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Conformation of Tunable Nanocylinders: Up to Sixth-Generation Dendronized Polymers via Graft-Through Approach by ROMP

Research output: Contribution to journalArticle

  • Fabien Dutertre
  • Ki Taek Bang
  • Emmanouil Vereroudakis
  • Benoit Loppinet
  • Sanghee Yang
  • Sung Yun Kang
  • George Fytas
  • Tae Lim Choi
Original languageEnglish
Pages (from-to)3342-3350
Number of pages9
JournalMacromolecules
Volume52
Issue number9
Early online date23 Apr 2019
DOIs
DateAccepted/In press - 15 Apr 2019
DateE-pub ahead of print - 23 Apr 2019
DatePublished (current) - 14 May 2019

Abstract

Well-defined dendronized polymers (denpols) bearing high-generation dendron are attractive nano-objects as high persistency provides distinct properties, contrast to the random coiled linear polymers However, their syntheses via graft-through approach have been very challenging due to their structural complexity and steric hindrance retarding polymerization. Here, we report the first example of the synthesis of poly(norbornene) (PNB) containing ester dendrons up to the sixth generation (G6) by ring-opening metathesis polymerization. This is the highest generation ever polymerized among dendronized polymers prepared by graft-through approach, producing denpols with molecular weight up to 1960 kg/mol. Combination of size-exclusion chromatography, light scattering, and neutron scattering allowed a thorough structural study of these large denpols in dilute solution. A semiflexible cylinder model was successfully applied to represent both the static and dynamic experimental quantities yielding persistent length (l p ), cross-sectional radius (R cs ), and contour length (L). The denpol persistency seemed to increase with generation, with l p reaching 27 nm (Kuhn length 54 nm) for PNB-G6, demonstrating a rod-like conformation. Poly(endo-tricycle[4.2.2.0]deca-3,9-diene) (PTD) denpols exhibited larger persistency than the PNB analogues of the same generation presumably due to the higher grafting density of the PTD denpols. As the dendritic side chains introduce shape anisotropy into the denpol backbone, future work will entail a study of these systems in the concentrated solutions and melts.

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    Rights statement: This is the final published version of the article (version of record). It first appeared online via ACS at https://doi.org/10.1021/acs.macromol.9b00457 . Please refer to any applicable terms of use of the publisher.

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