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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Roy, Ram Kinkar | - |
dc.date.accessioned | 2021-10-12T11:32:13Z | - |
dc.date.available | 2021-10-12T11:32:13Z | - |
dc.date.issued | 2016 | - |
dc.identifier.uri | https://pubs.acs.org/doi/10.1021/acs.inorgchem.5b01257 | - |
dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2721 | - |
dc.description.abstract | Ligand H3SamiMixed(tBu) was composed of two different compartments, a redox-active 2-aminophenol and a salen salicylidene. Both compartments were linked via a benzyl linker. The ligand reacted with CuCl2·2H2O under air in the presence of Et3N and provided the corresponding monoradical-coordinated mononuclear Cu(II) complex (1). Complex 1, in solution, reacted with air and provided complex 2 via ligand-centered oxygenation at the benzyl-CH2 position. Both complexes were characterized via IR, mass spectrometry, X-ray single-crystal diffraction, variable-temperature magnetic susceptibility, cyclic voltammograms (CVs), and UV–vis/NIR spectroscopic techniques. X-ray crystallographic analyses clearly showed almost equally distorted square planar geometry around the Cu(II) atom in both complexes. However, the bending of the radical-containing C6 ring compared to the N1–Cu1–O1 plane was different in both complexes. While complex 1 was paramagnetic and showed a ferromagnetic coupling between the dx2–y2 magnetic orbital of Cu(II) ion and the pz orbital of coordinated π-radical, complex 2 was diamagnetic by experiencing a strong antiferromagnetic coupling between the two magnetic orbitals. UV–vis/NIR spectra of the complexes were dominated by charge-transfer transitions. CVs of the complexes showed two reversible one-electron oxidations and one reversible one-electron reduction. E1/2ox2 and E1/2red1 potentials were different in both complexes, while E1/2ox1 values were almost the same and the process corresponded to the formation of phenoxyl radical. Theoretical studies were also performed to understand the magnetic coupling phenomena, and TD-DFT calculations were employed for the assignment of charge-transfer absorption bands. | en_US |
dc.language.iso | en | en_US |
dc.publisher | ACS | en_US |
dc.subject | Chemistry | en_US |
dc.subject | Charge transfer | en_US |
dc.subject | Ligands | en_US |
dc.subject | Oxidation | en_US |
dc.subject | Quantum mechanics | en_US |
dc.subject | Mathematical methods | en_US |
dc.title | Effect of Geometrical Distortion on the Electronic Structure: Synthesis and Characterization of Monoradical-Coordinated Mononuclear Cu(II) Complexes | en_US |
dc.type | Article | en_US |
Appears in Collections: | Department of Chemistry |
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