D. M. Andrada, C. Foroutan-Nejad, „Energy components in energy decomposition analysis (EDA) are path functions; why does it matter?”, Phys. Chem. Chem. Phys.
Y. Poronik, G. V. Baryshnikov, I. Deperasińska, E. M. Espinoza, J. A. Clark, H. Ågren, D. Gryko, V. I. Vullev, „Deciphering the unusual fluorescence in weakly coupled bis-nitro-pyrrolo[3,2-b]pyrroles”, Commun. Chem.
Ł. Łukasiewicz, M. Rammo, C. Stark, M. Krzeszewski, D. Jacquemin, A. Rebane, D. T. Gryko, „Ground‐ and Excited‐State Symmetry Breaking and Solvatofluorochromism in Centrosymmetric Pyrrolo[3,2‐ b ]pyrroles Possessing two Nitro Groups”, ChemPhotoChem
K. Gutkowski, K. Skonieczny, M. Bugaj, D. Jacquemin, D. T. Gryko, „N‐Arylation of Diketopyrrolopyrroles with Aryl Triflates”, Chem. Asian J.
O. Morawski, D. T. Gryko, A. Sobolewski, Ł. Kielesiński, „Highly Polarized Coumarin Derivatives Revisited: Solvent-controlled Competition Between Proton Coupled Electron Transfer and Twisted Intramolecular Charge Transfer”, Chem. Eur. J.
A. Minotto, P. A. Haigh, Ł. Łukasiewicz, E. Lunedei, D. T. Gryko, I. Darwazeh, F. Cacialli, „Visible light communication with efficient far-red/near-infrared polymer light-emitting diodes”, Light-Sci. Appl.
P.-T. Chou, S.-M. Tseng, F. Ambicki, I. Deperasińska, D. T. Gryko, Y. Poronik, „How an Eight-Membered Ring Alters the Rhodamine Chromophore”, J. Org. Chem.
Y. Qin, C. Schnedermann, M. Tasior, D. T. Gryko, D. G. Nocera, „Direct Observation of Different One- and Two-Photon Fluorescent States in a Pyrrolo[3,2-b]pyrrole Fluorophore”, J. Phys. Chem. Lett.
K. Skonieczny, I. Papadopoulos, D. Thiel, K. Gutkowski1, P. Haines, P. M. McCosker, A. D. Laurent, P. A. Keller, T. Clark, D. Jacquemin, D. M. Guldi, D. T. Gryko, „How To Make Nitroaromatic Compounds Glow: Next‐Generation Large X‐Shaped, Centrosymmetric Diketopyrrolopyrroles”, Angew. Chem. Int. Ed.
A. Nowak-Król, B. Koszarna, M. Krzeszewski, T. D. Lohrey, J. Arnold, D. T. Gryko, „Access to Corrole-Appended Persubstituted Benzofurans by a Multicomponent Reaction: The Dual Role of p-Chloranil”, Org. Lett.
M. Tasior, O. Vakuliuk, D. Koga, B. Koszarna, K. Górski, M. Grzybowski, Ł. Kielesiński, M. Krzeszewski, D. T. Gryko, „Method for the Large-Scale Synthesis of Multifunctional 1,4-Dihydro-pyrrolo[3,2-b]pyrroles”, J. Org. Chem.
M. Grzybowski, B. Sadowski, H. Butenschön, D. T. Gryko, „Synthetic Applications of Oxidative Aromatic Coupling – from Biphenols to Nanographenes”, Angew. Chem. Int. Ed.
D. C. Young, M. Tasior, A. D. Laurent, Ł. Dobrzycki, M. K. Cyrański, N. Tkachenko, D. Jacquemin, D. T. Gryko, „Photostable orange-red fluorescent unsymmetrical diketopyrrolopyrrole–BF2 hybrids”, J. Mater. Chem. C
Z. Szakács, M. Tasior, D. T. Gryko, E. Vauthey, „Change of Quadrupole Moment upon Excitation and Symmetry Breaking in Multibranched Donor‐Acceptor Dyes”, ChemPhysChem
T. Kim, W. Kim, O. Vakuliuk, D. T. Gryko, D. Kim, „Two-Step Charge Separation Passing Through the Partial Charge-Transfer State in a Molecular Dyad”, J. Am. Chem. Soc.
M. Pieczykolan, J.Czaban-Jóźwiak, M. Malinska, K. Woźniak, R. Dorta, A. Rybicka, A. Kajetanowicz, K. Grela, „The Influence of Various N-Heterocyclic Carbene Ligands on Activity of Nitro-Activated Olefin Metathesis Catalysts”, Molecules
M. Pieczykolan, B. Sadowski, D. T. Gryko, „An Efficient Method for the Programmed Synthesis of Multifunctional Diketopyrrolopyrroles”, Angew. Chem. Int. Ed.
J. Lewtak, B. Koszarna, M. Charyton, D. T. Gryko, „Extending a porphyrin chromophore via fusion with naphthalene”, J. Porphyr. Phthalocya.
S. Hatanaka, T. Ono, Y. Yano, D. T. Gryko, Y. Hisaeda, „Tris(pentafluorophenyl)borane-pyrrolo[3,2-b]pyrrole Hybrids: Solid-State Structure and Crystallization-Induced Enhanced Emission”, ChemPhotoChem
B. Sadowski, D. Stewart, A. Phillips, T. Grusenmeyer, J. Haley, T. Cooper, D. T. Gryko, „From Dipyrrolonaphthyridinediones to Quinazolinoindolizinoindolizinoquinazolines”, J. Org. Chem.
I. Benkyi, O. Staszewska-Krajewska, D. T. Gryko, M. Jaszuński, A. Stanger, D. Sundholm, „The Interplay of Aromaticity and Antiaromaticity in N-Doped Nanographenes”, J. Phys. Chem. A.