A molecular Kuhn-scale model is presented for the stress relaxation dynamics of entangled polymer networks. The governing equation of the model is given by the general form of the linearized Langevin equation. Based on the fluctuation-dissipation theorem, the stress relaxation modulus is derived using the normal mode representation. The entanglements are introduced as additional entropic springs connecting internal beads of the network strands. The validity of the model is assessed by comparing predicted stress relaxation modulus and viscoelastic storage and loss moduli with the estimates from molecular dynamics (MD) simulations, using the same computer models. A finite element procedure is proposed and used to assemble the network connectivity matrix, and its numerically solved eigenvalues are used to predict the linear stress relaxation dynamics. Both perfect (fully polymerized stoichiometric) and imperfect networks with different soluble and dangling structures and loops are studied using mapped Kuhn-scale network models with up to several dozen thousand Kuhn segments. It is shown that for the overlapping ranges of times and frequencies, the model predictions and MD estimates agree well.

In recent years, the development of nanoreactors, such as micellar nanoreactors (MNRs) for catalytic transformations, has gained significant attention due to their potential in enhancing reaction rates, selectivity, efficiency, and, as importantly, the ability to conduct organic chemistry in aqueous solutions. Among these, the copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) reaction represents a pivotal transformation and is widely used in the synthesis of bioconjugates, pharmaceuticals, and advanced materials. This study aims toward advancing our understanding of the design and utilization of polymeric amphiphiles containing tris-triazole ligands as an integral element for CuAAC reactions within MNRs. Specifically, our investigation delves into three critical factors that influence the reaction rate within MNRs: hydrophobicity, architectural configuration of the polymeric ligands, and their concentration. Utilizing the high molecular precision of dendritic amphiphiles, we synthesized polymeric ligands with two distinct architectures, namely, PEG-ditris-triazole amphiphile (DTA) and PEG-monotris-triazole amphiphile (MTA), and explored their CuAAC reactivity through coassembly with commercially available Pluronic P123 amphiphiles. The results indicate that the architecture and the concentration of the polymeric ligands play more dominant roles in influencing the reaction rate than the hydrophobicity of the dendritic blocks. Notably, while MNRs assembled from solely DTA showed a dampened reaction rate, spiking P123 micelles with DTA yielded an MNR with significantly faster rates. Moreover, P123 MNRs spiked with the synthesized MTA demonstrated increased CuAAC reaction rates compared to those spiked with the DTA, and they even outperformed the widely used Tris(benzyltriazolylmethyl)amine ligand. These findings provide valuable insights into the design principles of polymer-based ligands for constructing reactive MNRs and other types of nanoreactors for efficient catalytic transformations.

It has been a long-term goal to understand the molecular orientation in films of conjugated polymers, which is crucial to their efficient exploitation. Here, we show that the surface energies determine the crystal orientation in films of model conjugated polymers, substituted polythiophenes crystallized on substrates. We systematically increase the surface energy of edge-on crystals formed at the vacuum interface by attaching polar groups to the ends of the polymer side chains. This suppresses crystallization at the vacuum interface, resulting in a uniform face-on crystal orientation induced by the graphene substrate in polythiophene films as thick as 200 nm, which is relevant for devices. Surprisingly, face-on crystal orientation is attained in the modified polythiophenes crystallized even on amorphous surfaces. Furthermore, for the samples with still competing interfacial interactions, the crystal orientation can be switched in the same sample, depending on the crystallization conditions. Thus, we report a fundamental understanding and control of the equilibrium crystal orientation in films of conjugated polymers.

The conjugated polymer's backbone conformation dictates the delocalization of electrons, ultimately affecting its optoelectronic properties. Most conjugated polymers can be viewed as semirigid rods with their backbone embedded among long alkyl side chains. Thus, it is challenging to experimentally quantify the conformation of a conjugated backbone. Here, we performed contrast variation neutron scattering on rigid conjugated donor-acceptor (D-A) diketopyrrolopyrrole (DPP) polymers with selectively deuterated side chains to measure the conjugated backbone conformation. We first synthesized DPP-based polymers with deuterated side chains, confirmed by NMR and FTIR. Using contrast variation neutron scattering, we found that the DPP-based conjugated polymers are much more rigid than poly(3-alkylthiophenes), with persistence length ( ) at 16-18 nm versus 2-3 nm. More importantly, in contrast to the relatively flexible poly(3-alkylthiophenes) whose backbone is more flexible than the whole polymer, we found that the backbone of DPP-based polymers has the same value compared to the whole polymer chain. This indicates that side chain interference on backbone conformation is not present for the semirigid polymer, which is further confirmed by coarse-grained molecular dynamics (CG-MD) simulations. Our work provides a novel protocol to probe polymer's backbone conformation and paradigm-shifting understanding of the backbone conformation of semirigid conjugated polymers.

