Fluorene bridged cyclic nitrogen heterocyclic carbene silver complex and its preparation method and application
A nitrogen heterocycle and complex technology, applied in the field of metal organic chemistry, to achieve the effect of obvious fluorescence photosensitive effect
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[0033] Preparation of 2,7-dibromofluorene (W)
[0034]Dissolve the raw material fluorene (5.000 g, 30.0 mmol) in a three-necked flask and dissolve it in 30 ml of chloroform, place the three-necked flask in an ice-water bath and cool it to below 0°C, measure the liquid bromine (3.6 ml, 70.0 mmol) was dissolved in 5 ml of chloroform and placed in a constant pressure funnel, and the liquid bromine was slowly added dropwise with stirring. After 30 min, the dropwise addition was completed, the ice-water bath was removed, and the mixture was stirred at room temperature for 4 h. The reaction was stopped after 24 h, and a white solid was obtained by suction filtration under reduced pressure. The solid white product was rinsed with methanol to obtain 2,7-dibromofluorene (W) as a white crystal. Yield: 7.210 g (79%). Melting point: 208-210˚C. 1 H NMR (400MHz, DMSO- d 6 ): δ 1.60 (t, 6H, C H 2 ), 2.90 (m, 4H, C H 2 ), 7.65 (m, 2H, Ar H ),7.78(d, 2H, Ar H ), 7.86(d, 2H, Ar H )...
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