Rodríguez Rafael, Naranjo Cristina, Kumar Anil, Dhbaibi Kais, Matozzo Paola, Camerel Franck, Vanthuyne Nicolas, Gómez Rafael, Naaman Ron, Sánchez Luis, Crassous Jeanne
Institut des Sciences Chimiques de Rennes, University of Rennes, CNRS, ISCR, UMR 6226, F-35000, Rennes, France.
Departamento de Química Orgánica, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Ciudad Universitaria s/n, 28040, Madrid, Spain.
Chemistry. 2023 Nov 13;29(63):e202302254. doi: 10.1002/chem.202302254. Epub 2023 Oct 5.
Self-assembling features, chiroptical activity, and spin filtering properties are reported for 2,15- and 4,13-disubstituted [6]helicenes decorated in their periphery with 3,4,5-tris(dodecyloxy)-N-(4-ethynylphenyl)benzamide moieties. The weak non-covalent interaction between these units conditions the corresponding circularly polarized luminescence and spin polarization. The self-assembly is overall weak for these [6]helicene derivatives that, despite the formation of H-bonding interactions between the amide groups present in the peripheral moieties, shows very similar chiroptical properties both in the monomeric or aggregated states. This effect could be explained by considering the steric effect that these groups could generate in the growing of the corresponding aggregate formed. Importantly, the self-assembling features also condition chiral induced spin selectivity (CISS effect), with experimental spin polarization (SP) values found between 35-40 % for both systems, as measured by magnetic-conducting atomic force microscopy (AFM) technique.
据报道,在其外围装饰有3,4,5-三(十二烷氧基)-N-(4-乙炔基苯基)苯甲酰胺基团的2,15-和4,13-二取代[6]螺烯具有自组装特性、手性光活性和自旋过滤特性。这些单元之间的弱非共价相互作用决定了相应的圆偏振发光和自旋极化。对于这些[6]螺烯衍生物,自组装总体较弱,尽管外围部分存在的酰胺基团之间形成了氢键相互作用,但在单体或聚集状态下都表现出非常相似的手性光性质。这种效应可以通过考虑这些基团在相应聚集体生长过程中可能产生的空间效应来解释。重要的是,自组装特性也决定了手性诱导自旋选择性(CISS效应),通过磁导原子力显微镜(AFM)技术测量,两个系统的实验自旋极化(SP)值均在35-40%之间。