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Fibrillar structure of self-assemblies formed from heterocomplementary monomers linked through sextuple hydrogen-bonding arrays

✍ Scribed by E. Buhler; S. J. Candau; J. Schmidt; Y. Talmon; E. Kolomiets; J.-M. Lehn


Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
875 KB
Volume
45
Category
Article
ISSN
0887-6266

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✦ Synopsis


Abstract

The nanostructure of the fibrillar supramolecular aggregates generated in decane solutions of homoditopic heterocomplementary monomers forming sextuple hydrogen‐bond‐mediated self‐assemblies was investigated by small‐angle neutron scattering and cryogenic‐temperature transmission electron microscopy. The persistence length (L~p~) of the fibrillar aggregates was found to be ∼18 nm, as inferred from combined measurements of the radius of gyration and of the contour length. The values of both the weight‐average molecular weight and the mass per unit length of the fibers suggest that the latter consist of few aggregated monomolecular wires. At T = 25 °C, the formation of branched aggregates occurs around the crossover concentration, C*, between the dilute and semidilute regimes, whereas the classical behavior of equilibrium polymers is observed at T = 65 °C. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 45: 103–115, 2007