We acknowledge funding support from the University of Akron and the National Science Foundation under grant DMR-2042494.

<ol>
	<li>Geyer, R., Jambeck, J. R., Law, K. L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Production,+use,+and+fate+of+all+plastics+ever+made.">Production, use, and fate of all plastics ever made.</a> Science Advances. 3 (7), 1700782 (2017).</li><li>Barnes, D. K. A., Galgani, F., Thompson, R. C., Barlaz, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Accumulation+and+fragmentation+of+plastic+debris+in+global+environments.">Accumulation and fragmentation of plastic debris in global environments.</a> Philosophical Transactions of the Royal Society B: Biological Sciences. 364 (1526), 1985-1998 (2009).</li><li>Zheng, J., Suh, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Strategies+to+reduce+the+global+carbon+footprint+of+plastics.">Strategies to reduce the global carbon footprint of plastics.</a> Nature Climate Change. 9 (5), 374-378 (2019).</li><li>Coates, G. W., Getzler, Y. D. Y. L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Chemical+recycling+to+monomer+for+an+ideal,+circular+polymer+economy.">Chemical recycling to monomer for an ideal, circular polymer economy.</a> Nature Reviews Materials. 5 (7), 501-516 (2020).</li><li>Odian, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Ring-opening+Polymerization.">Ring-opening Polymerization.</a> Principles of Polymerization. , 544-618 (2004).</li><li>Zhu, J. B., Watson, E. M., Tang, J., Chen, E. Y. X. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+synthetic+polymer+system+with+repeatable+chemical+recyclability.">A synthetic polymer system with repeatable chemical recyclability.</a> Science. 360 (6387), 398-403 (2018).</li><li>Xiong, W., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Geminal+dimethyl+substitution+enables+controlled+polymerization+of+penicillamine-derived+&#946;-thiolactones+and+reversed+depolymerization.">Geminal dimethyl substitution enables controlled polymerization of penicillamine-derived &#946;-thiolactones and reversed depolymerization.</a> Chem. 6 (7), 1831-1843 (2020).</li><li>Abel, B. A., Snyder, R. L., Coates, G. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Chemically+recyclable+thermoplastics+from+reversible-deactivation+polymerization+of+cyclic+acetals.">Chemically recyclable thermoplastics from reversible-deactivation polymerization of cyclic acetals.</a> Science. 373 (6556), 783-789 (2021).</li><li>Neary, W. J., Isais, T. A., Kennemur, J. G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Depolymerization+of+bottlebrush+polypentenamers+and+their+macromolecular+metamorphosis.">Depolymerization of bottlebrush polypentenamers and their macromolecular metamorphosis.</a> Journal of the American Chemical Society. 141 (36), 14220-14229 (2019).</li><li>Feist, J. D., Xia, Y. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Enol+ethers+are+effective+monomers+for+ring-opening+metathesis+polymerization:+Synthesis+of+degradable+and+depolymerizable+poly(2,3-dihydrofuran).">Enol ethers are effective monomers for ring-opening metathesis polymerization: Synthesis of degradable and depolymerizable poly(2,3-dihydrofuran).</a> Journal of the American Chemical Society. 142 (3), 1186-1189 (2020).</li><li>Hong, M., Chen, E. Y. X. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Completely+recyclable+biopolymers+with+linear+and+cyclic+topologies+via+ring-opening+polymerization+of+&#947;-butyrolactone.">Completely recyclable biopolymers with linear and cyclic topologies via ring-opening polymerization of &#947;-butyrolactone.</a> Nature Chemistry. 8 (1), 42-49 (2016).</li><li>Shi, C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Design+principles+for+intrinsically+circular+polymers+with+tunable+properties.">Design principles for intrinsically circular polymers with tunable properties.