Charge Transport through Peptides in Single‐Molecule Electrical Measurements

Charge transport across the peptide chains is one of the vital processes in the biological systems, so understanding their charge transport properties is an indispensable prerequisite to explain the complex biochemical phenomenon. Here, we review the charge transport mechanism, the influence of the special groups and the experimental conditions on the charge transport through the peptide backbone by employing the single‐molecule electrical measurements. Besides, we further review the recent progresses in charge transport properties of supramolecular interaction among the adjacent peptide chains. Finally, we discuss some experimental and theoretical contradictions existing in the charge transport through peptides and provide new inspiration for the future development of the bioelectronics at the single‐molecule scale.     

Vacuum-free fabrication of high-performance semitransparent perovskite solar cells via e-glue assisted lamination process

From a base material of conductive polymer(poly-(3,4-ethylenedioxythiophene):poly(styrenesulfonate),PEDOT:PSS),a flexible and high-conductivity(as low as 45Ω/sq)transparent electrode was fabricated on polydimethylsiloxane elastomer by an acid treatment and transfer process.Combined with the D-sorbitol-doped PEDOT:PSS electric glue,we successfully demonstrated a vacuum-free and ambient lamination fabrication process for semi-transparent perovskite solar cells using triple cation Cs_(0.05)(MA_(0.17)FA_(0.83))_(0.95)Pb(I_(0.83)Br_(0.17))_3perovskite.By this manufacturing-friendly lamination process,we fabricated semitransparent perovskite solar cell devices with power conversion efficiencies up to 16.4%and variable transparencies.     

Tertiary Amines Differentiated from Primary and Secondary Amines by Active Ester‐Functionalized Hexabenzoperylene in Field Effect Transistors

Herein, we report two novel derivatives of hexabenzoperylene (HBP) that are functionalized with ester groups. Methyl acetate functionalized HBP ( 1 ) in single crystals self‐assembles into a supramolecular nanosheet, which has a two‐dimensional π‐stack of HBP sandwiched between two layers of ester groups. With the same self‐assembly motif, active ester‐functionalized HBP ( 2 ) in field effect transistors has enabled differentiation of tertiary amines from primary and secondary amines, in agreement with the fact that active ester reacts with primary and secondary amines but not with tertiary amines to form amides.     

Effect of Butyl α-Hydroxymethyl Acrylate Monomer Structure on the Morphology Produced via Aqueous Emulsion Polymerization-induced Self-assembly

Polymerization-induced self-assembly(PISA) is an efficient and versatile method to afford polymeric nano-objects with polymorphic morphologies. Compared to dispersion PISA syntheses based on soluble monomers, the vast majority of emulsion PISA formulations using insoluble monomers leads to kinetically-trapped spheres. Herein, we present aqueous emulsion PISA formulations generating worms and vesicles besides spheres. Two monomers with different butyl groups, n-butyl(n BHMA) and tert-butyl(t BHMA) α-hydroxymethyl acrylate, and thus possessing different water solubilities were synthesized via Baylis-Hillman reaction. Photoinitiated aqueous emulsion polymerizations of n BHMA and t BHMA employing poly(ethylene glycol) macromolecular chain transfer agents(macro-CTAs, PEG45-CTA, and PEG113-CTA) at 40 °C were systematically investigated to evaluate the effect of monomer structure and solubility on the morphology of the generated block copolymer nano-objects. Higher order morphologies including worms and vesicles were readily accessed for t BHMA, which has a higher water solubility than that of n BHMA. This study proves that plasticization of the core-forming block by water plays a key role in enhancing chain mobility required for morphological transition in emulsion PISA.     

Efficient removal of As(V) from simulated arsenic-contaminated wastewater via a novel metal–organic framework material: Synthesis,structure, and response surface methodology

