Quirós-Ovies Ramiro, Vázquez Sulleiro Manuel, Vera-Hidalgo Mariano, Prieto Javier, Gómez I Jénnifer, Sebastián Víctor, Santamaría Jesús, Pérez Emilio M
IMDEA Nanociencia, Ciudad Universitaria de Cantoblanco, C/Faraday 9, 28049, Madrid, Spain.
CEITEC Masaryk University, Kamenice 5, 62500, Brno, Czech Republic.
Chemistry. 2020 May 20;26(29):6629-6634. doi: 10.1002/chem.202000068. Epub 2020 Mar 31.
Most air-stable 2D materials are relatively inert, which makes their chemical modification difficult. In particular, in the case of MoS , the semiconducting 2 H-MoS is much less reactive than its metallic counterpart, 1T-MoS . As a consequence, there are hardly any reliable methods for the covalent modification of 2 H-MoS . An ideal method for the chemical functionalization of such materials should be both mild, not requiring the introduction of a large number of defects, and versatile, allowing for the decoration with as many different functional groups as possible. Herein, a comprehensive study on the covalent functionalization of 2 H-MoS with maleimides is presented. The use of a base (Et N) leads to the in situ formation of a succinimide polymer layer, covalently connected to MoS . In contrast, in the absence of base, functionalization stops at the molecular level. Moreover, the functionalization protocol is mild (occurs at room temperature), fast (nearly complete in 1 h), and very flexible (11 different solvents and 10 different maleimides tested). In practical terms, the procedures described here allow for the chemist to manipulate 2 H-MoS in a very flexible way, decorating it with polymers or molecules, and with a wide range of functional groups for subsequent modification. Conceptually, the spurious formation of an organic polymer might be general to other methods of functionalization of 2D materials, where a large excess of molecular reagents is typically used.
大多数空气稳定的二维材料相对惰性,这使得它们的化学修饰变得困难。特别是对于二硫化钼(MoS₂)而言,半导体性的2H-MoS₂比其金属性对应物1T-MoS₂的反应活性要低得多。因此,几乎没有任何可靠的方法对2H-MoS₂进行共价修饰。对于此类材料的化学功能化而言,理想的方法应该既温和(不需要引入大量缺陷)又通用(允许尽可能多地用不同官能团进行修饰)。在此,本文展示了一项关于用马来酰亚胺对2H-MoS₂进行共价功能化的全面研究。使用碱(Et₃N)会导致原位形成与MoS₂共价连接的琥珀酰亚胺聚合物层。相比之下,在没有碱的情况下,功能化停留在分子水平。此外,功能化方案温和(在室温下进行)、快速(1小时内几乎完成)且非常灵活(测试了11种不同溶剂和10种不同马来酰亚胺)。实际上,这里描述的方法允许化学家以非常灵活的方式操控2H-MoS₂,用聚合物或分子以及各种官能团对其进行修饰以便后续改性。从概念上讲,有机聚合物的虚假形成可能对于二维材料的其他功能化方法具有普遍性,在这些方法中通常使用大量过量的分子试剂。