Carbazole-embedded p-benziporphyrinoid: synthesis, structure and a reversible chemodosimeter for mercury(II) ions.

The first carbazole-embedded p-benziporphyrinoid is synthesized by a [3+1] acid-catalyzed condensation between appropriate coupling partners. The macrocycle 1 exhibited orange emission and showed a large Stokes shift of 5831 cm-1. Intriguingly, it shows a selective affinity towards Hg2+ ions over other metal-ions in a reversible manner. Job's plot confirmed the 1 : 1 stoichiometry with unambiguous confirmation of both 1 and 1-Hg by single crystal X-ray analysis.

Stable Inner 2H Tautomer of N-Confused-like Porphyrin Embedded with a Carbazole Subunit: Synthesis, Metal Coordination, and Magnetic and Anion Sensing Studies.

A new class of N-confused porphyrin 1 embedded with a carbazole subunit was prepared via [3 + 1] acid-catalyzed condensation of appropriate precursors. 1 underwent smooth metal complexation with Pd(II) and Cu(II) salts to provide the corresponding diamagnetic 1-Pd and paramagnetic 1-Cu, respectively. The single-crystal X-ray structure of 1-Pd is evident with a square-planar Pd-center through C-H activation of inverted pyrrole. Superconducting quantum interference device analysis combined with electron paramagnetic resonance (EPR) results provided insights into the paramagnetic nature of 1-Cu. Further, a ratiometric enhancement of near-IR fluorescence at 746 nm was found to be reversible upon adding CN- and F- ions. The solid-state structure of 1-Pd confirms that the anionic species is due to NH deprotonation.