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921.
A modified Takemoto catalyst enabled the asymmetric Michael addition of carbazolones to 2‐chloroacrylonitrile to afford 3,3‐disubstituted carbazolones with excellent enantioselectivity. This method was successfully applied to total syntheses of three Kopsia alkaloids which featured an unprecedented MnIII‐mediated oxidative cyclization to create the caged ring system and a SmI2‐mediated reductive coupling as key steps.  相似文献   
922.
Reported is a modular one‐step three‐component synthesis of tetrahydroisoquinolines using a Catellani strategy. This process exploits aziridines as the alkylating reagents, through palladium/norbornene cooperative catalysis, to enable a Catellani/Heck/aza‐Michael addition cascade. This mild, chemoselective, and scalable protocol has broad substrate scope (43 examples, up to 90 % yield). The most striking feature of this protocol is the excellent regioselectivity and diastereoselectivity observed for 2‐alkyl‐ and 2‐aryl‐substituted aziridines to access 1,3‐cis‐substituted and 1,4‐cis‐substituted tetrahydroisoquinolines, respectively. Moreover, this is a versatile process with high step and atom economy.  相似文献   
923.
Pestalustaines A (1) and B (2), one unique sesquiterpene possessing an unusual 5/6/7-fused tricyclic ring system and one unprecedented coumarin derivative bearing 6/6/5/5-fused tetracyclic ring system, were isolated from the plant-derived Pestalotiopsis adusta. Their structures with absolute configurations were established by extensive NMR analysis, X-ray crystallography, and CD spectra associated with TD-DFT calculation. Hypothetical biosynthetic pathways for compounds 1 and 2 are proposed. Compounds 1 and 2 showed weak to moderate cytotoxic activities against three human tumor cell lines HeLa, HCT116, and A549, whose IC50 values were ranged from 21.01 to 55.43?μM.  相似文献   
924.
A novel H2S-responsive fluorescent probe Rh-Lyso-H2S has been designed and synthesized. The Rh-Lyso-H2S shows high sensitivity and selectivity toward H2S, with a limit of detection of 3.36?×?10?7?M. The reason is that Rh-Lyso-H2S changed from a stable non-conjugated closed-ring lactone conformation with weak fluorescence to a conjugated open-ring conformation with strong fluorescence in the presence of H2S. The Rh-Lyso-H2S has a good lysosome-targeting capacity and is used to detect lysosomal H2S in living cells, which is driven via the protonation of its basic morpholine moiety by acidic lysosomes. Rh-Lyso-H2S is triggered by H2S via removing the thiophenecarboxylate group, and the corresponding activated mechanism of Rh-Lyso-H2S toward H2S is proposed.  相似文献   
925.
In this work, hybrid conductive fillers of carbon black (CB) and carbon nanotubes (CNTs) were introduced into polylactide (PLA)/thermoplastic poly(ether)urethane (TPU) blend (70/30 by weight) to tune the phase morphology and realize rapid electrically actuated shape memory effect (SME). Particularly, the dispersion of conductive fillers, the phase morphology, the electrical conductivities and the shape memory properties of the composites containing CB or CB/CNTs were comparatively investigated. The results suggested that both CB and CNTs were selectively localized in TPU phase, and induced the morphological change from the sea-island structure to the co-continuous structure. The presence of CNTs resulted in a denser CB/CNTs network, which enhanced the continuity of TPU phase. Because the formed continuous TPU phase provided stronger recovery driving force, the PLA/TPU/CB/CNTs composites showed better shape recovery properties compared with the PLA/TPU/CB composites at the same CB content. Moreover, the CB and CNTs exerted a synergistic effect on enhancing the electrical conductivities of the composites. As a result, the prepared composites exhibited excellent electrically actuated SME and the shape recovery speed was also greatly enhanced. This work demonstrated a promising strategy to achieve rapid electrically actuated SME via the addition of hybrid nanoparticles with self-networking ability in binary PLA/TPU blends over a much larger composition range.  相似文献   
926.
