Abyazisani Maryam, MacLeod Jennifer M, Lipton-Duffin Josh
School of Chemistry, Physics and mechanical Engineering , Queensland University of Technology , 2 George Street , Brisbane , QLD 4000 , Australia.
Institute for Future Environments , Queensland University of Technology , 2 George Street , Brisbane , QLD 4000 , Australia.
ACS Nano. 2019 Aug 27;13(8):9270-9278. doi: 10.1021/acsnano.9b03812. Epub 2019 Jul 15.
Ullmann coupling is one of the most frequently employed methodologies for producing π-conjugated surface-confined polymers. One unfortunate side product of the reaction is the creation of metal halide islands formed from liberated halogen atoms. Following the coupling reaction, these halide islands can account for a large proportion of the substrate surface area and thus inhibit domain growth and effectively poison the catalyst. Here, we describe an efficient and reliable methodology for removing the halogen byproduct at room temperature by exposure to a beam of atomic hydrogen; this action removes the halogen atoms in a matter of minutes, with minimal impact to the polymer structure. We also find that it is possible under certain circumstances to preserve the pre-exposure epitaxy after removal of the halogen. This finding provides a convenient and straightforward technique for addressing the most often-cited drawback of the on-surface Ullman coupling methodology and provides access to a previously inaccessible parameter space for these types of experiments.
乌尔曼偶联是制备π共轭表面受限聚合物最常用的方法之一。该反应一个不幸的副产物是由释放出的卤素原子形成金属卤化物岛。偶联反应之后,这些卤化物岛会占据很大一部分基底表面积,从而抑制畴生长并有效毒化催化剂。在此,我们描述了一种高效且可靠的方法,即在室温下通过暴露于原子氢束来去除卤素副产物;此操作在几分钟内就能去除卤素原子,对聚合物结构的影响极小。我们还发现,在某些情况下,去除卤素后有可能保留曝光前的外延结构。这一发现为解决表面乌尔曼偶联方法最常被提及的缺点提供了一种简便直接的技术,并为这类实验提供了一个以前无法进入的参数空间。