278
Halila, S., Manguian, M., Fort, S., Cottaz, S., Hamaide, T., Fleury, E., & Driguez, H. (2008).
Syntheses of well-defined glyco-polyorganosiloxanes by “click” chemistry and their surfactant properties. Macromolecular Chemistry and Physics, 209(12), 1282–1290. https://doi.
org/10.1002/macp.200700629.
Hamurcu, E. E., & Baysal, B. M. (1993). Interpenetrating polymer networks of
poly(dimethylsiloxane) preparation and characterization. Polymer, 34(24), 5163–5167. https://
doi.org/10.1016/0032-3861(93)90264-b.
Hanamura, H., & Nemoto, N. (2014). Synthesis and optical properties of poly(tetramethylsila
rylenesiloxane) derivative bearing diphenylcyclopentadithiophene moiety. Polymer, 55(26),
6672–6679. https://doi.org/10.1016/j.polymer.2014.10.048.
Hanamura, H., Hattori, R., Maruyama, R., & Nemoto, N. (2014). Synthesis and characterization of
poly(tetramethylsilarylenesiloxane) derivatives bearing benzodithiophene moieties. Reactive
and Functional Polymers, 84, 60–67. https://doi.org/10.1016/j.reactfunctpolym.2014.09.007.
Hauser, E. A. (1955). The colloid science of silica and silicones. Clays and Clay Minerals, 4,
45–53. https://doi.org/10.1346/ccmn.1955.0040107.
Hessberger, T., Braun, L. B., Serra, C. A., & Zentel, R. (2018). Microfluidic preparation of liquid
crystalline elastomer actuators. Journal of Visualized Experiments, 135, e57715. https://doi.
org/10.3791/57715.
Hetzer, R. H., Kümmerlen, F., Wirz, K., & Blunk, D. (2014). Fire testing a new fluorine-free AFFF
based on a novel class of environmentally sound high performance siloxane surfactants. Fire
Safety Science, 11, 1261–1270. https://doi.org/10.3801/iafss.fss.11-1261.
Hill, R. M. (1998). Superspreading. Current Opinion in Colloid & Interface Science, 3(3),
247–254. https://doi.org/10.1016/s1359-0294(98)80068-x.
Hill, R. M. (1999). Silicone surfactants. New York: Marel Dekker, INC.
Hill, R. M. (2002). Silicone surfactants New developments. Current Opinion in Colloid & Interface
Science, 7(5–6), 255–261. https://doi.org/10.1016/s1359-0294(02)00068-7.
Hong, M., Chen, J., & Chen, E. Y. X. (2018). Polymerization of polar monomers mediated by
main-group Lewis acid-base pairs. Chemical Reviews, 118(20), 10551–10616. https://doi.
org/10.1021/acs.chemrev.8b00352.
Hoyle, C. E., & Bowman, C. N. (2010). Thiol-ene click chemistry. Angewandte Chemie,
International Edition, 49(9), 1540–1573. https://doi.org/10.1002/anie.200903924.
Hron, P. (2003). Hydrophilisation of silicone rubber for medical applications. Polymer
International, 52(9), 1531–1539. https://doi.org/10.1002/pi.1273.
Https://brandt.co/ Silicone Based Surfactants.
Hu, J. S., Zhang, B. Y., He, X. Z., & Cheng, C. S. (2004). Synthesis, structure and characterization
of side chain cholesteric liquid crystalline polysiloxanes. Liquid Crystals, 31(10), 1357–1365.
https://doi.org/10.1080/02678290410001718980.
Huang, Y., Yi, S., Lv, Z., & Huang, C. (2016). Facile fabrication of superhydrophobic coatings based on two silica sols. Colloid & Polymer Science, 294(9), 1503–1509. https://doi.
org/10.1007/s00396-016-3912-9.
Hubbert, C., Breunig, M., Carroll, K. J., Rominger, F., & Hashmi, A. S. K. (2014). Simple synthesis
of new mixed isocyanide-NHC-platinum(II) complexes and their catalytic activity. Australian
Journal of Chemistry, 67(3), 469. https://doi.org/10.1071/ch13546.
Hurduc, N., Macovei, A., Paius, C., Raicu, A., Moleavin, I., Branza-Nichita, N., Hamel, M., &
Rocha, L. (2013). Azo-polysiloxanes as new supports for cell cultures. Materials Science and
Engineering: C, 33(4), 2440–2445. https://doi.org/10.1016/j.msec.2013.01.012.
Hurduc, N., Donose, B. C., Macovei, A., Paius, C., Ibanescu, C., Scutaru, D., Hamel, M., BranzaNichita, N., & Rocha, L. (2014). Direct observation of athermal photofluidisation in azopolymer films. Soft Matter, 10(26), 4640–4647. https://doi.org/10.1039/c4sm00397g.
Iacob, M., Racles, C., Dascalu, M., Tugui, C., Lozan, V., & Cazacu, M. (2019). Nanomaterials
developed by processing iron coordination compounds for biomedical application. Journal of
Nanomaterials, 2592974. https://doi.org/10.1155/2019/2592974.
