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151.
Ardeshir Khazaei Maryam Kiani Borazjani Shahnaz Saednia Mohammad Kiani Borazjani Maryam Golbaghi 《合成通讯》2013,43(10):1544-1553
A highly efficient procedure for etherification and oxidation of aromatic alcohol is described using unsupported and supported P2O5 on alumina and/or silica gel. The silica gel and alumina proved to be the most suitable support among the supports examined in our experiments. It was illustrated that the etherification and oxidative performance in reactions depend largely upon variables including reaction temperature, the nature of the P2O5 used (supported or unsupported P2O5), and whether solvent-free conditions are applied. It was shown that P2O5 not only can convert the aromatic alcohols into corresponding ethers and/or aldehyde and ketone but also can convert aromatic ethers into aldehyde or ketone via oxidative cleavage. Finally, quantum mechanical calculations were performed to rationalized these events, and it was indicated that aldehyde and ketone are more favorable products on the basis of the heat of formation (ΔHf).
152.
In this article a new coated platinum Cu2+ ion selective electrode based on 2-((2-(2-(2-(2-hydroxy-5-methoxybenzylideneamino)phenyl)disufanyl)phenylimino) methyl)-4-methoxyphenol Schiff base (L1) as a new ionophore is described. This sensor has a wide linear range of concentration (1.2 × 10−7-1.0 × 10−1 mol L−1) and a low detection limit of 9.8 × 10−8 mol L−1of Cu(NO3)2. It has a Nernstian response with slope of 29.54 ± 1.62 mV decade−1 and it is applicable in the pH range of 4.0-6.0 without any divergence in potentioal. The coated electrode has a short response time of approximately 9 s and is stable at least for 3.5 months. The electrode shows a good selectivity for Cu2+ ion toward a wide variety of metal ions. The proposed sensor was successfully applied for the determination of Cu2+ ion in different real and environmental samples and as indicator electrode for potentiometric titration of Cu2+ ion with EDTA. 相似文献
153.
Dashteh Mohammad Baghery Saeed Zolfigol Mohammad Ali Khazaei Ardeshir 《Molecular diversity》2022,26(5):2407-2426
Molecular Diversity - Three-component reaction of aldehydes with 3-(1H-indol-3-yl)-3-oxopropanenitrile and 1H-1,2,4-triazol-5-amine under the solvent-free condition at 70 °C was... 相似文献
154.
Shiwei Tao Dr. Baris Demir Dr. Ardeshir Baktash Yutong Zhu Dr. Qingbing Xia Prof. Yalong Jiao Yuying Zhao Dr. Tongen Lin Dr. Ming Li Dr. Miaoqiang Lyu Prof. Ian Gentle Prof. Lianzhou Wang Dr. Ruth Knibbe 《Angewandte Chemie (International ed. in English)》2023,62(39):e202307208
The irreversibility of anion intercalation-deintercalation is a fundamental issue in determining the cycling stability of a dual-ion battery (DIB). In this work, we demonstrate that using a partially fluorinated carbonate solvent can drive a beneficial fluorinated secondary interphase layer formation. Such layer facilitates reversible anion (de−)intercalation processes by impeding solvent molecule co-intercalation and the associated graphite exfoliation. The enhanced reversibility of anion transport contributes to the overall cycling stability for a Zn-graphite DIB—a high Coulombic efficiency of 98.5 % after 800 cycles, with an attractive discharge capacity of 156 mAh g−1 and a mid-point discharge voltage of ≈1.7 V (at 0.1 A g−1). In addition, the formed fluorinated secondary interphase suppresses the self-discharge behavior, preserving 29 times of the capacity retention rate compared to the battery with a commonly used carbonate solvent, after standing for 24 hours. This work provides a simple and effective strategy for addressing the critical challenges in graphite-based DIBs and contributes to fundamental understanding to help accelerate their practical application. 相似文献