Revisiting poly(vinyl chloride) reactivity in the context of chemical recycling.

Poly(vinyl chloride) (PVC) is one of the highest production volume polymers due to its many applications, and it is one of the least recycled due to its chemical structure and frequent formulation with additives. Developing efficient PVC recycling techniques would enable PVC waste to be reused or repurposed in other processes. Within this context, the literature on PVC modification offers considerable insight into versatile reaction pathways, potentially inspiring new approaches for repurposing PVC waste into value-added products. This perspective provides an overview of PVC functionalization through a lens of chemical recycling, discussing various PVC reactivity trends and their applications with a critical assessment and future outlook of their recycling implications.

Substituent Impact on Quinoxaline Performance and Degradation in Redox Flow Batteries.

Aqueous redox flow batteries (RFBs) are attractive candidates for low-cost, grid-scale storage of energy from renewable sources. Quinoxaline derivatives represent a promising but underexplored class of charge-storing materials on account of poor chemical stability in prior studies (with capacity fade rates >20%/day). Here, we establish that 2,3-dimethylquinoxaline-6-carboxylic acid (DMeQUIC) is vulnerable to tautomerization in its reduced form under alkaline conditions. We obtain kinetic rate constants for tautomerization by applying Bayesian inference to ultraviolet-visible spectroscopic data from operating flow cells and show that these rate constants quantitatively account for capacity fade measured in cycled cells. We use density functional theory (DFT) modeling to identify structural and chemical predictors of tautomerization resistance and demonstrate that they qualitatively explain stability trends for several commercially available and synthesized derivatives. Among these, quinoxaline-2-carboxylic acid shows a dramatic increase in stability over DMeQUIC and does not exhibit capacity fade in mixed symmetric cell cycling. The molecular design principles identified in this work set the stage for further development of quinoxalines in practical, aqueous organic RFBs.

Using waste poly(vinyl chloride) to synthesize chloroarenes by plasticizer-mediated electro(de)chlorination.

New approaches are needed to both reduce and reuse plastic waste. In this context, poly(vinyl chloride) (PVC) is an appealing target as it is the least recycled high-production-volume polymer due to its facile release of plasticizers and corrosive HCl gas. Herein, these limitations become advantageous in a paired-electrolysis reaction in which HCl is intentionally generated from PVC to chlorinate arenes in an air- and moisture-tolerant process that is mediated by the plasticizer. The reaction proceeds efficiently with other plastic waste present and a commercial plasticized PVC product (laboratory tubing) can be used directly. A simplified life-cycle assessment reveals that using PVC waste as the chlorine source in the paired-electrolysis reaction has a lower global warming potential than HCl. Overall, this method should inspire other strategies for repurposing waste PVC and related polymers using electrosynthetic reactions, including those that take advantage of existing polymer additives.

Theoretical and Experimental Investigation of Functionalized Cyanopyridines Yield an Anolyte with an Extremely Low Reduction Potential for Nonaqueous Redox Flow Batteries.

Cyanopyridines and cyanophenylpyridines were investigated as anolytes for nonaqueous redox flow batteries (RFBs). The three isomers of cyanopyridine are reduced at potentials of -2.2 V or lower vs. ferrocene+/0 (Fc+/0 ), but the 3-CNPy⋅- radical anion forms a sigma-dimer that is re-oxidized at E≈-1.1 V, which would lead to poor voltaic efficiency in a RFB. Bulk electrochemical charge-discharge cycling of the cyanopyridines in acetonitrile and 0.50 M [NBu4 ][PF6 ] shows that 2-CNPy and 4-CNPy lose capacity quickly under these conditions, due to irreversible chemical reaction/decomposition of the radical anions. Density-functional theory (DFT) calculations indicated that adding a phenyl group to the cyanopyridines would, for some isomers, limit dimerization and improve the stability of the radical anions, while shifting their E1/2 only about +0.10 V relative to the parent cyanopyridines. Among the cyanophenylpyridines, 3-CN-6-PhPy and 3-CN-4-PhPy are the most promising as anolytes. They exhibit reversible reductions at E1/2 =-2.19 and -2.22 V vs. ferrocene+/0 , respectively, and retain about half of their capacity after 30 bulk charge-discharge cycles. An improved version of 3-CN-6-PhPy with three methyl groups (3-cyano-4-methyl-6-(3,5-dimethylphenyl)pyridine) has an extremely low reduction potential of -2.50 V vs. Fc+/0 (the lowest reported for a nonaqueous RFB anolyte) and loses only 0.21 % of capacity per cycle during charge-discharge cycling in acetonitrile.

