In:
Israel Journal of Chemistry, Wiley, Vol. 51, No. 10 ( 2011-11), p. 1052-1066
Kurzfassung:
In this account we report on the self‐assembly of bis(merocyanine) dyes into helical nanorods by emphasizing the kinetic pathways and the mechanistic aspects leading to chiral amplification. A complex self‐assembly sequence of these dipolar dyes into well‐defined helical nanorod structures has been revealed spectroscopically by time‐dependent circular dichroism (CD) spectroscopy and microscopically by atomic force microscopy (AFM). This self‐assembly sequence proceeds over several kinetically formed supramolecular intermediates, which are distinguished by their morphology and (chir)optical properties. Moreover, the kinetics for the formation of homochiral nanorods was studied, revealing that chiral amplification mechanisms can operate at different stages of self‐assembly to afford energetically favored structures. The rates of these processes decrease strongly with decreasing chiral bias in the monomers or decreasing fraction of chiral co‐monomers in mixtures of chiral and achiral monomers. For the fully equilibrated nanorods, however, strong chiral amplification directed by the “majority‐rules” or “sergeants‐and‐soldiers” effect is observed.
Materialart:
Online-Ressource
ISSN:
0021-2148
,
1869-5868
DOI:
10.1002/ijch.201100023
Sprache:
Englisch
Verlag:
Wiley
Publikationsdatum:
2011
ZDB Id:
2066481-3
