Amine Boranes Dehydrogenation Mediated by an Unsymmetrical Iridium Pincer Hydride: (PCN) vs (PCP) Improved Catalytic Performance

The IrIII hydride (tBuPCN)IrHCl (1) containing the tridendate unsymmetrical pincer ligand tBuPCN- {tBuPCN(H) = 1-[3-[(di-tert-butylphosphino)methyl]phenyl]-1H-pyrazole} has been exploited as ammonia borane (NH3BH3, AB) and amine boranes dehydrogenation catalyst in THF solution at ambient temperature. 1 releases one H2 equivalent per AB equivalent, with concomitant cyclic poly(aminoboranes) formation [B-(cyclotriborazanyl)-amine-borane (BCTB) and cyclotriborazane (CTB)] as the final "spent fuel". 1 has been found to have superior catalytic activity than its symmetrical analogue (tBuPCP)IrHCl, with recorded TOF values of 580 h-1 (AB in THF) and 401 h-1 (DMAB in toluene) at ambient temperature. The reaction has been analyzed experimentally through multinuclear [11B, 31P{1H}, 1H] NMR and IR spectroscopy, kinetic rate measurements, and kinetic isotope effect determination with deuterated AB isotopologues. The hydride/borohydride intermediate (tBuPCN)IrH(η2-BH4) (2) is the catalyst resting state formed during the dehydrogenation process; it is detected by a variableerature multinuclear NMR of the reaction course (in the 190-323 K range). A DFT modeling of the reaction mechanism using DMAB as substrate has been performed with the geometry optimization in toluene at the M06 level of theory. The combination of the kinetic and computational data reveals that a simultaneous B-H/N-H activation occurs in the presence of 1, after the preliminary amine borane coordination to the metal center. © 2018 American Chemical Society.

Авторы
Luconi L.1 , Osipova E.S.2 , Giambastiani G.1, 3, 4 , Peruzzini M.1 , Rossin A.1 , Belkova N.V.2 , Filippov O.A.2 , Titova E.M. 2, 5 , Pavlov A.A.2 , Shubina E.S.2
Журнал
Издательство
American Chemical Society
Номер выпуска
18
Язык
Английский
Страницы
3142-3153
Статус
Опубликовано
Том
37
Год
2018
Организации
  • 1 Istituto di Chimica Dei Composti Organometallici - Consiglio Nazionale Delle Ricerche (ICCOM - CNR), Via Madonna del Piano 10, Sesto Fiorentino, 50019, Italy
  • 2 A.N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences (INEOS RAS), Vavilova Str. 28, Moscow, 119991, Russian Federation
  • 3 Institute of Chemistry and Processes for Energy Environment and Health (ICPEES), UMR 7515 CNRS, University of Strasbourg (UdS), 25, rue Becquerel, Cedex 02, Strasbourg, 67087, France
  • 4 Kazan Federal University, Kremlyovskaya Str. 18, Kazan, 420008, Russian Federation
  • 5 Peoples' Friendship University of Russia (RUDN University), 6 Miklukho-Maklay St, Moscow, 117198, Russian Federation
Ключевые слова
Ammonia; Boron compounds; Computation theory; Dehydrogenation; Hydrides; Iridium compounds; Kinetics; Reaction intermediates; Steel beams and girders; Temperature; Toluene; Catalyst resting state; Catalytic performance; Computational data; Dehydrogenation catalysts; Geometry optimization; Kinetic isotope effects; Reaction mechanism; Variable temperature; Catalyst activity
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/6413/