Synthesis and Detection of Pesticides of Luminescent Metal-organic Framework Based on Carboxyl-decorating Tetraphenylethylene

A water-stable porous anionic metal-organic framework(MOF), [(CH_3)_2NH_2][In(TCPP)_(4/3)]_n·(2DMF)_n(3H_2O)_n(1, TCPP = 1,1,2,2-tetra(4-carboxylbiphenyl)ethylene), was synthesized. Here, compound 1 showed extremely high sensitivity and selectivity to current general-purpose pesticide 2,6-dichloro-4-nitroaniline(DCN) in aqueous solution. The fluorescence intensity of compound 1 could be decreased as much as 80% by 6 mL DCN, and it was almost completely quenched only with 20 mL DCN. The results indicate that compound 1 can act as a fluorescent probe for DCN.     

Enhanced Activity of Enzyme Immobilized on Hydrophobic ZIF-8 Modified by Ni2+ Ions

The development of efficient enzyme immobilization to promote their recyclability and activity is highly desirable. Zeolitic imidazolate framework-8 (ZIF-8) has been proved to be an effective platform for enzyme immobilization due to its easy preparation and biocompatibility. However, the intrinsic hydrophobic characteristic hinders its further development in this filed. Herein, a facile synthesis approach was developed to immobilize pepsin (PEP) on the ZIF-8 carrier by using Ni²⁺ ions as anchor (ZIF-8@PEP-Ni). By contrast, the direct coating of PEP on the surface of ZIF-8 (ZIF-8@PEP) generated significant conformational changes. Electrochemical oxygen evolution reaction (OER) was employed to study the catalytic activity of immobilized PEP. The ZIF-8@PEP-Ni composite attains remarkable OER performance with an ultralow overpotential of only 127 mV at 10 mA cm⁻², which is much lower than the 690 and 919 mV overpotential values of ZIF-8@PEP and PEP, respectively.     

一个富路易斯碱位配合物的合成、结构及对痕量Ag+的荧光检测

通过溶剂热方法合成了一个由氢键拓展的携带路易斯碱位的三维超分子配位聚合物：{[Cd（HTZ-IP）（HPYTZ）（H₂O）₂]·5H₂O}_n（HTZ-H₂IP=5-（5-四氮唑基）间苯二甲酸;HPYTZ=3,5-（4-吡啶基）-1,2,4-三唑]。X射线单晶衍射结果表明,中心镉离子由含氮杂环羧酸配体和富氮辅助配体连接成"有悬挂手臂"的一维链,而链间则凭借配位水和2个配体的氢键作用拓展成三维超分子化合物。有趣的是配合物存在大量裸露的未配位的N原子,此N原子具有路易斯碱性质,能与路易斯酸性质的Ag⁺有效结合,从而引起配合物的荧光猝灭。该性质能在无色溶液中有效检测10^-4~10^-6 mol·L^-1范围内的痕量Ag⁺离子。     

A New Manganese Coordination Polymer Based on Azobenzene Tetracarboxylate and Auxiliary Pyridine Ligand: Synthesis,Crystal Structure and Magnetic Property

A new manganese coordination polymer(CP)has been synthesized under hydrothermal conditions.It’s formula is{Mn2(Oaobtc)(bpe)(H₂O)₄]}n,where H4Oobtc represents oxide azobenzene 2,2',3,3'-tetracarboxyl acid,and bpe is 1,2-bis(4-pyridine)ethylene.It was characterized by elemental analysis,infrared spectrum and X-ray single-crystal diffraction.The coordination polymer crystallizes in the monoclinic system,space group P2₁/c.The central ion was coordinated with H₄Oobtc ligands using bridging model,and carboxylic group connects two adjacent Mn(Ⅱ)ions into dimer units.The oxygen from carboxylates connect these dimer units into a one-dimensional(1D)chain,and N atoms from the bpe further expanded them into three-dimensional(3D)supramolecular edifice,eventually.Variable-temperature magnetic measurements of CP 1 indicate the presence of weak antiferromagnetic exchange between two nearest Mn(Ⅱ)ions with J=–0.367 cm^-1.     

Self-reciprocal and self-conjugate-reciprocal irreducible factors of xn − λ and their applications

In this paper, we present some necessary and sufficient conditions under which an irreducible polynomial is self-reciprocal (SR) or self-conjugate-reciprocal (SCR). By these characterizations, we obtain some enumeration formulas of SR and SCR irreducible factors of $x^n-\lambda$, $\lambda \in {\mathbb{F}}_q^{⁎}$, over ${\mathbb{F}}_q$, which are just open questions posed by Boripan et al. (2019). We also count the numbers of Euclidean and Hermitian LCD constacyclic codes and show some well-known results on Euclidean and Hermitian self-dual constacyclic codes in a simple and direct way.     

Permutation trinomials over Fq3

We consider four classes of polynomials over the fields ${\mathbb{F}}_{q^3}$, $q=p^h$, $p>3$, $f_1(x)=x^{q^2+q-1}+A{x}^{q^2-q+1}+Bx$, $f_2(x)=x^{q^2+q-1}+A{x}^{q^3-q^2+q}+Bx$, $f_3(x)=x^{q^2+q-1}+A{x}^{q^2}-Bx$, $f_4(x)=x^{q^2+q-1}+A{x}^q-Bx$, where $A,B\in {\mathbb{F}}_q$. We find sufficient conditions on the pairs $(A,B)$ for which these polynomials permute ${\mathbb{F}}_{q^3}$ and we give lower bounds on the number of such pairs.     