Glass Transition Temperatures of Individual Submicrometer Atmospheric Particles: Direct Measurement via Heated Atomic Force Microscopy Probe.

The phase (solid, semisolid, or liquid) of atmospheric aerosols is central to their ability to take up water or undergo heterogeneous reactions. In recent years, the unexpected prevalence of viscous organic particles has been shown through field measurements and global atmospheric modeling. The aerosol phase has been predicted using glass transition temperatures (Tg), which were estimated based on molecular weight, oxygen:carbon ratio, and chemical formulae of organic species present in atmospheric particles via studies of bulk materials. However, at the most important sizes for cloud nucleation (∼50-500 nm), particles are complex mixtures of numerous organic species, inorganic salts, and water with substantial particle-to-particle variability. To date, direct measurements of Tg have not been feasible for individual atmospheric particles. Herein, nanothermal analysis (NanoTA), which uses a resistively heated atomic force microscopy (AFM) probe, is combined with AFM photothermal infrared (AFM-PTIR) spectroscopy to determine the Tg and composition of individual particles down to 76 nm in diameter at ambient temperature and pressure. Laboratory-generated proxies for organic aerosol (sucrose, ouabain, raffinose, and maltoheptaose) had similar Tg values to bulk Tg values measured with differential scanning calorimetry (DSC) and the Tg predictions used in atmospheric models. Laboratory-generated phase-separated particles and ambient particles were analyzed with NanoTA + AFM-PTIR showing intraparticle variation in composition and Tg. These results demonstrate the potential for NanoTA + AFM-PTIR to increase our understanding of viscosity within submicrometer atmospheric particles with complex phases, morphologies, and compositions, which will enable improved modeling of aerosol impacts on clouds and climate.

A Nonaqueous Redox-Matched Flow Battery with Charge Storage in Insoluble Polymer Beads.

We describe the nonaqueous redox-matched flow battery (RMFB), where charge is stored on redox-active moieties covalently tethered to non-circulating, insoluble polymer beads and charge is transferred between the electrodes and the beads via soluble mediators with redox potentials matched to the active moieties on the beads. The RMFB reported herein uses ferrocene and viologen derivatives bound to crosslinked polystyrene beads. Charge storage in the beads leads to a high (approximately 1.0-1.7 M) effective concentration of active material in the reservoirs while preventing crossover of that material. The relatively low concentration of soluble mediators (15 mM) eliminates the need for high-solubility molecules to create high energy density batteries. Nernstian redox exchange between the beads and redox-matched mediators was fast relative to the cycle time of the RMFB. This approach is generalizable to many different redox-active moieties via attachment to the versatile Merrifield resin.

Rethinking Catalyst Trapping in Ni-Catalyzed Thieno[3,2-b]thiophene Polymerization.

Catalyst-transfer polymerization (CTP) is a chain-growth method used to synthesize conjugated polymers. Although CTP works well for most donor-type monomers, the polymerization stalls with thieno[3,2-b]thiophene when using Ni catalysts. Previous reports have rationalized this result by suggesting that the catalyst is trapped in a Ni0 π-complex with the highly electron-rich arene. In this study, evidence is provided that the catalyst trap is more likely a NiII complex that arises from oxidative insertion of Ni0 into the C-S bonds of thieno[3,2-b]thiophene. This result is consistent with the known reactivity of Ni0 complexes toward S-heteroarenes and is supported herein by 31P nuclear magnetic resonance spectra acquired in situ, as well as data collected from small-molecule model reactions and density-functional theory simulations of the polymerization. We propose that this C-S insertion pathway and related off-cycle reactions may be relevant to understanding or enabling the CTP of other monomers with fused thiophenes.

