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Stratingh Institute for Chemistry

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  1. 2019
  2. Kumar, S., Soni, S., Leach, I., Faraji, S., Feringa, B. L., Rudolf, P., & Chiechi, R. C. (2019). Eliminating Fatigue in Surface-Bound Spiropyrans. The Journal of Physical Chemistry. C: Nanomaterials and Interfaces, 123(42), 25908-25914. https://doi.org/10.1021/acs.jpcc.9b05889
  3. Elangovan, S., Afanasenko, A., Haupenthal, J., Sun, Z., Liu, Y., Hirsch, A. K. H., & Barta, K. (2019). From Wood to Tetrahydro-2-benzazepines in Three Waste-Free Steps: Modular Synthesis of Biologically Active Lignin-Derived Scaffolds. ACS central science, 5(10), 1707-1716. https://doi.org/10.1021/acscentsci.9b00781
  4. Tierney, M. M., Crespi, S., Ravelli, D., & Alexanian, E. J. (2019). Identifying Amidyl Radicals for Intermolecular C-H Functionalizations. Journal of Organic Chemistry, 84(20), 12983-12991. https://doi.org/10.1021/acs.joc.9b01774
  5. Pfeifer, L., Scherubl, M., Fellert, M., Danowski, W., Cheng, J., Pol, J., & Feringa, B. L. (2019). Photoefficient 2(nd) generation molecular motors responsive to visible light. Chemical Science, 10(38), 8768-8773. https://doi.org/10.1039/c9sc02150g
  6. Tosi, F., Stuart, M. C. A., Wezenberg, S. J., & Feringa, B. L. (2019). Salen-Based Amphiphiles: Directing Self-Assembly in Water by Metal Complexation. Angewandte Chemie (International ed. in English), 58(42), 14935–14939. https://doi.org/10.1002/anie.201908010
  7. Hung Tan Pham, N. V., Rizzo, H. G., Havenith, R. W. A., & Minh Tho Nguyen, N. V. (2019). BxGe120/+ Clusters with x=1-4: Germanium Tubes Stabilized by Three and Four Boron Dopants. Journal of Physical Chemistry C, 123(40), 24676-24684. https://doi.org/10.1021/acs.jpcc.9b05483
  8. Kolarski, D., Sugiyama, A., Breton, G., Rakers, C., Ono, D., Schulte, A., Tama, F., Itami, K., Szymanski, W., Hirota, T., & Feringa, B. L. (2019). Controlling the Circadian Clock with High Temporal Resolution through Photodosing. Journal of the American Chemical Society, 141(40), 15784-15791. https://doi.org/10.1021/jacs.9b05445
  9. Vargova, D., Perez, J. M., Harutyunyan, S. R., & Sebesta, R. (2019). Trapping of chiral enolates generated by Lewis acid promoted conjugate addition of Grignard reagents to unreactive Michael acceptors by various electrophiles. Chemical Communications, 55(78), 11766-11769. https://doi.org/10.1039/c9cc05041h
  10. Azevedo, H. S., Braunschweig, A. B., Chiechi, R. C., Fernandez, Y. D., Gildersleeve, J. C., Godula, K., Hartmann, L., Miura, Y., Schmidt, S., Turnbull, W. B., & Zhou, D. (2019). Glycan interactions on glycocalyx mimetic surfaces: general discussion. Faraday Discussions, 219, 183-188. https://doi.org/10.1039/C9FD90063B
  11. Hoorens, M. W. H., Ourailidou, M. E., Rodat, T., van der Wouden, P. E., Kobauri, P., Kriegs, M., Peifer, C., Feringa, B. L., Dekker, F. J., & Szymanski, W. (2019). Light-controlled inhibition of BRAFV600E kinase. European Journal of Medicinal Chemistry, 179, 133-146. https://doi.org/10.1016/j.ejmech.2019.06.042
  12. Azevedo, H. S., Braunschweig, A. B., Chiechi, R. C., Claridge, S. A., Cronin, L., Fernandez, Y. D., Feizi, T., Hartmann, L., Huang, M., Miura, Y., Palma, M., Qiu, X., Ravoo, B. J., Schmidt, S., Turnbull, W. B., Werner, C., Zheng, Z., & Zhou, D. (2019). New directions in surface functionalization and characterization: General discussion. Faraday Discussions, 219, 252-261. https://doi.org/10.1039/C9FD90064K
  13. Braunschweig, A., Byrne, J. P., Chiechi, R., Fernandez, Y. D., Gildersleeve, J., Godula, K., Hartmann, L., Mahon, C., Miura, Y., Nelson, A., Schmidt, S., Turnbull, W. B., Valles, D., Yu, J., & Zhou, D. (2019). Preparation of multivalent glycan micro- and nano-arrays: general discussion. Faraday Discussions, 219, 128-137. https://doi.org/10.1039/C9FD90062D
  14. de Vries, R., Viel, J., Oudshoorn, R., Kuipers, O., & Roelfes, G. (2019). Selective Modification of RiPPs via Diels-Alder Cycloadditions on Dehydroalanine Residues. Chemistry, 25(55), 12698–12702. https://doi.org/10.1002/chem.201902907
