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Vibration-reorientation dynamics, structural changes and its interrelation with the phase transition in polycrystalline [Cr(OC(NH₂)₂)₆](BF₄)₃.

作者信息

Górska Natalia, Mikuli Edward, Łabanowska Maria, Kurdziel Magdalena

机构信息

Faculty of Chemistry, Jagiellonian University, Ingardena 3, 30-060 Kraków, Poland.

Faculty of Chemistry, Jagiellonian University, Ingardena 3, 30-060 Kraków, Poland.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2016 Feb 5;154:237-242. doi: 10.1016/j.saa.2015.10.032. Epub 2015 Oct 24.

Abstract

Polycrystalline hexakis(urea-O)chromium(III) tetrafluoroborate possesses in the temperature range of 295-105 K one solid-solid phase transition at T(C) ≈ 255 K. Analysis of the band shapes associated with the ν(as)(CN) and δ(as)(NH2) vibrational modes of the Fourier transform infrared absorption (FT-IR) spectra, registered in the temperature range of 295-10 K, indicated existence of fast (τ(R) ≈ 10(-12) s) reorientational motion of the protons from NH2 groups belonging to OC(NH2)2 (urea) ligands, which does not suddenly change at T(C). Moreover, splitting of the IR bands associated with the ν(as)(NH), ν(s)(NH) and ν(as)(BF)F2/ν(s)(CN) modes at T(C) indicated that this phase transition is associated with a change of crystal structure. Similar analysis of the Raman scattering bands (FT-RS), associated with the δ(s)(FBF)E, ν(s)(BF)A and ν(as)(BF)F2/ν(s)(CN) vibrational modes, indicated fast reorientation of the BF4(−) ions, which does not suddenly change at T(C), and additionally confirmed structural character of this phase transition. Results obtained from vibrational spectroscopy measurements are compatible with that obtained by electron paramagnetic resonance spectroscopy (EPR) measurements in function of temperature, where rapid narrowing of the EPR line in the vicinity of the T(C) was observed.

摘要

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