Using JPP to Identify Ni Bidentate Phosphine Complexes In Situ.

Identifying intermediates of Ni-containing reactions can be challenging due to the high reactivity of Ni complexes and their sensitivity toward air and moisture. Many Ni bidentate phosphine complexes are diamagnetic and can be analyzed in situ via 31P NMR spectroscopy, but the oxidation state of Ni is difficult to determine using 31P chemical shift analysis alone. The J-coupling between P atoms, JPP, has been proposed to correlate with oxidation state, but few investigations have looked at how JPP is affected by parameters such as length of the linker or identity of the phosphine or other ligands. The present investigation into the JPP values of Ni bidentate phosphine complexes with two-carbon and three-carbon linkers shows that the JPP values observed in 31P NMR spectra, |JPP|, are competent indicators of the oxidation state at Ni. For complexes with two-carbon linkers, |JPP| > 40 Hz is typical of Ni0 while |JPP| < 30 Hz is typical of NiII; this trend is reversed for complexes with three-carbon linkers. Additionally, the Lewis acidity of the Ni and Lewis basicity of the phosphine ligand affect JPP predictably. For example, increased P-to-Ni donation arising from more-donating phosphines or more-withdrawing ligands trans to the P atoms causes a more negative JPP. These results should enable the oxidation state of Ni and properties of ligands in Ni bidentate phosphine complexes to be determined in situ during reactions containing these species.

Giving superabsorbent polymers a second life as pressure-sensitive adhesives.

An estimated 6.3 billion metric tons of post-consumer polymer waste has been produced, with the majority (79%) in landfills or the environment. Recycling methods that utilize these waste polymers could attenuate their environmental impact. For many polymers, recycling via mechanical processes is not feasible and these materials are destined for landfills or incineration. One salient example is the superabsorbent material used in diapers and feminine hygiene products, which contain crosslinked sodium polyacrylates. Here we report an open-loop recycling method for these materials that involves (i) decrosslinking via hydrolysis, (ii) an optional chain-shortening via sonication, and (iii) functionalizing via Fischer esterification. The resulting materials exhibit low-to-medium storage and loss moduli, and as such, are applicable as general-purpose adhesives. A life cycle assessment demonstrates that the adhesives synthesized via this approach outcompete the same materials derived from petroleum feedstocks on nearly every metric, including carbon dioxide emissions and cumulative energy demand.

100th Anniversary of Macromolecular Science Viewpoint: Redefining Sustainable Polymers.

Although Staudinger realized makromoleküles had enormous potential, he likely did not anticipate the consequences of their universal adoption. With 6.3 billion metric tons of plastic waste now contaminating our land, water, and air, we are facing an environmental and public health crisis. Synthetic polymer chemists can help create a more sustainable future, but are we on the right path to do so? Herein, a comprehensive literature survey reveals that there has been an increased focus on "sustainable polymers" in recent years, but most papers focus on biomass-derived feedstocks. In contrast, there is less focus on polymer end-of-life fates. Moving forward, we suggest an increased emphasis on chemical recycling, which sees value in plastic waste and promotes a closed-loop plastic economy. To help keep us on the path to sustainability, the synthetic polymer community should routinely seek the systems perspective offered by life cycle assessment.

Construction from Destruction: Hydrogel Formation from Triggered Depolymerization-Based Release of an Enzymatic Catalyst.

