Publications

  1. Color Polymorphism and Room Temperature Phosphorescence of 4-Bromo-2,7-Di-Tert-Butyl- 9-Methoxypyrene
    Olaf W. Morawski, Jerzy Karpiuk, Marek Grzybowski
    ChemPhysChem 2023, 25, e202400457
    DOI: 10.1002/cphc.202400457
    Graphical abstract
  2. Strong Chiroptical Effects in the Absorption and Emission of Macrocycles Based on the 2,5-Diaminoterephthalate Minimal Fluorophore
    Krzysztof Nowak, Olaf Morawski, Francesco Zinna, Gennaro Pescitelli, Lorenzo Di Bari, Marcin Górecki, Marek Grzybowski
    Chem. Eur. J. 2023, 29, e202300932
    DOI: 10.1002/chem.202300932
    Graphical abstract
  3. Fluorene analogues of xanthenes – low molecular weight near-infrared dyes
    Marek Grzybowski, Olaf Morawski, Krzysztof Nowak, Paula Garbacz
    Chem. Commun. 2022, 58, 5455-5458
    DOI: 10.1039/D2CC00561A
    Graphical abstract
  4. Tuning the aromatic backbone twist in dipyrrolonaphthyridinediones
    Bartłomiej Sadowski, Dominik Mierzwa, Seongsoo Kang, Marek Grzybowski, evgen M. Poronik, Andrzej L. Sobolewski, Dongho Kim, Daniel T. Gryko
    Chem. Commun. 2022, 58, 3697-3700
    DOI: 10.1039/D1CC06863F
    Graphical abstract
  5. Synthesis of Tetraaryl-, Pentaaryl-, and Hexaaryl-1,4-dihydropyrrolo[3,2-b]pyrroles
    Maciej Krzeszewski, Mariusz Tasior, Marek Grzybowski, Daniel T. Gryko
    Org. Synth. 2021, 98, 242-262
    DOI: 10.15227/orgsyn.098.0242
    Graphical abstract
  6. Covalent Self-Labeling of Tagged Proteins with Chemical Fluorescent Dyes in BY-2 Cells and Arabidopsis Seedlings
    Ryu J Iwatate, Akira Yoshinari, Noriyoshi Yagi, Marek Grzybowski, Hiroaki Ogasawara, Mako Kamiya, Toru Komatsu, Masayasu Taki, Shigehiro Yamaguchi, Wolf B Frommer, Masayoshi Nakamura
    Plant Cell 2020, 32, 3081-3094
    DOI: 10.1105/tpc.20.00439
  7. Method for the Large-Scale Synthesis of Multifunctional 1,4-Dihydro-pyrrolo[3,2-b]pyrroles
    Mariusz Tasior, Olena Vakuliuk, Daiki Koga, Beata Koszarna, Krzysztof Górski, Marek Grzybowski, Łukasz Kielesiński, Maciej Krzeszewski, Daniel T. Gryko
    J. Org. Chem. 2020, 85, 13529–13543
    DOI: 10.1021/acs.joc.0c01665
    Graphical abstract
  8. Effects of Amino Group Substitution on the Photophysical Properties and Stability of Near-Infrared Fluorescent P-Rhodamines
    Marek Grzybowski, Masayasu Taki, Keiji Kajiwara, Shigehiro Yamaguchi
    Chem. Eur. J. 2020, 26, 7912-7917
    DOI: 10.1002/chem.202000957
    Graphical abstract
  9. Synthetic Applications of Oxidative Aromatic Coupling—From Biphenols to Nanographenes
    Marek Grzybowski, Bartłomiej Sadowski, Holger Butenschön, Daniel T. Gryko
    Angew. Chem. Int. Ed. 2019, 59, 2998-3027
    DOI: 10.1002/anie.201904934
    Graphical abstract
  10. A Highly Photostable Near-Infrared Labeling Agent Based on a Phospha-rhodamine for Long-Term and Deep Imaging
    Marek Grzybowski, Masayasu Taki, Kieko Senda, Yoshikatsu Sato, Tetsuro Ariyoshi, Yasushi Okada, Ryosuke Kawakami, Takeshi Imamura, Shigehiro Yamaguchi
    Angew. Chem. Int. Ed. 2018, 57, 10137-10141
    DOI: 10.1002/anie.201804731
    Graphical abstract
  11. A far-red fluorescent probe based on a phospha-fluorescein scaffold for cytosolic calcium imaging
    Hiroaki Ogasawara, Marek Grzybowski, Riho Hosokawa, Yoshikatsu Sato, Masayasu Taki, Shigehiro Yamaguchi
    Chem. Commun. 2018, 54, 299-302
    DOI: 10.1039/C7CC07344E
    Graphical abstract
  12. Selective Conversion of P=O-Bridged Rhodamines into P=O-Rhodols: Solvatochromic Near-Infrared Fluorophores
    Marek Grzybowski, Masayasu Taki, Shigehiro Yamaguchi
    Chem. Eur. J. 2017, 23, 13028-13032
    DOI: 10.1002/chem.201703456
    Graphical abstract
  13. π-Expanded Dipyrrolonaphthyridinediones with Large Two-Photon Absorption Cross-Section Values
    Bartłomiej Sadowski, Hanayo Kita, Marek Grzybowski, Kenji Kamada, Daniel T. Gryko
    J. Org. Chem. 2017, 82, 7254–7264
    DOI: 10.1021/acs.joc.7b00831
    Graphical abstract
  14. Synthesis and optical properties of water-soluble diketopyrrolopyrroles
    Marek Grzybowski, Eliza Glodkowska-Mrowka, Guillame Clermont, Mireille Blanchard-Desce, Daniel T. Gryko
    Chem. Heterocycl. Comp. 2017, 53, 72–77