</a> Chem. 7 (11), 2896-2912 (2021).</li><li>Neary, W. J., Kennemur, J. G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Polypentenamer+renaissance:+Challenges+and+opportunities.">Polypentenamer renaissance: Challenges and opportunities.</a> ACS Macro Letters. 8 (1), 46-56 (2019).</li><li>Ols&#233;n, P., Odelius, K., Albertsson, A. -. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Thermodynamic+presynthetic+considerations+for+ring-opening+polymerization.">Thermodynamic presynthetic considerations for ring-opening polymerization.</a> Biomacromolecules. 17 (3), 699-709 (2016).</li><li>Sathe, D., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Olefin+metathesis-based+chemically+recyclable+polymers+enabled+by+fused-ring+monomers.">Olefin metathesis-based chemically recyclable polymers enabled by fused-ring monomers.</a> Nature Chemistry. 13 (8), 743-750 (2021).</li><li>Scherman, O. A., Walker, R., Grubbs, R. H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Synthesis+and+characterization+of+stereoregular+ethylene-vinyl+alcohol+copolymers+made+by+ring-opening+metathesis+polymerization.">Synthesis and characterization of stereoregular ethylene-vinyl alcohol copolymers made by ring-opening metathesis polymerization.</a> Macromolecules. 38 (22), 9009-9014 (2005).</li><li>You, W., Hugar, K. M., Coates, G. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Synthesis+of+alkaline+anion+exchange+membranes+with+chemically+stable+imidazolium+cations:+Unexpected+cross-linked+macrocycles+from+ring-fused+ROMP+monomers.">Synthesis of alkaline anion exchange membranes with chemically stable imidazolium cations: Unexpected cross-linked macrocycles from ring-fused ROMP monomers.</a> Macromolecules. 51 (8), 3212-3218 (2018).</li><li>Chen, H., Shi, Z., Hsu, T. G., Wang, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Overcoming+the+low+driving+force+in+forming+depolymerizable+polymers+through+monomer+isomerization.">Overcoming the low driving force in forming depolymerizable polymers through monomer isomerization.</a> Angewandte Chemie International Edition. 60 (48), 25493-25498 (2021).</li><li>Sathe, D., Chen, H., Wang, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Regulating+the+thermodynamics+and+thermal+properties+of+depolymerizable+polycyclooctenes+through+substituent+effects.">Regulating the thermodynamics and thermal properties of depolymerizable polycyclooctenes through substituent effects.</a> Macromolecular Rapid Communications. , (2022).</li><li>Vogel, A. I., Furniss, B. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Vogel's Textbook of Practical Organic Chemistry. , (2003).</li><li>Pirrung, M. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Following+the+Reaction.">Following the Reaction.</a> The Synthetic Organic Chemist's Companion. , 93-105 (2007).</li><li>Royzen, M., Yap, G. P. A., Fox, J. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+Photochemical+synthesis+of+functionalized+trans-cyclooctenes+driven+by+metal+complexation.">A Photochemical synthesis of functionalized trans-cyclooctenes driven by metal complexation.</a> Journal of the American Chemical Society. 130 (12), 3760-3761 (2008).</li><li>Chiang, Y., Kresge, A. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Mechanism+of+hydration+of+simple+olefins+in+aqueous+solution.+cis-+and+trans-Cyclooctene.">Mechanism of hydration of simple olefins in aqueous solution. cis- and trans-Cyclooctene.</a> Journal of the American Chemical Society. 107 (22), 6363-6367 (1985).</li><li>Fang, Y., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Studies+on+the+stability+and+stabilization+of+trans-cyclooctenes+through+radical+inhibition+and+silver+(I)+metal+complexation.">Studies on the stability and stabilization of trans-cyclooctenes through radical inhibition and silver (I) metal complexation.</a> Tetrahedron. 75 (32), 4307-4317 (2019).</li></ol>

