Selective Removal of Denatured Proteins Using MOF Nanopores.

Here we present, for the first time, the selective adsorption of denatured proteins using a metal-organic framework (MOF), demonstrating promising potential for protein purification. Typical proteins, such as lysozyme and carbonic anhydrase B, enter the pores of MIL-101 through their narrow apertures when they are denatured to an unfolded state. Selective adsorption is achieved by finely tuning two key features: the sizes of the aperture and cage of the MOF nanopores, which are responsible for sorting unfolded polypeptide chains and inhibiting the translocation of the native form into the pores, respectively. By leveraging this selective adsorption, we successfully purified a mixture of native and denatured proteins by adding MOF to the mixture, achieving a native purity of over 99%.

Fabrication of Self-Expanding Metal-Organic Cages Using a Ring-Openable Ligand.

Metal-organic cages (MOCs), which are formed via coordination-driven assembly, are being extensively developed for various applications owing to the utility of their accessible molecular-sized cavity. While MOC structures are uniquely and precisely predetermined by the metal coordination number and ligand configuration, tailoring MOCs to further modulate the size, shape, and chemical environment of the cavities has become intensively studied for a more efficient and adaptive molecular binding. Herein, we report self-expanding MOCs that exhibit remarkable structural variations in cage size and flexibility while maintaining their topology. A cyclic ligand with an oligomeric chain tethering the two benzene rings of stilbene was designed and mixed with RhII ions to obtain the parent MOCs. These MOCs were successfully transformed into expanded MOCs via the selective cleavage of the double bond in stilbene. The expanded MOCs could effectively trap multidentate N-donor molecules in their enlarged cavity, in contrast to the original MOCs with a narrow cavity. As the direct synthesis of expanded MOCs is impractical because of the entropically disfavored structures, self-expansion using ring-openable ligands is a promising approach that allows precision engineering and the production of functional MOCs that would otherwise be inaccessible.

Fabrication of Double-Stranded Vinyl Polymers Mediated by Coordination Nanochannels.

Although double-stranded structures are commonly found in biopolymers, a general and versatile methodology for fabricating double-stranded synthetic polymers has not yet been developed. Here, we report a new approach for synthesizing double-stranded polymers composed of polystyrene and poly(methyl methacrylate). We conducted crosslinking radical polymerization inside a metal-organic framework (MOF), which had one-dimensional channels with diameters similar to the thickness of two polymer chains. Effective spatial constraint within the MOF pores facilitated highly regulated crosslinking reactions between two polymer chains with extended conformations. Remarkably, the obtained double-stranded polymers were soluble in many organic solvents, even at a high crosslinking ratio (20%), unlike conventional crosslinked polymers. Notably, this stable duplex topology, which was inaccessible using previous methods, endowed the double-stranded vinyl polymers with unusual properties in the solution and bulk states. By designing the properties of the MOF nanochannels, the proposed technique can contribute to the development of a wide range of synthetic polymer duplexes.

Metal-Organic Frameworks as Versatile Media for Polymer Adsorption and Separation.