  15. Klein, J. E. M. N., Knizia, G., & Rzepa, H. S. (2019). Epoxidation of Alkenes by Peracids: From Textbook Mechanisms to a Quantum Mechanically Derived Curly-Arrow Depiction. Chemistryopen, 8(10), 1244-1250. https://doi.org/10.1002/open.201900099
  16. Wan, I. C. S., Witte, M. D., & Minnaard, A. J. (2019). From d- to l-Monosaccharide Derivatives via Photodecarboxylation-Alkylation. Organic letters, 21(18), 7669-7673. https://doi.org/10.1021/acs.orglett.9b03016
  17. Reeßing, F., Stuart, M. C. A., Samplonius, D. F., Dierckx, R. A. J. O., Feringa, B. L., Helfrich, W., & Szymanski, W. (2019). A light-responsive liposomal agent for MRI contrast enhancement and monitoring of cargo delivery. Chemical communications (Cambridge, England), 55(72), 10784-10787. https://doi.org/10.1039/c9cc05516a
  18. Nishimura, R., Fujimoto, A., Yasuda, N., Morimoto, M., Nagasaka, T., Sotome, H., Ito, S., Miyasaka, H., Yokojima, S., Nakamura, S., Feringa, B. L., & Uchida, K. (2019). Object Transportation System Mimicking the Cilia of Paramecium aurelia Making Use of the Light-Controllable Crystal Bending Behavior of a Photochromic Diarylethene. Angewandte Chemie-International Edition, 58(38), 13308-13312. https://doi.org/10.1002/anie.201907574
  19. Browne, W. (2019). Resonance Raman spectroscopy and its application in bioinorganic chemistry. In R. Louro, & R. Crichton (Eds.), Practical Approaches to Biological Inorganic Chemistry (2 ed., pp. 275-324). Elsevier. https://doi.org/10.1016/B978-0-444-64225-7.00008-0
  20. Mutter, N. L., Volarić, J., Szymanski, W., Feringa, B. L., & Maglia, G. (2019). Reversible Photocontrolled Nanopore Assembly. Journal of the American Chemical Society, 141(36), 14356-14363. https://doi.org/10.1021/jacs.9b06998
  21. Tosi, F., Stuart, M. C. A., Smit, H., Chen, J., & Feringa, B. L. (2019). Reorganization from Kinetically Stable Aggregation States to Thermodynamically Stable Nanotubes of BINOL-derived Amphiphiles in Water. Langmuir, 35(36), 11821-11828. https://doi.org/10.1021/acs.langmuir.9b01989
  22. Guo, Y., & Harutyunyan, S. R. (2019). Highly Enantioselective Catalytic Addition of Grignard Reagents to N-Heterocyclic Acceptors. Angewandte Chemie-International Edition, 58(37), 12950-12954. https://doi.org/10.1002/anie.201906237
  23. Steen, J. S., Knizia, G., & Klein, J. E. M. N. (2019). Sigma-Noninnocence: Masked Phenyl-Cation Transfer at Formal Ni-IV. Angewandte Chemie-International Edition, 58(37), 13133-13139. https://doi.org/10.1002/anie.201906658
  24. Liu, J., Garman, M. P., Dong, J., van der Zee, B., Qiu, L., Portale, G., Hummelen, J. C., & Koster, L. J. A. (2019). Doping Engineering Enables Highly Conductive and Thermally Stable n-Type Organic Thermoelectrics with High Power Factor. ACS Applied Energy Materials, 2(9), 6664-6671. https://doi.org/10.1021/acsaem.9b01179
  25. Vezie, M. S., Azzouzi, M., Telford, A. M., Hopper, T. R., Sieval, A. B., Hummelen, J. C., Fallon, K., Bronstein, H., Kirchartz, T., Bakulin, A. A., Clarke, T. M., & Nelson, J. (2019). Impact of Marginal Exciton-Charge-Transfer State Offset on Charge Generation and Recombination in Polymer: Fullerene Solar Cells. ACS Energy Letters, 4(9), 2096-2103. https://doi.org/10.1021/acsenergylett.9b01368
  26. Porto-Carrero, W., Cupani, A., Veenstra, M. J., Dorbec, M., Eykens, L., & Ormerod, D. (2019). Volume intensified dilution of a ring-closing metathesis in ethyl acetate by means of a membrane-assisted process in solvent recycle. Journal of Chemical Technology and Biotechnology, 94(9), 2990-2998. https://doi.org/10.1002/jctb.6109
  27. Ivasyshyn, V., Smit, H., & Chiechi, R. C. (2019). Synthesis of a Hominal Bis(difluoromethyl) Fragment. ACS Omega, 4(9), 14140-14150. https://doi.org/10.1021/acsomega.9b02131
  28. Konstantinidou, M., Magari, F., Sutanto, F., Uenver, M., Jumde, V., Klebe, G., Hirsch, A., & Doemling, A. (2019). Design of a multi-component reaction scaffold with inhibitory activity on aspartic proteases. Abstracts of Papers of the American Chemical Society, 258.