A patent application (PCT/US2021/050044) has been filed for this work.

The tCBCO monomers can be prepared from a common precursor: the [2+2] photocycloadduct of maleic anhydride and 1,5-cyclooctadiene, anhydride 1. Since the crude anhydride 1 is difficult to purify but can be hydrolyzed readily, the crude photoreaction mixture is subjected to methanolysis conditions to yield the readily isolable methyl ester-acid 2. The recrystallization of 2 after column chromatography is key to obtaining the pure trans-c...

The versatile and robust nature of synthetic polymers has made them a ubiquitous fixture of modern human existence. On the flip side, the same robust and environmentally resistant properties make polymer waste exceedingly persistent. This, together with the fact that a large fraction of all synthetic polymers ever made has ended up in landfills1, has raised legitimate concerns about their environmental effects2. Additionally, the open-loop nature of the traditional polymer economy has caused a steady consumption of petrochemical resources and a mounting carbon footprint3. Promising routes to a closed-loop polymer economy are, thus, highly sought after.
Chemical recycling to monomer (CRM) is one such route. The advantage of CRM over traditional recycling is that it leads to the regeneration of monomers that can be used to manufacture pristine polymers, as opposed to mechanical recycling of materials with deteriorating properties over multiple processing cycles. Polymers based on ring-opening polymerizations have appeared as especially attractive routes to CRM materials4. The thermodynamics of polymerization is typically an interplay between two opposing factors: the enthalpy of polymerization (&#916;Hp, which is typically negative and favors polymerization) and the entropy of polymerization (&#916;Sp, which is also typically negative but disfavors polymerization), with the ceiling temperature (Tc)&#160;being the temperature at which these two factors balance each other out5. For a polymer to be capable of CRM under practical and economically beneficial conditions, the right balance of &#916;Hp and &#916;Sp must be achieved. Cyclic monomers allow a convenient means to tune these factors via the selection of the appropriate ring size and geometry, since here, &#916;Hp is primarily determined by the ring strain of the cyclic monomers4,5. As a result, CRM polymers with a wide variety of monomers have been reported of late6,7,8,9,10,11. Out of these systems, ROMP polymers prepared from cyclopentenes are particularly promising due to the rather cheap starting material required and the hydrolytic and thermal stability of the polymers. Additionally, in the absence of a metathesis catalyst, the depolymerization is kinetically unfeasible, affording high thermal stability despite a low Tc12. However, cyclopentenes (and other monomers based on small cyclic structures) pose a key challenge-they cannot be readily functionalized, as the presence of functional groups on the backbone can affect the thermodynamics of polymerization in drastic, and sometimes unpredictable, ways13,14.
Recently, we reported a system that overcomes some of these challenges15. Inspired by examples of low-strain fused ring cyclooctenes in the literature16,17, a new CRM system was designed based on ROMP polymers of trans-cyclobutane fused cyclooctenes (tCBCO) (Figure 1A). The tCBCO monomers could be prepared at a gram scale from the [2+2] photo cycloadduct of maleic anhydride and 1,5-cyclooctadiene, which could be readily functionalized to achieve a diverse set of substituents (Figure 1B). The resulting monomers had ring strains comparable to cyclopentene (~5 kcal&#183;mol&#8722;1, as calculated using DFT). Thermodynamic studies revealed a low &#916;Hp (&#8722;1.7 kcal&#183;mol&#8722;1 to &#8722;2.8 kcal&#183;mol&#8722;1), which was offset by a low &#916;Sp (&#8722;3.6 kcal&#183;mol&#8722;1&#183;K&#8722;1 to &#8722;4.9 kcal&#183;mol&#8722;1&#183;K&#8722;1), allowing the preparation of high molecular weight polymers (at high monomer concentrations) and near quantitative depolymerization (&#62;90%, under dilute conditions) at ambient temperatures in the presence of Grubbs II catalyst (G2). It was also demonstrated that materials with diverse thermomechanical properties could be obtained while preserving the ease of polymerization/depolymerization. This ability was further exploited to prepare a soft elastomeric network (which could also be readily depolymerized), as well as a rigid thermoplastic (with tensile properties comparable to polystyrene).
One drawback with this system was the need for high monomer concentrations to access high molecular weight polymers. At the same time, due to extensive chain transfer and cyclization reactions, the polymerization was uncontrolled in nature. This was addressed in a subsequent work via photochemical isomerization of the Z-alkene in the tCBCO monomers to prepare highly strained E-alkene tCBCO monomers18. These monomers could be rapidly polymerized in a living manner at low initial monomer concentrations (&#8805;25 mM) in the presence of Grubbs I catalyst (G1) and excess triphenylphosphine (PPh3). The polymers could then be depolymerized to yield the Z-alkene form of the monomers. This has created opportunities to access new depolymerizable polymer architectures, including block copolymers and graft/bottlebrush copolymers.
In this work, detailed protocols are outlined for the synthesis of tCBCO monomers with different functional groups and their polymerization, as well as the depolymerization of the resulting polymers. Additionally, protocols for the preparation of dogbone samples of a soft elastomeric network and their depolymerization, as well as compression molding of the N-phenylimide substituted rigid thermoplastic polymer, are also described. Finally, protocols for the photoisomerization of a tCBCO monomer to its strained E-alkene tCBCO form and its subsequent living ROMP are also discussed.

