Acid Chloride Research Articles

Bis-tris-based polyester nanofiltration membranes fabricated via one-step interfacial polymerization for desalination

To obtain high-performance polyester (PE) nanofiltration (NF) membranes for desalination, most PE NF membranes are fabricated with high aqueous monomer concentration, or high reaction temperature, or long reaction time. The interfacial polymerization (IP) reaction rate between hydroxyl groups and acyl chloride groups is promoted but the cost of membrane fabrication is also increased. In this work, Bis-tris (bis(2-hydroxyethyl)-amino-tris(hydroxymethyl)methane) with rich hydroxyl groups is first utilized as an aqueous monomer to fabricate PE membranes under conventional IP conditions. The fabricated Bis-tris PE membranes feature strong hydrophilicity, excellent electronegativity, and ultra-thin selective layers, which are conducive to improving desalination performance. The optimized Bis-tris PE membrane shows excellent water permeance of 22.5 L m−2 h−1 bar−1 and a satisfactory Na2SO4 rejection of 96.9 %. Additionally, the Bis-tris PE membrane displays superior long-term stability and chlorine resistance under 96 h cross-flow filtration. This research enlightens the promising potential of Bis-tris as a novel and economic aqueous monomer for the fabrication of high-performance PE NF membranes.

A recoverable hydrophilic deep eutectic solvent for efficient extraction of polyphenolic compounds from raspberry root.

Green deep eutectic solvents (DESs) are widely used to extract bioactive components from plant biomass; however, hydrophilic DES and bioactive component isolation methods have not been developed. In this study, we synthesized hydrophilic DES (CL-CA-DES) using citric acid and choline chloride. We combined this with environmentally friendly anion- and cation-exchange resin column chromatographic isolation methods. This approach extracted and isolated four polyphenolic compounds (catechins, epicatechins, procyanidin B1, and procyanidin B2) from raspberry root and efficiently recovered the hydrophilic DES. CL-CA-DES extracted significantly higher contents of catechin and procyanidin B2 from raspberry root compared to other solvents. It also extracted substantially higher contents of epicatechin compared to butyl alcohol, 70% ethanol, and water, but there was no significant difference when compared with acetone and ethyl acetate. Additionally, CL-CA-DES extracted significantly higher contents of procyanidin B1 compared to butyl alcohol, water, and ethyl acetate, with no significant difference when compared with 70% ethanol and acetone. The isolation efficiency of the bioactive components in the raspberry root extract by anion- and cation-exchange resin column chromatography was higher than that of the organic solvent extraction and precipitation generation methods, and the method was effective in recovering CL-CA-DES with a recovery rate higher than 60%. In conclusion, this study developed a new method for the efficient recovery of hydrophilic CL-CA-DES, which can be used for isolating polyphenolic compounds from raspberry root.

Enhanced photocatalytic hydrogen evolution using dual templates of sulfur-doped carbon nitride

The band structure of semiconducting photocatalysts plays a crucial role in determining their charge carrier transport characteristics and photocatalytic activity. In this work, a simple method to modulate the band structures of carbon nitride by infusing dopants and porous materials is experimentally demonstrated. A combination of trithiocyanuric acid and ammonium chloride to calcinate in an air environment, sulfur dopants and a significant amount of porosity are infused into carbon nitride concurrently. The sulfur-doped and porous carbon nitride material shows remarkable performance in photocatalytic hydrogen production, achieving a maximum hydrogen evolution rate of 4516.84 μmol g−1 h−1. Furthermore, infusion of sulfur dopants and abundant porous into carbon nitride allows for substantial and continuous tuning of the conduction and valence band positions. The band structures modulation enhanced the optical absorption in visible light region, making it suitable for efficient solar energy conversion. The findings of this work are feasible to pave a foundation for future clean energy technology.

Silencing of GhSINAT5 Reduces Drought Resistance and Salt Tolerance in Cotton.

