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231225s2018 xx |||||o 00| ||eng c |
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|a 10.1107/S1600577518009517
|2 doi
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|a pubmed24n0960.xml
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|a eng
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| 100 |
1 |
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|a Zhang, Kaili
|e verfasserin
|4 aut
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|a Improved charge transfer multiplet method to simulate M- and L-edge X-ray absorption spectra of metal-centered excited states
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|c 2018
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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| 500 |
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|a Date Completed 06.09.2018
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|a Date Revised 06.09.2018
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|a published: Print-Electronic
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|a Citation Status PubMed-not-MEDLINE
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|a Charge transfer multiplet (CTM) theory is a computationally undemanding and highly mature method for simulating the soft X-ray spectra of first-row transition metal complexes. However, CTM theory has seldom been applied to the simulation of excited-state spectra. In this article, the CTM4XAS software package is extended to simulate M2,3- and L2,3-edge spectra for the excited states of first-row transition metals and also interpret CTM eigenfunctions in terms of Russell-Saunders term symbols. These new programs are used to reinterpret the recently reported excited-state M2,3-edge difference spectra of photogenerated ferrocenium cations and to propose alternative assignments for the electronic state of these cations responsible for the spectroscopic features. These new programs were also used to model the L2,3-edge spectra of FeII compounds during nuclear relaxation following photoinduced spin crossover and to propose spectroscopic signatures for their vibrationally hot states
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|a Journal Article
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|a X-ray spectroscopy
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|a electronic structure
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| 650 |
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|a multiplet simulations
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| 650 |
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4 |
|a valence excited states
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| 700 |
1 |
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|a Girolami, Gregory S
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Vura-Weis, Josh
|e verfasserin
|4 aut
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| 773 |
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|i Enthalten in
|t Journal of synchrotron radiation
|d 1994
|g 25(2018), Pt 5 vom: 01. Sept., Seite 1600-1608
|w (DE-627)NLM09824129X
|x 1600-5775
|7 nnns
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| 773 |
1 |
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|g volume:25
|g year:2018
|g number:Pt 5
|g day:01
|g month:09
|g pages:1600-1608
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| 856 |
4 |
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|u http://dx.doi.org/10.1107/S1600577518009517
|3 Volltext
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