The Milstein Bipyridyl PNN Pincer Complex of Ruthenium Becomes a Noyori-Type Catalyst under Reducing Conditions

被引:32
作者
Dawe, Louise N. [1 ]
Karimzadeh-Younjali, Morteza [1 ]
Dai, Zengjin [1 ]
Khaskin, Eugene [2 ]
Gusev, Dmitry G. [1 ]
机构
[1] Wilfrid Laurier Univ, Dept Chem & Biochem, Waterloo, ON N2L 3C5, Canada
[2] Okinawa Inst Sci & Technol, Onna, Okinawa 9040495, Japan
基金
加拿大自然科学与工程研究理事会;
关键词
METAL-LIGAND COOPERATION; SECONDARY ALCOHOLS; BOND ACTIVATION; AROMATIZATION-DEAROMATIZATION; DEHYDROGENATIVE BORYLATIONS; EFFICIENT HYDROGENATION; ALKENE HYDROBORATION; ESTER HYDROGENATION; BASIS-SETS; MECHANISM;
D O I
10.1021/jacs.0c06518
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hydrogenation of the dearomatized PNN ligand of the Milstein bipyridyl complex RuH(CO)[PNN] (2) gives a square-pyramidal Ru(II) product RuH(CO)[pPNN] (5). The central ring of the pPNN ligand is a piperidine. A minor byproduct of the hydrogenation reaction is complex 6 which has a dimeric structure made of two Ru(II) fragments each possessing a partly hydrogenated PNN ligand. The structures of 5 and 6 have been elucidated by NMR spectroscopy and X-ray crystallography. The PNN ligand of 2 is also hydrogenated under the conditions of the catalytic dehydrogenative coupling of ethanol to ethyl acetate. No direct evidence of the aromatized dihydride RuH2(CO)[PNN] (4) was found in this study. However, treating RuHCl(CO)[PNN] with Li[HBEt3] or reacting 2 with H-2 at low temperature resulted in a structurally characterized hydride-bridged dimer (7) bearing intact aromatized bipyridyl ligands. M06-L/def2-QZVP DFT calculations provided insights into the thermodynamics of the stoichiometric reactions of this work and into the nature of the intermediates of the catalytic ester hydrogenation facilitated by RuH2(CO)[pPN(H)N] (8) formed from 5 under H-2.
引用
收藏
页码:19510 / 19522
页数:13
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