The SEVEN IN ABSENTIA (SINA) E3 ubiquitin ligase is widely involved in drought and salt stress in plants. However, the biological function of the SINA proteins in cotton is still unknown. This study aimed to reveal the function of GhSINAT5 through biochemical, genetic and molecular approaches. GhSINAT5 is expressed in several tissues of cotton plants, including roots, stems, leaves and cotyledons, and its expression levels are significantly affected by polyethylene glycol, abscisic acid and sodium chloride. When GhSINAT5 was silenced in cotton plants, drought and salinity stress occurred, and the length, area and volume of the roots significantly decreased. Under drought stress, the levels of proline, superoxide dismutase, peroxidase and catalase in the GhSINAT5-silenced cotton plants were significantly lower than those in the non-silenced control plants, whereas the levels of hydrogen peroxide and malondialdehyde were greater. Moreover, the expression of stress-related genes in silenced plants under drought stress suggested that GhSINAT5 may play a positive role in the plant response to drought and salt stress by regulating these stress response-related genes. These findings not only deepen our understanding of the mechanisms of drought resistance in cotton but also provide potential targets for future improvements in crop stress resistance through genetic engineering.

Capsaicin mimic-based antifouling and antibacterial polyester nanofiltration membranes with tunable crosslinked structures

Polyester thin-film composite (PE TFC) nanofiltration membranes based on the interfacial polymerization (IP) of polyols/polyphenols and acyl chloride continue to attract considerable attention for textile wastewater treatment due to their excellent antifouling properties. Herein, N-(5-methyl acrylamide-2,3,4 hydroxy benzyl) acrylamide (AMTHBA), a polyphenol-inspired capsaicin derivative, was first utilized as an aqueous monomer for the preparation of antifouling and antibacterial PE TFC membranes via the IP process. The moderate reactivity of AMTHBA and its unique solubility enabled a rational control of the crosslinking density of PE membranes, allowing the formation of structures from loose to dense through an adjustment of the AMTHBA concentration. The densely crosslinked AM-TMC PE membrane exhibited favorable desalination performance, with a water permeance of 21.8 L m−2 h−1 bar−1 and a Na2SO4 rejection of 83.8 %. The loosely crosslinked AM-TMC PE membrane exhibited excellent dye/salt separation performance, with high dye rejections (e.g., 98.5 % for MB) and low salt rejections (e.g., 4.0 % for NaCl), as well as high water permeance (30.4 L m−2 h−1 bar−1). In contrast, the capsaicin-containing PE TFC membranes also demonstrated markedly enhanced resistance to bacterial growth and organic fouling. These findings indicate that AM-TMC PE membranes present novel avenues for the advancement of task-specific separation membranes.

Enhancing the Electrical Conductivity and Long-Term Stability of PEDOT:PSS Electrodes through Sequential Treatment with Nitric Acid and Cesium Chloride.

Solution-processable poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) is an important polymeric conductor used extensively in organic flexible, wearable, and stretchable optoelectronics. However, further enhancing its conductivity and long-term stability while maintaining its superb mechanical properties remains challenging. Here, a novel post-treatment approach to enhance the electrical properties and stability of sub-20-nm-thin PEDOT:PSS films processed from solution is introduced. The approach involves a sequential post-treatment with HNO3 and CsCl, resulting in a remarkable enhancement of the electrical conductivity of PEDOT:PSS films to over 5500 S cm-1, along with improved carrier mobility. The post-treated films exhibit remarkable air stability, retaining over 85% of their initial conductivity even after 270 days of storage. Various characterization techniques, including X-ray photoelectron spectroscopy, atomic force microscopy, Raman spectroscopy, Hall effect measurements, and grazing incidence wide angle X-ray scattering, coupled with density functional theory calculations, provide insights into the structural changes and interactions responsible for these improvements. To demonstrate the potential for practical applications, the ultrathin PEDOT:PSS films are connected to an inorganic light-emitting diode with a battery, showcasing their suitability as transparent electrodes. This work presents a promising approach for enhancing the electrical conductivity of PEDOT:PSS while offering a comprehensive understanding of the underlying mechanisms that can guide further advances.