C. Racles et al.
Halila, S., Manguian, M., Fort, S., Cottaz, S., Hamaide, T., Fleury, E., & Driguez, H. (2008).
Syntheses of well-defined glyco-polyorganosiloxanes by “click” chemistry and their surfactant properties. Macromolecular Chemistry and Physics, 209(12), 1282–1290. https://doi.
org/10.1002/macp.200700629.
Hamurcu, E. E., & Baysal, B. M. (1993). Interpenetrating polymer networks of
poly(dimethylsiloxane) preparation and characterization. Polymer, 34(24), 5163–5167. https://
doi.org/10.1016/0032-3861(93)90264-b.
Hanamura, H., & Nemoto, N. (2014). Synthesis and optical properties of poly(tetramethylsila
rylenesiloxane) derivative bearing diphenylcyclopentadithiophene moiety. Polymer, 55(26),
6672–6679. https://doi.org/10.1016/j.polymer.2014.10.048.
Hanamura, H., Hattori, R., Maruyama, R., & Nemoto, N. (2014). Synthesis and characterization of
poly(tetramethylsilarylenesiloxane) derivatives bearing benzodithiophene moieties. Reactive
and Functional Polymers, 84, 60–67. https://doi.org/10.1016/j.reactfunctpolym.2014.09.007.
Hauser, E. A. (1955). The colloid science of silica and silicones. Clays and Clay Minerals, 4,
45–53. https://doi.org/10.1346/ccmn.1955.0040107.
Hessberger, T., Braun, L. B., Serra, C. A., & Zentel, R. (2018). Microfluidic preparation of liquid
crystalline elastomer actuators. Journal of Visualized Experiments, 135, e57715. https://doi.
org/10.3791/57715.
Hetzer, R. H., Kümmerlen, F., Wirz, K., & Blunk, D. (2014). Fire testing a new fluorine-free AFFF
based on a novel class of environmentally sound high performance siloxane surfactants. Fire
Safety Science, 11, 1261–1270. https://doi.org/10.3801/iafss.fss.11-1261.
Hill, R. M. (1998). Superspreading. Current Opinion in Colloid & Interface Science, 3(3),
247–254. https://doi.org/10.1016/s1359-0294(98)80068-x.
Hill, R. M. (1999). Silicone surfactants. New York: Marel Dekker, INC.
Hill, R. M. (2002). Silicone surfactants New developments. Current Opinion in Colloid & Interface
Science, 7(5–6), 255–261. https://doi.org/10.1016/s1359-0294(02)00068-7.
Hong, M., Chen, J., & Chen, E. Y. X. (2018). Polymerization of polar monomers mediated by
main-group Lewis acid-base pairs. Chemical Reviews, 118(20), 10551–10616. https://doi.
org/10.1021/acs.chemrev.8b00352.
Hoyle, C. E., & Bowman, C. N. (2010). Thiol-ene click chemistry. Angewandte Chemie,
International Edition, 49(9), 1540–1573. https://doi.org/10.1002/anie.200903924.
Hron, P. (2003). Hydrophilisation of silicone rubber for medical applications. Polymer
International, 52(9), 1531–1539. https://doi.org/10.1002/pi.1273.
Https://brandt.co/ Silicone Based Surfactants.
Hu, J. S., Zhang, B. Y., He, X. Z., & Cheng, C. S. (2004). Synthesis, structure and characterization
of side chain cholesteric liquid crystalline polysiloxanes. Liquid Crystals, 31(10), 1357–1365.
https://doi.org/10.1080/02678290410001718980.
Huang, Y., Yi, S., Lv, Z., & Huang, C. (2016). Facile fabrication of superhydrophobic coatings based on two silica sols. Colloid & Polymer Science, 294(9), 1503–1509. https://doi.
org/10.1007/s00396-016-3912-9.
Hubbert, C., Breunig, M., Carroll, K. J., Rominger, F., & Hashmi, A. S. K. (2014). Simple synthesis
of new mixed isocyanide-NHC-platinum(II) complexes and their catalytic activity. Australian
Journal of Chemistry, 67(3), 469. https://doi.org/10.1071/ch13546.
Hurduc, N., Macovei, A., Paius, C., Raicu, A., Moleavin, I., Branza-Nichita, N., Hamel, M., &
Rocha, L. (2013). Azo-polysiloxanes as new supports for cell cultures. Materials Science and
Engineering: C, 33(4), 2440–2445. https://doi.org/10.1016/j.msec.2013.01.012.
Hurduc, N., Donose, B. C., Macovei, A., Paius, C., Ibanescu, C., Scutaru, D., Hamel, M., BranzaNichita, N., & Rocha, L. (2014). Direct observation of athermal photofluidisation in azopolymer films. Soft Matter, 10(26), 4640–4647. https://doi.org/10.1039/c4sm00397g.
Iacob, M., Racles, C., Dascalu, M., Tugui, C., Lozan, V., & Cazacu, M. (2019). Nanomaterials
developed by processing iron coordination compounds for biomedical application. Journal of
Nanomaterials, 2592974. https://doi.org/10.1155/2019/2592974.
C. Racles et al.