2006
DOI: 10.1021/ja065334o
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Rotational Reorganization of Doped Cholesteric Liquid Crystalline Films

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Cited by 204 publications
(195 citation statements)
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References 49 publications
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“…The realization of such chiral 'algebra' is even more rewarding given the disparate nature of the involved influences: a threedimensional force of physical nature, operating in centimetrelength scales, facing the chemical effect of a supramolecular level modifier. Notice that this finding is entirely different from previous successful attempts to photomodulate chiral modifierbased influences in doped ferroelectric 38 or cholesteric liquid crystals 39 , or to modify the helicoidal structure of cholesteric liquid crystals by means of an achiral external mechanical field 40 . Unveiled as a new dynamical scenario of chirality control, our contribution should also be envisaged, upon transference of the monolayer into a solid support, as a new strategy for stereocontrol of chemical reactions and responses at chiral surfaces 41,42 .…”
Section: Articlecontrasting
confidence: 86%
“…The realization of such chiral 'algebra' is even more rewarding given the disparate nature of the involved influences: a threedimensional force of physical nature, operating in centimetrelength scales, facing the chemical effect of a supramolecular level modifier. Notice that this finding is entirely different from previous successful attempts to photomodulate chiral modifierbased influences in doped ferroelectric 38 or cholesteric liquid crystals 39 , or to modify the helicoidal structure of cholesteric liquid crystals by means of an achiral external mechanical field 40 . Unveiled as a new dynamical scenario of chirality control, our contribution should also be envisaged, upon transference of the monolayer into a solid support, as a new strategy for stereocontrol of chemical reactions and responses at chiral surfaces 41,42 .…”
Section: Articlecontrasting
confidence: 86%
“…63,64 The chiral information expressed by the system comprising helicate 1 and its diastereomers allowed us to track separately the reversible ligand-exchange and imine-exchange processes occurring within this mixture of structures. The sorting of this dynamic library 14 during crystallization provided a novel example of the conversion of a complex mixture of diastereomers into a single pair of enantiomers, driven by the lower solubility of the latter.…”
Section: Discussionmentioning
confidence: 99%
“…A remarkable example has been reported on recently by Feringa and coworkers. 19,20 They described the rotational reorganization of cholesteric liquid crystalline films as the result of the conversion of a chiral molecular motor dopant to an isomer with a different helical twisting power, leading to a change in the cholesteric pitch. The direction of this reorganization is correlated to the sign of the change in helical twisting power of the dopant.…”
mentioning
confidence: 99%