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951.
952.
A Selective RhI‐Catalyzed Substrate‐Controlled C−C Bond Activation of Benzyl Sulfonamide/Alcohol‐Tethered Alkylidenecyclopropanes 下载免费PDF全文
Kai Chen Jia‐Xin Liu Dr. Xiang‐Ying Tang Prof. Min Shi 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(33):11549-11553
Benzyl sulfonamide/alcohol‐tethered alkylidenecyclopropanes undergo a rhodium‐catalyzed and substrate‐controlled selective C?C bond activation, producing three types of common organic structural units: benzo[c]azepine/oxepines, dihydronaphthalen‐1‐amines, and conjugated dienes. Epoxidation and aromatization of these products to construct two useful compounds have also been achieved. 相似文献
953.
Rational Design of an Ultrasensitive and Highly Selective Chemodosimeter by a Dual Quenching Mechanism for Cysteine Based on a Facile Michael‐Transcyclization Cascade Reaction 下载免费PDF全文
Xiangmin Li Yongjun Zheng Hongjuan Tong Rui Qian Dr. Lin Zhou Prof. Dr. Guixia Liu Prof. Dr. Yun Tang Prof. Dr. Hao Li Prof. Dr. Kaiyan Lou Prof. Dr. Wei Wang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(27):9247-9256
Differentiation of biologically important thiols, such as cysteine (Cys), homocysteine (Hcy), and glutathione (GSH) is still a challenging task. Herein, we present a novel fluorescent chemodosimeter capable of selectively detecting Cys over other biothiols including Hcy and GSH and other amino acids by a facile thiol‐Michael addition/transcyclization rearrangement cascade click process. The unique transcyclization step is critical for the selectivity as a result of the kinetically favorable formation of a six‐membered ring with the Cys Michael adduct. Moreover, the probe adopts a distinctive dual quenching mechanism—photoinduced electron transfer (PET) and photoinduced intramolecular charge transfer (ICT) to deliver a drastic turn‐on fluorescence response only at the Cys‐selective transcylization step. The judicious selection of strong electron‐withdrawing naphthalimide fluorophore with maleimide group enhances the electrophilicity and thus reactivity for the cascade process leading to fast detection and ultrasensitivity with a detection limit of 2.0 nm (S/N=3). The probe has demonstrated its practical utility potential in Cys imaging in live cells. 相似文献
954.
L LinHui Ye YanLin Jiang DongXing Hua Hui Zheng Tao Li ZhiHuan Ge YuCheng Li XiangQing Lou JianLing Cao ZhongXin Song YuShou Xiao Jun Li QiTe Qiao Rui You HaiBo Chen RuiJiu Xu HuShan Wang JianSong Guo ZhongYan Zhang XueYing Li Chen Hu ZhengGuo Chen RuoFu Wang Meng Xu ZhiGuo Yue Ke Tang Bin Zang YongDong Zhang XueHeng Yao XiangWu Chen JinDa Bai Zhen 《中国科学:物理学 力学 天文学(英文版)》2011,54(1):136-140
Knockout reaction experiment was carried out by using the 6He beams at 61.2 MeV/u impinging on a CH2 target. The α core fragments at forward angles were detected in coincidence with the recoiled protons at larger angles. From this exclusive measurement the valence nucleon knockout mechanism and the core knockout mechanism can be distinguished by the relation between the polar angles of the core fragments and the recoiled protons, respectively. It is demonstrated that the core knockout mechanism may result in some strong contamination to the real invariant mass spectrum.
相似文献955.
