Mechanoresponsive polymers with intense red emission are highly desirable in view of the strong penetrability and high resolution of red luminescence. Herein we introduce the sensitized luminescence ...of rare-earth Eu(III) complexes into the mechanochemiluminescence from polymeric dioxetane in a covalent way. By controlling the energy-transfer process from mechanically broken dioxetane to the Eu(III) center, bright red emission from transparent poly(methyl acrylate) films was achieved for the first time. Importantly, mechanoluminescence sensitivity is greatly improved, enabling the location and timing of bond scission with high resolution. A sensitive stretchable device with the polymer film as an emissive layer was fabricated by a facile surface-engineering method, which can emit patterned red light upon deformation. This sensitized mechanoluminescence design thus expands the useful space of luminescent stress probes.
Physically associated hydrogels based on strong hydrophobic interactions often have attractive mechanical properties that combine processability with elasticity. However, there is a need to study ...such interactions and understand their relation to the macroscopic hydrogel properties. Therefore, we use the surfactant sodium dodecyl sulfate (SDS) and urea as reagents that disrupt hydrophobic interactions. The model hydrogel is based on a segmented copolymer between poly(ethylene glycol) (PEG) and hydrophobic dimer fatty acid (DFA). We show that both agents influence viscoelastic properties, dynamics, and relaxation processes of the model hydrogel. In particular, the relaxation time is significantly reduced by urea, as compared to SDS, whereas the surfactant causes a decrease of the modulus of the hydrogel more efficiently. The reversibility of the effects of SDS and urea can be exploited, for instance, by using an injectable sol that solidifies when the SDS or urea diffuses out of the sample. Surfactant-induced processability may be advantageous in future applications of hydrophobically assembled physical hydrogels.
Nanocomposite hydrogels based on carbon nanotubes (CNTs) are known to possess remarkable stiffness, electrical, and thermal conductivity. However, they often make use of CNTs as fillers in covalently ...cross‐linked hydrogel networks or involve direct cross‐linking between CNTs and polymer chains, limiting processability properties. Herein, nanocomposite hydrogels are developed, in which CNTs are fillers in a physically cross‐linked hydrogel. Supramolecular nanocomposites are prepared at various CNT concentrations, ranging from 0.5 to 6 wt%. Incorporation of 3 wt% of CNTs leads to an increase of the material's toughness by over 80%, and it enhances electrical conductivity by 358%, compared to CNT‐free hydrogel. Meanwhile, the nanocomposite hydrogels maintain thixotropy and processability, typical of the parent hydrogel. The study also demonstrates that these materials display remarkable cytocompatibility and support cell growth and proliferation, while preserving their functional activities. These supramolecular nanocomposite hydrogels are therefore promising candidates for biomedical applications, in which both toughness and electrical conductivity are important parameters.
Supramolecular nanocomposite hydrogels are fabricated starting from a hydrophobically assembled physical gel and multi‐walled carbon nanotubes. Prepared nanocomposites are characterized by improved tensile toughness and electrical conductivity, due to dispersed nanotubes. Moreover, these supramolecular nanocomposites are fully processable and recoverable. Being also cytocompatible and able to support cell growth and proliferation, these gels are suitable for biomedical applications.
The formation of isocyanurate via cyclotrimerization of isocyanates is widely reported to provide a variety of polyurethane materials with improved chemical and physical properties such as ...weatherability, mechanical properties, thermal stability and flame retardancy. The demand for development of effective and selective catalysts for cyclotrimerization of isocyanates has been increasing. This review comprehensively summarizes catalysts for the cyclotrimerization of isocyanates that have been reported in peer‐reviewed publications and provides a valuable guideline for choosing suitable catalysts to match specific requirements. The catalysts are categorized into two main classes: catalysts operating via a Lewis basic cyclotrimerization mechanism and metal‐containing catalysts. Catalyst structures, reaction conditions, reaction time, catalytic effectivity as well as types of isocyanates whose trimerization is catalyzed are described in detail. In addition, featuring the findings and viewpoints from mechanistic studies, this review aims to stimulate the design and development of new, more efficient catalysts, and to guide further study of the trimerization mechanism with different classes of catalysts.
Catalysts in Industry: This review explores catalysts that are reported in peer‐reviewed literature from 1956 till now. Catalysts for isocyanate cyclotrimerization are categorized into two main classes: catalysts operating via a Lewis basic cyclotrimerization mechanism and metal‐containing catalysts. In addition to catalyst structures and reaction conditions, this review also discusses the detailed catalytic mechanisms of different types of catalysts.