  29. Afanasenko, A., Hannah, R., Yan, T., Elangovan, S., & Barta, K. (2019). Ruthenium and Iron-Catalysed Decarboxylative N-alkylation of Cyclic α-Amino Acids with Alcohols: Sustainable Routes to Pyrrolidine and Piperidine Derivatives. Chemsuschem, 12(16), 3801-3807. https://doi.org/10.1002/cssc.201901499
  30. Krause, S., Bon, V., Du, H., Dunin-Borkowski, R. E., Stoeck, U., Senkovska, I., & Kaskel, S. (2019). The impact of crystal size and temperature on the adsorption-induced flexibility of the Zr-based metal-organic framework DUT-98. Beilstein Journal of Nanotechnology, 10, 1737-1744. https://doi.org/10.3762/bjnano.10.169
  31. Mondol, R., & Otten, E. (2019). Structure and bonding in reduced boron and aluminium complexes with formazanate ligands. Dalton Transactions, 48(37), 13981-13988 . https://doi.org/10.1039/c9dt02831e
  32. Zhang, Q., Deng, Y-X., Luo, H-X., Shi, C-Y., Geise, G. M., Feringa, B. L., Tian, H., & Qu, D-H. (2019). Assembling a Natural Small Molecule into a Supramolecular Network with High Structural Order and Dynamic Functions. Journal of the American Chemical Society, 141(32), 12804-12814. https://doi.org/10.1021/jacs.9b05740
  33. Rauche, M., Ehrling, S., Krause, S., Senkovska, I., Kaskel, S., & Brunner, E. (2019). New insights into solvent-induced structural changes of C-13 labelled metal-organic frameworks by solid state NMR. Chemical Communications, 55(62), 9140-9143. https://doi.org/10.1039/c9cc04298a
  34. Kamphuis, A. J., Milocco, F., Koiter, L., Pescarmona, P., & Otten, E. (2019). Highly selective single-component formazanate ferrate(II) catalysts for the conversion of CO2 into cyclic carbonates. Chemsuschem, 12(15), 3635-3641. https://doi.org/10.1002/cssc.201900740
  35. Simhadri, C., Daze, K. D., Douglas, S. F., Milosevich, N., Monjas, L., Dev, A., Brown, T. M., Hirsch, A. K. H., Wulff, J. E., & Hof, F. (2019). Rational Adaptation of L3MBTL1 Inhibitors to Create Small-Molecule Cbx7 Antagonists. ChemMedChem, 14(15), 1444-1456. https://doi.org/10.1002/cmdc.201900021
  36. Leung, F. K-C., Kajitani, T., Stuart, M. C. A., Fukushima, T., & Feringa, B. L. (2019). Dual-Controlled Macroscopic Motions in A Supramolecular Hierarchical Assembly of Motor Amphiphiles. Angewandte Chemie (International ed. in English), 58(32), 10985-10989. https://doi.org/10.1002/anie.201905445
  37. Sun, Z., Buwalda, D., & Barta, K. (2019). Two-step catalytic conversion of lignocellulose to alkanes. RSC Advances, 9(41), 23727-23734. https://doi.org/10.1039/c9ra03174j
  38. Maglia, G., & Browne, W. (2019). Editorial overview: Reprogramming biology: from biopolymers to complex systems. Current Opinion in Biotechnology, 58, v-vi. https://doi.org/10.1016/j.copbio.2019.08.002
  39. Reessing, F., & Szymanski, W. (2019). Following nanomedicine activation with magnetic resonance imaging: Why, how, and what's next? Current Opinion in Biotechnology, 58, 9-18. https://doi.org/10.1016/j.copbio.2018.10.008
  40. Syari'ati, A., Kumar, S., Zahid, A., Ali El Yumin, A., Ye, J., & Rudolf, P. (2019). Spectroscopy Study of Structural Defects in Molybdenum disulfide (MoS2) Grown by Chemical Vapor Deposition (CVD). Chemical Communications, 55(70), 10384-10387. https://doi.org/10.1039/C9CC01577A
