on liquid crystalline elastomer
materials. Nanoscale, 5(12), 5225–5240. https://doi.org/10.1039/c3nr00037k.
Jonas, G., & Stadler, R. (1994). Carbohydrate modified polysiloxanes II. Synthesis via hydrosilation of mono-, di-and oligosaccharide allylglycosides. Acta Polymerica, 45(1), 14–20. https://
doi.org/10.1002/actp.1994.010450104.
Jones, L., & Tighe, B. (2004). Silicone hydrogel contact lens materials update – Part 2. http://www.
siliconehydrogels.org/editorials/index_august.asp
Junge, K., Möller, K., Wendt, B., Das, S., Goerdes, D., Thurow, K., & Beller, M. (2012).
Enantioselective zinc-catalyzed hydrosilylation of ketones using pybox or pybim ligands.
Chemistry, an Asian Journal, 7(2), 314–320. https://doi.org/10.1002/asia.201100561.
Kaneko, Y., Toyodome, H., Mizumo, T., Shikinaka, K., & Iyi, N. (2014). Preparation of a sulfogroup- containing rod-like polysilsesquioxane with a hexagonally stacked structure and
its proton conductivity. Chemistry—A European Journal, 20(30), 9394–9399. https://doi.
org/10.1002/chem.201402011.
Katsuki, K., Kaneko, K., Kaneko, K., Kato, R., Miyamoto, N., & Hanasaki, T. (2019). Design and
phase transition behavior of siloxane-based monomeric and dimeric liquid crystals bearing
cholesteryl mesogenic groups. Journal of Organometallic Chemistry, 886, 34–39. https://doi.
org/10.1016/j.jorganchem.2019.02.016.
Kolb, E. S., Gaudiana, R. A., & Mehta, P. G. (1996). A new polymeric triarylamine and its use as
a charge transport layer for polymeric LEDs. Macromolecules, 29(7), 2359–2364. https://doi.
org/10.1021/ma951021u.
Kornbluh, R., & Pelrine, R. (2008). High-performance acrylic and silicone elastomers. In F. Carpi,
D. De Rossi, R. Kornbluh, R. Pelrine, & P. Sommer-Larsen (Eds.), Dielectric elastomers
as electromechanical transducers: Fundamentals, materials, devices, models and applications of an emerging electroactive polymer technology (pp. 33–42). https://doi.org/10.1016/
b978-0-08-047488-5.00004-6.
Kowalewska, A., & Nowacka, M. (2015). Synthesis of ladder silsesquioxanes by in situ polycondensation of cyclic tetravinylsiloxanetetraols. Silicon, 7(2), 133–146. https://doi.org/10.1007/
s12633-014-9209-z.
Kuo, A. C. M. (1999). Poly(dimethylsiloxane). In Polymer data handbook (pp. 411–435). Oxford:
Oxford University Press.
Kupareva, A., Mäki-Arvela, P., Grénman, H., Eränen, K., & Murzin, D. Y. (2013). Base-catalyzed
transformations of tetramethyldisiloxane. Industrial and Engineering Chemistry Research,
52(30), 10080–10088. https://doi.org/10.1021/ie401711b.
11 Reactive and Functional Silicones for Special Applications
IARC. (1999). Surgical implants and other foreign bodies. World Heal. Organ. – Int. Agency Res.
Cancer, 74.
Igarashi, M., Matsumoto, T., Kobayashi, T., & Sato, K. (2014). Hydrosilylation of allyl derivatives with T, D and M type hydrosilanes. Journal of Organometallic Chemistry, 749, 421–427.
https://doi.org/10.1016/j.jorganchem.2013.10.014.
Ishiwari, F., Okabe, G., Ogiwara, H., Kajitani, T., Tokita, M., Takata, M., & Fukushima, T. (2018).
Terminal functionalization with a triptycene motif that dramatically changes the structural
and physical properties of an amorphous polymer. Journal of the American Chemical Society,
140(41), 13497–13502. https://doi.org/10.1021/jacs.8b09242.
