Diels-Alder Polymerization Research Articles

Wavy Graphene Nanoribbons Containing Periodic Eight-Membered Rings for Light-Emitting Electrochemical Cells.

Precision graphene nanoribbons (GNRs) offer distinctive physicochemical properties that are highly dependent on their geometric topologies, thereby holding great potential for applications in carbon-based optoelectronics and spintronics. While the edge structure and width control has been a popular strategy for engineering the optoelectronic properties of GNRs, non-hexagonal-ring-containing GNRs remain underexplored due to synthetic challenges, despite offering an equally high potential for tailored properties. Herein, we report the synthesis of a wavy GNR (wGNR) embedding periodic eight-membered rings into its carbon skeleton, which is achieved by the A2B2-type Diels-Alder polymerization between dibenzocyclooctadiyne (6) and dicyclopenta[e,l]pyrene-5,11-dione derivative (8), followed by a selective Scholl reaction of the obtained ladder-type polymer (LTP) precursor. The obtained wGNR, with a length of up to 30 nm, is thoroughly characterized by solid-state NMR, FT-IR, Raman, and UV-Vis spectroscopy with the support of DFT calculations. The non-planar geometry of wGNR efficiently prevents the inter-ribbon π-π aggregation, leading to photoluminescence in solution. Consequently, the wGNR can function as an emissive layer for organic light-emitting electrochemical cells (OLECs), offering a proof-of-concept exploration in implementing luminescent GNRs into optoelectronic devices. The fast-responding OLECs employing wGNR will pave the way for advancements in OLEC technology and other optoelectronic devices.

Synthesis and Thermo-Selective Recycling of Diels-Alder Cyclopentadiene Thermoplastics.

Catalyst-free and reversible step-growth Diels-Alder (DA) polymerization has a wide range of applications in polymer synthesis and is a promising method for fabricating recyclable thermoplastics. The effectiveness of polymerization and depolymerization relies on the chemical building blocks, often utilizing furan as the diene and maleimide as the dienophile. Compared to the traditional diene-dienophile or two-component approach that requires precise stoichiometry, cyclopentadiene (Cp) can serve dual roles via self-dimerization. This internally balanced platform offers a route to access high-molecular-weight polymers and a dynamic handle for polymer recycling, which has yet to be explored. Herein, through a reactivity investigation of different telechelic Cp derivatives, the uncontrolled cross-linking of Cp was addressed, revealing the first successful DA homopolymerization. To demonstrate the generality of our methodology, we synthesized and characterized six Cp homopolymers with backbones derived from common thermoplastics, such as poly(dimethylsiloxane), hydrogenated polybutadiene, and ethylene phthalate. Among these materials, the hydrogenated polybutadiene-Cp analog can be thermally depolymerized (Mn = 68 to 23 kDa) and repolymerized to the parent polymer (Mn = 68 kDa) under solvent- and catalyst-free conditions. This process was repeated over three cycles without intermediate purification, confirming the efficient thermo-selective recyclability. The varied degradable properties of the other four Cp-incorporated thermoplastics were also examined. Overall, this work provides a general methodology for accessing a new class of reversible homopolymers, potentially expanding the design and construction of sustainable thermoplastics.

Radio Frequency Joule Heating for Healing and Reversible Adhesion Enabled by Dynamic Covalent Bonds

Herein, radio frequency (RF) Joule heating is used to trigger dynamic covalent bond exchange in a furan‐maleimide Diels–Alder polymer (DAP). Prior work shows that carbon susceptors can be incorporated into materials and undergo Joule heating when exposed to an electric field. Herein, carbon nanotubes (CNTs) are added to the DAP to make the material responsive to RF fields, and to enable selective, noncontact healing behavior of DAP after electric field exposure. After healing, mechanical testing is conducted to compare the tensile strength and toughness of the healed samples with the mechanical properties of the original, undamaged samples. A 96.2% recovery in tensile strength and an 83.2% recovery in toughness are observed. Also, RF heating of DAP/CNT enables repeated bonding and debonding of the material, allowing for adhesion and deadhesion on demand.

