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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
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
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
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
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
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
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
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
Aspects of molecular chirality at metal surfaces
Ernst, K. H. (2009). Aspects of molecular chirality at metal surfaces. Zeitschrift für Physikalische Chemie, 223(1-2), 37-51. https://doi.org/10.1524/zpch.2009.6023
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. https://doi.org/10.1002/chem.202102069
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
Heterochiral to homochiral transition in pentahelicene 2D crystallization induced by second-layer nucleation
Mairena, A., Zoppi, L., Seibel, J., Troster, A. F., Grenader, K., Parschau, M., … Ernst, K. H. (2017). Heterochiral to homochiral transition in pentahelicene 2D crystallization induced by second-layer nucleation. ACS Nano, 11(1), 865-871. https://doi.org/10.1021/acsnano.6b07424
Unification of the matrix notation in molecular surface science
Merz, L., & Ernst, K. H. (2010). Unification of the matrix notation in molecular surface science. Surface Science, 604(11-12), 1049-1054. https://doi.org/10.1016/j.susc.2010.03.023
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