Littlewood-Paley算子交换子在加权Herz型Hardy空间上的有界性

研究了Littlewood-Paley算子交换子gψ,b在加权Herz型Hardy空间上的性质,并证明了gψ,b在某些条件下是HKa,pq(ω1,ω2)到Ka,pq(ω1,ω2)和HKa,pq(ω1,ω2)到WKa,pq(ω1,ω2)上的有界算子.     

Didepside Formation by the Nonreducing Polyketide Synthase Preu6 of Preussia isomera Requires Interaction of Starter Acyl Transferase and Thioesterase Domains

Orsellinic acid (OA) derivatives are produced by filamentous fungi using nonreducing polyketide synthases (nrPKSs). The chain-releasing thioesterase (TE) domains of such nrPKSs were proposed to also catalyze dimerization to yield didepsides, such as lecanoric acid. Here, we use combinatorial domain exchanges, domain dissections and reconstitutions to reveal that the TE domain of the lecanoric acid synthase Preu6 of Preussia isomera must collaborate with the starter acyl transferase (SAT) domain from the same nrPKS. We show that artificial SAT-TE fusion proteins are highly effective catalysts and reprogram the ketide homologation chassis to form didepsides. We also demonstrate that dissected SAT and TE domains of Preu6 physically interact, and SAT and TE domains of OA-synthesizing nrPKSs may co-evolve. Our work highlights an unexpected domain–domain interaction in nrPKSs that must be considered for the combinatorial biosynthesis of unnatural didepsides, depsidones, and diphenyl ethers.     

Modular Synthesis of a Tridecasaccharide Motif of Bacteroides vulgatus Lipopolysaccharides against Inflammatory Bowel Diseases through an Orthogonal One-Pot Glycosylation Strategy

Lipopolysaccharides from Bacteroides vulgatus represent interesting targets for the treatment of inflammatory bowel diseases. However, efficient access to long, branched and complex lipopolysaccharides remains challenging. Herein, we report the modular synthesis of a tridecasaccharide from Bacteroides vulgates through an orthogonal one-pot glycosylation strategy based on glycosyl ortho-(1-phenylvinyl)benzoates, which avoids the issues of thioglycoside-based one-pot synthesis. Our approach also features: 1) 5,7-O-di-tert-butylsilylene-directed glycosylation for stereoselective construction of the α-Kdo linkage; 2) hydrogen-bond-mediated aglycone delivery for the stereoselective formation of β-mannosidic bonds; 3) remote anchimeric assistance for stereoselective assembly of the α-fucosyl linkage; 4) several orthogonal one-pot synthetic steps and strategic use of orthogonal protecting groups to streamline oligosaccharide assembly; 5) convergent [1+6+6] one-pot synthesis of the target.     

Growing ZIF-8 Seeds on Charged COF Substrates toward Efficient Propylene-Propane Separation Membranes

We report a covalent organic framework (COF) induced seeding strategy to fabricate metal–organic framework (MOF) membranes. Contrary to graphene oxide nuclei-depositing substrate, COF substrate has uniform pore size, high microporosity and abundant functional groups. We designed a series of charged COF nanosheets to induce the formation of ZIF-8@COF nanosheet seeds with high aspect ratio over 150, which were readily processed into a compact and uniform seed layer. The resulting ZIF-8 membranes with thickness down to 100 nm exhibit an ultrahigh C₃H₆/C₃H₈ separation performance and superior long-term stability. Our strategy is also validated by fabricating ultrathin ZIF-67 and UiO-66 membranes.     

Impact of fluorine on the phase behavior of bis-p-tolyl propane in supercritical CO2, 1,1-difluoroethane,and 1,1,1,2-tetrafluoroethane

Fluorine substitution on a solute can have a significant effect on solute solubility in a given solvent and fluorine substitution on a solvent can also have a significant effect on solvent quality. The effect of fluorine is demonstrated with the phase behavior data for bis(p-tolyl)propane (BTP) compared to bis(p-tolyl)hexafluoropropane (BTHFP) in supercritical carbon dioxide, 1,1-difluoroethane (F152a), and 1,1,1,2-tetrafluoroethane (F134a). Semifluorinated BTHFP is more soluble than non-fluorinated BTP in all three solvents, especially CO₂. The CO₂–BTP system exhibits solid solubility behavior while the CO₂–BTHFP system exhibits liquid–liquid–vapor (LLV) behavior near the critical point of CO₂. Although the two dipolar hydrofluorocarbons (HFC) are better solvents than CO₂ for these two aromatic solid compounds, F152a is the superior HFC solvent, especially for BTP, because F152a has a smaller molar volume and a larger effective dipole moment than F134a. LLV behavior is also observed for the F134a–BTP system near the critical point of F134a although the F134a–BTHFP, F152a–BTP, and F152a–BTHFP systems all appear to exhibit type-I phase behavior and no liquid–liquid immiscibility near the respective critical points.     