Aryl ether-free polymer electrolytes for electrochemical and energy devices.

Anion exchange polymers (AEPs) play a crucial role in green hydrogen production through anion exchange membrane water electrolysis. The chemical stability of AEPs is paramount for stable system operation in electrolysers and other electrochemical devices. Given the instability of aryl ether-containing AEPs under high pH conditions, recent research has focused on quaternized aryl ether-free variants. The primary goal of this review is to provide a greater depth of knowledge on the synthesis of aryl ether-free AEPs targeted for electrochemical devices. Synthetic pathways that yield polyaromatic AEPs include acid-catalysed polyhydroxyalkylation, metal-promoted coupling reactions, ionene synthesis via nucleophilic substitution, alkylation of polybenzimidazole, and Diels-Alder polymerization. Polyolefinic AEPs are prepared through addition polymerization, ring-opening metathesis, radiation grafting reactions, and anionic polymerization. Discussions cover structure-property-performance relationships of AEPs in fuel cells, redox flow batteries, and water and CO2 electrolysers, along with the current status of scale-up synthesis and commercialization.

Fast Self-Healing at Room Temperature in Diels-Alder Elastomers.

Despite being primarily categorized as non-autonomous self-healing polymers, we demonstrate the ability of Diels-Alder polymers to heal macroscopic damages at room temperature, resulting in complete restoration of their mechanical properties within a few hours. Moreover, we observe immediate partial recovery, occurring mere minutes after reuniting the fractured surfaces. This fast room-temperature healing is accomplished by employing an off-stoichiometric maleimide-to-furan ratio in the polymer network. Through an extensive investigation of seven Diels-Alder polymers, the influence of crosslink density on self-healing, thermal, and (thermo-)mechanical performance was thoroughly examined. Crosslink density variations were achieved by adjusting the molecular weight of the monomers or utilizing the off-stoichiometric maleimide-to-furan ratio. Quasistatic tensile testing, dynamic mechanical analysis, dynamic rheometry, differential scanning calorimetry, and thermogravimetric analysis were employed to evaluate the individual effects of these parameters on material performance. While lowering the crosslink density in the polymer network via decreasing the off-stoichiometric ratio demonstrated the greatest acceleration of healing, it also led to a slight decrease in (dynamic) mechanical performance. On the other hand, reducing crosslink density using longer monomers resulted in faster healing, albeit to a lesser extent, while maintaining the (dynamic) mechanical performance.

Controlled Degradation of Polycaprolactone Polymers through Ultrasound Stimulation.

This study describes the development of an ultrasound-responsive polymer system that provides on-demand degradation when exposed to high-intensity focused ultrasound (HIFU). Diels-Alder cycloadducts were used to crosslink polycaprolactone (PCL) polymers and underwent a retro Diels-Alder reaction when stimulated with HIFU. Two Diels-Alder polymer compositions were explored to evaluate the link between reverse reaction energy barriers and polymer degradation rates. PCL crosslinked with isosorbide was also used as a non-Diels-Alder-based control polymer. An increase of HIFU exposure time and amplitude correlated with an increase of PCL degradation for Diels-Alder-based polymers. Ultrasound imaging during HIFU allowed for real-time visualization of the on-demand degradation through cavitation-based mechanisms. The temperature surrounding the sample was monitored with a thermocouple during HIFU stimulation; a minimal increase in temperature was observed. PCL polymers were characterized using Fourier transform infrared (FTIR) spectroscopy, nuclear magnetic resonance (NMR), differential scanning calorimetry (DSC), optical profilometry, and mechanical testing. PCL degradation byproducts were identified by mass spectrometry, and their cytocompatibility was evaluated in vitro. Overall, this study demonstrated that HIFU is an effective image-guided, external stimulus to control the degradation of Diels-Alder-based PCL polymers on-demand.

