Conjugated ligand-bridged ferrocene and ruthenium acetylene end group compound and preparation method and application thereof
A technology of ferrocene and compound, applied in the field of ferrocene and ruthenium acetylene terminal compound and its preparation, achieving the effect of broad application prospect
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Embodiment 1
[0028] A preparation method of a conjugated ligand (phenyl) bridged ferrocene and ruthenium acetylene end group compound, the above conjugated ligand bridged ferrocene and ruthenium acetylene end group compound is 1,4-phenyl The bridged ferrocene and ruthenium acetylene terminal compound specifically comprises the following steps: under nitrogen protection, 0.34mmol pentamethylcyclopentadienyl (1,2-bisdiphenylphosphine ethane) ruthenium chloride Cp * Dissolve Ru(dppe)Cl (227mg), 0.28mmol 4-trimethylsilylethynylphenylferrocene (100mg), 5.58mmol potassium fluoride (321mg) in a mixed solution of 20ml methanol and 3-4ml tetrahydrofuran , the system was heated and refluxed for 24 hours, cooled to room temperature, filtered with suction, the solid was washed with 10ml of methanol and 10ml of n-hexane, and then separated by column chromatography. The eluent was acetone and petroleum ether with a volume ratio of 1:10, and finally separated 180 mg of yellow solid was obtained, yield 6...
Embodiment 2
[0037] A method for preparing a ferrocene and ruthenium acetylene terminal compound bridged by a conjugated ligand (phenyl) is 1,3-benzene The ferrocene and ruthenium acetylene end group compound of radical bridging specifically comprise the following steps: under nitrogen protection, 0.34mmol pentamethylcyclopentadienyl (1,2-bisdiphenylphosphine ethane) chlorination Ruthenium Cp * Dissolve Ru(dppe)Cl (227mg), 0.28mmol 3-trimethylsilylethynylphenylferrocene (100mg), 5.58mmol potassium fluoride (321mg) in a mixed solution of 20ml methanol and 3-4ml tetrahydrofuran , the system was heated and refluxed for 24 hours, cooled to room temperature, filtered with suction, the solid was washed with 10ml of methanol and 10ml of n-hexane, and then separated by column chromatography. The eluent was acetone and petroleum ether with a volume ratio of 1:10, and finally separated 169 mg of pale yellow solid was obtained, yield 63%.
[0038]
[0039] The proton nuclear magnetic resonance spe...
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