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An organized combination of stiff and elastic domains within a single material can synergistically tailor bulk mechanical properties. However, synthetic methods to achieve such sophisticated architectures remain elusive. We report a rapid, facile, and environmentally benign method to pattern strong and stiff semicrystalline phases within soft and elastic matrices using stereo-controlled ring-opening metathesis polymerization of an industrial monomer, cis -cyclooctene. Dual polymerization catalysis dictates polyolefin backbone chemistry, which enables patterning of compositionally uniform materials with seamless stiff and elastic interfaces. Visible light–induced activation of a metathesis catalyst results in the formation of semicrystalline trans polyoctenamer rubber, outcompeting the formation of cis polyoctenamer rubber, which occurs at room temperature. This bottom-up approach provides a method for manufacturing polymeric materials with promising applications in soft optoelectronics and robotics.

We summarize the recent approaches to macrocycle-based anion extraction, including those based on calix[4]pyrroles, and so-called “Texas-sized” molecular boxes.

Access to multimaterial polymers with spatially localized properties and robust interfaces is anticipated to enable new capabilities in soft robotics, such as smooth actuation for advanced medical and manufacturing technologies. Here, orthogonal initiation is used to create interpenetrating polymer networks (IPNs) with spatial control over morphology and mechanical properties. Base catalyzes the formation of a stiff and strong polyurethane, while blue LEDs initiate the formation of a soft and elastic polyacrylate. IPN morphology is controlled by when the LED is turned "on", with large phase separation occurring for short time delays (≈1-2 min) and a mixed morphology for longer time delays (5 min), which is supported by dynamic mechanical analysis, small angle X-ray scattering, and atomic force microscopy. Through tailoring morphology, tensile moduli and fracture toughness can be tuned across ≈1-2 orders of magnitude. Moreover, a simple spring model is used to explain the observed mechanical behavior. Photopatterning produces "multimorphic" materials, where morphology is spatially localized with fine precision (100 µm), while maintaining a uniform chemical composition throughout to mitigate interfacial failure. As a final demonstration, the fabrication of hinges represents a possible use case for multimorphic materials in soft robotics.

Summary Light has emerged as a prominent stimulus to both generate and manipulate polymeric materials across multiple length scales. Compared with other external stimuli, light-mediated approaches enable unprecedented control over when and where chemical transformations occur (i.e., spatiotemporal control). To date, the majority of established protocols rely on individual wavelengths of light (∼monochromatic), which does not harness the full potential of light-matter interactions. This review summarizes the nascent progress in utilizing multiple discrete wavelengths of light as a tool to create and alter soft matter. The concepts are structured in an effort to provide a roadmap to foster new directions in light-based polymer materials chemistry. The physical organic nature of wavelength selectivity is first detailed in the introduction to provide key mechanistic insight and lay a foundation for further developments. Next, an overview of chromophores that undergo various light-driven transformations is presented, followed by their utility in polymer platforms for controlled synthesis, property manipulation, and advanced manufacturing. The review concludes with a summary and outlook on the exciting future of wavelength-selective light-matter interactions in polymer science.

Strong and well-engineered interfaces between dissimilar materials are a hallmark of natural systems but have proven difficult to emulate in synthetic materials, where interfaces often act as points of failure. In this work, curing reactions that are triggered by exposure to different wavelengths of visible light are used to produce multimaterial objects with tough, well-defined interfaces between chemically distinct domains. Longer-wavelength (green) light selectively initiates acrylate-based radical polymerization, while shorter-wavelength (blue) light results in the simultaneous formation of epoxy and acrylate networks through orthogonal cationic and radical processes. The improved mechanical strength of these interfaces is hypothesized to arise from a continuous acrylate network that bridges domains. Using printed test structures, interfaces were characterized through spatial resolution of their chemical composition, localized mechanical properties, and bulk fracture strength. This wavelength-selective photocuring of interpenetrating polymer networks is a promising strategy for increasing the mechanical performance of 3D-printed objects and expanding light-based additive manufacturing technologies.