Toughening and Stiffening in Thermoreversible Diels–Alder Polymer Network Blends

The thermophysical properties, mechanical behavior, and healing performance of Diels–Alder-based polymer networks can be tuned widely by changing the molar mass, functionality, and stoichiometric ratio of the multifunctional diene (e.g., furan) and dienophile (e.g., maleimide) monomers. Blending furan-functionalized monomers with a high and low molar mass opens a new dimension in tuning the properties of the resulting reversible polymer network blends (RPNBs), containing different ratios of elastomeric and thermoset phases, with low and high crosslink densities and glass transitions below and above room temperature, respectively. Increasing the thermoset content up to 20 wt % raises the gel transition temperature (Tgel), relaxation time (τ), rubbery plateau modulus, ultimate stress, and Young’s modulus of the stiffened elastomers, while the strain at fracture and self-healing efficiency remained mostly unchanged. Conversely, the addition of up to 20 wt % of the elastomer phase drastically toughens the thermosets because of stress dissipation, which can suppress the stress concentration in the phase-separated network blends. The blends showed higher stress and strain at break while retaining similar Young’s moduli. The toughness increases up to an order of magnitude at 50 wt %, compared to the pure thermoset. The phase-separated morphologies were evidenced by the presence of the Tg’s of the pure networks in DSC and DMA.

Easy Integrability and Data Processing of a Soft Tactile Array Sensor Through Reconfiguration

Most soft tactile sensors require a large number of wires to read the sensed data and complex algorithms to treat them. This makes the integration of soft tactile sensors challenging in full robotic systems. In order to simplify the integration of those soft devices, a new type of soft tactile array sensor is proposed. The sensitive keys of the sensor are made of three different self-healing Diels–Alder (DA) conductive polymers. The key positions in the sensor array are optimized in order to maximize the sensor accuracy in detecting pressed key positions and limit the number of wires required to read the sensor data. Since DA polymers are used, the keys are robustly connected to each other, ensuring high interfacial strength and conductivity while allowing reconfiguration. The reversible covalent bonds of the DA polymer allow the keys to be cut and healed back together to reform another tactile sensor tailored for another application with full recovery of the initial mechanical and electrical properties. In this work, two study cases are investigated: a keypad and a position sensor. The novel soft tactile array could reach an accuracy as low as 1.31% for the keypad and 3.8% for the position sensor compared with the developed sensor model. The keypad has a 90% success rate, whereas the position sensor has a 64% success rate.

Reconfigurable, Multi-Material, Voxel-Based Soft Robots

Voxel-based robots are aggregations of soft and simple building blocks that have been extensively evolved and simulated to perform various tasks, like walking, jumping or swimming. However, real-life voxel-based robots are rather scarce because of their challenging design and assembly. With the current materials and assembling methods, the interfaces between the soft multi-material voxels are prone to failure. This work proposes to make voxels out of reversible Diels-Alder polymers, which are available in a broad range of mechanical properties. By doing so, the covalent bonds at the multi-material interface ensure strong chemical connections, while allowing for reconfiguration. A first voxel-based gripper is thus robustly assembled, then disassembled, using its pieces (voxels) for reassembling another robot, i.e. a voxel-based walking robot. This reconfigurable property allows iterative validation of the simulated voxel-based robots and fine-tuning of the simulations parameters in a sustainable and economical way. Both physical voxel-based robots show similar behaviors as their simulations with root-mean-square errors down to 10.4%.

Photoredox Diels–Alder ladder polymerization

Ladder polymers with highly saturated backbones are prepared using a photoredox-catalyzed radical cation Diels–Alder polymerization.

Design of Surface-Aligned Main-Chain Liquid-Crystal Networks Prepared under Ambient, Light-Free Conditions Using the Diels-Alder Cycloaddition.

