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排序方式: 共有1330条查询结果,搜索用时 31 毫秒
71.
Yingying Wang Zhuangdong Yuan Yunjie Guo Xuxiao Ma Zitong Meng Jingquan Sha Haifeng Zhang 《无机化学与普通化学杂志》2020,646(20):1696-1701
Two dinuclear LnIII-based clusters, namely [Dy2L2(NO3)2(DME)4] ( 1 ) and [Gd2L2(NO3)2(DME)4] ( 2 ) [H2L = (E)-2-((2-hydroxybenzylidene)amino)phenol] were obtained under hydrothermal condition. Two LnIII ions are bridged by two phenolic hydroxyl oxygen atoms, and the distances of them are 3.829 Å (Dy1–Dy1A) and 3.860 Å (Gd1–Gd1A). Two Dy1–O–Dy1A and Gd1–O–Gd1A angles are 109.4° and 109.8°, respectively. Magnetic studies reveal a weak antiferromagnetic interaction between Gd ions in complex 2 , and single-molecule magnet behavior for 1 with Ueff = 49.9 K and τ0 = 1.54 × 10–6 s. 相似文献
72.
Guangxian Su Dr. Qizhao Li Dr. Masatoshi Ishida Dr. Chengjie Li Dr. Feng Sha Prof. Dr. Xin-Yan Wu Lu Wang Dr. Glib Baryshnikov Prof. Dr. Dawei Li Prof. Dr. Hans Ågren Prof. Dr. Hiroyuki Furuta Prof. Dr. Yongshu Xie 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(4):1553-1557
An N-confused phlorin isomer bearing a dipyrrin moiety at the α-position of the confused pyrrole ring ( 1 ) was synthesized. PdII and BIII coordination at the peripheral prodigiosin-like moiety of 1 afforded the corresponding complexes 2 and 3 . Reflux of 2 in triethylamine (TEA) converted the meso-phenyl into the PdII-coordinating phenoxy group to afford 4 . Under the same reaction conditions, TEA was linked to the α-position of the dipyrrin unit in 3 as an N,N-diethylaminovinyl group to afford 5 . Furthermore, peripheral coordination of BIII in 3 and 5 improved the planarity of the phlorin macrocycle and thus facilitated the coordination of AgIII at the inner cavity to afford 3-Ag and 5-Ag , respectively. These results provide an effective approach for developing unique porphyrinoids through peripheral coordination. 相似文献
73.
水滑石(LDHs)是一种阴离子黏土材料,由于其主体层板厚度的可调性,使其在光/电催化、电池、超级电容器、传感器以及生物医药等领域都具有广泛应用。降低层厚至单层可使材料的物理化学性质发生根本改变,从而优化催化性能。近期研究表明,利用自上而下,自下而上的方法,可以实现单层LDHs类材料的合成,但是受限于产量(g级)以及成本设备等问题,目前规模化制备高质量单层LDHs类材料还没有工业案例。成核晶化隔离法是目前唯一规模化合成纳米LDHs的工业化方法,具有成本低,产量可吨级放大等优点。本综述从合成方法、表征手段、应用三个角度讨论了单层及超薄LDHs的精准调控,详细论述了近期关于单层及超薄LDHs合成突破以及LDHs的规模化生产进展,并对其性能进行了总结,为后续设计高性能单层LDHs提供思路。 相似文献
74.
75.
Kai Wu Kang Li Sha Chen Ya‐Jun Hou Yu‐Lin Lu Jing‐Si Wang Mei‐Juan Wei Mei Pan Cheng‐Yong Su 《Angewandte Chemie (International ed. in English)》2020,59(7):2639-2643
A nanocage coupling effect from a redox RuII‐PdII metal–organic cage (MOC‐16) is demonstrated for efficient photochemical H2 production by virtue of redox–guest modulation of the photo‐induced electron transfer (PET) process. Through coupling with photoredox cycle of MOC‐16, tetrathiafulvalene (TTF) guests act as electron relay mediator to improve the overall electron transfer efficiency in the host–guest system in a long‐time scale, leading to significant promotion of visible‐light driven H2 evolution. By contrast, the presence of larger TTF‐derivatives in bulk solution without host–guest interactions results in interference with PET process of MOC‐16, leading to inefficient H2 evolution. Such interaction provides an example to understand the interplay between the redox‐active nanocage and guest for optimization of redox events and photocatalytic activities in a confined chemical nanoenvironment. 相似文献
76.
