Self-catalytic synthesis of hydrophilic polypyrrole/tellurium nanocomposite and its capacitance performance

Journal of Solid State Electrochemistry - A hydrophilic polypyrrole/tellurium (PPy/Te) nanocomposite was synthesized by a facile approach in which H2TeO3 was used as the oxidizing agent of pyrrole...     

Thioether‐derived Macrocycle for Peptide Secondary Structure Fixation

Recently, we developed methods to stabilize peptides into various secondary structures, including α‐helix, type III turn and β‐hairpin via proper thioether based macrocyclization. These conformationally constrained peptidomimetics confer enhanced biophysical properties and provide a valuable avenue towards clinically‐relevant therapeutic molecules. In this personal account, thioether‐derived macrocyclization methods developed by our group for stabilization of α‐helix, type‐III β turn and β‐hairpin conformations are discussed.     

自由Rota-Baxter代数的因子分解

近年来,Rota-Baxter代数在数学和物理学中有着广泛的应用,受到越来越多的关注,自由Rota-Baxter代数分别用括号字,根树以及Motzkin路径得到了构造.因子分解在代数学中是一个很重要的问题.本文主要考虑用括号字构造的自由RotaBaxter代数,得到了自由Rota-Baxter代数中基元素的因子分解.     

Global dynamics of a Vector‐Borne disease model with two delays and nonlinear transmission rate

In this paper, we investigate a Vector‐Borne disease model with nonlinear incidence rate and 2 delays: One is the incubation period in the vectors and the other is the incubation period in the host. Under the biologically motivated assumptions, we show that the global dynamics are completely determined by the basic reproduction number R₀. The disease‐free equilibrium is globally asymptotically stable if R₀≤1; when R₀>1, the system is uniformly persistent, and there exists a unique endemic equilibrium that is globally asymptotically. Numerical simulations are conducted to illustrate the theoretical results.     

Quadratic properties of least-squares solutions of linear matrix equations with statistical applications

Assume that a quadratic matrix-valued function \(\psi (X) = Q - X^{\prime }PX\) is given and let \(\mathcal{S} = \left\{ X\in {\mathbb R}^{n \times m} \, | \, \mathrm{trace}[\,(AX - B)^{\prime }(AX - B)\,] = \min \right\} \) be the set of all least-squares solutions of the linear matrix equation \(AX = B\). In this paper, we first establish explicit formulas for calculating the maximum and minimum ranks and inertias of \(\psi (X)\) subject to \(X \in {\mathcal S}\), and then derive from the formulas the analytic solutions of the two optimization problems \(\psi (X) =\max \) and \(\psi (X)= \min \) subject to \(X \in \mathcal{S}\) in the Löwner partial ordering. As applications, we present a variety of results on equalities and inequalities of the ordinary least squares estimators of unknown parameter vectors in general linear models.     

Precise large deviations for sums of random vectors with dependent components of consistently varying tails

Let {X _i = (X _1,i ,...,X _m,i )^?, i ≥ 1} be a sequence of independent and identically distributed nonnegative m-dimensional random vectors. The univariate marginal distributions of these vectors have consistently varying tails and finite means. Here, the components of X ₁ are allowed to be generally dependent. Moreover, let N(·) be a nonnegative integer-valued process, independent of the sequence {X _i , i ≥ 1}. Under several mild assumptions, precise large deviations for S _n = Σ _i=1 ⁿ X _i and S _N(t) = Σ _i=1 ^N(t) X _i are investigated. Meanwhile, some simulation examples are also given to illustrate the results.     

定量核磁共振氢谱法测定枸橼酸托法替布片的有效含量

建立了枸橼酸托法替布片中有效含量的定量核磁共振氢谱测定方法。以托法替布化学位移δ 7.13为定量峰,3,5-二甲基吡唑化学位移δ 5.73为内标峰,氘代二甲亚砜（DMSO-D6）为溶剂,使用核磁共振谱仪采集混合物的氢谱,对枸橼酸托法替布片中的有效成分进行定量测定。该方法专一性强,在0.793～7.925 mg/mL范围内呈现良好的线性关系（r2=0.998 4）。精密度、重复性和稳定性的相对标准偏差（RSD）分别为0.82%、1.7%和0.67%。该方法测得的枸橼酸托法替布片中托法替布的质量分数为2.25%,其结果与高效液相色谱法基本一致。定量核磁共振氢谱法具有操作方便简单,可同时进行定性与定量,检测时间短,无需对照品等优势,可用于枸橼酸托法替布片有效含量的测定。     

Inside Cover: Acid-catalyzed Disulfide-mediated Reversible Polymerization for Recyclable Dynamic Covalent Materials (Angew. Chem. Int. Ed. 11/2023)

Poly(1,2-dithiolane)s are a family of intrinsically recyclable polymers due to their dynamic covalent disulfide linkages. Despite the common use of thiolate-initiated anionic ring-opening polymerization (ROP) under basic condition, cationic ROP is still not exploited. Here we report that disulfide bond can act as a proton acceptor, being protonated by acids to form sulfonium cations, which can efficiently initiate the ROP of 1,2-dithiolanes and result in high-molecular-weight (over 1000 kDa) poly(disulfide)s. The reaction can be triggered by adding catalytic amounts of acids and non-coordinating anion salts, and completed in few minutes at room temperature. The acidic conditions allow the applicability for acidic monomers. Importantly, the reaction condition can be under open air without inert protection, enabling the nearly quantitative chemical recycling from bulk materials to original monomers.     

Solvent-Free Heterogeneous Catalytic Hydrogenation of Polyesters to Diols

The utilization of carbon resources stored in plastic polymers through chemical recycling and upcycling is a promising approach for mitigating plastic waste. However, most current methods for upcycling suffer from limited selectivity towards a specific valuable product, particularly when attempting full conversion of the plastic. We present a highly selective reaction route for transforming polylactic acid (PLA) into 1,2-propanediol utilizing a Zn-modified Cu catalyst. This reaction exhibits excellent reactivity (0.65 g g_cat⁻¹ h⁻¹) and selectivity (99.5 %) towards 1,2-propanediol, and most importantly, can be performed in a solvent-free mode. Significantly, the overall solvent-free reaction is an atom-economical reaction with all the atoms in reactants (PLA and H₂) fixed into the final product (1,2-propanediol), eliminating the need for a separation process. This method provides an innovative and economically viable solution for upgrading polyesters to produce high-purity products under mild conditions with optimal atom utilization.     

Two-dimensional Supramolecular Polymers Based on Selectively Recognized Aromatic Cation-π and Donor-Acceptor Motifs for Photocatalytic Hydrogen Evolution

Two-dimensional (2D) organic polymers have recently received considerable interest, especially those whose architectures are held together via supramolecular engineering. However, current approaches toward supramolecular 2D structures usually suffer from mutual interference of noncovalent interactions and lack of intrinsic functions. Herein, we report well-regulated 2D supramolecular polymers (2DSPs) through an aromatics-selective recognition strategy of cation-π and donor-acceptor (D-A) motifs, which are derived from C₄-symmetric cationic monomers and electron-withdrawing molecules. By subtly designing the strength and direction of noncovalent driving forces, the mutual interference between cation-π and D-A interactions is effectively avoided, enabling the construction of 2DSPs in aqueous solution. On this basis, the resultant 2DSPs possess boosted photocatalytic hydrogen evolution activity at a rate of 600 μmol g⁻¹ h⁻¹, which is mainly ascribed to the specific stacking mode of cation-π/D-A motifs and the ordered 2D structures.