High-pressure vapor–liquid and vapor–liquid–liquid equilibria in the carbon dioxide + 1-heptanol system

Vapor–liquid equilibria (VLE) and vapor–liquid–liquid equilibria (VLLE) data for the carbon dioxide + 1-heptanol system were measured at 293.15, 303.15, 313.15, 333.15 and 353.15 K. Phase behavior measurements were made in a high-pressure visual cell with variable volume, based on the static-analytic method. The pressure range under investigation was between 0.58 and 14.02 MPa. The Soave–Redlich–Kwong (SRK)-EOS coupled with Huron–Vidal (HV) mixing rules and a reduced UNIQUAC model, was used in a semi-predictive approach, in order to represent the complex phase behavior (critical curve, LLV line, isothermal VLE, LLE, and VLLE) of the system. The topology of phase behavior is qualitatively correct predicted.     

Comparative study on different carbon nanotube materials in terms of transparent conductive coatings

We compared conductive transparent carbon nanotube coatings on glass substrates made of differently produced single-wall (SWNT), double-wall, and multiwall carbon nanotubes. The airbrushing approach and the vacuum filtration method were utilized for the fabrication of carbon nanotube films. The optoelectronic performance of the carbon nanotube film was found to strongly depend on many effects including the ratio of metallic-to-semiconducting tubes, dispersion, length, diameter, chirality, wall number, structural defects, and the properties of substrates. The electronic transportability and optical properties of the SWNT network can be significantly altered by chemical doping with thionyl chloride. Hall effect measurements revealed that all of these thin carbon nanotube films are of p-type probably due to the acid reflux-based purification and atmospheric impurities. The competition between variable-range hoping and fluctuation-assisted tunneling in the functionized carbon nanotube system could lead to a crossover behavior in the temperature dependence of the network resistance.     

Effect of chain density and conformation on protein adsorption at PEG-grafted polyurethane surfaces

Polyurethanes were modified using monobenzyloxy polyethylene glycol (BPEG) which possesses a bulky hydrophobic benzyloxy group at one end and a hydroxyl group at the other end as a preconstructed BPEG layer, and poly(ethylene glycol) (PEG) and monomethoxyl poly(ethylene glycol) (MPEG) with various chain lengths as fillers. Our objective was to investigate the effect of PEG graft density and conformation on protein adsorption at PEGlated surface. The graft density was estimated by a chemical titration method. The combination of ATR-FTIR, AFM and titration results provide evidences that the graft density can be increased by backfilling PEG or MPEG to a BPEG layer. However, fibrinogen and albumin adsorption significantly increased on all surfaces after PEG or MPEG backfilling. We conclude that the conformation of hydrophobic benzyloxy end groups of the BPEG layer plays a key role. The benzyloxy end groups of preconstructed PEG chains stretch to the surface after PEG backfilling, which possibly accounts for the observed increase in protein adsorption. The BPEG conformation change after backfilling with PEG or MPEG was also suggested by contact angles. Additionally, protein adsorption was slightly influenced by the length of filler, suggesting a change in surface morphology.     

Disulfide bond creates a small connecting loop in aminoxy peptide backbone

Disulfide-bond formation between the side chains of cysteine-cysteine pairs is often critical to the folding behavior, stability, and functionality of proteins. In this paper, we report that sulfur atoms can be introduced into the amide groups of aminoxy peptides to form a novel type of disulfide bridge, which creates a connecting loop in the peptide backbone.     

Optical properties of ultrashort semiconducting single-walled carbon nanotube capsules down to sub-10 nm

Single-walled carbon nanotubes (SWNTs) are typically long (greater than or approximately equal 100 nm) and have been well established as novel quasi one-dimensional systems with interesting electrical, mechanical, and optical properties. Here, quasi zero-dimensional SWNTs with finite lengths down to the molecular scale (7.5 nm in average) were obtained by length separation using a density gradient ultracentrifugation method. Different sedimentation rates of nanotubes with different lengths in a density gradient were taken advantage of to sort SWNTs according to length. Optical experiments on the SWNT fractions revealed that the UV-vis-NIR absorption and photoluminescence peaks of the ultrashort SWNTs blue-shift up to approximately 30 meV compared to long nanotubes, owing to quantum confinement effects along the length of ultrashort SWNTs. These nanotube capsules essentially correspond to SWNT quantum dots.