The sequence of copolymers is of significant importance to their material properties, yet controlling the copolymer sequence remains a challenge. Previously, we have shown that polymer chains with sufficient stiffness and intermolecular attractions can undergo an emergent, polymerization-driven nematic alignment of nascent oligomers during a step-growth polymerization process. Both the extent of alignment and the point in the reaction at which it occurs impact the kinetics and the sequence development of the growing polymer. Of particular interest is the emergence of a characteristic block length in the ensemble of sequences, resulting in unusually peaked block length distributions. Here we explore the emergence of this characteristic block length over time and investigate how changes in activation energy, solution viscosity, and monomer density influence the sequence and block length distributions of stiff copolymers undergoing step-growth polymerization. We find that emergent aggregation and nematic ordering restrict the availability of longer chains to form bonds, thereby altering the propensity of chains to react in a length dependent fashion, which changes as the reaction progresses, and promoting the formation of chains and blocks of a characteristic length. Further, we demonstrate that the characteristic length scale which emerges is sensitive to the relative time scales of reaction kinetics and reactant diffusion, shifting in response to changes in the activation energy of the reaction and the viscosity of the solvent. Our observations suggest the potential for biasing characteristic lengths of sequence repeats in stiff and semiflexible copolymer systems by targeting specific nonbonded interactions and reaction kinetics through the informed adjustment of reaction conditions and the selection or chemical modification of monomer species.

Silicone bottlebrush copolymers and networks derived from cyclic carbosiloxanes are reported and shown to have enhanced properties and recyclability compared with traditional dimethylsiloxane-based materials. The preparation of these materials is enabled by the synthesis of well-defined heterotelechelic macromonomers with Si-H and norbornene chain ends via anionic ring-opening polymerization of the hybrid carbosiloxane monomer 2,2,5,5-tetramethyl-2,5-disila-1-oxacyclopentane. These novel heterotelechelic α-Si-H/ω-norbornene macromonomers undergo efficient ring-opening metathesis copolymerization to yield functional bottlebrush polymers with accurate control over molecular weight and functional-group density. Si-H groups retained at the ends of side-chains after ring-opening metathesis copolymerization allow for the preparation of supersoft networks via hydrosilylation with cross-linkers such as tetrakis[dimethyl(vinyl)silyl]orthosilicate. In contrast to traditional PDMS systems, the incorporation of poly(carbosiloxane) side chains allows the resulting networks to be recycled back to the original monomer (>85% recovery) via depolymerization at elevated temperatures (250 °C) in the presence of base catalysts (potassium hydroxide and tetramethylammonium hydroxide). The recovered monomer was successfully repolymerized through anionic ring-opening polymerization with no decrease in structural fidelity or activity. In summary, this combination of unique (macro)monomer design and bottlebrush architecture creates new opportunities in sustainable practices by offering a robust, recyclable alternative to commercial silicone-based materials.

A range of charge-stabilized aqueous polyurethane (PU) dispersions comprising hard segments formed from hydrogenated methylene diphenyl diisocyanate (HMDI) with dimethylolpropionic acid (DMPA) and ethylenediamine, and soft segments of poly(tetramethylene oxide) of different molecular weights are synthesized. Characterization of the dispersions by mass spectrometry, gel permeation chromatography, small-angle X-ray scattering, atomic force microscopy, and infrared spectroscopy shows that they are composed of PUs self-assembled into spherical particles (primary population) and supramolecular structures formed by hydrogen-bonded HMDI and DMPA acid-rich fragments (secondary population). Analysis of the scattering patterns of the dispersions, using a structural model based on conservation of mass, reveals that the proportion of supramolecular structures increases with DMPA content. It is also found that the PU particle radius follows the predictions of the particle surface charge density model, originally developed for acrylic statistical copolymers, and is controlled by hydrophile (DMPA) content in the PU molecules, where an increase in PU acidity results in a decrease in particle size. Moreover, there is a critical fractional coverage of hydrophiles stabilizing the particle surface for a given polyether soft-segment molecular weight, which increases with the polyether molecular weight, confirming that more acid groups are required to stabilize a more hydrophobic composition.

