Use of the self-assembly of tyrosine-containing bolaamphiphile molecules as a reactive template for metal deposition

Jinyoung Kwak, Soo In Park, Sang Yup Lee

Research output: Contribution to journalArticle

17 Citations (Scopus)

Abstract

A novel bolaamphiphile molecule exploiting biochemical functionality was synthesized and self-assembled to form a spherical reactive template for the preparation of composite metallic nanoshells. A tyrosine-containing bolaamphiphile, bis(N-alpha-amido-tyrosine)-1,7-heptane dicarboxylate, self-assembles instantaneously in an aqueous solution forming nanoscaled spheres. Instantaneous assembly of the prepared bolaamphiphile is driven by the polarity and stacking of phenol moiety in tyrosine. Through spectroscopic investigations, molecular interactions such as hydrogen bonding and π-π stacking of aromatic rings were found to induce the self-assembly of the molecule. The phenol moiety of tyrosine is exposed to the surface of the spherical assembly due to its polarity. Under basic conditions, the spherical assembly was used as a reactive template on which metal clusters were deposited. The surface-exposed phenol group reduced the silver ions to solid clusters, and these clusters were further exploited as catalysts for the gold layer deposition. This study illustrates that the bolaamphiphilic molecule with designed biochemical functionality provides a facile way to prepare supramolecular structures with chemical activity.

Original languageEnglish
Pages (from-to)70-75
Number of pages6
JournalColloids and Surfaces B: Biointerfaces
Volume102
DOIs
Publication statusPublished - 2013 Feb 1

Fingerprint

tyrosine
Self assembly
Phenols
Tyrosine
self assembly
templates
Phenol
Metals
phenols
Molecules
assembly
metals
Nanoshells
molecules
polarity
Molecular interactions
Heptane
Heptanes
Hydrogen bonds
Silver

All Science Journal Classification (ASJC) codes

  • Biotechnology
  • Surfaces and Interfaces
  • Physical and Theoretical Chemistry
  • Colloid and Surface Chemistry

Cite this

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abstract = "A novel bolaamphiphile molecule exploiting biochemical functionality was synthesized and self-assembled to form a spherical reactive template for the preparation of composite metallic nanoshells. A tyrosine-containing bolaamphiphile, bis(N-alpha-amido-tyrosine)-1,7-heptane dicarboxylate, self-assembles instantaneously in an aqueous solution forming nanoscaled spheres. Instantaneous assembly of the prepared bolaamphiphile is driven by the polarity and stacking of phenol moiety in tyrosine. Through spectroscopic investigations, molecular interactions such as hydrogen bonding and π-π stacking of aromatic rings were found to induce the self-assembly of the molecule. The phenol moiety of tyrosine is exposed to the surface of the spherical assembly due to its polarity. Under basic conditions, the spherical assembly was used as a reactive template on which metal clusters were deposited. The surface-exposed phenol group reduced the silver ions to solid clusters, and these clusters were further exploited as catalysts for the gold layer deposition. This study illustrates that the bolaamphiphilic molecule with designed biochemical functionality provides a facile way to prepare supramolecular structures with chemical activity.",
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Use of the self-assembly of tyrosine-containing bolaamphiphile molecules as a reactive template for metal deposition. / Kwak, Jinyoung; Park, Soo In; Lee, Sang Yup.

In: Colloids and Surfaces B: Biointerfaces, Vol. 102, 01.02.2013, p. 70-75.

Research output: Contribution to journalArticle

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AB - A novel bolaamphiphile molecule exploiting biochemical functionality was synthesized and self-assembled to form a spherical reactive template for the preparation of composite metallic nanoshells. A tyrosine-containing bolaamphiphile, bis(N-alpha-amido-tyrosine)-1,7-heptane dicarboxylate, self-assembles instantaneously in an aqueous solution forming nanoscaled spheres. Instantaneous assembly of the prepared bolaamphiphile is driven by the polarity and stacking of phenol moiety in tyrosine. Through spectroscopic investigations, molecular interactions such as hydrogen bonding and π-π stacking of aromatic rings were found to induce the self-assembly of the molecule. The phenol moiety of tyrosine is exposed to the surface of the spherical assembly due to its polarity. Under basic conditions, the spherical assembly was used as a reactive template on which metal clusters were deposited. The surface-exposed phenol group reduced the silver ions to solid clusters, and these clusters were further exploited as catalysts for the gold layer deposition. This study illustrates that the bolaamphiphilic molecule with designed biochemical functionality provides a facile way to prepare supramolecular structures with chemical activity.

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