Issue 5, 2013
From the journal:

New Journal of Chemistry

Exploring hydrogen bonding and weak aromatic interactions induced assembly of adenine and thymine functionalised naphthalenediimides†

Nagarjun Narayanaswamy,a   M. B. Avinasha  and  T. Govindaraju*a  

* Corresponding authors

a Bioorganic Chemistry Laboratory, New Chemistry Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Jakkur, Bangalore 560064, India
E-mail: tgraju@jncasr.ac.in
Fax: +91 8022082627

Abstract

Adenine and thymine functionalised naphthalenediimide (NDI) conjugates and complementary peptide nucleic acid (PNA) dimers are designed to exploit complementary hydrogen bonding and aromatic interactions for controllable molecular organization. These nucleobase appended NDIs organized into well-defined fibers, nanoribbons, porous spheres, belts and petal-like 2D sheets.

Graphical abstract: Exploring hydrogen bonding and weak aromatic interactions induced assembly of adenine and thymine functionalised naphthalenediimides

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Article information

DOI
https://doi.org/10.1039/C3NJ00060E
Article type
Letter
Submitted
14 Jan 2013
Accepted
12 Mar 2013
First published
13 Mar 2013

New J. Chem., 2013,37, 1302-1306

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Exploring hydrogen bonding and weak aromatic interactions induced assembly of adenine and thymine functionalised naphthalenediimides

N. Narayanaswamy, M. B. Avinash and T. Govindaraju, New J. Chem., 2013, 37, 1302 DOI: 10.1039/C3NJ00060E

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