Molecular recognition is of paramount importance for modern chemical processes and has now been achieved for small molecules using well-established host-guest chemistry and adsorption-science principles. In contrast, technologies for recognizing polymer structure are relatively undeveloped. Conventional polymer separation methods, which are mostly limited in practice to size-exclusion chromatography and reprecipitation, find it difficult to recognize minute structural differences in polymer structures as such small structural alterations barely influence the polymer characteristics, including molecular size, polarity, and solubility. Therefore, most of the polymeric products being used today contain mixtures of polymers with different structures as it is challenging to completely control polymer structures during synthesis even with state-of-the-art substitution and polymerization techniques. In this context, development of novel techniques that can resolve the challenges of polymer recognition and separation is in great demand, as these techniques hold the promise of a new paradigm in polymer synthesis, impacting not only materials chemistry but also analytical and biological chemistry.In biological systems, precise recognition and translation of base monomer sequences of mRNA are achieved by threading them through small ribosome tunnels. This principle of introducing polymers into nanosized channels can possibly help us design powerful polymer recognition and separation technologies using metal-organic frameworks (MOFs) as ideal and highly designable recognition media. MOFs are porous materials comprising organic ligands and metal ions and have been extensively studied as porous beds for gas separation and storage. Recently, we found that MOFs can accommodate large polymeric chains in their nanopores. Polymer chains can spontaneously infiltrate MOFs from neat molten and solution phases by threading their terminals into MOF nanochannels. Polymer structures can be recognized and differentiated due to such insertion processes, resulting in the selective adsorption of polymers on MOFs. This enables the precise recognition of the polymer terminus structure, resulting in the perfect separation of a variety of terminal-functionalized polymers that are otherwise difficult to separate by conventional polymer separation methods. Furthermore, the MOFs can recognize polymer shapes, thus enabling the large-scale separation of high purity cyclic polymers from the complex crude mixtures of linear polymers, which are used as precursor materials in common cyclization reactions. In solution-phase adsorption, many factors, including molecular weight, terminal groups, polymer shape, polymer-MOF interaction, and coexisting solvent molecules, influence the selective adsorption behavior; this yields a new liquid chromatography-based polymer separation technology using an MOF as the stationary phase. MOF-packed columns, in which a novel separation mode based on polymer insertion into the MOF operates under a dynamic insertion/rejection equilibrium at the liquid/solid interface, exhibited excellent polymer separation capability. The polymer recognition principle described in this study thus has a high probability for realizing previously unfeasible polymer separations based on monomer composition and sequences, stereoregularity, regioregularity, helicity, and block sequences in synthetic polymers and biomacromolecules.

Outcomes of dogs with progressive myelomalacia treated with hemilaminectomy or with extensive hemilaminectomy and durotomy.

OBJECTIVE: To evaluate the ability of extensive hemilaminectomy and durotomy (EHLD) to control progressive myelomalacia (PMM) in dogs. STUDY DESIGN: Retrospective clinical study. ANIMALS: Twenty-eight client owned dogs that underwent EHLD (n = 10) or HL alone (n = 18). METHODS: After diagnosis by MRI, dogs were immediately treated with HL alone or EHLD at the site of intramedullary hyperintensity on T2-weighted (T2W)-MRI. Medical records were retrospectively reviewed. Follow-up data were collected via telephone interviews with the referring veterinarian and a standardized questionnaire. Postoperative survival outcome between groups was compared (log-rank test) by using Cox's proportional hazard analysis with baseline characteristics entered as covariates. RESULTS: The survival rate was higher in the EHLD group (P = .03) compared with the HL-alone group. Eleven of 18 dogs treated with HL survived, while seven of 18 dogs died (median, 5 days after surgery). In the EHLD group, 10 of 10 dogs survived postoperatively. Baseline characteristics were not associated with postoperative survival outcomes. According to multivariate analysis, EHLD was the independent factor associated with an increase in survival rate (P = .0002). CONCLUSION: EHLD durotomy at the intramedullary hyperintense region on T2W-MRI improved the survival rate of dogs with PMM compared with dogs treated with standard HL. CLINICAL SIGNIFICANCE: This study provides evidence that supports treatment with EHLD in dogs with PMM. Additional prospective studies are required.

[Comparison of two cases of type 2 autoimmune pancreatitis].

We describe two cases of type 2 autoimmune pancreatitis (AIP). A 39-year-old man presented to our hospital with complaints of epigastric and back pain. Pancreatic enzyme levels were elevated, but serum levels of immunoglobulins G and G4 (IgG and IgG4) were normal. Computed tomography (CT) showed diffuse pancreatic enlargement, and endoscopic retrograde pancreatography revealed diffuse narrowing of the pancreatic duct. Endoscopic ultrasound-guided fine-needle aspiration (EUS-FNA) revealed granulocytic epithelial lesions and very few IgG4-positive cells. Colonoscopy revealed ulcerative colitis. Type 2 AIP was diagnosed, and 5-aminosalicylic acid (5-ASA) and prednisolone were administered. The clinical course has since been favorable, and the prednisolone dose is currently being reduced. A 47-year-old woman presented to our hospital with complaints of bloody stools. Colonoscopy revealed ulcerative colitis. CT depicted diffuse pancreatic enlargement with a capsule-like rim. Pancreatic enzyme levels were elevated, but serum levels of IgG and IgG4 were normal. On magnetic resonance cholangiopancreatography, the pancreatic duct could not be delineated. No pathological findings of type 2 AIP were obtained on EUS-FNA. Type 2 AIP was suspected, and 5-ASA and steroid enemas were administered. To date, recurrence has not been observed, and 5-ASA management continues. The two cases differed with regard to sex of patient, clinical course, pathological findings, and treatment.

