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Growth dynamics and electron reflectivity in ultrathin films of chiral heptahelicene on metal (100) surfaces studied by spin-polarized low energy electron microscopy
Baljozović, M., Fernandes Cauduro, A. L., Seibel, J., Mairena, A., Grass, S., Lacour, J., … Ernst, K. H. (2021). Growth dynamics and electron reflectivity in ultrathin films of chiral heptahelicene on metal (100) surfaces studied by spin-polarized low energy electron microscopy. Physica Status Solidi B: Basic Research, 258(12), 2100263 (8 pp.). https://doi.org/10.1002/pssb.202100263
Stereoisomeric influence on 2D lattice structure: Achiral <I>meso</I>-tartaric acid <I>versus</I> chiral tartaric acid
Behzadi, B., Parschau, M., Romer, S., & Ernst, K. H. (2006). Stereoisomeric influence on 2D lattice structure: Achiral meso-tartaric acid versus chiral tartaric acid. Surface and Interface Analysis, 38(12-13), 1607-1610. https://doi.org/10.1002/sia.2426
Adsorption mode of the chiral modifier cinchonidine on Au(1 1 1)
Behzadi, B., Ferri, D., Baiker, A., & Ernst, K. H. (2007). Adsorption mode of the chiral modifier cinchonidine on Au(1 1 1). Applied Surface Science, 253(7), 3480-3484. https://doi.org/10.1016/j.apsusc.2006.07.084
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
Amplification of chirality in two-dimensional molecular lattices
Ernst, K. H. (2008). Amplification of chirality in two-dimensional molecular lattices. Current Opinion in Colloid and Interface Science, 13(1-2), 54-59. https://doi.org/10.1016/j.cocis.2007.08.011
Differences in two-dimensional crystal structures: racemic and enantiopure heptahelicene on Cu(111)
Ernst, K. H., Parschau, M., & Fasel, R. (2004). Differences in two-dimensional crystal structures: racemic and enantiopure heptahelicene on Cu(111). e-Journal of Surface Science and Nanotechnology, 2, 136-140. https://doi.org/10.1380/ejssnt.2004.136
Expression and amplification of chirality in two-dimensional molecular crystals
Ernst, K. H. (2008). Expression and amplification of chirality in two-dimensional molecular crystals. Chimia, 62(6), 471-475. https://doi.org/10.2533/chimia.2008.471
Intermediate structures in two-dimensional molecular self-assembly
Ernst, K. H. (2010). Intermediate structures in two-dimensional molecular self-assembly. Frontiers of Physics in China, 5(4), 340-346. https://doi.org/10.1007/s11467-010-0106-7
Stereochemistry of 2D molecular crystallization
Ernst, K. H. (2014). Stereochemistry of 2D molecular crystallization. Chimia, 68(1-2), 49-53. https://doi.org/10.2533/chimia.2014.49
Supramolecular chiral films
Ernst, K. H., Fasel, R., & Kuster, Y. (2002). Supramolecular chiral films. In A. Lakhtakia, G. Dewar, & M. W. McCall (Eds.), Proceedings of SPIE: Vol. 4806. Complex mediums III: beyond linear isotropic dielectrics (pp. 248-257). https://doi.org/10.1117/12.472991
Pasteur’s Experiment Performed at the Nanoscale: Manual Separation of Chiral Molecules, One by One
Ernst, K. H., Baumann, S., Lutz, C. P., Seibel, J., Zoppi, L., & Heinrich, A. J. (2015). Pasteur’s Experiment Performed at the Nanoscale: Manual Separation of Chiral Molecules, One by One. Nano Letters, 15(8), 5388-5392. https://doi.org/10.1021/acs.nanolett.5b01762
Molecular chirality in surface science
Ernst, K. H. (2013). Molecular chirality in surface science. Surface Science, 613, 1-5. https://doi.org/10.1016/j.susc.2013.03.014
Alfred Werner's coordination chemistry: new insights from old samples
Ernst, K. H., Wild, F. R. W. P., Blacque, O., & Berke, H. (2011). Alfred Werner's coordination chemistry: new insights from old samples. Angewandte Chemie International Edition, 50(46), 10780-10787. https://doi.org/10.1002/anie.201104477
Molecular chirality at surfaces
Ernst, K. H. (2012). Molecular chirality at surfaces. Physica Status Solidi B: Basic Research, 249(11), 2057-2088. https://doi.org/10.1002/pssb.201248188
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
Chiral autocatalysis and mirror symmetry breaking
Gellman, A. J., & Ernst, K. H. (2018). Chiral autocatalysis and mirror symmetry breaking. Catalysis Letters, 148(6), 1610-1621. https://doi.org/10.1007/s10562-018-2380-x
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
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, 27(54), 13523-13526. https://doi.org/10.1002/chem.202102069
Conglomerate aggregation of 7,12,17‐trioxa[11]helicene into homochiral two‐dimensional crystals on the Cu(100) surface
Irziqat, B., Berger, J., Cebrat, A., Mendieta-Moreno, J. I., Sundar, M. S., Bedekar, A. V., & Ernst, K. H. (2022). Conglomerate aggregation of 7,12,17‐trioxa[11]helicene into homochiral two‐dimensional crystals on the Cu(100) surface. Helvetica Chimica Acta, 105(12), e202200114 (8 pp.). https://doi.org/10.1002/hlca.202200114
Chiral reconstruction of Cu(110) after adsorption of fumaric acid
Karageorgaki, C., Passerone, D., & Ernst, K. H. (2014). Chiral reconstruction of Cu(110) after adsorption of fumaric acid. Surface Science, 629, 75-80. https://doi.org/10.1016/j.susc.2014.01.010