Cyclic Conjugation Effects in Cyclacenes

Abstract

Cyclic conjugation is studied in Hückel and Möbius cyclacenes as well as in a few other related open-chain and cyclic belt-shaped hydrocarbons (e.g., zig-zag cyclarenes). the main conclusions are that (a) the energy effect of the conjugation along the perimeter of cyclacenes is relatively large, (b) conjugation along the 6 -, 10 - and 14-membered cycles has a much greater effect, in spite of the fact that these cycles embrace bonds that formally are not involved in cyclic conjugation. Möbius cyclacenes are non-alternant hydrocarbons and their odd-cycles have a significant contribution to conjugation. the contribution of conjugation in individual cycles to the total resonance energy is briefly discussed.     

Effects of LiF on the Structure and Properties of Ba0.85Ca0.15Zr0.1Ti0.9O3 Lead‐Free Piezoelectric Ceramics

Preparation of Ba_0.85Ca_0.15Zr_0.1Ti_0.9O₃ (BCZT) lead‐free piezoelectric ceramics with different amounts of LiF (BCZT‐xLiF) was done, and the effects of the LiF doping on the phase transition behavior and the electrical properties of the resulting ceramic were investigated. The experimental results showed that the polymorphic rhombohedral‐tetragonal phase transition temperature was found shifted toward room temperature with the Li doping. The study showed that BCZT lead‐free piezoelectric ceramic with improved performance properties at room temperature can be achieved by shifting the polymorphic phase transition point nearer room temperature through the addition of LiF.     

Evolution and stability of 2-mercaptobenzimidazole inhibitor film upon Al alloy 6061

Journal of Applied Electrochemistry - Organic corrosion inhibitors have become competent alternatives to hazardous chrome conversion coatings due to their rapid adsorption over metal surfaces in...     

Effects of mutations in the calcium-binding sites of recoverin on its calcium affinity: evidence for successive filling of the calcium binding sites

A molecule of the photoreceptor Ca²⁺-binding protein recoverincontains four potential EF-hand Ca²⁺-binding sites, of whichonly two, the second and the third, are capable of binding calciumions. We have studied the effects of substitutions in the second,third and fourth EF-hand sites of recoverin on its Ca²⁺-bindingproperties and some other characteristics, using intrinsic fluorescence,circular dichroism spectroscopy and differential scanning microcalorimetry.The interaction of the two operating binding sites of wild-typerecoverin with calcium increases the protein's thermal stability,but makes the environment around the tryptophan residues moreflexible. The amino acid substitution in the EF-hand 3 (E121Q)totally abolishes the high calcium affinity of recoverin, whilethe mutation in the EF-hand 2 (E85Q) causes only a moderatedecrease in calcium binding. Based on this evidence, we suggestthat the binding of calcium ions to recoverin is a sequentialprocess with the EF-hand 3 being filled first. Estimation ofCa²⁺-binding constants according to the sequential binding schemegave the values 3.7 x 10⁶ and 3.1 x 10⁵ M^–1 for thirdand second EF-hands, respectively. The substitutions in theEF-hand 2 or 3 (or in both the sites simultaneously) do notdisturb significantly either tertiary or secondary structureof the apo-protein. Amino acid substitutions, which have beendesigned to restore the calcium affinity of the EF-hand 4 (G160D,K161E, K162N, D165G and K166Q), increase the calcium capacityand affinity of recoverin but also perturb the protein structureand decrease the thermostability of its apo-form.     

Anodic stripping voltammetric measurement of trace heavy metals at antimony film carbon paste electrode

The antimony film carbon paste electrode (SbF-CPE) was prepared in situ on the carbon paste substrate electrode as a “mercury-free” electrochemical sensor. Its aptitude for measuring some selected trace heavy metals has been demonstrated in combination with square-wave anodic stripping voltammetry in non-deaerated model solutions of 0.01 M hydrochloric acid with pH 2. Some important operational parameters, such as deposition potential, deposition time, and concentration of antimony ions were optimized, and the electroanalytical performance of the SbF-CPE was critically compared with both bismuth film carbon paste electrode (BiF-CPE) and mercury film carbon paste electrode (MF-CPE) using Cd(II) and Pb(II) as test metal ions. In comparison with BiF-CPE and MF-CPE, the SbF-CPE exhibited superior electroanalytical performance in more acidic medium (pH 2) associated with favorably low hydrogen evolution, improved stripping response for Cd(II), and moreover, stripping signals corresponding to Cd(II) and Pb(II) at the SbF-CPE were slightly narrower than those observed at bismuth and mercury counterparts. In addition, the comparison with antimony film electrode prepared at the glassy carbon substrate electrode displayed higher stripping current response recorded at the SbF-CPE. The newly developed sensor revealed highly linear behavior in the examined concentration range from 5 to 50 μg L⁻¹, with limits of detection (3σ) of 0.8 μg L⁻¹ for Cd(II), and 0.2 μg L⁻¹ for Pb(II) in connection with 120 s deposition step, offering good reproducibility of ±3.8% for Cd(II), and ±1.2% for Pb(II) (30 μg L⁻¹, n = 10). Preliminary experiments disclosed that SbF-CPE and MF-CPE exhibit comparable performance for measuring trace concentration levels of Zn(II) in acidic medium with pH 2, whereas its detection with BiF-CPE was practically impossible. Finally, the practical applicability of SbF-CPE was demonstrated via measuring Cd(II) and Pb(II) in a real water sample.     

