Daniel T. Gryko
Researcher Next ID · RN-041378
Researcher · Chemistry
Institute of Organic Chemistry
Warsaw, Poland
- Works count
- 593
- Citation count
- 16,021
- H-index
- 64
- i10-index
- 284
Research interests
Publications
Visible light communication with efficient far-red/near-infrared polymer light-emitting diodes
Light Science & Applications · 2020 · https://doi.org/10.1038/s41377-020-0314-z
Synthetic Applications of Oxidative Aromatic Coupling—From Biphenols to Nanographenes
Angewandte Chemie International Edition · 2019 · https://doi.org/10.1002/anie.201904934
On-surface synthesis of a nitrogen-embedded buckybowl with inverse Stone–Thrower–Wales topology
Nature Communications · 2018 · https://doi.org/10.1038/s41467-018-04144-5
The Tetraarylpyrrolo[3,2-b]pyrroles—From Serendipitous Discovery to Promising Heterocyclic Optoelectronic Materials
Accounts of Chemical Research · 2017 · https://doi.org/10.1021/acs.accounts.7b00275
The Tetraarylpyrrolo[3,2-b]pyrroles—From Serendipitous Discovery to Promising Heterocyclic Optoelectronic Materials
Accounts of Chemical Research · 2017 · https://doi.org/10.1021/acs.accounts.7b00275
The Tetraarylpyrrolo[3,2-b]pyrroles—From Serendipitous Discovery to Promising Heterocyclic Optoelectronic Materials
Accounts of Chemical Research · 2017 · https://doi.org/10.1021/acs.accounts.7b00275
Synthesis of Corroles and Their Heteroanalogs
Chemical Reviews · 2016 · https://doi.org/10.1021/acs.chemrev.6b00434
Recent advances in the synthesis of indolizines and their π-expanded analogues
Organic & Biomolecular Chemistry · 2016 · https://doi.org/10.1039/c6ob00985a
Symmetry‐Breaking Charge Transfer and Hydrogen Bonding: Toward Asymmetrical Photochemistry
Angewandte Chemie International Edition · 2016 · https://doi.org/10.1002/anie.201608567
Diketopyrrolopyrroles: Synthesis, Reactivity, and Optical Properties
Advanced Optical Materials · 2015 · https://doi.org/10.1002/adom.201400559
π-Expanded coumarins: synthesis, optical properties and applications
Journal of Materials Chemistry C · 2014 · https://doi.org/10.1039/c4tc02665a
Oxidative aromatische Kupplung und Scholl‐Reaktion im Vergleich
Angewandte Chemie · 2013 · https://doi.org/10.1002/ange.201210238
Comparison of Oxidative Aromatic Coupling and the Scholl Reaction
Angewandte Chemie International Edition · 2013 · https://doi.org/10.1002/anie.201210238
Imidazo[1,2-a]pyridines Susceptible to Excited State Intramolecular Proton Transfer: One-Pot Synthesis via an Ortoleva–King Reaction
The Journal of Organic Chemistry · 2012 · https://doi.org/10.1021/jo300643w
Synthesis of π-extended porphyrins via intramolecular oxidative coupling
Chemical Communications · 2012 · https://doi.org/10.1039/c2cc31279d
Photoactive corrole-based arrays
Chemical Society Reviews · 2009 · https://doi.org/10.1039/b805230c
Corrole−Fullerene Dyads: Formation of Long-Lived Charge-Separated States in Nonpolar Solvents
Journal of the American Chemical Society · 2008 · https://doi.org/10.1021/ja804665y
Efficient Synthesis of meso-Substituted Corroles in a H2O−MeOH Mixture
The Journal of Organic Chemistry · 2006 · https://doi.org/10.1021/jo060007k
Electrochemistry and Spectroelectrochemistry of meso-Substituted Free-Base Corroles in Nonaqueous Media: Reactions of (Cor)H3, [(Cor)H4]+, and [(Cor)H2]-
Inorganic Chemistry · 2006 · https://doi.org/10.1021/ic051729h
Photophysical characterization of free-base corroles, promising chromophores for light energy conversion and singlet oxygen generation
New Journal of Chemistry · 2005 · https://doi.org/10.1039/b507979a
Recent advances in the chemistry of corroles and core-modified corroles
Journal of Porphyrins and Phthalocyanines · 2004 · https://doi.org/10.1142/s1088424604000465
Recent Advances in the Synthesis of Corroles and Core-Modified Corroles
European Journal of Organic Chemistry · 2002 · https://doi.org/10.1002/1099-0690(200206)2002:11<1735::aid-ejoc1735>3.0.co;2-k
Refined methods for the synthesis of meso-substituted A3- and trans-A2B-corrolesElectronic supplementary information (ESI) available: table describing attempts to optimize the reaction of MesDPM 30 with aldehyde 11. See http://www.rsc.org/suppdata/ob/b2/b208950e/
Organic & Biomolecular Chemistry · 2002 · https://doi.org/10.1039/b208950e
A Simple and Versatile One-Pot Synthesis of meso-Substituted trans-A2B-Corroles
The Journal of Organic Chemistry · 2001 · https://doi.org/10.1021/jo010146w
Current projects
No projects listed.