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Hierarchical Self‐Assembly of Curved Aromatics: From Donor–Acceptor Porphyrins to Triply Periodic Minimal Surfaces.
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- Angewandte Chemie, 2024, v. 136, n. 9, p. 1, doi. 10.1002/ange.202316243
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Hierarchical Self‐Assembly of Curved Aromatics: From Donor–Acceptor Porphyrins to Triply Periodic Minimal Surfaces.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 9, p. 1, doi. 10.1002/anie.202316243
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- Article
Complexes of N‐Confused Porphyrin Derivatives as Ortho‐Metallating Ligands. Synthesis, Structure, Redox Properties, and Chirality.
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- Advanced Science, 2024, v. 11, n. 2, p. 1, doi. 10.1002/advs.202306696
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π‐Extended Hexapyrrolylbenzenes: Exploring Charge‐Transfer Phenomena in Donor‐Acceptor Propellers.
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- Chemistry - A European Journal, 2023, v. 29, n. 67, p. 1, doi. 10.1002/chem.202302429
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Dinor[7]helicene and Beyond: Divergent Synthesis of Chiral Diradicaloids with Variable Open‐Shell Character.
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- Angewandte Chemie, 2023, v. 135, n. 38, p. 1, doi. 10.1002/ange.202309238
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Dinor[7]helicene and Beyond: Divergent Synthesis of Chiral Diradicaloids with Variable Open‐Shell Character.
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- Angewandte Chemie International Edition, 2023, v. 62, n. 38, p. 1, doi. 10.1002/anie.202309238
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Tridecacyclene Tetraimide: An Easily Reduced Cyclooctatetraene Derivative.
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- Angewandte Chemie, 2022, v. 134, n. 38, p. 1, doi. 10.1002/ange.202207486
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Tridecacyclene Tetraimide: An Easily Reduced Cyclooctatetraene Derivative.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 38, p. 1, doi. 10.1002/anie.202207486
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Naphthalimide‐Fused Dipyrrins: Tunable Halochromic Switches and Photothermal NIR‐II Dyes.
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- Advanced Science, 2022, v. 9, n. 19, p. 1, doi. 10.1002/advs.202105886
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- Article
Helicity Modulation in NIR‐Absorbing Porphyrin‐Ryleneimides.
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- Angewandte Chemie, 2022, v. 134, n. 18, p. 1, doi. 10.1002/ange.202200781
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- Article
Helicity Modulation in NIR‐Absorbing Porphyrin‐Ryleneimides.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 18, p. 1, doi. 10.1002/anie.202200781
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- Article
An Open‐Shell Coronoid with Hybrid Chichibabin–Schlenk Conjugation.
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- Angewandte Chemie, 2021, v. 133, n. 41, p. 22670, doi. 10.1002/ange.202109273
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- Article
An Open‐Shell Coronoid with Hybrid Chichibabin–Schlenk Conjugation.
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- Angewandte Chemie International Edition, 2021, v. 60, n. 41, p. 22496, doi. 10.1002/anie.202109273
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- Article
Porphyrin‐Ryleneimide Hybrids: Low‐Bandgap Acceptors in Energy‐Transfer Cassettes.
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- Chemistry - An Asian Journal, 2020, v. 15, n. 18, p. 2763, doi. 10.1002/asia.202000897
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- Article
Porphyrin‐Ryleneimide Hybrids: Low‐Bandgap Acceptors in Energy‐Transfer Cassettes.
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- Chemistry - An Asian Journal, 2020, v. 15, n. 18, p. 2854, doi. 10.1002/asia.202000762
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- Article
Cover Feature: Conformation‐Dependent Response to the Protonation of Diphenanthrioctaphyrin(1.1.1.0.1.1.1.0): A Route to Pseudorotaxane‐Like Structures (Chem. Eur. J. 39/2020).
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- Chemistry - A European Journal, 2020, v. 26, n. 39, p. 8480, doi. 10.1002/chem.202002880
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- Article
Conformation‐Dependent Response to the Protonation of Diphenanthrioctaphyrin(1.1.1.0.1.1.1.0): A Route to Pseudorotaxane‐Like Structures.
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- Chemistry - A European Journal, 2020, v. 26, n. 39, p. 8555, doi. 10.1002/chem.202000940
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- Article
Aromatic and Antiaromatic Pathways in Triphyrin(2.1.1) Annelated with Benzo[b]heterocycles.
