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Adsorption of cyanogen chloride over Al- and Ga-doped BN nanotubes
Superlattices and Microstructures, 2014Ali Reza Soltani, Mohammad Taghi Baei
exaly +2 more sources
, 2021
An efficient sensor was produced to detect toxic cyanogen gas even in the presence of water, oxygen, and nitrogen molecules due to the significant sensitivity and selectivity of the desired BC3NTs.
Rezvan Rahimi, M. Solimannejad
semanticscholar +1 more source
An efficient sensor was produced to detect toxic cyanogen gas even in the presence of water, oxygen, and nitrogen molecules due to the significant sensitivity and selectivity of the desired BC3NTs.
Rezvan Rahimi, M. Solimannejad
semanticscholar +1 more source
Cyanogen bromide cleavage of proteins in salt and buffer solutions
Analytical Biochemistry, 2010Yaroslav A Andreev +2 more
exaly +2 more sources
Cyanogenic and non-cyanogenic glycosides from Manihot esculenta
Phytochemistry, 1995In addition to lotaustralin and linamarin, a novel cyanogenic glycoside, 2-((6-O-(beta-D-apiofuranosyl)-beta-D-glucopyranosyl)oxy)-2-met hylbutanenitrile , two novel non-cyanogenic glycosides, (2S)-((6-O-(beta-D-apiofuranosyl)-beta-D- glucopyranosyl)oxy)butane and 2-((6-O-(beta-D-apiofuranosyl)-beta-D-glucopyranosyl)oxy)propane, and a simple non ...
H, Prawat +9 more
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Toxicon, 2000
The cyanogenic glycosides belong to the products of secondary metabolism, to the natural products of plants. These compounds are composed of an alpha-hydroxynitrile type aglycone and of a sugar moiety (mostly D-glucose). The distribution of the cyanogenic glycosides (CGs) in the plant kingdom is relatively wide, the number of CG-containing taxa is at ...
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The cyanogenic glycosides belong to the products of secondary metabolism, to the natural products of plants. These compounds are composed of an alpha-hydroxynitrile type aglycone and of a sugar moiety (mostly D-glucose). The distribution of the cyanogenic glycosides (CGs) in the plant kingdom is relatively wide, the number of CG-containing taxa is at ...
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The force fields of cyanogen halides. III. Cyanogen bromide and cyanogen iodine
Spectrochimica Acta Part A: Molecular Spectroscopy, 1978Abstract Following work determining the force fields of FCN and ClCN a related treatment for BrCN and ICN leads to the force fields indicated in Table 1 and giving the agreement with experiment shown by Tables 3, 4 and 5 for BrCN and Tables 7 and 8 for ICN. Table 6 gives the agreement of B 0 values for all isotopic molecules with r e values for
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CI.—Cyanogen bromide and cyanogen
J. Chem. Soc., Trans., 1913Augustus Edward Dixon, John Taylor
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