Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 14694-95-2, is researched, Molecular C54H45ClP3Rh, about Stability of silicones modified with PEO-silane amphiphiles: Impact of structure and concentration, the main research direction is silicone PEO silane amphiphile concentration.Computed Properties of C54H45ClP3Rh.
The efficacy of poly (ethylene oxide) (PEO)-based surface-modifying additives (SMAs), following the bulk-modification of silicones, requires sustained, water-driven PEO migration to the surface to achieve hydrophilicity and subsequent reduction of protein adsorption. Herein, a condensation cure silicone was modified with PEO-silane amphiphile SMAs (5-100 μmol per 1 g silicone) comprised of an oligo (di-Me siloxane) (ODMS) tether, PEO segment and optional triethoxysilane (TEOS) crosslinkable group. This allowed us to confirm that the TEOS crosslinkable group was not necessary and that the ODMS tether (m = 13 or 30) could sufficiently phys. anchor the amphiphile in the silicone network. Surface hydrophilicity was examined before and after aqueous conditioning, as well as mass loss and water uptake after conditioning. Overall, silicones modified with all amphiphilic SMAs produced increasingly hydrophilic surfaces and their hydrophilicity was maintained following conditioning. At all concentrations, all amphiphilic SMA modified silicones had minimal water uptake and mass loss, comparable to that of unmodified silicone. Finally, silicones modified with all amphiphilic SMAs ≥25 μmol exhibited exceptional protein resistance that was not appreciably diminished after conditioning.
Different reactions of this compound(Tris(triphenylphosphine)chlororhodium)Computed Properties of C54H45ClP3Rh require different conditions, so the reaction conditions are very important.
Reference:
Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate