Observation of the Transition from Triple Bonds to Single Bonds between Ru-Ge Bonding in RuGeO(CO) n - (n=3-5)

被引:0
|
作者
Zhang, Ziheng [1 ,2 ]
Ling, Zicheng [1 ]
Ju, Bangmin [2 ]
Li, Gang [2 ]
Yuan, Qinqin [1 ]
Cheng, Longjiu [1 ]
Xie, Hua [2 ]
Jiang, Ling [2 ]
机构
[1] Anhui Univ, Dept Chem, Key Lab Funct Inorgan Mat Anhui Prov, Hefei 230601, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Mol React Dynam, Dalian 116023, Peoples R China
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2024年 / 15卷 / 27期
基金
中国国家自然科学基金;
关键词
INFRARED PHOTODISSOCIATION SPECTROSCOPY; METAL-CARBONYL CATIONS; CO OXIDATION; MONONUCLEAR; ACTIVATION; GERMANIUM; ENERGIES;
D O I
10.1021/acs.jpclett.4c01532
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This work reports the observation and characterization of heterobinuclear transition-metal main-group metal oxide carbonyl complex anions, RuGeO(CO)(n) - (n = 3-5), by combining mass-selected photoelectron velocity map imaging spectroscopy and quantum chemistry calculations. The experimentally determined vertical electron detachment energy of RuGeO(CO)(3)(-) surpasses those of RuGeO(CO)(4)(-) and RuGeO(CO)(5)(-), which is attributed to distinctive bonding features. RuGeO(CO)(3)(-) manifests one covalent sigma and two Ru-to-Ge dative pi bonds, contrasting with the sole covalent sigma bond present in RuGeO(CO)(4)(-) and RuGeO(CO)(5)(-). Unpaired spin density distribution analysis reveals a 17-electron configuration at the Ru center in RuGeO(CO)(3)(-) and an 18-electron configuration in RuGeO(CO)(4)(-) and RuGeO(CO)(5)(-). This work closes a gap in the quantitative physicochemical characterization of heteronuclear oxide carbonyl complexes, enhancing our insights into catalytic processes of CO/GeO on the metal surface at the molecular level.
引用
收藏
页码:6952 / 6957
页数:6
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