In situ encapsulation of capsaicinoids in MIL-88A as a food-grade nanopreservative for meat safety

The biocompatible MIL-88A metal-organic framework (MOF), synthesized from food-grade fumaric acid and ferric chloride, was introduced for the efficient one-step in situ encapsulation of capsaicinoids as a nanopreservative. The resulting MIL-88A@Caps nanoparticles can load 61.43 mg/g of capsaicinoids, surpassing conventional MOF-based encapsulation. The potent MIL-88A@Caps nanoformulations synergize the intrinsic antimicrobial properties of MIL-88A and capsaicinoids. At the same concentration (0.5 mg/mL), MIL-88A@Caps was highly effective against S. aureus and Salmonella, with inhibition rates of 94.90 ± 0.58% and 94.30 ± 1.24%, respectively, compared to MIL-88A (62.28 ± 5.04% and 70.46 ± 1.96%) and capsaicinoids (63.68 ± 1.25% and 49.53 ± 1.22%), respectively. Model precooked-chicken preservation experiments revealed that MIL-88A@Caps significantly delayed spoilage parameters compared to untreated samples, with more favorable viable counts (8.08 lgCFU/g), pH value (6.60 ± 0.02), TVB-N value (8.59 ± 0.21 mg/100 g), and color changes on day 9. Our findings yield a green nanopreservative for meat safety.

Investigation study of methyl violet photodegradation over alginate-carboxymethyl cellulose/titanium(IV) oxide/covalent organic frameworks bio-nanocomposite beads under ultraviolet irradiation

Concerned about water treatment, it is of great importance to present new approaches for improving photocatalytic activity. Since photocatalysis is ubiquitous in almost all chemical manufacturing processes, the development of photocatalytic systems carries significance for our environment. In this regard, three different amounts of covalent organic frameworks decorated with titanium(IV) oxide nanoparticles (TiO2/COF hybrids) in Alginate-Carboxymethyl cellulose (Alg-CMC) blend matrix were prepared under ultrasound irradiation, which Citric acid and Calcium chloride acted as two green cross-linkages. Based on the physio-chemical analyses of these bio-nanocomposite (bio-NC) beads, the Alg-CMC blend polymer appeared to be the best candidate for a disparity of TiO2/COF hybrids. Not only did COF aid to increase the distribution of TiO2 nanoparticles, but it declined the bandgap energies. The resultant Alg-CMC/TiO2/COF (TiO2/COF = 15:6) bio-NC beads demonstrated efficient photodegradation activity towards Methyl violet (MV) under Ultraviolet light. The obtained results of scavenger studies indicated that superoxide radicals and electron agents played a major role in MV degradation. Further investigation confirmed that single oxygen addition and N-de-methylation could be two important pathways for the decomposition of MV by these bio-NC beads.

Silk sericin-coated polyamide thin-film composite membranes to simultaneously improve anti-scaling properties, long-term storage, and waste-to-resource recovery

