Premium
Helicity‐Encoded Molecular Strands: Efficient Access by the Hydrazone Route and Structural Features
Author(s) -
Schmitt JeanLouis,
Stadler AdrianMihail,
Kyritsakas Nathalie,
Lehn JeanMarie
Publication year - 2003
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/hlca.200390137
Subject(s) - chemistry , crystallography , stacking , hydrazone , helicity , stereochemistry , pyridine , folding (dsp implementation) , organic chemistry , particle physics , electrical engineering , engineering , physics
Control over the folding of molecular strands may be achieved by appropriate choice of the constituting subunits, in particular for chains of specific heterocycles such as sequences of directly connected pyridine (py) and pyrimidine (pym) rings, which are known to fold into extended helical structures. Since the hydrazone (hyz) group represents an isomorphic analogue of a py site, the condensation of hydrazine and carboxaldehyde derivatives of pym offers a very efficient approach to strands incorporating hyz instead of py units and constituted by sequences of alternating hyz and pym groups. A series of such strands of different lengths, up to ten hyz units, i.e. , 1 – 7 , were synthesized. Their spectral properties indicate that they fold indeed into helical shapes. Extensive characterization was performed in solution by 1 HNMR spectroscopy and in the solid state by determination of the crystal structures of eight such strands. They all display the expected helical geometry with up to 3 1 / 3 turns and direct stacking contacts. The efficiency and flexibility of the synthetic approach as well as its wide potential for generation of diversity through lateral decoration make the (hyzpym) subunit a particularly attractive helicity codon.