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111.
Weidong Shang Sheng‐Nan Su Rong Shi Ze‐Dong Mou Guo‐Qiang Yu Xia Zhang Dawen Niu 《Angewandte Chemie (International ed. in English)》2021,60(1):385-390
We here report glycosyl sulfoxides appended with an aryl iodide moiety as readily available, air and moisture stable precursors to glycosyl radicals. These glycosyl sulfoxides could be converted to glycosyl radicals by way of a rapid and efficient intramolecular radical substitution event. The use of this type of precursors enabled the synthesis of various complex C‐linked glycoconjugates under mild conditions. This reaction could be performed in aqueous media and is amenable to the synthesis of glycopeptidomimetics and carbohydrate‐DNA conjugates. 相似文献
112.
José Carlos Velasco Calderón Shang Jiang Prof. Dr. Samir H. Mushrif 《Chemphyschem》2021,22(21):2222-2230
The addition of aprotic solvents results in higher reactivities and selectivities in many key aqueous phase biomass reactions, including the acid-catalyzed conversion of fructose to 5-hydroxyl methyl furfural (HMF). The addition of certain co-solvents inhibits the formation of humins via preferential solvation of key functional groups and can alter reaction kinetics. An important factor in this context is the relative stability of the hydronium ion (the catalyst) in the vicinity of the biomass moiety as compared to that in bulk, as it could determine its efficacy in the protonation step. Hence, in the present work, molecular dynamics (MD) simulations of HMF (the model product) and fructose (the model reactant) in acidic water and water-DMSO mixtures are performed to analyze their interaction with the hydronium ions. We show that the presence of DMSO favors the interaction of the hydronium ion with fructose, whereas it has a detrimental effect on the interaction of hydronium ion with HMF. Well-tempered metadynamics (WT-MTD) simulations are performed to determine the relative stability of the hydronium ion in the immediate vicinity of fructose and HMF, as compared to that in the bulk solvent phase, as a function of solvent composition. We find that DMSO improves the stabilization of the hydronium ions in the first solvation shell of fructose compared to that in the bulk solvent. On the other hand, hydronium ions become less stable in the immediate vicinity of HMF, as the concentration of DMSO increases. 相似文献
113.
Yan Meng Ding Congcong Shu Xiaoyan Liu Yi Yang Jingjun Wei Guilin Zhang Zhentao Xie Yi Lu Xirui 《Journal of Radioanalytical and Nuclear Chemistry》2021,329(1):401-410
Journal of Radioanalytical and Nuclear Chemistry - To long-term immobilization of secondary iodine-waste, iodine loaded silver-coated silica-gel (AgIs), glass-powder was used to directly solidify... 相似文献
114.
115.
WIA-PA协议是一种新型工业级无线传感器网络国际标准。当WIA-PA网络内节点数目增多时,传统的参考广播同步算法RBS以及改进型ERBS算法网络开销非常大。针对这一严峻的问题,提出了一种能量有效的局部最优时间同步算法。该算法对相邻的接收节点在多个参考广播消息的条件下求取平均相位偏差,然后对此平均相位偏差进行最大后验估计,最后根据此估计值调整本地时钟。仿真结果表明,本文所提时间同步算法在同步精度方面比RBS约提高168%,比ERBS约提高24%;同时,同步过程中的网络能耗也大大减少。 相似文献
116.
采用固相反应法制备了系列样品TixNi1-xFe2O4 (x=0.0, 0.1, 0.2, 0.3, 0.4). 室温下的X射线衍射谱表明样品全部为(A)[B]2O4型单相立方尖晶石结构, 属于空间群Fd3m. 样品的晶格常数随Ti掺杂量的增加而增大. 样品在10 K温度下的比饱和磁化强度σS随着Ti掺杂量x的增加逐渐减小. 研究发现, 当Ti掺杂量x≥ 0.2时, 磁化强度σ随温度T的变化曲线出现两个转变温度TL和TN. 当温度低于TN时, 磁化强度明显减小; 当温度达到TN时, dσ/dT具有最大值. σ-T曲线的这些特征表明, 由于Ti掺杂在样品中出现了附加的反铁磁结构. 这说明样品中的Ti离子不是无磁性的+4价离子, 而是以+2和+3价态存在, 其离子磁矩的方向与Fe和Ni离子的磁矩方向相反. 利用本课题组提出的量子力学方势垒模型拟合样品在10 K温度下的磁矩, 得到了Ti, Fe和Ni三种阳离子在(A)位和[B]位的分布情况, 并发现在所有掺杂样品中, 80%的Ti离子以+2价态占据尖晶石结构的[B]位. 相似文献
117.
