The Effects of Benzene on the Structure and Properties of Triethylamine Hydrochloride/Chloroaluminate

The effects of benzene (C6H6) on the radial distribution function, coordination number, spatial distribution function, physical and chemical properties such as density, viscosity, conductivity and transport properties of triethylamine hydrochloride /chloroaluminate ([Et3NH] Cl/AlCl3) ionic liquid were studied by first principle and molecular dynamics simulation. The stable geometry and electronic properties of benzene and ionic liquids, as well as their optimized adsorption on Cu (111) surface were obtained. The density, viscosity and conductivity obtained agreed well with the experimental values. It is found that the adsorption of cations, anions and benzene on Cu (111) surface is physical adsorption, and the adsorption capacity is [Et3NH] > C6H6 > Al2Cl7−. With the increase of benzene concentration, the density of the system decreases gradually, the interaction between cations and anions gradually weakens, resulting in the decrease of viscosity, the enhancement of diffusion and the increase of conductivity. Since the diffusion and adsorption capacity of benzene are greater than that of electroactive ion of Al2Cl7−, benzene would be easier to adsorb on the protruding part of the electrode surface, so as to reduce the effective surface area of the cathode, slow down the reduction speed of Al2Cl7− on the cathode surface and increase the over-potential, so the grain refined deposition layers can be obtained in electrodeposition.

Chemical inhibition of lycopene β-cyclases unmask operation of phytoene synthase 2 in ripening tomato fruits

In ripening tomato fruits, the leaf-specific carotenoids biosynthesis mediated by phytoene synthase 2 (PSY2) is replaced by a fruit-specific pathway by the expression of two chromoplast-specific genes: phytoene synthase 1 (PSY1) and lycopene-β-cyclase (CYCB). Consequently, mutations in those two and other genes contributing to intermediate steps render the ripened tomato fruits bereft of lycopene. To decipher whether PSY2-mediated pathway also operates in ripening fruits, we blocked the in vivo activity of lycopene-β-cyclases by injecting CPTA (2-(4-Chlorophenylthio) triethylamine hydrochloride), an inhibitor of lycopene-β-cyclases. The injection of CPTA induced accumulation of lycopene in leaves, immature-green and ripening fruits. Even, in tomato mutants deficient in fruit-specific carotenoid biosynthesis such as V7 and r (PSY1), and ζ-carotene isomerase (ZISO), CPTA triggered lycopene accumulation. The CPTA-treated ziso mutant fruits, where PSY1 remains functional, accumulated phytoene and phytofluene. Conversely, CPTA-treated PSY1-knockout mutant (r3756) fruits did not accumulate phytoene and phytofluene. CPTA-treated fruits were enriched in lycopene-derived volatiles and had reduced ABA levels. The lycopene accumulation was associated with the partial transformation of chloroplasts to chromoplasts bearing thread-like crystalline structures, indicating lycopene accumulation. Our study shows that inhibition of lycopene β-cyclases unmasks the operation of a parallel carotenoid biosynthetic pathway mediated by PSY2 in ripening tomato fruits.

Mixed Chlorometallate Ionic Liquids as C4 Alkylation Catalysts: A Quantitative Study of Acceptor Properties

The acceptor properties of mixed chlorometallate ionic liquids for isobutane-butene alkylation (C4 alkylation) reaction were studied. These ionic liquids were prepared by mixing metal chlorides with either triethylamine hydrochloride or 1-butyl-3-methylimidazolium chloride in various molar ratios. Using triethylphosphine oxide as a probe, Gutmann Acceptor Numbers (AN) of the catalysts were determined, and the Lewis acidity of mixed chlorometallate ionic liquids was quantitatively measured. Additionally, AN value was developed to determine the relationship between Lewis acidity and catalytic selectivity. The favorite AN value for the C4 alkylation reaction should be around 93.0. The [(C2H5)3NH]Cl–AlCl3−CuCl appears to be more Lewis acidity than that of [(C2H5)3NH]Cl–AlCl3. The correlation of the acceptor numbers to speciation of the mixed chlorometallate ionic liquids has also been investigated. [AlCl4]−, [Al2Cl7]−, and [MAlCl5]− (M = Cu, Ag) are the main anionic species of the mixed chlorometallate ILs. While the presence of [(C2H5)3N·M]+ cation always decreases the acidity of the [(C2H5)3NH]Cl−AlCl3−MCl ionic liquids.

Manganese(III) Porphyrin as Electrocatalyst for Hydrogen Evolution Reaction

5,10,15,20-tetraphenyl-21H,23H-porphine manganese(III) chloride (Mn(TPP)Cl) has been evaluated as electrocatalyst for Hydrogen Evolution Reaction (HER) in the presence of triethylamine hydrochloride (Et3NHCl) as source of proton. The direct reduction of Et3NHCl on vitreous carbon electrode occurs at Ep -1.6 V vs Ag/AgCl in [Bu4N][BF4]-CH3CN. Interestingly, in the presence of Mn(TPP)Cl as electrocatalyst the reduction potential shifts to -1.20 V. Based on gas chromatography analysis, the formation of H2 gas, with a current efficiency of ca. 58% after 2 h, is observed with a yield of 8 μmoles and a turnover of 2.5. However, the chemical yield at carbon electrode was about 35%. These results reflect the exquisite electrocatalytic efficiency of Mn(TPP)Cl in Hydrogen Evolution Reaction (HER).

Triethylamine-based catalysts for the melt polymerization of carbonate monomers

Triethylamine hydrochloride and triethylamine catalyze the melt polymerization of carbonate monomers faster than stannous octoate.

The ferrocene effect: enhanced electrocatalytic hydrogen production using meso-tetraferrocenyl porphyrin palladium(ii) and copper(ii) complexes

Copper(ii) and palladium(ii) meso-tetraferrocenylporphyrins (CuTFcP and PdTFcP) were employed as catalysts for electrochemical proton reduction in DMF using trifluoroacetic acid (TFA) or triethylamine hydrochloride (TEAHCl) as acids.