On U(n)-invariant strongly convex complex Finsler metrics

Science China Mathematics - In this paper, we obtain a necessary and sufficient condition for a U(n)-invariant complex Finsler metric F on domains in ?n to be strongly convex, which also...     

The induction of PANoptosis in KRAS-mutant pancreatic ductal adenocarcinoma cells by a multispecific platinum complex

Science China Chemistry - Oncogenic KRAS reprograms pancreatic ductal adenocarcinoma (PDAC) cells to a state that is awfully resistant to apoptosis. An alternative coping strategy is to trigger a...     

Multi-emissive 1D Cd(II) polymers with a biphenyl bridged bisazamacrocycle for ratiometric discrimination of nitroaromatics and selective visual detection of picric acid

Three one-dimensional ladder-like coordination polymers consisting of Cd₆ metalloring as the building unit, {[Cd₄LCl₄]·3H₂O}_n ( 1 ), {[Cd₃L(ClO₄)(H₂O)]ClO₄·3H₂O}_n ( 2 ), and {[Cd₆(L)₂(NO₃)₂(CH₃OH)(H₂O)](NO₃)₂·2CH₃OH·5H₂O}_n ( 3 ), were solvothermally constructed from a carboxylic functionalized bisazamacrocyclic ligand 4,4′-bis((4,7-bis(2-carboxyethyl)-1,4,7-triazacyclonon-1-yl)methyl)-1,1′-biphenyl (H₄L). These compounds dispersed in ethanol show the multiple emissions originating from the monomeric and intramolecularly overlapping biphenyl moieties which could be sensitively quenched by picric acid (PA) and 4-nitrophenol (4-NP) through the effective fluorescence resonance energy transfer process. The differential fluorescent responses of each compound on exposure to PA and 4-NP individually make the convenient ratiometric discrimination of two analytes based on the fluorescent intensity ratio (I₃₂₀/I₃₆₀) attainable, and 1 and 2 as ratiometric chemosensors for PA present a broad linear detection range from 4 to 300 μM with detection limits of 0.84 and 0.93 μM, respectively. Furthermore, the blue light emission of 1 under an ultraviolet lamp could be selectively quenched by PA even in the presence of all other interfering nitroaromatic pollutants, which empowers the fast visual detection of PA by naked eye.     

Self-supported metal sulphide nanocrystals-assembled nanosheets on carbon paper as efficient counter electrodes for quantum-dot-sensitized solar cells

Developing efficient counter electrodes (CEs) and quantum dots made of earth-abundant and non-toxic elements is essential but still challenging for quantum dot-sensitized solar cells (QDSSCs). Here, we report a facile strategy to prepare self-supported and robust CoS₂ and NiS nanocrystals-assembled nanosheets directly grown on carbon paper (MSx NS@CP) as efficient counter electrodes for QDSSCs. Such CEs integrate the merits of fast electron transfer from interconnected conductive scaffold, efficient mass transfer from hierarchically vertical nanosheet on 3D open substrate, as well as abundant highly active catalytic sites from metal sulphide nanocrystal units. As a result, QDDSCs based on such CoS₂ NS@CP and NiS NS@CP CEs achieve a PCE of 8.88% and 7.53%, respectively. The detailed analyses suggest that CoS₂ NS@CP has the highest catalytic activity and shows the lowest charger transfer resistance, leading to the highest PCE. These findings may inspire the design and exploration of other self-supported efficient CEs by integrating highly active catalysts onto 3D conductive networks for efficient QDSSCs.     

~(236)U Multi-modal Fission Paths on a Five-dimensional Deformation Surface

In this paper, we develop a new path search algorithm which considers all the degrees of freedom and apply it on our calculated five-dimensional potential energy surface(PES) of~(236) U. Asymmetric and symmetric fission paths and barriers are obtained.     

Preparation of stable and superior flux GO/LDH/PDA‐based nanofiltration membranes through electrostatic self‐assembly for dye purification

Graphene oxide (GO) has triggered significant attention as a new type of self‐assembly membrane material. However, the low filtration flux and unstable performance of GO membrane limit its practical application. Hence, in this work, layered double hydroxides (LDHs), as a 2D material with double‐layer channel structure and positive electricity, were self‐assembled with GO at weight ratio of 7:3 by electrostatic interaction. Then, the GO/LDH hybrids combined with polydopamine (PDA) to obtain stable and high‐flux GO‐based membranes through vacuum filtration and the structure and morphology of as‐prepared samples were characterized by FT‐IR, XRD, XPS, and SEM. Furthermore, the separation performance and surface electronegativity of membranes were tested via pure water flux, rejection efficiency, recycle experiments, and zeta potential. Results revealed that the stability and flux of composite membrane were enhanced significantly compared with neat GO‐based membrane. Further, the dye rejection rate of methylene blue (MB) is higher than Congo red (CR) and rhodamine B (Rh B) and reached to 99.8%.     