A polyamide thin-film composite (PA-TFC) membrane, which is one of the widely used for desalination and water softening processes, features a lot of carboxyl groups inevitably formed by hydrolysis of unreacted acyl chlorides after interfacial polymerization. However, since carboxyl groups interact with multivalent cations and thereby cause membrane scaling, it is desirable to reduce the density of carboxyl groups on the membrane surface. In this regard, silk sericin (SS) can be an excellent alternative to modifying the surface characteristics to mitigate scaling because it has various hydrophilic amino acids with a much lower density of carboxyl groups per unit mass. Given the properties, we prepared anti-scaling TFC membranes by coating SS on the PA active layer. According to the result, the SS-PA-TFC (16.4% decrease) significantly reduced the flux decline to half of the PA-TFC (36.7% decrease) during the 48-h scaling test under the condition for heterogeneous gypsum crystal nucleation. More importantly, the comparison of operation duration until cleaning obviously revealed the anti-scaling properties of the SS-PA-TFC, which was evidenced by about 7.5 times longer duration than the PA-TFC. Furthermore, the cyclic scaling test in 19 mM CaSO4 showed that the SS-PA-TFC (3.6%) could decrease the irreversible fouling to about one-fifth of the PA-TFC (15.9%). This outstanding anti-scaling performance of the SS-PA-TFC stemmed from the less negatively charged (‐40.8 and ‐28.1 mV for the PA-TFC and SS-PA-TFC, respectively) and much more hydrophilic surface (52.2° and 18.2° for the contact angles of the PA-TFC and SS-PA-TFC, respectively). Suprisingly, the above-mentioned anti-scaling properties of the SS-PA-TFC membrane were achieved without the trade-off between water flux and salt rejection thanks to a very thin SS coating layer (ca. 16 nm). Apart from the anti-scaling properties, SS coating also improved long-term storage and waste-to-resource recovery.

Protective effects of alpha-lipoic acid and alagebrium chloride against testicular dysfunction induced by varicocele and advanced glycation end (AGE) – Rich diet in a rat mode

Heat stress from varicocele can heighten oxidative stress in the testes, impacting sperm function and male fertility. Antioxidant therapy is explored as a remedy for varicocele, while dietary factors like processed foods, sugar, and saturated fats correlate with male infertility. Advanced glycation end products (AGEs), generated through glycation processes, can provoke oxidative stress, inflammation, and adverse health consequences. Alpha-lipoic acid (ALA), a versatile antioxidant, may alleviate oxidative stress and counteract the impact of AGEs, potentially by enhancing glucose reabsorption. Alagebrium chloride (ALT711), an anti-AGE compound, exhibits promise in cardiovascular disease by disrupting AGE cross-links. This study investigates the effects of ALA and ALT-711 on testicular function in varicocele and AGEs animal models. Both AGE and varicocele were found to alter the natural trends, leading to abnormal patterns in sperm parameters, testicular functional tests, as well as the expression of CML, RAGE, and TNF-α proteins. However, the administration of ALA or ALT711 helped mitigate these effects. While ALA demonstrated a slightly greater overall benefit compared to ALT, the difference was not statistically significant.

Layered heterogeneous polyamide-hydrazide based reverse osmosis membranes with enhanced separation performance

It is the goal of membrane science to continuously overcome the trade-off between permeability and selectivity of reverse osmosis (RO) membranes. In this study we propose a strategy based on the pore characteristics of cyclobutane-1,2,3,4-tetracarboxylic acid chloride (BTC) and trimesoyl chloride (TMC) crosslinked with cyclobutane-1,2,3,4-tetracarbohydrazide (CBTH) for constructing layered heterostructures of polyamide-hydrazide membranes. By using BTC and TMC successively, the porous BTC-CBTH polyamide was employed as the bottom layer, and the dense TMC-CBTH polyamide as the top layer, creating an RO membrane with a “sparse and dense” heterogeneous structure. This layered heterostructure ingeniously differentiates the structure and function of the selective layer of the RO membrane, enabling the loose bottom layer and the dense top layer to respectively perform the tasks of support and separation. The permeability coefficient of the prepared RO membrane reached 3.82 L⋅m−2⋅h−1⋅bar−1, which was enhanced by 29 % compared with that of the polyamide-hydrazide membrane prepared by single-step interfacial polymerization, while the rejection of NaCl was maintained at 99.13 %. The heterogeneous layered construction strategy effectively improves the permeability and selectivity of the RO membrane, and provides a universal solution for consistently overcoming the “trade-off” effect in RO membranes.

