A promising solution to address the challenges in plastics sustainability is to replace current polymers with chemically recyclable ones that can depolymerise into their constituent monomers for circular use of materials. Despite the progress, few depolymerisable polymers exhibit the excellent thermal stability and strong mechanical properties of traditional polymers. Here we report a series of chemically recyclable polymers that show excellent thermal stability (decomposition temperature > 370 ºC) and tunable mechanical properties. The polymers are formed via ring-opening metathesis polymerisation of cyclooctene with a trans-cyclobutane installed at the 5,6-positions. The additional ring converts the nondepolymerisable polycyclooctene into a depolymerisable polymer by reducing the ring strain energy in the monomer (from 8.2 kcal/mol in unsubstituted cyclooctene to 4.9 kcal/mol in the fused ring). The fusedring monomer enables a broad scope of functionalities to be incorporated, providing access to chemically recyclable elastomers and plastics that show promise as next-generation sustainable materials. Main TextSynthetic polymers, including synthetic rubber and synthetic plastics, have been used in nearly every aspect of our daily lives. The dominance of synthetic polymers is largely driven by their excellent stability and processability as well as their versatile mechanical properties. However, due to their high durability, waste materials composed of these polymers have accumulated in the ocean and have caused serious concerns for marine ecosystems 1 . In addition, since 90% of these polymers are derived from nite fossil feedstocks, the production of these materials is unsustainable if they cannot be recycled and reused 2 .

Though numerous applications require degradable polymers, there are surprisingly few polymer systems that combine superior stability and controllable degradability. Particularly, the degradability of a conventional degradable polymer is typically enabled by cleavable groups on the backbone, which can be attacked by stimuli in ambient conditions, causing undesirable material deterioration. Here we report a general strategy to overcome this issue: "locking" the degradability during handling and use of the polymers and "unlocking" it when degradation is needed. This strategy is demonstrated with a cyclobutane-fused lactone (CBL) polymer. The cyclobutane keeps polymer backbone intact under conditions that hydrolyze the lactone and allows the ester group to be recovered when undesirable hydrolysis occurs. When backbone degradation is needed, the degradability can be unlocked by mechanochemical activation that converts the polyCBL into a linear polyester. The rare combination of two intrinsically conflicting properties, i.e., backbone stability and accessible degradability, can make this polymer a potential option for new sustainable materials.

The synthesis of two new heteroleptic Cu(I) photosensitizers (PS), [Cu(Xantphos)(NN)]PF (NN = biq = 2,2'-biquinoline, dmebiq = 2,2'-biquinoline-4,4'-dimethyl ester; Xantphos = 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene), along with the associated structural, photophysical, and electrochemical properties, are described. The biquinoline diimine ligand extends the PS light absorbing properties into the visible with a maximum absorption at 455 and 505 nm for NN = biq and dmebiq, respectively, in CHCl solvent. Following photoexcitation, both Cu(I) PS are emissive at low energy, albeit displaying stark differences in their excited state lifetimes (τ = 410 ± 5 (biq) and 44 ± 4 ns (dmebiq)). Cyclic voltammetry indicates a Cu-based HOMO and NN-based LUMO for both complexes, whereby the methyl ester substituents stabilize the LUMO within [Cu(Xantphos)(dmebiq)] by ∼0.37 V compared to the unsubstituted analogue. When combined with HO, N,N-dimethylaniline (DMA) electron donor, and cis-[Rh(NN)Cl]PF (NN = Mebpy = 4,4'-dimethyl-2,2'-bipyridine, bpy = 2,2'-bipyridine, dmebpy = 2,2'-bipyridine-4,4'-dimethyl ester) water reduction catalysts (WRC), photocatalytic H evolution is only observed using the [Cu(Xantphos)(biq)] PS. Furthermore, the choice of cis-[Rh(NN)Cl] WRC strongly affects the catalytic activity with turnover numbers (TON = mol H per mol Rh catalyst) of 25 ± 3, 22 ± 1, and 43 ± 3 for NN = Mebpy, bpy, and dmebpy, respectively. This work illustrates how ligand modification to carefully tune the PS light absorbing, excited state, and redox-active properties, along with the WRC redox potentials, can have a profound impact on the photoinduced intermolecular electron transfer between components and the subsequent catalytic activity.

The successful implementation of redox flow battery (RFB) technology requires the development of highly stable and soluble catholyte and anolyte materials that could be used in aqueous media. In this work, we investigated a highly soluble derivative of ferrocene1,1′-bis(sulfonate)ferrocene dianion disodium saltas a possible catholyte in an all-anionic RFB design. Based on the results of cyclic voltammetry and charge/discharge cycling experiments, we determined that this compound can be unstable and prone to a nucleophilic attack by anions in certain supporting electrolytes. However, it is stable in neutral pH solutions with weak nucleophilic anions like nitrate. These findings are fundamental for the future development of improved RFB materials.

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