(28)    R. Navrátil, S. Wiedbrauk, J. Jašík, H. Dube*, J. Roithová*, Phys. Chem. Chem. Phys. 2018, accepted. Transforming Hemithioindigo from a Two-Way to a One-Way Molecular Photoswitch by Isolation in the Gas Phase.

(27)    A. Gerwien, T. Reinhardt, P. Mayer, H. Dube*, Org. Lett. 2018, 1, 232-235. Synthesis of Double-Bond Substituted Hemithioindigo Photoswitches. doi: 10.1021/acs.orglett.7b03574

(26)    C. Petermayer, S. Thumser, F. Kink, P. Mayer, H. Dube*, J. Am. Chem. Soc. 2017, 139, 15060-15067. Hemiindigo - Highly Bistable Photoswitching at the Biooptical Window. doi: 10.1021/jacs.7b07531

(25)    L. A. Huber, K. Hoffmann, S. Thumser, N. Böcher, P. Mayer, H. Dube*, Angew. Chem. 2017129, 14728-14731; Angew. Chem. Int. Ed. 2017, 56, 14536-14539. Direct Observation of Hemithioindigo-Motor Unidirectionality. doi: 10.1002/anie.201708178   Highlighted in Synfacts 2018, 14, 0080 (doi: 10.1055/s-0036-1591087) and Laborpraxis 2017, 41, 34-35.  Molekulare Motoren – Auf dem Weg zu smarten Nanomaschinen.

(24)    S. Wiedbrauk, B. Maerz, E. Samoylova, P. Mayer, W. Zinth, H. Dube*, J. Phys. Chem. Lett. 2017, 8, 1585-1592. Ingredients to TICT Formation in Donor Substituted Hemithioindigo. doi: 10.1021/acs.jpclett.7b00371

(23)    F. Kink, M. Polo Collado, S. Wiedbrauk, P. Mayer, H. Dube*, Chem. Eur. J. 2017, 23, 6237-6243. Bistable Photoswitching of Hemithioindigo with Green and Red Light - Entry Point to Advanced Molecular Digital Information Processing. (Frontispiece) doi: 10.1002/chem.201700826

(22)    M. Schildhauer, H. Dube*, Nachr. Chem. 2016, 64, 1049-1053. Immer vorwärts, nie zurück. doi: 10.1002/nadc.20164046972

(21)    M. Guentner, E. Uhl, P. Mayer, H. Dube*, Chem. Eur. J. 2016, 22, 16433-16436. Photocontrol of Polar Aromatic Interactions by a bis-Hemithioindigo Based Helical Receptor. doi: 10.1002/chem.201604237

(20)    S. Wiedbrauk, B. Maerz, E. Samoylova, A. Reiner, F. Trommer, P. Mayer, W. Zinth, H. Dube*, J. Am. Chem. Soc. 2016, 138, 12219-12227. Twisted Hemithioindigo Photoswitches:  Solvent Polarity  Determines the Type of Light-Induced Rotations. doi: 10.1021/jacs.6b05981

(19)    M. Guentner, M. Schildhauer, S. Thumser, P. Mayer, D. Stephenson, P. J. Mayer, H. Dube*, Nat. Commun. 2015, 6, 8406. Sunlight Powered kHz Rotation of a Hemithioindigo Based Molecular Motor. doi: 10.1038/ncomms9406

(18)    S. Wiedbrauk, H. Dube*, Tetrahedron Lett. 2015, 56, 4266-4274. Hemithioindigo - an Emerging Photoswitch. doi: 10.1016/j.tetlet.2015.05.022

(17)    B. Maerz, S. Wiedbrauk, S. Oesterling, E. Samoylova, A. Nenov, P. Mayer, R. de Vivie-Riedle, W. Zinth, H. Dube*, Chem. Eur. J. 2014, 20, 13984-13992. Making Fast Photoswitches Faster - Using Hammett Analysis to Understand the Limit of Donor-Acceptor Approaches for Faster Hemithioindigo Photoswitches. doi: 10.1002/chem.201403661


Before Munich:

(16)    B. Kasumaj, H. Dube, N. Zölch, F. Diederich, G. Jeschke, J. Magn. Reson. 2012, 223, 187-197. Relaxation and modulation interference effects in two-pulse electron spin echo envelope modulation (ESEEM). (Abstract)