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- Chemistry - A European Journal, 2019, v. 25, n. 68, p. 15477, doi. 10.1002/chem.201903863
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Front Cover: C−H and C−M Activation, Aromaticity Tuning, and Co⋅⋅⋅Ru Interactions Confined in the Azuliporphyrin Framework (Chem. Eur. J. 64/2019).
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- Chemistry - A European Journal, 2019, v. 25, n. 64, p. 14475, doi. 10.1002/chem.201904035
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- Article
C−H and C−M Activation, Aromaticity Tuning, and Co⋅⋅⋅Ru Interactions Confined in the Azuliporphyrin Framework.
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- Chemistry - A European Journal, 2019, v. 25, n. 64, p. 14479, doi. 10.1002/chem.201904036
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- Article
C−H and C−M Activation, Aromaticity Tuning, and Co⋅⋅⋅Ru Interactions Confined in the Azuliporphyrin Framework.
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- Chemistry - A European Journal, 2019, v. 25, n. 64, p. 14536, doi. 10.1002/chem.201903215
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- Article
Stereocontrolled Synthesis of Chiral Heteroaromatic Propellers with Small Optical Bandgaps.
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- Angewandte Chemie International Edition, 2019, v. 58, n. 15, p. 4929, doi. 10.1002/anie.201900175
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Back Cover: Stereocontrolled Synthesis of Chiral Heteroaromatic Propellers with Small Optical Bandgaps (Angew. Chem. Int. Ed. 15/2019).
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- Angewandte Chemie International Edition, 2019, v. 58, n. 15, p. 5136, doi. 10.1002/anie.201902135
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- Article
Electron‐Deficient Bipyrrole Boomerangs: Bright Fluorophores Obtained via Double C−H Bond Activation.
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- Chemistry - A European Journal, 2018, v. 24, n. 29, p. 7525, doi. 10.1002/chem.201801199
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- Article
Helicenophyrins: Expanded Carbaporphyrins Incorporating Aza[5]helicene and Heptacyclic S‐Shaped Aza[5]helicene Motifs.
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- Angewandte Chemie, 2018, v. 130, n. 15, p. 4094, doi. 10.1002/ange.201800879
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- Article
Helicenophyrins: Expanded Carbaporphyrins Incorporating Aza[5]helicene and Heptacyclic S‐Shaped Aza[5]helicene Motifs.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 15, p. 4030, doi. 10.1002/anie.201800879
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- Article
Pyridine-Fused Bis(Norcorrole) through Hantzsch-Type Cyclization: Enhancement of Antiaromaticity by an Aromatic Bridge.
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- Angewandte Chemie, 2017, v. 129, n. 36, p. 10950, doi. 10.1002/ange.201705715
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- Article
Pyridine-Fused Bis(Norcorrole) through Hantzsch-Type Cyclization: Enhancement of Antiaromaticity by an Aromatic Bridge.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 36, p. 10810, doi. 10.1002/anie.201705715
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- Article
Dipyrrin-Bis( N-Confused Porphyrin) Conjugate: Synthesis, Synergetic Ligation and Chirality Sensing.
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- Chemistry - An Asian Journal, 2017, v. 12, n. 6, p. 643, doi. 10.1002/asia.201700129
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- Article
Distributional effects of flood risk management--a cross-country comparison of preflood compensation.
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- Ecology & Society, 2016, v. 21, n. 4, p. 200, doi. 10.5751/ES-08648-210426
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- Article
An Electron-Deficient Azacoronene Obtained by Radial π Extension.
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- Angewandte Chemie, 2016, v. 128, n. 47, p. 14878, doi. 10.1002/ange.201608400
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An Electron-Deficient Azacoronene Obtained by Radial π Extension.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 47, p. 14658, doi. 10.1002/anie.201608400
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- Article
Octulene: A Hyperbolic Molecular Belt that Binds Chloride Anions.
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- Angewandte Chemie, 2016, v. 128, n. 45, p. 14278, doi. 10.1002/ange.201608384
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- Article
Octulene: A Hyperbolic Molecular Belt that Binds Chloride Anions.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 45, p. 14072, doi. 10.1002/anie.201608384
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- Article
Reversible Carbon-Carbon Bond Breaking and Spin Equilibria in Bis(pyrimidinenorcorrole).
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- Angewandte Chemie, 2016, v. 128, n. 42, p. 13336, doi. 10.1002/ange.201607237
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- Article
Reversible Carbon-Carbon Bond Breaking and Spin Equilibria in Bis(pyrimidinenorcorrole).
