The effect of Mn oxidation state on metal core electron excitations in manganese dimers: a time-dependent density functional investigation

2009 ◽  
Vol 11 (27) ◽  
pp. 5634 ◽  
Author(s):  
Adrian R. Jaszewski ◽  
Rob Stranger ◽  
Ronald J. Pace
Keyword(s):  
Oxidation State ◽  
Density Functional ◽  
Time Dependent ◽  
Metal Core ◽  
Core Electron ◽  
Functional Investigation ◽  
Electron Excitations ◽  
Dependent Density

Time-Dependent DFT Studies of Metal Core-Electron Excitations in Mn Complexes

2008 ◽  
Vol 112 (44) ◽  
pp. 11223-11234 ◽  
Author(s):  
Adrian R. Jaszewski ◽  
Rob Stranger ◽  
Ronald J. Pace
Keyword(s):  
Time Dependent ◽  
Dft Studies ◽  
Metal Core ◽  
Core Electron ◽  
Electron Excitations

Spectroscopic and time-dependent density functional investigation of the role of structure on the acid-base effects of citrinin detection

2017 ◽  
Vol 29 (3) ◽  
pp. 715-723 ◽  
Author(s):  
Michael Appell ◽  
Kervin O. Evans ◽  
David L. Compton ◽  
Lijuan C. Wang ◽  
Wayne B. Bosma
Keyword(s):  
Density Functional ◽  
Time Dependent ◽  
Acid Base ◽  
Functional Investigation ◽  
Dependent Density

Time dependent density functional investigation of the near-edge absorption spectra of V2O5

2006 ◽  
Vol 8 (37) ◽  
pp. 4300 ◽  
Author(s):  
R. De Francesco ◽  
M. Stener ◽  
M. Caus? ◽  
D. Toffoli ◽  
G. Fronzoni
Keyword(s):  
Absorption Spectra ◽  
Density Functional ◽  
Time Dependent ◽  
Edge Absorption ◽  
Functional Investigation ◽  
Dependent Density

Benchmark of Simplified Time-Dependent Density Functional Theory for UV-Vis Spectral Properties of Porphyrinoids

2019 ◽  
Author(s):  
Kamal Batra ◽  
Stefan Zahn ◽  
Thomas Heine
Keyword(s):  
Density Functional Theory ◽  
Density Functional ◽  
Large Scale ◽  
Absolute Error ◽  
Time Dependent ◽  
Basis Set ◽  
Basis Sets ◽  
Functional Theory ◽  
Framework Materials ◽  
Dependent Density

<p>We thoroughly benchmark time-dependent density- functional theory for the predictive calculation of UV/Vis spectra of porphyrin derivatives. With the aim to provide an approach that is computationally feasible for large-scale applications such as biological systems or molecular framework materials, albeit performing with high accuracy for the Q-bands, we compare the results given by various computational protocols, including basis sets, density-functionals (including gradient corrected local functionals, hybrids, double hybrids and range-separated functionals), and various variants of time-dependent density-functional theory, including the simplified Tamm-Dancoff approximation. An excellent choice for these calculations is the range-separated functional CAM-B3LYP in combination with the simplified Tamm-Dancoff approximation and a basis set of double-ζ quality def2-SVP (mean absolute error [MAE] of ~0.05 eV). This is not surpassed by more expensive approaches, not even by double hybrid functionals, and solely systematic excitation energy scaling slightly improves the results (MAE ~0.04 eV). </p>

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