Alexander Sunder

Glycidol represents a latent cyclic AB2-type monomer that can be polymerized in a ring-opening multibranching polymerization (ROMBP). Hyperbranched aliphatic polyethers with controlled molecular weights and narrow molecular weight distribution have been prepared via anionic polymerization of glycidol with rapid cation-exchange equilibrium. 1,1,1-Tris(hydroxymethyl)propane (TMP) was partially deprotonated (10%) and used as initiator for the anionic polymerization carried out under slow addition conditions to minimize polymerization without initiator as well as cyclization. 13C NMR spectra were employed to assess the degree of branching (DB), which was in the range 0.53−0.59. 13C NMR, MALDI-TOF mass spectrometry, vapor pressure osmometry (VPO), and GPC were used to characterize molecular weights and polydispersities of the polyols formed, showing good agreement. n for the polymers prepared was in the range 15−83 (M̄n = 1250−6500), and M̄w/M̄n obtained was 1.13−1.47, being exceptionally low for hyperbranched polymers. MALDI-TOF spectra evidenced complete attachment of the hyperbranched structures to the TMP initiator and the absence of macrocyclics as well as hyperbranched macromolecules without initiator, due to the slow addition. The hyperbranched polyethers prepared showed Tg's between −20 and − 26 °C.

This article summarizes basic principles and recent progress in the field of cascade-branched polymers. Methods for the preparation of macromolecules with hyperbranched structures are presented and compared concerning the extent of control over molecular weights and polydispersity. Step-growth and recently developed chain-growth strategies as well as enzyme and transition metal catalyzed polymerizations are discussed with respect to mechanism and future potential.

Polar dyes can be solubilized in apolar media—molecular nanocapsules with hydrophilic interiors have been prepared (see schematic representation) using polyglycerols with narrow polydispersity and simple esterification with fatty acids. These unimolecular micelles offer attractive potential for a variety of applications ranging from controlled drug release to the design of microreactors and catalysts.

ADVERTISEMENT RETURN TO ISSUEPREVCommunicationNEXTAn Approach to Glycerol Dendrimers and Pseudo-Dendritic PolyglycerolsRainer Haag, Alexander Sunder, and Jean-François StumbéView Author Information Freiburger Materialforschungszentrum und Institut für Makromolekulare Chemie, Albert-Ludwigs-Universität, Stefan-Meier-Strasse 21, 79104 Freiburg, Germany Cite this: J. Am. Chem. Soc. 2000, 122, 12, 2954–2955Publication Date (Web):March 10, 2000Publication History Received14 December 1999Published online10 March 2000Published inissue 1 March 2000https://pubs.acs.org/doi/10.1021/ja994363ehttps://doi.org/10.1021/ja994363erapid-communicationACS PublicationsCopyright © 2000 American Chemical SocietyRequest reuse permissionsArticle Views3421Altmetric-Citations189LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-AlertscloseSupporting Info (1)»Supporting Information Supporting Information SUBJECTS:Alcohols,Dendrons,Organic polymers,Physical and chemical properties,Polymers Get e-Alerts

Polar dyes can be solubilized in apolar media-molecular nanocapsules with hydrophilic interiors have been prepared (see schematic representation) using polyglycerols with narrow polydispersity and simple esterification with fatty acids. These unimolecular micelles offer attractive potential for a variety of applications ranging from controlled drug release to the design of microreactors and catalysts.