Chen Sun Ya‐Hui Guo Sha‐Sha Han Jing‐Zhao Li Kuan Jiang Lin‐Feng Dong Qi‐Long Liu Cheng‐Yang Yue Xiao‐Wu Lei 《Angewandte Chemie (International ed. in English)》2020,59(38):16465-16469
Considering the instability and low photoluminescence quantum yield (PLQY) of blue‐emitting perovskites, it is still challenging and attractive to construct single crystalline hybrid lead halides with highly stable and efficient blue light emission. Herein, by rationally introducing d10 transition metal into single lead halide as new structural building unit and optical emitting center, we prepared a bimetallic halide of [(NH4)2]CuPbBr5 with new type of three‐dimensional (3D) anionic framework. [(NH4)2]CuPbBr5 exhibits strong band‐edge blue emission (441 nm) with a high PLQY of 32 % upon excitation with UV light. Detailed photophysical studies indicate [(NH4)2]CuPbBr5 also displays broadband red light emissions derived from self‐trapped states. Furthermore, the 3D framework features high structural and optical stabilities at extreme environments during at least three years. To our best knowledge, this work represents the first 3D non‐perovskite bimetallic halide with highly efficient and stable blue light emission. 相似文献
77.
Wen-Jie Shi Dan Liu Xin Li Dr. Sha Bai Prof. Yao-Yu Wang Prof. Dr. Ying-Feng Han 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(29):7853-7861
The incorporation of functional groups into the cavity of discrete supramolecular coordination cages (SCCs) will bring unique functions and applications. Here, three dicarboxylate ligands (H2 L1 Cl, H2 L2 Cl and H2 L3 Cl) containing N-heterocyclic carbene (NHC) precursors as linkers were introduced to construct SCCs by combining with two C3-symmertic (CpZr)3(μ3-O)(μ2-OH)3 clusters as three-connect vertices, resulted in a series of rugby-like V2E3 (V=vertex, E=edge) type homoleptic cages ( SCC-1 , SCC-2 and SCC-3 ). However, V4E6-type tetrahedral cages ( SCC-4 and SCC-5 ), incorporating six Au-NHC moieties, were obtained when the corresponding NHC-gold(I) functionalized ligands (H2 L1 Au, H2 L2 Au) were applied. For the first time, we present a trackable CpZr-involved cage to cage conversion to generate a heteroleptic V2E3 cage ( SCC-6 ) from two homoleptic cages ( SCC-2 and SCC-5 ) with different geometries of V2E3 and V4E6. The heteroleptic assembly SCC-6 can also be formed upon a subcomponent displacement strategy. The structural transformation and reassembly processes were detected and monitored by 1H NMR spectroscopy and electrospray-ionization mass spectrometry. The formation of heteroleptic assembly was further supported by single crystal X-ray diffraction analysis. Moreover, homoleptic cage SCC-2 possesses a trigonal bipyramidal cationic cavity allowing the encapsulation of a series of sulfonate anionic guests. 相似文献
78.
A local gradient estimate for positive solutions of porous medium equations on complete noncompact Riemannian manifolds under the Ricci flow is derived. Moreover, a global gradient estimate for such equations on compact Riemannian manifolds is also obtained. 相似文献
79.
Theoretical Analysis of Interference Nanolithography of Surface Plasmon Polaritons without a Match Layer
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Interference nanolithography techniques based on long-range surface plasmon polaritons (LR-SPP) are hardly ever achieved by experiments at present. One key reason is that suitable liquid materials are difflcult to find as the match layer connects the metal film and the resist. We redesign a Kretschmann-Raether structure for interference lithography. A polymer layer is coated under the metal film, and an air layer is placed between the polymer layer and the resist layer. This design not only avoids the above-mentioned question of the match layer, but also can form a soft contact between the polymer layer and the resist layer and can protect the exposure pattern. Simulation results confirm that a device with an appropriately thick polymer layer can form high intensity and contrast interference fringes with a critical dimension of about λ/7 in the resist. In addition, the fabrication of the device is very easy. 相似文献
80.
Total syntheses of nine novel phospholipids were accomplished to facilitate the identification and biological testing of compounds that are generated upon oxidative cleavage of arachidonate and linoleate esters of 2-lysophosphatidylcholine, the two most abundant polyunsaturated phospholipids in low-density lipoprotein. An efficient general synthesis exploiting 2-lithiofuran as a 4-oxo-2-butenoyl carbanion equivalent provided phospholipids containing gamma-keto-alpha,beta-unsaturated carbonyl functional arrays. By exploiting facile cis-trans isomerizations, two commercially available cis alkenes, (2Z)-2-butene-1,4-diol and 2,5-dihydrofuran, could be employed as starting materials for preparing the Horner-Wadsworth-Emmons reagent 4-(diethoxyphosphoryl)-2E-butenal, a valuable building block for the synthesis of 2,4-dienals. The reagent was exploited in a total synthesis of 13-oxotridec-9E,11E-dienoic acid, confirming the identity of this product that is generated upon autoxidation of linoleic acid and by decomposition of 13-hydroperoxy-9,11-octadecadienoate (13-HPODE), especially in the presence of redox active transition metal ions, cytochrome p-450, or hydroperoxide lyase. 相似文献