Metal Complexes of 5,15‐Porphyrinquinones: Systematic Study of Crystal Structure, Electronic Structure, and Lewis Acidity

• Published in: European journal of inorganic chemistry Vol. 2020; no. 36; pp. 3507 - 3516
• Main Authors: Yamashita, Ken‐ichi, Hirano, Daisuke, Sugiura, Ken‐ichi
• Format: Journal Article
• Language: English
• Published: WEINHEIM Wiley 30.09.2020; Wiley Subscription Services, Inc
• Subjects: Absorption spectra; Chemistry; Chemistry, Inorganic & Nuclear; Coordination compounds; Coupling (molecular); Crystal structure; Electronic structure; Inorganic chemistry; Lewis acids; Metal ions; Metal‐metal interactions; Molecular orbitals; Physical Sciences; Porphyrinoids; Porphyrins; Quinones; Science & Technology; Transition metals; Ultraviolet spectra; Transition metals; COPPER(II); PORPHYRINS; Lewis acids; NICKEL(II) COMPLEXES; COORDINATION; DIOXOPORPHYRINS; Metal-metal interactions; Porphyrinoids; Quinones; NMR; MESO-OXIDATION; PARAMAGNETIC-SUSCEPTIBILITY; EVANS METHOD
• ISSN: 1434-1948; 1099-0682
• DOI: 10.1002/ejic.202000527

We conducted the first systematic study on the synthesis, structure, and properties of various divalent metal complexes (NiII, CuII, ZnII, PdII, PtII, and PbII) of 5,15‐porphyrinquinone (PQ, a quinone compound of porphyrin) for diversifying the chemistry of traditional quinone‐metal complexes. Similar to electron‐accepting nature of PQ, the metal complexes studied here also exhibit it. NiII, PdII, and PtII complexes favor face‐to‐face stacked structures in the crystals, thus inducing effective PtII–PtII interaction, which has not been observed in the porphyrin analogues to date. Ultraviolet‐visible (UV/Vis) absorption spectra of the metal complexes vary widely depending on the metal ion and owing to the effective d(metal)–π(PQ) coupling in their molecular orbitals. Quantitative analyses of the axial ligation on the central metal ions (NiII and CuII) revealed significantly larger binding constants than those of the porphyrin analogues, indicating significant enhancement of their Lewis acidities due to the strong electron‐withdrawing nature of PQ. Aimed at the expansion of the chemistry of quinone‐metal complexes, the systematic study of divalent metal complexes of 5,15‐porphyrinquinone revealed their strong electron‐accepting nature and metal–metal interaction (for Pt), effective d(metal)–π(ligand) coupling in their molecular orbital, and their great enhancement of the Lewis acidity of the central metals.