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◆ Journal of the American Chemical Society2026-01-02· Chemistry

Diverse N <sub>2</sub> Functionalization Enabled by an Unsymmetric Dititanium Complex

Yi-Fei Huang, Yun‐Shu Cui, Si‐Jun Xie, Ye Lü, Feng Liu, Dan-Dan Zhai, Zhang‐Jie Shi

原始摘要(英文原文)· Original abstract
Di- and multinuclear metal cooperation plays a pivotal role in small-molecule activation and functionalization. Herein, we report a symmetric phenoxide-bridged ligand that supports an unsymmetric dititanium dinitrogen complex featuring side-on/end-on N 2 coordination. This complex possessed a strongly nucleophilic (N 2 ) 4– moiety that readily underwent diverse derivatizations to construct N–C, N–Si, and N–P bonds. Particularly noteworthy are the complex’s reactivities with α,ω-dihaloalkanes, which selectively generate structurally distinct N -heterocyclic compounds, showing the potential in constructing diverse N -contained heterocycles directly from N 2 .
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Diverse N <sub>2</sub> Functionalization Enabled by an Unsymmetric Dititanium Complex — 科研速览 Science Skim