We report a simple procedure for rapid, visible light-mediated, controlled radical polymerization in aqueous solutions. Based on the photoelectron transfer reversible addition–fragmentation chain transfer (PET–RAFT) polymerization, fast chain propagation at room temperature in water was achieved in the presence of reductant and without prior deoxygenation. A systematic study correlating irradiation intensity and polymerization kinetics, enabled by in situ nuclear magnetic resonance spectroscopy, provided optimized reaction conditions. The versatility of this procedure was demonstrated through a rapid triblock copolymer synthesis, and incorporation of water-labile activated esters for direct conjugation of hydrophilic small molecules and proteins. In addition, this technique boasts excellent temporal control and provides a wide range of macromolecular materials with controlled molecular weights and narrow molecular weight distributions.

Boron dipyrromethenes (BODIPYs) are versatile dyes with diverse structures and associated optoelectronic properties. Their integration into soft materials (polymers) has enabled a myriad of applications from biological/environmental (e.g., imaging, sensing, and therapy) to organic electronic devices and synthesis/degradation. The story herein is meant to guide the reader from the bottom-up, starting with general syntheses of BODIPYs, followed by a discussion of photophysical and electrochemical properties as they relate to structure. These structure–property relationships are then connected to three light driven transformations that are central to the utility of BODIPYs in materials science: (1) electron/energy transfer; (2) triplet formation, and (3) photolysis. Next, the synthetic integration of BODIPYs as structural motifs in both π-conjugated and non-π-conjugated polymers is described, along with prescribed methods to tailor their optoelectronic properties. These properties are then correlated to recent utility of BODIPYs within polymer science, both fundamental – examination of polymer dynamics and self-assembly – and applied – biomedicine, optoelectronics, chemosensors, small molecule photoredox catalysis, and photo-polymerization and -degradation. The end of this review provides a summary of the rich history and outlook on the exciting future opportunities for this burgeoning field of BODIPYs in polymer chemistry.

This paper describes a correlation between charge extraction and energy-level alignment at the interface of polymeric hole transport layers and perovskite active layers. By tailoring the composition of the conjugated backbone of the hole transport material, energy levels between perovskites and hole transport layers are varied. Matching the band alignment at perovskite/hole transport interfaces dramatically improved charge extraction and thus device performance. Time-resolved microwave conductivity measurements, performed to elucidate hole transfer kinetics, suggest that hole transport layer energy levels greatly influence hole extraction efficiency at this interface, a finding that agrees well with device performance metrics. Furthermore, photoluminescence, Mott-Schottky, and space charge limited current measurements support that energy-level alignment between the hole transport layer and perovskite active layer enables more efficient hole extraction and transport at the device interface. The insight surrounding hole extraction in inverted perovskite devices will help design effective hole transport materials, which, in turn, facilitates the production of more efficient solar cells.

Access to clean drinking water is a recognized societal need that touches on the health and livelihood of millions of people worldwide. This is providing an incentive to develop new water-treatment technologies. Traditional technologies, while widespread, are usually inefficient at removing organic pollutants from sewage or so-called grey water. Macrocycle-containing covalent polymer networks have begun to attract attention in the context of water treatment owing to the inherent stability provided by the polymer backbones and their ability to capture micropollutant guests as the result of tunable macrocycle-based host-guest interactions. In this Minireview, we summarize recent advances (from 2016 to mid-2020) involving the removal of organic micropollutants from water using macrocycle-containing covalent polymer networks. An overview of future challenges within this subfield is also provided.

