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New Tridentate Ligand Affords a Long-Lived 3MLCT Excited State in a Ru(II) Complex: DNA Photocleavage and 1O2 Production.
Lanquist, Austin P; Piechota, Eric J; Wickramasinghe, Lanka D; Marques Silva, Alexia; Thummel, Randolph P; Turro, Claudia.
Afiliação
  • Lanquist AP; Department of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio 43210, United States.
  • Piechota EJ; Department of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio 43210, United States.
  • Wickramasinghe LD; Department of Chemistry, University of Houston, Houston, Texas 77004, United States.
  • Marques Silva A; Department of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio 43210, United States.
  • Thummel RP; Department of Chemistry, University of Houston, Houston, Texas 77004, United States.
  • Turro C; Department of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio 43210, United States.
Inorg Chem ; 62(39): 15927-15935, 2023 Oct 02.
Article em En | MEDLINE | ID: mdl-37733276
ABSTRACT
Two new complexes, [Ru(tpy)(qdppz)](PF6)2 (1; qdppz = 2-(quinolin-8-yl)dipyrido[3,2-a2',3'-c]phenazine, tpy = 2,2'6',2″-terpyridine) and [Ru(qdppz)2](PF6)2 (2), were investigated for their potential use as phototherapeutic agents through their ability to photosensitize the production of singlet oxygen, 1O2, upon irradiation with visible light. The complexes exhibit strong Ru(dπ) → qdppz(π*) metal-to-ligand charge transfer (MLCT) absorption with maxima at 485 and 495 nm for 1 and 2 in acetone, respectively, red-shifted from the Ru(dπ) → tpy(π*) absorption at 470 nm observed for [Ru(tpy)2]2+ (3) in the same solvent. Complexes 1 and 3 are not luminescent at room temperature, but 3MLCT emission is observed for 2 with maximum at 690 nm (λexc = 480 nm) in acetone. The lifetimes of the 3MLCT states of 1 and 2 were measured using transient absorption spectroscopy to be ∼9 and 310 ns in methanol, respectively, at room temperature (λexc = 490 nm). The bite angle of the qdppz ligand is closer to octahedral geometry than that of tpy, resulting in the longer lifetime of 2 as compared to those of 1 and 3. Arrhenius treatment of the temperature dependence of the luminescence results in similar activation energies, Ea, from the 3MLCT to the 3LF (ligand-field) state for the two complexes, 2520 cm-1 in 1 and 2400 cm-1 in 2. However, the pre-exponential factors differ by approximately two orders of magnitude, 2.3 × 1013 s-1 for 1 and 1.4 × 1011 s-1 for 2, which, together with differences in the Huang-Rhys factors, lead to markedly different 3MLCT lifetimes. Although both 1 and 2 intercalate between the DNA bases, only 2 is able to photocleave DNA owing to its 1O2 production upon irradiation with ΦΔ = 0.69. The present work highlights the profound effect of the ligand bite angle on the electronic structure, providing guidelines for extending the lifetime of 3MLCT Ru(II) complexes with tridentate ligands, a desired property for a number of applications.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Revista: Inorg Chem Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Revista: Inorg Chem Ano de publicação: 2023 Tipo de documento: Article