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Polymerization‐induced self‐assembly (PISA) has emerged as a scalable one‐pot technique to prepare block copolymer (BCP) nanoparticles. Recently, a PISA process, that results in poly(l‐lactide)‐b‐poly(ethylene glycol) BCP nanoparticles coined ring‐opening polymerization (ROP)‐induced crystallization‐driven self‐assembly (ROPI‐CDSA), was developed. The resulting nanorods demonstrate a strong propensity for aggregation, resulting in the formation of 2D sheets and 3D networks. This article reports the synthesis of poly(N,N‐dimethyl acrylamide)‐b‐poly(l)‐lactide BCP nanoparticles by ROPI‐CDSA, utilizing a two‐step, one‐pot approach. A dual‐functionalized photoiniferter is first used for controlled radical polymerization of the acrylamido‐based monomer, and the resulting polymer serves as a macroinitiator for organocatalyzed ROP to form the solvophobic polyester block. The resulting nanorods are highly stable and display anisotropy at higher molecular weights (>12k Da) and concentrations (>20% solids) than the previous report. This development expands the chemical scope of ROPI‐CDSA BCPs and provides readily accessible nanorods made with biocompatible materials. [ABSTRACT FROM AUTHOR]

Electron tomography holds great promise as a tool for investigating the 3D morphologies and internal structures of metal‐organic framework‐based protein biocomposites (protein@MOFs). Understanding the 3D spatial arrangement of proteins within protein@MOFs is paramount for developing synthetic methods to control their spatial localization and distribution patterns within the biocomposite crystals. In this study, the naturally occurring iron oxide mineral core of the protein horse spleen ferritin (Fn) is leveraged as a contrast agent to directly observe individual proteins once encapsulated into MOFs by electron microscopy techniques. This methodology couples scanning electron microscopy, transmission electron microscopy, and electron tomography to garner detailed 2D and 3D structural interpretations of where proteins spatially lie in Fn@MOF crystals, addressing the significant gaps in understanding how synthetic conditions relate to overall protein spatial localization and aggregation. These findings collectively reveal that adjusting the ligand‐to‐metal ratios, protein concentration, and the use of denaturing agents alters how proteins are arranged, localized, and aggregated within MOF crystals. [ABSTRACT FROM AUTHOR]

Enzymes present a promising green chemistry alternative for accelerating chemical reactions in industry. However, many industrial applications require harsh synthetic conditions (i.e. high temperature and/or organic solvents), causing enzymes to denature. Metal–organic frameworks (MOFs) offer a promising method to overcome the structural limitations of potentially revolutionary enzymes through enzymatic immobilization. However, for high activity of immobilized enzymes to be achieved, a comprehensive understanding of the factors influencing enzyme performance is critical. While extensive efforts have demonstrated that final MOF properties such as crystallinity, porosity, and network defects significantly influence enzyme activity, here we propose a separate, but equally impactful, factor in determining enzyme@MOF activity: enzyme folding in prenucleation clusters. To investigate both MOF structural property and enzyme folding factors, two model enzymes, glucose oxidase and catalase, were encapsulated into ZIF-8. The biocomposite formation and prenucleation clusters were examined through electron microscopy, advanced spectroscopy, and scattering techniques, respectively. Results from these studies indicate enzyme folding with MOF precursors is a crucial aspect to consider when pairing enzymes with selected MOF precursors. To assist in this consideration, we provide alternative strategies for retaining enzyme activity in denaturing conditions. Finally, a roadmap is provided for tuning activity of immobilized enzymes, paving the way for industrial-scale production of enzyme@MOFs. [ABSTRACT FROM AUTHOR]

Metal–organic frameworks offer a diverse landscape of building blocks to design high performance materials for implications in almost every major industry. With this diversity stems complex crystallization mechanisms with various pathways and intermediates. Crystallization studies have been key to the advancement of countless biological and synthetic systems, with MOFs being no exception. This review provides an overview of the current theories and fundamental chemistry used to decipher MOF crystallization. We then discuss how intrinsic and extrinsic synthetic parameters can be used as tools to modulate the crystallization pathway to produce MOF crystals with finely tuned physical and chemical properties. Experimental and computational methods are provided to guide the probing of MOF crystal formation on the molecular and bulk scale. Lastly, we summarize the recent major advances in the field and our outlook on the exciting future of MOF crystallization. [ABSTRACT FROM AUTHOR]