Surface-aligned liquid-crystal networks (LCNs) offer a solution for developing functional materials capable of performing a range of tasks, including actuation, shape memory, and surfaces patterning. Here we show that Diels-Alder cycloaddition can be used to prepare the backbone of planar aligned LCNs under mild ambient conditions without the addition of additives or UV irradiation. The mechanical properties of the networks have robust viscoelastic modulus and stiffness with a reversible local free volume change upon physical aging. This study shows new opportunities to design surface-aligned LCNs based on additive free step-growth Diels-Alder polymerization and enables the potential to incorporate a wider range of photochromic materials into LCNs.

Precise Structural Regulation and Band-Gap Engineering of Curved Graphene Nanoribbons.

Graphene nanoribbons (GNRs)─quasi-one-dimensional graphene cutouts─have drawn growing attention as promising candidates for next-generation electronic and spintronic materials. Theoretical and experimental studies have demonstrated that the electronic and magnetic properties of GNRs critically depend on their widths and edge topologies. Thus, the preparation of structurally defined GNRs is highly desirable not only for their fundamental physicochemical studies but also for their future technological development in carbon-based nanoelectronics. In the past decade, significant efforts have been made to construct a wide variety of GNRs with well-defined widths and edge structures via bottom-up synthesis. In addition to extensively studied planar GNRs consisting of armchair, zigzag, or gulf edges, curved GNRs (cGNRs) bearing cove ([4]helicene unit) or fjord ([5]helicene unit) regions along the ribbon edges have received increasing interest after we presented the first attempt to synthesize the fully cove-edged GNRs in 2015. Profiting from their novel edge topologies, cGNRs usually exhibit an unprecedented narrow band gap and high carrier transport mobility in comparison to the planar GNRs with similar widths. Moreover, cGNRs with particular out-of-plane-distorted structures are expected to provide further opportunities in nonlinear optics and asymmetric catalysis. However, the synthesis of cGNRs bearing cove or fjord edges remains underdeveloped due to the absence of efficient synthetic strategies/methods and suitable molecular precursor design.In this Account, we present the recent advances in the bottom-up synthesis and characterization of structurally defined cGNRs containing cove or fjord edges, mainly from our research group. First, the synthetic strategies toward cGNRs bearing cove edges are described, including the design of molecular monomers and polymer precursors as well as the corresponding polymerization methods, such as Ullmann coupling, Yamamoto coupling, A2B2-type Diels-Alder polymerization, followed by Scholl-type cyclodehydrogenation. The synthesis of typical model compounds is also described to support the understanding of the related cGNRs. In addition, the synthesis of cGNRs containing fjord edges from other research groups via the regioselective Scholl reaction, Hopf cyclization or regioselective photochemical cyclodehydrochlorination approach is presented. Second, we discuss the optoelectronic properties of the as-synthesized cGNRs and reveal the design principle to obtain cGNRs with high charge carrier mobilities. Finally, the challenges and prospects in the design and synthesis of cGNRs are offered. We anticipate that this Account will further stimulate the development of cGNRs through a collaborative effort between different disciplines.

Impact of crosslinker on stereochemistry of a dynamic covalent polymer network: A molecular dynamics simulation

We studied the effect of crosslinking density, ϕc, crosslinker length, m, and crosslinker flexibility on endo to exo adduct ratio in Diels–Alder polymer networks. The fraction of endo attachments, ψendo, increased with an increase of ϕc due to suppression of exo adducts at the early time-limiting stage of the network formation, as also observed in our recently published experimental study [1]. Polymer networks formed with flexible crosslinkers demonstrated a linear growth of ψendo with ϕc for all values of m. ψexo of networks with stiff crosslinkers sharply grew in the range of lower ϕc (ϕc<0.6) and plateaued at ϕc>0.6.

Solution Synthesis and Characterization of a Long and Curved Graphene Nanoribbon with Hybrid Cove-Armchair-Gulf Edge Structures.

