Source:http://linkedlifedata.com/resource/pubmed/id/17441138
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2007-4-18
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pubmed:abstractText |
Two novel discotic macrocycles, substituted cyclohexa-m-phenylene (CHP) and cyclo-3,6-trisphenanthrylene (CTP), and the linear oligomer 3,3':6',3''-terphenanthrene (TP) as a model substance have been synthesized by repetitive cross-coupling reactions. To correlate the molecular design with the supramolecular architecture and the established macroscopic order, 2D wide-angle X-ray scattering experiments were performed on mechanically extruded filaments. At room temperature in their crystalline phases, all three compounds revealed columnar assemblies in which the macrocycles self-organized by pi-stacking interactions. The degree of macroscopic order was found to depend upon the planarity and stiffness of the aromatic core. The flexible CHP ring showed a poor macroscopic order of the columnar structures and a low isotropization temperature, whereas the more-planar, less-flexible CTP self-assembled into well-defined superstructures. The larger pi-stacking area and the more-pronounced intermolecular interactions for CTP led to the formation of a mesophase over a very large temperature range. The surprising columnar organization of the "open" TP system was explained by back-folding of the molecule into a ringlike structure.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:status |
PubMed-not-MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
1861-471X
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
8
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pubmed:volume |
2
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
51-6
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pubmed:year |
2007
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pubmed:articleTitle |
Columnar mesophase formation of cyclohexa-m-phenylene-based macrocycles.
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pubmed:affiliation |
Max-Planck-Institut für Polymerforschung, Ackermannweg 10, D-55128 Mainz, Germany.
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pubmed:publicationType |
Journal Article
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