Bioreducible polymeric mRNA carriers are an emerging family of vectors for gene delivery and vaccine development. A few bioreducible systems have been generated through aqueous‐phase ring‐opening polymerization of lipoic acid derivatives, however this methodology limits hydrophobic group incorporation and functionality into resulting polymers. Herein, a poly(active ester)disulfide polymer is synthesized that can undergo facile aminolysis with amine‐containing substrates under stoichiometric control and mild reaction conditions to yield a library of multifunctional polydisulfide polymers. Functionalized polydisulfide polymer species form stable mRNA‐polymer nanoparticles for intracellular delivery of mRNAs in vitro. Alkyl‐functionalized polydisulfide‐RNA nanoparticles demonstrate rapid cellular uptake and excellent biodegradability when delivering EGFP and OVA mRNAs to cells in vitro. This streamlined polydisulfide synthesis provides a new facile methodology for accessing multifunctional bioreducible polymers as biomaterials for RNA delivery and other applications. [ABSTRACT FROM AUTHOR]

Liquid‐Phase (Scanning) Transmission Electron Microscopy (LP‐(S)TEM) has become an essential technique to monitor nanoscale materials processes in liquids in real‐time. Due to the pressure difference between the liquid and the microscope vacuum, bending of the silicon nitride (SiNx) membrane windows generally occurs. This causes a spatially varying liquid layer thickness that makes interpretation of LP‐(S)TEM results difficult due to a locally varying achievable resolution and diffusion limitations. To mediate these difficulties, it is shown: 1) how to quantitatively map liquid layer thickness for any liquid at less than 0.01 e− Å−2 total dose; 2) how to dynamically modulate the liquid thickness by tuning the internal pressure in the liquid cell, co‐determined by the Laplace pressure and the external pressure. It is demonstrated that reproducible inward bulging of the window membranes can be realized, leading to an ultra‐thin liquid layer in the central window area for high‐resolution imaging. Furthermore, it is shown that the liquid thickness can be dynamically altered in a programmed way, thereby potentially overcoming the diffusion limitations towards achieving bulk solution conditions. The presented approaches provide essential ways to measure and dynamically adjust liquid thickness in LP‐(S)TEM experiments, enabling new experiment designs and better control of solution chemistry. [ABSTRACT FROM AUTHOR]

Liquid phase transmission electron microscopy has become a powerful tool for imaging the structure and dynamics of materials in solution. Direct observation of material formation, modification and operation has provided unique insights into the chemistry that governs the structure–property relationships of materials with myriad applications including optical, magnetic and electronic materials. However, full control over the reaction environment inside the microscope, especially the solution temperature and concentration of reactants, remains challenging and has limited the application of this high-resolution methodology. Here we present the 'Stream Liquid Heating Holder', a complete system for liquid phase experiments at elevated temperature inside the transmission electron microscope. This system features a unique on-chip flow channel combined with a microheater. The channel enables direct flow over the imaging area and rapid replenishment of the solution inside the Nano-cell with simultaneous heating to more than 100 °C. The capabilities of the system are demonstrated by studying the liquid flow dynamics and comparing the temperature dependent etching kinetics of silica nanoparticles by in situ liquid phase electron microscopy to in-flask experiments. [ABSTRACT FROM AUTHOR]

Graphene liquid cells (GLCs) for transmission electron microscopy (TEM) enable high‐resolution, real‐time imaging of dynamic processes in water. Large‐scale implementation, however, is prevented by major difficulties in reproducing GLC fabrication. Here, a high‐yield method is presented to fabricate GLCs under millimeter areas of continuous graphene, facilitating efficient GLC formation on a TEM grid. Additionally, GLCs are located on the grid using correlated light‐electron microscopy (CLEM), which reduces beam damage by limiting electron exposure time. CLEM allows the acquisition of reliable statistics and the investigation of the most common shapes of GLCs. In particular, a novel type of liquid cell is found, formed from only a single graphene sheet, greatly simplifying the fabrication process. The methods presented in this work—particularly the reproducibility and simplicity of fabrication—will enable future application of GLCs for high‐resolution dynamic imaging of biomolecular systems. [ABSTRACT FROM AUTHOR]