The driving of rapid polymerizations with visible to near-infrared light will enable nascent technologies in the emerging fields of bio- and composite-printing. However, current photopolymerization strategies are limited by long reaction times, high light intensities, and/or large catalyst loadings. The improvement of efficiency remains elusive without a comprehensive, mechanistic evaluation of photocatalysis to better understand how composition relates to polymerization metrics. With this objective in mind, a series of methine- and aza-bridged boron dipyrromethene (BODIPY) derivatives were synthesized and systematically characterized to elucidate key structure-property relationships that facilitate efficient photopolymerization driven by visible to far-red light. For both BODIPY scaffolds, halogenation was shown as a general method to increase polymerization rate, quantitatively characterized using a custom real-time infrared spectroscopy setup. Furthermore, a combination of steady-state emission quenching experiments, electronic structure calculations, and ultrafast transient absorption revealed that efficient intersystem crossing to the lowest excited triplet state upon halogenation was a key mechanistic step to achieving rapid photopolymerization reactions. Unprecedented polymerization rates were achieved with extremely low light intensities (

Light-driven 3D printing to convert liquid resins into solid objects (i.e., photocuring) has traditionally been dominated by engineering disciplines, yielding the fastest build speeds and highest resolution of any additive manufacturing process. However, the reliance on high-energy UV/violet light limits the materials scope due to degradation and attenuation (e.g., absorption and/or scattering). Chemical innovation to shift the spectrum into more mild and tunable visible wavelengths promises to improve compatibility and expand the repertoire of accessible objects, including those containing biological compounds, nanocomposites, and multimaterial structures. Photochemistry at these longer wavelengths currently suffers from slow reaction times precluding its utility. Herein, novel panchromatic photopolymer resins were developed and applied for the first time to realize rapid high-resolution visible light 3D printing. The combination of electron-deficient and electron-rich coinitiators was critical to overcoming the speed-limited photocuring with visible light. Furthermore, azo-dyes were identified as vital resin components to confine curing to irradiation zones, improving spatial resolution. A unique screening method was used to streamline optimization (e.g., exposure time and azo-dye loading) and correlate resin composition to resolution, cure rate, and mechanical performance. Ultimately, a versatile and general visible-light-based printing method was shown to afford (1) stiff and soft objects with feature sizes, Liquid resins that rapidly harden upon exposure to low-energy visible light are developed and applied to high-resolution projection-based 3D printing across the color spectrum.

Calix[4]pyrrole (C4P)-based systems have been extensively explored as binding agents for anions and ion pairs. However, their capacity to act as molecular containers for neutral species remains underexplored. We report here the molecular recognition of pyrazine N,N′-dioxide (PZDO) using a series of aryl extended C4Ps including three α,α-diaryl substituted C4Ps (receptors 1–3), an α,β-diaryl substituted C4P (receptor 4) and an α,α,α,α-tetraaryl substituted C4P (receptor 5). Single crystal structural analyses of the 2 : 1 host–guest complexes between receptors 1–3 and PZDO revealed that the C4P subunits exist in an unusual partial cone conformation and that the PZDO guest is held within electron-rich cavities formed by the lower rims of the individual C4P macrocycle. In contrast, receptor 5 was seen to adopt the cone conformation in the solid state, allowing one PZDO molecule to be accommodated inside the upper-rim cavity. Evidence for guest-directed self-assembly is also seen in the solid state. Evidence for C4P–PZDO interactions in CD3CN/CD3OD solution came from 1H NMR spectroscopic titrations. Electrostatic potential maps created by means of density functional theory calculations were constructed. Density functional theory calculations were also performed to analyse the energetics of various limiting binding modes. On the basis of these studies, it is inferred that interactions between the ‘two-wall’ C4P derivatives (i.e. receptors 1–4) and PZDO involve a complex binding mode that differs from what has been seen in previous host–guest complexes formed between C4Ps and N-oxides. The present study thus paves the way for the further design of C4P-based receptors with novel recognition features., The molecular recognition of pyrazine N,N′-dioxide by aryl extended 'two-walled' calix[4]pyrrole-based receptors is seen to stabilise two different binding modes in the solid state.

This work introduces an integrated photonic system that enables curing of a visible-light-curable resin for chip-based 3D printing. Curing of multiple mm-scale regions is achieved via an integrated optical phased array operating at 632.8 nm.

