X-ray photoelectronic spectra and electronic structure of coordination compounds of the Eu complexes with the mixed ligands
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KOROCHENTSEV, V., , , OSMUSHKO, I., VOVNA, V., MIROCHNIK, A., ZOLOTUKHINA, A., KOROCHENTCEVA, V.. X-ray photoelectronic spectra and electronic structure of coordination compounds of the Eu complexes with the mixed ligands. In: Physical Methods in Coordination and Supramolecular Chemistry, 24-26 octombrie 2012, Chişinău. Chisinau, Republic of Moldova: 2012, XVII, p. 37.
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Physical Methods in Coordination and Supramolecular Chemistry
XVII, 2012
Conferința ""Physical Methods in Coordination and Supramolecular Chemistry""
Chişinău, Moldova, 24-26 octombrie 2012

X-ray photoelectronic spectra and electronic structure of coordination compounds of the Eu complexes with the mixed ligands


Pag. 37-37

Korochentsev V.1, 1, Osmushko I.1, Vovna V.1, Mirochnik A.2, Zolotukhina A.1, Korochentceva V.1
 
1 Far East Federal University, Vladivostok,
2 Institute of Chemistry, Russian Academy of Sciences, Vladivostok
 
 
Disponibil în IBN: 26 mai 2020


Rezumat

Electronic structure of chelate Eu(III) complexes was investigated by means of XRay photoelectron spectroscopy (PES) and DFT ( B3LYP) calculations. We studied the geometrical structure and nature of occupied orbitals. An influence of the ligand replacement (dbm – dibenzoilmethanate, acr - acrilate, macr - metacrilate) on an electronic structure was also investigated. Results The obtained experimental data and the results of quantum chemical calculations allowed us to make a reliable assignment of the spectral peaks which correspond to valence electrons. Concentration of elements in Eu (acr)3 → Eu (dbm)(acr)2 → Eu (dbm)2(acr) → Eu(dbm)3 → Eu (dbm)2(macr) → Eu(dbm)(macr)2 → E (macr)3 is given in Table 1. In Eu(acr)3 as well as in all other studied compounds, first six MO’s are purely ligand orbitals of π-type localized on C-atoms. Next five MO with energies from 11.79 eV to 12.42 eV have contributions from f AO of Eu(III). Ionization from these orbitals (fig. 1) forms the first intensive peak on the spectrum.tabelTable 1. Element concentration in Eu(III) complexes.figureFig.1. Eu(acr)3 valence area.

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<description xml:lang='en' descriptionType='Abstract'><p>Electronic structure of chelate Eu(III) complexes was investigated by means of XRay photoelectron spectroscopy (PES) and DFT ( B3LYP) calculations. We studied the geometrical structure and nature of occupied orbitals. An influence of the ligand replacement (dbm &ndash; dibenzoilmethanate, acr - acrilate, macr - metacrilate) on an electronic structure was also investigated. Results The obtained experimental data and the results of quantum chemical calculations allowed us to make a reliable assignment of the spectral peaks which correspond to valence electrons. Concentration of elements in Eu (acr)3 &rarr; Eu (dbm)(acr)2 &rarr; Eu (dbm)2(acr) &rarr; Eu(dbm)3 &rarr; Eu (dbm)2(macr) &rarr; Eu(dbm)(macr)2 &rarr; E (macr)3 is given in Table 1. In Eu(acr)3 as well as in all other studied compounds, first six MO&rsquo;s are purely ligand orbitals of &pi;-type localized on C-atoms. Next five MO with energies from 11.79 eV to 12.42 eV have contributions from f AO of Eu(III). Ionization from these orbitals (fig. 1) forms the first intensive peak on the spectrum.</p><p>tabel</p><p>Table 1. Element concentration in Eu(III) complexes.</p><p>figure</p><p>Fig.1. Eu(acr)3 valence area.</p></description>
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