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- Angewandte Chemie International Edition, 2016, v. 55, n. 42, p. 13142, doi. 10.1002/anie.201607237
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- Article
Nitration of Norcorrolatonickel(II): First Observation of a Diatropic Current in a System Comprising a Norcorrole Ring.
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- Chemistry - A European Journal, 2016, v. 22, n. 12, p. 4231, doi. 10.1002/chem.201504584
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- Article
Towards Norcorrin: Hydrogenation Chemistry and the Heterodimerization of Nickel(II) Norcorrole.
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- Chemistry - A European Journal, 2015, v. 21, n. 21, p. 7790, doi. 10.1002/chem.201500736
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- Article
Bis(N-Confused Porphyrin) as a Semirigid Receptor with a Chirality Memory: A Two-Way Host Enantiomerization through Point-to-Axial Chirality Transfer.
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- Chemistry - A European Journal, 2015, v. 21, n. 6, p. 2547, doi. 10.1002/chem.201405598
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- Article
Enantiomer Resolution of Intrinsically Chiral C21-Alkylated N-Confused Porphyrin Complexes.
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- Chemistry - A European Journal, 2011, v. 17, n. 3, p. 1009, doi. 10.1002/chem.201000534
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- Article
Glückszahl Sieben: Charakterisierung stabiler, T-förmiger Kupfer(II)-Komplexe von [32]Heptaphyrinen.
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- Angewandte Chemie, 2010, v. 122, n. 8, p. 1399, doi. 10.1002/ange.200905577
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Lucky Seven: Characterization of Stable T-Shaped Copper(II) Complexes of [32]Heptaphyrins.
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- Angewandte Chemie International Edition, 2010, v. 49, n. 8, p. 1359, doi. 10.1002/anie.200905577
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- Article
Helical Bis(N-Confused Porphyrins) with Subunits Fused by Double Orthometalation with Platinum: Adaptability of an Apparently Rigid System.
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- Angewandte Chemie International Edition, 2009, v. 48, n. 46, p. 8736, doi. 10.1002/anie.200904289
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- Article
Synthesis, Characterization, and Chirality of Dimeric N-Confused Porphyrin-Zinc Complexes: Toward the Enantioselective Synthesis of Bis(porphyrinoid) Systems.
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- Angewandte Chemie International Edition, 2007, v. 46, n. 39, p. 7432, doi. 10.1002/anie.200701860
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Synthesis and Characterization of a Cyclic Bis-silver(I) Assembly of Four 2-Aza-21-carbaporphyrinatosilver(III) SubunitsThis work was supported by the Polish Ministry of Scientific Research and Information Technology (Grant 3 T09A 16228).
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- Angewandte Chemie International Edition, 2005, v. 44, n. 39, p. 6417, doi. 10.1002/anie.200502208
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Synthesis and Characterization of a Cyclic Bis-silver(I) Assembly of Four 2-Aza-21-carbaporphyrinatosilver(III) Subunits.
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- Angewandte Chemie, 2005, v. 117, n. 39, p. 6575, doi. 10.1002/ange.200502208
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Synthesis and Characterization of a Directly Linked N-Confused Porphyrin DimerThe author thanks Dr. M. Stępień for his help in the X-ray crystal structure analysis and for helpful discussions. This work was supported by the State Committee for Scientific Research of Poland (Grant No. 3 09A 155 15)
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- Angewandte Chemie International Edition, 2004, v. 43, n. 42, p. 5655, doi. 10.1002/anie.200461361
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Synthesis and Characterization of a Directly Linked N-Confused Porphyrin DimerThe author thanks Dr. M. Stępień for his help in the X-ray crystal structure analysis and for helpful discussions. This work was supported by the State Committee for Scientific Research of Poland (Grant No. 3 09A 155 15)
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- Angewandte Chemie, 2004, v. 116, n. 42, p. 5773, doi. 10.1002/ange.200461361
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- Article
Synthesis, Crystallographic and Spectroscopic Studies of Dimeric Cu<sup>I</sup> Complexes with Schiff-Base-Containing Triazole Ligands.
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- European Journal of Inorganic Chemistry, 2003, v. 2003, n. 8, p. 1548
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Nickel Complexes of 21-Oxaporphyrin and 21, 23-Dioxaporphyrin.
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- Chemistry - A European Journal, 1997, v. 3, n. 2, p. 268, doi. 10.1002/chem.19970030216
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- Article