Search results for "Intervalence charge transfer"
showing 4 items of 4 documents
The Ti-influence on the tourmaline color
2008
Titanium was examined in different black tourmalines by spectrophotometric analyses in the region between 12500 and 27000 cm-1 (800-370 nm) using a microscope spectrophotometer MPV-5P, Leitz (Germany), and chemically analyzed on an electron microprobe Camebax Microbeam, Cameca (France) in WDS Mode. Fourteen tourmaline samples with their face oriented parallel to the principal axis, cut and polished down to thin sections, showed polarized spectra of two broad absorption bands at approximately 14000 cm-1 (715 nm) and 24000 cm-1 (417 nm). Precision thickness measurements were used to calculate the absorption coefficients α. For the absorption around 24000 cm-1, a linear correlation was observe…
Synthesis by solution combustion of inorganic blue pigments MFe2(P2O7)2: Influence of the cation M (Zn2+, Co2+, Cu2+, and Mg2+) on their optical prop…
2020
Abstract The aim of this work is to find the effect of the cation M (Zn2+, Co2+, Cu2+, and Mg2+) on the optical properties of MFe2(P2O7)2 synthesized by solution combustion. The crystal structure of the powders was determined by X-ray diffraction (XRD), Infrared spectroscopy (IR), and Raman spectroscopy. The presence of Fe2+ and Fe3+ ions in the pigments was studied using Mossbauer spectroscopy (MS), these spectra showed at 298 K three well-defined Mossbauer doublets belonging to octahedral S1 site and S3 site of Fe3+ and trigonal prismatic S2 site of Fe2+, confirming the formation of ZnFe2(P2O7)2, CoFe2(P2O7)2 and MgFe2(P2O7)2 structures, while in CuFe2(P2O7)2 there is no presence of trigo…
Oligonuclear Ferrocene Amides: Mixed‐Valent Peptides and Potential Redox‐Switchable Foldamers
2010
Trinuclear ferrocene tris-amides were synthesized from an Fmoc- or Boc-protected ferrocene amino acid, and hydrogen-bonded zigzag conformations were determined by NMR spectroscopy, molecular modelling, and X-ray diffraction. In these ordered secondary structures orientation of the individual amide dipole moments approximately in the same direction results in a macrodipole moment similar to that of α-helices composed of α-amino acids. Unlike ordinary α-amino acids, the building blocks in these ferrocene amides with defined secondary structure can be sequentially oxidized to mono-, di-, and trications. Singly and doubly charged mixed-valent cations were probed experimentally by Vis/NIR, param…
How Hydrogen Bonds Affect Reactivity and Intervalence Charge Transfer in Ferrocenium‐Phenolate Radicals
2016
The ferrocenyl-phenol 2,4-di-tert-butyl-6-(ferrocenylcarbamoyl)phenol (H-1) forms intramolecular hydrogen bonds which are absent in its constitutional isomer 2,6-di-tert-butyl-4-(ferrocenylcarbamoyl)phenol (H-2). Their corresponding bases 1– and 2– show intra- and intermolecular NH···O hydrogen bonds, respectively. The phenolate 1– is reversibly oxidized to 1·, whereas 2– only undergoes a quasi-reversible oxidation to 2·, which suggests a higher reactivity. The radical pools of 1· and 2· formed by the oxidation/deprotonation of H-1 and H-2 have been probed by (rapid-freeze) electron paramagnetic resonance (EPR) spectroscopy and by spin-trapping techniques to elucidate the types of radicals …