Chronic toxicity of nanodiamonds can disturb development and reproduction of Acheta domesticus L.

The use of nanodiamonds in numerous materials designed for industry and medicine is growing rapidly. Consequently health and environmental risks associated with the exposure of humans and other biota to nanodiamonds-based materials are of the utmost importance. Scarcity of toxicological data for these particles led us to examine the potentially deleterious effects of nanodiamonds in model insect species, Acheta domesticus (Orthoptera) chronically exposed to ND in its diet. Organism-level end-point indices (lifespan, body weight, consumption, caloric value of faeces, reproduction) revealed adverse changes in the treated crickets in comparison with the control. Preliminary studies of oxidative stress level in the offspring of ND-treated crickets suggest toxicity of these particles limited to the exposed individuals. EPR analysis showing increase of radical signal in the faeces of ND-fed crickets led us to propose novel mechanism of nanodiamonds toxicity that is discussed in the light of literature data. CAPSULE: Development and reproduction of Acheta domesticus can be disturbed by the chronic exposure to nanodiamonds.

Evaluation of in vivo graphene oxide toxicity for Acheta domesticus in relation to nanomaterial purity and time passed from the exposure.

Graphene and its oxidized form-graphene oxide (GO) have become exceptionally popular in industry and medicine due to their unique properties. However, there are suspicions that GO can cause adverse effects. Therefore, comprehensive knowledge on its potential toxicity is essential. This research assesses the in vivo toxicity of pure and manganese ion contaminated GO, which were injected into the hemolymph of Acheta domesticus. The activity of catalase (CAT) and gluthiathione peroxidases (GSTPx) as well as heat shock protein (HSP 70) and total antioxidant capacity (TAC) levels were measured at consecutive time points-1h, 24h, 48h and 72h after injection. Neither pure GO nor GO contaminated with manganese were neutral to the organism. The results proved the intensification of oxidative stress after GO injection, which was confirmed by increased enzyme activity. The organism seems to cope with this stress, especially in the first 24h after injection. In the following days, increasing HSP 70 levels were observed, which might suggest the synthesis of new proteins and the removal of old and damaged ones. With that in mind, the potential toxicity of the studied material, which could lead to serious and permanent damage to the organism, should still be taken into consideration.

Size effects in the conduction electron spin resonance of anthracite and higher anthraxolite.

Electron paramagnetic resonance spectroscopy of conduction electrons, i.e. Conduction Electron Spin Resonance (CESR), is a powerful tool for studies of carbon samples. Conductive samples cause additional effects in CESR spectra that influence the shape and intensity of the signals. In cases where conduction electrons play a dominant role, whilst the influence of localized paramagnetic centres is small or negligible, the effects because of the spins on conduction electrons will dominate the spectra. It has been shown that for some ratios of the bulk sample sizes (d) to the skin depth (δ), which depend on the electrical conductivity, additional size effects become visible in the line asymmetry parameter A/|B|, which is the ratio of the maximum to the absolute, minimum value of the resonance signal. To study these effects the electrical direct current-conductivity and CESR measurements are carried out for two amorphous bulk coal samples of anthracite and a higher anthraxolite. The observed effects are described and discussed in terms of the Dyson theory. Copyright © 2015 John Wiley & Sons, Ltd.

Exchange interactions and electron delocalization in the mixed-valence cluster V(4)(IV)V(2)(V)O(7)(OC(2)H(5))(12).

The mixed-valence cluster compound V4IVV2VO7(OC2H5)12 was studied by X-band electron paramagnetic resonance (EPR) in the temperature range of 4.2-293 K. According to X-ray diffraction study, the crystal structure of the compound was described by a R3m space group at 295 K (four d1 electrons are equally delocalized on all vanadium ions) and changed to a P21/n space group on cooling the crystals to 173 K (the electrons are preferably localized on the four equatorial vanadium ions). The EPR spectra originate from the S = 1 total spin states with the fine structure averaged to a single Lorentzian line and from the S = 2 total spin states with fine structure partly averaged in the temperature range of 295-200 K and well averaged below 45-50 K. The states of S = 1 and S = 2 of comparable energy (DeltaE approximately 2 cm(-1); ES=1 < ES=2) were shown to be the lowest ones. The VIV <--> VV unpaired electron transfers together with isotropic Heisenberg exchange were shown to determine the total spin states composition and the intracluster dynamics of the compound. Two types of electron transfers were assumed: the single-jump transfer leading to the averaged configurations of the V4IVV2V <--> V3IVVV VIVVV type and to the splitting of the total spin states by intervals comparable in magnitude with the isotropic exchange parameter J approximately 100 cm-1 and the double-jump transfer resulting in dynamics. Temperature dependence of the transition rates nutr was observed. In the range of 295-210 K, the value of nutr = (0.5-0.6) x 10(10) s(-1) is sufficient for averaging the fine structure of the S = 1 states, and below 45 K the value of nutr approximately 1.5 x 10(10) s(-1) also averages the fine structure of the S = 2 state. A change in the localization plane of the VIV ions in the temperature range of 40-50 K was discovered.

Low-temperature single-crystal Raman and neutron-diffraction study of the hydrogenous ammonium copper(II) Tutton salt and the deuterated analogue in the metastable state.

Low-temperature (15 K) single-crystal neutron-diffraction structures and Raman spectra of the salts (NX4)2[Cu(OX2)6](SO4)2, where X=H or D, are reported. This study is concerned with the origin of the structural phase change that is known to occur upon deuteration. Data for the deuterated salt were measured in the metastable state, achieved by application of 500 bar of hydrostatic pressure at approximately 303 K followed by cooling to 281 K and the subsequent release of pressure. This allows for the direct comparison between the hydrogenous and deuterated salts, in the same modification, at ambient pressure and low temperature. The Raman spectra provide no intimation of any significant change in the intermolecular bonding. Furthermore, structural differences are few, the largest being for the long Cu-O bond, which is 2.2834(5) and 2.2802(4) A for the hydrogenous and the deuterated salts, respectively. Calorimetric data for the deuterated salt are also presented, providing an estimate of 0.17(2) kJ/mol for the enthalpy difference between the two structural forms at 295.8(5) K. The structural data suggest that substitution of hydrogen for deuterium gives rise to changes in the hydrogen-bonding interactions that result in a slightly reduced force field about the copper(II) center. The small structural differences suggest different relative stabilities for the hydrogenous and deuterated salts, which may be sufficient to stabilize the hydrogenous salt in the anomalous structural form.

Pressure-controlled plasticity of Cu(H2O)6(2+) complex and phase transition in Cs2Cu(ZrF6)2*6H2O.

The X-band EPR study of a polycrystalline Cs2Cu(ZrF6)2*6H2O demonstrates a feature of plasticity of the Jahn-Teller Cu(H2O)6 complex in the crystal lattice of this compound. The temperature- and pressure-induced evolution of the spectra shows that the copper complex is extremely sensitive to these factors, which due to the ferroelastic properties of the compound studied modify the internal tetragonal and orthorhombic strains acting on the complex. It is supported by the analysis of the temperature dependencies of the principal values of the g-factor under various pressures, indicating that the complex varies its shape adapting it to the varied conditions. A pressure-induced phase transition is discovered.