Single Unit Monomer Insertion Research Articles

Orthogonal Radical and Cationic Single-Unit Monomer Insertions for Engineering Polymer Architectures.

The single-unit monomer insertion (SUMI), derived from living/controlled polymerization, can be directly functionalized at the end or within the chain of polymers prepared by living/controlled polymerization, offering potential applications in the preparation of polymers with complex architectures. Many scenarios demand the simultaneous incorporation of monomers suitable for different polymerization methods into complex polymers. Therefore, it becomes imperative to utilize SUMI technologies with diverse mechanisms, especially those that are compatible with each other. Here, we reported the orthogonal SUMI technique, seamlessly combining radical and cationic SUMI approaches. Through the careful optimization of monomer and chain transfer agent pairs and adjustments to reaction conditions, we can efficiently execute both radical and cationic SUMI processes in one pot without mutual interference. The utilization of orthogonal SUMI pairs facilitates the integration of radical and cationic reversible addition-fragmentation chain transfer (RAFT) polymerization in various configurations. This flexibility enables the synthesis of diblock, triblock, and star polymers that incorporate both cationically and radically polymerizable monomers. Moreover, we have successfully implemented a mixing mechanism of free radicals and cations in RAFT step-growth polymerization, resulting in the creation of a side-chain sequence-controlled polymer brushes.

Orthogonal Radical and Cationic Single‐Unit Monomer Insertions for Engineering Polymer Architectures

AbstractThe single‐unit monomer insertion (SUMI), derived from living/controlled polymerization, can be directly functionalized at the end or within the chain of polymers prepared by living/controlled polymerization, offering potential applications in the preparation of polymers with complex architectures. Many scenarios demand the simultaneous incorporation of monomers suitable for different polymerization methods into complex polymers. Therefore, it becomes imperative to utilize SUMI technologies with diverse mechanisms, especially those that are compatible with each other. Here, we reported the orthogonal SUMI technique, seamlessly combining radical and cationic SUMI approaches. Through the careful optimization of monomer and chain transfer agent pairs and adjustments to reaction conditions, we can efficiently execute both radical and cationic SUMI processes in one pot without mutual interference. The utilization of orthogonal SUMI pairs facilitates the integration of radical and cationic reversible addition‐fragmentation chain transfer (RAFT) polymerization in various configurations. This flexibility enables the synthesis of diblock, triblock, and star polymers that incorporate both cationically and radically polymerizable monomers. Moreover, we have successfully implemented a mixing mechanism of free radicals and cations in RAFT step‐growth polymerization, resulting in the creation of a side‐chain sequence‐controlled polymer brushes.

Controlled switching thiocarbonylthio end-groups enables interconvertible radical and cationic single-unit monomer insertions and RAFT polymerizations

To emulate the ordered arrangement of monomer units found in natural macromolecules, single-unit monomer insertion (SUMI) have emerged as a potent technique for synthesizing sequence-controlled vinyl polymers. Specifically, numerous applications necessitate vinyl polymers encompassing both radically and cationically polymerizable monomers, posing a formidable challenge due to the distinct thiocarbonylthio end-groups required for efficient control over radical and cationic SUMIs. Herein, we present a breakthrough in the form of interconvertible radical and cationic SUMIs achieved through the manipulation of thiocarbonylthio end-groups. The transition from a trithiocarbonate (for radical SUMI) to a dithiocarbamate (for cationic SUMI) is successfully accomplished via a radical-promoted reaction with bis(thiocarbonyl) disulfide. Conversely, the reverse transformation utilizes the reaction between dithiocarbamate and bistrithiocarbonate disulfide under a cationic mechanism. Employing this strategy, we demonstrate a series of synthetic examples featuring discrete oligomers containing acrylate, maleimide, vinyl ether, and styrene, compositions unattainable through the SUMI of a single mechanism alone.

Synthesis of Dendrimer-Like Molecules with Partial Carbon Chain via Iterative Single Unit Monomer Insertions.

Carbon-chain dendritic polymers hold unique properties and promising applications. However, synthesizing carbon-chain dendrimers, beyond conjugated ones, remains a challenge. Here, the use of the iterative single unit monomer insertion technique for synthesizing 2.5 generation partial-carbon-chain dendrimers (G2.5) is described, utilizing bismaleimide as the core, a maleimide-trithiocarbonate conjugate as the branching unit, and indene as the spacer unit, following a divergent growth strategy. The optimized conditions for synthesizing the maleimide-trithiocarbonate branching unit are a bismaleimide to trithiocarbonate ratio of 5:1 and a reaction time of 30 min. The structures are verified using 1H nuclear magnetic resonance, gel permeation chromatography, and matrix-assisted laser desorption/ionization-time of flight mass spectra. A four-arm star polymer is then synthesized using the G2.5 as the core. This synthesis of a partial-carbon-chain dendrimer establishes a foundational step toward creating all-carbon-chain ones and may open new application avenues in material science.

