Preparation of Lewis acid ionic liquids for one-pot synthesis of benzofuranol from pyrocatechol and 3-chloro-2-methylpropene

Several Lewis acid ionic liquids (LAILs) with different acidic scales were synthesised and used as catalysts for the synthesis of benzofuranol by condensation of pyrocatechol and 3-chloro-2-methylpropene in one pot. The catalytic activity of these ionic liquids was correlated with their Lewis acidity. Low to moderate conversion with excellent selectivity to benzofuranol was obtained in the presence of the appropriate LAILs. Compared to the two-step synthetic method currently used in industry, a higher yield plateau (81.1%) of benzofuranol was achieved in the presence of [BMIm][AlCl₄] IL as catalyst at 418 K after 4 h. Furthermore, the catalyst is readily separated from the resultant products via decantation and could be reused after treatment in vacuum.     

Robust model-based predictive control of exothermic chemical reactor

A case study of the robust model-based predictive control (MPC) of an exothermic continuous stirred tank reactor (CSTR) with uncertain parameters is presented. Three robust MPC approaches are considered and the simulation results are compared in terms of quality of control performance and total consumption of coolant. The results reveal the main benefits of the considered approaches and confirm that the robust MPC can bring about a reduction in consumption of the coolant.     

Effect of alkylated diphenylamine on thermal-oxidative degradation behavior of poly-<Emphasis Type="Italic">α</Emphasis>-olefin

An oil-soluble antioxidant, alkylated diphenylamine (ADPA), was prepared by alkylation of diphenylamine. The influence of ADPA on the thermal-oxidative stability of poly-α-olefin (PAO8) was evaluated by thermogravimetry (TG). For comparison, the thermal-oxidative stability of PAO8 with zinc dialkyl dithiophosphate (ZDDP) was also investigated. Activation energy (E_a)of the corresponding thermal-oxidative degradation process was evaluated by the Flynn-Wall-Ozawa (FWO) and Kissinger-Akahira-Sunose (KAS) methods. To demonstrate the reliability of the kinetic study, the antioxidant performance of ADPA and ZDDP in PAO8 was also studied by the pressure drop (PDT) and accelerated oxidation (AOT) tests. The results indicate that ADPA has better antioxidant ability than ZDDP in increasing the E_a value and enhancing the oxidative stability of PAO8. Good correlation between the applied test methods was established.     

Density of lithium fluoride—lithium carbonate-based molten salts

The density of the LiF-Li₂CO₃ melts system was measured using the Archimedean method. Using the quadratic regression orthogonal design with two factors, a regression equation for the density of LiF-Li₂CO₃ melts was obtained in which the concentration of LiF and temperature were considered. The results indicated that the density of the LiF-Li₂CO₃ melts decreased with either increasing the concentration of LiF or increasing temperature; a linear relation was observed between density and temperature. In addition, the influences of NaF, KF, NaCl, and KCl additives on the densities of the given systems were studied. The addition of NaF and KF increased the density of the melts, whereas NaCl and KCl resulted in an initial increase and subsequent decrease with an increasing additive concentration. The density attained a maximum at NaCl and KCl mass fraction of approximately 15%.     

Efficient method for the synthesis of polysubstituted 2,6-dicyanoanilines by one-pot three-component tandem reaction of malononitrile with <Emphasis Type="Italic">α</Emphasis>,<Emphasis Type="Italic">β</Emphasis>-unsaturated imines

A facile and efficient one-pot synthesis of polysubstituted benzenes was achieved via the Michael addition of malononitrile with α,β-unsaturated imines and a sequential tandem reaction. This reaction generates polysubstituted 2,6-dicyanoanilines in high yields (15 examples, isolated yields of 57–91 %), and proceeds under mild reaction conditions (60°C, 10 min). In addition, a possible mechanism accounting for the reaction is proposed.     

The significance of a second adsorption phase with weakly adsorbed species for the calculation of the surface concentrations of a mixture: methanol–DME and methanol–ethene adsorption in SAPO-34

With the calorimetric (adsorption heat versus coverage) curve also measured together with the adsorption isotherm, the simultaneous use of both curves showed that there were two phases of adsorption in the adsorption of methanol, dimethyl ether, ethene and propane in SAPO-34. The dual-site Langmuir equation gave good fits to the adsorption data to support the interpretation that a second (type 2) adsorption phase occurred in the high-pressure region in addition to a first (type 1) adsorption phase on the acid sites at lower pressures. Adsorption experiments and calculations using binary gas mixtures showed that due to the existence of two types of adsorption, the multicomponent Langmuir isotherm equation (Langmuir competitive adsorption model) calculated incorrect surface concentrations when the concentrations were high. In contrast, the ideal adsorbed solution theory (IAST) calculated correct surface concentrations in the adsorption of mixtures.     

A Zinc(II) Photocage Based on a Decarboxylation Metal Ion Release Mechanism for Investigating Homeostasis and Biological Signaling

Metal ion signaling in biology has been studied extensively with ortho‐nitrobenzyl photocages; however, the low quantum yields and other optical properties are not ideal for these applications. We describe the synthesis and characterization of NTAdeCage, the first member in a new class of Zn²⁺ photocages that utilizes a light‐driven decarboxylation reaction in the metal ion release mechanism. NTAdeCage binds Zn²⁺ with sub‐pM affinity using a modified nitrilotriacetate chelator and exhibits an almost 6 order of magnitude decrease in metal binding affinity upon uncaging. In contrast to other metal ion photocages, NTAdeCage and the corresponding Zn²⁺ complex undergo efficient photolysis with quantum yields approaching 30 %. The ability of NTAdeCage to mediate the uptake of ⁶⁵Zn²⁺ by Xenopus laevis oocytes expressing hZIP4 demonstrates the viability of this photocaging strategy to execute biological assays.     

New approach for natural products screening by real-time monitoring of hemoglobin hydrolysis using quartz crystal microbalance

The hemoglobin (Hb) released from erythrocytes is a primary nutritive component for many blood-feeding parasites. The aspartic protease cathepsin D is a hemoglobinase that is involved in the Hb degradation process and is considered an interesting target for chemotherapy intervention. However, traditional enzymatic assays for studying Hb degradation utilize spectrophotometric techniques, which do not allow real-time monitoring and can present serious interference problems. Herein, we describe a biosensor using simple approach for the real-time monitoring of Hb hydrolysis as well as an efficient screening method for natural products as enzymatic inhibitors using a quartz crystal microbalance (QCM) technique. Hemoglobin was anchored on the quartz crystal surface using mixed self-assembled monolayers. The addition of the enzyme caused a mass change (frequency shift) due to Hb hydrolysis, which was monitored in real time. From the frequency change patterns of the Hb-functionalized QCM, we evaluated the enzymatic reaction by determining the kinetic parameters of product formation (k_cat). The QCM enzymatic assay using immobilized human Hb was shown to be an excellent approach for screening possible inhibitors in complex mixtures, opening up a new avenue for the discovery of novel inhibitors.