Metalloporphyrinyl-Phosphonates with Serrated Chain Structures: Exfoliation and NIR Photothermal Effect

Near-infrared (NIR) photothermal materials have received significant attention due to their potential applications in photothermal therapy, diagnosis, and imaging. In this work, we constructed three mixed-ligand metal phosphonates, namely, Co(Ni-H6TPPP)(phen)(H2O)2 (CoNi), Ni(Ni-H6TPPP)(phen)(H2O)2 (NiNi), and Co(Co-H6TPPP)(phen)(H2O)2 (CoCo), where H10TPPP is 5,10,15,20-tetrakis(p-phenylphosphonic acid)-porphyrin and phen is 1,10-phenanthroline. These compounds are isostructural showing 1D serrated chain structures in which the porphyrin rings are stacked between the chains with pi-pi interactions. All displayed a broad absorption from the UV-vis to NIR (ca. 1500 nm) regions in the solid state. Interestingly, the chains in these compounds can be chemically exfoliated in water by adjusting the pH, forming interwoven nanostrands/nanosheets with thicknesses of one to several chains. The photothermal effect was observed for CoNi, NiNi, and CoCo in the solid state and in HEPES solution (pH = 7.4) upon 808 nm laser irradiation, among which CoCo showed the highest photothermal conversion efficiency. The important role of the cobalt(II) ion in the porphyrin ring and phenylphosphonic unit in extending pi-electron delocalization and enhancing the absorption in the NIR region in CoCo is revealed by theoretical calculations.

Automated summary

Three mixed-ligand metal phosphonates were constructed, and the chains in these compounds could be dispersed in water by adjusting the pH, forming interwoven nanostrands/nanosheets. The photothermal effect was observed for these compounds both in solid state and in HEPES solution upon 808 nm laser irradiation, and CoCo showed the highest photothermal conversion efficiency. Theoretical calculations revealed the important role of cobalt(II) ion in extending pi-electron delocalization and enhancing NIR absorption in CoCo.