Departamento de Química Orgánica, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Ciudad Universitaria, s/n, 28040, -Madrid, Spain.
Angew Chem Int Ed Engl. 2023 Mar 27;62(14):e202218572. doi: 10.1002/anie.202218572. Epub 2023 Feb 20.
The synthesis and self-assembling features of N-annulated perylenebisimides (N-PBIs) 2-4 are reported and compared with the complex self-assembly of N-PBI 1. The studies presented herein demonstrate that increasing the length of the alkyl spacer separating the central aromatic core of the dye and the peripheral side chains cancels the differentiation on the corresponding supramolecular polymerization. Thus, only 2 is able to form two different supramolecular polymorphs. The formation of kinetically trapped monomeric species is observed for all the N-PBIs 2-4. These metastable species, constituted by intramolecularly H-bonded pseudocycles of 7, 8, 9, or 10 members for compounds 1, 2, 3, and 4, respectively, provoke kinetically controlled supramolecular polymerizations that can be accelerated by the addition of seeds. The results presented herein shed light on the intricate process of differentiation in self-assembly.
本文报道了 N-稠合苝二酰亚胺(N-PBIs)2-4 的合成和自组装特性,并将其与 N-PBI 1 的复杂自组装进行了比较。本文的研究表明,增加染料中心芳核与外围侧链之间的间隔烷基链的长度会取消对相应超分子聚合的区分。因此,只有 2 能够形成两种不同的超分子多晶型物。对于所有的 N-PBIs 2-4,都观察到动力学捕获的单体物种的形成。这些处于亚稳状态的物种,分别由化合物 1、2、3 和 4 中的分子内氢键形成的 7、8、9 或 10 成员的拟环组成,引发动力学控制的超分子聚合,通过添加晶种可以加速该聚合。本文的结果阐明了自组装中复杂的分化过程。