scholarly journals The electronic structure of thorium monoxide: Ligand field assignment of states in the range 0–5 eV

2018 ◽  
Vol 40 (2) ◽  
pp. 430-446 ◽  
Author(s):  
Leonid A. Kaledin ◽  
Alexey L. Kaledin ◽  
Michael C. Heaven
Keyword(s):  
Electronic Structure ◽  
Ligand Field ◽  
Thorium Monoxide

The electronic structure of LaO: Ligand field versus ab initio calculations

1995 ◽  
Vol 103 (18) ◽  
pp. 8004-8013 ◽  
Author(s):  
Joël Schamps ◽  
Mohammed Bencheikh ◽  
Jean‐Claude Barthelat ◽  
Robert W. Field
Keyword(s):  
Electronic Structure ◽  
Ab Initio Calculations ◽  
Ab Initio ◽  
Ligand Field ◽  
Field Versus

The electronic structure of LaF: A multiconfiguration ligand field calculation

1987 ◽  
Vol 87 (5) ◽  
pp. 2898-2912 ◽  
Author(s):  
Harold Schall ◽  
Michael Dulick ◽  
Robert W. Field
Keyword(s):  
Electronic Structure ◽  
Ligand Field ◽  
Field Calculation

scholarly journals Multireference Description of Nickel–Aryl Homolytic Bond Dissociation Processes in Photoredox Catalysis

2020 ◽  
Author(s):  
David Cagan ◽  
Gautam Stroscio ◽  
Alexander Cusumano ◽  
Ryan Hadt
Keyword(s):  
Electronic Structure ◽  
Excited State ◽  
Charge Transfer ◽  
Density Functional ◽  
Single Photon ◽  
Ligand Field ◽  
Initial Population ◽  
Bond Dissociation ◽  
Ligand Charge Transfer ◽  
Triplet Excited States

<p>Multireference electronic structure calculations consistent with known experimental data have elucidated a novel mechanism for photo-triggered Ni(II)–C homolytic bond dissociation in Ni 2,2’-bipyridine (bpy) photoredox catalysts. Previously, a thermally assisted dissociation from the lowest energy triplet ligand field excited state was proposed and supported by density functional theory (DFT) calculations that reveal a barrier of ~30 kcal mol<sup>-1</sup>. In contrast, multireference ab initio calculations suggest this process is disfavored, with barrier heights of ~70 kcal mol<sup>-1</sup>, and highlight important ligand noninnocent contributions to excited state relaxation and bond dissociation processes that are not captured with DFT. In the multireference description, photo-triggered Ni(II)–C homolytic bond dissociation occurs via initial population of a singlet Ni(II)-to-bpy metal-to-ligand charge transfer (<sup>1</sup>MLCT) excited state followed by intersystem crossing and aryl-to-Ni(III) charge transfer, overall a formal two-electron transfer process driven by a single photon. This results in repulsive triplet excited states from which spontaneous homolytic bond dissociation can occur, effectively competing with relaxation to the lowest energy, nondissociative triplet Ni(II) ligand field excited state. These findings guide important electronic structure considerations for the experimental and computational elucidation of the mechanisms of ground and excited state cross-coupling catalysis mediated by Ni heteroaromatic complexes.</p>

ChemInform Abstract: LIGAND FIELD SPECTRUM AND THE ELECTRONIC STRUCTURE OF THE HEXACYANOCHROMATE(3-) ION

1984 ◽  
Vol 15 (38) ◽  
Author(s):  
L. G. VANQUICKENBORNE ◽  
L. HASPESLAGH ◽  
M. HENDRICKX ◽  
J. VERHULST
Keyword(s):  
Electronic Structure ◽  
Ligand Field ◽  
Field Spectrum

Manipulation of the heme electronic structure by external stimuli and ligand field

ICAME 2011 ◽  
2013 ◽  
pp. 319-329
Author(s):  
Yoshiki Ohgo ◽  
Masashi Takahashi ◽  
Kazuyuki Takahashi ◽  
Yukiko Namatame ◽  
Hisashi Konaka ◽  
...  
Keyword(s):  
Electronic Structure ◽  
Ligand Field ◽  
Heme Electronic Structure ◽  
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