Pyrazole carbodithiolate-driven iterative RAFT single-additions.

In this Communication, we comprehensively investigated substituent effects relevant to iterative reversible activation fragmentation chain transfer (RAFT) single unit monomer insertion (SUMI) reactions. Through the use of the pyrazole carbodithiolate (PCDT) "Z-group" as the chain transfer component in RAFT SUMI, we show the importance of "Z-group" effects and its interplay with "R-group" (the carbon-centred radical precursor) effects. We also expanded the scope of RAFT SUMI to new monomer types and sequences thereof. As such, the C-S bond dissocation/reformation steps were found to be crucial factors in SUMI, and it was found that general substituent effects must be wholistically examined for every step of this reaction. This stands in contrast with conventional knowledge of RAFT polymerisation, where the main consideration is often centred around the propagation stage, i.e., the key C-C bond formation step. Indeed, contrary to SUMI, the latter characteristic was observed in the analogous alternating copolymerisation.

Development of Sequence‐Controlled, Degradable, and Cytocompatible Oligomers with Explicit Fragmentation Pathways

Back Cover: In Article 2200788, Feiyue Xing, Yingshan Zhou, Pu Xiao, and co-workers demonstrate the preparation of novel sequence-controlled pentamers by single unit monomer insertion. The oligomers are degradable due to the ester bonds of 5,6-benzo-2-methylene-1,3-dioxepane undergoing radical ring-opening polymerization. The well-defined structures of the degraded products are fully confirmed by specific fragmentation pathways and show no cytotoxicity for the potential biomedical applications.

Cationic Single-Unit Monomer Insertion (cSUMI): From Discrete Oligomers to the α-/ω-End and In-Chain Sequence-Regulated Polymers

Single-unit monomer insertion (SUMI) has become an important strategy for the synthesis of sequence-controlled vinyl polymers due to its strong versatility and high efficiency. However, all reported SUMI processes are based on a free-radical mechanism, resulting in a limited number of monomer types being applicable to SUMI or a limited number of sequences of structural units that SUMI can synthesize. Herein, we developed a novel SUMI based on a cationic mechanism (cSUMI), which operates through a degenerative (similar to radical SUMI) but cationic chain transfer process. By optimizing the chain transfer agent (CTA) and monomer pairs, a high-efficiency cSUMI was achieved for vinyl ether and styrene monomers. Based on this reaction, a range of discrete oligomers containing vinyl ether and styrene moieties, and even α-/ω-end and in-chain sequence-regulated polymers were synthesized, most of which cannot be achieved by radical SUMI. In addition, we explored the application of these sequence-regulated polymers in the preparation of miktoarm star polymers, delivery of photosensitizers, and solubilization of fluorescence probes. The development of SUMI with a new mechanism will certainly broaden the scope of structures and sequences in precise vinyl-based polymers.

Photoinduced RAFT Step‐Growth Polymerization toward Degradable Living Polymer Networks

Comprehensive SummaryThe application of reversible degenerative radical polymerization (RDRP) in the construction of polymer networks (PNs) provides a facile and convenient way to fabricate 3D objects with the ability to be posttransformed. However, the polymerization mechanism mainly relies on chain‐growth polymerization, which limits its wide application for various polymeric materials with different functionalities. Here, we present a method toward PNs by utilizing a photoinduced RAFT step‐growth polymerization, which is based on a RAFT single unit monomer insertion (SUMI) reaction between a xanthate and an alkyl vinyl group. Benefiting from this reaction, a pendant RAFT agent can be generated in each repeat unit of the backbone during the polymerization. These reactivatable dormant species can be further used for the postfunctionalization of PNs prepared by step‐growth polymerization of multifunctional monomers. Moreover, the prepared PNs are degradable owing to the introduction of ester groups, providing an avenue toward degradable and stimuli‐responsive materials.

Solid-phase synthesis of iterative RAFT single unit monomer insertion adducts

In this article, we disclose the use of a solid-phase methodology to synthesise iterative RAFT single unit monomer insertion (SUMI) adducts.

Development of Sequence-Controlled, Degradable, and Cytocompatible Oligomers with Explicit Fragmentation Pathways.