    DOI: 10.1007/s10593-017-2023-y
    Graphical abstract
  15. Modulation of Symmetry-Breaking Intramolecular Charge-Transfer Dynamics Assisted by Pendant Side Chains in π-Linkers in Quadrupolar Diketopyrrolopyrrole Derivatives
    Woojae Kim, Jooyoung Sung, Marek Grzybowski, Daniel T. Gryko, Dongho Kim
    J. Chem. Phys. Lett. 2016, 7, 3060–3066
    DOI: 10.1021/acs.jpclett.6b01248
    Graphical abstract
  16. Z-Shaped Pyrrolo[3,2-b]pyrroles and Their Transformation into π-Expanded Indolo[3,2-b]indoles
    Rafał Stężycki, Marek Grzybowski, Guillaume Clermont, Mireille Blanchard-Desce, Daniel T. Gryko
    Chem. Eur. J. 2016, 22, 5198-5203
    DOI: 10.1002/chem.201505052
    Graphical abstract
  17. Dipyrrolonaphthyridinediones – structurally unique cross-conjugated dyes
    Marek Grzybowski, Irena Deperasińska, Maciej Chotkowski, Marzena Banasiewicz, Artur Makarewicz, Bolesław Kozankiewicz, Daniel T. Gryko
    Chem. Commun. 2016, 52, 5108-5111
    DOI: 10.1039/C6CC01017B
    Graphical abstract
  18. Solvatofluorochromic, non-centrosymmetric π-expanded diketopyrrolopyrrole
    Marek Grzybowski, Artur Jeżewski, Irena Deperasińska, Daniel H. Friese, Marzena Banasiewicz, Vincent Hugues, Bolesław Kozankiewicz, Mireille Blanchard-Desce, Daniel T. Gryko
    Org. Biomol. Chem. 2016, 14, 2025-2033
    DOI: 10.1039/C5OB02583D
    Graphical abstract
  19. Phospha-fluorescein: a red-emissive fluorescein analogue with high photobleaching resistance
    Aiko Fukazawa, Shinji Suda, Masayasu Taki, Eriko Yamaguchi, Marek Grzybowski, Yoshikatsu Sato, Tetsuya Higashiyama, Shigehiro Yamaguchi
    Chem. Commun. 2016, 52, 1120-1123
    DOI: 10.1039/C5CC09345G
    Graphical abstract
  20. Polar Diketopyrrolopyrrole-Imidazolium Salts as Selective Probes for Staining Mitochondria in Two-Photon Fluorescence Microscopy
    Marek Grzybowski, Eliza Glodkowska-Mrowka, Vincent Hugues, Wojciech Brutkowski, Mireille Blanchard-Desce, Daniel T. Gryko
    Chem. Eur. J. 2015, 21, 9101-9110
    DOI: 10.1002/chem.201500738
    Graphical abstract
  21. Diketopyrrolopyrroles: Synthesis, Reactivity, and Optical Properties
    Marek Grzybowski, Daniel T. Gryko
    Adv. Opt. Mater. 2015, 3, 280-320
    DOI: 10.1002/adom.201400559
    Graphical abstract
  22. Hydrogen-bonded diketopyrrolopyrrole (DPP) pigments as organic semiconductors
    Eric Daniel Głowacki, Halime Coskun, Martin A. Blood-Forsythe, Uwe Monkowius, Lucia Leonat, Marek Grzybowski, Daniel Gryko, Matthew Schuette White, Alán Aspuru-Guzik, Niyazi Serdar Sariciftci
    Organic Electronics 2014, 15, 3521-3528
    DOI: 10.1016/j.orgel.2014.09.038
    Graphical abstract
  23. Two-Photon-Induced Fluorescence in New π-Expanded Diketopyrrolopyrroles
    Marek Grzybowski, Vincent Hugues, Mireille Blanchard-Desce, Daniel T. Gryko
    Chem. Eur. J. 2014, 20, 12493-12501
    DOI: 10.1002/chem.201402569
    Graphical abstract
  24. Excited-State Dynamics of an Environment-Sensitive Push–Pull Diketopyrrolopyrrole: Major Differences between the Bulk Solution Phase and the Dodecane/Water Interface
    Sabine Richert, Sandra Mosquera Vazquez, Marek Grzybowski, Daniel T. Gryko, Alexander Kyrychenko, Eric Vauthey
    J. Phys. Chem. B 2014, 118, 9952–9963
    DOI: 10.1021/jp506062j
    Graphical abstract
  25. Comparison of Oxidative Aromatic Coupling and the Scholl Reaction
    Marek Grzybowski, Kamil Skonieczny, Holger Butenschön, Daniel T. Gryko
    Angew. Chem. Int. Ed. 2013, 52, 9900-9930
    DOI: 10.1002/anie.201210238
    Graphical abstract
  26. Strong two-photon absorption enhancement in a unique bis-porphyrin bearing a diketopyrrolopyrrole unit
    Agnieszka Nowak-Król, Marek Grzybowski, Jerzy Romiszewski, Mikhail Drobizhev, Geoffrey Wicks, Maciej Chotkowski, Aleksander Rebane, Ewa Górecka, Daniel T Gryko
    Chem. Commun. 2013, 49, 8368-8370
    DOI: 10.1039/C3CC44728F
    Graphical abstract
  27. Bright, Color-Tunable Fluorescent Dyes Based on π-Expanded Diketopyrrolopyrroles
    Marek Grzybowski, Eliza Glodkowska-Mrowka, Tomasz Stoklosa, Daniel T. Gryko
    Org. Lett. 2012, 14, 2670–2673
    DOI: 10.1021/ol300674v
    Graphical abstract