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Geometric distortions of octahedral cations and tetrahedral anions in disordered [Cu(bpy)3]CrO4·7.5H2O crystal : a comparative study.
Autorzy
Rok wydania
2010
Czasopismo
Numer woluminu
29
Strony
2574-2581
DOI
10.1016/j.poly.2010.06.003
Kolekcja
Język
Angielski
Typ publikacji
Artykuł
A novel copper(II) chromate complex of the formula [Cu(bpy)3][CrO4]·7.5H2O (1) (bpy = 2,2′-bipyridine) was prepared in the crystalline form and characterized by X-ray diffraction and spectroscopic methods (EPR, FIR-IR, NIR–Vis–UV). Two non-equivalent [Cu(bpy)3]2+ groups in the form of tetragonally elongated octahedron are built into the hydrogen-bonded network. The tetragonality parameter T is 0.9830 and 0.9876 for Cu(1) and Cu(2) centers, respectively, points to the significant Jahn–Teller (JT) distortion in the tris-bipyridine copper(II) cations. The EPR parameters g1, g2 and g3 are equal to 2.168, 2.159 and 2.072, respectively, correspond to the Cu–N bond directions oscillating between long and short distances. The chromate moiety is a non-coordinated to the metal center and forms a very distorted tetrahedron with three bond lengths in the range 1.617(2)–1.629(2) Å. The O(3A) and O(3B) atoms execute reorientational motion between two equilibrium arrangements with equal probability. The related geometric distortion, Δr, is 0.097 Å. The Gaussian analysis of single crystal electronic spectra was based on the four d–d bands assigned for Cu(II) center to the 2A1g(dx2−y2) → 2A2g(dz2), 2B1g(dxy), 2B2g(dxz) and 2B3g(dyz) transitions in D2h symmetry.
Słowa kluczowe
Chromate(VI) and copper(II) complexes, X-ray diffraction, EPR, IR and UV–Vis–NIR spectroscopy, Single crystal electronic spectra at 4.2 K, Gaussian analysis
Adres publiczny
https://doi.org/10.1016/j.poly.2010.06.003
Strona internetowa wydawcy
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