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An efficient synthetic strategy that includes protection–modification–deprotection consequence was successfully developed to obtain novel water-soluble, amphiphilic, surface-active maltodextrin-based glycosilicones.

We devise a high-carrier-mobility hole-transport layer with less hole loss, obtained via doping poly(9-vinylcarbazole) into poly[(9,9-dioctylfluorenyl-2,7-diyl)-alt-(4,4′-(N-(4-butylphenyl)))], achieving high external quantum efficiency QLEDs (22.7%).

Rubber materials are the key components of flexible optoelectronic devices, especially for the light-emitting diodes based on arrays of inorganic nanowires (NWs). This paper reports on polydimethylsiloxane-graft-polystyrene (PDMS-St) as a new flexible substrate of GaP NW array structures. The NWs were encapsulated by the newly introduced G-coating method to substitute the inefficient mainstream spin-coating. To further exploit the flexibility and the stretchability of the NW/PDMS-St structures, the ferrocenyl-containing polymethylhydrosiloxane was synthesized and successfully used as an electrode for the NWs. In order to make an alternative highly efficient transparent electrode, a new application of conductive single-walled carbon nanotubes was demonstrated. The novel materials and methods demonstrated unsurpassed mechanical stability of the fabricated flexible electronic devices.

The platinum-catalyzed self-cross-linking of polymethylhydrosiloxane at RT in air was performed for the first time and proved by 1H, 13C, and 29Si SSNMR and swelling measurements. Quantum chemical modeling of possible structures was investigated. Platinum (0) and (ii) complexes were used as catalysts between the Si-H groups of polymethylhydrosiloxane. Karstedt's catalyst leads to Si-O-Si and Si-Si bond formation, but cis-[PtCl2(BnCN)2] generates predominantly Si-O-Si cross-links. cis-[PtCl2(BnCN)2] allows creating high-quality silicone rubbers without visible mechanical defects. This cross-linking approach can be used to obtain new Si-H-containing silicone materials.

Cyclic organosilicon triperoxides were found to be vinyl-selective free-radical initiators for thermal curing at 100–180 °C of vinyl-terminated polydimethylsiloxane and trimethylsilyl-terminated polymethylhydrosiloxane producing homogeneous transparent silicone rubbers with antibacterial properties. The usage of the cyclic organosilicon triperoxides as the curing agents does not require free radical inhibitors in comparison with diacyl- and dialkyl peroxides. Among the tested compounds, the peroxide with the Me–Si–Me fragment and two cyclohexane rings is a much more active curing agent (180 °C, c = 0.22 M, τcuring = 45 min) than other organosilicon peroxides. Cured silicone samples from mixtures with vinyl-terminated polysiloxane and silicone hydride have improved mechanical properties: peroxides provide more than 200% elongation, and compression sets of the samples are less than 1%. The prepared silicone rubbers showed pronounced antibacterial activity.