Mono- and bis-Pd(ii) complexes of N-confused dithiahexaphyrin(1.1.1.1.1.0) with the absorption and aromaticity modulated by Pd(ii) coordination, macrocycle contraction and ancillary ligands.

To further enrich the coordination chemistry of hexaphyrins and probe the underlying property-structural correlations, N-confused dithiahexaphyrin(1.1.1.1.1.0) (1) with 26 π-electron Hückel aromaticity was synthesized. Based on its unprecedented two unsymmetrical cavities, five palladium complexes 2, 3, 4-Ph, 4-Cl and 5 have been successfully synthesized under various coordinations. Thus, two mono-Pd(ii) complexes 2 and 3 with the Pd(ii) atom coordinated in the two different cavities were obtained by treating 1 with palladium reagents PdCl, and (PPh)PdCl respectively. On this basis, bis-Pd(ii) complexes 4-Ph and 4-Cl were synthesized by treating 2 and 3 with (PPh)PdCl and PdCl, respectively. As a result, both 4-Ph and 4-Cl contain two Pd(ii) atoms coordinated within the two cavities, with one of the Pd(ii) atoms further coordinated to a triphenylphosphine ligand in addition to an anionic ancillary ligand of Ph and Cl, respectively. Notably, a further contracted mono-Pd(ii) complex 5 was synthesized by treating 1 with Pd(PPh) by eliminating one of the -carbon atoms together with the corresponding CF moiety. These complexes present tunable 26 π aromaticity and NIR absorption up to 1060 nm. This work provides an effective approach for developing distinctive porphyrinoid Pd(ii) complexes from a single porphyrinoid, without resorting to tedious syntheses of a series of porphyrinoid ligands.