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Fateme Banihashemi Amr F. M. Ibrahim Ali Akbar Babaluo Jerry Y. S. Lin 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(8):2541-2545
Highly b‐oriented, closely packed, MFI zeolite films are prepared on seeded stainless‐steel plates using organic template‐free, secondary growth solutions, containing aluminum sulfate as a crystallization agent. The number of a‐oriented twin crystals is significantly reduced, and even eliminated, simply by restricting the pH value of the secondary growth solution to the narrow range of 11.1–11.3. Values of pH can be adjusted through the controlled addition of (NH4)2SO4 or H2SO4 to secondary growth solutions of the composition (1 SiO2:0.57 NaOH:137.5 H2O:0.0050 (Al2(SO4)3?18 H2O)) or by simply decreasing the molar composition of NaOH with no extra additives. 相似文献
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Yu Duan Zi‐You Yu Shao‐Jin Hu Xu‐Sheng Zheng Chu‐Tian Zhang Hong‐He Ding Bi‐Cheng Hu Qi‐Qi Fu Zhi‐Long Yu Xiao Zheng Jun‐Fa Zhu Min‐Rui Gao Shu‐Hong Yu 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(44):15919-15924
The anode oxygen evolution reaction (OER) is known to largely limit the efficiency of electrolyzers owing to its sluggish kinetics. While crystalline metal oxides are promising as OER catalysts, their amorphous phases also show high activities. Efforts to produce amorphous metal oxides have progressed slowly, and how an amorphous structure benefits the catalytic performances remains elusive. Now the first scalable synthesis of amorphous NiFeMo oxide (up to 515 g in one batch) is presented with homogeneous elemental distribution via a facile supersaturated co‐precipitation method. In contrast to its crystalline counterpart, amorphous NiFeMo oxide undergoes a faster surface self‐reconstruction process during OER, forming a metal oxy(hydroxide) active layer with rich oxygen vacancies, leading to superior OER activity (280 mV overpotential at 10 mA cm?2 in 0.1 m KOH). This opens up the potential of fast, facile, and scale‐up production of amorphous metal oxides for high‐performance OER catalysts. 相似文献
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Xiangyu Zhang James C. Anderson 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(50):18208-18213
The total synthesis of representative members of the schizozygine alkaloids, (+)‐vallesamidine and (+)‐14,15‐dehydrostrempeliopine, were completed from a late‐stage divergent intermediate. The synthesis took advantage of efficient nitro‐group reactions with the A/B/C ring skeleton constructed concisely on a gram scale through an asymmetric Michael addition, nitro‐Mannich/lactamisation, Tsuji–Trost allylation, and intramolecular C?N coupling reaction. Other key features of the synthesis are a novel [1,4] hydride transfer/Mannich‐type cyclisation to build ring E and a diastereoselective ring‐closing metathesis reaction to construct ring D. This approach gave access to a late‐stage C14,C15 alkene divergent intermediate that could be simply transformed into (+)‐vallesamidine, (+)‐14,15‐dehydrostrempeliopine, and potentially other schizozygine alkaloids and unnatural derivatives. 相似文献
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