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Mirror Helices and Helicity Switch at Surfaces Based on Chiral Triangular‐Shape Oligo(phenylene ethynylenes)
Author(s) -
Aparicio Fátima,
García Fátima,
Fernández Gustavo,
Matesanz Emilio,
Sánchez Luis
Publication year - 2011
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201001596
Subject(s) - stereocenter , supramolecular chemistry , crystallography , phenylene , chirality (physics) , supramolecular chirality , isodesmic reaction , polymerization , self assembly , helicity , chemistry , materials science , stereochemistry , enantioselective synthesis , polymer , nanotechnology , crystal structure , physics , computational chemistry , chiral symmetry , organic chemistry , density functional theory , nambu–jona lasinio model , quantum mechanics , particle physics , quark , catalysis
The self‐assembly of triangular‐shaped oligo(phenylene ethynylenes) (OPEs), peripherally decorated with chiral and linear paraffinic chains, is investigated in bulk, onto surfaces and in solution. Whilst the X‐ray diffraction data for the chiral studied systems display a broad reflection centered at 2 θ ∼20° ( λ =Cu Kα ), the higher crystallinity of OPE 3 , endowed with three linear decyl chains, results in a diffractrogram with a number of well‐resolved reflections that can be accurately indexed as a columnar packing arranged in 2D oblique cells. Compounds ( S )‐ 1 a and ( R )‐ 1 b —endowed with ( S ) ‐ and ( R )‐3,7‐dimethyloctyloxy chains—transfer their chirality to the supramolecular structures formed upon their self‐assembly, and give rise to helical nanostructures of opposite handedness. A helicity switch is noticeable for the case of chiral ( S )‐ 2 decorated with ( S )‐2‐methylnonyloxy chains which forms right‐handed helices despite it possesses the same stereoconfiguration for their stereogenic carbons as ( S )‐ 1 a that self‐assembles into left‐handed helices. The stability and the mechanism of the supramolecular polymerization in solution have been investigated by UV/Vis experiments in methylcyclohexane. These studies demonstrate that the larger the distance between the stereogenic carbon and the aromatic framework is, the more stable the aggregate is. Additionally, the self‐assembly mechanism is conditioned by the peripheral substituents: whereas compounds ( S )‐ 1 a and ( R )‐ 1 b self‐assemble in a cooperative manner with a low degree of cooperativity, the aggregation of ( S )‐ 2 and 3 is well described by an isodesmic model. Therefore, the interaction between the chiral coil chains conditions the handedness of the helical pitch, the stability of the supramolecular structure and the supramolecular polymerization mechanism of the studied OPEs.