<table><tbody><tr><td>1 and 3 dram vials</td><td>VWR</td><td>66011-041, 66011-100</td><td></td></tr><tr><td>1,4-butanediol</td><td>Sigma-Aldrich</td><td>240559-100G</td><td></td></tr><tr><td>1,5-cyclooctadiene</td><td>ACROS</td><td>AC297120010</td><td></td></tr><tr><td>1-butanol</td><td>Fisher</td><td>A399-1</td><td></td></tr><tr><td>20 mL scintillation vials</td><td>VWR</td><td>66022-081</td><td></td></tr><tr><td>Acetic Anhydride</td><td>Alfa-Aesar</td><td>AAL042950B</td><td></td></tr><tr><td>Acetone</td><td>Fisher</td><td>A18-20</td><td></td></tr><tr><td>Aluminum backed TLC plates</td><td>Silicycle</td><td>TLA-R10011B-323</td><td></td></tr><tr><td>Ammonium hydroxide</td><td>Fisher</td><td>A669-212</td><td></td></tr><tr><td>Aniline</td><td>TCI</td><td>A0463500G</td><td></td></tr><tr><td>BD precisionglide (18 G)</td><td>Fisher</td><td></td><td></td></tr><tr><td>Chloroform</td><td>Fisher</td><td>C298-4</td><td></td></tr><tr><td>Column for circulation (to be packed with silver nitrate treated silica gel)</td><td></td><td></td><td>Approximately 1 cm radius and 25 cm long, with inner thread on either end</td></tr><tr><td>d-Chloroform</td><td>Cambridge Isotopes</td><td>DLM-7-100</td><td></td></tr><tr><td>Dichloromethane</td><td>VWR</td><td>BDH1113-19L</td><td></td></tr><tr><td>EDC.HCl; 3-(3-dimethylaminopropyl)-1-ethyl-carbodiimide hydrochloride</td><td>Chemimpex</td><td>00050</td><td></td></tr><tr><td>Ethyl Acetate</td><td>Fisher</td><td>E145-20</td><td></td></tr><tr><td>Ethyl Vinyl Ether</td><td>Sigma-Aldrich</td><td>422177-250ML</td><td></td></tr><tr><td>Glass chromatography columns</td><td>Fabricated in-house</td><td>D = 20 mm, L= 450 mm and D = 40 mm, L = 450 mm</td><td>The columns are fitted with a teflon stopcock at one end and a 24/40 ground glass joint to accommodate a solvent reservoir if needed.</td></tr><tr><td>Grubbs Catalyst 1st Generation (M102)</td><td>Sigma-Aldrich</td><td>579726-1G</td><td></td></tr><tr><td>Grubbs Catalyst 2nd Generation (M204)</td><td>Sigma-Aldrich</td><td>569747-100MG</td><td></td></tr><tr><td>Hexanes</td><td>Fisher</td><td>H292-20</td><td></td></tr><tr><td>Hydraulic press</td><td>Carver Instruments</td><td>#3912</td><td>Coupled with temperature control modules (see below)</td></tr><tr><td>Hydrochloric acid</td><td>Fisher</td><td>AA87617K4</td><td></td></tr><tr><td>Maleic Anhydride</td><td>ACROS</td><td>AC125240010</td><td></td></tr><tr><td>Methanol</td><td>Fisher</td><td>A412-20</td><td></td></tr><tr><td>Micro essential Hydrion pH paper (1-13 pH)</td><td>Fisher</td><td>14-850-120</td><td></td></tr><tr><td>Normject Luer Lock syringes (1, 3 and 10 mL)</td><td>VWR</td><td>89174-491, 53547-014 and 53547-010</td><td></td></tr><tr><td>Photoreactor chamber</td><td>Rayonet</td><td>RPR-100</td><td></td></tr><tr><td>QuadraPure TU (catalyst scavenger)</td><td>Sigma-Aldrich</td><td>655422-5G</td><td></td></tr><tr><td>Quartz tubes</td><td>Favricated in-house</td><td>D=2&quot;, L=12.5&quot; and D=1.5&quot;, L=10.5&quot;</td><td></td></tr><tr><td>Rotavap</td><td>Buchi</td><td></td><td></td></tr><tr><td>SciLog Accu Digital Metering Pump MP- 40</td><td>Parker</td><td></td><td>500 mL capacity</td></tr><tr><td>Siliaflash Irregular Silica, F60</td><td>Silicycle</td><td>R10030B-25KG</td><td></td></tr><tr><td>Silver Nitrate</td><td>ACROS</td><td>AC197680050</td><td></td></tr><tr><td>Sodium hydroxide</td><td>VWR</td><td>BDH9292-2.5KG</td><td></td></tr><tr><td>Steel Mold</td><td>Fabricated in-house</td><td>Overall dimensions of mold cavity: length 20 mm, width 7 mm and depth 1 mm; gauge dimensions: length 10 mm, width 3 mm)</td><td></td></tr><tr><td>Steel Plates</td><td>Fabricated in-house</td><td>100 mm x 150 mm x 1 mm</td><td></td></tr><tr><td>Teflon Mold (6-cavities)</td><td>Fabricated in-house</td><td>Overall cavity dimensions: length 25 mm, width 8.35 mm and depth 0.8 mm; gauge dimensions: length 5 mm, width 2 mm)</td><td></td></tr><tr><td>Teflon Sheets (0.005&quot; thick)</td><td>McMaster-Carr</td><td>8569K61</td><td></td></tr><tr><td>Temperature Control Modules</td><td>Omega</td><td>C9000A and C9000</td><td>&amp;deg;C units (two modules, one for top and one for bottom)</td></tr><tr><td>Triphenyl Phosphine</td><td>TCI</td><td>T0519500G</td><td></td></tr><tr><td>UV lamps</td><td>Rayonet</td><td>RPR2537A and RPR3000A</td><td></td></tr><tr><td>Vacuum pump</td><td>Welch Duoseal</td><td></td><td></td></tr><tr><td>Whatman Filter Paper (grade 2)</td><td>VWR</td><td>09-810F</td><td>filter paper</td></tr></tbody></table>