Insights into the simultaneous chronopotentiometric stripping measurement of indium(III), thallium(I) and zinc(II) in acidic medium at the in situ prepared antimony film carbon paste electrode

The simultaneous measurement of microgram per liter concentration levels of indium(III), thallium(I) and zinc(II) at the antimony film carbon paste electrode (SbF-CPE) is demonstrated. The antimony film was deposited in situ on a carbon paste substrate electrode and employed in chronopotentiometric stripping mode in deoxygenated solutions of 0.01 M hydrochloric acid (pH 2). The chronopotentiometric stripping performance of the SbF-CPE was studied and compared with constant current chronopotentiometric stripping and anodic stripping voltammetric operation. In comparison with its bismuth and mercury counterparts, the SbF-CPE exhibited advantageous electroanalytical performance; namely, at the bismuth film electrode, the measurement of zinc(II) was practically impossible due to hydrogen evolution, whereas the mercury film electrode exhibited a poorly developed signal for thallium(I). The SbF-CPE revealed favorable calculated LoDs (3σ) of 1.4 μg L⁻¹ for thallium(I) and 2.4 μg L⁻¹ for indium(III) along with good linear response in the examined concentration range from 10 to 100 μg L⁻¹ with correlations coefficients (R²) of 0.992 for thallium(I) and 0.994 for indium(III) associated with a 120 s deposition time. The chronopotentiometric stripping performance of the SbF-CPE was characterized also by satisfactory reproducibility of 1.62% for indium(III), 3.96% for thallium(I) and 2.11% for zinc(II) (c = 40 μg L⁻¹, n = 11).     

Composites of poly(vinyl acetate) filled with calcium carbonate: Microscopy,diffractometry and thermophysical properties

Calcium carbonate (CaCO₃) is used as filler in poly(vinyl acetate)(PVAc) composites to enhance the mechanical properties. The filler is often commercially surface treated with stearic acid to optimize the interfacial bonding and wetting. The effects of the interface on properties were studied using scanning electron microscopy (SEM) of films with initial and deformed morphologies. Plasticizing additives cause a significant change in the appearance of the films and a reduction in the glass transition temperature of the matrix from 40°C to ≈ 18°C, which was not altered by further addition of the filler. A PVAc composite fracture surface shows the particles adhering well to the matrix, suggesting good adhesion and reinforcement. The SEM study is complemented by WAXD, SEM/X-SEM, XPS, and thermal analysis.     

Ecological Example of Conditioned Flavor Aversion in Plant–Herbivore Interactions: Effect of Terpenes of Eucalyptus Leaves on Feeding by Common Ringtail and Brushtail Possums

We investigated the hypothesis that feeding deterrence of common ringtail possums (Pseudocheirus peregrinus) and common brushtail possums (Trichosurus vulpecula) by Eucalyptus terpenes (in this case 1,8-cineole) is a result of a conditioned flavor aversion (CFA), due to the association of terpenes with postingestive effects of another group of Eucalyptus toxins, the diformylphloroglucinol compounds (DFPCs). Wild-caught common ringtail and common brushtail possums showed a dose-dependent reduction in food intake when 1,8-cineole was added to the diet. However, after continued exposure over 12 days to increasing amounts of cineole in the diet, both species substantially increased their intakes of cineole relative to control animals. This indicated that the aversion to cineole was a conditioned response rather than a physiological limitation in their ability to detoxify terpenes. Subsequent exposure to a diet including both cineole and jensenone (a simple DFPC also found in Eucalyptus and considered to cause postingestive emesis) in corresponding amounts was able to recondition the dose-dependent aversion. Consequently, animals that had been given jensenone showed an aversion to cineole-rich diets that matched the behavior of animals in the control group. This supported our hypothesis that the effect of terpenes on feeding of these marsupial folivores on Eucalyptus is due to a CFA. Possums can cope with levels of terpenes in the diet that far exceed those occurring naturally. The role of terpenes in marsupial folivore–Eucalyptus interactions appears to be to act as a cue to levels of toxic DFPCs in the leaves, rather than acting as toxins in their own right.     

Integrated Approach for Supporting Sustainable Water Resources Management of Irrigation Based on the WEFN Framework

Irrigated agriculture plays a vital role for the socio-economic development of the Mediterranean area, although it has significant impacts on both water and energy resources. Therefore, in a context in which water resources are also experiencing increasing pressures, there is an urgent need for supporting their sustainable management. This may be an extremely challenging task, especially at the local scale, due to the several interconnected dynamics affecting the state of a complex irrigation system. In fact, multiple actors are involved in decision-making processes, and the use of natural resources (and their mutual interactions) strongly depends on their behaviors, which affect the system as a whole. In this context, the present study proposes an integrated methodology, based on the Water Energy Food Nexus (WEFN), specifically focused on the sustainable management of water resources for irrigation. Firstly, a model based on Causal Loop Diagrams (CLD) is developed in order to get a deep insight into the key dynamics behind a complex irrigation system. Secondly, three indices based on the “footprint” concept are identified, in order to synthesize such dynamics. The integration of these two approaches support investigating the whole system and, particularly, understanding the influence of multiple decisional actors on it, as well as the role of a set of key drivers and constraints. This might also allow drawing some relevant conclusions, useful for supporting effective decisions oriented to a sustainable water resources management. Specific reference is made to a case study, the Capitanata irrigation system, located in the Southern Italy.