The third industrial revolution has brought mankind into the information age. The development of information storage materials has played a key role in this transformation. Such materials have seen use in many application areas, including computing, logistics, and medicine. Information storage materials run the gamut from magnetic information storage media to molecular-based information storage materials. Among these, fluorescent-based information storage materials are of particular interest due to their unique properties, including an ability to store information with high levels of security, maintain mechanical stability, and respond to appropriately chosen external stimuli. In this review, we focus on recent advances involving the preparation and study of fluorescent materials-based information storage codes. For organisational purposes, these codes are treated according to the dimensionality of the code system in question, namely 1D-, 2D-, and 3D-type codes. The present review is designed to provide a succinct summary of what has been accomplished in the area, while outlining existing challenges and noting directions for future development.

The development and application of novel activated furan copolymers is reported. The platform provides a colorimetric method for sensing amines in aqueous media through the generation of a highly colored donor acceptor Stenhouse adduct (DASA). Furthermore, the resulting DASA polymer conjugates, which are obtained after amine sensing, are characterized to determine fundamental structure property relationships for this emerging class of negative photochromic species.

With 3D printing, the desire is to be "limited only by imagination," and although remarkable advancements have been made in recent years, the scope of printable materials remains narrow compared to other forms of manufacturing. Light-driven polymerization methods for 3D printing are particularly attractive due to unparalleled speed and resolution, yet the reliance on high-energy UV/violet light in contemporary processes limits the number of compatible materials due to pervasive absorption, scattering, and degradation at these short wavelengths. Such issues can be addressed with visible-light photopolymerizations. However, these lower-energy methods often suffer from slow reaction times and sensitivity to oxygen, precluding their utility in 3D printing processes that require rapid hardening (curing) to maximize build speed and resolution. Herein, multifunctional thiols are identified as simple additives to enable rapid high-resolution visible-light 3D printing under ambient (atmospheric O2 ) conditions that rival modern UV/violet-based technology. The present process is universal, providing access to commercially relevant acrylic resins with a range of disparate mechanical responses from strong and stiff to soft and extensible. Pushing forward, the insight presented within this study will inform the development of next-generation 3D-printing materials, such as multicomponent hydrogels and composites.

Water swollen polymer networks are attractive for applications ranging from tissue regeneration to water purification. For water purification, charged polymers provide excellent ion separation properties. However, many ion exchange membranes (IEMs) are brittle, necessitating the use of thick support materials that ultimately decrease throughput. To this end, a series of double network hydrogels (DNHs), synthesized with varied composition to decrease water content, are examined as robust membrane materials for water purification. One network contains fixed anionic charges, while the other comprises a copolymer with different ratios of hydrophobic ethyl acrylate (EA) and hydrophilic dimethyl acrylamide (DMA) repeat units. Characterizing water content and mechanical performance in free standing DNH films reveals a ~5× decrease in water content, while increasing ultimate stress and strain by ~3.5× and ~4.5× for 90:5 EA:DMA relative to pure DMA. Salt transport properties relevant to water purification, including permeability, solubility, and diffusivity, are measured and show improved performance upon reducing water content. Overall, the ability to simultaneously reduce water content, increase mechanical integrity, and decrease salt transport rates highlights the potential of DNHs for membrane applications.

Driving rapid polymerizations with visible to near-infrared (NIR) light will enable nascent technologies in the emerging fields of bio- and composite-printing. However, current photopolymerization strategies are limited by long reaction times, high light intensities, and/or large catalyst loadings. Improving efficiency remains elusive without a comprehensive, mechanistic evaluation of photocatalysis to better understand how composition relates to polymerization metrics. With this objective in mind, a series of methine- and aza-bridged boron dipyrromethene (BODIPY) derivatives were synthesized and systematically characterized to elucidate key structure-property relationships that facilitate efficient photopolymerization driven by visible to NIR light. For both BODIPY scaffolds, halogenation was shown as a general method to increase polymerization rate, quantitatively characterized using a custom real-time infrared spectroscopy setup. Furthermore, a combination of steady-state emission quenching experiments, electronic structure calculations, and ultrafast transient absorption revealed that efficient intersystem crossing to the lowest excited triplet state upon halogenation was a key mechanistic step to achieving rapid photopolymerization reactions. Unprecedented polymerization rates were achieved with extremely low light intensities (< 1 mW/cm2) and catalyst loadings (< 50 μM), exemplified by reaction completion within 60 seconds of irradiation using green, red, and NIR light-emitting diodes.