A novel metal–organic framework material {[N(C₂H₅)₃][Zn₂(ptmda)₂(μ₂-H₂O)]·(H₂O)_0.5}_n { GUT-3 ; H₂ptmda is 4,4′-([p-tolylazanediyl]bis [methylene])dibenzoic acid} was successfully synthesized using the hydrothermal method and characterized by X-ray diffraction, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy. GUT-3 has a two-dimensional network based on dinuclear [Zn₂(ptmda)₂(μ₂-H₂O)]⁻ building units which formed an eightfold interpenetration network in GUT-3 molecules. Hirshfeld surface analysis revealed that H–H, C–H, and O–H bonds accounted for the majority of intermolecular interactions. Moreover, the interactions between GUT-3 and As(V) – the form of As(V) is AsO₄³⁻ – were analyzed in aqueous solutions in a batch system to study the effect of pH, concentration, adsorbent dose, adsorption time, adsorption temperature, and shaking speed. The kinetic and isotherm data of arsenic adsorption on GUT-3 were accurately modeled by pseudo-second-order, Langmuir (q_m = 33.91 mg/g), and Freundlich models. The Box–Behnken response surface method was used to optimize the adsorption conditions of As(V) from the simulated arsenic-contaminated wastewater. The effect of various experimental parameters and optimal experimental conditions was ascertained using the quadratic model.     

Fault Tolerant Multi-Party Authenticated Quantum Conference Against Collective Noise

International Journal of Theoretical Physics - With the advent of new science and technology, teleconference, which allows multiple participants to communicate directly without being constrained by...     

Absolute control of helicity at the C-termini in quinoline oligoamide foldamers by chiral oxazolylaniline moieties

Absolute one-handed chiral quinoline tetramers andoctamers containing different oxazolylanilines at the C-terminus have been synthesized.The absolute one-handed sense and diastereomeric excess values were valued by^1H NMR.X-ray crystal diffractionand CD studies reveal that the S-oxazolylaniline always induces a P-handed helicity and the absolute helicity is driven by the stable three-center hydrogen bonding between protons in the amide and N atoms in oxazolylaniline and adjacent quinoline ring.CPL investigations demonstrated that S-CQn-a-d are CPL active and its g(lum)values are dependent on its length.Interestingly,the sizes of the substituents in the chiral centers are different,howeve r,they exert no effect on the dissymmetric factors g(abs)and g(lum)of quinoline oligoamide foldamers.     

Design and development of self-repairable and recyclable crosslinked poly(thiourethane-urethane) via enhanced aliphatic disulfide chemistry

Thermoset polymer elastomers that are capable of autonomous repairability upon physical damage at ambient temperature are highly desirable because of their thermal and environmental resistance, outstanding mechanical toughness and stability. To aim at this goal, we demonstrated that tris(diethylamino)phosphine was initially proven as an efficient catalyst for the aliphatic disulfide exchange at mild condition. By making use of the aliphatic disulfide bond reshuffling and elasticity of polyurethane elastomers, the inherently cross-linked polysulfide-based poly(thiourethane-urethane) elastomers were prepared and exhibited the ability to mend without extrinsic stimuli in the presence of phosphorus catalyst at room temperature after artificially damaged. The self-healing efficiency via the mechanical recovery approach was investigated to be mainly dependent upon the cross-linking density of polysulfide and hard segments chemistry, which in turns determined the molecular chain diffusion and reshuffling that was corroborated by the stress-relaxation study. The thermoset elastomer based on asymmetric diisocynate showed a maximum self-healing efficiency of 85.6% compared to 71.6% for the elastomer with symmetric monomer building blocks. The self-healable polymer was confirmed to be recyclable and reprocessable through a cut-compression processing cycle under a quite mild pressure and temperature thanks to the disulfide bond reshuffling. Meanwhile, the recycled thermoset elastomer well maintained the mechanical properties to its original material.     

Mathematical studies of the solution of Burgers' equations by Adomian decomposition method

In this paper, a novel Adomian decomposition method (ADM) is developed for the solution of Burgers' equation. While high level of this method for differential equations are found in the literature, this work covers most of the necessary details required to apply ADM for partial differential equations. The present ADM has the capability to produce three different types of solutions, namely, explicit exact solution, analytic solution, and semi-analytic solution. In the best cases, when a closed-form solution exists, ADM is able to capture this exact solution, while most of the numerical methods can only provide an approximation solution. The proposed ADM is validated using different test cases dealing with inviscid and viscous Burgers' equations. Satisfactory results are obtained for all test cases, and, particularly, results reported in this paper agree well with those reported by other researchers.     

Collective sustained oscillations in excitable small-world networks: the moderate fundamental loop or the minimum Winfree loop?

Nonlinear Dynamics - The problem of self-sustained oscillations in excitable complex networks is the central issue under investigation, among which the exploration of the key factors in determining...