A novel samarium(ii) complex bearing a dianionic bis(phenolate) cyclam ligand: synthesis, structure and electron-transfer reactions. Issue 9 (28th January 2016)

• Record Type: Journal Article
• Authors: Maria, Leonor; Soares, Marina; Santos, Isabel C.; Sousa, Vânia R.; Mora, Elsa; Marçalo, Joaquim; Luzyanin, Konstantin V.
• Is Part Of: Dalton transactions. Volume 45:Issue 9(2016)
• Page Start: 3778
• Page End: 3790
• Publication Date: 2016-01-28
• Subjects: Chemistry, Inorganic -- Periodicals; Chemistry, Physical and theoretical -- Periodicals; Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/c5dt04647e
• Languages: English
• ISSNs: 1477-9226

Abstract

Abstract : A novel divalent samarium complex anchored on a dianionic bis(phenolate) ligand is reported and reactivity studies demonstrate that it is highly effective in inducing single-electron transfer processes. Abstract : The reaction of the hexadentate dianionic 1, 4, 8, 11-tetraazacyclotetradecane-based bis(phenolate) ligand, ( t Bu2 ArO)2 Me2 -cyclam 2−, with [SmI2 (thf)2 ] in thf resulted in the formation of the divalent samarium complex [Sm(κ 6 -{( t Bu2 ArO)2 Me2 -cyclam})] (1 ). X-ray diffraction studies revealed that after recrystallization from n -hexane/thf complex1 has a monomeric structure and does not contain thf molecules coordinated to the Sm(ii ) center. However, UV-vis and 1 H NMR spectroscopy of1 evidenced the formation of thf-solvated complexes in neat thf. Reductive studies show that complex1 can act as a single electron-transfer reagent and form well-defined Sm(iii ) species. The reaction of1 with several substrates, namely, TlBPh4, pyridine N -oxide, OPPh3, SPPh3 and bipyridines, are reported. Spectroscopy studies, including NMR, and single crystal X-ray diffraction data are in agreement with the formation of cationic Sm(iii ) species, monochalcogenide bridged Sm(iii ) complexes and Sm(iii ) complexes with bipyridine radical ligand, respectively.