Litcius/Paper detail

One-Electron (2c/1e) Tin···Tin Bond Stabilized by <i>ortho</i>-Phenylenediamido Ligands

Kaiyip Chan, Fei Ying, Dongyu He, Li Yang, Yanxia Zhao, Jing Xie, Ji‐Hu Su, Biao Wu, Xiao‐Juan Yang

2024Journal of the American Chemical Society14 citationsDOI

Abstract

Odd-electron bonds, i.e., the two-center, three-electron (2c/3e), or one-electron (2c/1e) bonds, have attracted tremendous interest owing to their novel bonding nature and radical properties. Herein, complex [K(THF) 6 ][LSn:···Sn:L] ( 1 ), featuring the first and unsupported 2c/1e Sn···Sn σ-bond with a long distance (3.2155(9) Å), was synthesized by reduction of stannylene [LSn:] (L = N, N -dpp- o -phenylene diamide) with KC 8 . The one-electron Sn–Sn bond in 1 was confirmed by the crystal structure, DFT calculations, EPR spectroscopy, and reactivity studies. This compound can be viewed as a stabilized radical by delocalizing to two metal centers and can readily mediate radical reactions such as C–C coupling of benzaldehyde.

Topics & Concepts

ChemistryTinReactivity (psychology)Electron paramagnetic resonanceElectron deficiencyBenzaldehydeCrystallographyMetalMedicinal chemistryPhotochemistryCatalysisOrganic chemistryNuclear magnetic resonanceAlternative medicineMedicinePathologyPhysicsSynthesis and characterization of novel inorganic/organometallic compoundsOrganometallic Complex Synthesis and CatalysisOrganoboron and organosilicon chemistry