Catalytic activity of a new dioxidomolybdenum() complex with a bipodal NO-donor ligand in sulfur compound oxidation
A new dinuclear dioxidomolybdenum( vi ) complex [(MoO 2 ) 2 (BPA) 2 (μ-O)] was synthesized by the reaction between the tridentate N 2 O-donor ligand N -(2-hydroxybenzyl)- N -(pyridin-2-ylmethyl)amine (HBPA) and molybdenum trioxide (MoO 3 ). This complex was analyzed by FT-IR, UV-visible, ESI-MS, ele...
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Published in | New journal of chemistry Vol. 47; no. 3; pp. 14123 - 14133 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Published |
31.07.2023
|
Online Access | Get full text |
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Summary: | A new dinuclear dioxidomolybdenum(
vi
) complex [(MoO
2
)
2
(BPA)
2
(μ-O)] was synthesized by the reaction between the tridentate N
2
O-donor ligand
N
-(2-hydroxybenzyl)-
N
-(pyridin-2-ylmethyl)amine (HBPA) and molybdenum trioxide (MoO
3
). This complex was analyzed by FT-IR, UV-visible, ESI-MS, elemental (CHN), thermogravimetric and electrochemical analyses. The crystal structure was solved by single crystal X-ray diffraction, which shows two non-equivalent molybdenum(
vi
) ions bridge-coordinated by an oxido ligand. The complex was studied using DFT calculations, resulting in a molecular structure with a geometry similar to the one obtained by X-ray diffraction. The dinuclear dioxidomolybdenum(
vi
) complex [(MoO
2
)
2
(BPA)
2
(μ-O)] was evaluated as a catalyst in the reaction involving the oxidation of sulfur compounds, at 25 and 50 °C, using hydrogen peroxide as an oxidant and acetonitrile as a solvent. The catalyst is able to oxidize thioanisole, diphenyl sulfide and dibenzothiophene producing sulfoxide and sulfone with conversions of 94%, 76% and 27%, respectively.
A new dinuclear dioxidomolybdenum(
vi
) complex [(MoO
2
)
2
(BPA)
2
(μ-O)] was synthesized and evaluated as a catalyst in the reaction involving the oxidation of sulfur compounds. |
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Bibliography: | For ESI and crystallographic data in CIF or other electronic format see DOI 2217613 Electronic supplementary information (ESI) available: Tables TS1-TS6 and Fig. S1-S6. CCDC https://doi.org/10.1039/d2nj06227e |
ISSN: | 1144-0546 1369-9261 |
DOI: | 10.1039/d2nj06227e |