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• W4237110530 endingPage "5229" @default.
• W4237110530 startingPage "5215" @default.
• W4237110530 abstract "Presented herein are synthetic, structural, and reactivity studies delineating the characteristics of the niobaziridine hydride functional group as it pertains to the stabilization of trisanilide niobium complexes of the type Nb(N[R]Ar)3 (1R, Ar = 3,5-Me2C6H3). Utilization of the N-isopropyl anilide ligand, N[i-Pr]Ar, results in the niobaziridine hydride dimer [Nb(H)(η2-Me2C═NAr)(N[i-Pr]Ar)2]2 ([2i-Pr-H]2). Dimer [2i-Pr-H]2 is thermally unstable at room temperature and decomposes via ortho-metalation and i-Pr radical ejection to a species containing a Nb−Nb bond. The ligand variant N[Np]Ar (Np = neopentyl) provides the room-temperature-stable niobaziridine hydride monomer Nb(H)(η2-t-Bu(H)C═NAr)(N[Np]Ar)2 (2Np-H). Thermal decomposition of 2Np-H at elevated temperature (75 °C) provides the neopentyl imido complex Nb(NNp)(Ar)(N[Np]Ar)2 (5Np). H/D isotopic labeling studies provide evidence for reversible β-H elimination interconverting 2Np-H and its trisanilide tautomer [Nb(N[Np]Ar)3] (1Np), with the latter thereby implicated as an intermediate during the 2Np-H → 5Np conversion. Reactivity studies between 2Np-H and certain small-molecule substrates confirm that the niobaziridine hydride group can effectively mask a reactive d2 Nb(III) trisanilide center. However, 2Np-H exhibits insertion chemistry when treated with a variety of unsaturated organic substrates, thus demonstrating a pronounced tendency to additionally function as a Lewis acidic, early transition metal hydride species. A general mechanism accounting for the divergent reactivity of 2Np-H is proposed. Niobaziridine hydride complexes derived from the amido ligands N[CH2Ad]Ar, N[Cy]Ar, and NCy2 (Ad = 1-adamantyl, Cy = cyclohexyl) are also presented, and their thermal behavior and reaction chemistry are compared with those of 2Np-H. In addition, the radical anion of 2Np-H is reported and compared with the neutral d1 molybdaziridine hydride complex Mo(H)(η2-Me2C═NAr)(N[i-Pr]Ar)2 (3i-Pr-H), to which it is isoelectronic." @default.
• W4237110530 created "2022-05-12" @default.
• W4237110530 creator A5022058969 @default.
• W4237110530 creator A5024174359 @default.
• W4237110530 creator A5035397949 @default.
• W4237110530 creator A5040222176 @default.
• W4237110530 creator A5080206718 @default.
• W4237110530 date "2010-10-15" @default.
• W4237110530 modified "2023-10-01" @default.
• W4237110530 title "Niobaziridine Hydrides" @default.
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