Zeolites are the catalytic workhorses of the refinery and chemicals production industry. Their inherent micropores lead to remarkable shape-selectivity, but also present diffusion limitations on reactions. One scalable approach to further their functionality is to introduce mesopores into the individual zeolite crystal by base leaching. Using cryogenic transmission electron microscopy (cryo-TEM), we are able to capture the pore formation process in ZSM-5 zeolites in the solution state, first forming mesopores, to eventually yielding hollow crystals. Electron tomography indicates that the larger pores in the initial leaching stages tend to exist at the boundary between the aluminum-rich shell and the aluminum-poor core, while multiple small pores are also present within the aluminum-poor core. This indicates that pore formation is based on crystalline and chemical inhomogeneities at the single crystal level. [ABSTRACT FROM AUTHOR]

There has been much interest in the construction of soft nanomaterials in solution due to a desire to emulate the exquisite structure and function of Nature's equivalents (e.g. enzymes, viruses, proteins and DNA). Nature's soft nanomaterials are capable of selectivity, precision and efficiency in areas such as information storage and replication, transportation and delivery, and synthesis and catalysis. To this end, the use of small molecules, amphiphiles, colloids, and polymers have been investigated for the development of advanced materials in myriad fields of biomedicine and synthetic chemistry. Two major challenges are faced in this area of research: the reproducible, scalable and precise synthesis of such constructs and the reliable, accurate and in-depth analysis of these materials. This tutorial review will focus on this second aspect and provide a guide for the characterisation and analysis of soft nanomaterials in solution using scattering and microscopic techniques. [ABSTRACT FROM AUTHOR]

Segregation and templating approaches have been honed by billions of years of evolution to direct many complex biological processes. Nature uses segregation to improve biochemical control by organizing reactants into defined, well-regulated environments, and the transfer of genetic information is a primary function of templating. The ribosome, wherein messenger RNA is translated into polypeptides, combines both techniques to allow for ideal biopolymer syntheses. Herein is presented a biomimetic segregation/templating approach to synthetic radical polymerization. Polymerization of a nucleobase-containing vinyl monomer in the presence of a complementary block copolymer template of low molecular weight yields high molecular weight (Mw up to ~400,000 g mol?1), extremely low polydispersity (?1.08) daughter polymers. Control is attained by segregation of propagating radicals in discrete micelle cores (via cooperative assembly of dynamic template polymers). Significantly reduced bimolecular termination, combined with controlled propagation along a defined number of templates, ensures unprecedented control to afford well-defined high molecular weight polymers. [ABSTRACT FROM AUTHOR]

Self-complementary tweezer-molecules based on a naphthalenediimide core self-assemble into supramolecular dimers through mutual π–π-stacking and hydrogen bonding. The resulting motif is extremely stable in solution (Ka = 105 M−1), and its attachment to one terminal position of a poly(ethylene glycol) chain leads to a doubling of the polymer's apparent molecular weight. [ABSTRACT FROM AUTHOR]

The design and synthesis of a tuneable and reversible morphology switching copolymer system is reported. The kinetics of the transition under a range of conditions has been explored, as has the stabilization of the resultant structures. [ABSTRACT FROM AUTHOR]

The self-assembly of block copolymers into 1D, 2D and 3D nano- and microstructures is of great interest for a wide range of applications. A key challenge in this field is obtaining independent control over molecular structure and hierarchical structure in all dimensions using scalable one-pot chemistry. Here we report on the ring opening polymerization-induced crystallization-driven self-assembly (ROPI-CDSA) of poly-L-lactide-block-polyethylene glycol block copolymers into 1D, 2D and 3D nanostructures. A key feature of ROPI-CDSA is that the polymerization time is much shorter than the self-assembly relaxation time, resulting in a non-equilibrium self-assembly process. The self-assembly mechanism is analyzed by cryo-transmission electron microscopy, wide-angle x-ray scattering, Fourier transform infrared spectroscopy, and turbidity studies. The analysis revealed that the self-assembly mechanism is dependent on both the polymer molecular structure and concentration. Knowledge of the self-assembly mechanism enabled the kinetic trapping of multiple hierarchical structures from a single block copolymer. A key challenge in the self-assembly of block copolymers is obtaining independent control over molecular structure and hierarchical structure in all dimensions using scalable one-pot chemistry. Here the authors show the ring opening polymerization-induced crystallization-driven self-assembly of poly-L-lactide-block-polyethylene glycol block copolymers into 1D, 2D and 3D nanostructures. [ABSTRACT FROM AUTHOR]