Particle and field-theoretic simulations are both commonly used methods to study the equilibrium properties of polymeric materials. Yet despite the formal equivalence of the two methods, no comprehensive comparisons of particle and field-theoretic simulations exist in the literature. In this work, we seek to fill this gap by performing a systematic and quantitative comparison of particle and field-theoretic simulations. In our comparison, we consider four representative polymeric systems: a homopolymer melt/solution, a diblock copolymer melt, a polyampholyte solution, and a polyelectrolyte gel. For each of these systems, we first demonstrate that particle and field-theoretic simulations are equivalent and yield exactly the same results for the pressure and the chemical potential. We next quantify the performance of each method across a range of different conditions including variations in chain length, system density, interaction strength, system size, and polymer volume fraction. The outcome of these calculations is a comprehensive look into the performance of each method and the systems and conditions when either particle or field-theoretic simulations are preferred. We find that field-theoretic simulations are equal to or faster than particle simulations for nearly all of the systems and conditions examined. In many situations, field-theoretic simulations are several orders of magnitude faster than particle simulations, especially if the polymer chains are long, the system density is high, and long-range Coulombic interactions are present. We also demonstrate that field-theoretic simulations are considerably faster at calculating the chemical potential and bypass the challenges associated with particle-based Widom insertion techniques. Taken together, our results provide quantitative evidence that field-theoretic simulations can reach and sample equilibrium considerably faster than particle simulations while simultaneously producing equivalent results.

Boosting the transport and selectivity properties of membranes based on polymers of intrinsic microporosity (PIMs) toward one specific working analyte of interest is challenging. In this work, a novel family of PIM membranes, prepared by casting and exhibiting optima mechanical properties and high thermal stability, was synthesized from 4,4'-(2,2,2-trifluoro-1-phenylethane-1,1-diyl) bis(benzene-1,2-diol) and two tetrafluoro-nitrile derivatives. Gas permeability measurements evidenced a CO/CH selectivity up to 170% relative to the reference polymer, PIM-1, in agreement with their calculated fractional free volume and the analysis of the textural properties by N and CO gas adsorption. Besides, the chemical modification by acid hydrolysis of the PIM membranes favored the permeability for lithium ions (LiCl 2M, 6 × 10 cm·s) compared to other alkali metal analogs such as sodium (NaCl 2M, 7.38 × 10 cm·s) and potassium (KCl 2M, 1.05 × 10 cm·s). Moreover, the complete mitigation of the crossover of redox species with higher molecular sizes than the ions from alkali metal salts was confirmed by using benchtop NMR methods. Additionally, the modified PIM membranes were measured in a symmetric electrochemical flow cell using an aqueous electrolyte by combining lithium ferro/ferricyanide redox compounds and lithium chloride. The electrochemical tests showed low polarization, high-rate capability, and capacity retention values of 99% when cycled at 10 mA·cm for over 50 cycles. Based on these results, these polymers could be used as highly selective and conducting membranes in electrodialysis for lithium separation and lithium-based redox flow batteries and as a protective layer in high-energy density lithium metal batteries.

Nanoconfinement has been recognized to induce significant changes in the physical properties of polymeric films when their thickness is less than 100 nm. Despite extensive research on the effect of nanoconfinement on nonconjugated polymers, studies focusing on the confinement effects on dynamics and associated electronic and mechanical properties for semiconductive and semirigid conjugated polymers remain limited. In this study, we conducted a comprehensive investigation into the nanoconfinement effects on both p- and n-type conjugated polymers having varying chain rigidity under different degrees of confinement. Using the flash differential scanning calorimetry technique, it was found that the increased molecular mobility with decreasing film thickness, as indicated by the depression of glass transition temperature ( ) from its bulk values, was directly proportional to chain rigidity. This relationship between chain rigidity and enhanced segmental mobility was further corroborated through molecular dynamics simulations. Thinner films exhibited a higher degree of crystallinity for all conjugated polymers, and a significant reduction of more than 50% in elastic modulus was observed for films with approximately 20 nm thickness compared to those of 105 nm thickness, particularly for highly rigid conjugated polymers. Interestingly, we found that the charge mobility remained independent of film thickness, with all samples demonstrating good charge mobility regardless of the different film thicknesses for devices measured here. Nanoconfined conjugated polymer thin films exhibited a combination of mechanical compliance and good charge carrier mobility properties, making them promising candidates for the next generation of flexible and portable organic electronics. From an engineering standpoint, confinement could be an effective strategy to tailor the dynamics and mechanical properties without significant loss of electronic property.

