化学
齿合度
硼
平面的
平方(代数)
方位(导航)
结晶学
立体化学
晶体结构
有机化学
地图学
计算机科学
计算机图形学(图像)
地理
几何学
数学
作者
Yutaka Mondori,Yasuhiro Yamauchi,Takahiro Kawakita,Sensuke Ogoshi,Yuta Uetake,Yasuo Takeichi,Hidehiro Sakurai,Yoichi Hoshimoto
摘要
Transition metals are known to work as electron donors toward electron-accepting heavier-group-13 elements (Al, Ga, and In), called Z-type ligands. However, complexes with boron-based Z-type ligands are stable only in the presence of additional coordination units (the so-called "supported-ligand" strategy). Here, we report the synthesis and characterization of square-planar Ni(0) complexes that bear tris(perfluoroaryl)boranes as monodentate Z-type ligands, even though such coordination geometry has been traditionally associated with Ni(II) species based on the well-established ligand-field theory. A combined theoretical and experimental approach revealed a mixed covalent/dative character for the Ni-B bonds. This strategy uses frustrated L/Z-ligand pairs that combine sterically encumbered electron-donating (L-type) and electron-accepting ligands to form noncovalent interactions over L-M-Z units to achieve unprecedented low-valent transition metal species with monodentate Z-type ligands.
科研通智能强力驱动
Strongly Powered by AbleSci AI