Biomimetic systems that undergo macroscopic phase transformations by transducing and amplifying external cues are highly desirable for applications such as self-healing. Here, we report self-assembly of polyelectrolyte complexes into a vesicular structure that can accommodate hydrophilic guest molecules, including enzymes. Triggered depolymerization of one of the polyelectrolyte molecules in the complex causes the vesicle to disassemble and release its contents. Such a triggered release of enzymes causes molecular-scale events to be amplified due to the enzyme's catalytic properties. This feature has been utilized to demonstrate construction of hydrogels from the destruction of nanoscopic polymeric vesicles. The design principles developed here are broadly adaptable to other triggerable depolymerization motifs reported in the literature.

Functionalized and Degradable Polyphthalaldehyde Derivatives.

Polymers that depolymerize back to monomers can be repeatedly chemically recycled, thereby reducing their environmental impact. Polyphthalaldehyde is a metastable polymer that can rapidly and quantitatively depolymerize due to its low ceiling temperature. However, the effect of substitution on the physical and chemical properties of polyphthalaldehyde derivatives has not been systematically studied. Herein, we investigate the cationic polymerization of seven o-phthalaldehyde derivatives and demonstrate that judicious choice of substituent results in materials with a wide range of ceiling temperatures (<-60 to 106 °C) and decomposition temperatures (109-196 °C). We anticipate that these new polymers and their derivatives will enable researchers to access degradable materials with tunable thermal, physical, and chemical properties.

The History of Palladium-Catalyzed Cross-Couplings Should Inspire the Future of Catalyst-Transfer Polymerization.

Conjugated polymers are the workhorse materials in organic electronics, a field that is rapidly growing to encompass energy storage devices such as supercapacitors and batteries. The highest-performing materials today have incredibly diverse structures and are accessed via step-growth polymerizations. This method results in limited control over the polymer's molecular weight, sequence, and dispersity, all of which can significantly impact device performance. The discovery of catalyst-transfer polymerization (CTP) in 2004 was predicted to change this landscape. Instead, nearly 14 years later, the CTP scope remains mostly limited to polymerizing small, electron-rich monomers. There is a pronounced gap between the rich array of structures utilized in organic electronics and what can be polymerized in a living, chain-growth fashion via CTP. Here, we suggest that palladium precatalysts could bridge this gap based on their huge versatility in the small-molecule cross-coupling literature. We highlight specific ancillary ligands from the small-molecule literature that we anticipate are candidates for enabling diverse conjugated polymer syntheses based on nearly a decade of research into the CTP mechanism. In addition, we describe several recent promising examples of CTP mediated by Pd precatalysts that serve as inspiration for the future. We present this Perspective as a call-to-action to advance organic electronics with CTP.

Ring-Walking in Catalyst-Transfer Polymerization.

Catalyst-transfer polymerization (CTP) has emerged as a useful method for synthesizing conjugated polymers with control over their length, sequence, and end-groups. However, the extent to which the polymerizations are living and chain-growth (or not) is highly catalyst and monomer dependent. Few studies have elucidated the impact of these identities on the stability and reactivity of the key intermediate, especially under polymerization-relevant conditions. We developed herein a simple experiment to identify catalyst stability and ring-walking ability using in situ-generated polymers. The combined results show that the ancillary ligand, metal, and polymer identity all play a crucial role. While each catalyst studied walks efficiently over large distances in poly(thiophene), the trends observed for poly(phenylene) highlight the differing roles of transition metal and ancillary ligand identities. The insights gained herein should be useful for extending CTP to other monomer and copolymer scaffolds.

Matchmaking in Catalyst-Transfer Polycondensation: Optimizing Catalysts based on Mechanistic Insight.

