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101.
针对新型装甲装备通用质量特性评价指标体系难以确定的问题,在明确评价指标体系构建原则的基础上,结合新型装甲装备特点,确定了通用质量特性初始评价指标及指标筛选要求,运用QFD将新型装甲装备通用质量特性需求映射为评价指标筛选要求,采用粗糙集理论(Rough Set Theory,RST)确定了指标筛选重要度,考虑到关联度的不确定性及多个专家估计值的平均值和估计值的波动程度,将贝叶斯理论引入关系矩阵的确定中,用区间数确定了关联度,进行了评价指标筛选,构建了新型装甲装备通用质量特性评价指标体系,为新型装甲装备通用质量特性评价奠定了基础。 相似文献
102.
103.
Ultrafast solvation dynamics at internal sites of staphylococcal nuclease investigated by site-directed mutagenesis 下载免费PDF全文
Internal solvation of protein was studied by site-directed mutagenesis,with which an intrinsically fluorescent probe,tryptophan,is inserted into the desired position inside a protein molecule for ultrafast spectroscopic study.Here we review this unique method for protein dynamics research.We first introduce the frontiers of protein solvation,site-directed mutagenesis,protein stability and characteristics,and the spectroscopic methods.Then we present time-resolved spectroscopic dynamics of solvation dynamics inside cavities of active sites.The studies are carried out on a globular protein,staphylococcal nuclease.The solvation at sites inside the protein molecule’s cavities clearly reveals characteristics of the local environment.These solvation behaviors are directly correlated to enzyme activity. 相似文献
104.
Dr. Liuyi Li Dr. Zhilin Chen Dr. Hong Zhong Prof. Dr. Ruihu Wang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(11):3050-3060
Two urea‐based porous organic frameworks, UOF‐1 and UOF‐2, were synthesized through a urea‐forming condensation of 1,3,5‐benzenetriisocyanate with 1,4‐diaminobenzene and benzidine, respectively. UOF‐1 and UOF‐2 possess good hydrophilic properties and high scavenging ability for palladium. Their palladium polymers, PdII/UOF‐1 and PdII/UOF‐2, exhibit high catalytic activity and selectivity for Suzuki–Miyaura cross‐coupling reactions and selective reduction of nitroarenes in water. The catalytic reactions can be efficiently performed at room temperature. Palladium nanoparticles with narrow size distribution were formed after the catalytic reaction and were well dispersed in UOF‐1 and UOF‐2. XPS analysis confirmed the coordination of the urea oxygen atom with palladium. SEM and TEM images showed that the original network morphology of UOF‐1 and UOF‐2 was maintained after palladium loading and catalytic reactions. 相似文献
105.
Zhen Zhao Vincent H. Crespi James D. Kubicki Daniel J. Cosgrove Linghao Zhong 《Cellulose (London, England)》2014,21(2):1025-1039
The effect of surface hydrophobicity and side-chain variation on xyloglucan adsorption onto cellulose microfibrils (CMF) is investigated via molecular dynamics simulations. A molecular model of CMF with (100), (010), (1–10), (110) and (200) crystal faces was built. We considered xylogluco-oligosaccharides (XGO) with three repeating units, namely (XXXG)3, (XXLG)3, and (XXFG)3 (where each (1,4)-β-d-glucosyl residue in the backbone is given a one-letter code according to its substituents: G = β-d-Glc; X = α-d-Xyl-(1,6)-β-d-Glc; L = β-d-Gal-(1,2)-α-d-Xyl-(1,6)-β-d-Glc; F = α-l-Fuc-(1,2)-β-d-Gal-(1,2)-α-d-Xyl-(1,6)-β-d-Glc). Our work shows that (XXXG)3 binds more favorably to the CMF (100) and (200) hydrophobic surfaces than to the (110), (010) and (1–10) hydrophilic surfaces. The origin of this behavior is attributed to the topography of hydrophobic CMF surface, which stabilizes (XXXG)3 in flat conformation. In contrast, on the rough hydrophilic CMF surface (XXXG)3 adopts a less favorable random-coil conformation to facilitate more hydrogen bonds with the surface. Extending the xyloglucan side chains from (XXXG)3 to (XXLG)3 hinders their stacking on the CMF hydrophobic surface. For (XXFG)3, the interaction with the hydrophobic surface is as strong as (XXXG)3. All three XGOs have similar binding to the hydrophilic surface. Steered molecular dynamics simulation was performed on an adhesive model where (XXXG)3 was sandwiched between two CMF hydrophobic surfaces. Our analysis suggests that this sandwich structure might help provide mechanical strength for plant cell walls. Our study relates to a recently revised model of primary cell walls in which extensibility is largely determined by xyloglucan located in limited regions of tight contact between CMFs. 相似文献
106.