The potential of near-infrared spectroscopy (NIRS) for the quality control of traditional Chinese medicine has been evaluated. Seven quantitative parameters, andrographolide, deoxyandrographolide, dehydroandrographolide, neoandrographolide, moisture, ash content, and alcohol-soluble extract of Andrographis paniculata, were evaluated by NIRS. The reference values of andrographolides were determined by high-performance liquid chromatography, and the others were obtained using the standard methods of the 2015 Chinese Pharmacopoeia. The predicted values were determined by a quantitative model using NIRS based on partial least square regression. Different spectral preprocessing methods, spectral ranges, and optimum number of factors were selected to optimize the models. All models were estimated by the combination of various parameters, including the correlation coefficient of calibration for andrographolide, deoxyandrographolide, dehydroandrographolide, neoandrographolide, moisture, ash content, alcohol-soluble extract (values of 0.980, 0.984, 0.989, 0.983, 0.987, 0.988, 0.979, respectively), root mean square error of calibration (values of 0.156, 0.038, 0.050, 0.029, 0.604, 0.431, 0.135, respectively), root mean square error of prediction (values of 0.169, 0.041, 0.050, 0.033, 0.280, 0.493, 0.140, respectively), root mean square error of cross-validation (values of 0.626, 0.114, 0.158, 0.046, 1.145, 0.774, 0.508, respectively), and ratio of standard deviation to standard error of prediction (values of 4.583, 4.690, 4.796, 4.899, 4.899, 4.690, 5.099, respectively). The results show that the calibration models by NIRS are reliable and can be applied for the quantification for seven parameters from A. paniculata for quality control in traditional Chinese medicine production and processing.  相似文献   
927.
α-NaFeO2 layered LiNi1/3Co1/3Mn1/3O2 cathode materials were synthesized by mechanical milling accompanied by the solid phase sintering. The sample exhibited a good crystallinity and layered structure while sintered at 900°C, which can be further improved by adding a pre-sintering process at 500°C before high temperature sintering. The sample with a pre-sintering process presents an average particle size about 0.6 μm, and a hexagonal crystalline structure. The optimally fabricated sample showed a first charge capacity of 210.2 mA h/g, discharge capacity of 171.2 mA h/g with a current rate of 0.2 C within the voltage range of 2.7~4.5 V. With increasing the current rate to 1 C, the charge–discharge capacity faded quickly during the cycling process, which can be partially recovered while operated at a low current rate. However, the capacity fading at a current rate of 2 C was largely irreversible. The evolution of the surface chemical states was evaluated using X-ray photoelectron spectroscopy on the charged and discharged samples to understand the high rate capacity fading.  相似文献   
928.
用"化学让大自然丰富多彩、色彩斑斓——天然色素的五彩世界""化学很魔幻——揭秘化学小魔术""化学让我们生活得更智慧、更安全、更健康——引导大众消除生活误区""化学也诗意——以诗入‘化’——打造诗意化学科普"和"化学让大自然更为奇特绝妙——走进大自然,学习化学知识,感悟化学的魅力"五个主题,介绍了中国科学技术大学化学实验教学中心在化学科普教育内容方面的一些探索和经验。  相似文献   
929.
Nanoparticles are able to be excreted from both apical and basolateral sides after taken up by cells. Compared to nanospheres, nanorods preferred basolateral exocytosis to apical exocytosis.  相似文献   
930.
Inspired by the cubic Mn4CaO5 cluster of natural oxygen‐evolving complex in Photosystem II, tetrametallic molecular water oxidation catalysts, especially M4O4 cubane‐like clusters (M=transition metals), have aroused great interest in developing highly active and robust catalysts for water oxidation. Among these M4O4 clusters, however, copper‐based molecular catalysts are poorly understood. Now, bio‐inspired Cu4O4 cubanes are presented as effective molecular catalysts for electrocatalytic water oxidation in aqueous solution (pH 12). The exceptional catalytic activity is manifested with a turnover frequency (TOF) of 267 s?1 for [(LGly‐Cu)4] at 1.70 V and 105 s?1 for [(LGlu‐Cu)4] at 1.56 V. Electrochemical and spectroscopic study revealed a successive two‐electron transfer process in the Cu4O4 cubanes to form high‐valent CuIII and CuIIIO. intermediates during the catalysis.  相似文献   
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