Sequence-defined and degradable polymers can mimic biopolymers, such as peptides and DNA, to undertake life-supporting functions in a chemical way. The design and development of well-structured oligomers/polymers is the most concern for the public, even to further uncover their degradation process illustrating the degraded products and their properties. However, seldom investigation has been reported on the aforementioned aspects. In this work, the alternating photo-reversible addition-fragmentation chain-transfer (photo-RAFT) single unit monomer insertion (SUMI) of different N-substituted maleimides and thermal radical ring-opening SUMI of a cyclic ketene acetal monomer (i.e., 5,6-benzo-2-methylene-1,3-dioxepane (BMDO)) is adopted, to produce two degradable pentamers owing to the conversion of the exo-methylene group of BMDO into ester bonds along the main chains of the prepared products. Moreover, the possible degraded approach of pentamers is studied by combining high-resolution mass spectrometry (HRMS) and liquid chromatography-mass spectrometry (LC-MS) for the first time. This work also sheds light on the precise structures and cytotoxicity of SUMI products and their degraded compounds, proposing a detailed and credible outlook for biomedical applications.

PET-RAFT single unit monomer insertion of β-methylstyrene derivatives: RAFT degradation and reaction selectivity.

Reversible addition-fragmentation chain transfer (RAFT) single unit monomer insertion (SUMI) of β-methylstyrene derivatives into diverse RAFT agents presented fast reaction kinetics, but significant degradation of the SUMI products occurred due to a hydrogen abstraction reaction. Fortunately, such degradation can be suppressed through appropriate design of initial RAFT agents attributed to effective chain transfer and selective photoactivation.

How does the single unit monomer insertion technique promote kinetic analysis of activation and initiation in photo-RAFT processes?

The single unit monomer insertion technique provides a simple platform for the kinetic investigation of early stage of photo-RAFT process that comprises photo-activation of initial RAFT agents and addition of RAFT leaving radicals to the monomers.

Sequential and alternating RAFT single unit monomer insertion: model trimers as the guide for discrete oligomer synthesis

A complete set of model trimers and their synthetic kinetics are established to guide the synthesis of diverse sequence-defined polymers.

A 20th anniversary perspective on the life of RAFT (RAFT coming of age)

AbstractRAFT (reversible addition–fragmentation chain transfer) polymerization, making use of thiocarbonylthio transfer agents, was announced to the world just over 21 years ago. RAFT arose out of a desire to achieve perfection in polymers (or at least to define and limit the imperfections) and to invent living radical polymerization. However, living radical polymerization cannot be and never was. This perspective looks at RAFT after 21 years of development. Is RAFT a mature technology? We briefly summarize areas of current interest focusing on what is happening at CSIRO and point to where RAFT is going in areas such as RAFT free from exogenous initiators (photoRAFT, PET‐RAFT, eRAFT), new RAFT agents, RAFT for sequence‐defined polymers and RAFT single unit monomer insertion, RAFT emulsion polymerization and RAFT polymerization‐induced self‐assembly (PISA), RAFT‐crosslinking polymerization and the industrial applications of RAFT. © 2019 Society of Chemical Industry

Self-Assembly of Monolayer Vesicles via Backbone-Shiftable Synthesis of Janus Core–Shell Bottlebrush Polymer

We report the self-assembly of monolayer vesicles from Janus core–shell bottlebrush polymers. A route was developed to synthesize doubly grafted bottlebrush copolymers (DGBCPs) possessing A-b-B and B′-b-C side chains on a single repeating unit. Graft-through ring-opening metathesis polymerization of a norbornene moiety installed by single unit monomer insertion allowed us to place the backbone on any repeating unit of the core (B and B′) block. By decorating each core chain end with different chains via reversible addition–fragmentation chain transfer polymerization, we can obtain nanoobjects with an asymmetric B core and a phase-separated A/C shell. We demonstrate that polystyrene-branch-polystyrene′ and polylactide-b-polystyrene-branch-polystyrene′-b-poly(n-butyl acrylate) macromonomers can be successfully synthesized and polymerized to produce DGBCPs in high yields (81–94% conversion) with an absolute molar mass of 149–395 kg mol–1 and a dispersity of 1.18–1.38. In a solvent slightly more selective to A than C, self-assembly of monolayer vesicles with diameter of <100 nm was observed by transmission electron microscopy. Dissipative particle dynamics simulations suggest that increasing the backbone length and moving the backbone toward the B′/C interface increases the backbone bending energy and favors a lower curvature. The spontaneous curvature appears to prefer a particular layer radius, avoiding bilayer formation.

Selective and Rapid Light-Induced RAFT Single Unit Monomer Insertion in Aqueous Solution.