Chiral Induction in Buckminsterfullerene Using a Metal-Organic Framework.

Chiral induction is an emerging topic of interest in various areas of chemistry because of its relationship to the elusive mechanism of spontaneous symmetry breaking in nature. Buckminsterfullerene (C60 ) with the shape of a highly symmetric truncated icosahedron has rarely been referred for chiral induction due to the difficult symmetry breaking. In this work, we demonstrate that a chiral metal-organic framework (MOF) can provide a key field for chiral induction. C60 could be incorporated into the chiral nanochannels of the MOF using an in situ self-assembly strategy. The circular dichroism spectra of the resulting nanocomposites showed an intense chiral signal in the absorption region of C60 . Experimental and theoretical studies showed that this unprecedented chiral induction of C60 was attributed to hybridization of the molecular orbitals through a close association with the pore surface of the MOF. Our method can endow highly symmetric achiral compounds with chirality, paving the new way toward fabrication of novel chiral nanomaterials.

Metal-Organic Frameworks for Practical Separation of Cyclic and Linear Polymers.

The purification step in the manufacturing of cyclic polymers is difficult as complete fractionation to eliminate linear impurities requires considerable effort. Here, we report a new polymer separation methodology that uses metal-organic frameworks (MOFs) to discriminate between linear and cyclic polyethylene glycols (PEGs) via selective polymer insertion into the MOF nanopores. Preparation of a MOF-packed column allowed analytical and preparative chromatographic separation of these topologically distinct pairs. In addition, gram-scale PEGs with only cyclic structures were successfully obtained from a crude reaction mixture by using MOF as an adsorbent.

Scalable and Precise Synthesis of Armchair-Edge Graphene Nanoribbon in Metal-Organic Framework.

Graphene nanoribbons (GNRs), narrow and straight-edged stripes of graphene, attract a great deal of attention because of their excellent electronic and magnetic properties. As of yet, there is no fabrication method for GNRs to satisfy both precision at the atomic scale and scalability, which is critical for fundamental research and future technological development. Here, we report a methodology for bulk-scale synthesis of GNRs with atomic precision utilizing a metal-organic framework (MOF). The GNR was synthesized by the polymerization of perylene (PER) or its derivative within the nanochannels of the MOF. Molecular dynamics simulations showed that PER was uniaxially aligned along the nanochannels of the MOF through host-guest interactions, which allowed for regulated growth of the nanoribbons. A series of characterizations of the GNR, including NMR, UV/vis/NIR, and Raman spectroscopy measurements, confirmed the formation of the GNR with well-controlled edge structure and width.

Recognition of Polymer Terminus by Metal-Organic Frameworks Enabling Chromatographic Separation of Polymers.

Unlike commonly used molecular recognition techniques, recognition of polymer structures requires an additional aspect of extremely high recognition ability, by which marginal structural differences can be identified in a large polymer chain. Herein we show that metal-organic frameworks (MOFs) can recognize polymer terminal structures, thus enabling the first reported chromatographic separation of polymers. End-functionalized polyethylene glycols (PEGs) are selectively inserted into the MOF channel, the insertion kinetics being dependent on the projection size of the PEG terminus. This size-selective insertion mechanism facilitates precise discrimination of end-functionalized PEGs using liquid chromatography (LC). An MOF-packed column thus provides an efficient and easily accessible method for the separation of such end-functionalized polymers using conventional LC systems.

Controlling the Packing of Metal-Organic Layers by Inclusion of Polymer Guests.

The preparation of metal-organic structures with a controlled degree of disorder is currently one of the most promising fields of materials science. Here, we describe the effect of guest polymer chains on the transformation of a metal-organic framework (MOF). Heating a pillared MOF at a controlled temperature resulted in the exclusive removal of the pillar ligands, while the connectivity of the metal-organic square-grid layers was maintained. In the absence of a polymer, 2D-layers rearranged to form a new crystalline phase. In contrast, the presence of a polymer in the MOF inhibited totally the recrystallization, leading to a turbostratic phase with layers threaded and maintained apart by the polymer chains. This work demonstrates a new synthetic approach toward the preparation of anisotropic metal-organic materials with controlled disorder. It also reveals how guests can dramatically modify the conversion of host MOFs, even though no chemical reaction occurs between them.