Catalyst-transfer polycondensation (CTP) has emerged as a useful living, chain-growth polymerization method for synthesizing conjugated (hetero)arene-based polymers with targetable molecular weights, narrow dispersities, and controllable copolymer sequences-all properties that significantly influence their performance in devices. Over the past decade, several phosphine- and carbene-ligated Ni- and Pd-based precatalysts have been shown to be effective in CTP. One current limitation is that these traditional CTP catalysts lead to nonliving, non-chain-growth behavior when complex monomer scaffolds are utilized. Because these monomers are often found in the highest-performing materials, there is a significant need to identify alternative CTP catalysts. Recent mechanistic insight into CTP has laid the foundation for designing new catalysts to expand the CTP monomer scope. Building off this insight, we have designed and implemented model systems to identify effective catalysts by understanding their underlying mechanistic behaviors and systematically modifying catalyst structures to improve their chain-growth behavior. In this Account, we describe how each catalyst parameter-the ancillary ligand(s), reactive ligand(s), and transition metal-influences CTP. As an example, ancillary ligands often dictate the turnover-limiting step of the catalytic cycle, and perhaps more importantly, they can be used to promote the formation of the key intermediate (a metal-arene associative complex) and its subsequent reactivity. The fidelity of this intermediate is central to the mechanism for the living, chain-growth polymerization. Reactive ligands, on the other hand, can be used to improve catalyst solubility and accelerate initiation. Additional advantages of the reactive ligand include providing access points for postpolymerization modification and synthesizing polymers directly off surfaces. While the most frequently used CTP catalysts contain nickel, palladium-based catalysts exhibit a higher functional group tolerance and broader substrate scope (e.g., monomers with boron, magnesium, tin, and gold transmetalating agents). Overall, we anticipate that applying the tools and lessons detailed in this Account to other monomers should facilitate a better "matchmaking" process that will lead to new catalyst-transfer polycondensations.

Developing a Gel-Based Sensor Using Crystal Morphology Prediction.

The stimuli-responsive nature of molecular gels makes them appealing platforms for sensing. The biggest challenge is in identifying an appropriate gelator for each specific chemical or biological target. Due to the similarities between crystallization and gel formation, we hypothesized that the tools used to predict crystal morphologies could be useful for identifying gelators. Herein, we demonstrate that new gelators can be discovered by focusing on scaffolds with predicted high aspect ratio crystals. Using this morphology prediction method, we identified two promising molecular scaffolds containing lead atoms. Because solvent is largely ignored in morphology prediction but can play a major role in gelation, each scaffold needed to be structurally modified before six new Pb-containing gelators were discovered. One of these new gelators was developed into a robust sensor capable of detecting lead at the U.S. Environmental Protection Agency limit for paint (5000 ppm).

My maize and blue brick road to physical organic chemistry in materials.

Similar to Dorothy's journey along the yellow brick road in The Wizard of Oz, this perspective carves out the path I took from my early childhood fascinations with science through my independent career at the University of Michigan (maize and blue). The influential research projects and mentors are highlighted, including some fortuitous experimental results that drew me into the field of supramolecular chemistry, specifically, and organic materials, broadly. My research group's efforts toward designing new sensors based on small molecule gelators are described. In particular, I highlight how our design strategy has evolved as we learn more about molecular gelators. This perspective concludes with some predictions about where molecular gels, as well as my personal and professional life, are headed.

Impact of Preferential π-Binding in Catalyst-Transfer Polycondensation of Thiazole Derivatives.

Polymerizing electron-deficient arenes in a controlled, chain-growth fashion remains a significant challenge despite a decade of research on catalyst-transfer polycondensation. The prevailing hypothesis is that the chain-growth mechanism stalls at a strongly associated metal-polymer π-complex, preventing catalyst turnover. To evaluate this hypothesis, we performed mechanistic studies using thiazole derivatives and identified approaches to improve their chain-growth polymerization. These studies revealed a surprisingly high barrier for chain-walking toward the reactive C-X bond. In addition, a competitive pathway involving chain-transfer to monomer was identified. This pathway is facilitated by ancillary ligand dissociation and N-coordination to the incoming monomer. We found that this chain-transfer pathway can be attenuated by using a rigid ancillary ligand, leading to an improved polymerization. Combined, these studies provide mechanistic insight into the challenges associated with electron-deficient monomers as well as ways to improve their living, chain-growth polymerization. Our mechanistic studies also revealed an unexpected radical anion-mediated oligomerization in the absence of catalyst, as well as a surprising oxidative addition into the thiazole C-S bond in a model system.