Nano Archive

Nanostaircase formation in the solid state from self-assembling synthetic terephthalamides with a common molecular scaffold

Ray, Sudipta and Hegde, Raghurama P. and Das, Apurba Kumar and Shamala, N. and Banerjee, Arindam (2006) Nanostaircase formation in the solid state from self-assembling synthetic terephthalamides with a common molecular scaffold. Tetrahedron, 62 (41). 9603 - 9609.

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Official URL: http://www.sciencedirect.com/science/article/B6THR...

Abstract

The design and construction of nanostructured materials using proper self-assembling molecular building blocks is a real challenge to scientists. Here, we present the formation of a new nano-architecture, i.e., nanostaircase in the solid state by using molecular building blocks, which are amenable to self-assembly in a directed manner to form the specific nanostructure. The molecular building blocks are terephthalamides 1–4, which are bis-terephthalamides of methyl esters of various α-amino acids including l-leucine 1, d-leucine 2, l-isoleucine 3, and α-aminoisobutyric acid (Aib) 4. All terephthalamides presented here, irrespective of their different side chain residues or stereochemistry, self-assemble to form supramolecular nanostaircase structures in crystals. Each terephthalamide contains two good hydrogen-bond donors and two hydrogen-bond acceptors. Two N–HO hydrogen bonds and C–Hπ interactions are responsible for the formation and stabilization of the nanostaircase structures in crystals. The molecular building blocks are packed orthogonally to each other in crystals and this arrangement can help the formation of nanostaircase structure upon self-assembly.

Item Type:Article
Uncontrolled Keywords:C–Hπ interactions; Nanostaircase; Terephthalamide; Self-assembly; Hydrogen bonds
Subjects:Material Science > Nanofabrication processes and tools
Biomedical Science > Nanomedicine
ID Code:5759
Deposited By:SPI
Deposited On:24 Jul 2009 10:03
Last Modified:24 Jul 2009 10:03

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