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Carbon-Based Oxamate Cobalt(III) Complexes as Bioenzyme Mimics for Contaminant Elimination in High Backgrounds of Complicated Constituents

机译:碳基草酸盐钴(III)复合物作为生物酶模拟物在复杂成分的高背景下消除污染物

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摘要

Complex wastewater with massive components is now a serious environmental issue facing humanity. Selective removal of low-concentration contaminants in mixed constituents holds great promise for increasing water supplies. Bioenzymes like horseradish peroxidase exhibit oxidizing power and selectivity. Here, we manufactured its mimic through immobilizing non-heme oxamate anionic cobalt(III) complex ([CoIII(opba)], opba = o-phenylenebis(oxamate)) onto pyridine (Py) modified multiwalled carbon nanotubes ([CoIII(opba)]-Py-MWCNTs, MWCNTs = multiwalled carbon nanotubes), where MWCNTs captured substrates and Py functioned as the fifth ligand. We chose typical azo dye (C.I. Acid Red 1) and antibiotic (ciprofloxacin) as model substrates. Without •OH, this catalyst could detoxify target micropollutants efficiently at pH from 8 to 11. It also remained efficient in repetitive tests, and the final products were non-poisonous OH-containing acids. Combined with radical scavenger tests and electron paramagnetic resonance result, we speculated that high-valent cobalt-oxo active species and oxygen atom transfer reaction dominated in the reaction pathway. According to density functional theory calculations, the electron spin density distribution order showed that electron-withdrawing ligand was beneficial for inward pulling the excess electron and lowering the corresponding energy levels, achieving an electrophilic-attack enhancement of the catalyst. With target removal property and recyclability, this catalyst is prospective in water detoxication.
机译:具有大量成分的复杂废水现已成为人类面临的严重环境问题。选择性去除混合成分中的低浓度污染物具有增加水供应的巨大希望。辣根过氧化物酶等生物酶具有氧化能力和选择性。在这里,我们通过固定非血红素草酸酯阴离子钴(III)([Co III (opba)] -,opba = o-phenylenebis(oxamate) )置于吡啶(Py)修饰的多壁碳纳米管上[[Co III (opba)] - -Py-MWCNT,MWCNT =多壁碳纳米管),其中MWCNT捕获了底物, Py充当第五配体。我们选择典型的偶氮染料(C.I.酸性红1)和抗生素(环丙沙星)作为模型底物。如果没有•OH,则该催化剂可以在8至11的pH值下有效地将目标微污染物解毒。在重复测试中,该催化剂也仍然有效,并且最终产物为无毒的OH酸。结合自由基清除剂测试和电子顺磁共振结果,我们推测高价钴氧合活性物种和氧原子转移反应在反应路径中占主导地位。根据密度泛函理论计算,电子自旋密度分布阶数表明吸电子配体有利于向内拉动多余的电子并降低相应的能级,从而实现了催化剂的亲电攻击增强。具有目标去除性能和可回收性,该催化剂有望用于水脱毒。

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