Name: synthesis of cyclic polymers and characterization of their diffusive motion in the melt state at the single molecule level
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Description: Watch this Scientific Journal Video about Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level at JoVE.com

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.).

1. Synthesis of Monofunctional and Bifunctional Poly(THF)
<ol>
	<li>Monofunctional poly(THF)
	<ol>
		<li>Flame dry a 2-neck 100-ml round-bottom flask. Vacuum and fill the flask with nitrogen (3 cycles).</li>
		<li>Add distilled tetrahydrofuran (THF) (50 ml) to the flask. Put the flask in a water bath at 20 &#176;C and equilibrate the temperature.</li>
		<li>Add methyl triflate (0.5 mmol) to the flask by a syringe. Stir the mixture for 5-10 min at 20 &#176;C.</li>
		<li>Add N-phenyl pyrrolidine...

<ol>
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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.
<p ...

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
Cyclic polymer dynamics has been investigated using both synthetic and naturally occurring molecules by means of ensemble averaged experimental methods such as nuclear magnetic resonance (NMR), light scattering, and viscosity measurements.7-9 However, these studies often suffer from impurity molecules in the samples.10 Furthermore, spatiotemporal heterogeneities of the motion of individual molecules caused by inherent structural heterogeneity of entangled polymers are often hidden behind the ensemble averaging in these studies. In order to characterize molecular level dynamics of cyclic polymers, a synthesis method that provides high purity cyclic polymers and an experimental and analysis methods that allow for quantitative characterization of molecular motion at the single molecule level have to be developed. Here, we will show a method to synthesize high-purity cyclic and dicyclic poly(THF)s that incorporate a fluorophore unit using an electrostatic self-assembly and covalent fixation (ESA-CF) process11-13 and a method to analyze the motion of the individual fluorophore-incorporated polymer chains using a combination of mean-squared displacement (MSD) and cumulative distribution function (CDF) analyses.
A proper data processing has been shown to be essential for the accurate characterization of the diffusive motion. With an adequate MSD and CDF analyses, a multiple-mode diffusion of the cyclic and dicyclic polymers in the melt and semi-dilute solution of the linear polymer chains has been revealed,14-16 suggesting the significant effects of the topological states of the polymers on the diffusive motion of the chains under entangled conditions.17 While the experimental and analytical approaches to characterize the motion of the cyclic polymers are described in this protocol, the same method can be used to quantitatively characterize the diffusive motion in many other heterogeneous systems. The approach would be especially suitable when multiple diffusion components existing in the samples are to be analyzed.

