Novel Lanthanide(III) Porphyrin-Based Metal–Organic Frameworks: Structure, Gas Adsorption, and Magnetic Properties

[Image: see text] The present work focuses on the hydrothermal synthesis and properties of porous coordination polymers of metal–porphyrin framework (MPF) type, namely, {[Pr(4)(H(2)TPPS)(3)]·11H(2)O}(n) (UPJS-10), {[Eu/Sm(H(2)TPPS)]·H(3)O(+)·16H(2)O}(n) (UPJS-11), and {[Ce(4)(H(2)TPPS)(3)]·11H(2)O}(n) (UPJS-12) (H(2)TPPS = 4,4′,4″,4‴-(porphyrin-5,10,15,20-tetrayl)tetrakisbenzenesulfonate(4-)). The compounds were characterized using several analytical techniques: infrared spectroscopy, thermogravimetric measurements, elemental analysis, gas adsorption measurements, and single-crystal structure analysis (SXRD). The results of SXRD revealed a three-dimensional open porous framework containing crossing cavities propagating along all crystallographic axes. Coordination of H(2)TPPS(4–) ligands with Ln(III) ions leads to the formation of 1D polymeric chains propagating along the c crystallographic axis. Argon sorption measurements at −186 °C show that the activated MPFs have apparent BET surface areas of 260 m(2) g(–1) (UPJS-10) and 230 m(2) g(–1) (UPJS-12). Carbon dioxide adsorption isotherms at 0 °C show adsorption capacities up to 1 bar of 9.8 wt % for UPJS-10 and 8.6 wt % for UPJS-12. At a temperature of 20 °C, the respective CO(2) adsorption capacities decreased to 6.95 and 5.99 wt %, respectively. The magnetic properties of UPJS-10 are characterized by the presence of a close-lying nonmagnetic ground singlet and excited doublet states in the electronic spectrum of Pr(III) ions. A much larger energy difference was suggested between the two lowest Kramers doublets of Ce(III) ions in UPJS-12. Finally, the analysis of X-band EPR spectra revealed the presence of radical spins, which were tentatively assigned to be originating from the porphyrin ligands.