A simple and efficient method to construct a hyperbranched multicyclic polymer is introduced. First, a tailored trithiocarbonate with two terminal anthracene units and three azide groups is successfully synthesized, and this multifunctional trithiocarbonate is used as chain transfer agent (CTA) to afford anthracene-telechelic polystyrene (PS) via reversible addition-fragmentation chain transfer (RAFT) polymerization. After that, linear PS is irradiated under 365 nm UV light to achieve the cyclization process. The monocyclic polymer further reacts with sym-dibenzo-1,5-cyclooctadiene-3,7-diyne via "A +B " strategy based on a self-accelerating click reaction to produce hyperbranched multicyclic polymer. The structures and properties of the polymers are characterized by nuclear magnetic resonance (NMR), gel permeation chromatography (GPC), UV-vis spectrophotometry, and triple-detection size-exclusion chromatography (TD-SEC). The number of monocyclic units of the resultant hyperbranched multicyclic polymer reaches about 21 based on multi-angle laser light scattering (MALLS) measurements. The plot of intrinsic viscosity versus molecular weight reveals that the α value of the unique hyperbranched multicyclic polymer is lower than both hyperbranched polymers and cyclic polymers.
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http://dx.doi.org/10.1002/marc.201900164 | DOI Listing |
Macromol Rapid Commun
July 2019
Hefei National Laboratory for Physical Sciences at the Microscale, CAS Key Laboratory of Soft Matter Chemistry, Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei, Anhui, 230026, China.
J Phys Chem B
March 2014
Key Laboratory of Space Applied Physics and Chemistry of Ministry of Education, Department of Applied Chemistry, School of Science, Northwestern Polytechnical University, Xi'an, 710072, P. R. China.
Terminal index (TI) was presented as a new characteristic parameter for quantitative description of branched and cyclic topology of highly branched soluble polymers derived from A2 + B3 stepwise polymerization. TI is defined as the ratio of terminal units of an A2 + B3 type highly branched polymer to those in its perfect hyperbranched counterpart. TI is concisely represented as T/(D + L), which can be conveniently calculated from a quantitative NMR spectrum.
View Article and Find Full Text PDFEnviron Sci Technol
March 2011
School of Chemical & Biomolecular Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.
While current carbon capture and sequestration (CCS) technologies for large point sources can help address the impact of CO(2) buildup on global climate change, these technologies can at best slow the rate of increase of the atmospheric CO(2) concentration. In contrast, the direct CO(2) capture from ambient air offers the potential to be a truly carbon negative technology. We propose here that amine-based solid adsorbents have significant promise as key components of a hypothetical air capture process.
View Article and Find Full Text PDFAcc Chem Res
August 2009
Institut für Technische and Makromolekulare Chemie, Bundesstrasse 45, 20146 Hamburg, Germany.
The recent confirmation that polycondensations (and other step-growth polymerizations) of difunctional monomers involve cyclization reactions at any concentration and at any stage of the polymerization also has consequences for three-dimensional polycondensations on multifunctional monomers. It is demonstrated that tree-shaped (hyperbranched) oligomers are gradually transformed into star-shaped polymers with a cyclic core, when the conversion increases. Polycondensations of "a(2) + b(3)" or "a(2) + b(4)" monomer combinations yield multicyclic polymers, when gelation can be avoided.
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