Facile scalable one-flow synthesis of ionizable cationic lipid library as precursors of nanoparticle carriers

A variety of ionizable and cationic lipids have been synthesized as precursors for nanoparticle carriers. However, the laborious synthetic routes in batch reactors often involve the use of toxic and carcinogenic agents, as well as challenge of removing gaseous byproducts. In this study, we present facile one-flow micro-reaction process that enables the synthesis of 11 ionizable lipids as well as 7 cationic lipids, including the well-known DODAP and DOTAP. These lipids can be scaled up to produce approximately ∼10g/h by using a straightforward size-up approach. The development of the lipid library was involved generating highly moisture-sensitive acyl chloride at 25 °C for 1.5 min. The toxic byproducts such as HCl, CO2 and CO were subsequently removed using a liquid–gas separator. The esterification with dimethylamino-1,2-diol at 25 °C for 3 min, monitored in-line with FTIR, completed the process. Additionally, the synthesized ionizable lipids were converted to cationic lipids with methyl sulfate, chloride ions via dimethyl sulfate and Steglich esterification in a continuous flow system. Finally, the produced DODAP was transformed into a uniform-sized LNPs (64 nm, PDI 0.07) and liposomal nanoparticles (72 nm, PDI 0.05) while DOTAP was converted to liposomes (55 nm, PDI 0.08) using a custom micro-mixer. This efficient platform for lipid synthesis significantly contributes to the practical applications of lipid-based nanomedicines.

Palladium-Catalyzed Decarbonylative Nucleophilic Halogenation of Acyl Fluorides and Chlorides: Synthesis of Aryl Halides via Reductive Elimination of the C–X (X = I, Br, and Cl) Bond and Mechanistic Implications

Palladium-Catalyzed Decarbonylative Nucleophilic Halogenation of Acyl Fluorides and Chlorides: Synthesis of Aryl Halides via Reductive Elimination of the C–X (X = I, Br, and Cl) Bond and Mechanistic Implications

Enhanced performance of amine and thiol chemically modified graphene oxide for effective removal of Hg(II), Pb(II), and Cr(VI) from aqueous solution

This study describes a novel adsorbent with a multidentate ligand that was facilely fabricated by covalently bonding 4-amino-3-hydrazino-5-mercapto-1,2,4-triazole on graphene oxide (AHMT-PRGO). The AHMT-PRGO nano-adsorbent was used for the effective removal of Hg(II), Pb(II), and Cr(VI) from wastewater. The AHMT-PRGO nano-adsorbent was synthesized by a nucleophilic substitution reaction between GO acyl chloride and AHMT chelating ligand in the presence of tetrabutyl-ammonium bromide as a catalyst. The successful modifications were confirmed via several spectroscopic and electron microscopy instrumentations including UV–Vis, FTIR, Raman, XRD, XPS, SEM, and TEM. The maximum adsorption capacities of Hg(II), Cr(VI), and Pb(II) on the AHMT-PRGO nano-adsorbent were 370.0, 136.2, and 109.6 mg/g, respectively, exceeding those of most previously reported adsorbents. Additionally, the equilibrium contact times for Hg(II), Pb(II), and Cr(VI) were 60, 30, and 400 min, respectively. In a mixture of nine heavy metal ions containing 250 ppm of each ion, the AHMT-PRGO nano-adsorbent exhibited high selectivity for Hg(II) ions. Furthermore, the AHMT-PRGO nano-adsorbent showed high stability over five adsorption–desorption cycles. Additionally, the AHMT-PRGO nano-adsorbent was successfully applied to remove heavy metal ions from real water samples. The novelty of AHMT-PRGO lies in the combination of a multidentate ligand for strong and selective binding with the high surface area and stability offered by covalently bonded graphene oxide. This combination offers potential advantages over traditional adsorbents in terms of adsorption capacity, selectivity, and reusability.