118.
Fault tolerant deterministic secure quantum communication using logical Bell states against collective noise
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This study proposes two novel fault tolerant deterministic secure quantum communication(DSQC) schemes resistant to collective noise using logical Bell states. Either DSQC scheme is constructed based on a new coding function, which is designed by exploiting the property of the corresponding logical Bell states immune to collective-dephasing noise and collective-rotation noise, respectively. The secret message can be encoded by two simple unitary operations and decoded by merely performing Bell measurements, which can make the proposed scheme more convenient in practical applications.Moreover, the strategy of one-step quanta transmission, together with the technique of decoy logical qubits checking not only reduces the influence of other noise existing in a quantum channel, but also guarantees the security of the communication between two legitimate users. The final analysis shows that the proposed schemes are feasible and robust against various well-known attacks over the collective noise channel. 相似文献
119.
Xian‐Kai Wan Shang‐Fu Yuan Zhi‐Wei Lin Prof. Dr. Quan‐Ming Wang 《Angewandte Chemie (International ed. in English)》2014,53(11):2923-2926
The chirality of a gold nanocluster can be generated from either an intrinsically chiral inorganic core or an achiral inorganic core in a chiral environment. The first structural determination of a gold nanocluster containing an intrinsic chiral inorganic core is reported. The chiral gold nanocluster [Au20(PP3)4]Cl4 (PP3=tris(2‐(diphenylphosphino)ethyl)phosphine) has been prepared by the reduction of a gold(I)–tetraphosphine precursor in dichloromethane solution. Single‐crystal structural determination reveals that the cluster molecular structure has C3 symmetry. It consists of a Au20 core consolidated by four peripheral tetraphosphines. The Au20 core can be viewed as the combination of an icosahedral Au13 and a helical Y‐shaped Au7 motif. The identity of this Au20 cluster is confirmed by ESI‐MS. The chelation of multidentate phosphines enhances the stability of this Au20 cluster. 相似文献
120.
Balancing the Rate of Cluster Growth and Etching for Gram‐Scale Synthesis of Thiolate‐Protected Au25 Nanoclusters with Atomic Precision
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Xun Yuan Bin Zhang Zhentao Luo Qiaofeng Yao Prof. David Tai Leong Prof. Ning Yan Prof. Jianping Xie 《Angewandte Chemie (International ed. in English)》2014,53(18):4623-4627
We report a NaOH‐mediated NaBH4 reduction method for the synthesis of mono‐, bi‐, and tri‐thiolate‐protected Au25 nanoclusters (NCs) with precise control of both the Au core and thiolate ligand surface. The key strategy is to use NaOH to tune the formation kinetics of Au NCs, i.e., reduce the reduction ability of NaBH4 and accelerate the etching ability of free thiolate ligands, leading to a well‐balanced reversible reaction for rapid formation of thermodynamically favorable Au25 NCs. This protocol is facile, rapid (≤3 h), versatile (applicable for various thiolate ligands), and highly scalable (>1 g Au NCs). In addition, bi‐ and tri‐thiolate‐protected Au25 NCs with adjustable ratios of hetero‐thiolate ligands were easily obtained. Such ligand precision in molecular ratios, spatial distribution and uniformity resulted in richly diverse surface landscapes on the Au NCs consisting of multiple functional groups such as carboxyl, amine, and hydroxy. Analysis based on NMR spectroscopy revealed that the hetero‐ligands on the NCs are well distributed with no ligand segregation. The unprecedented synthesis of multi‐thiolate‐protected Au25 NCs may further promote the practical applications of functional metal NCs. 相似文献