4.8 Article

Nano- and microstructuration of supramolecular materials driven by H-bonded uracil.2,6-diamidopyridine complexes

Journal

NANOSCALE
Volume 5, Issue 19, Pages 8837-8851

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c3nr01711g

Keywords

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Funding

  1. EU through the ERC Starting Grant COLORLANDS project
  2. FRS-FNRS (FRFC) [2.4.550.09]
  3. FRS-FNRS (MIS) [F.4.505.10.F]
  4. Loterie Nationale
  5. Science Policy Office of the Belgian Federal Government [BELSPO-IAP 7/05]
  6. TINTIN ARC project [09/14-023]
  7. MIUR through the FIRB Futuro in Ricerca (SUPRACARBON) [RBFR10DAK6]
  8. University of Namur

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In the last few decades, multiple H-bonded arrays have been shown to be versatile tools to prepare functional supramolecular materials. Supramolecular complexes formed by uracil (Ur) and 2,6-diamidopyridine (DAP) developed by Lehn are the first examples of multiple H-bonded systems governing the formation of supramolecular polymers in solution. Although a large variety of complementary multiple H-bonded complexes has been prepared, the use of the heteromolecular Ur.DAP complex still remains very promising due to its ease of preparation and its intermediate association strength that ensures a dynamical character to the self-assembly and self-organisation processes. In this feature article, we report a detailed account on the results that our group has obtained in this field by designing and engineering a novel library of shape persistent molecular modules able to transfer their geometrical information to the final supramolecular architectures through the formation of Ur.DAP complexes both at the nanoscopic and microscopic levels.

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