Method Article

Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level

DOI:

10.3791/54503

September 26th, 2016

In This Article

Summary

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A protocol for the synthesis and characterization of diffusive motion of cyclic polymers at the single molecule level is presented.

Abstract

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We demonstrate a method for the synthesis of cyclic polymers and a protocol for characterizing their diffusive motion in a melt state at the single molecule level. An electrostatic self-assembly and covalent fixation (ESA-CF) process is used for the synthesis of the cyclic poly(tetrahydrofuran) (poly(THF)). The diffusive motion of individual cyclic polymer chains in a melt state is visualized using single molecule fluorescence imaging by incorporating a fluorophore unit in the cyclic chains. The diffusive motion of the chains is quantitatively characterized by means of a combination of mean-squared displacement (MSD) analysis and a cumulative distribution function (CDF) analysis. The cyclic polymer exhibits multiple-mode diffusion which is distinct from its linear counterpart. The results demonstrate that the diffusional heterogeneity of polymers that is often hidden behind ensemble averaging can be revealed by the efficient synthesis of the cyclic polymers using the ESA-CF process and the quantitative analysis of the diffusive motion at the single molecule level using the MSD and CDF analyses.

Introduction

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Cyclic polymers are unique in that they do not have chain ends. They often exhibit unusual behaviors which is distinct from their linear counterpart, including increased thermal stability of polymer micelles by a linear-to-cyclic conversion,1,2 and spatial organization of DNA in bacterial cells by a loop formation.3 Topological interactions between the cyclic chains are believed to be the critical factor for such unusual behaviors.4,5 Therefore, characterizing the motion and relaxation of cyclic polymers under entangled conditions has been an important research topic in polymer science for decades.6

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Protocol

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1. Synthesis of Monofunctional and Bifunctional Poly(THF)

  1. Monofunctional poly(THF)
    1. Flame dry a 2-neck 100-ml round-bottom flask. Vacuum and fill the flask with nitrogen (3 cycles).
    2. Add distilled tetrahydrofuran (THF) (50 ml) to the flask. Put the flask in a water bath at 20 °C and equilibrate the temperature.
    3. Add methyl triflate (0.5 mmol) to the flask by a syringe. Stir the mixture for 5-10 min at 20 °C.
    4. Add N-phenyl pyrrolidine (4-6 equiv.) to the flask by a syringe. Stir the mixture for 30-60 min.
    5. Completely remove the solvent under reduced pressure (ca. 100 Torr)....

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Results

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The perylene diimide-incorporated 4-armed star and 8-shaped dicyclic poly(THF)s were synthesized using the electrostatic self-assembly and covalent fixation (ESA-CF) process (Figure 1, Figure 2). Time-lapse single-molecule fluorescence images were measured for the 4-armed (Figure 3a) and 8-shaped (Figure 3b) polymers. The time-lapse fluorescence images (Figure 3) show spatially isolated bright and sharp s.......

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Discussion

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The 4-armed and 8-shaped polymers were prepared via the ESA-CF protocol (Figure 1), which is a critical step for the synthesis.12,24 Monofunctional and bifunctional linear poly(THF)s with N-phenylpiperidinium end groups were synthesized according to the previous procedure.11 The ion exchange was carried out by reprecipitation of an acetone solution of a polymer precursor with triflate counteranions into an aqueous solution containing an excess amount of carboxylate.

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Disclosures

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The authors have nothing to disclose.

Acknowledgements

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This work was supported by a Grant-in-Aid for Scientific Research No. 22750122 (S.H.), No. 26288099 (T.Y.), and No. 23350050 (Y.T.) of the Japan Society for the Promotion of Science. S.H. is grateful for The Kurata Memorial Hitachi Science and Technology Foundation. The research reported in this publication was supported by the King Abdullah University of Science and Technology (S.H.).

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Materials
THFGodo
Wakosil C-300Wako Pure Chemical Industries
AcetoneGodo
TolueneGodo
n-HexaneGodo
CHCl3Kanto Chemical
Bio-Beads S-X1Bio-Rad
Methyl triflateNacalai Tesque
Triflic anhydrideNacalai Tesque
Potassium HydroxideWako Pure Chemical Industries
EthanolWako Pure Chemical Industries
Poly(tetrahydrofuran)Aldrich
ChloroformWako Pure Chemical Industries
Immersion oilCargilleType 37 / Type A
Equipment
2-Neck 100-ml round-bottom flask
Flask
Beaker
Funnel
Filter paperWhatman
Reflux condenser
Syringe
Water bath
Magnetic stirrer
Rotary evaporator
Microscope cover slips (24 x 24 mm, No. 1)Matsunami GlassCO22241
Staining jarAS ONE Corporation1-7934-01
Ultrasonic cleanerVWR International 142-0047
Inverted microscopeOlympusIX71
Ar-Kr ion laserCoherentInnova 70C
Berek compensatorNewport5540
Excitation filterSemrockLL01-488-12.5
Dichloric mirrorOmega optical500DRLP
Emission filterSemrockBLP01-488R-25
Lens and mirrorThorlabs
EM-CCD cameraAndor TechnologyiXon
Objective lens (100X, N.A. = 1.3)OlympusUPLFLN 100XOP
Objective heaterBioptechs
Preparative GPCJapan Analytical IndustryLC-908

References

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  1. Honda, S., Yamamoto, T., Tezuka, Y. Topology-Directed Control on Thermal Stability: Micelles Formed from Linear and Cyclized Amphiphilic Block Copolymers. J. Am. Chem. Soc. 132 (30), 10251-10253 (2010).
  2. Honda, S., Yamamoto, T., Tezuka, Y.

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Tags

Cyclic PolymersSingle Molecule ImagingMean Squared DisplacementCumulative Distribution FunctionElectrostatic Self AssemblyCovalent FixationPolymer Melt StateDiffusive Motion AnalysisTopological PolymersFluorescence Microscopy

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