The fabrication of well-defined, multifunctional polymer brushes under ambient conditions is described. This facile method uses light-mediated, metal-free atom-transfer radical polymerization (ATRP) to grow polymer brushes with only microliter volumes required. Key to the success of this strategy is the dual action of N-phenylphenothiazine (PTH) as both an oxygen scavenger and polymerization catalyst. Use of simple glass cover slips results in a high degree of spatial and temporal control and allows for multiple polymer brushes to be grown simultaneously. The preparation of arbitrary 3D patterns and functional/emissive polymer brushes demonstrates the practicality and versatility of this novel strategy.

A stimuli-responsive invisible ink for time-dependent encryption of information is reported. Consisting of a pillar[5]arene-based supramolecular network grafted with spiropyran moieties, these materials display time-dependent photochromic behavior with tailorable fading rates. Ultraviolet (UV) light results in isomerization of the colorless spiropyran to the corresponding colored merocyanine, while visible light or heat causes the reverse isomerization with a rate that is dependent on the density of host-guest crosslinks. The kinetics of discoloration are a function of merocyanine aggregation, which becomes more pronounced as the host-guest crosslink density is increased, leading to a reduced conversion rate and slower time-dependent fading. The degree of crosslinking, and hence the fading rate, may be modulated via the addition of unbound pillar[5]arene host or nitrile guest as competitors. Time-dependent information encryption is enabled by combining selective placement of host and guest competitors and UV patterning. UV patterning provides an initially "false" image that does not reveal the desired information, and it is only after a given time that the encrypted data appears. This work provides a unique approach to enhance the security of information storage associated with offline portable data encryption.

The synthesis, device fabrication, and electric poling of novel amino-functionalized fulleropyrrolidines in polymer solar cells is reported. Systematically varying the tether lengths between the fullerene cage and tertiary amines provides insight into enhanced device efficiency and stability after poling. DFT calculations in an external electric field result in alignment of molecular dipole moments, which corroborates our hypothesis that electrotropic polarization causes an increased built-in electrostatic potential difference across the device, and results in enhance performance.

Fundamental to the field of organic electronics is the understanding that structure begets function. For conjugated polymers, monomer structure determines overall energy levels while also influencing interchain interactions. These interchain interactions induce aggregation and creates higher order morphology, greatly influencing the ultimate performance of electronic devices. Understanding the interplay of morphological changes with device efficiency is imperative to improving the performance of organic electronics with minor differences in molecular structure, linear versus branched side-chains, carbon versus silicon bridgehead atoms or hydrogen versus fluorine substitution, having dramatic effects on the energetics, aggregation, morphology, and, ultimately, performance of these materials. This report highlights the power of minor structural changes in conjugated polymers and the associated design rules for the preparation of next generation electronic materials.

While perovskite solar cells have invigorated the photovoltaic research community due to their excellent power conversion efficiencies (PCEs), these devices notably suffer from poor stability. To address this crucial issue, a solution-processable organic chemical inhibition layer (OCIL) was integrated into perovskite solar cells, resulting in improved device stability and a maximum PCE of 16.3%. Photoenhanced self-doping of the fulleropyrrolidine mixture in the interlayers afforded devices that were advantageously insensitive to OCIL thickness, ranging from 4 to 190 nm. X-ray photoelectron spectroscopy (XPS) indicated that the fulleropyrrolidine mixture improved device stability by stabilizing the metal electrode and trapping ionic defects (i.e., I–) that originate from the perovskite active layer. Moreover, degraded devices were rejuvenated by repeatedly peeling away and replacing the OCIL/Ag electrode, and this repeel and replace process resulted in further improvement to device stability with minimal variation of device efficiency., Fulleropyrrolidines trap inherent ion contamination, passivate electrodes, enable “repeel and replace” to refresh device interface, and overcome the intrinsic instability of perovskite devices.

