Bidirectional noninnocence of hinge-like deprotonated bis-lawsone on selective ruthenium platform: a function of varying ancillary ligands. Issue 27 (28th June 2022)

• Record Type: Journal Article
• Authors: Arya, Yogita; Bera, Sudip Kumar; Priego, José Luis; Jiménez-Aparicio, Reyes; Lahiri, Goutam Kumar
• Is Part Of: Dalton transactions. Volume 51:Issue 27(2022)
• Page Start: 10441
• Page End: 10456
• Publication Date: 2022-06-28
• Subjects: Chemistry, Inorganic -- Periodicals; Chemistry, Physical and theoretical -- Periodicals; Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/d2dt01466a
• Languages: English
• ISSNs: 1477-9226

Abstract

Abstract : Deprotonated bis-lawsone-based discreate ruthenium complexes beyond 3d metal/Ga-derived systems and their bidirectional (fractional) noninnocence have been highlighted. Abstract : The present work aimed to obtain discrete heavier metal complexes of unperturbed deprotonated bis-lawsone (hinge-like H2 L = 2, 2′-bis(3-hydroxy-1, 4-napthoquinone). This is primarily due to its limited examples with lighter metal ions (Co, Zn, and Ga) and the fact that our earlier approach with the osmium ion facilitated its functionalisation. Herein, we demonstrated the successful synthesis and structural characterisation of L 2− -derived diruthenium [(bpy)2 Ru II (μ-L 2− )Ru II (bpy)2 ](ClO4 )2 [1 ](ClO4 )2 ( S = 0), (acac)2 Ru III (μ-L 2− )Ru III (acac)2 2 ( S = 1) and monoruthenium (pap)2 Ru(L 2− ) 3 ( S = 0) derivatives (bpy = 2, 2′-bipyridine, acac = acetylacetonate, and pap = 2-phenylazopyridine). The crystal structures established that (i) O, O − /O, O − donating five-membered bis-bidentate and O −, O − donating seven-membered bidentate chelating modes of deprotonated L 2− in rac (ΔΔ/ΛΛ) diastereomeric [1 ](ClO4 )2, 2 and 3, respectively. (ii) The L 2− bridging unit in [1 ](ClO4 )2, 2 and 3 underwent twisting its two naphthoquinone rings with respect to the ring connecting C–C bond by 73.01°, 62.15° and 59.12°, respectively. (iii) Intermolecular π–π interactions (∼3.5 Å) between the neighbouring molecules. The paramagnetic complex 2 ( S = 1) with two non-interacting Ru(iii ) ( S = 1/2) ions exhibited weak antiferromagnetic coupling only at very low temperatures. In agreement with the magnetic results, 2 displayed typical Ru III -based anisotropic EPR in CH3 CN (< g >/Δ g : 2.314/0.564) but without any forbidden g 1/2 signal at 120 K. The complexes exhibited multiple redox processes in CH3 CN in the experimental potential window of ± 2.0 V versus SCE. The analysis of the redox steps via a combined experimental and theoretical (DFT/TD-DFT) approach revealed the involvement of L 2− to varying extents in both the oxidative and reductive processes as a consequence of its bidirectional redox non-innocent feature. The mixing of the frontier orbitals of the metal ion and L 2− due to their closeness in energy indeed led to the resonating electronic form in certain redox states instead of any precise electronic structural state.