A method of grafting well-defined and hydrolytically stable surface structures onto cross-linked poly(dimethylsiloxane) (PDMS) has been developed. In the first step, argon microwave plasma was used to introduce Si-H groups onto the surface. In the second step, allyltetrafluoroethyl ether was grafted to these Si-H groups using a platinum-catalyzed hydrosilylation reaction. The influences of the plasma parameters of power, pressure, and treatment time on the surface composition, both before and after the hydrosilylation step, were investigated by X-ray photoelectron spectroscopy and contact angle measurements. It was found that the pressure had little influence on the results, whereas the power and treatment time determined the rate of change in surface composition during the plasma treatment. The graft yield reached a plateau value corresponding to about 5% grafted molecules in the analyzed surface region. Hydrosilylation grafting of PDMS is a promising method to obtain biomaterials with hydrolytically stable structures covalently bound to the surface.
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http://dx.doi.org/10.1021/bm015654u | DOI Listing |
PLoS One
December 2024
Division of Ophthalmology, Department of Special Surgery, Faculty of Medicine, Jordan University of Science & Technology, Irbid, Jordan.
Purpose: The emulsification of silicone oil (SO) remains poorly understood. In the present study, we investigated the physical properties of unused pharmaceutical SO samples under various conditions. Moreover, clinical correlations with the patients' SO samples were assessed.
View Article and Find Full Text PDFJ Phys Chem A
January 2025
Departamento de Química Física y Química Inorgánica, Facultad de Ciencias─I.U. CINQUIMA, Paseo de Belén, 7, 47011 Valladolid, Spain.
The conformational space of 3-chloropropionic acid has been studied under the isolated conditions of a supersonic expansion using Stark-modulated free-jet absorption millimeter-wave and centimeter-wave chirped-pulse Fourier transform microwave spectroscopy techniques. The rotational spectra originating from the three most stable conformers including Cl and Cl isotopologues were observed in both experiments using helium expansion while a partial conformational relaxation involving skeletal rearrangements takes place in an argon expansion. The rotational parameters, geometries, and energy order were determined from the experiment, allowing a comparison with quantum chemical predictions.
View Article and Find Full Text PDFJ Phys Chem A
October 2024
Department of Chemistry, Amherst College, P.O. Box 5000, Amherst, Massachusetts 01002-5000, United States.
The and isomers of the chiral tagging candidate molecule, 2-fluoro-3-(trifluoromethyl)oxirane, as well as the lowest energy gas-phase heterodimer of each with the argon atom, are characterized via quantum chemistry calculations and microwave rotational spectroscopy from 5 to 18 GHz and their ground state, vibrationally averaged structures, are determined. Apart from the / nature of the ring substitution and small differences in the dihedral angle specifying the rotation of the trifluoromethyl group, the two oxirane molecules and their respective argon complexes each have remarkable structural similarity. In contrast, the binding mode of argon to the oxirane, while similar for the two complexes here, is distinct from those modes observed in previous argon-fluorooxirane species.
View Article and Find Full Text PDFJ Phys Chem A
October 2024
Department of Chemistry, Amherst College, P.O. Box 5000, Amherst, Massachusetts 01002-5000, United States.
Microwave spectra of both the and isomers of 1,2,3,3,3-pentafluoropropene along with all three of the singly substituted C isotopologues for each are obtained using broadband chirped-pulse Fourier transform microwave spectroscopy from 2.0-18.1 GHz.
View Article and Find Full Text PDFMolecules
August 2024
Department of Chemical and Environment Engineering, Faculty of Chemical Technology and Engineering, West Pomeranian University of Technology in Szczecin, Pułaskiego,10, 70-322 Szczecin, Poland.
The adsorption properties of microporous carbon materials modified with iron citrate were investigated. The carbon materials were produced based on resorcinol-formaldehyde resin, treated in a microwave assisted solvothermal reactor, and next carbonized in the tube furnace at a temperature of 700 °C under argon atmosphere. Iron citrate was applied as a modifier, added to the material precursor before the synthesis in the reactor, in the quantity enabling to obtain the nanocomposites with C:Fe mass ratio equal to 10:1.
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