Organic bulk heterojunction (BHJ) solar cells require broad absorption of the incident solar spectrum by the donor and acceptor in the blend. Fullerene derivatives with covalently linked dyes, referred to as dyads, were designed to have strong optical absorption and appropriate electronic levels for electron transfer with common donor polymers in BHJs. Dyads with dyes based on diketopyrrolopyrrole and benzothiadiazole were synthesized using either a methanofullerene or a fulleropyrrolidine linkage. The performance of these dyad acceptors in BHJ solar cells with poly(3-hexylthiophene) (P3HT) and a low optical gap co-polymer of thiophene and diketopyrrolopyrrole (PDPP2FT) were examined. Although the solar power conversion efficiencies were low, charge generation from the molecular dye in the dyad could be observed in BHJs with PDPP2FT. The low power conversion efficiency was attributed to the morphology of the BHJs based on grazing incidence wide angle X-ray scattering patterns. Density functional theory was used to examine the charge transfer states between the donor and the dyad. The lowest energy charge-transfer state was found to be a transition from the donor polymer to the fullerene portion of the dyad.

The efficient operation of polymer- and perovskite-based photovoltaic devices depends on selective charge extraction layers that are placed between the active layer and electrodes. Herein, we demonstrate that integration of a tetra-n-butyl ammonium iodide-doped zwitterionic fulleropyrrolidine derivative, C60-SB, as a cathode modification interlayer significantly improves the photovoltaic device performance. Compared to the intrinsic (undoped) zwitterionic material, which is an efficient interlayer itself, the doped interlayers further improve average power conversion efficiencies from 8.37% to 9.68% in polymer-based devices and from 12.53% to 15.31% in perovskite-based devices. Ultraviolet photoelectron spectroscopy revealed that doping increases the interfacial dipole at the C60-SB/Ag interface, i.e., reduces the effective work function of the resultant composite cathode. This effect originates from the population of negative polaron states in C60-SB by extrinsic charges that prevent directional charge t...

A simple, inexpensive, and modular method to directly illuminate NMR samples for in situ analysis of photochemical transformations is reported. The versatility of this technique is demonstrated by analyzing the light-induced propagating front for small-molecule photoswitches and the kinetics of photocontrolled living radical polymerizations. In situ measurements allow oxygen-sensitive and rapid photoevents to be studied in detail, leading to reliable determination of photoswitching quantum yields and polymerization rates. By systematically tuning light intensity, a direct relationship between propagation rate and intensity is revealed. Of particular note is the facile translation of the conditions identified through this NMR analysis to analogous benchtop experiments with insight into the nature of the photoreactive species.

A signature of photo‐mediated controlled polymerizations is the ability to modulate the rate of polymerization by turning the light source ‘on’ and ‘off.’ However, in many reported systems, growth can be reproducibly observed during dark periods. In this study, emerging photo‐mediated controlled radical polymerizations are evaluated with in situ 1H NMR monitoring to assess their behavior in the dark. Interestingly, it is observed that Cu‐mediated systems undergo long‐lived, linear growth during dark periods in organic media.\ud \ud

The design, synthesis, and characterization of solution-processable polymers for organic light emitting diode (OLED) applications are presented. Theoretical calculations were employed to identify a carbazole-pyrimidine based building block as an optimized host material for the emissive layer of an idealized OLED stack. Efficient, free radical homopolymerization and copolymerization with a novel methacrylate-based heteroleptic iridium(III) complex leads to a library of nonconjugated polymers with pendant semiconductors. Optoelectronic characterization reveals impressive photoluminescence quantum yield (PLQY) values exceeding 80% and single-layer OLEDs show optimal performance for copolymers containing 6 mol % of iridium comonomer dopant.

