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排序方式: 共有95条查询结果,搜索用时 31 毫秒
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Bianca Stoean Dumitrita Rugina Monica Focsan Ana-Maria Craciun MÎdÎlina Nistor Tamas Lovasz Alexandru Turza Ioan-Dan Porumb Emese Gl Castelia Cristea Luminita Silaghi-Dumitrescu Simion Astilean Luiza Ioana Gaina 《International journal of molecular sciences》2021,22(6)
We report here the synthesis and structural characterization of novel cationic (phenothiazinyl)vinyl-pyridinium (PVP) dyes, together with optical (absorption/emission) properties and their potential applicability as fluorescent labels. Convective heating, ultrasound irradiation and mechanochemical synthesis were considered as alternative synthetic methodologies proficient for overcoming drawbacks such as long reaction time, nonsatisfactory yields or solvent requirements in the synthesis of novel dye (E)-1-(3-chloropropyl)-4-(2-(10-methyl-10H-phenothiazin-3-yl)vinyl)pyridin-1-ium bromide 3d and its N-alkyl-2-methylpyridinium precursor 1c. The trans geometry of the newly synthesized (E)-4-(2-(7-bromo-10-ethyl-10H-phenothiazin-3-yl)vinyl)-1-methylpyridin-1-ium iodide 3b and (E)-1-methyl-4-(2-(10-methyl-10H-phenothiazin-3-yl)vinyl)pyridin-1-ium tetrafluoroborate 3a′ was confirmed by single crystal X-ray diffraction. A negative solvatochromism of the dyes in polar solvents was highlighted by UV-Vis spectroscopy and explanatory insights were supported by molecular modeling which suggested a better stabilization of the lowest unoccupied molecular orbitals (LUMO). The photostability of the dye 3b was investigated by irradiation at 365 nm in different solvents, while the steady-state and time-resolved fluorescence properties of dye 3b and 3a′ in solid state were evaluated under one-photon excitation at 485 nm. The in vitro cytotoxicity of the new PVP dyes on B16-F10 melanoma cells was evaluated by WST-1 assay, while their intracellular localization was assessed by epi-fluorescence conventional microscopy imaging as well as one- and two-photon excited confocal fluorescence lifetime imaging microscopy (FLIM). PVP dyes displayed low cytotoxicity, good internalization inside melanoma cells and intense fluorescence emission inside the B16-F10 murine melanoma cells, making them suitable staining agents for imaging applications. 相似文献
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超声波法制备纳米粉体工艺 总被引:1,自引:0,他引:1
本文阐述了超声波和超声化学的基本原理;讨论了超声化学法在纳米粉体材料制备中的应用;展望超声技术在纳米氧化铁制备中的应用前景。 相似文献
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将机械力化学与超声波化学相结合制备出高纯度、结晶性良好的尖晶石型ZnAl_2O_4纳米颗粒。分析了样品的表面形貌、晶体结构及微观结构。研究结果表明:当焙烧温度为600~900℃时,ZnO与γ-Al_2O_3固相反应制备出高纯度、结晶性良好的尖晶石型ZnAl_2O_4纳米颗粒。随着焙烧温度的升高,材料的致密度增大,结晶度提高,平均孔径依次增大,比表面积明显下降,孔隙率降低。 相似文献
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The interaction between molten gallium and the hydrocarbon medium induced by ultrasonic energy—can gallium carbide be formed? 下载免费PDF全文
Vijay Bhooshan Kumar Manuel Monte Olivier Mathon Sakura Pascarelli Ze'ev Porat Aharon Gedanken 《Journal of the American Ceramic Society》2017,100(7):3305-3315
Ultrasonic irradiation of molten gallium in organic liquids (decane, dodecane, etc.) results in dispersion of the gallium into nanometric spheres. These were examined by several analytical methods XRD, DSC, Raman and IR spectroscopy) as well as electron microscopy (SEM, TEM) and found to be composed of Ga and C. The DSC analysis indicates that the Ga has possibly reacted with carbon, while the Raman spectrum of the product demonstrates a strong additional peak that could not be identified. This work explores the possibility that the product is gallium carbide or another gallium‐carbon complex. To investigate the nature of the product, we performed detailed extended X‐ray absorption fine structure (EXAFS) and X‐ray absorption near‐edge structure (XANES) analyses. On the basis of DSC, IR, and Raman it appear to be formation of GaC, whereas the analysis by EXAFS and XANES demonstrated that the gallium is found to be in a higher reduced state (almost metallic), supported by carbon. The question that remains open in addition to the one related to the formation of galium carbide is whether a complex structure, including oxygen contamination is involved in the layers surrounding the Ga as indicated by the EXAFS results. 相似文献
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用超声化学法制备纳米Fe颗粒包覆的Nd2Fe14B复合粉体,将其在Ar气保护下经放电等离子烧结(SPS),得到Nd2Fe14B/α-Fe纳米晶复合磁体.Fe名义质量分数为5%的烧结磁体具有较高的磁性能:Br=0.86 T,Hci=683.8 kA/m,(BH)max=95.92 kJ/m3.烧结前对复合粉末进行适当的高能球磨,能促进显微组织进一步细化,增强软磁相与硬磁相之间的交换耦合,使相同Fe含量和烧结工艺的磁体Br和(BH)max分别提高到0.94 T和113.6 kJ/m3. 相似文献