Wang Caixia, Jian Jiwen, Li Zhen Hua, Chen Mohua, Wang Guanjun, Zhou Mingfei
Collaborative Innovation Center of Chemistry for Energy Materials, Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysts and Innovative Materials, Fudan University , Shanghai 200433, China.
J Phys Chem A. 2015 Sep 3;119(35):9286-93. doi: 10.1021/acs.jpca.5b07089. Epub 2015 Aug 25.
The infrared spectra of mass-selected Ni(O2)n(+) (n = 2-4) and their argon-tagged complexes are measured by infrared photodissociation spectroscopy in the gas phase. The experimental spectra provide distinctive patterns allowing the determination of their geometric and electronic structures by comparison with the simulated vibrational spectra from density functional theory calculations. The Ni(O2)2Ar2 cation complex was determined to have D2h symmetry involving a Ni(O2)2(+) core ion with two equivalent superoxide ligands side-on bound to a Ni(3+) cation center. The higher Ni(O2)3(+) and Ni(O2)4(+) cation complexes were determined to have structures with a chemically bound Ni(O2)2(+) core ion that is weakly coordinated by neutral O2 molecule(s).
通过气相红外光解离光谱法测量了质量选择的Ni(O₂)ₙ⁺(n = 2 - 4)及其氩标记配合物的红外光谱。实验光谱提供了独特的模式,通过与密度泛函理论计算得到的模拟振动光谱进行比较,可以确定它们的几何结构和电子结构。[Ni(O₂)₂Ar₂]⁺阳离子配合物被确定具有D₂h对称性,涉及一个Ni(O₂)₂⁺核心离子,两个等效的超氧配体以侧基方式与一个Ni³⁺阳离子中心结合。更高的Ni(O₂)₃⁺和Ni(O₂)₄⁺阳离子配合物被确定具有化学结合的Ni(O₂)₂⁺核心离子结构,该核心离子由中性O₂分子弱配位。