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Positive and negative regulation of carbon nanotube catalysts through encapsulation within macrocycles

机译:通过大环内的包封对碳纳米管催化剂的正负调节

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摘要

One of the most attractive applications of carbon nanomaterials is as catalysts, due to their extreme surface-to-volume ratio. The substitution of C with heteroatoms (typically B and N as p- and n-dopants) has been explored to enhance their catalytic activity. Here we show that encapsulation within weakly doping macrocycles can be used to modify the catalytic properties of the nanotubes towards the reduction of nitroarenes, either enhancing it (n-doping) or slowing it down (p-doping). This artificial regulation strategy presents a unique combination of features found in the natural regulation of enzymes: binding of the effectors (the macrocycles) is noncovalent, yet stable thanks to the mechanical link, and their effect is remote, but not allosteric, since it does not affect the structure of the active site. By careful design of the macrocycles’ structure, we expect that this strategy will contribute to overcome the major hurdles in SWNT-based catalysts: activity, aggregation, and specificity.
机译:碳纳米材料最吸引人的应用之一是催化剂,因为它们具有极高的表面体积比。已经研究了用杂原子(通常是B和N为p型和n型掺杂剂)取代C的作用,以增强其催化活性。在这里,我们表明弱掺杂大环内的封装可用于改变纳米管的催化性能,以降低硝基芳烃的含量,从而增强(n掺杂)或减慢其速度(p掺杂)。这种人工调节策略提供了酶自然调节中发现的特征的独特组合:效应子(大环)的结合是非共价的,但由于机械连接的缘故却是稳定的,并且它们的作用很小,但不是变构的,因为它确实不影响活动站点的结构。通过仔细设计大环化合物的结构,我们预计该策略将有助于克服基于SWNT的催化剂的主要障碍:活性,聚集和特异性。

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