Curved graphene nanoribbons (GNRs) with hybrid edge structures have recently attracted increasing attention due to their unique band structures and electronic properties as a result of their nonplanar conformation. This work reports the solution synthesis of a long and curved multi‐edged GNR (cMGNR) with unprecedented cove–armchair–gulf edge structures. The synthesis involves an efficient A2B2‐type Diels–Alder polymerization between a diethynyl‐substituted prefused bichrysene monomer (3b) and a dicyclopenta[e,l]pyrene‐5,11‐dione derivative (6) followed by FeCl3‐mediated Scholl oxidative cyclodehydrogenation of the obtained polyarylenes (P1). Model compounds 1a and 1b are first synthesized to examine the suitability and efficiency of the corresponding polymers for the Scholl reaction. The successful formation of cMGNR from polymer P1 bearing prefused bichrysene units is confirmed by FTIR, Raman, and solid‐state NMR analyses. The cove‐edge structure of the cMGNR imparts the ribbon with a unique nonplanar conformation as revealed by density functional theory (DFT) simulation, which effectively enhances its dispersibility in solution. The cMGNR has a narrow optical bandgap of 1.61 eV, as estimated from the UV–vis absorption spectrum, which is among the family of low‐bandgap solution‐synthesized GNRs. Moreover, the cMGNR exhibits a carrier mobility of ≈2 cm2 V−1 s−1 inferred from contact‐free terahertz spectroscopy.

Thermodynamics and Stereochemistry of Diels–Alder Polymer Networks: Role of Crosslinker Flexibility and Crosslinking Density

Dynamic covalent polymer networks crosslinked through Diels–Alder (DA) reactions are promising self-healing, 3D-printable materials that have the unique ability to reshuffle their dynamic bonds in ...

Self‐Healable Hydrophobic Material Based on Anthracenyl Functionalized Fluorous Block Copolymers via Reversible Addition‐Fragmentation Chain Transfer Polymerization and Rapid Diels–Alder Reaction

AbstractRecently, among the available approaches to develop self‐healable materials, 1,2,4‐triazoline‐3,5‐dione (TAD)‐based Diels–Alder (DA) chemistry has gained tremendous attention, becuase this DA reaction is very rapid under ambient conditions. This study delineates developing a self‐healing hydrophobic fluorinated polymer utilizing dynamic and rapid TAD‐DA chemistry. For this purpose, block copolymers of 2‐hydroxyethyl methacrylate (HEMA) and 2,2,2‐trifluoroethylmethacrylate (TFEMA) are prepared via reversible addition‐fragmentation chain transfer polymerization. Subsequently, the pendant hydroxyl groups of the HEMA repeat units are modified with anthracenyl functionality via esterification with 9‐anthracenecarboxylic acid. The tailor‐made polymer‐bearing anthracenyl pendants are subsequently crosslinked via a rapid DA reaction using a bifunctional TAD derivative at room temperature (r.t.). Differential scanning calorimetry (DSC) analysis is performed to interpret the thermoreversible behavior of the TAD‐derived DA polymer. The self‐healing characteristics of this TAD‐derived DA conjugate are studied by monitoring the healing of a notched surface via AFM analysis. Interestingly, the TAD conjugated fluoropolymers are hydrophobic, as evidenced by the water contact angle analysis. Such TAD‐derived DA fluoropolymer conjugates with remarkable hydrophobic characteristics and excellent self‐healing features can pave a new direction in the potential materials for specialty paints, coatings, and adhesives.

A Diels-Alder polymer platform for thermally enhanced drug release toward efficient local cancer chemotherapy

