Summerfield Alex, Baldoni Matteo, Kondratuk Dmitry V, Anderson Harry L, Whitelam Stephen, Garrahan Juan P, Besley Elena, Beton Peter H
School of Physics and Astronomy, University of Nottingham, Nottingham, NG7 2RD, UK.
School of Chemistry, University of Nottingham, Nottingham, NG7 2RD, UK.
Nat Commun. 2019 Jul 3;10(1):2932. doi: 10.1038/s41467-019-11009-y.
The regular packing of atoms, molecules and nanoparticles provides the basis for the understanding of structural order within condensed phases of matter. Typically the constituent particles are considered to be rigid with a fixed shape. Here we show, through a combined experimental and numerical study of the adsorption of cyclic porphyrin polymers, nanorings, on a graphite surface, that flexible molecules can exhibit a rich and complex packing behaviour. Depending on the number of porphyrin sub-units within the nanoring we observe either a highly ordered hexagonal phase or frustrated packing driven by directional interactions which for some arrangements is combined with the internal deformation of the cyclic polymer. Frustration and deformation occur in arrays of polymers with ten sub-units since close packing and co-alignment of neighbouring groups cannot be simultaneously realised for nanorings with this internal symmetry.
原子、分子和纳米粒子的规则堆积为理解凝聚态物质内部的结构有序性提供了基础。通常,组成粒子被认为是具有固定形状的刚性粒子。在此,我们通过对环状卟啉聚合物(纳米环)在石墨表面吸附的实验与数值相结合的研究表明,柔性分子能够展现出丰富而复杂的堆积行为。根据纳米环内卟啉亚基的数量,我们观察到要么是高度有序的六方相,要么是由方向相互作用驱动的受挫堆积,对于某些排列而言,这种相互作用还伴随着环状聚合物的内部变形。具有十个亚基的聚合物阵列中会出现受挫和变形现象,因为对于具有这种内部对称性的纳米环,相邻基团的紧密堆积和共排列无法同时实现。