The utility of Meldrum's activated furan (MAF) for the colorimetric detection of sub ppm levels of amines in solution, on solid supports, and as vapors is reported. MAF is synthesized in one step from inexpensive and commercially available starting materials and exhibits high selectivity for primary and secondary amines in the presence of competing nucleophiles. The reaction between activated furans and amines results in a distinct color change, discernable by the naked eye. UV/Vis absorption spectroscopy was utilized to monitor reactions in solution and determine detection limits. Additionally, solutions of MAF were useful as stains for thin layer chromatography and for monitoring solid-phase synthesis of peptides and peptidomimetics. Finally, MAF was used to detect volatile amines released from fish samples, demonstrating potential for food spoilage applications.

The modular synthesis of asymmetric rylenes from naphthalic anhydride derivatives is presented. Imidization, Suzuki–Miyaura coupling and cyclodehydrogenation reactions are utilized for the generation of novel functional rylenes with these three core transformations providing significant flexibility over the final structure. The combination of simple purification and high yields enables access to asymmetric rylenes with functional handles at the imide-position and site-specific incorporation of bay position substituents. The resulting library of perylenes and bisnapthalimide-anthracene derivatives showcase the presented methodology and the ability to tune optoelectronic and electrochemical properties.

A new di-tert-butyl acrylate (diTBA) monomer for controlled radical polymerization is reported. This monomer complements the classical use of tert-butyl acrylate (TBA) for synthesis of poly(acrylic acid) by increasing the density of carboxylic acids per repeat unit, while also increasing the flexibility of the carboxylic acid side-chains. The monomer is well behaved under Cu(II)-mediated photoinduced controlled radical polymerization and delivers polymers with excellent chain-end fidelity at high monomer conversions. Importantly, this new diTBA monomer readily copolymerizes with TBA to further the potential for applications in areas such as dispersing agents and adsorbents. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017, 55, 801–807

ConspectusConjugated polymer zwitterions (CPZs) are neutral, hydrophilic, polymer semiconductors. The pendent zwitterions, viewed as side chain dipoles, impart solubility in polar solvents for solution processing, and open opportunities as interfacial components of optoelectronic devices, for example, between metal electrodes and organic semiconductor active layers. Such interlayers are crucial for defining the performance of organic electronic devices, e.g., field-effect transistors (OFETs), light-emitting diodes (OLEDs), and photovoltaics (OPVs), all of which consist of multilayer structures. The interlayers reduce the Schottky barrier height and thus improve charge injection in OFETs and OLEDs. In OPVs, the interlayers serve to increase the built-in electric potential difference (Vbi) across the active layer, ensuring efficient extraction of photogenerated charge carriers.In general, polar and even charged electronically active polymers have gained recognition for their ability to modify metal/semicond...

The synthesis of hydrophilic conjugated polymers typically relies on organometallic coupling methodologies. Here we present an approach to prepare polar poly(arylene–vinylene)s (PAVs) in water using the Horner–Wadsworth–Emmons (HWE) reaction. The additional preparation of discrete arylene vinylene (AVs) afforded insight into HWE kinetics and regioselectivity. Nine novel PAVs and AVs were synthesized, characterized by UV–vis absorption and ultraviolet photoelectron spectroscopy, and studied for their utility in sensing and photovoltaic applications.

A novel library of tunable negative photochromic compounds, donor-acceptor Stenhouse adducts (DASAs), is reported. Tailoring the electron deficient "acceptor" moiety yielded DASAs that can be activated with mild visible and far red light. The effect of acceptor composition on reactivity, absorption, equilibrium, and cyclability is exploited for the design of high performance photoswitches. The structural changes to the carbon acid acceptor also provide access to new, more structurally diverse DASA derivatives by facilitating the ring-opening reaction with electron deficient amine donors.

A modular synthesis of Donor-Acceptor Stenhouse Adduct (DASA) polymer conjugates is described. Pentafluorophenyl-ester chemistry is employed to incorporate aromatic amines into acrylate and methacrylate copolymers, which are subsequently coupled with activated furans to generate polymers bearing a range of DASA units in a modular manner. The effect of polymer glass transition temperature on switching kinetics is studied, showing dramatic rate enhancements in going from a glassy to a rubbery matrix. Moreover, tuning the DASA absorption profile allows for selective switching, as demonstrated by ternary photopatterning, with potential applications in rewriteable data storage.

