K
Ke-Li Han
Researcher at Dalian Institute of Chemical Physics
Publications - 492
Citations - 30389
Ke-Li Han is an academic researcher from Dalian Institute of Chemical Physics. The author has contributed to research in topics: Excited state & Potential energy surface. The author has an hindex of 82, co-authored 491 publications receiving 26199 citations. Previous affiliations of Ke-Li Han include University of Minnesota & California Institute of Technology.
Papers
More filters
Journal ArticleDOI
Theoretical perspective on the reaction mechanism from arylpentazenes to arylpentazoles: new insights into the enhancement of cyclo-N5 production.
TL;DR: A potential solution to the enhancement of cyclo-N5 yield is proposed by scrutinizing the complete reaction pathways and substituent effects of arylpentazole.
Journal ArticleDOI
Spin-orbit effect in the energy pooling reaction O2(aΔ1)+O2(aΔ1)→O2(bΣ1)+O2(XΣ3)
TL;DR: In this article, the spin-orbit induced transition probability as a function of collision energy is calculated for the energy pooling reaction, and the rate constant obtained from a uniform J-shifting approach is compared with the existing theoretical and experimental data.
Journal ArticleDOI
Nonadiabatic quantum reactive scattering of the OH(A Σ2+)+D2
TL;DR: The theoretical results of nonadiabatic time-dependent wave-packet calculation are in good agreement with the existing experimental data.
Journal ArticleDOI
Generation of an Isolated Sub-100 Attosecond Pulse in a Two-Color Laser Field
TL;DR: In this article, a phase-stabilized few-cycle laser pulse and its subharmonic laser were combined to obtain a broadened continuum spectrum of 190 eV and an isolated 85 attosecond (as) pulse.
Journal ArticleDOI
An acyl group makes a difference in the reactivity patterns of cytochrome P450 catalyzed N-demethylation of substituted N,N-dimethylbenzamides-high spin selective reactions.
TL;DR: It is shown that the above mechanistic differences between the two reaction series of DMA and DMBA are caused by the ability of the para substituent to maintain a conjugation path between the C-H reaction center and the aryl moiety.