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61. 200 lat chemii związków aromatycznych

59. Donor–Acceptor Oligopyrroles and Beyond. Functional Aromatics via Naphthalimide Fusion

57. π-Conjugated Oligoradicaloids & Anions. Aromaticity, Magnetism, and Non-covalent Interactions

55. π-Conjugated Oligoradicaloids & Anions. Aromaticity, Magnetism, and Non-covalent Interactions

53. Donor–Acceptor Oligopyrroles and Beyond. Functional Aromatics via Naphthalimide Fusion

51. Krzywizny i wnęki w chemii związków aromatycznych

49. Curved nanocarbons and heterocycles: from intriguing π systems to supramolecular interactions

47. Curved nanocarbons and heterocycles: from intriguing π systems to supramolecular interactions

45. Donor–Acceptor Oligopyrroles: from Modular Dyes to Supramolecular Systems

43. Nowe strategie syntezy złożonych struktur aromatycznych. Topologia, krzywizny i funkcje

41. Carbon-Rich π-Aromatic Surfaces. Topology, Curvature, and Function

39. Carbon-Rich π-Aromatic Surfaces. Topology, Curvature, and Function

37. Synthetic Approaches to Curved Aromatic Molecules

35. Carbon-Rich Cavities in Macrocyclic and Curved Aromatics

33. Donor–Acceptor Oligopyrroles. A Modular Approach toward Heteronanocarbons

31. Peripherally Fused Azacoronenes. From Synthetic Challenges to Engineered Properties

29. Curvature vs. π-Conjugation: New Routes to Chiral and Low-Bandgap Systems

27. New Synthetic Approaches to Complex Aromatic Molecules (Liebig Lecture)

25. New Synthetic Approaches to Complex Aromatic Molecules (Liebig Lecture)

23. New Synthetic Approaches to Complex Aromatic Molecules (Liebig Lecture)

21. From Coronoid Macrocyles to Stable Open-Shell Systems

19. Helically Curved Oligopyrroles: Boomerangs, Snowflakes, Propellers

17. From Coronoid Macrocyles to Stable Biradicaloid Systems

15. Bending and Fusion: Synthetic Approaches to Tunable Aromatic Chromophores

13. Synthetic Approaches to Pyrrole-based Donor−Acceptor Oligomers

11. Bending Aromatic Molecules with Transition Metal-Mediated Reactions. The Fold-in Method and Beyond

9. Bending Aromatics From Electron-Deficient Nanographenoids to Hydrocarbon-Based Anion Receptors

7. Polycyclic Heteroaromatics in Two and Three Dimensions Design, Synthesis, and Properties

5. Designing New Carbon-Rich Molecules. Inspirations from Heterocyclic and Macrocyclic Chemistry

3. Distorted Heteroaromatics. Synthesis, Reactivity, and Electronic Structure 

1. Distorted Heteroaromatics: Synthesis and Self-Assembly