GC×GC/qMS analyses of Campomanesia guazumifolia (Cambess.) O. Berg essential oils and their antioxidant and antimicrobial activity

The present study investigated the essential oil obtained from Campomanesia guazumifolia (Cambess.) O. Berg, an aromatic plant used in Brazilian folk medicine. The chemical composition was performed by GC×GC/qMS. The antioxidant and antimicrobial activities were evaluated by DPPH and BCB and, MIC assays, respectively. Sixty-eight compounds were identified in the oil, where the major compounds were bicyclogermacrene (15%), globulol (5%) and spathulenol (5%). Sesquiterpene hydrocarbons (29 compounds) and oxygenated sesquiterpenes (20 compounds) were the most representative classes of terpenes. DPPH (IC₅₀ value 26.1 ± 0.5 μg/mL) and BCB (68.3 ± 1.5%) values indicated a significant antioxidant activity. The essential oil strongly inhibited Staphylococcus aureus (MIC 15 ± 0.1 μg/mL), Escherichia coli (MIC 25 ± 0.2 μg/mL) and Candida albicans (MIC 5 ± 0.1 μg/mL). The results give a deeper understanding of the chemical composition and report for the first time the antioxidant and antimicrobial potential of the C. guazumifolia essential oil.     

Plants as resources for organic molecules: Facing the green and sustainable future today

Over the last century, the conventional and linear production system has significantly influenced the socio-environment globally. The transition to a more circular production system, aiming at maintaining the value of products and resources for as long as possible, is an opportunity to create innovative processes that are regenerative by intention. This means replacing the end-of-life concept with restoration, renewable energy use and by- or co-products as well as eliminating toxic chemicals by developing and using redesigned materials, procedures and business models. In this context, the main objective of this paper is to present a critical overview related to the most recent green and sustainable extraction or separation approaches to remove organic molecules from plant-derived resources, specifically agro-industrial and forestry waste using circular processing systems in operation in the last four years.     

New Rare‐Earth Metal Germanides RE2Ge9 (RE = Nd,Sm) by Thermal Decomposition of High‐Pressure Phases REGe5

The rare‐earth metal germanides RE₂Ge₉ (RE = Nd, Sm) have been prepared by thermal decomposition of the metastable high‐pressure phases REGe₅ at ambient pressure. The compounds adopt an orthorhombic unit cell with a = 396.34(4) pm; b = 954.05(8) pm and c = 1238.4(1) pm for Nd₂Ge₉ and a = 395.46(7) pm; b = 946.4(2) pm and c = 1232.1(3) pm for Sm₂Ge₉. Crystal structure refinements reveal space group Pmmn (No. 59) for Nd₂Ge₉. The atomic pattern resembles an ordered defect variety of the pentagermanide motif REGe₅ (RE = La; Nd, Sm, Gd, Tb) comprising corrugated germanium layers. These condense into a three‐dimensional network interconnected by eight‐coordinated germanium atoms. The resulting framework channels along [100] enclose the neodymium atoms. With respect to the atomic arrangement of the pentagermanides, half of the interlayer germanium atoms are eliminated in an ordered way so that occupied and empty germanium columns alternate along [001]. The rare‐earth metal atoms of both types of compounds, REGe₅ and RE₂Ge₉, exhibit the electronic states 4f ³ and 4f ⁵ (oxidation state +3) for neodymium and samarium, respectively, evidencing that the modification of the germanium network leaves the electron configuration of the metal atoms unaffected.     

Magnetically Aligned Supramolecular Hydrogels

The magnetic‐field‐induced alignment of the fibrillar structures present in an aqueous solution of a dipeptide gelator, and the subsequent retention of this alignment upon transformation to a hydrogel upon the addition of CaCl₂ or upon a reduction in solution pH is reported. Utilising the switchable nature of the magnetic field coupled with the slow diffusion of CaCl₂, it is possible to precisely control the extent of anisotropy across a hydrogel, something that is generally very difficult to do using alternative methods. The approach is readily extended to other compounds that form viscous solutions at high pH. It is expected that this work will greatly expand the utility of such low‐molecular‐weight gelators (LMWG) in areas where alignment is key.     