  41. Yan, X., & Harutyunyan, S. R. (2019). Catalytic enantioselective addition of organometallics to unprotected carboxylic acids. Nature Communications, 10, [3402]. https://doi.org/10.1038/s41467-019-11345-z
  42. Park, S-Y., Yang, J-S., Li, Z., Deng, P., Zhu, X., Young, D., Ericsson, M., Andringa, R. L. H., Minnaard, A. J., Zhu, C., Sun, F., Moody, D. B., Morris, A. J., Fan, J., & Hsu, V. W. (2019). The late stage of COPI vesicle fission requires shorter forms of phosphatidic acid and diacylglycerol. Nature Communications, 10, [3409]. https://doi.org/10.1038/s41467-019-11324-4
  43. van der Vlag, R., Guo, H., Hapko, U., Eleftheriadis, N., Monjas, L., Dekker, F. J., & Hirsch, A. K. H. (2019). A combinatorial approach for the discovery of drug-like inhibitors of 15-lipoxygenase-1. European Journal of Medicinal Chemistry, 174, 45-55. https://doi.org/10.1016/j.ejmech.2019.04.021
  44. Wegeberg, C., Browne, W. R., & McKenzie, C. J. (2019). cis Donor Influence on O-O Bond Lability in Iron(III) Hydroperoxo Complexes: Oxidation Catalysis and Ligand Transformation. Inorganic Chemistry, 58(14), 8983-8994. https://doi.org/10.1021/acs.inorgchem.9b00247
  45. Sinha, N., Heijnen, D., Feringa, B. L., & Organ, M. G. (2019). Murahashi Cross‐Coupling at −78 °C: A One-Pot Procedure for Sequential C-C/C-C, C-C/C-N, and C-C/C-S Cross-Coupling of Bromo-Chloro-Arenes. Chemistry, 25(39), 9180-9184. https://doi.org/10.1002/chem.201901678
  46. Barbieri, A., Kasper, J. B., Mecozzi, F., Lanzalunga, O., & Browne, W. R. (2019). Origins of Catalyst Inhibition in the Manganese-Catalysed Oxidation of Lignin Model Compounds with H2O2. Chemsuschem, 12(13), 3126-3133. https://doi.org/10.1002/cssc.201900689
  47. Mishra, V. K., Buter, J., Blevins, M. S., Witte, M. D., Van Rhijn, I., Moody, D. B., Brodbelt, J. S., & Minnaard, A. J. (2019). Total Synthesis of an Immunogenic Trehalose Phospholipid from Salmonella Typhi and Elucidation of Its sn-Regiochemistry by Mass Spectrometry. Organic letters, 21(13), 5126-5131. https://doi.org/10.1021/acs.orglett.9b01725
  48. Sorbelli, D., Comprido, L. N. D. S., Knizia, G., Hashmi, A. S. K., Belpassi, L., Belanzoni, P., & Klein, J. E. M. N. (2019). Cationic Gold(I) Diarylallenylidene Complexes: Bonding Features and Ligand Effects. Chemphyschem, 20(13), 1671-1679. https://doi.org/10.1002/cphc.201900411
  49. Liu, Y., Afanasenko, A., Elangovan, S., Sun, Z., & Barta, K. (2019). Primary Benzylamines by Efficient N-Alkylation of Benzyl Alcohols Using Commercial Ni Catalysts and Easy-to-Handle Ammonia Sources. ACS Sustainable Chemistry & Engineering , 7(13), 11267-11274. https://doi.org/10.1021/acssuschemeng.9b00619
  50. Liu, J., Shi, Y., Dong, J., Nugraha, M. I., Qiu, X., Su, M., Chiechi, R. C., Baran, D., Portale, G., Guo, X., & Koster, L. J. A. (2019). Overcoming Coulomb Interaction Improves Free-Charge Generation and Thermoelectric Properties for n-Doped Conjugated Polymers. ACS Energy Letters, 4(7), 1556-1564. https://doi.org/10.1021/acsenergylett.9b00977
  51. Kortekaas, L., & Browne, W. R. (2019). The evolution of spiropyran: fundamentals and progress of an extraordinarily versatile photochrome. Chemical Society Reviews, 48(12), 3406-3424. https://doi.org/10.1039/c9cs00203k
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