Theories of interpreting polymer physics and rheology at the molecular level from experiments, including small-angle scattering, typically rely on the assumption that polymer chains possess a Gaussian configuration distribution. This assumption frequently fails to describe features of real polymer molecules both at equilibrium (when polymers have nonlinear topology or heterogeneous chemistry) and out of equilibrium (when they are subjected to nonlinear deformations). To better describe non-Gaussian polymer conformation distributions, we propose a moments analysis based on the Gram-Charlier expansion as a natural framework for describing structure and scattering from non-Gaussian polymers. The expansion describes the conformation distribution in terms of cumulants (equivalent to moments of the distribution) of the underlying segment density distribution function, providing low-dimensional descriptors that can be inferred directly from measured scattering in a way that is agnostic to a polymer's topology, chemistry, or state of deformation. We use this framework to show that cumulants can be used to "fingerprint" non-Gaussian conformation distributions of polymers either at equilibrium (applied to sequence-defined heteropolymers) or out of equilibrium (applied to polymers experiencing nonlinear deformation due to flow). We anticipate that this new analysis method will provide a general framework for examining nonideal polymer configurations and the properties that arise from them.

Polyolefins, including high-density polyethylene (HDPE) and isotactic polypropylene (iPP), account for over half of the worldwide plastics market and have wide-ranging applications. Recycling of these materials is hindered due to separation difficulties as co-mingled blends of HDPE and iPP often exhibit brittle mechanical behavior because phase separated domains detach under stress due to low interfacial adhesion. Motivated to improve mechanical properties of mixed recyclates during processing, this work examines the effect of shear on the crystallization kinetics and rheological properties of HDPE-iPP blends utilizing a combination of differential scanning calorimetry (DSC), rheo-Raman spectroscopy, polarized optical microscopy, and scanning electron microscopy (SEM). In the quiescent experiments, the crystallization temperature as a function of blend composition exhibits a distinct decrease when the iPP forms the droplet phase, as expected, due to fractionated crystallization. In the presence of shear, we find elongated domains due to high capillary number. Unexpectedly, we find a compositional dependence to the flow-induced crystallization (FIC) of iPP: stronger FIC is observed in all blends compared to the pure iPP. Moreover, the flow completely counteracts the reduced crystallization arising from fractionated crystallization, indicating that the flow is able to induce nucleation in droplets to an extent such that it offsets the reduction in active nucleating agents in finite size droplets. We attribute these effects to differing microflow fields in the various morphologies as the iPP domains deform under shear.

We investigate the thermal and mechanical properties of poly(ethylene glycol), PEG, networks with either solely covalent epoxy bonds (single networks, SNs) or coexisting epoxy and iron-catecholate bonds (dual networks, DNs). The latter has recently been shown to be a promising material that combines mechanical strength with significant deformability. Here, we address the previously unexplored effects of the temperature and PEG precursor molar mass on the mechanical properties of the networks. We focus on PEG molar masses of 500 g/mol, where crystallization is suppressed, and 1000 g/mol, where some weak crystals are formed. SNs soften with an increasing PEG molar mass. Heating reversibly softens the DN, but it has a minimal effect on SNs. Nonlinear shear deformation of the DN breaks iron-catecholate bonds, and subsequent recovery upon shear cessation occurs to a long-time steady-state modulus whose value is almost triple the original one, likely due to the formation of tris-complexes versus initial sterically or kinetically trapped bis-complexation. The response under elongation indicates that the DN with sacrificial bonds is stiffer and more extensible than the other networks. These results may provide guidelines for designing dual networks with tunable mechanics at the molecular level.

