All Stories

  1. Cover Feature: Accepting to Donate: NDI-Based Small Molecule as a Donor for Bulk Heterojunction Binary Solar Cells (Eur. J. Org. Chem. /2020)
  2. Accepting to Donate: NDI-Based Small Molecule as a Donor for Bulk Heterojunction Binary Solar Cells
  3. Electronic Modulation of Terrylene Diimides Leading to Core-Twisting, Tunable Emission and Intermolecular Interactions
  4. NIR absorbing ortho-π-extended perylene bisimide as a promising material for bulk heterojunction organic solar cells
  5. A cell-permeant small molecule for the super-resolution imaging of the endoplasmic reticulum in live cells
  6. A tris-(manganese(iii))corrole–porphyrin–corrole triad: synthesis, characterization and catalytic epoxidation
  7. Aminophenyl-substituted cobalt(iii) corrole: a bifunctional electrocatalyst for the oxygen and hydrogen evolution reactions
  8. Corrole-BODIPY Dyad as Small-Molecule Donor for Bulk Heterojunction Solar Cells
  9. Metal-free Annulation at the Ortho- and Bay-Positions of Perylene Bisimide Leading to Lateral π-Extension with Strong NIR Absorption
  10. Sterically hindered 5,15-tetraphenylbenzene-porphyrins: syntheses, structures, atropisomerism and photophysical properties
  11. Selective Imaging of Lipids in Adipocytes by Using an Imidazolyl Derivative of Perylene Bisimide
  12. The Curious Case of a Parasitic Twin of the Corroles
  13. A Curious Case of Parasitic Twin of Corroles
  14. Modulation of the power conversion efficiency of organic solar cells via architectural variation of a promising non-fullerene acceptor
  15. Evidence for a [17] π-Electronic Full-Fledged Non-innocent Gallium(III)-Corrole Radical
  16. Zwitterionic BODIPYs with large stokes shift: small molecular biomarkers for live cells
  17. Porphyrin based push–pull conjugates as donors for solution-processed bulk heterojunction solar cells: a case of metal-dependent power conversion efficiency
  18. A facile and visual approach for the detection of trace level ammonia vapours under ambient conditions
  19. Novel structurally tuned DAMN receptor for “in situ” diagnosis of bicarbonate in environmental waters
  20. First Example of a Modular Porphyrinoid Assembly Capable of Stabilizing Different Metal Ions in a Single Molecular Scaffold
  21. Corrole-BODIPY Dyads: Synthesis, Structure, and Electrochemical and Photophysical Properties
  22. Perylenebisimide-based multi-modal cyanide recognition: molecular logic gate deciphering magnetic memory units
  23. Reusable and specific proton transfer signalling by inorganic cyanide in solution and solid phase
  24. Dual-mode chemodosimetric response of dibromo-BODIPY with anions
  25. Gallium(iii)corrole–BODIPY hybrid: novel photophysical properties and first observation of B–F⋯F interactions
  26. A selective fluoride sensor and a digital processor with “Write–Read–Erase–Read” behaviour
  27. Novel Azepino-perylenebisimides: Synthesis, Structure, and Properties
  28. Aliphatic Amine Discrimination by Pentafluorophenyl Dibromo BODIPY
  29. Visible-Light Activation of the Bimetallic Chromophore–Catalyst Dyad: Analysis of Transient Intermediates and Reactivity toward Organic Sulfides
  30. Unsymmetrical Perylenebisimides
  31. A molecular Boolean mimic with OR, NOR, YES and INH functions: dual-ion recognition driven fluorescence “turn on”
  32. A new meso–meso directly-linked corrole–porphyrin–corrole hybrid: synthesis and photophysical properties
  33. Selective iodide chemosensing through a redox-active Cu-corrole
  34. Thienyl-linked pyrenes: new green-emitting triads
  35. Exclusive fluoride ion recognition and fluorescence “turn-on” response with a label-free DMN Schiff base
  36. Temperature-Dependent Conformational Change of meso -Hexakis(pentafluorophenyl) [28]Hexaphyrins(1.1.1.1.1.1) into Möbius Structures †
  37. Unambiguous Identification of Möbius Aromaticity for meso -Aryl-Substituted [28]Hexaphyrins(1.1.1.1.1.1)
  38. 2,5-Thienylene-Bridged Triangular and Linear Porphyrin Trimers
  39. 2,5-Thienylene-Bridged Triangular and Linear Porphyrin Trimers
  40. Smaragdyrin–Azobenzene Conjugates: Syntheses, Structure, and Spectral and Electrochemical Properties
  41. meso-meso-Linked Corrole Dimers with Modified Cores: Synthesis, Characterization, and Properties
  42. Aromatic Core-Modified Twisted Heptaphyrins[1.1.1.1.1.1.0]:  Syntheses and Structural Characterization
  43. Core-Modified Expanded Porphyrins with Large Third-Order Nonlinear Optical Response
  44. Figure-eight aromatic core-modified octaphyrins with six meso links: syntheses and structural characterization
  45. Syntheses of Core-Modified Corroles by Three Different [3 + 1] Methodologies
  46. Oxasmaragdyrin–Ferrocene and Oxacorrole–Ferrocene Conjugates: Synthesis, Structure, and Nonlinear Optical Properties
  47. Core-Modified Hexaphyrins; Characterization of Two- and Four-Ring Inverted 26 π Aromatic Macrocycles
  48. Modified Corroles with One Meso-Free Carbon: Synthesis and Characterization
  49. Porphyrins in Photodynamic Therapy - A Search for Ideal Photosensitizers
  50. Core modified oxybenziporphyrins: new aromatic ligands for metal–carbon bond activationElectronic supplementary information (ESI) available: See FAB mass, UV-Vis, 1H, 2D NMR spectra. http://www.rsc.org/suppdata/cc/b1/b111155h/
  51. First structural characterization of core modified 10,15-meso aryl azuliporphyrins: observation of C–H⋯π interaction between pyrrole β-CH and mesityl ring