depolymerizable olefinic polymers based on fused-ring cyclooctene monomers

The growing consumption of synthetic polymers and the accumulation of polymer waste have led to a pressing need for new routes to sustainable materials. Achieving a closed-loop polymer economy via chemical recycling to monomer (CRM) is one such promising route. Our group recently reported a new CRM system based on polymers prepared by ring-opening metathesis polymerization (ROMP) of trans-cyclobutane fused cyclooctene (tCBCO) monomers. This system offers several key advantages, including the ease of polymerization at ambient temperatures, quantitative depolymerization to monomers under mild conditions, and a broad range of functionalities and thermomechanical properties. Here, we outline detailed protocols for the preparation of tCBCO-based monomers and their corresponding polymers, including the preparation of elastic polymer networks and compression molding of linear thermoplastic polymers. We also outline the preparation of high ring strain E-alkene tCBCO monomers and their living polymerization. Finally, the procedures for the depolymerization of linear polymers and polymer networks are also demonstrated.

Discussed here are representative results previously published15,18,19. Figure 5 shows the GPC traces for polymer P1 prepared by conventional ROMP with G2 (red curve)15 and living ROMP of EM1&#160;with G1/PPh3 (black)18</...

Watch this Scientific Journal Video about Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers at JoVE.com

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers

Here, we describe protocols for the preparation of trans-cyclobutane fused cyclooctenes (tCBCO),&#160;their polymerization to prepare depolymerizable olefinic polymers, and the depolymerization of these polymers under mild conditions. Additionally, protocols for the preparation of depolymerizable networks and compression molding of rigid linear plastics based on this system are described.

The growing consumption of synthetic polymers and the accumulation of polymer waste have led to a pressing need for new routes to sustainable materials. ...

depolymerizable-olefinic-polymers-based-on-fused-ring-cyclooctene

Research

JoVE Journal

Chemistry

3.2K Views.  University of Akron. Here, we describe protocols for the preparation of trans-cyclobutane fused cyclooctenes (tCBCO), their polymerization to prepare depolymerizable olefinic polymers, and the depolymerization of these polymers under mild conditions. Additionally, protocols for the preparation of depolymerizable networks and compression molding of rigid linear plastics based on this system are described.

Video: Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers

Anionic Polymerization of an Amphiphilic Copolymer for Preparation of Block Copolymer Micelles Stabilized by &#960;-&#960; Stacking Interactions

In this study, an amphiphilic copolymer that includes a core-forming block with phenyl groups was synthesized by living anionic polymerization of phenyl glycidyl ether (PheGE) on methoxy-polyethylene glycol (mPEG-b-PPheGE). Characterization of the copolymer revealed a narrow molecular distribution (PDI &#60; 1.03) and confirmed the degree of polymerization of mPEG122-b-(PheGE)15. The critical micelle concentration of the copolymer was evaluated using an established fluorescence method with the aggregation behavior evaluated by dynamic light scattering and transmission electronic microscopy. The potential of the copolymer for use in drug delivery applications was evaluated in a preliminary manner including in vitro biocompatibility, loading and release of the hydrophobic anti-cancer drug doxorubicin (DOX). A stable micelle formulation of DOX was prepared with drug loading levels up to 14% (wt%), drug loading efficiencies &#62; 60% (w/w) and sustained release of drug over 4 days under physiologically relevant conditions (acidic and neutral pH, presence of albumin). The high drug loading level and sustained release is attributed to stabilizing &#960;-&#960; interactions between DOX and the core-forming block of the micelles.

The key steps of living anionic polymerization of phenyl glycidyl ether (PheGE) on methoxy-polyethylene glycol (mPEG-b-PPheGE) are described. The resulting block copolymer micelles (BCMs) were loaded with doxorubicin 14% (wt%) and sustained release of drug over 4 days under physiologically relevant conditions was obtained.

In this study, an amphiphilic copolymer that includes a core-forming block with phenyl groups was synthesized by living anionic polymerization of phenyl ...

