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Hazaana S. Aafrin Joseph Ancemma Selvasekarapandian S. Naachiyar R. Meera Vignesh N. Muniraj 《Journal of Solid State Electrochemistry》2023,27(2):539-557
Journal of Solid State Electrochemistry - In the present work, biopolymer electrolytes based on agar–agar (AA) and lithium chloride (LiCl) have been prepared using solution casting technique... 相似文献
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Maruthibabu Paidikondala Vignesh Kumar Rangasami Ganesh N. Nawale Tommaso Casalini Giuseppe Perale Sandeep Kadekar Gaurav Mohanty Turkka Salminen Oommen P. Oommen Oommen P. Varghese 《Angewandte Chemie (International ed. in English)》2019,58(9):2815-2819
Circulating nucleic acids, such as short interfering RNA (siRNA), regulate many biological processes; however, the mechanism by which these molecules enter the cell is poorly understood. The role of extracellular‐matrix‐derived polymers in binding siRNAs and trafficking them across the plasma membrane is reported. Thermal melting, dynamic light scattering, scanning electron microscopy, and computational analysis indicate that hyaluronic acid can stabilize siRNA via hydrogen bonding and Van der Waals interactions. This stabilization facilitated HA size‐ and concentration‐dependent gene silencing in a CD44‐positive human osteosarcoma cell line (MG‐63) and in human mesenchymal stromal cells (hMSCs). This native HA‐based siRNA transfection represents the first report on an anionic, non‐viral delivery method that resulted in approximately 60 % gene knockdown in both cell types tested, which correlated with a reduction in translation levels. 相似文献
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Vignesh R. A. Shalini Kumari Puja Poddar Dibakar Dhara Souvik Maiti 《Macromolecular bioscience》2020,20(8)
Multicellular tumor spheroid (MCTS) mimics microenvironment for tumor formation and provides predictive insight for in vivo tests. The hanging drop (HD) method of spheroid generation is cost effective, but it is limited by a long time duration for spheroid development and a low rate of formation of larger spheroids. Toward addressing those limitations, thermoresponsive copolymers with poly(N‐isopropylacrylamide) (p(NIPA)) backbone are developed, to be used as additives in the MCTS formation via HD method. Upon investigation it is found that in the presence of the polymer, robust and compact spheroids are formed in a short duration of 48 h. Larger spheroids (350–600 µm) can be formed by increasing the number of cells. Spheroids are characterized for their 3D shape and different cellular layers, and drug uptake study is done to prove the efficacy of the spheroids generated in drug screening. 相似文献
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S. Iniyan Juanna Ren Swapnil Deshmukh K. Rajeswaran G. Jegan Hua Hou Vembu Suryanarayanan Vignesh Murugadoss Murugavel Kathiresan Ben Bin Xu Zhanhu Guo 《Chemical record (New York, N.Y.)》2023,23(12):e202300317
Due to the increasing global energy demands, scarce fossil fuel supplies, and environmental issues, the pursued goals of energy technologies are being sustainable, more efficient, accessible, and produce near zero greenhouse gas emissions. Electrochemical water splitting is considered as a highly viable and eco-friendly energy technology. Further, electrochemical carbon dioxide (CO2) reduction reaction (CO2RR) is a cleaner strategy for CO2 utilization and conversion to stable energy (fuels). One of the critical issues in these cleaner technologies is the development of efficient and economical electrocatalyst. Among various materials, metal-organic frameworks (MOFs) are becoming increasingly popular because of their structural tunability, such as pre- and post- synthetic modifications, flexibility in ligand design and its functional groups, and incorporation of different metal nodes, that allows for the design of suitable MOFs with desired quality required for each process. In this review, the design of MOF was discussed for specific process together with different synthetic methods and their effects on the MOF properties. The MOFs as electrocatalysts were highlighted with their performances from the aspects of hydrogen evolution reaction (HER), oxygen evolution reaction (OER), and electrochemical CO2RR. Finally, the challenges and opportunities in this field are discussed. 相似文献
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Dr. Stuart K. Langley Dr. Kuduva R. Vignesh Dr. Boujemaa Moubaraki Prof. Gopalan Rajaraman Prof. Keith S. Murray 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(16):4156-4165
We report four new complexes based on a {LnIII6} wheel structure, three of which possess a net toroidal magnetic moment. The four examples consist of {TbIII6} and {HoIII6} wheels, which are rare examples of non DyIII based complexes possessing a toroidal magnetic ground state, and a {DyIII6} complex which improves its toroidal structure upon lowering the crystallographic symmetry from trigonal (R ) to triclinic (P ). Notably the toroidal moment is lost for the trigonal {ErIII6} analogue. This suggests the possibility of utilizing the popular concept of oblate and prolate electron density of the ground state MJ levels of lanthanide ions to engineer toroidal moments. 相似文献
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Monica S. Esther Santhoshi Dhas C. Ravi Venkatesh R. Sivakumar R. Vignesh R. Ferby V. Anslin 《Journal of Solid State Electrochemistry》2022,26(5):1271-1290
Journal of Solid State Electrochemistry - Herein, we have analyzed for the first time on the synergetic effect of NiO and MnOx towards electrochromic behaviour in comparison with pristine NiO films... 相似文献
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Dr. Ramasamy Jayarajan Hediyala B. Chandrashekar Aishwarya K. Dalvi Prof. Dr. Debabrata Maiti 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(50):11426-11430
The horizon of ultrasound-assistance has been expanded to palladium-catalyzed distal C−H functionalization of arenes. Compared to thermal conditions, operationally simple ultrasound mediated distal C−H functionalization occurred with a shorter reaction time and enhanced reactivity of reactants to give superior yields with improved selectivity both in terms of meta:others and mono:di. A wide variety of meta-functionalizations such as olefination, alkylation, acetoxylation, allylation and cyanation were successfully carried out under ambient temperature. 相似文献
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The reaction of hydroxylamine hydrochloride with ethyl 3‐aroyl‐1‐cyano‐4‐hydroxy‐2,4,6‐triarylcyclohexanecarboxylate has led to the formation of ethyl 2‐[amino(hydroxyimino)methyl]‐3‐aryl‐5‐(hydroxyimino)‐5‐arylpentanoate via a tandem ring opening and oximation process. The structures of the products are confirmed by NMR and X‐ray techniques, and the conformational features of the product arrived at are compared with a molecular dynamics simulation study. 相似文献