Using a pyrazolate-bridged dinucleating ligand that provides two proximate pincer-type PNN binding sites ("two-in-one pincer"), different synthetic routes have been developed towards its dicobalt(I) complex 2 that features a twice deprotonated ligand backbone and two weakly activated terminal N substrate ligands directed into the bimetallic pocket. Protonation of 2 is shown to occur at the ligand scaffold and to trigger conversion to a tetracobalt(I) complex 4 with two end-on μ -bridging N ; in THF 4 is labile and undergoes temperature-dependent N /triflate ligand exchange. These pyrazolate-based systems combine the potential of exhibiting both metal-metal and metal-ligand cooperativity, viz. two concepts that have emerged as promising design motifs for molecular N fixation catalysts. Complex 2 serves as an efficient (pre)catalyst for the reductive silylation of N into N(SiMe ) (using KC and Me SiCl), yielding up to 240 equiv N(SiMe ) per catalyst.
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http://dx.doi.org/10.1002/anie.202101387 | DOI Listing |
Acc Chem Res
November 2023
Beijing National Laboratory for Molecular Sciences (BNLMS), Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry, Peking University, Beijing 100871, China.
ConspectusThe activation and functionalization of N to form nitrogen-element bonds have long posed challenges to industrial, biological, and synthetic chemists. The first transition-metal dinitrogen complex prepared by Allen and Senoff in 1965 provoked researchers to explore homogeneous N fixation. Despite intensive research in the last six decades, efficient and quantitative conversion of N to diazenido and hydrazido species remains problematic.
View Article and Find Full Text PDFDalton Trans
March 2023
Department of Chemistry, Fudan University, No. 2005, Songhu Road, Shanghai 200438, China.
Compared with Si-C(sp and sp) bonds bearing neighboring π-bond hyperconjugative interactions, the activation of robust Si-C(sp) bonds has proved to be a challenge. Herein, two distinct Si-C(sp) bond cleavages have been realized by rare-earth-mediated and nucleophilic addition of unsaturated substrates. The reactions of TpY[κ-(C,N)-CH(SiHPh)SiMeNSiMe](THF) (1) with CO or CS gave two endocyclic Si-C bond cleavage products, TpY[κ-(O,N)-OCCH(SiHPh)SiMeNSiMe](THF) (2) and TpY[κ-(S,N)-SSiMeNSiMe](THF) (3), respectively.
View Article and Find Full Text PDFInorg Chem
December 2022
Facultad de Ciencias, Departamento de Química Inorgánica, Instituto de Síntesis Química y Catálisis Homogénea, Universidad de Zaragoza, CSIC, Zaragoza 50009, Spain.
The catalytic system [Ir(CFCO)(κ-NSi)] [; NSi = (4-methylpyridin-2-yloxy)dimethylsilyl]/B(CF) promotes the selective reduction of CO with tertiary silanes to the corresponding bis(silyl)acetal. Stoichiometric and catalytic studies evidenced that species [Ir(CFCOO-B(CF))(κ-NSi)] (), [Ir(κ-NSi)][HB(CF)] (), and [Ir(HCOO-B(CF))(κ-NSi)] () are intermediates of the catalytic process. The structure of has been determined by X-ray diffraction methods.
View Article and Find Full Text PDFInorg Chem
June 2021
School of Chemical and Physical Sciences, Victoria University of Wellington, P.O. Box 600, Wellington 6012, New Zealand.
We report the synthesis of aromatic germanimines [(HMDS)Ge═NAr] (Ar = Ph, Mes, Dipp; Mes = 2,4,6-MeCH, Dipp = 2,6-PrCH) and an investigation into their associated reactivity. [(HMDS)Ge═NPh] decomposes above -30 °C, while [(HMDS)Ge═NDipp] engages in an intramolecular reaction at 60 °C. [(HMDS)Ge═NMes] was shown to rearrange via a 1,3-silyl migration to give [(HMDS){(SiMe)(Mes)N}Ge(NSiMe)] in a 1:7 equilibrium mixture at room temperature.
View Article and Find Full Text PDFChemistry
June 2020
Department of Chemistry, Shanghai Key Laboratory of, Molecular Catalysis and Innovative Materials, Fudan University, Shanghai, 200433, P. R. China.
A new method for the modification of a silylamino ligand has been developed through mono and dual C(sp )-H/Si-H cross-dehydrocoupling with silanes. The reaction of [LY{η -(C,N)-CH Si(Me )NSiMe }] (L=bis(2,6-diisopropylphenyl)-β-diketiminato, L' (1 '); L=tris(3,5-dimethylpyrazolyl)borate, Tp (1 )) with 2 equivalents of PhSiH in toluene gave the complexes [LY{η -(C,N)-C(SiH Ph) Si(Me )NSiMe }] (L=L' (2 ); L=Tp (2 )). Moreover, 1 reacted with the secondary silanes Ph SiH and Et SiH to afford the corresponding mono C-H activation products [Tp Y{η -(C,N)-CH(SiHR )Si(Me )NSiMe }] (R=Ph (4 b); R=Et (4 c)).
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