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			<td height="21" style="height:21px;width:320px;">Materials</td>
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			<td height="21" style="height:21px;width:320px;">THF</td>
			<td style="width:240px;">Godo</td>
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			<td></td>
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			<td height="21" style="height:21px;width:320px;">Wakosil C-300</td>
			<td style="width:240px;">Wako Pure Chemical Industries</td>
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			<td height="21" style="height:21px;width:320px;">Acetone</td>
			<td style="width:240px;">Godo</td>
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			<td height="21" style="height:21px;width:320px;">Toluene</td>
			<td style="width:240px;">Godo</td>
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			<td height="21" style="height:21px;width:320px;">n-Hexane</td>
			<td style="width:240px;">Godo</td>
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			<td height="21" style="height:21px;width:320px;">CHCl3</td>
			<td style="width:240px;">Kanto Chemical</td>
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			<td height="21" style="height:21px;width:320px;">Bio-Beads S-X1</td>
			<td style="width:240px;">Bio-Rad</td>
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			<td height="21" style="height:21px;width:320px;">Methyl triflate</td>
			<td style="width:240px;">Nacalai Tesque</td>
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			<td height="21" style="height:21px;width:320px;">Triflic anhydride</td>
			<td style="width:240px;">Nacalai Tesque</td>
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			<td height="21" style="height:21px;width:320px;">Potassium Hydroxide</td>
			<td style="width:240px;">Wako Pure Chemical Industries</td>
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			<td height="21" style="height:21px;width:320px;">Ethanol</td>
			<td style="width:240px;">Wako Pure Chemical Industries</td>
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			<td height="21" style="height:21px;width:320px;">Poly(tetrahydrofuran)</td>
			<td style="width:240px;">Aldrich</td>
			<td style="width:119px;"></td>
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			<td height="21" style="height:21px;width:320px;">Chloroform</td>
			<td style="width:240px;">Wako Pure Chemical Industries</td>
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			<td height="21" style="height:21px;width:320px;">Immersion oil</td>
			<td style="width:240px;">Cargille</td>
			<td style="width:119px;">Type 37 / Type A</td>
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			<td height="21" style="height:21px;width:320px;">Equipment</td>
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			<td height="21" style="height:21px;width:320px;">2-Neck 100-mL round-bottom flask</td>
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			<td height="21" style="height:21px;width:320px;">Flask</td>
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			<td height="21" style="height:21px;width:320px;">Beaker</td>
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			<td height="21" style="height:21px;width:320px;">Funnel</td>
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			<td height="21" style="height:21px;width:320px;">Filter paper</td>
			<td style="width:240px;">Whatman</td>
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			<td height="21" style="height:21px;width:320px;">Reflux condenser</td>
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			<td height="21" style="height:21px;width:320px;">Syringe</td>
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			<td height="21" style="height:21px;width:320px;">Water bath</td>
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			<td height="21" style="height:21px;width:320px;">Magnetic stirrer</td>
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			<td height="21" style="height:21px;width:320px;">Rotary evaporator</td>
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			<td height="21" style="height:21px;width:320px;">Microscope cover slips (24 x 24 mm, No. 1)</td>
			<td style="width:240px;">Matsunami Glass</td>
			<td style="width:119px;">CO22241</td>
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			<td height="21" style="height:21px;width:320px;">Staining jar</td>
			<td style="width:240px;">AS ONE Corporation</td>
			<td style="width:119px;">1-7934-01</td>
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			<td height="21" style="height:21px;width:320px;">Ultrasonic cleaner</td>
			<td style="width:240px;">VWR International&#160;</td>
			<td style="width:119px;">142-0047</td>
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			<td height="21" style="height:21px;width:320px;">Inverted microscope</td>
			<td style="width:240px;">Olympus</td>
			<td style="width:119px;">IX71</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:320px;">Ar-Kr ion laser</td>
			<td style="width:240px;">Coherent</td>
			<td style="width:119px;">Innova 70C</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:320px;">Berek compensator</td>
			<td style="width:240px;">Newport</td>
			<td align="right" style="width:119px;">5540</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:320px;">Excitation filter</td>
			<td style="width:240px;">Semrock</td>
			<td style="width:119px;">LL01-488-12.5</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:320px;">Dichloric mirror</td>
			<td style="width:240px;">Omega optical</td>
			<td style="width:119px;">500DRLP</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:320px;">Emission filter</td>
			<td style="width:240px;">Semrock</td>
			<td style="width:119px;">BLP01-488R-25</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:320px;">Lens and mirror</td>
			<td style="width:240px;">Thorlabs</td>
			<td style="width:119px;"></td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:320px;">EM-CCD camera</td>
			<td style="width:240px;">Andor Technology</td>
			<td style="width:119px;">iXon</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:320px;">Objective lens (x100, N.A. = 1.3)</td>
			<td style="width:240px;">Olympus</td>
			<td style="width:119px;">UPLFLN 100XOP</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:320px;">Objective heater</td>
			<td style="width:240px;">Bioptechs</td>
			<td style="width:119px;"></td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:320px;">Preparative GPC</td>
			<td style="width:240px;">Japan Analytical Industry</td>
			<td style="width:119px;">LC-908</td>
			<td></td>
		</tr>
	</tbody>
</table>

synthesis of cyclic polymers and characterization of their diffusive motion in the melt state at the single molecule level

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.

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...

Watch this Scientific Journal Video about Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level at JoVE.com

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

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

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 ...