Oxidative chemical vapor deposition (oCVD) stands as an attractive approach for the synthesis, engineering, and integration of conjugated polymers for advanced electronic and optoelectronic applications. In oCVD, the oxidant significantly influences the conformational and optoelectronic properties of the resulting conjugated polymer thin films. In this work, triflate salts of iron(III) and copper(II) (Fe(OTf) and Cu(OTf), respectively) are investigated for the first time as suitable alternative oxidants to the widely used iron(III) chloride (FeCl) for the oCVD of conjugated polymers. Structural and compositional characterizations of the resulting thin films evidenced the successful polymerization of cobalt(II) 5,15-diphenyl porphyrin using either Fe(OTf) or Cu(OTf). Along with an intermolecular dehydrogenative C-C coupling reaction, the occurrence of side reactions, such as the inclusion of -CF groups and demetalation and subsequent insertion of copper(II) in the porphyrin macrocycle when using Cu(OTf), were evidenced. Interestingly, the inclusion of -CF groups into the polymer backbone when using triflate salts results in a deepening of the frontier energy levels, while the insertion of copper(II) contributes to a reduction in the band gap energy. This work demonstrates that the careful selection of the oxidant agent in oCVD enables fine-tuning the optoelectronic properties of conjugated polymers to suit specific application requirements.

A unique case of sterically constrained crystallization arises in bottlebrush polymers bearing semicrystalline side chains. Bottlebrushes with grafted side chains can form crystalline structures governed by the complex interplay between side chain packing and backbone confinement. The confinement effect can be readily tuned by varying the side chain grafting density, thus affording control over the crystallization behavior of these systems. In this work, the grafting density effect on the crystallization behavior of molecular bottlebrushes comprising poly(ethylene oxide) (PEO) side chains grafted to a methacrylate backbone was systematically studied. Thermal analysis using differential scanning calorimetry showed that the bottlebrush polymers displayed suppressed crystallization temperatures, lower melting temperatures, and reduced crystallinities compared to linear homopolymer PEO. The crystalline morphology was investigated using polarized light, atomic force, and scanning electron microscopy. Isothermal crystallization experiments revealed a nonmonotonous dependence of the nucleation density on the side chain grafting density. The grafting density effect was also investigated using self-seeding experiments, revealing an increased clearing temperature and memory retention at higher grafting densities. This work highlights how grafting density influences the crystallization behavior of semicrystalline bottlebrushes, providing information for the processing and application of these unique polymers.

Drying oils like linseed oil are composed of multifunctional triglyceride molecules that can cure through three-dimensional free-radical polymerization into complex polymer networks. In the context of oil paint conservation, it is important to understand how factors like paint composition and curing conditions affect the chemistry and network structure of the oil polymer network and subsequently the links between the structure and long-term paint stability. Here, we employed time-resolved ATR-FTIR spectroscopy and comprehensive data analysis to study the curing behavior of five types of drying oil and the effects of curing temperature as well as the presence of a curing catalyst (PbO). Extracted concentration curves of key reactive functional groups point to a phase transition similar to a gel point that is especially pronounced in the presence of PbO, after which curing reactivity slows down dramatically. Analysis of kinetic parameters suggests that PbO induces a network structure with a more heterogeneous cross-link density, and the ATR-FTIR spectra indicate lower levels of oxidation in those cases. Finally, lower temperatures appear to favor the formation of carboxylic acid groups in oil mixtures with PbO.

Starting from a generic model based on the thermodynamics of mixing and abstracted from the chemistry and microscopic details of solution components, three consistent and complementary computational approaches are deployed to investigate the general condition for polymer cononsolvency in binary mixed solvents at the order. The study reveals χ - χ + χ as the underlying universal parameter that regulates cononsolvency, where χ is the immiscibility parameter between the α- and β-component. Two disparate cononsolvency regimes are identified for χ - χ + χ < 0 and χ - χ + χ > 2, respectively, based on the behavior of the second osmotic virial coefficient at varying solvent mixture composition . The predicted condition is verified using self-consistent field calculations by directly examining the polymer conformational transition as a function of . It is further shown that in the regime χ - χ + χ < 0, the reentrant polymer conformation transition is driven by maximizing the solvent-cosolvent contact, but in the regime χ - χ + χ > 2, it is driven by promoting polymer and cosolvent contact. In-between the two regimes when neither effect is dominant, a monotonic response of polymer conformation to is observed. Effects of the mean-field approximation on the predicted condition are evaluated by comparing the mean-field calculations with computer simulations. It shows that the fluctuation effects lead to a higher threshold value of χ - χ + χ in the second regime, where local enrichment of cosolvent in polymer proximity plays a critical role.

