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Schlagwörter:
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Zusammenfassung:
Various acrylates [E-phenylpropenoate, E-3(4′-nitrophenyl)propenoate, E-3(2′,5′-difluorphenyl)propenoate, E-3(2′-thienyl)propenoate, E-3(4′-imidazolyl)propenoate or E-2,3-dimethylpropenoate] were successfully intercalated into Ca(II)Fe(III) layered double hydroxide (CaFe–LDH) verified by a range of instrumental methods. The possible arrangements for the organic anions were suggested on the basis of basal spacing data, layer thickness and the dimensions of the quantum chemically optimised structures of the acrylate ions. Using the acrylate−CaFe–LDHs as reactant-filled nanoreactors, photoinitiated topotactic [2 + 2] cyclisation reactions followed by IR spectroscopy could be performed with many representatives [E-phenylpropenoate-, E-3(4′-nitrophenyl)propenoate-, E-3(2′,5′-difluorphenyl)propenoate- or E-3(2′-thienyl)propenoate−CaFe–LDHs] resulting in cyclobutane derivatives within the layers of the host material indicating that there were domains where the intercalated anions were in close proximity to each other and in proper arrangement for the reaction to occur.
