Chemical composition and possible in vitro phytotoxic activity of Helichrsyum italicum (Roth) Don ssp. italicum

The chemical composition of the essential oil of Helichrysum italicum (Roth) Don ssp. italicum, collected in the National Park of Cilento and Diano Valley, Southern Italy, was studied by means of GC and GC/MS. Forty four compounds of 45 constituents were identified in the oil, mainly oxygenated sesquiterpenes. The essential oil was evaluated for its potential in vitro phytotoxic activity against germination and early radicle elongation of radish and garden cress. The radicle elongation of radish was significantly inhibited at the highest doses tested, while germination of both seeds was not affected.     

Crystal structure and hydrogen bonding study of (10E)-2,2-dimethyl-3,4-dihydro-2H-benzo[g]chromene-5,10-dione 10-oxime derived from α-lapachone

The compound (10E)-2,2-dimethyl-3,4-dihydro-2H-benzo[g]chromene-5,10-dione-10-oxime (1) was synthesized from a-lapachone and hydroxylamine chloride in alkaline medium. Single-crystals suitable for X-ray diffraction measurements were grown from an ethanol solution, and the crystal structure of the title molecule is reported for the first time. The title molecule was also characterized by 1H- and 13C-NMR in CDCl? solution, FTIR and MS. The crystal structure of 1 shows an E stereochemistry and dimers formed through classical hydrogen bonds.     

General linear response formula for non integrable systems obeying the Vlasov equation

Long-range interacting N-particle systems get trapped into long-living out-of-equilibrium stationary states called quasi-stationary states (QSS). We study here the response to a small external perturbation when such systems are settled into a QSS. In the N → ∞ limit the system is described by the Vlasov equation and QSS are mapped into stable stationary solutions of such equation. We consider this problem in the context of a model that has recently attracted considerable attention, the Hamiltonian mean field (HMF) model. For such a model, stationary inhomogeneous and homogeneous states determine an integrable dynamics in the mean-field effective potential and an action-angle transformation allows one to derive an exact linear response formula. However, such a result would be of limited interest if restricted to the integrable case. In this paper, we show how to derive a general linear response formula which does not use integrability as a requirement. The presence of conservation laws (mass, energy, momentum, etc.) and of further Casimir invariants can be imposed a posteriori. We perform an analysis of the infinite time asymptotics of the response formula for a specific observable, the magnetization in the HMF model, as a result of the application of an external magnetic field, for two stationary stable distributions: the Boltzmann-Gibbs equilibrium distribution and the Fermi-Dirac one. When compared with numerical simulations the predictions of the theory are very good away from the transition energy from inhomogeneous to homogeneous states.     

Divalent metal vinylphosphonate layered materials: compositional variability, structural peculiarities, dehydration behavior, and photoluminescent properties

A family of M-VP (M = Ni, Co, Cd, Mn, Zn, Fe, Cu, Pb; VP = vinylphosphonate) and M-PVP (M = Co, Cd; PVP = phenylvinylphosphonate) materials have been synthesized by hydrothermal methods and characterized by FT-IR, elemental analysis, and thermogravimetric analysis (TGA). Their structures were determined either by single crystal X-ray crystallography or from laboratory X-ray powder diffraction data. The crystal structure of some M-VP and M-PVP materials is two-dimensional (2D) layered, with the organic groups (vinyl or phenylvinyl) protruding into the interlamellar space. However, the Pb-VP and Cu-VP materials show dramatically different structural features. The porous, three-dimensional (3D) structure of Pb-VP contains the Pb center in a pentagonal pyramid. A Cu-VP variant of the common 2D layered structure shows a very peculiar structure. The structure of the material is 2D with the layers based upon three crystallographically distinct Cu atoms; an octahedrally coordinated Cu(2+) atom, a square planar Cu(2+) atom and a Cu(+) atom. The latter has an unusual co-ordination environment as it is 3-coordinated to two oxygen atoms with the third bond across the double bond of the vinyl group. Metal-coordinated water loss was studied by TGA and thermodiffractometry. The rehydration of the anhydrous phases to give the initial phase takes place rapidly for Cd-PVP but it takes several days for Co-PVP. The M-VP materials exhibit variable dehydration-rehydration behavior, with most of them losing crystallinity during the process.     

Classification,Toxicity and Bioactivity of Natural Diterpenoid Alkaloids

Diterpenoid alkaloids are natural compounds having complex structural features with many stereo-centres originating from the amination of natural tetracyclic diterpenes and produced primarily from plants in the Aconitum, Delphinium, Consolida genera. Corals, Xenia, Okinawan/Clavularia, Alcyonacea (soft corals) and marine sponges are rich sources of diterpenoids, despite the difficulty to access them and the lack of availability. Researchers have long been concerned with the potential beneficial or harmful effects of diterpenoid alkaloids due to their structural complexity, which accounts for their use as pharmaceuticals as well as their lousy reputation as toxic substances. Compounds belonging to this unique and fascinating family of natural products exhibit a broad spectrum of biological activities. Some of these compounds are on the list of clinical drugs, while others act as incredibly potent neurotoxins. Despite numerous attempts to prepare synthetic products, this review only introduces the natural diterpenoid alkaloids, describing ‘compounds’ structures and classifications and their toxicity and bioactivity. The purpose of the review is to highlight some existing relationships between the presence of substituents in the structure of such molecules and their recognised bioactivity.     

Wavelength dispersive X‐ray fluorescence (WDXRF) and chemometric investigation of human hair after cosmetic treatment

Variations in the chemical composition of 63 different human and 6 different synthetic hair samples were investigated using wavelength dispersive X‐ray fluorescence (WDXRF) spectra profiles. To evaluate the effect of cosmetic treatment on the strands, the human hair samples were bleached, but the synthetic ones were not. To better investigate the data, exploratory analyses were calculated using principal component analysis for the WDXRF spectra. Eight normalizations/standardizations were applied in the WDXRF to verify the clustering tendency. Bleaching was tested, because it is one way in which people mask their real hair color. After the data were standardized, an enhancement of the data discrimination was verified. Furthermore, the explained variance was higher in the first principal components. The WDXRF spectra were able to distinguish samples with distinct features, including synthetic, dyed, and straightened hair. The findings of this study hold promise for forensics due to desirable aspects such as nondestructivity and the possibility of a large hair sample database.