Green Synthesis of Alzheimer's Disease Probes Aftobetin and Analogues Enabled by Flow Technology and Heterogeneous Photocatalysis.

Aftobetin is a non-invasive diagnosis probe of Alzheimer's disease, that can bind with aggregated β-amyloid peptide in eye's lenses, used for early diagnosis of Alzheimer's disease in a rapid and painless mode. The reported synthesis of this probe fell short in the aspects of greenness and economy due to the involvement of toxic Chromium(IV) oxidant, noble palladium catalyst, elevated reaction temperature, the long reaction time as well as the cumbersome workup. Herein, a holistic optimization of the synthetic process was achieved via the employment of flow technology and heterogenous photocatalysis. Firstly, the integration of heterogenous carbon nitrides photocatalysis and circulation flow technology furnished the air oxidation of alcohol and nickel catalyzed C-N coupling at 20-g scale, thus avoiding the use of toxic Chromium and precious palladium species respectively. Flow-intensified esterification between acyl chloride and alcohol, just taking 30 seconds replaced the Steglich esterification of 6 hours, also avoiding the generation of difficult-to-remove dicyclohexylurea. Finally, C-N coupling, esterification and Knoevenagel condensation were telescoped together, thus simplifying the reaction workup. This fully-flow protocol led to the on-demand synthesis of eight probes.

Iron-Catalyzed Friedel-Crafts-type 3,5-Diacylation of Indoles.

The exploration of remote functionalization of indoles is impeded by the inherently dominant reactivity intrinsic to the pyrrole moiety. Herein, we delineate a novel strategy facilitated by Lewis acid mediation, enabling the remote C-H functionalization, which culminates in the synthesis of an array of selectively functionalized indole derivatives, encompassing 3-trifluoroacetyl and 5-benzoyl motifs, utilizing trifluoroacetic anhydride and various acyl chlorides. Notably, the protocol exhibits versatility, as epitomized by the extension of C5-acylation to alkylation and sulfonation reactions. This methodology is distinguished by its exemplary regio- and chemo-selectivity, extensive substrate scope, commendable tolerance to a diverse array of functional groups, and the employment of comparatively mild reaction conditions.

Cu(OTf)2-mediated acylation and direct N-transacylation of sulfonamides

Metal triflate-catalyzed acylation of sulfonamides and direct transacylation of N-acylsulfonamides have been investigated. The acylation of sulfonamides proceeds efficiently in the presence of a catalytic amount of Cu(OTf)2 (0.001 equiv) using either carboxylic anhydrides or acyl chlorides as the acylating agents. Alternative catalysts suitable for this transformation include Al(OTf)3, Fe(OTf)3, Ga(OTf)3, In(OTf)3, and Er(OTf)3. In the presence of Cu(OTf)2 (0.2 equiv), N-acylsulfonamides undergo direct transacylation in excess acyl chlorides (10 equiv) to furnish new N-acylsulfonamides through exchange of N-acyl groups. Ga(OTf)3, Fe(OTf)3, and In(OTf)3 are similarly reactive in catalyzing such transacylation transformations. The reaction conditions are mild and operationally convenient. A variety of functional groups including halogeno, keto, nitro, cyano, ether, and carboxylic ester are tolerated, providing the corresponding monoacylated N-acylsulfonamides in good to excellent yields.

Affinity Constants of Bovine Serum Albumin for 5 nm Gold Nanoparticles (AuNPs) with ω-Functionalized Thiol Monolayers Determined by Fluorescence Spectroscopy.

