polarized light microscope eclipse 50i pol (Nikon)
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polarized light microscope eclipse 50i pol
Polarized Light Microscope Eclipse 50i Pol, supplied by Nikon, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/polarizing+microscope+eclipse+50i+pol/pm39835460__ja4c14775_si_001-16-9-8
Average 90 stars, based on 1 article reviews
Polarized Light Microscope Eclipse 50i Pol, supplied by Nikon, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/polarizing+microscope+eclipse+50i+pol/pm39835460__ja4c14775_si_001-16-9-8
Average 90 stars, based on 1 article reviews
polarized light microscope eclipse 50i pol - by Bioz Stars,
2026-09
90/100 stars
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Microscopy:Article Title: Iron-Catalyzed Selective B–H Activation for 4/5-fold Methylation and Arylation of Carboranes Article Snippet: GC-MS analyses were performed on Agilent GC-MS 6890N. .. Melting points were measured using a Article Title: Trifluoromethylation of Anthraquinones for n-Type Organic Semiconductors in Field Effect Transistors. Article Snippet: This study puts forth a new design of n-type organic semiconductors, which has trifluoromethylethynyl groups attached to 9,10-anthraquinone at different positions.. These electron-deficient anthraquinones are synthesized by trifluoromethylation of the corresponding trimethylsilyl-protected alkynes with fluoroform-derived CuCF3, and their π-π stacking in the crystals is tunable by varying the positions of trifluoromethylethynyl groups.. It is found that most of these trifluoromethylated anthraquinones function as n-type semiconductors in solution-processed field effect transistors with electron mobility of up to 0.28 cm2 V−1 s−1. Article Title: Mechanically triggered reversible stepwise tricolor switching and thermochromism of anthracene- o -carborane dyad †Electronic supplementary information (ESI) available: UV-vis absorption and fluorescence spectra, DFT calculations. See DOI: 10.1039/c8sc00833g Article Snippet: UV-vis absorption spectra were recorded on a HITACHI U-3900H and the fluorescence spectra were recorded on a HITACHI F-4500 spectrofluorometer and a FluoroLog-3 (Horiba-Jobin-Yvon, Edison, NJ, USA) fluorescence spectrophotometer. .. Melting points were measured using a Article Title: Highly-efficient solid-state emission of tethered anthracene-o-carborane dyads and their visco- and thermo-chromic luminescence properties Article Snippet: A facile and efficient method is described to greatly improve the emission efficiency of anthracene-o-carborane dyad by linking two o-carborane building blocks together through tailored alkyl linkages.. Improvement of the emission efficiency of the tethered anthracene-o-carborane dyads was achieved with the quantum yield up to 40.8% and 51.4% for BCAC4 and BCAC6 respectively, in contrast to that of CAH (4.3%) and CAA (36%), demonstrating that the cooperation advocates that one plus one is much bigger than two.. In addition, these developed emissive AIE luminogens exhibit impressive response to the environmental stimuli of viscosity and temperature. Article Title: Iridium-Catalyzed Annulation of o -Carboranyl Carboxylic Acids with Alkynes: Synthesis of Carborano-Isocoumarins. Article Snippet: An efficient iridium-catalyzed formal [4+2] annulation of carboranyl carboxylic acids with alkynes is developed, resulting in the facile synthesis of a new class of carboranoisocoumarin derivatives.. The carboxyl group not only serves as a directing group to control the regioselectivity but also ingeniously becomes a part of the final products.. The reaction mechanism involves sequential carboxyl-directed B(4)-H metalation, alkyne insertion, and reductive elimination. Article Title: Multifunctional luminescent molecules of o -carborane-pyrene dyad/triad: flexible synthesis and study of the photophysical properties Article Snippet: The development of organic single-molecule multiple photoluminescence compounds hold a great promise for advanced opt-electronic devices, optical probes and temperature sensors.. The pyrenyl-substituted o-carborane, CSP and CDP, were obtained via a modified nickel-catalyzed cross-coupling reaction in satisfactory yields.. 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