Effective cholesteric liquid crystal inducers based on axially chiral alleno-acetylenes
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[1] F. Diederich,et al. A shape-persistent alleno-acetylenic macrocycle with a modifiable periphery: synthesis, chiroptical properties and H-bond-driven self-assembly into a homochiral columnar structure. , 2013, Chemical communications.
[2] M. Goh,et al. Chirality transfer from atropisomeric chiral inducers to nematic and smectic liquid crystals – synthesis and characterization of di- and tetra-substituted axially chiral binaphthyl derivatives , 2012 .
[3] F. Diederich,et al. 1,2-Di(phenylethynyl)ethenes with axially chiral, 2,2'-bridged 1,1'-binaphthyl substituents: potent cholesteric liquid-crystal inducers. , 2012, Organic & biomolecular chemistry.
[4] Yan Wang,et al. Light‐Driven Chiral Molecular Switches or Motors in Liquid Crystals , 2012, Advanced materials.
[5] D. Broer,et al. Irreversible visual sensing of humidity using a cholesteric liquid crystal. , 2012, Chemical communications.
[6] Nathalie Katsonis,et al. Controlling chirality with helix inversion in cholesteric liquid crystals , 2012 .
[7] F. Diederich,et al. Allenes in molecular materials. , 2012, Angewandte Chemie.
[8] Xiaodong Shi,et al. Synthesis of allene triazole through iron catalyzed regioselective addition to propargyl alcohols. , 2012, Chemical communications.
[9] K. Akagi,et al. Dynamic photoswitching of helical inversion in liquid crystals containing photoresponsive axially chiral dopants. , 2012, Journal of the American Chemical Society.
[10] Augustine Urbas,et al. Reversible visible-light tuning of self-organized helical superstructures enabled by unprecedented light-driven axially chiral molecular switches. , 2012, Journal of the American Chemical Society.
[11] F. Diederich,et al. Enantiopure, monodisperse alleno-acetylenic cyclooligomers: effect of symmetry and conformational flexibility on the chiroptical properties of carbon-rich compounds. , 2011, Chemistry.
[12] A. Ferrarini,et al. Chirality transfer across length-scales in nematic liquid crystals: fundamentals and applications. , 2011, Chemical Society reviews.
[13] Ana G. Petrovic,et al. Enantiomerically pure alleno-acetylenic macrocycles: synthesis, solid-state structures, chiroptical properties, and electron localization function analysis. , 2010, Chemistry.
[14] Ana G. Petrovic,et al. Amplification of chirality in monodisperse, enantiopure alleno-acetylenic oligomers. , 2010, Angewandte Chemie.
[15] F. Diederich,et al. N-arylated 3,5-dihydro-4H-dinaphtho[2,1-c:1',2'-e]azepines: axially chiral donors with high helical twisting powers for nonplanar push-pull chromophores. , 2009, Chemistry.
[16] F. Diederich,et al. 1,3-Diethynylallenes (DEAs): enantioselective synthesis, absolute configuration, and chiral induction in 1,1,4,4-tetracyanobuta-1,3-dienes (TCBDs). , 2008, Chemistry.
[17] Ben L Feringa,et al. Amplification of chirality in liquid crystals. , 2006, Organic & biomolecular chemistry.
[18] Nathalie Katsonis,et al. Molecular machines: Nanomotor rotates microscale objects , 2006, Nature.
[19] B. Feringa,et al. Macroscopic expression of the chirality of amino alcohols by a double amplification mechanism in liquid crystalline media. , 2005, Journal of the American Chemical Society.
[20] Shengming Ma,et al. Some typical advances in the synthetic applications of allenes. , 2005, Chemical reviews.
[21] B. Feringa,et al. Direct visual detection of the stereoselectivity of a catalytic reaction. , 2004, Angewandte Chemie.
[22] J. W. Doane,et al. A New High Twisting Power Material for Use as a Single Asymmetric Dopant in Cholesteric Displays with a Temperature Independence of the Helical Twisting Power , 2004 .
[23] H. Chow,et al. A highly selective synthesis of diarylethynes and their oligomers by a palladium-catalyzed Sonogashira coupling reaction under phase transfer conditions. , 2001, The Journal of organic chemistry.
[24] D. Seebach,et al. TADDOLs with Unprecedented Helical Twisting Power in Liquid Crystals. Preliminary communication , 1997 .
[25] C. Rosini,et al. Conformational Analysis of Some trans-4,5-Diaryl-1,3-dioxolanes by CD Spectroscopy and Induction of Cholesteric Mesophases in Nematic Solvents: A Correlation between Twisting Power and Structure of the Dopant , 1997 .
[26] G. Moro,et al. Shape model for ordering properties of molecular dopants inducing chiral mesophases , 1996 .
[27] Moro,et al. Simple molecular model for induced cholesteric phases. , 1996, Physical review. E, Statistical physics, plasmas, fluids, and related interdisciplinary topics.