A detailed understanding of the binding of serum proteins to small (dcore <10 nm) nanoparticles (NPs) is essential for the mediation of protein corona formation in next generation nanotherapeutics. While a number of studies have investigated the details of protein adsorption on large functionalized NPs, small NPs (with a particle surface area comparable in size to the protein) have not received extensive study. This study determined the affinity constant (Ka) of BSA when binding to three different functionalized 5 nm gold nanoparticles (AuNPs). AuNPs were synthesized using three ω-functionalized thiols (mercaptoethoxy-ethoxy-ethanol (MEEE), mercaptohexanoic acid (MHA), and mercaptopentyltrimethylammonium chloride (MPTMA)), giving rise to particles with three different surface charges. The binding affinity of bovine serum albumin (BSA) to the different AuNP surfaces was investigated using UV-visible absorbance spectroscopy, dynamic light scattering (DLS), and fluorescence quenching titrations. Fluorescence titrations indicated that the affinity of BSA was actually highest for small AuNPs with a negative surface charge (MHA-AuNPs). Interestingly, the positively charged MPTMA-AuNPs showed the lowest Ka for BSA, indicating that electrostatic interactions are likely not the primary driving force in binding of BSA to these small AuNPs. Ka values at 25 °C for MHA, MEEE, and MPTMA-AuNPs were 5.2 ± 0.2 × 107, 3.7 ± 0.2 × 107, and 3.3 ± 0.16 × 107 M-1 in water, respectively. Fluorescence quenching titrations performed in 100 mM NaCl resulted in lower Ka values for the charged AuNPs, while the Ka value for the MEEE-AuNPs remained unchanged. Measurement of the hydrodynamic diameter (Dh) by dynamic light scattering (DLS) suggests that adsorption of 1-2 BSA molecules is sufficient to saturate the AuNP surface. DLS and negative-stain TEM images indicate that, despite the lower observed Ka values, the binding of MPTMA-AuNPs to BSA likely induces significant protein misfolding and may lead to extensive BSA aggregation at specific BSA:AuNP molar ratios.

Obtention of Suitable Pregnant Leach Solution (PLS) for Copper Solvent Extraction Plants from Copper Concentrate Using Hydrogen Peroxide and Iodine in a Sulfuric Acid–Chloride Medium

Copper leaching presents an environmentally friendly alternative to traditional sulfide ore processing methods. This study investigates an efficient leaching process for copper concentrate, utilizing a solution of sulfuric acid (H2SO4) and potassium iodide (KI) in a chloride medium (NaCl), enhanced by hydrogen peroxide (H2O2) at room temperature. A significant aspect of this research was optimizing the KI concentration to minimize iodide sublimation into iodine gas (I2). Through the experimental design, the optimal dosages of reagents were determined, leading to maximized copper extraction of approximately 27% in 45 min of testing at room temperature. The results showed that it is possible to obtain a suitable pregnant leach solution (PLS) (i.e., in the range of 3 to 8 g/L of Cu) for treatment in available copper solvent extraction (SX) plants with a cost of less than 4.5 USD/t Cu, according to the economic analysis carried out. The results of this study determine the most effective operational conditions for leaching and ensure a suitable PLS for SX plants in a cost-effective and environmentally friendly manner. This approach could significantly contribute to more sustainable practices in the mining and processing of copper ores.

Synthesis of Trisubstituted Furans from Activated Alkenes by P(III)/P(V) Redox Cycling Catalysis.

The organocatalytic formation of an underrepresented family of trisubstituted and tetrasubstituted furans from activated alkenes and acyl chlorides is reported. In a reaction sequence based on P(III)/P(V) redox cycling catalysis, the cyclic phosphine catalysts react with diacylethenes or acyl acrylates in Michael addition, followed by acylation and either an intramolecular Wittig reaction or a ring closure reaction, liberating the furans. The formed phosphine oxides are reduced in situ by phenylsilane as a terminal reductant. In the first step, 12 diacylethenes were converted to the respective trisubstituted furans. The reaction of acyl acrylates showed a surprising, catalyst-dependent alternate reaction forming tetrasubstituted furans. Two additional methods were developed, giving 14 trisubstituted furans using a phospholene catalyst and an additional 6 tetrasubstituted furans using a phosphetane catalyst. This encompassed 19 newly described compounds.