Literature DB >> 19852501

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

Hui Shao1, Tuan Nguyen, Natalie C Romano, David A Modarelli, Jon R Parquette.   

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.

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Year:  2009        PMID: 19852501     DOI: 10.1021/ja906377q

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  13 in total

1.  Redox-sensitive reversible self-assembly of amino acid-naphthalene diimide conjugates.

Authors:  Wathsala Liyanage; Paul W Rubeo; Bradley L Nilsson
Journal:  Interface Focus       Date:  2017-10-20       Impact factor: 3.906

2.  Responsive organogels formed by supramolecular self assembly of PEG-block-allyl-functionalized racemic polypeptides into β-sheet-driven polymeric ribbons.

Authors:  Jiong Zou; Fuwu Zhang; Yingchao Chen; Jeffery E Raymond; Shiyi Zhang; Jingwei Fan; Jiahua Zhu; Ang Li; Kellie Seetho; Xun He; Darrin J Pochan; Karen L Wooley
Journal:  Soft Matter       Date:  2013-07-10       Impact factor: 3.679

3.  Exploiting the interactions of aromatic units for folding and assembly in aqueous environments.

Authors:  B A Ikkanda; B L Iverson
Journal:  Chem Commun (Camb)       Date:  2016-06-14       Impact factor: 6.222

4.  Time-Dependent Solid State Polymorphism of a Series of Donor-Acceptor Dyads.

Authors:  Cameron Peebles; Paul M Alvey; Vincent Lynch; Brent L Iverson
Journal:  Cryst Growth Des       Date:  2014-01-02       Impact factor: 4.076

5.  More than meets the eye: conformational switching of a stacked dialkoxynaphthalene-naphthalenetetracarboxylic diimide (DAN-NDI) foldamer to an NDI-NDI fibril aggregate.

Authors:  Cameron Peebles; Rebecca Piland; Brent L Iverson
Journal:  Chemistry       Date:  2013-07-12       Impact factor: 5.236

6.  Red aqueous room-temperature phosphorescence modulated by anion-π and intermolecular electronic coupling interactions.

Authors:  Fengbo Liu; Hai Yang; Dongdong Sun; Fang Gao; Xiongzhi Zhang; Zhiyong Zhao; Xie Han; Simin Liu
Journal:  Chem Sci       Date:  2022-05-25       Impact factor: 9.969

7.  Multi-responsive Hydrogels Derived from the Self-assembly of Tethered Allyl-functionalized Racemic Oligopeptides.

Authors:  Xun He; Jingwei Fan; Fuwu Zhang; Richen Li; Kevin A Pollack; Jeffery E Raymond; Jiong Zou; Karen L Wooley
Journal:  J Mater Chem B       Date:  2014-12-14       Impact factor: 6.331

8.  A nanomesh scaffold for supramolecular nanowire optoelectronic devices.

Authors:  Lei Zhang; Xiaolan Zhong; Egon Pavlica; Songlin Li; Alexander Klekachev; Gvido Bratina; Thomas W Ebbesen; Emanuele Orgiu; Paolo Samorì
Journal:  Nat Nanotechnol       Date:  2016-07-25       Impact factor: 39.213

9.  Synthesis and Liquid Crystalline Properties of Unsymmetrically Substituted Naphthalenediimides with a Polar Headgroup: Effect of Amide Hydrogen Bonding and Alkyl Chain Length.

Authors:  Namdev V Ghule; Rajesh S Bhosale; Sidhanath V Bhosale; Turlapati Srikanth; Nandiraju V S Rao; Sheshanath V Bhosale
Journal:  ChemistryOpen       Date:  2017-11-15       Impact factor: 2.911

10.  Energy transfer within responsive pi-conjugated coassembled peptide-based nanostructures in aqueous environments.

Authors:  Herdeline Ann M Ardoña; John D Tovar
Journal:  Chem Sci       Date:  2014-12-05       Impact factor: 9.825

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