Dual Photoreactive Ternary Ruthenium(II) Terpyridyl Complexes: A Comparative Study on Visible-Light-Induced Single-Step Dissociation of Bidentate Ligands and Generation of Singlet Oxygen

• Published in: Inorganic chemistry Vol. 63; no. 32; pp. 14998 - 15015
• Main Authors: Chatterjee, Pritha, Mishra, Ramranjan, Chawla, Sakshi, Sonkar, Avinash Kumar, De, Arijit K., Patra, Ashis K.
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 12-08-2024
• ISSN: 0020-1669; 1520-510X; 1520-510X
• DOI: 10.1021/acs.inorgchem.4c01727

The versatile and tunable ligand-exchange dynamics in ruthenium­(II)-polypyridyl complexes imposed by the modulation of the steric and electronic effects of the coordinated ligands provide an unlimited scope for developing phototherapeutic agents. The photorelease of a bidentate ligand from the Ru-center is better suited for potent Ru­(II)-based photocytotoxic agents with two available labile sites for cross-linking with biological targets augmented with possible phototriggered 1O2 generation. Herein, we introduced a phenyl-terpyridine (ptpy) ligand in the octahedral Ru­(II) core of [Ru­(ptpy)­(L–L)­Cl]+ to induce structural distortion for the possible photorelease of electronically distinct bidentate ligands (L–L). For a systematic study, we designed four Ru­(II) polypyridyl complexes: [Ru­(ptpy)­(L–L)­Cl]­(PF6), ([1]–[4]), where L–L = 1,2-bis­(phenylthio)­ethane (SPH) [1], N,N,N′,N′-tetramethylethylenediamine (TMEN) [2], N1,N2-diphenylethane-1,2-diimine (BPEDI) [3], and bis­[2-(diphenylphosphino)­phenyl]­ether (DPE-Phos) [4]. The detailed photochemical studies suggest a single-step dissociation of L–L from the bis-thioether (SPH) complex [1] and diamine (TMEN) complex [2], while no photosubstitution was observed for [3] and [4]. Complex [1] and [2] demonstrated a dual role, involving both photosubstitution and 1O2 generation, while [3] and [4] solely exhibited poor to moderate 1O2 production. The interplay of excited states leading to these behaviors was rationalized from the lifetimes of the 3MLCT excited states by using transient absorption spectroscopy, suggesting intricate relaxation dynamics and 1O2 generation upon excitation. Therefore, the photolabile complexes [1] and [2] could potentially act as dual photoreactive agents via the phototriggered release of L–L (PACT) and/or 1O2-mediated PDT mechanisms, while [4] primarily can be utilized as a PDT agent.