Abstract

Using different porogens and crosslinkers for 3-O-methacryloyl-1,2;5,6-di-O-isopropylidene-α-D-glucofuranose, porous polymer beads having surface areas of up to 300 m 2 g -1 were synthesized by suspension polymerization. After subsequent removal of the protecting groups, a hydrophilic sugar-containing resin was obtained. In the case when the initial polymer had only very small pores, after hydrolysis, an almost non-porous resin was recovered. With initially large pores, the pore structure of the resin remained unchanged. For resins with medium pore sizes, the pore volume and surface area of the unprotected resin were dependent of the degree of hydrolysis. In fact a linear relationship between surface area and degree of hydrolysis could be observed. Furthermore, this relationship was reversible, i.e. after reprotection of partly or fully hydrolyzed resins, the original pore structure of the protected polymer could be recovered. Depending on the degree of hydrolysis, porous resins of various hydrophilicity, containing reactive hydroxyl groups suitable for further derivatization have been synthesized.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.