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The reaction of NiCl2·6H2O with a hemilabile diaminodiamide ligand 4,7-diazadecanediamide gave a pale blue compound [Ni(C8H18N4O2)(H2O)2]·2C8H18N4O2
The reaction of NiCl2·6H2O with one equivalent hemilabile diaminodiamide ligand N,N′-bis β-carbamoylethyl)1,2-diamiN,N′-bis β-carbamoylethylpale blue compouN,N′-bis β-carbamoylethyl2·3H2O·4Cl (2).
The reaction of CuCl2·2H2O with one equivalent hemilabile diaminodiamide ligand N,N′-bis β-carbamoylethyl trans-1,2-diaminocyclohexane (1) gave a blue compouN,N′-bis β-carbamoylethyl trans-1,2-diaminocyclohexane
The formation of β-silicomulybic acid was used to determine silicate (detection limit 0.1 µM), and a phosphomolybdate hetropoly acid reduced to a blue compound was used to determine phosphate (detection limit 0.01 µM).
The leaves of Isatis subspecies synthesise indoxyl-forming substances, which are indican (Schunk 1855) and isatan B Beijerinck (1900), when they are exposed to the air, reflect the blue compound, indigo (Epstein et al. 1967 Gilbert et al. 2002), which is used in dying.
The church is a huge presence in Hollywood and anyone who has visited Los Angeles can attest to its looming power in real estate alone -- starting with its massive Celebrity Centre located on Franklin Avenue, and the enormous blue compound on Sunset Boulevard, which is home to the church's West Coast headquarters.
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Toxic (red) and non-toxic (blue) compounds are shown for the Scripps IC50 set (left) and NCGC IC50 set (right).
The formation of blue compounds derived from FC-reactive phenols was independent of the structures of the phenolic compounds, enabling quantification of the full complement of phenolics from plant extracts.
Figure 1 Advanced Dataset Graphs built for the "aquatic toxicity datasets, including the training set TR (red – 644 compounds), and two external sets TS, involving 339 (black) and 110 (blue) compounds respectively.
Figure 13 shows a screenshot of the CheS-Mapper viewer, with LogD values highlighted: the compounds are colored according to their feature value of LogD, compounds with low values are colored in blue, compounds with high values are colored in red.
Prussian blue compounds have potential advantages of high working potentials and multi-electron redox capacities as Na-ion battery cathodes; however, they suffer from their poor capacity utilization in aqueous electrolytes due to the blockage of the active lattice sites by coordinating and zeolitic water for Na insertion reaction.
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