ABSTRACT We reports a novel thermally enhanced drug release system synthesized via a dynamic Diels-Alder (DA) reaction to develop chemotherapy for pancreatic cancer. The anticancer prodrug was designed by tethering gemcitabine (GEM) to poly(furfuryl methacrylate) (PFMA) via N-(3-maleimidopropionyloxy)succinimide as a linker by DA reaction (PFMA-L-GEM). The conversion rate of the DA reaction was found to be approximately 60% at room temperature for 120 h. The reversible deconstruction of the DA covalent bond in retro Diels-Alder (rDA) reaction was confirmed by proton nuclear magnetic resonance, and the reaction was significantly accelerated at 90 °C. A PFMA-LGEM film containing magnetic nanoparticles (MNPs) was prepared for thermally enhanced release of the drug via the rDA reaction. Drug release was initiated by heating MNPs by alternating magnetic field. This enables local heating within the film above the rDA reaction temperature while maintaining a constant surrounding medium temperature. The MNPs/PFMA-L-GEM film decreased the viability of pancreatic cancer cells by 49% over 24 h. Our results suggest that DA/rDA-based thermally enhanced drug release systems can serve as a local drug release platform and deliver the target drug within locally heated tissue, thereby improving the therapeutic efficiency and overcoming the side effects of conventional drugs used to treat pancreatic cancer.

Influence of the Glass Transition Temperature and the Density of Crosslinking Groups on the Reversibility of Diels-Alder Polymer Networks.

The interest in self-healing, recyclable, and adaptable polymers is growing. This work addresses the reversibility of crosslink formation based on Diels-Alder reaction in copolymer networks containing furfuryl and maleimide groups, which represent the “diene” and the “dienophile,” respectively. The copolymers are synthesized by atom transfer radical polymerization (ATRP) and free radical polymerization. The diene bearing copolymers are crosslinked either with a small molecule containing two dienophiles or with a dienophile bearing copolymer. The influence of the crosslinking temperature on the Diels-Alder reaction is analyzed. Furthermore, the influence of the glass transition temperature and the influence of the density of crosslinking groups on the thermo-reversibility of crosslinking are investigated by temperature dependent infrared spectroscopy and differential scanning calorimetry. It is shown that the reversibility of crosslinking is strongly influenced by the glass transition temperature of the system.

Design of closed-loop recycling production of a Diels-Alder polymer from a biomass-derived difuran as a functional additive for polyurethanes.

Acetalization of biomass-derived 5-hydroxymethyl furfural (HMF) with pentaerythritol produced a difuran (HPH) monomer in the presence of an acid catalyst. A recyclable polymer was then synthesized by Diels-Alder reaction of bismaleimide and the HMF-derived difuran (HPH). A polyurethane, produced from the Diels-Alder polymer has a higher glass transition temperature than a polyurethane, produced from ethylene glycol. The polyurethane, containing Diels-Alder polymer also has a self-healing ability. The Diels-Alder polymer could be hydrolyzed under acidic acetate buffer at 60°C to produce the monomers for recycling. Each produced monomer was separated by solvent extraction, and the extracted monomers were recovered in different solvent fractions, such as aqueous, ethyl acetate, and acetone fractions. Techno economic analysis was used to assess the minimum selling price ($14.1 per kg) for the primary production of Diels-Alder polymer at a feed capacity of 400 tons per year. The economic viability of the primary recovery process for the most expensive recovered monomer, bismaleimide, was assessed by calculating the minimum selling price of the bismaleimide ($15.2 per kg). A circular closed-loop recycling production process for the Diels-Alder polymer was developed and this approach can produce the Diels-Alder polymer at $8.2 per kg when the feed capacity was 40 ktons per year.

Room Temperature Self-Healing in Soft Pneumatic Robotics: Autonomous Self-Healing in a Diels-Alder Polymer Network

Healable soft robotic systems have been developed by constructing flexible membranes out of Diels?Alder (DA) polymer networks. In these components, relatively large amounts of damage, on the centimeter scale, can be healed, provided that the temperature is increased to 80?90 ?C. This article presents a new DA polymer network that can heal at room temperature through a smart design of the network that increases the molecular mobility in the material. This new material is used to develop the first healable soft robotic prototype that can autonomously recover from severe, realistic damage. The soft pneumatic hand can recover from various types of injuries, including being cut completely in half, without the need for a temperature increase. After healing, the performance of the soft robotic prototype is recovered.