Facile preparation of supramolecular (ABAC)n multiblock copolymers from Hamilton wedge and barbiturate-functionalized RAFT agentsElectronic supplementary information (ESI) available: 1H and 13C NMR spectra of compound 2 and CTAs, 13C NMR spectra of Ba-PS-b-PnBuA-b-PS-Ba4 and HW-PI-HW4, ESI-TOF mass spectra of CTAs. See DOI: 10.1039/c3py01482g

Two original Hamilton wedge (HW)/barbiturate (Ba) functionalized symmetrical trithiocarbonates have been successfully synthesized and their capability to efficiently mediate the polymerization of styrene, n BuA and isoprene was investigated. Relying on supramolecular association of the recognition c...

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Main Authors Chen, Senbin, Deng, Yuanming, Chang, Xijun, Barqawi, Haitham, Schulz, Matthias, Binder, Wolfgang H
Format Journal Article
LanguageEnglish
Published 18.03.2014
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Abstract Two original Hamilton wedge (HW)/barbiturate (Ba) functionalized symmetrical trithiocarbonates have been successfully synthesized and their capability to efficiently mediate the polymerization of styrene, n BuA and isoprene was investigated. Relying on supramolecular association of the recognition couple, telechelic macromolecular building blocks subsequently afford the formation of novel supramolecular (ABAC) n multiblock copolymers, where A is in a glassy state, B and C in a rubbery state. The successful generation of the desired supramolecular structure was evidenced by 1 H NMR, ITC, viscometry, and DLS as well as DSC. The facile preparation of novel supramolecular (ABAC) n multiblock copolymers from Hamilton wedge and barbiturate functionalized H-bonding RAFT agents is reported.
AbstractList Two original Hamilton wedge (HW)/barbiturate (Ba) functionalized symmetrical trithiocarbonates have been successfully synthesized and their capability to efficiently mediate the polymerization of styrene, n BuA and isoprene was investigated. Relying on supramolecular association of the recognition couple, telechelic macromolecular building blocks subsequently afford the formation of novel supramolecular (ABAC) n multiblock copolymers, where A is in a glassy state, B and C in a rubbery state. The successful generation of the desired supramolecular structure was evidenced by 1 H NMR, ITC, viscometry, and DLS as well as DSC. The facile preparation of novel supramolecular (ABAC) n multiblock copolymers from Hamilton wedge and barbiturate functionalized H-bonding RAFT agents is reported.
Author Barqawi, Haitham
Chen, Senbin
Deng, Yuanming
Binder, Wolfgang H
Chang, Xijun
Schulz, Matthias
AuthorAffiliation Institute of Chemistry
Shenzhen University and Shenzhen Key Laboratory of Special Functional Materials
Chair of Macromolecular Chemistry
Martin-Luther University Halle-Wittenberg
Lanzhou University
Faculty of Natural Sciences II (Chemistry, Physics and Mathematics)
College of Materials Science and Engineering
College of Chemistry and Chemical Engineering
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Notes BuA-
b
13
Electronic supplementary information (ESI) available
C NMR spectra of compound
10.1039/c3py01482g
and CTAs
C NMR spectra of Ba-PS-
n
P
1
2
PS-Ba4 and HW-PI-HW4, ESI-TOF mass spectra of CTAs. See DOI
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References_xml – issn: 2011
  publication-title: Synthesis and Self-Assembly of Hydrogen-Bonded Supramolecular Polymers
  doi: Binder Enders Herbst Hackethal
– issn: 2007
  end-page: p 1-78
  publication-title: Advances in Polymer Science: Hydrogen Bonded Polymers
  doi: Binder Zirbs
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Title Facile preparation of supramolecular (ABAC)n multiblock copolymers from Hamilton wedge and barbiturate-functionalized RAFT agentsElectronic supplementary information (ESI) available: 1H and 13C NMR spectra of compound 2 and CTAs, 13C NMR spectra of Ba-PS-b-PnBuA-b-PS-Ba4 and HW-PI-HW4, ESI-TOF mass spectra of CTAs. See DOI: 10.1039/c3py01482g
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