Dr. Shuang Pan Dr. Haiyang Zou Aurelia C. Wang Dr. Zewei Wang Jiwoo Yu Chuntao Lan Qiliang Liu Prof. Zhong Lin Wang Prof. Tianquan Lian Prof. Juan Peng Prof. Zhiqun Lin 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(35):15052-15059
Despite recent progress in producing perovskite nanowires (NWs) for optoelectronics, it remains challenging to solution-print an array of NWs with precisely controlled position and orientation. Herein, we report a robust capillary-assisted solution printing (CASP) strategy to rapidly access aligned and highly crystalline perovskite NW arrays. The key to the CASP approach lies in the integration of capillary-directed assembly through periodic nanochannels and solution printing through the programmably moving substrate to rapidly guide the deposition of perovskite NWs. The growth kinetics of perovskite NWs was closely examined by in situ optical microscopy. Intriguingly, the as-printed perovskite NWs array exhibit excellent optical and optoelectronic properties and can be conveniently implemented for the scalable fabrication of photodetectors. 相似文献
107.
Zheng Huayan Narkhede Nilesh Han Linyi Zhang Huacheng Li Zhong 《Research on Chemical Intermediates》2020,46(3):1749-1769
Research on Chemical Intermediates - The reaction steps during methanol synthesis from CO2/H2 are influenced by the type of catalysts such as pure Cu and Zn-decorated Cu. In this study, density... 相似文献
108.
Hui Shao Xiaonan Gao Zhong‐Tian Wang Ziwei Gao Yu‐Ming Zhao 《Angewandte Chemie (International ed. in English)》2020,59(19):7419-7424
A divergent synthetic approach to six Ganoderma meroterpenoids, namely ganocins A–C, ganocochlearins C and D, and cochlearol T, has been developed for the first time. This synthetic route features a two‐phase strategy which includes early‐stage rapid construction of a common planar tricyclic intermediate followed by highly selective late‐stage transformations into various Ganoderma meroterpenoids. Key to the strategy are a bioinspired intramolecular hetero‐Diels–Alder reaction and Stahl‐type oxidative aromatization, allowing efficient formation of the common tricyclic phenol intermediate. A nucleophilic dearomatization of the phenol unit, combined with a regioselective 1,4‐reduction of the resulting dienone, enabled rapid access to ganocins B and C. Additionally, site‐selective Mukaiyama hydration, followed by an intramolecular oxa‐Michael addition/triflation cascade, served as a key strategic element in the chemical synthesis of ganocin A. 相似文献
109.
The crystal and molecular structures of the title compounds were determined by X-ray diffraction technique from diffractometer intensity measurements. It has been found that two homologous disulfides, bis(dimethoxythiophosphoryl) disulfide 1 and bis(dineopentoxythiophosphoryl) disulfide 2 , form different molecular and crystal structures with space groups C2/c and P&1macr;, respectively. These results were confirmed by 31P CP MAS NMR studies, which showed that under favorable conditions the solid state NMR may lead to determination of the number of crystallographically unique phosphorus atoms. Moreover, the variation of the disulfide S–S bond length versus torsional P–S–S–P angles was observed. 相似文献
110.
A redox-neutral Fe-catalyzed intramolecular C—H amidation of N-benzoyloxyureas is described.This methodology employs a simple iron complex in situ generated fro... 相似文献