Spin-orbit coupling in the oxidative activation of H-H by FeO+. Selection rules and reactivity effects

被引:239
|
作者
Danovich, D
Shaik, S
机构
[1] HEBREW UNIV JERUSALEM,DEPT ORGAN CHEM,INST CHEM,IL-91904 JERUSALEM,ISRAEL
[2] HEBREW UNIV JERUSALEM,MINERVA CTR COMPUTAT QUANTUM CHEM,IL-91904 JERUSALEM,ISRAEL
关键词
D O I
10.1021/ja963033g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Spin-orbit coupling (SOC) calculations are performed along the reaction pathway of the oxidation process, FeO+ + H-2 --> Fe+ + H2O (eq 1). Selection rules are derived for SOC between different spin situations, and are applied to understand the computed SOC patterns along the oxidation pathway, and their relationship to the electronic structure of the various species. The process involves two spin inversion (SI) junctions between sextet and quartet states: near the FeO+/H-2 cluster at the entrance channel, and near the Fe+/H2O cluster at the exit channel. The sextet-quartet SOC is significant at the reactant extreme (for FeO+), but decreases at the FeO+/H-2 cluster and continues to decrease until it becomes vanishingly small between the D-6-F-4 states of Fe+ at the product extreme. The results show that while the quartet surface provides a low-energy path, the SI junctions reduce the probability of the oxidation process significantly. In agreement with the deductions of Armentrout et al., (2c) the poor bond activation capability of the D-6 ground state of Fe+ in the reverse reaction is accounted for by the inefficient D-6-F-4 State mixing due to the expected poor SOC between the respective 4s(1)3d(6) and 3d(7) configurations. On the other hand, the F-4 excited state of Fe+ can activate H2O more efficiently since it can lead to the insertion intermediate (4)(HFeOH+) in a spin-conserving manner. Other findings of Schwarz et al.(1,2a) and Armentrout et al.(2c,d) are discussed in the light of the SOC patterns. The importance of the SOC at the exit channel is highlighted by comparing the product distribution of the reaction (eq 1) with analogous reactions of MO(+) species: when the ground state M(+) has a 4s(1)3(n-1) (Fe+, Mn+) electronic structure as opposed to those cases where the ground state electronic structure is 3d(n) (Co+, Ni+) and where no spin inversion is required. Predictions based on the understanding of the SOC patterns are made and compared with appropriate experimental data.
引用
收藏
页码:1773 / 1786
页数:14
相关论文
共 50 条
  • [31] Spin-orbit coupling and intersystem crossing in 4H-Pyran-4-thione:: CASSCF//TD-B3LYP study
    Lue Ling-Ling
    Liu Xin-Wen
    Yuan Kun
    Wang Yong-Cheng
    Wang Han-Qing
    CHINESE JOURNAL OF CHEMISTRY, 2007, 25 (10) : 1461 - 1466
  • [32] I + (H2O)2 → HI + (H2O)OH Forward and Reverse Reactions. CCSD(T) Studies Including Spin-Orbit Coupling
    Wang, Hui
    Li, Guoliang
    Li, Qian-Shu
    Xie, Yaoming
    Schaefer, Henry F., III
    JOURNAL OF PHYSICAL CHEMISTRY B, 2016, 120 (08): : 1743 - 1748
  • [33] REACTIVITY OF SPIN-ORBIT STATE-SELECTED KR+P-2(J) IONS WITH H-2, HD, AND D2
    ERVIN, KM
    ARMENTROUT, PB
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1986, 192 : 19 - PHYS
  • [34] Width dependence of the 0.5 × (2e2/h) conductance plateau in InAs quantum point contacts in presence of lateral spin-orbit coupling
    Partha Pratim Das
    Marc Cahay
    Shashikala Kalita
    Sib Sankar Mal
    Alok Kumar Jha
    Scientific Reports, 9
  • [35] Spin-orbit effects on the electronic spectroscopy of transition metal dihydrides H2M(CO)4 (M = Fe, Os)
    Vallet, V
    Strich, A
    Daniel, C
    CHEMICAL PHYSICS, 2005, 311 (1-2) : 13 - 18
  • [36] Reactions of Ta+ and W+ with H2, D2, and HD:: Effect of lanthanide contraction and spin-orbit interactions on reactivity and thermochemistry
    Zhang, XG
    Rue, C
    Shin, SY
    Armentrout, PB
    JOURNAL OF CHEMICAL PHYSICS, 2002, 116 (13): : 5574 - 5583
  • [37] Role of molecular distortions in the spin-orbit coupling between the singlet and triplet states of the 4π electron systems C4H4, C5H5+, and C3H3-
    Shiota, Y
    Kondo, M
    Yoshizawa, K
    JOURNAL OF CHEMICAL PHYSICS, 2001, 115 (20): : 9243 - 9254
  • [38] A THEORETICAL INTERPRETATION OF SUBSTITUENT EFFECTS ON H-H AND 13C-H SPIN COUPLING CONSTANTS FOR CH3X (CH2)2X AND CH2=CHX DERIVATIVES
    YONEZAWA, T
    MORISHIM.I
    FUJII, M
    KATO, H
    BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1969, 42 (05) : 1248 - +
  • [39] Effect of atomic configuration and spin-orbit coupling on thermodynamic stability and electronic bandgap of monolayer 2H-Mo1-xWxS2 solid solutions
    Atthapak, C.
    Ektarawong, A.
    Pakornchote, T.
    Alling, B.
    Bovornratanaraks, T.
    PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2021, 23 (24) : 13535 - 13543
  • [40] Width dependence of the 0.5 x (2e2/h) conductance plateau in InAs quantum point contacts in presence of lateral spin-orbit coupling
    Das, Partha Pratim
    Cahay, Marc
    Kalita, Shashikala
    Mal, Sib Sankar
    Jha, Alok Kumar
    SCIENTIFIC REPORTS, 2019, 9 (1)