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131.
A tunable optical rail is embedded into the cavity of a nonlinear-polarization-rotation(NPR) mode-locked fiber laser to generate a sampling pulse with different repetition frequencies and realize bit-rate-adaptive software synchronous optical sampling.Two ultrashort pulses(20.26677 and 20.22900 MHz) are derived,and a 100-MHz data signal is sampled twice with these pulses based on sum-frequency generation(SFG) in periodically poled lithium niobate(PPLN).The eye diagram is successfully recovered,and an estimated bit rate of 102.22 MHz is derived.This method is feasible for bit rates ranging from 200 MHz to 1 GHz,with <3% relative error. 相似文献
132.
利用二级轻气炮加载技术研究了碳水混合物的冲击压缩特性。研究发现:冲击压力p低于19.0 GPa时,石墨与水混合物冲击压缩特性明显不同于金刚石与水混合物的冲击压缩特性;p大于23 GPa后,它们的特性十分接近;当p为52.9 GPa时,石墨与水混合物表现出反常的冲击压缩特性,压力增加而体积出现膨胀,这与高压下碳与水发生化学反应产生气体相关。还对碳水混合物的相互作用势及混合法则的选取进行了讨论。 相似文献
133.
Jinkun Sun Yingjian Liu Jiayi Huang Jiatian Li Mengmeng Chen Xiaoyu Hu Yatao Liu Run Wang Yanan Shen Jingjing Li Xuecheng Chen Dong Qian Baigang An Zunfeng Liu 《Journal of Energy Chemistry》2021,(12):594-603
Increasing mechanical flexibility without sacrificing electrochemical performance of the electrode mate-rial is highly desired in the design of flexible electro... 相似文献
134.
The PdCl2-catalyzed allylation of heteroarenes is presented. Various heteroarenes including O-, N-, and S-based ones were allylated efficiently with a rich range of allylic acetates in the presence of only 2 mol % of PdCl2, without the need of bases/acids, additives, and external supporting ligands. In addition, the reactions were carried out under mild and simple conditions just by stirring the two reactants and catalyst in CH2Cl2 at 60 °C. Moreover, the by-product produced was non-toxic acetic acid. Thus, the method presented in this work provides a general, clean, and operationally simple approach for the functionalization of heteroarenes. Finally, a preliminary mechanistic study suggested that the Pd(II) may be reduced in situ by the heteroarenes to Pd(0), which serves as the active metal center to catalyze the following allylations of heteroarenes via a Tsuji–Trost pathway. 相似文献
135.
Polystyrene-bound diethanolamine based ionic liquids (PS-DHEEAB and PS-THEAB) were synthesized and applied for the chemical fixation of CO2 into cyclic carbonates without any additional co-catalyst and solvent. The effect of the catalysts with different number of hydroxyl group in the cation of the IL on the reaction was systematically investigated. Highest activity and selectivity were achieved in the presence of polystyrene supported diethanolamine ethyl bromide (PS-DHEEAB) in comparison with other catalysts employed. The catalyst was tough in stability and also found to be extended to a variety of terminal epoxides and aziridines. The relationship between high catalytic reactivity and the –OH functional groups was proposed. 相似文献
136.
A highly efficient protocol for the synthesis of aminopropyl functionalized ganglioside GM1b has been described. The full protected ganglioside GM1b was obtained in 71% yield within 5 h. The key feature of the synthetic approach was the use of sialic acid donor that was with a C-5 trichloroacetamide moiety and with a dibenzyl phosphite residue as leaving group at the anomeric carbon. The sialyl donor gave high yields and excellent α-anomeric selectivities with a wide variety of glycosyl acceptors ranging from C-3 or C-6 hydroxyls of galactoside to C-6 hydroxyl of glucosaminoside by using TMSOTf as catalyst in a mixture solution of acetonitrile and methylene chloride. 相似文献
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A detailed quantum chemical study is performed on the mechanism of ClOO + NO reaction at the B3LYP/6-311+G (2d) level of theory combined with CCSD (T) single point energy calculation. The possible product channels for the reaction are obtained and discussed on the basis of the singlet [ClNO3] potential energy surface. The calculation indicates that the dominant product for the title reaction is ClO + NO2 by the direct dissociation of the initial adduct, and the formation of the other products is much less likely since they are unfavorable kinetically. A comparison is also made between the title reaction and the analogous reaction of FO2 + NO to gain a deeper insight into the mechanism of the XO2 + NO reactions. 相似文献