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基于萘二酰亚胺修饰二肽的 1-D n 型纳米结构的自组装。

Self-assembly of 1-D n-type nanostructures based on naphthalene diimide-appended dipeptides.

机构信息

Department of Chemistry, The Ohio State University, 100 West 18th Avenue, Columbus, Ohio 43210, USA.

出版信息

J Am Chem Soc. 2009 Nov 18;131(45):16374-6. doi: 10.1021/ja906377q.

Abstract

n-Type 1D nanostructures are formed from the beta-sheet assembly of dipeptides bearing a 1,4,5,8-naphthalenetetracarboxylic acid diimide (NDI) side chain into either helical nanofibers or twisted nanoribbons. Amyloid-like 1-D helical nanofibers and twisted nanoribbons assemble in an aqueous solution depending on the placement of the NDI group. beta-Sheet-type hydrogen bonding and pi-pi association play important roles in directing the assembly process. A delicate balance between electrostatic repulsion and hydrophobic interactions is critical for self-assembly. Fluorescence lifetime and anisotropy experiments indicate that the nature of the intermolecular organization and packing within the nanostructures critically impacts intermolecular energy migration pi-electron delocalization.

摘要

n 型 1D 纳米结构是由带有 1,4,5,8-萘四羧酸二酰亚胺(NDI)侧链的二肽的β-折叠组装而成,形成螺旋纳米纤维或扭曲纳米带。在水溶液中,类似淀粉样的 1D 螺旋纳米纤维和扭曲纳米带根据 NDI 基团的位置组装。β-折叠型氢键和π-π 相互作用在指导组装过程中起着重要作用。静电排斥和疏水相互作用之间的微妙平衡对于自组装至关重要。荧光寿命和各向异性实验表明,纳米结构内分子间的组织和堆积的性质对分子间能量迁移π电子离域有重要影响。

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