Thanks to many promising properties, including biocompatibility and the ability to experience large deformations, poly(ethylene glycol) diacrylate (PEGDA) hydrogels are excellent candidate materials for a wide range of applications. Interestingly, the polymerization of PEGDA leads to a network microstructure that is fundamentally different from that of the "classic" polymeric gels. Specifically, PEGDA hydrogels comprise PEG chains that are interconnected by multifunctional densely grafted rod-like polyacrylates (PAs), which serve as cross-linkers. In this work, we derive a microstructurally motivated model that captures the essential features which enable deformation in PEGDA hydrogels: (1) entropic elasticity of PEG chains, (2) deformation of PA rods, and (3) PA-PA interactions. Expressions for the energy-density functions and the stress associated with each of the three contributions are derived. The model demonstrates the microstructural evolution of the network during loading and reveals the role of key microscopic quantities. To validate the model, we fabricate and compress PEGDA hydrogel discs. The model is in excellent agreement with our experimental findings for a broad range of PEGDA compositions. Interestingly, we show that the response of PEGDA hydrogels with short PEG chains and long PA rods is governed by PA-PA interactions, whereas networks with longer PEG chains are dominated by entropy. To enable design, we employ the model to investigate the influence of key microstructural quantities, such as the length of the PEG and the PA chains, on the macroscopic properties and response. The findings from this work pave the way to the efficient design of PEGDA hydrogels with tunable properties and behaviors, which will enable the optimization of their performance in various applications.

This work aims to systematically examine the topology effect on the self-assembly of block copolymers. Compositionally, symmetric polystyrene--polydimethylsiloxane block copolymers (BCPs) with different chain topologies (diblock, three-arm star-block, and four-arm star-block) and various molecular weights are synthesized. These purposely designed block copolymers are used as a model system to investigate the topology effect on order-to-disorder transition temperature ( ) by temperature-resolved small-angle X-ray scattering experiments. An increase of the is observed when the arm number of BCPs with equivalent arm length (i.e., molecular weight) is increased from one to four. Based on the random-phase approximation (RPA), Flory-Huggins interaction parameter (χ) is determined from the regression of the measured . The observation by differential scanning calorimetry also demonstrates the shifting of the endothermic peak from the order-to-disorder transition of star-blocks to the higher temperature region, consistent with the scattering experiments and the RPA prediction.

A series of polyimides (PIs) was synthesized from 6FDA and two -OH substituted diamines having bulky pendant phenyl, Ph, and trifluoromethyl, CF, groups as precursors for thermally rearranged polybenzoxazole, TR-PBO, membranes. One diamine had two pendant Ph substituents; in the other, the substituents were Ph and CF. Applying azeotropic and chemical cyclizations allowed the obtention of four -hydroxy (-OH) or/and -acetoxy (-OAc) substituted PIs depending on the imidization method. The PIs were labeled as 3Ph-OH, 4Ph-OH, or 3Ph-OAc and 4PH-OAc, respectively. Thermal rearrangements of all four precursors were investigated in the interval from 350 to 450 °C. The conversions to TR-PBO increased with temperature, and almost quantitative conversions were obtained at temperatures close to 450 °C, although -OH substituted PIs reached conversions slightly higher than those of -OAc PIs at a given temperature. The TR-polymers' fractional free volume (FFV) also increased with conversion but was higher for the -OAc substituted precursors. Despite the high TR-PBO conversions, self-supported uniform TR membranes with reasonable mechanical properties were obtained, except for 4Ph-OH. Gas separation behavior of the membranes significantly improved after the thermal treatment, and the final CO/CH permselectivities lay between the 1991 and 2008 Robeson upper bounds. Particularly, TR-membranes derived from -OAc precursors and with pendant CF group demonstrated better gas transport properties with values of = 1121 barrer and α = 29 for 3Ph-OAc derived membrane, which positioned it beyond the 2008 upper limit.

A new approach to ring-opening polymerization (ROP) based on C(sp)-C(sp) bond cleavage is reported. This process is based on the ability of Pd to promote both the β-carbon elimination of a bifunctional cyclobutanol precursor and the C-C coupling process with the resulting Pd-alkyl intermediate. Consequently, novel polyketone materials are obtained. Owing to the modular synthesis of the used cyclobutanol monomers, the present ROP reaction allows the introduction of substitution patterns in the polymeric chain that are not accessible by current polyketone synthesis methodologies. We have explored in detail the initiation, propagation, and termination steps of this new polymerization process.