基于氮氧自由基配体的锰和钴双核配合物的分子结构和磁性

合成了2个基于氮氧自由基配体且结构类似的双核配位化合物,其分子式分别为[Mn₂(hfac)₄(NIT-mo-pmy)₂](1)和[CO₂(hfac)₄(NIT-mo-pmy)₂](2),其中hfac=六氟乙酰丙酮,NIT-mo-pmy=2-(2-甲氧基-5′-嘧啶基)-4,4,5,5-四甲基咪唑啉基-3-氧-1-氧自由基。2个配合物均属于三斜晶系P1空间群,其双核配位单元进一步构筑为中心对称的平行四边形分子阵列。变温磁化率的测试表明,在2个配合物中,中心离子和氮氧自由基单元之间存在反铁磁交换作用。借助构效关系研究,分析了磁作用强度的差异。通过适当近似的磁化学模型,对Mn(Ⅱ)配合物的磁性行为进行了定量拟合,并与相关化合物磁作用强度进行了比对、分析。     

Two Carboxylato-bridged Binuclear Cobalt(Ⅱ) Complexes Pillared Coligands: Synthesis,Structures and Magnetic Properties

By adopting mixed-ligand strategy, two Co(Ⅱ) coordination polymers, [Co(phda)(itmb)(H_2O)_2]_n(1) and [Co(phda)(Hpytz)]_n(2)(H_2phda = 1,2-phenylenediacetate, itmb = 1-(imidazo-1-ly)-4-(1,2,4-triazol-1-yl methyl) benzene and Hpytz = 3,5-di(4-pyridyl)-1,2,4-triazolate), were hydrothermally synthesized and then characterized by elemental analysis, IR spectroscopy, thermogravimetric analysis(TGA), powder X-ray diffraction(PXRD) and single-crystal X-ray diffraction. The single-crystal X-ray diffraction reveals that two complexes feature carboxylato-bridged binuclear subunits extended further by the nitrogen-rich coligands to form different structures. Complex 1 containing phda-bridged binuclear cobalt is developed by itmb coligand to 1D double-stranded chain, whereas complex 2 exhibits 2D open bilayers, which result from the ribbon-like carboxylate chains pillared Hpytz coligands. In addition, the magnetic susceptibilities of both compounds were measured over the temperature range of 3～300 K, and the data were analyzed well using Mag Saki software. The best fitting parameters were κ = 0.98, λ =-100 cm~(-1), ? = 588 cm~(-1) and J = 0.6 cm~(-1) for complex 1 and κ = 0.86, λ =-110 cm~(-1), ? = 756.8 cm~(-1) and J =-1.25 cm~(-1) for complex 2. The results indicate the existence of weaker ferromagnetic interaction for complex 1 and antiferromagnetic interaction for complex 2 between the metal centers in the dinuclear metal units.     

Two N-donor Auxiliary Ligands Mediated Zn(Ⅱ) Coordination Polymers Incorporating 5-Nitro-1,2,3-benzenetricarboxylate Ligand: Syntheses,Crystal Structures,and Luminescent Properties

Two N-donor auxiliary ligands mediated Zn(Ⅱ) coordination polymers, namely, {[Zn(Hnbta)-(bimm)](3H_2O)}_n(1) and {[Zn_(1.5)(nbta)(pyim)(H_2O)](2H_2O)}_n(2)(H_3nbta = 5-nitro-1,2,3-benzenetricarboxylic acid, bimm = bis(imidazol-1-yl)methane and pyim = N-(4-pyridylmethyl)imidazole), have been prepared by the hydrothermal reaction. Their structures were determined by single-crystal X-ray diffraction analysis, elemental analyses and infrared spectra. Compound 1 possesses a one-dimensional(1D) chain structure, while compound 2 features a two-dimensional(2D) network. In addition, they both exhibit high thermal stabilities and photoluminescent properties in the solid, and can be explored as potential luminescent materials.     

Synergistic effect and mechanisms of ultrasound and AlOOH suspension on Al hydrolysis for hydrogen production

Ultrasound can accelerate and change the reaction process and is widely used in the field of hydrogen production and storage. In this study, ultrasound (US) and AlOOH suspension (AH) are used to promote hydrogen production from Al hydrolysis. The results indicate that both US and AH greatly shorten the induction time and enhance the hydrogen production rate and yield. The promoting effect of US and AH on Al hydrolysis originates from the acoustic cavitation effect and catalytic effect, respectively. When AH is used in combination with US, Al hydrolysis has the best hydrogen production performance and the hydrogen yield can reach 96.6 % within 1.2 h, because there is a synergistic effect on Al hydrolysis between AH and US. Mechanism analyses reveal that the micro-jets and local high temperature environment arising from acoustic cavitation improve the catalytic activity of AlOOH, while the suspended AlOOH particles enhance the cavitation effect of US. This work provides a novel and feasible method to promote hydrogen production from Al hydrolysis.