The Preparation and Properties of Thermo-reversibly Cross-linked Rubber Via Diels-Alder Chemistry

A method for using Diels Alder thermo-reversible chemistry as cross-linking tool for rubber products is demonstrated. In this work, a commercial ethylene-propylene rubber, grafted with maleic anhydride, is thermo-reversibly cross-linked in two steps. The pending anhydride moieties are first modified with furfurylamine to graft furan groups to the rubber backbone. These pendant furan groups are then cross-linked with a bis-maleimide via a Diels-Alder coupling reaction. Both reactions can be performed under a broad range of experimental conditions and can easily be applied on a large scale. The material properties of the resulting Diels-Alder cross-linked rubbers are similar to a peroxide-cured ethylene/propylene/diene rubber (EPDM) reference. The cross-links break at elevated temperatures (&#62; 150 &#176;C) via the retro-Diels-Alder reaction and can be reformed by thermal annealing at lower temperatures (50-70 &#176;C). Reversibility of the system was proven with infrared spectroscopy, solubility tests and mechanical properties. Recyclability of the material was also shown in a practical way, i.e., by cutting a cross-linked sample into small parts and compression molding them into new samples displaying comparable mechanical properties, which is not possible for conventionally cross-linked rubbers.

A simple two-step approach involving rubber modification and cross-linking yields fully reworkable, elastic rubber products.

A method for using Diels Alder thermo-reversible chemistry as cross-linking tool for rubber products is demonstrated. In this work, a commercial ...

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.

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 ...

A Simple and Efficient Protocol for the Catalytic Insertion Polymerization of Functional Norbornenes

Norbornene can be polymerized by a variety of mechanisms, including insertion polymerization whereby the double bond is polymerized and the bicyclic nature of the monomer is conserved. The resulting polymer, polynorbornene, has a very high glass transition temperature, Tg, and interesting optical and electrical properties. However, the polymerization of functional norbornenes by this mechanism is complicated by the fact that the endo substituted norbornene monomer has, in general, a very low reactivity. Furthermore, the separation of the endo substituted monomer from the exo monomer is a tedious task. Here, we present a simple protocol for the polymerization of substituted norbornenes (endo:exo ca. 80:20) bearing either a carboxylic acid or a pendant double bond. The process does not require that both isomers be separated, and proceeds with low catalyst loadings (0.01 to 0.02 mol%). The polymer bearing pendant double bonds can be further transformed in high yield, to afford a polymer bearing pendant epoxy groups. These simple procedures can be applied to prepare polynorbornenes with a variety of functional groups, such as esters, alcohols, imides, double bonds, carboxylic acids, bromo-alkyls, aldehydes and anhydrides.

We describe the catalytic insertion polymerization of 5-norbornene-2-carboxylic acid and 5-vinyl-2-norbornene to form functional polymers with a very high glass transition temperature.

Norbornene can be polymerized by a variety of mechanisms, including insertion polymerization whereby the double bond is polymerized and the bicyclic ...

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives

A facile method for the preparation of polycarbodiimide-based secondary structures (e.g., nano-rings, &#34;craters,&#34; fibers, looped fibers, fibrous networks, ribbons, worm-like aggregates, toroidal structures, and spherical particles) is described. These aggregates are morphologically influenced by extensive hydrophobic side chain-side chain interactions of the singular polycarbodiimide strands, as inferred by atomic force microscopy (AFM) and scanning electron microscopy (SEM) techniques. Polycarbodiimide-g-polystyrene copolymers (PS-PCDs) were prepared by a combination of synthetic methods, including coordination-insertion polymerization, copper(I)-catalyzed azide alkyne cycloaddition (CuAAC) &#34;click&#34; chemistry, and atom transfer radical polymerization (ATRP). PS-PCDs were found to form specific toroidal architectures at low concentrations in CHCl3. To determine the influence of a more polar solvent medium (i.e., THF and THF/EtOH) on polymer aggregation behavior, a number of representative PS-PCD composites have been tested to show discrete concentration-dependent spherical particles. These fundamental studies are of practical interest to the development of experimental procedures for desirable architectures by directed self-assembly in thin film. These architectures may be exploited as drug carriers, whereas other morphological findings represent certain interest in the area of novel functional materials.

Here, we present a protocol to prepare and visualize secondary structures (e.g., fibers, toroidal architectures, and nano-spheres) derived from helical polycarbodiimides. The morphology characterized by both atomic force microscopy (AFM) and scanning electron microscopy (SEM) was shown to depend on molecular structure, concentration, and the solvent of choice.

A facile method for the preparation of polycarbodiimide-based secondary structures (e.g., nano-rings, &#34;craters,&#34; fibers, looped fibers, fibrous ...