Elucidating Molecule–Plasmon Interactions in Nanocavities with 2 nm Spatial Resolution and at the Single‐Molecule Level

The fundamental understanding of the subtle interactions between molecules and plasmons is of great significance for the development of plasmon‐enhanced spectroscopy (PES) techniques with ultrahigh sensitivity. However, this information has been elusive due to the complex mechanisms and difficulty in reliably constructing and precisely controlling interactions in well‐defined plasmonic systems. Herein, the interactions in plasmonic nanocavities of film‐coupled metallic nanocubes (NCs) are investigated. Through engineering the spacer layer, molecule–plasmon interactions were precisely controlled and resolved within 2 nm. Efficient energy exchange interactions between the NCs and the surface within the 1–2 nm range are demonstrated. Additionally, optical dressed molecular excited states with a huge Lamb shift of ≈7 meV at the single‐molecule (SM) level were observed. This work provides a basis for understanding the underlying molecule–plasmon interaction, paving the way for fully manipulating light–matter interactions at the nanoscale.     

可获得高分辨率谱线信息的新型太阳极紫外成像仪

极紫外光谱观测和诊断是研究太阳大气基本物理过程的最重要手段之一。但因为波长短，很多可见光仪器的设计方案不再适用，且极紫外观测只能在太空中开展。国际上现有卫星上的太阳极紫外成像仪和光谱仪都有各自的不足，比如极紫外成像仪不能获得高光谱分辨率的谱线信息；狭缝式光谱仪通过扫描可得到活动区域的信息，但扫描时间过长，对于研究剧烈变化的太阳活动有很大的局限性。这些不足制约了对日冕物质抛射(CME)和耀斑等太阳活动的高精度观测及对其机理的研究：无法看到CME在内日冕的加速过程，而且无法将可见光看到的CME现象同极紫外看到的日面源区直接联系；缺少观测目标的视向速度信息，难以识别CME的触发过程。采用多级衍射成像方式的一种新型太阳极紫外成像仪，除实现传统极紫外成像仪功能外，还可以在太阳活动变化过程中同步获得全日面各区域的光谱信息。新型成像仪可以得到高光谱分辨率数据，用于反演低日冕的等离子体视向速度，获得全日面的速度分布，与同时得到的高空间分辨率图像相结合，可以识别太阳活动现象对应的物质运动, 为空间科学研究提供数据；因为没有狭缝和运动部件，可以实现对大视场的太阳活动区域的高时间分辨率成像，有利于捕捉日面活动的快速变化。新型成像仪采用无狭缝光谱分光成像的设计理念，即同一时间把一定光谱带宽的信息记录到一个二维的图像上，此过程可以看成是从某一个角度将空间和光谱数据立方体投影到一个面上，然后再利用反演得到空间分辨图像和光谱信息。多级光谱成像的光学设计与传统光谱仪最大的不同是其不存在逐行扫描的狭缝，这使得其能够同时获得大视场内太阳的空间信息和光谱信息。因为极紫外波段的特殊性，以及本仪器面向卫星遥感应用，不可能像可见光波段或者医用CT机一样实现很多衍射级的同时成像。因此，新型极紫外成像仪光学系统由反射镜、色散光栅和五个探测器组成，入射的太阳极紫外辐射经过光栅色散后分别由五个级次的探测器接收，其中四个探测器分部接收±1和±2衍射级图像，另外一个接收0级图像。空间信息可以直接从0级图像得到，而光谱信息则需要根据五个级次成像的反演结果得出。介绍了光学系统的设计以及反演算法，并分析了反演算法的误差。光路基于变间距光栅设计，可实现空间分辨率1.8 arcsec·pixel-1, 光谱分辨率7.8×10-3 nm·pixel-1，同时减小了体积和重量，适合空间应用。     

A Concise Total Synthesis of (−)‐Himalensine A

The daphniphyllum alkaloids are a structurally fascinating and remarkably diverse family of natural products. General strategies for the chemical synthesis of their challenging architectures are highly desirable for efficiently accessing these intriguing alkaloids and addressing their pharmaceutical potential. Herein, a concise strategy designed to provide general and diversifiable access to various daphniphyllum alkaloids is described and utilized in the asymmetric synthesis of (?)‐himalensine A, which was accomplished in 14 steps. Key features of this strategy include a Cu‐catalyzed nitrile hydration, a Heck reaction to construct the challenging 2‐azabicyclo[3.3.1]nonane motif, a Meinwald rearrangement reaction, six, pot‐economic reactions, and the minimal use of protecting groups, which significantly improved the overall synthetic efficiency.     

Recent advances on iron-catalyzed coupling reactions involving organolithium reagents

Several iron-catalyzed cross- and homo-coupling reactions involving organolithiums were developed to form diverse carbon-carbon bonds. The usefulness of this protocol was demonstrated by producing gram-scale products in good yields.