The photocatalyst Zn(II) meso-tetra(4-sulfonatophenyl)porphyrin (ZnTPPS) is found to substantially accelerate visible-light-initiated (red, yellow, green light) single unit monomer insertion (SUMI) of N,N-dimethylacrylamide into the reversible addition-fragmentation chain transfer (RAFT) agent, 4-((((2-carboxyethyl)thio)carbonothioyl)thio)-4-cyanopentanoic acid (RAFT1 ), in aqueous solution. Thus, under irradiation with red (633 nm) or yellow (593 nm) light with 50 mpm (moles per million mole of monomer) ZnTPPS at 30 °C, the rate enhancement provided by photoinduced energy or electron transfer (PET) is ≈sevenfold over the rate of direct photoRAFT-SUMI (without catalyst), which corresponds to achieving full and selective reaction in hours versus days. Importantly, the selectivity, as judged by the absence of oligomers, is retained. Under green light at similar power, higher rates of SUMI are also observed. However, the degree of enhancement provided by PET-RAFT-SUMI over direct photoRAFT-SUMI as a function of catalyst concentration is less and some oligomers are formed.

Single Unit Monomer Insertion: A Versatile Platform for Molecular Engineering through Radical Addition Reactions and Polymerization

Single unit monomer insertion (SUMI) is an emerging technology for precise polymer synthesis through a radical addition reaction mechanism with monomer additions occurring one at a time. It possess...

Upscaling single unit monomer insertion to synthesize discrete oligomers

ABSTRACTAs one of the emerging techniques for preparing discrete oligomers, the photo‐RAFT single unit monomer insertion (SUMI) process has shown its uniqueness and superiority in the control of both monomer sequence and stereochemistry. However, current precision polymer synthesis techniques are still burdened by the scalability challenges, such as low reaction yields, small product quantities, and long production times. Herein, we successfully established a practical protocol to address scalability problems in the photo‐RAFT SUMI processes. A series of discrete oligomers containing up to five monomer units were synthesized in batch and flow reactors by sequential and alternating SUMI of two monomers into a trithiocarbonate RAFT agent under mild reaction conditions and purified by automated flash chromatography. This protocol offers the process with large quantity (grams scale), excellent isolated yields (82%–95% for each step and 59% for five iterations), and short production time (several days for a pentamer). © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019, 57, 1947–1955

Discrete and Stereospecific Oligomers Prepared by Sequential and Alternating Single Unit Monomer Insertion

Natural biopolymers, such as DNA and proteins, have uniform microstructures with defined molecular weight, precise monomer sequence, and stereoregularity along the polymer main chain that affords them unique biological functions. To reproduce such structurally perfect polymers and understand the mechanism of specific functions through chemical approaches, researchers have proposed using synthetic polymers as an alternative due to their broad chemical diversity and relatively simple manipulation. Herein, we report a new methodology to prepare sequence-controlled and stereospecific oligomers using alternating radical chain growth and sequential photoinduced RAFT single unit monomer insertion (photo-RAFT SUMI). Two families of cyclic monomers, the indenes and the N-substituted maleimides, can be alternatively inserted into RAFT agents, one unit at a time, allowing the monomer sequence to be controlled through sequential and alternating monomer addition. Importantly, the stereochemistry of cyclic monomer insertion into the RAFT agents is found to be trans-selective along the main chains due to steric hindrance from the repeating monomer units. All investigated cyclic monomers provide such trans-selectivity, but analogous acyclic monomers give a mixed cis- and trans-insertion.

Light-Induced RAFT Single Unit Monomer Insertion in Aqueous Solution-Toward Sequence-Controlled Polymers.

First report on the sequential, visible light-initiated, single unit monomer insertion (SUMI) of N,N-dimethylacrylamide (DMAm) into the reversible addition fragmentation chain transfer (RAFT) agent, 4-((((2-carboxyethyl)thio)carbonothioyl)thio)-4-cyanopentanoic acid (CTA1 ), in aqueous solution is provided. The specificity for SUMI over formation of higher oligomers and/or RAFT agent-derived by-products is higher for longer irradiation wavelengths. Red light provides the cleanest product (selective SUMI), showing a linear pseudo-first order kinetic profile to high (>80%) conversion, but also the slowest reaction rate. Blue light provides a relatively rapid reaction, but also gives some by-products (<2%) and the kinetic profile displays a conversion plateau at >65% conversion. Higher specificity with red light is attributed to CTA1 absorbing at longer wavelengths than the SUMI product, which allows selective excitation of CTA1 . The use of a higher reaction temperature (65 °C vs ambient) results in a higher reaction rate and a reduction in oligomer formation.