Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/8838
Title: Arene-ruthenium(II)-phosphine complexes: Green catalysts for hydration of nitriles under mild conditions
Authors: Vyas, Komal M.
Singh, Rinky
Mobin, Shaikh M.
Mukhopadhyay, Suman
Issue Date: 2020
Publisher: Elsevier B.V.
Citation: Vyas, K. M., Mandal, P., Singh, R., Mobin, S. M., & Mukhopadhyay, S. (2020). Arene-ruthenium(II)-phosphine complexes: Green catalysts for hydration of nitriles under mild conditions. Inorganic Chemistry Communications, 112 doi:10.1016/j.inoche.2019.107698
Abstract: Three new arene-ruthenium(II) complexes were prepared by treating [{RuCl(µ-Cl)(η6-arene)}2] (η6-arene = p-cymene) dimer with tri(2-furyl)phosphine (PFu3) and 1,3,5-triaza-7-phosphaadamantane (PTA), respectively to obtain [RuCl2(η6-arene)PFu3] [Ru]-1, [RuCl(η6-arene)(PFu3)(PTA)]BF4 [Ru]-2 and [RuCl(η6-arene)(PFu3)2]BF4 [Ru]-3. All the complexes were structurally identified using analytical and spectroscopic methods including single-crystal X-ray studies. The effectiveness of resulting complexes as potential homogeneous catalysts for selective hydration of different nitriles into corresponding amides in aqueous medium and air atmosphere was explored. There was a remarkable difference in catalytic activity of the catalysts depending on the nature and number of phosphorus-donor ligands and sites available for catalysis. Experimental studies performed using structural analogues of efficient catalyst concluded a structural-activity relationship for the higher catalytic activity of [Ru]-1, being able to convert huge variety of aromatic, heteroaromatic and aliphatic nitriles. The use of eco-friendly water as a solvent, open atmosphere and avoidance of any organic solvent during the catalytic reactions prove the reported process to be truly green and sustainable. © 2019 Elsevier B.V.
URI: https://doi.org/10.1016/j.inoche.2019.107698
https://dspace.iiti.ac.in/handle/123456789/8838
ISSN: 1387-7003
Type of Material: Journal Article
Appears in Collections:Department of Chemistry

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