A light-mediated methodology to grow patterned, emissive polymer brushes with micron feature resolution is reported and applied to organic light emitting diode (OLED) displays. Light is used for both initiator functionalization of indium tin oxide and subsequent atom transfer radical polymerization of methacrylate-based fluorescent and phosphorescent iridium monomers. The iridium centers play key roles in photocatalyzing and mediating polymer growth while also emitting light in the final OLED structure. The scope of the presented procedure enables the synthesis of a library of polymers with emissive colors spanning the visible spectrum where the dopant incorporation, position of brush growth, and brush thickness are readily controlled. The chain-ends of the polymer brushes remain intact, affording subsequent chain extension and formation of well-defined diblock architectures. This high level of structure and function control allows for the facile preparation of random ternary copolymers and red–green–blue arrays to yield white emission., Emissive polymer brushes are grafted from conductive substrates via photocatalysis for organic light emitting diode displays. Color tunability, micron pixel features, thickness control, and diblocks are demonstrated.

Narrow band gap conjugated polymer zwitterions (CPZs) were synthesized by Suzuki polymerization and characterized to understand their electronic properties and utility as cathode modification layers in solar cells. The polymers were prepared from diketopyrrolopyrrole (DPP) and iso-indigo monomers containing sulfobetaine (SB) pendant groups, benefiting from an ion-rich aqueous phase in the polymerizations. UV–vis absorption spectroscopy revealed the optical energy gap value for the CPZs, ranging from 1.7 to 1.2 eV. Ultraviolet photoelectron spectroscopy of the CPZs as thin layers on Ag metal showed that the pendent zwitterions impart an interfacial dipole (Δ) to the metal and a work function reduction of ∼0.9 eV. OPVs fabricated using a conventional bulk heterojunction (BHJ) device architecture of ITO/PEDOT:PSS/(PTB7:PC71BM)/CPZ/Ag led to dramatic improvements in power conversion efficiency (PCE) values relative to devices having bare Ag cathodes (PCE

Ionic liquids (ILs) were utilized for the rapid air-stable Suzuki polymerization of polar zwitterionic thiophene monomers, precluding the need for volatile organic solvents, phosphine ligands and phase transfer catalysts typically used in conjugated polymer synthesis. Ten different ILs were examined, demonstrating the scope and limitations of their utility as solvents in this Suzuki polymerization. Imidazolium, pyridinium and pyrrolidinium ILs proved effective for these polymerizations, with top performance achieved using pyrrolidinium triflate, affording polymers with molecular weight values >30 kDa. The enhanced solubility of these conjugated polymer zwitterions (CPZs) in ILs, relative to organic solvents, led to higher molecular weight polymers than obtained using previously reported methods. CPZs synthesized in ILs proved effective as cathode modification layers in solar cells, giving rise to a power conversion efficiency (PCE) of 7.57% in bulk heterojunction devices.

We report a direct and facile synthesis of novel conjugated polymeric zwitterions (CPZs) as a simple route to electronically active homopolymers and copolymers containing dipole-inducing pendent zwitterions. Sulfobetaine-containing polythiophenes (PTSB-1 and PTSB-2) and alternating thiophene–benzothiadiazoles (PTBTSB-1 and PTBTSB-2) were prepared and characterized relative to alkylated polymer analogues (POT-a-T and POT-a-BT). The polar zwitterionic side chains make these polymers hydrophilic and salt-responsive, with interesting electronic properties that depend on zwitterion distance from the conjugated polymer backbone (tether length), as characterized by UV–vis absorption and ultraviolet photoelectron spectroscopy (UPS). Close proximity (CH2 spacer) of the sulfobetaine groups to the polymer backbone results in increased ionization potential and enlarged band gaps of 2.19 and 2.04 eV for PTSB-1 and PTBTSB-1, respectively. On Au and Ag surfaces, the zwitterionic pendent groups significantly alter the wo...