Transcription of Chirality from Metal-Organic Framework to Polythiophene.

Here, we report an unprecedented chirality transfer from a metal-organic framework (MOF) to a polymer. In this work, unsubstituted polythiophene (PTh) was prepared in the nanochannels of a chiral MOF. Circular dichroism spectroscopy revealed that nanoconfinement of the polymer chains could endow optically inactive PTh with a chiral nature. The thickness of polymer chain assemblies could be controlled by tuning the loading amount of PTh, which resulted in a drastic change in the chiroptical properties. Note that PTh liberated from the host still exhibited chirality even without the chiral support. Remarkably, the recovered PTh presented high thermal stability of chirality up to 250 °C. Our findings show that the encapsulation of the polymer chains in chiral MOFs is a simple and effective methodology not only to express the chirality of polymers but also to elucidate the inter- and intrachain chirality in polymer assemblies.

Hybridization of MOFs and polymers.

Metal-organic frameworks (MOFs) have received much attention because of their attractive properties. They show great potential applications in many fields. An emerging trend in MOF research is hybridization with flexible materials, which is the subject of this review. Polymers possess a variety of unique attributes, such as softness, thermal and chemical stability, and optoelectrical properties that can be integrated with MOFs to make hybrids with sophisticated architectures. Hybridization of MOFs and polymers is producing new and versatile materials that exhibit peculiar properties hard to realize with the individual components. This review article focuses on the methodology for hybridization of MOFs and polymers, as well as the intriguing functions of hybrid materials.

Opening of an Accessible Microporosity in an Otherwise Nonporous Metal-Organic Framework by Polymeric Guests.

The development of highly porous metal-organic frameworks (MOFs) is greatly sought after, due to their wide range of applications. As an alternative to the development of new structures, we propose to obtain new stable configurations for flexible MOFs by insertion of polymeric guests. The guests prevent the otherwise spontaneous closing of the host frameworks and result in stable opened forms. Introduced at a fraction of the maximal capacity, polymer chains cause an opening of the occupied nanochannels, and because of the MOF reticular stiffness, this opening is propagated to the neighboring nanochannels that become accessible for adsorption. Composites were obtained by in situ polymerization of vinyl monomers in the nanochannels of an otherwise nonporous MOF, resulting in homogeneously loaded materials with a significant increase of porosity (SBET = 920 m2/g). In addition, by limiting the accessible configurations for the framework and forbidding the formation of a reactive intermediate, the polymeric guest prevented the thermal degradation of the host MOF even at very low loading (as low as 3 wt %) and increased its stability domain by more than 200 °C.

Inorganic nanoparticles in porous coordination polymers.

Porous coordination polymers (PCPs) have been recently highlighted because of their high synthetic designability in structure and functions. Because of their ordered nanoporous structures with a large surface area and tunable pore surface functionality, PCPs have emerged as a significant class of nanoporous materials with potential applications in gas storage, separation, catalysis, and chemical sensing. Recent research has shown the utility of PCPs as host materials for the confinement of nanoparticles of inorganic polymers (IPs), such as metals, metal oxides, and metal chalcogenides. The fabrication of IP nanoparticles in PCPs (PCP⊃IP) has been studied for manifesting specific nanosized-dependent properties and host-guest synergistic functions. In this review, we describe the recent progress in the accommodation of IPs in the nanochannels of PCPs and the remarkable functions of the composite materials.

Nanostructuration of PEDOT in Porous Coordination Polymers for Tunable Porosity and Conductivity.

A series of conductive porous composites were obtained by the polymerization of 3,4-ethylenedioxythiophene (EDOT) in the cavities of MIL-101(Cr). By controlling the amount of EDOT loaded into the host framework, it was possible to modulate the conductivity as well as the porosity of the composite. This approach yields materials with a reasonable electronic conductivity (1.1 × 10(-3) S·cm(-1)) while maintaining high porosity (SBET = 803 m(2)/g). This serves as a promising strategy for obtaining highly nanotextured conductive polymers with very high accessibility for small gas molecules, which are beneficial to the fabrication of a chemiresistive sensor for the detection of NO2.

