Half-sandwich cycloruthenated complexes from aryloxazolines: synthesis, structures, and catalytic activities
Wei-Guo Jia1, Tai Zhang, Dong Xie
1College of Chemistry and Materials Science, Center for Nano Science and Technology, The Key Laboratory of Functional Molecular Solids, Ministry of Education, Anhui Laboratory of Molecular-Based Materials, Anhui Normal University, Wuhu, 241000, China. wgjiasy@mail.ahnu.edu.cn.
Abstract:
Seven half-sandwich cycloruthenated complexes [Ru(p-cymene)LCl] (2a-2g) (L = 2-phenyl-2-oxazoline (2a), 2-p-tolyl-4,5-dihydrooxazole (2b), 4,4-dimethyl-2-phenyl-2-oxazoline (2c), 2-(4-chlorophenyl)-4,5-dihydrooxazole (2d), 2-(4-bromophenyl)-4,5-dihydrooxazole (2e), 2-(4-fluorophenyl)-4,5-dihydrooxazole (2f) and 2-(4-nitrophenyl)-4,5-dihydrooxazole (2g)) were synthesized and characterized. All half-sandwich cycloruthenated complexes were fully characterized by (1)H and (13)C NMR spectra, elemental analyses and infrared spectroscopy. The molecular structures of 2a, 2d and 2e were confirmed by single-crystal X-ray diffraction methods. These half-sandwich cycloruthenated complexes were employed in nitroarene reduction using sodium borohydride (NaBH4) as a reducing agent in ethanol at room temperature. The catalytic results indicate that half-sandwich cycloruthenated complexes show promising catalytic activity in nitroarene reduction with a broad substrate and varied functional group compatibility.
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