Amphiphilic polyether-based block copolymers as crosslinkable ligands for Au-nanoparticles. Issue 31 (17th December 2014)

• Record Type: Journal Article
• Authors: Hörenz, Christoph; Rudolph, Tobias; Barthel, Markus J.; Günther, Ulrike; Schacher, Felix H.
• Is Part Of: Polymer chemistry. Volume 6:Issue 31(2015)
• Page Start: 5633
• Page End: 5642
• Publication Date: 2014-12-17
• Subjects: Polymers -- Periodicals; Macromolecules -- Periodicals; Polymerization -- Periodicals; 547.705
• DOI: 10.1039/c4py01434k
• Languages: English
• ISSNs: 1759-9954

Abstract

Abstract : We report on the synthesis of thiol-terminated, polyether-based block copolymers featuring a crosslinkable block and their use as ligands for Au-nanoparticles in organic solvents. Abstract : We report on the synthesis of thiol-terminated, polyether-based amphiphilic block copolymers with a hydrophilic poly(ethylene oxide) (PEO) segment and a second crosslinkable block of either poly(furfuryl glycidyl ether) (PFGE) or poly(allyl glycidyl ether) (PAGE). Both block copolymers could be synthesized with narrow dispersities ( Đ ≤ 1.07) via living anionic ring-opening polymerization (AROP). Introduction of the thiol-moiety enables the application of these block copolymers as ligands for the preparation of Au-nanoparticles (Au-NPs) by direct reduction of suitable precursors in N, N -dimethylacetamide (DMAc). The ligands of the obtained hybrid nanoparticles featuring an Au core and a block copolymer shell were crosslinked either via Diels–Alder reactions for the PFGE segment or via hydrosilylation chemistry targeting the PAGE segment. In this way, shell-crosslinked Au-NPs with enhanced stability against ligand exchange reactions in the presence of competitive ligands like alkyl thiols could be prepared.