High-level, restricted coupled cluster with singles, doubles, and perturbative triples calculations are performed to determine the ground electronic state of KO. In the absence of spin–orbit coupling, we find that the ground state is a state, with a state lying just over 200 cm−1 higher in energy. We ascertain that basis set extension, higher-order correlation energy, mass-velocity, and Darwin relativistic terms do not change this ordering. We then calculate the low-lying Ω states when spin–orbit coupling is turned on. The state undergoes an avoided crossing with the state, and we therefore designate the ground state as This state is essentially at short R, but essentially at long R; there is a corresponding state with the opposite behavior. These states have significantly different shapes and so spectroscopy from the adiabatic states. Finally, we calculate the dissociation energy of KO as and derive as
Skip Nav Destination
Article navigation
8 November 2002
Research Article|
November 08 2002
What is the ground electronic state of KO?
Edmond P. F. Lee;
Edmond P. F. Lee
Department of Applied Biology and Chemical Technology, Hong Kong Polytechnic University, Hung Hom, Hong Kong
Department of Chemistry, University of Southampton, Highfield, Southampton, United Kingdom, SO17 1BJ
Search for other works by this author on:
Pavel Soldán;
Pavel Soldán
Department of Chemistry, University of Durham, South Road, Durham, United Kingdom, DH1 3LE
Search for other works by this author on:
Timothy G. Wright
Timothy G. Wright
Spectroscopy of Complexes and Radicals (SOCAR) Group, Department of Chemistry, School of Chemistry, Physics and Environmental Science, University of Sussex, Falmer, Brighton, United Kingdom, BN1 9QJ
Search for other works by this author on:
J. Chem. Phys. 117, 8241–8247 (2002)
Article history
Received:
July 12 2002
Accepted:
August 12 2002
Citation
Edmond P. F. Lee, Pavel Soldán, Timothy G. Wright; What is the ground electronic state of KO?. J. Chem. Phys. 8 November 2002; 117 (18): 8241–8247. https://doi.org/10.1063/1.1511179
Download citation file:
Pay-Per-View Access
$40.00
Sign In
You could not be signed in. Please check your credentials and make sure you have an active account and try again.
Citing articles via
DeePMD-kit v2: A software package for deep potential models
Jinzhe Zeng, Duo Zhang, et al.
Beyond the Debye–Hückel limit: Toward a general theory for concentrated electrolytes
Mohammadhasan Dinpajooh, Nadia N. Intan, et al.
Related Content
The intermolecular potential energy surface of the He⋅NO + cationic complex
J. Chem. Phys. (February 2002)
Spectroscopy of Na + ⋅ Rg and transport coefficients of Na + in Rg(Rg=He–Rn)
J. Chem. Phys. (August 2003)
The Ã←X̃(1+1) REMPI spectrum and high-level ab initio calculations of the complex between NO and N 2
J. Chem. Phys. (December 2000)
Heavier alkali-metal monosulfides (KS, RbS, CsS, and FrS) and their cations
J. Chem. Phys. (October 2005)
Near-dissociation states and coupled potential curves for the HeN + complex
J. Chem. Phys. (August 2002)