Amidation,Esterification, and Thioesterification of a Carboxyl‐Functionalized Covalent Organic Framework

Three new post‐synthetic modification reactions, namely amidation, esterification, and thioesterification, were demonstrated on a novel highly crystalline two‐dimensional covalent organic framework (COF), COF‐616, bearing pre‐installed carboxyl groups. The strategy can be used to introduce a large variety of functional groups into COFs and the modifications can be carried out under mild reaction conditions, with high yields, and an easy work‐up protocol. As a proof of concept, various chelating functionalities were successfully incorporated into COF‐616 to yield a family of adsorbents for efficient removal of several contaminants in the water.     

Structure Determination of Alkynyl‐Protected Gold Nanocluster Au22(tBuC≡C)18 and Its Thermochromic Luminescence

An alkynyl‐protected gold nanocluster, Au₂₂(^tBuC≡C)₁₈ ( 1 ), has been synthesized and its structure has been determined by single‐crystal X‐ray diffraction. The molecular structure consists of a Au₁₃ cuboctahedron kernel and three [Au₃(^tBuC≡C)₄] trimeric staples. The cluster 1 has strong luminescence in the solid state with a 15 % quantum yield, and it displays interesting thermochromic luminescence as revealed by temperature‐dependent emission spectra. The enhanced room‐temperature emission is characterized as thermally activated delayed fluorescence.     

Overview of Polyvinyl Alcohol Nanocomposite Hydrogels for Electro‐Skin,Actuator, Supercapacitor and Fuel Cell

The properties of polyvinyl alcohol (PVA) nanocomposite hydrogels influenced by nanoparticles are reviewed. Various kinds of nanoparticles with excellent mechanical and electrical properties have been introduced into PVA hydrogel to produce stretchable and conductive PVA nanocomposite hydrogel. Understanding the mechanism between the matrix of PVA hydrogel and nanoparticles is therefore critical for the development of PVA nanocomposite hydrogels. This review focuses on the nanoparticles include carbon nanotubes, graphene oxide and metal nanoparticles, and describes the effects of nanoparticles on the mechanical and conductive properties of PVA nanocomposite hydrogels. A new promising area of soft stretchable PVA nanocomposite hydrogel is highlighted for possible applications. Finally, a brief outlook for future research is presented.     

Purification and antioxidant capacity analysis of anthocyanin glucoside cinnamic ester isomers from Solanum nigrum fruits

In a recent study, anthocyanins, which have a strong free radical‐scavenging activity, were examined for their potential to effectively prevent cancer. However, clinical trials are limited by the purity of the anthocyanin. Multiple methods are used to extract and purify anthocyanins. Based on previous work on Solanum nigrum, which is a widely distributed plant, in this study, DM130 macroporous resin, Sephadex LH20, and a C18 column were used to separate cis–trans anthocyanin isomers. These anthocyanins constitute the majority of total S. nigrum anthocyanins. The results showed that this “DM130‐LH20‐C18 system” can be used to obtain a cinnamic acid‐derived cis–trans anthocyanin, petunidin‐3‐(p‐coumaroyl)‐rutinoside‐5‐glucoside, with a purity of 98.5%, for effective quantitation. In order to determine the antioxidant ability of the petunidin‐3‐(p‐coumaroyl)‐rutinoside‐5‐glucoside cis–trans isomers, three ordinary methods were adopted. The maximum antioxidant ability of the cis–trans anthocyanin was dozens of times higher than that of vitamin C.     

Correction: Cu-catalyzed C–C bond formation of vinylidene cyclopropanes with carbon nucleophiles

Correction for ‘Cu-catalyzed C–C bond formation of vinylidene cyclopropanes with carbon nucleophiles’ by Jichao Chen et al., Chem. Sci., 2019, 10, 10601–10606.

We regret that in the original article the structure of compound 1 in Tables 1–3 was incorrect. The correct structure is given below.The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.     

Autocatalytic polymerization of selenium/polypyrrole nanocomposites as functional theranostic agents for multi-spectral photoacoustic imaging and photothermal therapy of tumor

The synchronization of diagnosis and treatment is a new trend in cancer treatment. Photoacoustic imaging (PAI) and photothermal therapy (PTT) are recognized as one of the perfect combinations. The autocatalytic polymerization of selenium/polypyrrole (Se@PPy) nanocomposites with a wide-absorption band at near-infrared region (NIR, 800 nm) has been developed in this paper. The wide optical absorption characteristics enable Se@PPy nanocomposites to achieve multi-spectral PAI. Ex vivo experiments show desirable photoacoustic ability of the Se@PPy nanocomposites at wavelengths ranging from 700 nm to 900 nm, which is better than that of commercial indocyanine green (ICG). Se@PPy nanocomposites have high photothermal conversion efficiency up to 36.3% as well as excellent photo-thermal stability. In vitro cytotoxicity test demonstrates that the Se@PPy nanocomposites have good bio-safety. Furthermore, the feasibility of Se@PPy nanocomposites for enhancing multi-spectral PAI guided PTT was verified on 4T1 tumor-bearing nude mice. Our results indicate that Se@PPy nanocomposites could be used as an effective theranostic agent for near-infrared light-mediated PAI and PTT of tumor.     

