Micro & nano letters | |
Electrical and optical properties of metal-sandwiched ZnO/Ti/Cu/Ti/ZnO transparent conductive thin film | |
article | |
Qijing Lin1  Na Zhao2  Zhuangde Jiang2  Qingzhi Meng2  Feng Chen2  | |
[1] Collaborative Innovation Center of High-End Manufacturing Equipment, Xi'an Jiaotong University;State Key Laboratory for Manufacturing Systems Engineering, Xi'an Jiaotong University;State Key Laboratory of Fluid Power and Mechatronic Systems, Zhejiang University;State Key Laboratory of Mechanical System and Vibration, Shanghai Jiaotong University | |
关键词: copper; titanium; zinc compounds; II-VI semiconductors; wide band gap semiconductors; metallic thin films; semiconductor thin films; sputter deposition; semiconductor-metal boundaries; transparency; electrical conductivity; rapid thermal annealing; surface morphology; electrical resistivity; electrical properties; optical properties; metal-sandwiched transparent conductive thin film; magnetron sputtering technology; rapid thermal annealing; surface morphologies; sheet resistance; figure of merit; temperature 100 degC to 400 degC; ZnO-Ti-Cu-Ti-ZnO; | |
DOI : 10.1049/mnl.2018.5234 | |
学科分类:计算机科学(综合) | |
来源: Wiley | |
【 摘 要 】
This study includes synthesis of some nitrogenous heterocyclic compounds linked to amino acid esters or heterocyclic amines that may have a potential activity as antimicrobial and/or cytotoxic. Quinolines are an important group of organic compounds that possess useful biological activity as antibacterial, antifungal and antitumor .8-Hydroxyquinoline (8-HQ) and numerous of its derivatives exhibit potent activities against fungi and bacteria which make them good candidates for the treatment of many parasitic and microbial infection diseases. These pharmacological properties of quinolones aroused our interest in synthesizing several new compounds featuring heterocyclic rings of the quinoline derivatives linked to amino acid ester or heterocyclic amine with the aim of obtaining a pharmacologically active compounds.O-alkylation has been done on( 8-hydroxyquinoline ) to get (O-alkylated ester) derivatives which are deesterfied to get acetic acid derivatives, then coupled with amino acid that have protected carboxyl group (amino acid esters) or heterocyclic amine by using conventional solution method for peptide synthesis as a coupling method. The proposed analogues were successfully synthesized and the processing of the reactions confirmed by TLC ,the synthesized analogues with the proposed structures as they were characterized and proved by melting point, infrared spectroscopy (IR) and elemental microanalysis. The tested analogues showed cytotoxic activity on the HEp-2 cell line (tumor of larynx) with inhibitory concentration percent of (IC %) range (32.43 % - 49.55%) and showed that the tested compounds had variable antimicrobial activities against selected bacteria and yeast when compared with selected standard drugs.
【 授权许可】
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