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Electrochemical polymerization of phenanthrene in mixed electrolytes of boron trifluoride diethyl etherate and concentrated sulfuric acid

机译:三氟化硼二乙醚和浓硫酸混合电解质中菲的电化学聚合

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摘要

A novel high-quality polyphenanthrene(PPH)film with electrical conductivity of 10~(-1)S cm~(-1)was synthesized electrochemically by direct anodic oxidation of phenanthrene in boron trifluoride diethyl etherate containing 10% concentrated sulfuric acid(v/v).The oxidation onset potential of phenanthrene in this medium was measured to be only 0.91 V versus saturated calomel electrode(SCE),which was lower than that determined in acetonitrile +0.1 mol L~(-1)Bu4NBF4(1.56 V versus SCE).As-formed PPH films from this medium showed good electrochemical behavior and stability.De-doped PPH films were thoroughly soluble in dimethylsulfoxide or CHCl3.The structure and morphology of the polymer were investigated using UV-visible and Fourier transform infrared(FTIR)spectroscopy and scanning electron microscopy.FTIR and ~1H NMR spectra showed that the PPH was grown via the coupling of the monomer mainly at the C_4,C_5,C_9 and C_(10)positions.Fluorescence spectral studies indicated that PPH was a blue-green light emitter.
机译:通过在10%浓硫酸(v / v)的三氟化硼二乙醚中将菲直接阳极氧化电化学合成了一种新型的电导率为10〜(-1)S cm〜(-1)的高质量聚菲(PPH)薄膜。 v)。相对于饱和甘汞电极(SCE),菲在该介质中的氧化起始电势仅为0.91 V,低于乙腈+0.1 mol L〜(-1)Bu4NBF4(1.56 V vs.由该介质形成的PPH膜表现出良好的电化学性能和稳定性,去掺杂的PPH膜可完全溶于二甲亚砜或CHCl3中,用紫外可见光和傅立叶变换红外光谱(FTIR)研究聚合物的结构和形态光谱和扫描电镜观察FTIR和〜1H NMR谱表明PPH是通过单体主要在C_4,C_5,C_9和C_(10)位置偶联而生长的。荧光光谱研究表明PPH是蓝色的。重新发光。

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