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Stereospecific on-surface cyclodehydrogenation of bishelicenes: preservation of handedness from helical to planar chirality
Irziqat, B., Cebrat, A., Baljozović, M., Martin, K., Parschau, M., Avarvari, N., & Ernst, K. H. (2021). Stereospecific on-surface cyclodehydrogenation of bishelicenes: preservation of handedness from helical to planar chirality. Chemistry: A European Journal. https://doi.org/10.1002/chem.202102069
Transition from homochiral clusters to racemate monolayers during 2D crystallization of trioxa[11] helicene on Ag(100)
Irziqat, B., Berger, J., Mendieta-Moreno, J. I., Sundar, M. S., Bedekar, A., & Ernst, K. H. (2021). Transition from homochiral clusters to racemate monolayers during 2D crystallization of trioxa[11] helicene on Ag(100). ChemPhysChem, 22(3), 293-297. https://doi.org/10.1002/cphc.202000853
Stereoselective on-surface cyclodehydrofluorization of a tetraphenylporphyrin and homochiral self-assembly
Chen, H., Tao, L., Wang, D., Wu, Z. Y., Zhang, J. L., Gao, S., … Gao, H. J. (2020). Stereoselective on-surface cyclodehydrofluorization of a tetraphenylporphyrin and homochiral self-assembly. Angewandte Chemie International Edition, 59(40), 17413-17416. https://doi.org/10.1002/anie.202005425
Near‐enantiopure trimerization of 9‐Ethynylphenanthrene on a chiralmetal surface
Stolz, S., Yakutovich, A. V., Prinz, J., Dienel, T., Pignedoli, C. A., Brune, H., … Widmer, R. (2020). Near‐enantiopure trimerization of 9‐Ethynylphenanthrene on a chiralmetal surface. Angewandte Chemie International Edition, 59(5), 18179-18183. https://doi.org/10.1002/anie.202006844
Peaks and more
Meyer, V. R. (2019). Peaks and more. Pure and Applied Chemistry, 91(2), 317-326. https://doi.org/10.1515/pac-2018-0711
Liquid crystalline filamentous biological colloids: analogies and differences
Nyström, G., & Mezzenga, R. (2018). Liquid crystalline filamentous biological colloids: analogies and differences. Current Opinion in Colloid and Interface Science, 38, 30-44. https://doi.org/10.1016/j.cocis.2018.08.004
Highly enantioselective adsorption of small prochiral molecules on a chiral intermetallic compound
Prinz, J., Gröning, O., Brune, H., & Widmer, R. (2015). Highly enantioselective adsorption of small prochiral molecules on a chiral intermetallic compound. Angewandte Chemie International Edition, 54(13), 3902-3906. https://doi.org/10.1002/anie.201410107
Self-assembly and two-dimensional spontaneous resolution of cyano-functionalized [7]helicenes on Cu(111)
Stöhr, M., Boz, S., Schär, M., Nguyen, M. T., Pignedoli, C. A., Passerone, D., … Diederich, F. (2011). Self-assembly and two-dimensional spontaneous resolution of cyano-functionalized [7]helicenes on Cu(111). Angewandte Chemie International Edition, 50(42), 9982-9986. https://doi.org/10.1002/anie.201102627
Homochiral conglomerates and racemic crystals in two dimensions: tartaric acid on Cu(110)
Romer, S., Behzadi, B., Fasel, R., & Ernst, K. H. (2005). Homochiral conglomerates and racemic crystals in two dimensions: tartaric acid on Cu(110). Chemistry: A European Journal, 11(14), 4149-4154. https://doi.org/10.1002/chem.200400962
Chirality transfer from single molecules into self-assembled monolayers
Fasel, R., Parschau, M., & Ernst, K. H. (2003). Chirality transfer from single molecules into self-assembled monolayers. Angewandte Chemie International Edition, 42(42), 5178-5181. https://doi.org/10.1002/anie.200352232