Iwakiri, N., Nishikawa, T., Kaneko, Y., & Kadokawa, J. I. (2009). Synthesis of amphiphilic polysiloxanes and their properties for formation of nano-aggregates. Colloid & Polymer Science,
287(5), 577–582. https://doi.org/10.1007/s00396-009-2005-4.
Ji, Y., Huang, Y. Y., Tajbakhsh, A. R., & Terentjev, E. M. (2009). Polysiloxane surfactants for the
dispersion of carbon nanotubes in nonpolar organic solvents. Langmuir, 25(20), 12325–12331.
https://doi.org/10.1021/la901622c.
Jia, H., Bai, X., Li, N., Yu, L., & Zheng, L. (2011). Siloxane surfactant induced self-assembly of
gold nanoparticles and their application to SERS. CrystEngComm, 13(20), 6179–6184. https://
doi.org/10.1039/c1ce05715d.
Jiang, H., Chensha, L., & Xuenzhen, H. (2013). Actuators based on liquid crystalline elastomer
materials. Nanoscale, 5(12), 5225–5240. https://doi.org/10.1039/c3nr00037k.
Jonas, G., & Stadler, R. (1994). Carbohydrate modified polysiloxanes II. Synthesis via hydrosilation of mono-, di-and oligosaccharide allylglycosides. Acta Polymerica, 45(1), 14–20. https://
doi.org/10.1002/actp.1994.010450104.
Jones, L., & Tighe, B. (2004). Silicone hydrogel contact lens materials update – Part 2. http://www.
siliconehydrogels.org/editorials/index_august.asp
Junge, K., Möller, K., Wendt, B., Das, S., Goerdes, D., Thurow, K., & Beller, M. (2012).
Enantioselective zinc-catalyzed hydrosilylation of ketones using pybox or pybim ligands.
Chemistry, an Asian Journal, 7(2), 314–320. https://doi.org/10.1002/asia.201100561.
Kaneko, Y., Toyodome, H., Mizumo, T., Shikinaka, K., & Iyi, N. (2014). Preparation of a sulfogroup- containing rod-like polysilsesquioxane with a hexagonally stacked structure and
its proton conductivity. Chemistry—A European Journal, 20(30), 9394–9399. https://doi.
org/10.1002/chem.201402011.
Katsuki, K., Kaneko, K., Kaneko, K., Kato, R., Miyamoto, N., & Hanasaki, T. (2019). Design and
phase transition behavior of siloxane-based monomeric and dimeric liquid crystals bearing
cholesteryl mesogenic groups. Journal of Organometallic Chemistry, 886, 34–39. https://doi.
org/10.1016/j.jorganchem.2019.02.016.
Kolb, E. S., Gaudiana, R. A., & Mehta, P. G. (1996). A new polymeric triarylamine and its use as
a charge transport layer for polymeric LEDs. Macromolecules, 29(7), 2359–2364. https://doi.
org/10.1021/ma951021u.
Kornbluh, R., & Pelrine, R. (2008). High-performance acrylic and silicone elastomers. In F. Carpi,
D. De Rossi, R. Kornbluh, R. Pelrine, & P. Sommer-Larsen (Eds.), Dielectric elastomers
as electromechanical transducers: Fundamentals, materials, devices, models and applications of an emerging electroactive polymer technology (pp. 33–42). https://doi.org/10.1016/
b978-0-08-047488-5.00004-6.
Kowalewska, A., & Nowacka, M. (2015). Synthesis of ladder silsesquioxanes by in situ polycondensation of cyclic tetravinylsiloxanetetraols. Silicon, 7(2), 133–146. https://doi.org/10.1007/
s12633-014-9209-z.
Kuo, A. C. M. (1999). Poly(dimethylsiloxane). In Polymer data handbook (pp. 411–435). Oxford:
Oxford University Press.
Kupareva, A., Mäki-Arvela, P., Grénman, H., Eränen, K., & Murzin, D. Y. (2013). Base-catalyzed
transformations of tetramethyldisiloxane. Industrial and Engineering Chemistry Research,
52(30), 10080–10088. https://doi.org/10.1021/ie401711b.
11 Reactive and Functional Silicones for Special Applications