π-Electron Conjugation in Two Dimensions

被引:224
作者
Gutzler, Rico [1 ]
Perepichka, Dmitrii F. [2 ,3 ]
机构
[1] Max Planck Inst Solid State Res, D-70569 Stuttgart, Germany
[2] McGill Univ, Dept Chem, Montreal, PQ H3A 0B8, Canada
[3] McGill Univ, Ctr Self Assembled Chem Struct, Montreal, PQ H3A 0B8, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
OPTICAL-PROPERTIES; COVALENT NETWORKS; ORGANIC POLYMERS; CARBON; NANOGRAPHENES; DERIVATIVES; CHEMISTRY; OLIGOMERS; GRAPHYNE; MOBILITY;
D O I
10.1021/ja408355p
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Organic oligomers and polymers with extended pi-conjugation are the fundamental building blocks of organic electronic devices. Novel routes are being explored to create tailor-made organic materials, and recent progress in organic chemistry and surface chemistry has led to the synthesis of planar 2D polymers. Here we show how extending pi-conjugation in the second dimension leads to novel materials with HOMO-LUMO gaps smaller than in ID polymers built from the same parent molecular repeat unit. Density functional theory calculations on experimentally realized 2D polymers grant insight into HOMO-LUMO gap contraction with increasing oligomer size and show fundamental differences between ID and 2D "band gap engineering". We discuss how the effects of cross-conjugation and dihedral twists affect the electronic gaps.
引用
收藏
页码:16585 / 16594
页数:10
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