Publications by authors named "Vjacheslav V Zuev"

We suggest a new method for postsynthesis modification of silicones containing silanol groups. It was found that trimethylborate is an effective catalyst for dehydrative condensation of silanol groups with the formation of ladder-like blocks. The utility of this approach was demonstrated on postsynthesis modification of poly-( poly(dimethylsiloxane)- ladder-like poly(phenylsiloxane)) and poly-( poly((3,3',3″-trifluoropropyl-methyl)siloxane)- ladder-like poly(phenylsiloxane) with a combination of linear and ladder-like blocks having silanol groups.

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H spin-diffusion solid-state NMR was utilized to elucidate the domain size in multiblock-copolymers (BCPs) poly-( poly(dimethylsiloxane)- ladder-like poly(phenylsiloxane)) and poly-( poly((3,3',3″-trifluoropropyl-methyl)siloxane)- ladder-like poly(phenylsiloxane). It was found that these BCPs form worm-like morphology with rigid cylinders dispersed in amorphous matrix. By using the combination of solid-state NMR techniques such as C CP/MAS, C direct-polarization MAS and 2D H EXSY, it was shown that the main factor which governs the diameter value of these rigid domains is the presence of interpenetrating segments of soft blocks.

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Multiblock copolymers containing linear polydimethylsiloxane or polymethyltrifluoropropylsiloxane and ladder-like polyphenylsiloxane were synthesized in a one-step pathway. The functional homopolymer blocks and final multiblock copolymers were characterized using solution and solid-state multinuclear H, C, F, and Si NMR spectroscopy. It was shown that the ladder-like block contains silanol units, which influence the adhesion properties of multiblock copolymers and morphology of their casted films.

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A set of aromatic-oxyaliphatic polyurethanes (PUs) with different mass fractions of components also containing fluorinated fragments was synthesized and studied using various solid-state NMR techniques and dielectric spectroscopy. In contrast to the common model suggested by Cooper and Tobolsky in 1966, the rigid domains of microphase separated PUs are formed, not only by units containing urethane bonds, but also by oxyethylene fragments that form a common rigid phase. The urethane bonds and oxyethylene fragments are incorporated into both rigid and soft phases.

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