A chemiluminescent mechanophore, bis(adamantyl-1,2-dioxetane), is used to investigate the covalent bond scission resulting from the sorption of chloroform by glassy poly(methyl methacrylate) (PMMA) ...networks. Bis(adamantyl)-1,2-dioxetane units incorporated as cross-linkers underwent mechanoluminescent scission, demonstrating that solvent ingress caused covalent bond scission. At higher cross-linking densities, the light emission took the form of hundreds of discrete bursts, widely varying in intensity, with each burst composed of 107–109 photons. Camera imaging indicated a relatively slow propagation of bursts through the material and permitted analysis of the spatial correlation between the discrete bond-breaking events. The implications of these observations for the mechanism of sorption and fracture are discussed.
Nanostructured polymer films with continuous, membrane-spanning pores from polymerizable hexagonal columnar discotic liquid crystals (LCs) were fabricated. A robust alignment method was developed to ...obtain homeotropic alignment of columns between glass surfaces by adding a small amount of a tri(ethylene glycol) modified analogue of the mesogen as a dopant that preferentially wets glass. The homeotropic LC alignment was fixated via a photoinitiated free radical copolymerization of a high-temperature tolerant trisallyl mesogen with a divinyl ester. Removal of the hydrogen-bonded template from the aligned columns afforded a nanoporous network with pores of nearly 1 nm in diameter perpendicular to the surface, and without noticeable collapse of the nanopores. The effect of pore orientation was demonstrated by an adsorption experiment in which homeotropic film showed a threefold increase in the initial uptake rate of methylene blue compared to planarly aligned films.
Biomimetic, strain‐stiffening materials are reported, made through self‐assembly and covalent fixation of small building blocks to form fibrous hydrogels that are able to stiffen by an order of ...magnitude in response to applied stress. The gels consist of semi‐flexible rodlike micelles of bisurea bolaamphiphiles with oligo(ethylene oxide) (EO) outer blocks and a polydiacetylene (PDA) backbone. The micelles are fibers, composed of 9–10 ribbons. A gelation method based on Cu‐catalyzed azide–alkyne cycloaddition (CuAAC), was developed and shown to lead to strain‐stiffening hydrogels with unusual, yet universal, linear and nonlinear stress–strain response. Upon gelation, the X‐ray scattering profile is unchanged, suggesting that crosslinks are formed at random positions along the fiber contour without fiber bundling. The work expands current knowledge about the design principles and chemistries needed to achieve fully synthetic, biomimetic soft matter with on‐demand, targeted mechanical properties.
Biomimetic, strain‐stiffening materials were made through self‐assembly and covalent fixation of small bisurea bolaamphiphile building blocks to form fibrous hydrogels. These gels are able to stiffen by an order of magnitude in response to applied stress.
A triazine based disc shaped molecule with two hydrolyzable units, imine and ester groups, was polymerized via acyclic diene metathesis in the columnar hexagonal (Colhex) LC phase. Fabrication of a ...cationic nanoporous polymer (pore diameter ∼1.3 nm) lined with ammonium groups at the pore surface was achieved by hydrolysis of the imine linkage. Size selective aldehyde uptake by the cationic porous polymer was demonstrated. The anilinium groups in the pores were converted to azide as well as phenyl groups by further chemical treatment, leading to porous polymers with neutral functional groups in the pores. The pores were enlarged by further hydrolysis of the ester groups to create ∼2.6 nm pores lined with −COONa surface groups. The same pores could be obtained in a single step without first hydrolyzing the imine linkage. XRD studies demonstrated that the Colhex order of the monomer was preserved after polymerization as well as in both the nanoporous polymers. The porous anionic polymer lined with −COOH groups was further converted to the −COOLi, −COONa, −COOK, −COOCs, and −COONH4 salts. The porous polymer lined with −COONa groups selectively adsorbs a cationic dye, methylene blue, over an anionic dye.
Multiple, coexisting hydrophobic compartments have been created in water using molecular self-sorting among mixtures of bolaamphiphiles with differently spaced urea groups in their hydrophobic parts. ...The selective incorporation of bisurea functionalized fluorescent probes showed that different bolaamphiphiles form separate populations of rod-like micelles, which dynamically coexist in solution, each micelle binding to its correspondingly functionalized guests.
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