High‐Loading Nano‐SnO2 Encapsulated in situ in Three‐Dimensional Rigid Porous Carbon for Superior Lithium‐Ion Batteries 下载免费PDF全文
Hairong Xue Dr. Jianqing Zhao Jing Tang Hao Gong Prof. Ping He Prof. Haoshen Zhou Prof. Yusuke Yamauchi Prof. Jianping He 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(14):4915-4923
Tin oxide nanoparticles (SnO2 NPs) have been encapsulated in situ in a three‐dimensional ordered space structure. Within this composite, ordered mesoporous carbon (OMC) acts as a carbon framework showing a desirable ordered mesoporous structure with an average pore size (≈6 nm) and a high surface area (470.3 m2 g?1), and the SnO2 NPs (≈10 nm) are highly loaded (up to 80 wt %) and homogeneously distributed within the OMC matrix. As an anode material for lithium‐ion batteries, a SnO2@OMC composite material can deliver an initial charge capacity of 943 mAh g?1 and retain 68.9 % of the initial capacity after 50 cycles at a current density of 50 mA g?1, even exhibit a capacity of 503 mA h g?1 after 100 cycles at 160 mA g?1. In situ encapsulation of the SnO2 NPs within an OMC framework contributes to a higher capacity and a better cycling stability and rate capability in comparison with bare OMC and OMC ex situ loaded with SnO2 particles (SnO2/OMC). The significantly improved electrochemical performance of the SnO2@OMC composite can be attributed to the multifunctional OMC matrix, which can facilitate electrolyte infiltration, accelerate charge transfer, and lithium‐ion diffusion, and act as a favorable buffer to release reaction strains for lithiation/delithiation of the SnO2 NPs. 相似文献
956.
Gold‐Catalyzed Fluorination–Hydration: Synthesis of α‐Fluorobenzofuranones from 2‐Alkynylphenol Derivatives 下载免费PDF全文
Qiang Wang Yu Jiang Run Sun Prof. Dr. Xiang‐Ying Tang Prof. Dr. Min Shi 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(41):14739-14745
The AuI‐catalyzed fluorination–hydration of 2‐alkynylphenol derivatives in the presence of Selectfluor [1‐chloromethyl‐4‐fluoro‐1,4‐diazoniabicyclo‐[2.2.2]octane bis(tetrafluoroborate)] has been developed. This method provides straightforward access to α‐fluorobenzofuranones with the construction of C?O, C=O, and C?F bonds in a single step on the basis of an AuI/AuIII redox catalytic cycle. Several control experiments, including the asymmetric variant of this reaction, were also conducted to gain insight into the reaction mechanism. 相似文献
957.
958.
Dr. Jiu Chen Prof. Dr. Qing Tang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(38):9925-9933
The recent successful growth of MoSi2N4 and WSi2N4 monolayers led to the discovery of a new class of the two-dimensional (2D) MA2Z4 materials with no known 3D layered allotropes, which renders great possibilities to integrate diverse properties by proper design of sandwiched “MZ2” building blocks and “A−Z” passivation layers. In this work, the dynamic stability, electronic properties, and surface reactivity of the new MA2Z4 family, in which M is Ti, Zr, Hf, V, Nb, Ta, Cr, Mo, W, A refers to Si or Ge, and Z is N, P or As, is theoretically probed. Among the proposed 54 possible combinations, about 42 compositions are dynamically stable, which vary from non-magnetic, anti-ferromagnetic, to ferromagnetic semiconductors, metals and half-metals. In particular, the VB (V, Nb, Ta) MA2Z4 possesses robust intrinsic ferromagnetism that is essential for spintronics applications. In regard to surface activity, most MA2Z4, particularly N- or P-terminated IVB and VB MA2Z4, have high catalytic potential for hydrogen evolution, and the ▵GH of non-magnetic MA2Z4 is highly correlated to the highest occupied p electronic states of the surface Z atoms. The photocatalytic activity is also evaluated. MoSi2N4 and WSi2N4 within 4 % tensile strain are capable of photocatalytic overall water splitting. The findings indicate the new 2D MA2Z4 family has fascinating properties and possesses strong potential for applications but not limited to electronics, spintronics and catalysts, which will stimulate the interests of experimental synthesis. 相似文献
959.
960.
Fei Lu Mengzhen Wang Na Li Prof. Bo Tang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(21):6422-6434
As an emerging class of inorganic metal oxides, organically functionalized polyoxometalates (POMs) or POM-based nanohybrids have been demonstrated promising potential for the inhibition of various cancer types by the virtue of their diversity in structures and significantly reduced toxicity. This contribution summarizes the latest achievement of POM-based nanomaterials in cancer diagnosis and various therapeutics to put forward our fundamental viewpoints on the design principles of modified POMs based on their application. In addition, major challenges and perspectives in this field are also discussed. We expect that this review will provide a valuable and systematic reference for the further development of POM-based nanomaterials. 相似文献