Abstract
The preparation of chiral functional materials with new, improved, and interesting properties is aided tremendously by control of the spatial arrangement of the functional units within them. The use of non-covalent interactions is absolutely critical in this regard, and the molecular–supramolecular balance has to be strictly controlled. The conducting, magnetic and optical properties of chiral materials whose function is profoundly influenced by supramolecular chemistry will be reviewed. Special emphasis is placed on the control of helical arrangements in liquid crystalline systems, in which both chiral induction and spontaneous resolution are important phenomena which can be controlled.
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Abbreviations
- hfac:
-
Hexafluoroacetylacetonate
- AFM:
-
atomic force microscopy
- CD:
-
circular dichroism
- CPL:
-
circularly polarised light
- CSA:
-
camphorsulphonic acid
- IR:
-
infrared
- LB:
-
Langmuir–Blodgett
- LC:
-
liquid crystal
- OPV:
-
oligophenylenevinylene
- PANI:
-
poly(aniline)
- PEDOT:
-
poly(ethylenedioxythiophene)
- Pc:
-
phthalocyanine
- PT:
-
poly(thiophene)
- SEM:
-
scanning electron microscopy
- TEM:
-
transmission electron microscopy
- TTF:
-
tetrathiafulvalene
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Acknowledgments
We warmly thank all the researchers that have contributed to the research in this area that has been performed in our laboratories, and to the organisations that finance our research at the present time: The European Commission for the Marie Curie RTN CHEXTAN (MRTN-CT-2004-512161), the Network of Excellence MAGMANet (515767-2) and the Integrated Project NAIMO (NMP4-CT-2004-500355), and the DGI, Spain (Projects No. BQU 2003-00760 and MAT 2003-04699). We also thank Dr. “Bert” Meijer (Eindhoven University of Technology, Holland) for supplying the graphics for Fig. 15.
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Amabilino, D.B., Veciana, J. Supramolecular Chiral Functional Materials. In: Crego-Calama, M., Reinhoudt, D.N. (eds) Supramolecular Chirality. Topics in Current Chemistry, vol 265. Springer, Berlin, Heidelberg. https://doi.org/10.1007/128_034
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