resumo
A series of nickel(II) complexes, namely, [Ni-II(La-c)(2)Cl-2] (1a-c ), [Ni-II(L-a,L-b)(3)](x)(2) {([2a](X)(2), [2b](X)(2)) (X = ClO4, I-3)}, [Ni-II(L-c(OH2)(2)]-(C1O(4))(2) ([3](ClO4)(2)) and [Ni-II{(L-a'b)(-)}(2)] (4a, 4b) featuring the redox-active tridentate azo-aromatic pincer ligand 2-(arylazo)-1,10-phenanthroline (L) were synthesized. The coordinated azo-aromatic ligand showed reversible hemilability depending on its formal oxidation state. On the one hand, in its native state, the unreduced ligand L shows bidentate coordination; the 1,10-phenanthroline moiety binds the central Ni(II) atom in a bidentate fashion, while the azo-chromophore remains pendent. On the other hand, the one-electron reduced ligand [L]('-) binds the nickel(II) atom in a tridentate fashion. In complexes 1, [2](2+), and [3](2+), the 1,10-phenanthroline moiety of the neutral unreduced azo-aromatic ligand L binds the central nickel(II) atom in a bidentate fashion, while the azo-chromophore remains pendent. The complex 4 is a singlet diradical species, where two monoanionic azo-anion radical ligands [L](.-) are bound to the central nickel(II) center in a tridentate fashion. Redox-induced reversible hemilability of the coordinated azo-aromatic ligand L was revealed from the interconversion of the synthesized complexes upon reduction and oxidation. Complex 1 upon reduction transformed to complex 4 with the loss of two chlorido ligands, whereas the complex 4 upon oxidation in the presence of excess chloride (LiCI) source transformed back to 1. Similarly, the complexes [2](2+) and 4 were also found to be interconvertible upon reduction and oxidation, respectively. Thorough experimental and density functional theory studies were performed to unveil the electronic structures of the synthesized complexes, and attempt was made to understand the redox-induced hemilability of the coordinated azo-aromatic ligand L.
palavras-chave
ELECTRON-TRANSFER SERIES; CATALYTIC ALCOHOL OXIDATION; TRANSITION-METAL-COMPLEXES; ACTIVE TRIS(AMIDO) LIGAND; ANION-RADICAL COMPLEXES; PLANAR NICKEL-COMPLEXES; SET MODEL CHEMISTRY; STRUCTURAL-CHARACTERIZATION; COORDINATION CHEMISTRY; PALLADIUM(II) COMPLEX
categoria
Chemistry
autores
Das, S; Sinha, S; Jash, U; Sikari, R; Saha, A; Barman, SK; Brandao, P; Paul, ND
nossos autores
Paula Cristina Ferreira da Silva Brandão
Investigador Auxiliaragradecimentos
The research was supported by DST (Project No. YSS/2015/001552). S.D. is thankful to UGC, S.S. is thankful to IIESTS, U.J. is thankful to DST-Inspire, and R.S. is thankful to UGC-RGNF for providing fellowship. We thank IIEST, Shibpur, for financial assistance. SAIF, IIESTS is duly acknowledged for providing single-crystal X-ray facility. P.B. thanks CICECO-Aveiro Institute of Materials, POCI-01-0145-FEDER-007679 (FCT Ref No. UID/CTM/50011/2013), financed by national funds through the FCT/MEC and when appropriate cofinanced by FEDER under the PT2020 Partnership Agreement. This paper is dedicated to Professor R. N. Mukherjee of Department of Chemistry, Indian Institute of Technology, Kanpur, on the occasion of his 65th birth anniversary.