Peer-reviewedCC BYPolymers
Comparison of the Reactivity of PDMS with Terminal Allyl and Vinyl Groups in the Hydrosilylation Reaction
- 1, Russian Academy of Sciences, Profsoyuznaya 70, 117393 Moscow, Russia; (V.G.); (F.K.); (S.A.); (K.B.); (K.B.); (A.M.)
Related
- Metal/Support Interfaces Overcome Reactivity Constraints of the Oxygen Reduction Reaction
- Reactivity and Selectivity of Photocatalytic Nitrate Reduction Reaction to Ammonia: Pt, Pd, Ir, and Rh Single Atoms on p-Type TiO2 Nanotubes.
- Utilization of heuristic approaches and molecular modelling to visualise chemical reactivity in small student groups
- Tailoring Liquid Crystalline Self‐Assembly and Photophysical Properties of Unsymmetrical Fluorenones via Polar Terminal Groups
- Well-defined alkali metal catalysts for selective reduction of functionalized esters and carbonyl compounds via hydrosilylation.
BibTeX
@article{gubarev2026comparison,
title = {{Comparison of the Reactivity of PDMS with Terminal Allyl and Vinyl Groups in the Hydrosilylation Reaction}},
author = {Valentin Gubarev and Fedor Krylov and Sofia Ardabevskaia and Kseniya Bezlepkina and Kirill Bakanov and Sergey Milenin and Aziz Muzafarov},
journal = {Polymers},
year = {2026},
month = sep,
url = {https://europepmc.org/article/PMC/PMC13666875},
note = {CC BY},
}
RIS
TY - JOUR
TI - Comparison of the Reactivity of PDMS with Terminal Allyl and Vinyl Groups in the Hydrosilylation Reaction
AU - Valentin Gubarev
AU - Fedor Krylov
AU - Sofia Ardabevskaia
AU - Kseniya Bezlepkina
AU - Kirill Bakanov
AU - Sergey Milenin
AU - Aziz Muzafarov
PY - 2026
DA - 2026/09/29
JO - Polymers
UR - https://europepmc.org/article/PMC/PMC13666875
SN - 2073-4360
ER -