کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5416668 | 1506891 | 2010 | 9 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
A relativistic DFT study of the electron affinity of the biscyclopentadienyl uranium complexes Cpâ2UX2
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
شیمی
شیمی تئوریک و عملی
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چکیده انگلیسی
Electron affinities (EA) of a series of biscyclopentadienyl uranium complexes Cpâ2UX2 (X2Â =Â (BH4)2, Me2, (NEt2)Cl and (OEt)2) related to the U(III)/U(IV) redox system were calculated using Density Functional Theory (DFT) in the framework of the relativistic Zero Order Regular Approximation (ZORA) coupled with the Conductor-like Screening Model (COSMO) for a realistic solvation approach, implemented in the ADF (Amsterdam Density Functional) package. A good correlation (r2Â =Â 0.992-0.996) is obtained between the calculated EA values at the ZORA/BP86/TZP and ZORA/BP86/TZ2P levels and the measured half-wave potentials in THF for the series of complexes under consideration. The importance of spin-orbit coupling and solvent effect which must be taken into account in order to achieve the good agreement between theory and experiment, as well as the basis set extension, are brought to light. The influence of the non aromatic ligands X2 on electron affinities was studied. The role of involved orbitals (singled occupied molecular orbital -SOMO- of anionic species or lowest unoccupied molecular orbital -LUMO- of neutral species) in the redox process is discussed.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Molecular Structure: THEOCHEM - Volume 954, Issues 1â3, 30 August 2010, Pages 115-123
Journal: Journal of Molecular Structure: THEOCHEM - Volume 954, Issues 1â3, 30 August 2010, Pages 115-123
نویسندگان
Aziz Elkechai, Samir Meskaldji, Abdou Boucekkine, Lotfi Belkhiri, Delphine Bouchet, Mohand Amarouche, Caroline Clappe, Didier Hauchard, Michel Ephritikhine,