Synthesis, Structure, and Properties of Supramolecular Photoswitches Based on Ammonioalkyl Derivatives of Crown-Ether Styryl Dyesстатья
Статья опубликована в высокорейтинговом журнале
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Дата последнего поиска статьи во внешних источниках: 12 января 2015 г.
Аннотация:The synthesis of new styryl dyes derived from 4-pyridine and 4-quinoline and having an ammonioalkyl N-substituent and a benzocrown-ether moiety of different size and with different sets of heteroatoms was developed. Spontaneous “head-to-tail” dimerization of these dyes via the formation of numerous hydrogen bonds between the terminal NH3+ groups and crown-ether moieties was detected in MeCN solutions. The stability constants of the dimeric complexes having pseudocyclic structure were studied by 1H NMR titration. The most stable complexes (logKd up to 8.2) were found in the case of dyes with the (aza)-18-crown-6-ether moiety, which is most complementary for binding a primary ammonium group. Stacking interaction of the conjugated systems in the dimeric complexes contributes to their stability to a much lesser extent. In dimeric complexes, the ethylene bonds of the dyes are pre-organized for stereospecific [2+2] photocycloaddition (PCA) induced by visible light. The PCA yields only rctt isomers of bis-crown-containing cyclobutane derivatives. The dyes were studied by X-ray diffraction; it was found that the dimeric arrangement is also retained in the crystalline state. The possibility of topochemical PCA of the dyes in single crystals without their destruction was demonstrated. The possibility of retro-PCA of the obtained cyclobutane derivatives to give the starting dyes was shown. The elucidated regularities of PCA can be used to fabricate optical data recording systems based on ammonioalkyl derivatives of crown-ether styryl dyes.