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Inside Cover: Hydrogen‐Bonding Induced Alternate Stacking of Donor (D) and Acceptor (A) Chromophores and their Supramolecular Switching to Segregated States (Chem. Eur. J. 32/2012)
Author(s) -
Das Anindita,
Molla Mijanur Rahaman,
Maity Bholanath,
Koley Debasis,
Ghosh Suhrit
Publication year - 2012
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Reports
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201290137
Subject(s) - chromophore , stacking , amide , chemistry , acceptor , supramolecular chemistry , hydrogen bond , linker , crystallography , photochemistry , organic chemistry , molecule , crystal structure , physics , computer science , condensed matter physics , operating system
Bis‐amide‐functionalized donor (D) and acceptor (A) chromophores with comparable distances between the two amide groups form alternate D–A stacking in the moderately nonpolar solvent tetrachloroethylene (TCE) to produce either a fibrillar gel or spherical reverse vesicles depending on linker length. In the highly nonpolar medium methylcyclohexane (MCH) alternately stacked D and A chromophores switch over to a segregated 1D assembly of individual building blocks. For more details, see the Full Paper by D. Koley, S. Ghosh et al. on page 9849 ff.