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将含二炔基的[2Fe2S]模型化合物[Fe2(μ-SCH2C≡CH)2(CO)6](A)和双叠氮单体2,6-(N3CH2)Py(B,Py=吡啶)与含碱性基团的双炔单体(2-Py CH2)N(CH2C≡CH)2(C,Py=吡啶)通过“点击反应”以不同比例进行共聚,得到了6种含不同碱基量的[FeFe]-氢化酶模型化合物功能聚合物Polymer-1~Polymer-6。通过红外光谱、硫元素分析、热重、扫描电镜和电化学对这些聚合物进行了表征。红外光谱和电化学研究表明二铁六羰基单元A以二铁五羰基的形式存在于聚合物中。在共聚过程中,增加单体C的含量能显著改变聚合物的形貌和增加其在有机溶剂中的溶解度,同时热稳定性也有所增加。这些聚合物在含有醋酸的DMF介质中催化质子还原的行为表明,通过单体C引入的碱性基团所形成的次级配位环境对二铁中心的催化性能有显著影响。
The dialkynyl-containing [2Fe2S] model compound [Fe2 (μ-SCH2C≡CH) 2 (CO) 6] (A) and the bisazide monomer 2,6- (N3CH2) Py Copolymerization with different alkyne group-containing alkyne monomer (2-Py CH2) N (CH2C≡CH) 2 (C, Py = pyridine) by “click reaction” Base amount of [FeFe] -hydrogenase model compound functional polymer Polymer-1 ~ Polymer-6. These polymers were characterized by infrared spectroscopy, elemental sulfur analysis, thermogravimetry, scanning electron microscopy and electrochemistry. Infrared spectroscopy and electrochemical studies showed that the iron hexacarbonyl unit A in the form of ferrocene pentacarbonyl in the polymer. In the copolymerization process, increasing the content of monomer C can significantly change the polymer morphology and increase its solubility in organic solvents, while thermal stability has also increased. The catalytic proton reduction behavior of these polymers in acetic acid-containing DMF media indicates that the secondary coordination environment formed by the basic groups introduced by monomer C has a significant effect on the catalytic performance of the diiron centers.