Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/147423
Title: Synthesis of vinyl iodide chain-end polymers via organocatalyzed chain-end transformation
Authors: Chang, Jun Jie
Pan, Matthew Houwen
Goto, Atsushi
Keywords: Science::Chemistry::Organic chemistry::Polymers
Issue Date: 2021
Source: Chang, J. J., Pan, M. H. & Goto, A. (2021). Synthesis of vinyl iodide chain-end polymers via organocatalyzed chain-end transformation. Chemical Communications, 57(9), 1105-1108. https://dx.doi.org/10.1039/D0CC07987A
Journal: Chemical Communications
Abstract: In the presence of alkynes (CH≡C–R2), iodide chain-end polymers (Polymer–I) were successfully transformed to vinyl iodide chain-end polymers (Polymer–CH=CR2–I) in a single step via organocatalysis. This reaction is completely metal-free and easy to carry out without using special reagents or special conditions. The polymers encompassed polyacrylates and polymethacrylate, and additional functionalities (e.g., OH and CF3) was also incorporated into the R2 moiety. The obtained Polymer–CH=CR2–I further served as a useful precursor for copper-catalyzed cross-coupling reactions with various thiols (R3–SH) to yield vinyl sulfide chain-end polymers (Polymer–CH=CR2–SR3) with various R3 moieties. Interestingly, under selected conditions, this organocatalysis also offered block-like copolymers containing a conjugated oligo-alkyne segment and a non-conjugated polyacrylate segment. Exploiting the unique structure, the block-like copolymer was used as an efficient dispersant of carbon nanotubes.
URI: https://hdl.handle.net/10356/147423
ISSN: 1364-548X
DOI: 10.1039/D0CC07987A
Rights: © 2021 The Author(s) (Royal Society of Chemistry). All rights reserved. This paper was published in Chemical Communications and is made available with permission of The Author(s) (Royal Society of Chemistry).
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SPMS Journal Articles

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