Controlled Photoredox Ring-Opening Polymerization of O-Carboxyanhydrides Mediated by Ni/Zn Complexes

Here, we describe an effective protocol that combines photoredox Ni/Ir catalysis with the use of a Zn-alkoxide for efficient ring-opening polymerization, allowing for the synthesis of isotactic poly(&#945;-hydroxy acids) with expected molecular weights (&#62;140 kDa) and narrow molecular weight distributions (Mw/Mn &#60; 1.1). This ring-opening polymerization is mediated by Ni and Zn complexes in the presence of an alcohol initiator and a photoredox Ir catalyst, irradiated by a blue LED (400 - 500 nm). The polymerization is performed at a low temperature (-15 &#176;C) to avoid undesired side reactions. The complete monomer consumption can be achieved within 4 - 8 hours, providing a polymer close to the expected molecular weight with narrow molecular weight distribution. The resulted number-average molecular weight shows a linear correlation with the degree of polymerization up to 1000. The homodecoupling 1H NMR study confirms that the obtained polymer is isotactic without epimerization. This polymerization reported herein offers a strategy for achieving rapid, controlled O-carboxyanhydrides polymerization to prepare stereoregular poly(&#945;-hydroxy acids) and its copolymers bearing various functional side-chain groups.

Controlled Photoredox Ring-Opening Polymerization of O-Carboxyanhydrides Mediated by Ni/Zn Complexes

A protocol for the controlled photoredox ring-opening polymerization of O-carboxyanhydrides mediated by Ni/Zn complexes is presented.

Here, we describe an effective protocol that combines photoredox Ni/Ir catalysis with the use of a Zn-alkoxide for efficient ring-opening polymerization, ...

Kinetics of Addition Polymerization to Polydimethylsiloxane

Source: <a href="https://www.jove.com/author/Kerry+M._Dooley">Kerry M. Dooley</a> and Michael G. Benton, Department of Chemical Engineering, Louisiana State University, Baton Rouge, LA
Polymers are molecules consisting of many repeating monomer units that are chemically bonded into long chains. They exhibit a broad range of physical properties, which are affected by their chemical structure, molecular weight and degree of polymerization. The polymer industry manufactures thousands of raw materials used in a broad variety of commercial products.1,2
The goal of this video is to perform an addition polymerization reaction and then evaluate the resulting product to understand how viscosity can be used to determine polymer molecular weight. Additionally, this experiment will investigate how molecular weight can be related to monomer conversion.

Synthesis of Polydimethylsiloxane via Addition Polymerization

Source: Kerry M. Dooley and Michael G. Benton, Department of Chemical Engineering, Louisiana State University, Baton Rouge, LA
Polymers are molecules ...

Education

JoVE Science Education

Engineering

Chemical Engineering

Free-Radical Chain Reaction and Polymerization of Alkenes

The conversion of alkenes to macromolecules called polymers is a reaction of high commercial importance. The structure of the polymer is defined by a repeating unit, while the terminal groups are considered insignificant. The average degree of polymerization represents the number of repeating units in the polymer molecule and is denoted by the subscript n.
<img alt="Figure1" src="/files/ftp_upload/11773/11773_PT_Figure_1.svg" style="text-align: center; height: 60px;" />
Alkenes undergo polymerization via a free-radical mechanism involving three steps: initiation, propagation, and termination.&#160;
Radicals are generated in the initiation step by heating a small quantity of free-radical initiators such as benzoyl peroxide. The benzoyloxy radical loses CO2 and forms a phenyl radical (Ph&#183;), which adds to the double bond of the alkene to initiate the polymerization process. One of the electrons of the alkene &#960; bond pairs with one electron from the phenyl radical to form a new C&#8211;C bond.
<img alt="Figure2" src="/files/ftp_upload/11773/11773_PT_Figure_2.svg" style="text-align: center; height: 60px;" />
<img alt="Figure3" src="/files/ftp_upload/11773/11773_PT_Figure_3.svg" style="text-align: center; height: 60px;" />
<img alt="Figure4" src="/files/ftp_upload/11773/11773_PT_Figure_4.svg" style="text-align: center; height: 80px;" />
In the propagation step, the carbon radical generated in the initiation step adds to another molecule of alkene to generate a new radical. The continuous addition of alkene monomers at the radical site yields the polymer.
<img alt="Figure5" src="/files/ftp_upload/11773/11773_PT_Figure_5.svg" style="text-align: center; height: 80px;" />
The termination step of the free-radical mechanism occurs via recombination or disproportionation. In a recombination step, two growing chains form a bond at their radical sites.
<img alt="Figure6" src="/files/ftp_upload/11773/11773_PT_Figure_6.svg" style="text-align: center; height: 60px;" />
In termination by disproportionation, a &#946;-hydrogen atom is transferred from one radical to another radical center, resulting in two non-radical products.
<img alt="Figure7" src="/files/ftp_upload/11773/11773_PT_Figure_7.svg" style="text-align: center; height: 300px;" />
The free-radical polymerization of ethylene yields low-density polyethylene (LDPE), where the low density is a consequence of significant branching in the polymer chains. Articles made from polymers surround us in various forms, such as food packaging materials, plastic bags, bottles, stationery, and automotive parts.

