Literature DB >> 15469265

Efficient photocurrent generation by self-assembled monolayers composed of 3 10-helical peptides carrying linearly spaced naphthyl groups at the side chains.

Kazuyuki Yanagisawa1, Tomoyuki Morita, Shunsaku Kimura.   

Abstract

Self-assembled monolayers (SAMs) were prepared on a gold substrate from a 310-helical peptide carrying three naphthyl groups at the side chain (SSN3B) or from the reference peptides carrying no or one naphthyl group. The 310-helical conformation of SSN3B in solution was confirmed by 1H NMR spectroscopy and geometry optimization. Cyclic voltammetry and infrared absorption-reflection spectroscopy showed vertical molecular orientation and a well-packed structure in the SSN3B SAM. Anodic photocurrent was successfully generated by the SSN3B SAM in the presence of triethanolamine, and the current intensity was found to be much larger than those by the other SAMs from peptides carrying one naphthyl group. It was therefore concluded that the linearly spaced naphthyl groups along the helical axis act as photosensitizer and electron-hopping site to promote photocurrent generation remarkably.

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Year:  2004        PMID: 15469265     DOI: 10.1021/ja0476011

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


  2 in total

1.  Unraveling the interplay of backbone rigidity and electron rich side-chains on electron transfer in peptides: the realization of tunable molecular wires.

Authors:  John R Horsley; Jingxian Yu; Katherine E Moore; Joe G Shapter; Andrew D Abell
Journal:  J Am Chem Soc       Date:  2014-08-20       Impact factor: 15.419

2.  An Orthogonal Dynamic Covalent Chemistry Tool for Ring-Opening Polymerization of Cyclic Oligochalcogenides on Detachable Helical Peptide Templates.

Authors:  Quentin Laurent; Naomi Sakai; Stefan Matile
Journal:  Chemistry       Date:  2022-05-04       Impact factor: 5.020

  2 in total

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