4.7 Article

Hybrid Polycarbosilane-Siloxane Dendrimers: Synthesis and Properties

期刊

POLYMERS
卷 13, 期 4, 页码 -

出版社

MDPI
DOI: 10.3390/polym13040606

关键词

dendrimers; synthesis of dendrimers; synthesis of hybrid carbosilane-siloxane structures; thermal properties

资金

  1. Russian Foundation for Basic Research (RFBR) [18-29-04037]
  2. Russian Science Foundation [18-13-00411]
  3. Russian Foundation for Basic Research [19-03-00779]
  4. Ministry of Science and Higher Education of the Russian Federation within the State assignment FSRC 'Crystallography and Photonics' RAS
  5. Ministry of Science and Higher Education of the Russian Federation in INEOS RAS
  6. Ministry of Science and Higher Education of the Russian Federation
  7. Russian Science Foundation [18-13-00411] Funding Source: Russian Science Foundation

向作者/读者索取更多资源

Carbosilane dendrimers of different generations were synthesized, with theoretical models and simulations confirming their monodispersity and almost spherical shape. Glass transition temperature was found to be independent of generation, but greatly affected by the chemical nature of terminal groups. The viscoelastic properties of high-generation dendrimers exhibited general trends with increasing generation, determined by the regular branching structure.
A series of carbosilane dendrimers of the 4th, 6th, and 7th generations with a terminal trimethylsilylsiloxane layer was synthesized. Theoretical models of these dendrimers were developed, and equilibrium dendrimer conformations obtained via molecular dynamics simulations were in a good agreement with experimental small-angle X-ray scattering (SAXS) data demonstrating molecule monodispersity and an almost spherical shape. It was confirmed that the glass transition temperature is independent of the dendrimer generation, but is greatly affected by the chemical nature of the dendrimer terminal groups. A sharp increase in the zero-shear viscosity of dendrimer melts was found between the 5th and the 7th dendrimer generations, which was qualitatively identical to that previously reported for polycarbosilane dendrimers with butyl terminal groups. The viscoelastic properties of high-generation dendrimers seem to follow some general trends with an increase in the generation number, which are determined by the regular branching structure of dendrimers.

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