DFT study of dihydrogen addition to molybdenum π-heteroaromatic complexes: a prerequisite step for the catalytic hydrodenitrogenation process. (15th September 2015)

• Record Type: Journal Article
• Authors: Fetisov, Evgenii O.; Gloriozov, Igor P.; Kissounko, Denis A.; Nechaev, Mikhail S.; Kahlal, Samia; Saillard, Jean-Yves; Oprunenko, Yuri F.
• Is Part Of: New journal of chemistry. Volume 39:Number 11(2015:Nov.)
• Page Start: 8915
• Page End: 8921
• Publication Date: 2015-09-15
• Subjects: Chemistry -- Periodicals; Chimie -- Périodiques; 540
• DOI: 10.1039/c5nj01585e
• Languages: English
• ISSNs: 1144-0546

Abstract

Abstract : The mechanism proceeds via consecutive steps of oxidative H2 addition, hydrogen metal-to-ligand transfer, accompanied by a change of metal–ligand hapticity. Abstract : The range of molybdenum hydride complexes that are sought to participate in the important catalytic hydrodenitrogenation process (HDN) of nitrogen containing polycyclic aromatic hydrocarbons were evaluated by DFT studies. The previously synthesized stable (η 6 -quinoline)Mo(PMe3 )3 complex1N, in which molybdenum is bonded to the heterocyclic ring, was chosen as a model. The hydrogenation of the quinone heterocycle, which was postulated as the initial step in the overall HDN reaction, is found to occur via three consecutive steps of the oxidative addition of dihydrogen to Mo in1N . Successive transfer of hydrogen atoms from the metal to the heterocycle leads to the ultimate formation of the tetrahydrido molybdenum intermediate Mo(PMe3 )4 H4 13 and 2, 2, 3, 3-tetrahydroquinoline C9 H11 N14 . All the involved intermediates and transition states have been fully characterized by DFT. This computational modeling of the hydrogenation of quinoline, as a part of extended HDN catalytic processes, provides a fundamental understanding of such mechanisms.