Photoinduced Electron Transfer within Supramolecular Donor-Acceptor Peptide Nanostructures under Aqueous Conditions

被引:70
作者
Sanders, Allix M. [1 ,4 ]
Magnanelli, Timothy J. [1 ]
Bragg, Arthur E. [1 ]
Tovar, John D. [1 ,2 ,3 ]
机构
[1] Johns Hopkins Univ, Dept Chem, Krieger Sch Arts & Sci, 3400 North Charles St, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Dept Mat Sci & Engn, Whiting Sch Engn, 3400 North Charles St, Baltimore, MD 21218 USA
[3] Johns Hopkins Univ, Inst NanoBioTechnol, 3400 North Charles St, Baltimore, MD 21218 USA
[4] NCI, Frederick, MD 21702 USA
基金
美国国家科学基金会;
关键词
PORPHYRIN-FULLERENE TRIAD; CHARGE SEPARATION; CONDUCTING-POLYMER; ENERGY-TRANSFER; STRUCTURAL RELAXATION; NEURITE OUTGROWTH; DYADS; LIGHT; NANOMATERIALS; RECOMBINATION;
D O I
10.1021/jacs.5b12001
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report the synthesis, self-assembly, and electron transfer capabilities of peptide-based electron donor acceptor molecules and supramolecular nanostructures. These modified peptides contain pi-conjugated oligothiophene electron donor cores that are peripherally substituted with naphthalene diimide electron acceptors installed via imidation of site-specific lysine residues. These molecules self-assemble into one-dimensional nanostructures in aqueous media, as shown through steady-state absorption, photoluminescence, and circular dichroism spectra, as well as transmission electron microscopy. Excitation of the oligothiophene donor moieties results in electron transfer to the acceptor units, ultimately creating polar, charge-separated states that persist for over a nanosecond as observed with transient absorption spectroscopy. This study demonstrates how transient electric fields can be engineered into aqueous nanomaterials of biomedical relevance through external, temporally controlled photonic inputs.
引用
收藏
页码:3362 / 3370
页数:9
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