Cadmium complex of 1,5-di(1-H-benzimidazolyl)pentane, and preparation method and application thereof
A technology of benzimidazole-based and cadmium complexes, which is applied in cadmium organic compounds, chemical instruments and methods, chemical/physical processes, etc., can solve the problems of weak and rare interactions, achieve mild conditions, high yield, The effect of broad application prospects
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Embodiment 1
[0025] Weigh 0.0156g (0.05mmol) of Cd(ClO 4 ) 2 ·6H 2 O was dissolved in 4 mL of acetonitrile, and then 4 mL of acetonitrile solution dissolved with 0.0152 g (0.05 mmol) of pbbm was added dropwise to the above solution to obtain a clear solution, which was allowed to stand for 14 days to obtain a colorless single crystal. Then washed with distilled water and acetonitrile, and dried. The yield was about 60% (calculated based on 1,5-bis(1-H-benzimidazolyl)pentane).
Embodiment 2
[0027] Weigh 0.0156g (0.05mmol) of Cd(ClO 4 ) 2 ·6H 2 O was dissolved in 2.5 mL of acetonitrile, and then 6 mL of acetonitrile solution dissolved with 0.0182 g (0.06 mmol) of pbbm was added dropwise into the above solution to obtain a clear solution, which was allowed to stand for 18 days to obtain a colorless single crystal. Then washed with distilled water and acetonitrile, and dried. The yield was about 57% (calculated based on 1,5-bis(1-H-benzimidazolyl)pentane).
Embodiment 3
[0029] Weigh 0.0156g (0.05mmol) of Cd(ClO 4 ) 2 ·6H 2 O was dissolved in 5 mL of acetonitrile, and then 3 mL of acetonitrile solution dissolved with 0.0228 g (0.075 mmol) of pbbm was added dropwise to the above solution to obtain a clear solution, which was allowed to stand for 20 days to obtain a colorless single crystal. Then washed with distilled water and acetonitrile, and dried.
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