一个各向异性磁稀释杂化钙钛矿系列[CH3NH3][CoxZn1-x(HCOO)3]

Inorganic-organic or hybrid perovskite materials, which are the complementary counterparts of pure inorganic perovskites, can provide many new opportunities in the researches of phase transitions, critical phenomena, and relevant properties, as they combine the characteristics of inorganic and organic components. Therefore, the hybrid perovskites of ammonium metal formate framework are very promising, and their properties have been found to be strongly dependent on the characteristics of the constituent metal ions and/or ammonium ions. Herein, we used solid solution strategies, borrowed from solid state chemistry, to investigate the anisotropic diluted magnetic hybrid perovskite system of [CH₃NH₃][Co_xZn_1-x(HCOO)₃], wherein the B-sites are occupied by the mixed metal ions of Co²⁺ and Zn²⁺. The solid solution compounds of this series in the range x = 0–1 (or the molar percent Co% = 0–100%) were successfully prepared using conventional solution chemistry methods. The resulting compounds were demonstrated to be iso-structural by using both single-crystal and powder X-ray diffraction analyses. The solid solution crystals belong to the orthorhombic space group Pnma, with the cell parameters being a = 8.3015(2)–8.3207(3) Å, b = 11.6574(4)–11.6811(5) Å, c = 8.1315(3)–8.1427(4) Å, and V = 787.89(5)–790.98(7) ų. The perovskite structure consists of a simple cubic anionic metal-formate framework and CH₃NH₃⁺ cations which are located in the framework cavities, with N―H···O hydrogen bonds formed between the framework and the cation. The members of this series showed negligible changes (< 0.4%) in their respective lattice and structural parameters. Thus, the prepared solid solution compounds constitute good molecule-based examples for the study of magnetic dilution under almost the same structural parameters and molecular geometries. Upon dilution, the magnetization per mole of Co at low temperatures and low fields was suppressed by the magnetic anisotropy of Co²⁺ and gradual destruction of the large spin canting between coupled Co²⁺ ions, in contrast to the magnetization enhancement observed in the isotropic diluted system of [CH₃NH₃][Mn_xZn_1-x(HCOO)₃] with the same perovskite structure. The percolation limit was estimated as (Co%)_P = 27(1)% (or x_P = 0.27(1)) from the magnetic data, which was slightly lower than that predicted by the percolation theory for a simple cubic lattice (31%); this trend was due to the strong magnetic anisotropy of the present system. In addition, rare incommensurate phase transitions were primarily detected below ~120 K for the pure Co and Zn members, which may also affect the magnetic properties of the materials.     

A self-optimizing inverse analysis method for estimation of cyclic elasto-plasticity model parameters

In this paper, a novel inverse analysis methodology call a Self-Optimizing Inverse Method (Self-OPTIM) has been presented, which inversely estimates cyclic elasto-plastic constitutive model parameters using global forces and displacement on the same partial boundaries and full-(or partial-) field displacement data. A novelty of the methodology is that it automatically self-estimates material parameters by updating “full-field” reference stresses and strains through two parallel nonlinear finite element simulations. Although a well-known classical cyclic plasticity model is chosen in this paper, it must be emphasized that the proposed Self-OPTIM method is a model-independent method, which means that any advanced model can be naturally integrated with the proposed methodology. Thus, using numerically generated test data of low-carbon steel specimens (AISI 1010), the proposed Self-OPTIM method has been verified showing its successful performance to estimate nonlinear isotropic and kinematic hardening parameters, yield stress, Young’s modulus and Poisson ratio. The effects of experimental noises from CCD camera and measurement errors of the boundary forces are also investigated for the Self-OPTIM method.     

平面张弦结构抗连续倒塌的动力分析

杆件由于爆炸、腐蚀等发生脆性破坏后引起剩余结构的振动和压杆由于失稳过程中的弹性突跳（Snap-through）引起的相邻结构振动是张弦结构倒塌过程中常伴生的两种动力现象。本文对第一种动力响应产生的原因、失效构件的模拟方法进行了分析,说明进行张弦结构抗连续倒塌的动力分析应采用初始条件法模拟构件的失效。根据张弦结构的特点,从构件失效和结构失效两方面提出了张弦结构倒塌失效的评估准则,并采用变换荷载路径法通过静力连续倒塌分析找出张弦结构各部分的关键构件;然后采用初始条件法按考虑几何非线性、阻尼比、材料非线性等分别模拟这些关键构件失效引起的动力响应,得到了平面张弦结构各部分构件失效的动力特性、动力放大系数和失效构件的位置,并对不同失效时间进行动力响应分析得到张弦结构动力效应与构件失效时间的关系曲线。最后给出张弦结构进行抗连续倒塌分析的一些结论和建议,如进行连续倒塌动力时程分析时初始失效杆件选取和失效时间取值以及弹性动力放大系数与塑性动力放大系数的区别等,为张弦结构的抗连续倒塌设计提供技术支持和参考。     

A full-duplex radio-over-fiber link with 12-tupling mm-wave generation and wavelength reuse for upstream signal

A full-duplex radio-over-fiber (RoF) link with a novel scheme to generate 60 GHz mm-waves from a 5 GHz RF signal source is investigated. In the RoF downlink, the required frequency of the RF oscillator is reduced greatly. Since the optical carrier is not modulated by downstream data, part of it is reused to carry upstream data and the upstream data is transmitted to the central station using optical single-sideband modulation. In this way, a single wavelength is used for both downstream and upstream transmissions. Based on this scheme, a full-duplex RoF link is built and its transmission performance is analyzed. Theoretical analysis and numerical simulation show that the downstream signal cannot only eliminate code form distortion caused by time shift of the code edges, but also reduce the influence of the fading effect as the 60 GHz DSB optical mm-wave signal is transmitted along the fiber, and the upstream signal is immune to both fading effect and time shift of the code edges.