Free-radical Polymerization Reaction of Alkenes

Wolnorodnikowa reakcja łańcuchowa i polimeryzacja alkenów

The conversion of alkenes to macromolecules called polymers is a reaction of high commercial importance. The structure of the polymer is defined by a ...

JoVE Core

Organic Chemistry

Unit 1

Reactions of Alkenes

KEY TERMS AND CONCEPTS

Olefin Metathesis Polymerization: Overview

Recently, the development of olefin metathesis polymerization advanced the field of polymer synthesis. Simply put, the reorganization of substituents on their double&#160;bonds between two olefins in the presence of a catalyst is known as the olefin metathesis reaction. The use of metathesis reaction for polymer synthesis is called olefin metathesis polymerization.
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists of a carbon-metal double bond, also known as carbene.
The olefin metathesis reaction follows the reversible mechanism as shown in the figure below:
<img alt="Figure1" src="/files/ftp_upload/12934/12934_PT_Figure_1.svg" style="text-align: center; height: 300px;" />
The general mechanism involves the reaction of Grubbs catalyst with an alkene in a [2+2] cycloaddition giving a four-membered metallacyclobutane intermediate which immediately undergoes a ring-opening reaction in a reverse manner to give back the starting material or by breaking different bonds to form a different carbene or a catalyst and a different alkene product.
The new catalyst undergoes [2+2] cycloaddition with a second alkene to form a new metallacyclobutane, giving the metathesis product and a new carbene complex. This new carbene complex is then ready to attack another molecule of starting material, and the cycle is repeated.
There are several ways the olefin metathesis has been implemented for polymer synthesis. However, ring-opening metathesis polymerization (ROMP) and acyclic diene metathesis (ADMET) are the most widely used for polymerization. ROMP is a chain growth, addition polymerization reaction, whereas ADMET is a step-growth, condensation polymerization reaction.

Polimeryzacja metatezy olefin: przegląd

Recently, the development of olefin metathesis polymerization advanced the field of polymer synthesis. Simply put, the reorganization of substituents on ...

Synthetic Polymers

Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)

Ring-opening metathesis polymerization or ROMP involves strained cycloalkenes as starting materials. The mechanism of ROMP proceeds by reacting cycloalkene with Grubbs catalyst to give metallacyclobutane intermediate which undergoes a ring-opening reaction to form new carbene. The new carbene reacts with another molecule of cycloalkene. Repetition of these steps leads to the formation of an unsaturated open-chain polymer product. All these steps are reversible, however, relieving the ring strain drives the reaction forward.
The characteristic feature of the ROMP is that the unsaturation present in the reactants is conserved in the products. The reactivity of cycloalkenes towards ROMP decreases with an increase in the ring size.
Poly(phenylene vinylene) (PPV), an important polymer having alternating phenyl and vinyl groups used for electro-optical applications, is prepared by ROMP reaction. Acetyl-substituted bicyclooctadiene undergoes ROMP in the presence of Grubbs catalyst and gives processable polymer which upon heating loses two moles of acetic acid and aromatizes to form poly(phenylene vinylene) polymer.
<img alt="Figure1" src="/files/ftp_upload/12935/12935_PT_Figure_1.svg" style="text-align: center; height: 95px;" />
Figure 1. ROMP synthesis of poly(phenylene vinylene).

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers

Podsumowanie

Przeglądaj więcej filmów

Rozdziały w tym wideo

Anionic Polymerization of an Amphiphilic Copolymer for Preparation of Block Copolymer Micelles Stabilized by π-π Stacking Interactions

The Preparation and Properties of Thermo-reversibly Cross-linked Rubber Via Diels-Alder Chemistry

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

A Simple and Efficient Protocol for the Catalytic Insertion Polymerization of Functional Norbornenes

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives

Controlled Photoredox Ring-Opening Polymerization of O-Carboxyanhydrides Mediated by Ni/Zn Complexes

Kinetics of Addition Polymerization to Polydimethylsiloxane

Wolnorodnikowa reakcja łańcuchowa i polimeryzacja alkenów

Polimeryzacja metatezy olefin: przegląd

Polimeryzacja metatezy olefin: polimeryzacja metatezy z otwarciem pierścienia (ROMP)