Marcin Lindner

Head of the group
Dr. Marcin Lindner

Assistants
Dr. eng. Krzysztof Bartkowski
Dr Urszula Klimczak

Post-doc
Dr. Sukhvinder Dhiman

PhD Students
M.Sc. eng. Julia Korczak
M.Sc. eng. Katarzyna Piasecka
M.Sc. Mohil Thanki
M.Sc. Jakub Wagner

FIRST TEAM
FENG.02.02-IP.05-0061/23
“Światło w (chiralnym) tunelu: nowe holistyczne podejście do uzyskiwania wydajnych i stabilnych urządzeń CP-OLED”

HORYZONT EUROPA
101182946-GHOST-HORIZON-MSCA-2023-SE-01
“Green Horizon on Organic Semiconductor Technologies (GHOST)”

NCN SONATINA 2024/52/C/ST5/00129
„Stable organic radicals capable of thermally activated delayed fluorescence – multi-purpose materials for optoelectronic applications”

NCN SONATA BIS 2023/50/E/ST5/00051
„Highly efficient NIR organic emitters with inverted singlet-triplet excited states (NIR-INVEST)”

NCN OPUS 2022/45/B/ST4/00800
„Ambipolar, bowl-shaped polyaromatic compounds with manifold, precisely arranged, nitrogen dopants. Unprecedented class of efficient OLED emitters (BOwLEDs)”

NCN PRELUDIUM 2022/45/N/ST4/00913
„Diaza-BF2-embedded N-polycyclic aromatic hydrocarbons – game changer in the domain of NIR TADF emitters”

D. Szeląg,   J. S. Cyniak,   J. Ażgin,   J. Wagner,   M. Lindner,   W. Wróblewski, A. Kasprzak, „Metal cations recognition by bowl-shaped N-pyrrolic polycyclic aromatic hydrocarbons”, Chem. Commun.

M. Grzelak, D. Kumar, M. A. Kochman, G. Wiosna-Sałyga, M. Morawiak, A. Kubas, P. Data, M. Lindner,  „Unprecedented roll-off ratio in high-performing red TADF OLED emitters featuring 2,3-Indole-annulated naphthalene imide and auxiliary donors”, Chem. Sci.

P. Govindharaj, A. J. Wierzba, K. Kęska, M. A Kochman, G. Wiosna-Sałyga, A. Kubas, P. Data, M. Lindner, „Regioisomerism vs Conformation: Impact of Molecular Design on the Emission Pathway in Organic Light-Emitting Device Emitters”, ACS Appl. Mater. Interfaces

K. Bartkowski, A. K. Gupta, T. Matulaitis, M. Morawiak, E. Zysman-Colman, M. Lindner, „Using pyrrolizine-fused bipolar PAHs as a new strategy towards efficient red and NIR emissive dyes”, Org. Chem. Front.

J. Wagner, D. Kumar, M. A. Kochman, T. Gryber, M. Grzelak,
A. Kubas, P. Data, M. Lindner, „Facile Functionalization of Ambipolar, Nitrogen-Doped PAHs toward Highly Efficient TADF OLED Emitters”, ACS Appl. Mater. Interfaces

W. Derkowski, D. Kumar, T. Gryber, M. Kochman, M. Morawiak, J. Wagner, A. Kubas, P. Data, M. Lindner, „V-shaped donor-acceptor organic emitters. A new approach towards efficient TADF OLED devices”, Chem. Commun.

K. Bartkowski, P. Zimmermann Crocomo, M. A. Kochman, D. Kumar, A. Kubas, P. Data, M. Lindner, „Tandem rigidification and π-extension as a key tool for the development of a narrow linewidth yellow hyperfluorescent OLED system”, Chem. Sci.

R. Kusy, M. Lindner, J. Wagner, K. Grela, „Ligand-to-metal ratio controls stereoselectivity:Highly functional group-tolerant, iridium-based,(E)-selective alkyne transfer semihydrogenation”, Chem Catalysis

J. Wagner, P. Zimmermann Crocomo, M. A. Kochman, A. Kubas, P. Data, M. Lindner, „Modular, n-Doped Concave PAHs for High-Performance OLEDs with Tunable Emission Mechanisms”, Angew. Chem. Int. Ed.

K. Dąbrowa, M. Lindner, A. Tyszka-Gumkowska, J. Jurczak, „Imino-thiolate-templated synthesis of a chloride-selective neutral macrocyclic host with a specific “turn-off–on” fluorescence response for hypochlorite”, Org. Chem. Front.

M. Hromadová, J. Sebera, M. Lindner, J. Gasior, G. Meszaros, O. Fuhr, M. Mayor, M. Valášek, V. Kolivoska, „Tuning the contact conductance of anchoring groups in single molecule junctions by molecular design”, Nanoscale

W. Wulfhekel, J. Homberg , M. Lindner, L. Gerhard, K. Edelmann, T. Frauhammer, Y. Nahas, M. Valsek, M. Mayor, „Six state molecular revolver mounted on a rigid platform”, Nanoscale

V. Kolivoška, J. Šebera, T. Sebechlebská, M. Lindner, J. Gasior, G. Mészáros, M. Mayor, M. Valášek, M. Hromadová, „Probabilistic mapping of single molecule junction configurations as a tool to achieve the desired geometry of asymmetric tripodal molecules”, Chem. Commun.

M. Lindner, A. Krasiński, J. Jurczak, „Facile, Stereocontrolled Synthetic Route towards Bis-functionalised Pyrrolizidines”, Synthesis

J. Jurczak, A. Sobczuk, K. Da̧browa, M. Lindner, P. Niedbała, „An Indirect Synthetic Approach toward Conformationally Constrained 20-Membered Unclosed Cryptands via Late-Stage Installation of Intraannular Substituents”, J. Org. Chem.

J. Jurczak, A. Sobczuk, K. Dąbrowa, M. Lindner, P. Niedbała, P. Stepniak, „Chirality of 20‐membered unclosed cryptand: Macroring distortion via lariat arm modification”, Chirality