The overall goal of this experiment is to characterize diffusional motion of topological polymers, especially cyclic polymers, under entangled conditions at the single molecule level. This method can help answer key questions in the field of polymer physics, such as topology-dependent spacio-temporal dynamics of polymers. The main advantage of this technique is that heterogeneous diffusion can be quantitatively characterized at the single-chain level, which is usually hidden behind on some level.To begin this procedure, dissolve perylene diimide salt in 150 milliliters of water, then dissolve monofunctional poly(THF)in four millimeters of acetone. Add the acetone solution drop-wise to the vigorously stirred aqueous solution. Collect the formed precipitate by vacuum filtration.Next, prepare a five milligram per milliliter solution of the precipitate in toluene. Reflux the solution for four hours. After allowing the solution to cool, completely remove the solvent under reduced pressure by rotary evaporation.When finished, dissolve the residue in a 2:1 mixture of n-hexane:acetone and filter the resulting solution through a plug of silica gel. Then add the filtered solution to ice cold water to precipitate the product. To prepare the polymer melt sample, add 100 microliters of non-labeled linear poly(THF)to a glass bottle and heat it to approximately 25 degrees celsius using a hair dryer.Prepare a 10 to the minus six molars solution of the fluorophore incorporated polymer solution in chloroform. Then add one microliter of this solution to 100 microliters of the non-labeled linear poly(THF)melt. After thoroughly mixing the sample with a pipette tip, evaporate the chloroform by heating with a hair dryer.Using a micro-pipette place 10 microliters of the sample on a cleaned cover slip. Place another cleaned cover slip on the sample and gently press the two cover slips together using plastic tweezers. Next, attach an objective heater to the objective lens of an inverted microscope and set the temperature to 30 degrees celsius.Place one drop of immersion oil on the lens and mount the sample on the microscope stage. Ensure that a sample thickness of approximately 10 micrometers is obtained by checking the axial position of the bottom and top surface of the sample. Then adjust the focus of the microscope to a few micrometers above the bottom surface of the sample.Following this, apply an electron multiplying or EM gain to a CCD camera in order to obtain a high quality fluorescent image of the single fluorophore. Now set a region of interest using the software controlling the camera. To optimize the experimental conditions, adjust the illumination area of the sample to approximately 20 micrometers in diameter using the diaphragm inserted in the excitation beam path.Set the excitation laser power at the sample to four to eight milliwatts by manually selecting an appropriate neutral density filter inserted in the excitation beam path. Finally, record 500 to 1000 fluorescence image sequences of the fluorophore incorporated polymer in the melt state at a 100 to 200 hertz frame rate. Time-lapse single molecule florescence images were measured for the four-armed and eight-shaped polymers and show spatially isolated bright and sharp spots due to the incorporation of the highly fluorescent perylene diimide fluorophore into the chains.The frequency histograms of the diffusion coefficient determined by mean-squared displacement analysis display broad distributions resulting from both the statistical error of the analysis and heterogeneity of the diffusion. The frequency histograms show clear deviations from the homogeneous diffusion model, which demonstrates heterogeneous diffusion of the polymer molecules. The single and double Gaussian models hit the experimentally obtained cumulative distribution functions well and demonstrate that the diffusion of the formed polymer is described by the broad distribution of the diffusion coefficient, whereas the eight-shaped polymer displays two distinct diffusion modes.Once mastered, the synthesis of polymers can be done in six hours and the single molecule immersion experiment can be done in several hours if they are performed properly. After it's development, this technique paved the way for researchers in the field of polymer science to explore polymer dynamics in crowded environments. After watching this video, you should have a good understanding of how to characterize diffusive motion of topological polymers under entangled condition at the single-chain level.Don't forget that working with lasers and organic solvents can be extremely hazardous and precautions such as laser safety and review of the MSDS should always be taken while performing this procedure.

Research

JoVE Journal

Chemistry

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Lipopolysaccharide (LPS) is the major cell surface molecule of gram-negative bacteria, deposited on the outer leaflet of the outer membrane bilayer. LPS ...

Synthesis of Hypervalent Iodonium Alkynyl Triflates for the Application of Generating Cyanocarbenes

The procedures described in this article involve the synthesis and isolation of hypervalent iodonium alkynyl triflates (HIATs) and their subsequent ...

Split-and-pool Synthesis and Characterization of Peptide Tertiary Amide Library

Peptidomimetics are great sources of protein ligands. The oligomeric nature of these compounds enables us to access large synthetic libraries on solid ...

Amide Coupling Reaction for the Synthesis of Bispyridine-based Ligands and Their Complexation to Platinum as Dinuclear Anticancer Agents

Amide coupling reactions can be used to synthesize bispyridine-based ligands for use as bridging linkers in multinuclear platinum anticancer drugs. ...

The Synthesis, Characterization and Reactivity of a Series of Ruthenium N-triphosPh Complexes

The Synthesis, Characterization and Reactivity of a Series of Ruthenium N-triphosPh Complexes

Herein we report the synthesis of a tridentate phosphine ligand N(CH2PPh2)3 (N-triphosPh) (1) via a phosphorus based Mannich reaction of the ...

Synthesis, Characterization, and Functionalization of Hybrid Au/CdS and Au/ZnS Core/Shell Nanoparticles

Plasmonic nanoparticles are an attractive material for light harvesting applications due to their easily modified surface, high surface area and large ...

Protocol for the Synthesis of Ortho-trifluoromethoxylated Aniline Derivatives

Protocol for the Synthesis of Ortho-trifluoromethoxylated Aniline Derivatives

Molecules bearing trifluoromethoxy (OCF3) group often show desired pharmacological and biological properties. However, facile synthesis of ...

Synthesis of Protein Bioconjugates via Cysteine-maleimide Chemistry

Synthesis of Protein Bioconjugates via Cysteine-maleimide Chemistry

The chemical linking or bioconjugation of proteins to fluorescent dyes, drugs, polymers and other proteins has a broad range of applications, such as the ...

Insights into the Interactions of Amino Acids and Peptides with Inorganic Materials Using Single-Molecule Force Spectroscopy

The interactions between proteins or peptides and inorganic materials lead to several interesting processes. For example, combining proteins with minerals ...

Using Cyclic Voltammetry, UV-Vis-NIR, and EPR Spectroelectrochemistry to Analyze Organic Compounds

Cyclic voltammetry (CV) is a technique used in the analysis of organic compounds. When this technique is combined with electron paramagnetic resonance ...