Domain wall relaxation,creep, sliding,and switching in superferromagnetic discontinuous Co(80)Fe(20)/Al(2)O3 multilayers

The ac susceptibility of a superferromagnetic discontinuous multilayer [Co(80)Fe20(1.4 nm)/Al(2)O3(3 nm)](10) is measured as a function of temperature, frequency, and field amplitude and compared to static and dynamic hysteresis loops. Its properties are successfully mapped onto the predicted [T. Nattermann, V. Pokrovsky, and V. M. Vinokur, Phys. Rev. Lett. 87, 197005 (2001)]] dynamical phase transitions, which link the relaxation, creep, sliding, and switching regimes of pinned domain walls.     

The optical theorem and forward glory effects in heavy-ion scattering

A detailed discussion of the optical theorem for heavy-ion scattering is given. It is pointed out that a careful application of this theorem to light heavy-ion systems may yield information about the nuclear interaction at distances corresponding to forward glory trajectories. Applications to several cases are presented.     

On the structure of inner ideals of nest algebras

IfA is a nest algebra andA _s=A ∩ A* , whereA* is the set of the adjoints of the operators lying inA, then the pair (A, A _s) forms a partial Jordan *-triple. Important tools when investigating the structure of a partial Jordan *-triple are its tripotents. In particular, given an orthogonal family of tripotents of the partial Jordan *-triple (A, A _s), the nest algebraA splits into a direct sum of subspaces known as the Peirce decomposition relative to that family. In this paper, the Peirce decomposition relative to an orthogonal family of minimal tripotents is used to investigate the structure of the inner ideals of (A, A _s), whereA is a nest algebra associated with an atomic nest. A property enjoyed by inner ideals of the partial Jordan *-triple (A, A _s) is presented as the main theorem. This result is then applied in the final part of the paper to provide examples of inner ideals. A characterization of the minimal tripotents as a certain class of rank one operators is also obtained as a means to deduce the principal theorem.     

Characterization of the volatile fraction emitted by Pinus spp. by one- and two-dimensional chromatographic techniques with mass spectrometric detection

The chemical composition of the needles of P. pinea, P. pinaster, P. halepensis, P. nigra, P. brutia, P. patula, P. radiata, P. taeda, P. elliotti, P. kesiya, P. sylvestris and P. eldarica was investigated. Headspace solid-phase microextraction and steam distillation extraction were used to collect the volatile fractions. Samples were analyzed using one-dimensional gas chromatography (1D-GC) and comprehensive two-dimensional gas chromatography (GC × GC) associated with a quadrupole and a time-of-flight mass detectors. Results showed that the analytical capabilities of 1D-GC are partially limited by the separation power of the columns. The higher sensibility and the absence of peak skewing of the time-of-flight mass analyzer, with the use of automated peak finding and deconvolution algorithms, allowed for the detection of trace components with qualitative full spectra and the extraction of true mass spectra from coeluting compounds, promoting their reliable identification and thus significantly improving results obtained by 1D-GC/MS, when using a quadrupole mass analyzer. The use of GC × GC resulted in enhanced separation efficiency and increased signal to noise ratio (sensitivity) of the analytes, maximizing mass spectra quality and improving compound detection and identification. This work shows the use of 1D-GC/ToFMS for the analysis of pine needles volatiles, achieving the detection of 177 compounds, that is more than twice the number previously identified by standard 1D-GC/MS. The analysis by GC × GC for the same sample allowed the detection of 212 compounds. The enantioselective GC × GC analysis performed for all the Pinus spp. under study achieved the detection of 422 different compounds. Cross-over phenomena according to operational conditions are highlighted and discussed.