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991.
992.
以波义耳研究燃烧的史实为背景,创新设计燃烧条件的探究实验,并提出“条件叠加式”燃烧条件探究新思路。以“燃灭控”为主线,一以贯之地显性化“条件是认识化学反应的一种基本视角”,落实“在一定条件下通过化学反应可以实现物质转化”的化学观念。基于调控化学反应思想创新设计“燃旺弱灭”反应控制视域,统整开展“情境”“活动”与“任务”三位一体的学习活动。重置教材实验的教学价值取向,结合燃烧的形式美、汉语言文字解读,将化学学科知识与美育、汉语言文化领域跨领域融合。 相似文献
993.
Dr. Aaron D. W. Kennedy Ray G. DiNardi Lucy L. Fillbrook Assoc. Prof. William A. Donald Assoc. Prof. Jonathon E. Beves 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(16):e202104461
A photoswitchable ligand and palladium(II) ions form a dynamic mixture of self-assembled metallosupramolecular structures. The photoswitching ligand is an ortho-fluoroazobenzene with appended pyridyl groups. Combining the E-isomer with palladium(II) salts affords a double-walled triangle with composition [Pd3L6]6+ and a distorted tetrahedron [Pd4L8]8+ (1 : 2 ratio at 298 K). Irradiation with 410 nm light generates a photostationary state with approximately 80 % of the E-isomer of the ligand and results in the selective disassembly of the tetrahedron, the more thermodynamically stable structure, and the formation of the triangle, the more kinetically inert product. The triangle is then slowly transformed back into the tetrahedron over 2 days at 333 K. The Z-isomer of the ligand does not form any well-defined structures and has a thermal half-life of 25 days at 298 K. This approach shows how a thermodynamically preferred self-assembled structure can be reversibly pumped to a kinetic trap by small perturbations of the isomer distribution using non-destructive visible light. 相似文献
994.
自抗扰控制技术在捷联惯导动基座初始对准中的应用研究 总被引:1,自引:1,他引:1
提出并设计了应用自抗扰控制技术(ADRC)的捷联惯性系统动基座初始对准方案。通过数字仿真,将卡尔曼滤波与自抗扰控制的性能进行了详细的比较,证明该方法具有对准时间快,精度高,抗干扰能力强等特点。 相似文献
995.
基于新型滤波器-HABF的SINS传递对准仿真 总被引:1,自引:0,他引:1
传统动基座传递对准主要采用扩展卡尔曼滤波技术。但在动基座传递对准的非线性、非高斯条件下,这种基于模型线性化和高斯假设的滤波方法在估计系统状态及其方差时误差较大且可能发散。混合退火粒子滤波针对非线性、非高斯系统状态的在线估计问题,提出一种新的基于序贯重要性抽样的粒子滤波算法。在滤波算法中,用状态参数分解和退火系数来产生重要性概率密度函数,此概率密度函数综合考虑了转移先验、似然、噪声的统计特性以及最新的观察数据,因此更接近于系统状态的后验概率。实验仿真结果表明,这种基于混合退火粒子滤波器不仅比扩展卡尔曼滤波提高了传递对准的精度,而且又比传统的粒子算法减少了时间。 相似文献
996.
HAN Jun GE Yun YAN Chao-guo 《高等学校化学研究》2006,22(4):537-542
IntroductionOver the past two decades, dendrimers have at-tracted considerable attention because of their inherentnovel structural features and their potential applicationsin various scientific and industrial fields such as cataly-sis or newmaterials, and… 相似文献
997.
Anna Tashchilova Nadezhda Podoplelova Alexey Sulimov Danil Kutov Ivan Ilin Mikhail Panteleev Khidmet Shikhaliev Svetlana Medvedeva Nadezhda Novichikhina Andrey Potapov Vladimir Sulimov 《Molecules (Basel, Switzerland)》2022,27(4)
In the modern world, complications caused by disorders in the blood coagulation system are found in almost all areas of medicine. Thus, the development of new, more advanced drugs that can prevent pathological conditions without disrupting normal hemostasis is an urgent task. The blood coagulation factor XIIa is one of the most promising therapeutic targets for the development of anticoagulants based on its inhibitors. The initial stage of drug development is directly related to computational methods of searching for a lead compound. In this study, docking followed by quantum chemical calculations was used to search for noncovalent low-molecular-weight factor XIIa inhibitors in a focused library of druglike compounds. As a result of the study, four low-molecular-weight compounds were experimentally confirmed as factor XIIa inhibitors. Selectivity testing revealed that two of the identified factor XIIa inhibitors were selective over the coagulation factors Xa and XIa. 相似文献
998.
Giacomo Picci Matthew T. Mulvee Claudia Caltagirone Vito Lippolis Antonio Frontera Rosa M. Gomila Jonathan W. Steed 《Molecules (Basel, Switzerland)》2022,27(4)
Three novel bis-urea fluorescent low-molecular-weight gelators (LMWGs) based on the tetraethyl diphenylmethane spacer—namely, L1, L2, and L3, bearing indole, dansyl, and quinoline units as fluorogenic fragments, respectively, are able to form gel in different solvents. L2 and L3 gel in apolar solvents such as chlorobenzene and nitrobenzene. Gelator L1 is able to gel in the polar solvent mixture DMSO/H2O (H2O 15% v/v). This allowed the study of gel formation in the presence of anions as a third component. An interesting anion-dependent gel formation was observed with fluoride and benzoate inhibiting the gelation process and H2PO4−, thus causing a delay of 24 h in the gel formation. The interaction of L1 with the anions in solution was clarified by 1H-NMR titrations and the differences in the cooperativity of the two types of NH H-bond donor groups (one indole NH and two urea NHs) on L1 when binding BzO− or H2PO4− were taken into account to explain the inhibition of the gelation in the presence of BzO−. DFT calculations corroborate this hypothesis and, more importantly, demonstrate considering a trimeric model of the L1 gel that BzO− favours its disruption into monomers inhibiting the gel formation. 相似文献
999.
Yingying Chen Xinchen Wang Xinyuan Ma Shuobin Liang Qianqian Gao Elena V. Tretyakova Yongmin Zhang Demin Zhou Sulong Xiao 《Molecules (Basel, Switzerland)》2022,27(4)
Betulinic acid (BA) and its derivatives exhibit a variety of biological activities, especially their anti-HIV-1 activity, but generally have only modest inhibitory potency against influenza virus. The entry of influenza virus into host cells can be competitively inhibited by multivalent derivatives targeting hemagglutinin. In this study, a series of hexa-, hepta- and octavalent BA derivatives based on α-, β- and γ-cyclodextrin scaffolds, respectively, with varying lengths of flexible oligo(ethylene glycol) linkers was designed and synthesized using a microwave-assisted copper-catalyzed 1,3-dipolar cycloaddition reaction. The generated BA-cyclodextrin conjugates were tested for their in vitro activity against influenza A/WSN/33 (H1N1) virus and cytotoxicity. Among the tested compounds, 58, 80 and 82 showed slight cytotoxicity to Madin-Darby canine kidney cells with viabilities ranging from 64 to 68% at a high concentration of 100 μM. Four conjugates 51 and 69–71 showed significant inhibitory effects on influenza infection with half maximal inhibitory concentration values of 5.20, 9.82, 7.48 and 7.59 μM, respectively. The structure-activity relationships of multivalent BA-cyclodextrin conjugates were discussed, highlighting that multivalent BA derivatives may be potential antiviral agents against influenza infection. 相似文献
1000.