ABSTRACT
Amphiphilic branched silica derivatives associated with oligomeric medium (ASiP) were obtained using tetraethoxysilane, polyoxyethylene glycol and low molecular weight polydimethylsiloxane. The creation of a silica core was based on tetraethoxysilane hydrolysis and condensation reactions by using water and a potassium diethylene glycolate as the catalyst. These reactions proceeded with the sequential participation of polyoxyethylene glycol and polydimethylsiloxane in parallel transetherification reactions. Microporous polymer film based on 2,4-toluene diisocyanate and block copolymers of propylene and ethylene oxides with terminal potassium-alcoholate groups were modified by ASiP. It has been shown that ASiP at the phase interface between thermodynamically incompatible macrochains performs the function of a link. It leads to a significant increase of intermolecular interactions and the supramolecular organization of the modified microporous polymers.
ABSTRACT
The hyperbranched polymers have drawn intensive attention in the design of macromolecules and functional materials because of their unique physical and chemical properties resulting from the branched architecture and the high number of functional groups. In the present study, by means of light scattering, viscosimetry, thermomechanical analysis, tensile stress-strain, mechanical loss tangent and water vapor permeability measurements, we demonstrate the hierarchical macromolecular organization of organoboron polyurethanes synthesized using sterically hindered amino ethers (AEBA) of boric acid. It is shown that the water vapor permeability of polyurethanes obtained on the basis of sterically hindered aminoethers of boric acid is due to the peculiarities of the chemical structure of AEBA, which can exhibit an ionomeric nature and the presence of steric hindrances created in the hyperbranched structure of AEBA, which can lead to an increase in free volume in such polyurethanes.