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Published in 2018 at "Reaction Kinetics, Mechanisms and Catalysis"
DOI: 10.1007/s11144-018-1445-6
Abstract: Selective hydrogenations of C6 dienic compounds bearing two or more conjugated double bonds in trans position using homogeneous ruthenium catalysts were performed. The following compounds of high purity (over 99%) were prepared: benzyl (2E,4E)-hexa-2,4-dienoate, (2E,4E)-hexa-2,4-dien-1-yl…
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Keywords:
hexa;
hydrogenation;
homogeneous ruthenium;
dienic compounds ... See more keywords
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Published in 2020 at "Case Studies in Thermal Engineering"
DOI: 10.1016/j.csite.2020.100589
Abstract: Abstract In this paper, the synthesis of BaFe12-2xCoxNixO19 (x = 0–0.2) materials at a calcination temperature of 950 °C using a co-precipitation method have been reported. The precursor concentrations of the mixture were varied to identify the optimum…
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Keywords:
barium hexa;
effect additions;
hexa;
magnetic properties ... See more keywords
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Published in 2017 at "Optik"
DOI: 10.1016/j.ijleo.2016.11.205
Abstract: Abstract The series of M-type Ba1-xSrxFe12O19 (x = 0.0, 0.2, 0.4, 0.6, 0.8, 1) have been fabricated using powder metallurgy route. The effects of strontium ions have been systematically investigated. The samples are sintered at 1200 °C for…
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Keywords:
magnetic optical;
hexa;
optical properties;
effect strontium ... See more keywords
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Published in 2017 at "Inorganic chemistry"
DOI: 10.1021/acs.inorgchem.7b00061
Abstract: Three types of unusual cagelike copper(II) methylsilsesquioxanes, namely, nona- [(MeSiO1.5)18(CuO)9] 1, hexa- [(MeSiO1.5)10(HO0.5)2(CuO)6(C12H8N2)2(MeSiO1.5)10(HO0.5)1.33(CH3COO0.5)0.67(CuO)6(C12H8N2)2] 2, [(MeSiO1.5)10(CuO)6(MeO0.5)2(C10H8N2)2] 3, and trinuclear [(MeSiO1.5)8(CuO)3(C10H8N2)2] 4, were obtained in 44%, 27%, 20%, and 16% yields, respectively. Nuclearity and structural fashion of…
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Keywords:
mesio1;
cuo;
hexa;
mesio1 cuo ... See more keywords
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Published in 2022 at "Frontiers in Molecular Biosciences"
DOI: 10.3389/fmolb.2022.892248
Abstract: Introduction: Tay–Sachs disease is an autosomal recessively inherited lysosomal storage disease that results from loss-of-function mutations in the HEXA gene coding β-hexosaminidase A. HEXA gene deficiency affects the central nervous system owing to GM2 ganglioside…
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Keywords:
hexa;
disease;
brain;
hexa neu3 ... See more keywords