(15)    H. Dube, J. Rebek, Jr., Angew. Chem. 2012, 124, 3261-3264, Angew. Chem. Int. Ed. 2012, 51, 3207-3210. Selective Guest Exchange in Encapsulation Complexes Using Different Light Inputs. (Abstract)

(14)    O. B. Berryman, H. Dube, J. Rebek, Jr., Isr. J. Chem. 2011, 51, 700-709. Photophysics Applied to Cavitands and Capsules. (Abstract)

(13)    D. Ajami, H. Dube, J. Rebek, Jr., J. Am. Chem. Soc. 2011, 133, 9689-9691. Boronic Acid Hydrogen Bonding in Encapsulation Complexes. (Abstract)

(12)    K. Tiefenbacher, H. Dube, D. Ajami, J. Rebek, Jr., Chem. Commun. 2011, 47, 7341-7343. A Transparent Photo-Responsive Organogel Based on a Glycoluril Supergelator. (Abstract)

(11)    D. Ajami, P. M. Tolstoy, H. Dube, S. Odermatt, B. Koeppe, J. Guo, H.-H. Limbach, J. Rebek, Jr., Angew. Chem. 2011, 123, 548-552. Angew. Chem. Int. Ed. 2011, 50, 528-531. Encapsulated Carboxylic Acid Dimers with Compressed Hydrogen Bonds. (Abstract)

(10)    F. Durola, H. Dube, D. Ajami, J. Rebek, Jr., Supramol. Chem. 2011, 23, 37-41. Control of Nanospaces with Molecular Devices. (Abstract)

(9)     H. Dube, F. Durola, J. Rebek, Jr., J. Chin. Chem. Soc. 2010, 57, 595-603. (InvitedPaper). Molecular Switching in Nanospaces. (Article)

(8)     H. Dube, M. R. Ams, J. Rebek, Jr., J. Am. Chem. Soc. 2010, 132, 9984-9985. Supramolecular Control of Fluorescence through Reversible Encapsulation. (Abstract)

(7)     H. Dube, D. Ajami, J. Rebek, Jr., Angew. Chem. 2010, 122, 3260-3263, Angew. Chem. Int. Ed. 2010, 49, 3192-3195. (selected as Hot Paper). Photochemical Control of Reversible Encapsulation. (Abstract)

(6)     R. Tschaggelar, B. Kasumaj, M. G. Santangelo, J. Forrer, P. Leger, H. Dube, F. Diederich, J. Harmer, R. Schuhmann, I. G. Rubio, G. Jeschke, J. Magn. Reson. 2009, 200, 81-87. Cryogenic 35 GHz Pulse ENDOR Probehead Accomodating Large Sample Sizes: Performance and Applications. (Abstract)

(5)     H. Dube, B. Kasumaj, C. Calle, B. Felber, M. Saito, G. Jeschke, F. Diederich, Chem. Eur. J. 2009, 15, 125-135. Probing Hydrogen Bonding to Bound Dioxygen in Synthetic Model Compounds for Myoglobin and Hemoglobin: The Importance of Precise Geometry. (Abstract)

(4)     H. Dube, B. Kasumaj, C. Calle, M. Saito, G. Jeschke, F. Diederich, Angew. Chem. 2008, 120, 2638-2642, Angew. Chem. Int. Ed. 2008, 47, 2600-2603. (Cover Page). Direct Evidence for a Hydrogen Bond to Bound Dioxygen in a Myoglobin/Hemoglobin Model System and in Cobalt Myoglobin by Pulse-EPR Spectroscopy. (Abstract) Featured in “Swiss Science Concentrates” in Chimia 2008, 62, No. 6, 529.

(3)     I. Sapountzis, H. Dube, R. Lewis, N. Gommermann, P. Knochel, J. Org. Chem. 2005, 70, 2445-2454. Synthesis of Functionalized Nitroarylmagnesium Halides via an Iodine-Magnesium Exchange. (Abstract)

(2)     H. Dube, N. Gommermann, P. Knochel, Synthesis 2004, 2015-2025. Synthesis of Chiral a-Aminoalkylpyrimidines Using an Enantioselective Three-Component Reaction. (Abstract)

(1)     I. Sapountzis, H. Dube, P. Knochel, Adv. Syn. Catal. 2004, 346, 709-712. Synthesis of Nitro-Substituted Polyfunctional Biphenyls by Negishi Cross-Coupling of o-Nitroarylzinc Reagents. (Abstract)