Peptide-Metal Organic Framework Swimmers that Direct the Motion toward Chemical Targets.

Highly efficient and robust chemical motors are expected for the application in microbots that can selectively swim toward targets and accomplish their tasks in sensing, labeling, and delivering. However, one of major issues for such development is that current artificial swimmers have difficulty controlling their directional motion toward targets like bacterial chemotaxis. To program synthetic motors with sensing capability for the target-directed motion, we need to develop swimmers whose motions are sensitive to chemical gradients in environments. Here we create a new intelligent biochemical swimmer by integrating metal organic frameworks (MOFs) and peptides that can sense toxic heavy metals in solution and swim toward the targets. With the aid of Pb-binding enzymes, the peptide-MOF motor can directionally swim toward PbSe quantum dots (QD) by sensing pH gradient and eventually complete the motion as the swimmer reaches the highest gradient point at the target position in solution. This type of technology could be evolved to miniaturize chemical robotic systems that sense target chemicals and swim toward target locations.

Radical Polymerization of Vinyl Monomers in Porous Organic Cages.

The radical polymerization of vinyl monomers was performed in a tetrahedral imine-linked organic cage with extrinsic porosity (CC3). Because of its dynamic and responsive packing structure, CC3 endowed the polymerization with specific behaviors. The adsorption of styrene triggered a change in the CC3 assembly, resulting in a monomer arrangement that was suitable for polymerization within the host matrix. The polymerization reaction was strongly dependent on the crystallinity of CC3 and was promoted by amorphization of the host in a cooperative manner, which is not possible with conventional rigid porous materials. Furthermore, CC3 can recognize the polarity of substrates, and thus polar monomers, such as methyl methacrylate and acrylonitrile, could not induce the structural changes in CC3 that are required for polymerization. This monomer specificity governed by the flexibility of CC3 is useful to the prevent incorporation of unfavorable monomers into the polymeric products.

Unraveling Inter- and Intrachain Electronics in Polythiophene Assemblies Mediated by Coordination Nanospaces.

Strong interchain interactions render unsubstituted polythiophene un-fusible, non-melting, and insoluble. Therefore, control of the packing structure, which has a profound effect on the optical and electronic properties of the polymer, has never been achieved. Unsubstituted polythiophene was prepared in the one-dimensional channels of [La(1,3,5-benzenetrisbenzoate)]n, where polymer chains form unprecedented assembly structures mediated by the host framework. It is noteworthy that the emission and carrier transport properties were drastically changed by varying the number of chains within a particular assembly. The response of the composite to additional guests is also examined as a method to use the composites as low-concentration sensors. Our findings show that the encapsulation of polymer chains in host materials is a facile method for understanding the intrinsic properties of conjugated polymers, along with controlling and enhancing their functions.

Confinement of single polysilane chains in coordination nanospaces.

Understanding the intrinsic properties of single conducting polymer chains is of interest, largely for their applications in molecular devices. In this study, we report the accommodation of single polysilane chains with hole-transporting ability in porous coordination polymers (PCPs), [Al(OH)(L)]n (1a; L = 2,6-naphthalenedicarboxylate, channel size = 8.5 × 8.5 Å(2), 1b; L = 4,4'-biphenyldicarboxylate, channel size = 11.1 × 11.1 Å(2)). Interestingly, the isolation of single polysilane chains increased the values of carrier mobility in comparison with that in the bulk state due to the elimination of the slow interchain hole hopping. Moreover, even when the chains are isolated one another, the main chain conformation of polysilane could be controlled by changing the pore environment of PCPs, as evidenced by Raman spectroscopy, solid-state NMR measurements, and molecular dynamics simulation. Hence, we succeeded in varying the conducting property of single polysilane chains. Additionally, polysilanes have a drawback, photodegradation under ultraviolet light, which should be overcome for the application of polysilanes. It is noteworthy that the accommodation of polysilane in the nanopores did not exhibit photodegradation. These results highlight that PCP-polysilane hybrids are promising candidates for further use in the field of molecular electronics.