Hydrogen Bond Donor Research Articles

Screening deep eutectic solvents as green solvents for efficient extraction of carbazole from model crude anthracene oil

Carbazole is a high value-added component of crude anthracene. Highly efficient and sustainable extraction solvents are extremely significant for carbazole separation. Deep eutectic solvents (DESs), as a new class of green solvents, have gained extensive attention from researchers in the field of separation. However, a large number of DESs are generated due to the enormous combinations of hydrogen bond acceptors (HBAs) and hydrogen bond donors (HBDs), which makes it challenging to identify the most suitable DES for specific separation process. Therefore, a reliable and effective method for DESs screening was highly desirable. In this work, a DESs screening method was proposed for the separation of carbazole. Initially, the COSMO-RS model was employed to calculate thermodynamic properties at infinite dilution. Subsequently, the liquid–liquid phase equilibrium behavior of prescreened DESs was further predicted by COSMO-RS to eliminate those that were miscible with toluene. Finally, the practical extraction performance of the top DES candidates was evaluated through experimental investigation. The results well validated the reliability of the screening method, identifying tetraethylammonium chloride/propionic acid (1:2) as the most promising DES for carbazole separation. Furthermore, the extraction mechanism was explored using FT-IR analysis and quantum chemical calculations.

Novel application of citric acid based natural deep eutectic solvent in drilling fluids for shale swelling prevention

Swelling of shale in clastic reservoirs poses a significant challenge, causing instability in wellbores. Utilizing water-based drilling mud with shale inhibitors is preferable for environmental reasons over oil-based mud. Ionic liquids (ILs) have garnered interest as shale inhibitors due to their customizable properties and strong electrostatic features. However, widely used imidazolium-based ILs in drilling fluids are found to be toxic, non-biodegradable, and expensive. Deep Eutectic Solvents (DES), considered a more economical and less toxic alternative to ILs, still fall short in terms of environmental sustainability. The latest advancement in this field introduces Natural Deep Eutectic Solvents (NADES), renowned for their genuine eco-friendliness. This study explores NADES formulated with citric acid (as a Hydrogen Bond Acceptor) and glycerine (as a Hydrogen Bond Donor) as additives in drilling fluids. The NADES based drilling mud was prepared according to API 13B-1 standards and their efficacy was compared with KCl, imidazolium based ionic liquid, and Choline Chloride: Urea-DES based mud. A thorough physicochemical characterization of the in-house prepared NADES is detailed. The research evaluates rheological, filtration and shale inhibition properties of the mud, demonstrating that NADES enhanced the yield point to plastic viscosity ratio (YP/PV), reduced mudcake thickness by 26%, and decreased filtrate volume by 30.1% at a 3% concentration. Notably, NADES achieved an impressive 49.14% inhibition of swelling and improved shale recovery by 86.36%. These outcomes are attributed to NADES’ ability to modify surface activity, zeta potential, and clay layer spacing which are discussed to understand the underlying mechanism. This sustainable drilling fluid promises to reshape the drilling industry by offering a non-toxic, cost-effective, and highly efficient alternative to conventional shale inhibitors, paving the way for environmentally conscious drilling practices.

Corrolato(oxo)antimony(V) Dimer with Hydrogen-Bond Donor Groups in Secondary Coordination Sphere as a Catalyst for Hydrogen Evolution Reaction.

The focus is on developing alternative molecular catalysts using main-group elements and implementing strategic improvements for sustainable hydrogen production. For this purpose, a FB corrole with a (2-(2-((4-methylphenyl)sulfonamido)ethoxy)phenyl) group inserted into the meso position (C-10) of the corrole, along with its high-valent (corrolato)(oxo)antimony(V) dimer, was synthesized. In the crystal structure analysis of the FB corrole and the (corrolato)(oxo)antimony(V) dimer complex, it was noted that the sulfonamido group in the ligand periphery sits atop the corrole ring. The electrochemical hydrogen evolution reaction (HER) of the (corrolato)(oxo)antimony(V) dimer was studied and compared with a previously reported (corrolato)(oxo)antimony(V) complex, which lacks hydrogen-bond donor groups in the secondary coordination sphere. The newly designed molecules, featuring hydrogen-bond donor groups in the secondary coordination sphere, demonstrated clear superiority in the electrochemical HER. Controlled potential electrolysis was employed to evaluate the charge accumulation associated with hydrogen generation in a homogeneous three-electrode system in the presence of 50 mM TFA. The produced hydrogen exhibits a Faradaic efficiency of approximately 80.96%, a turnover frequency (TOF) of 0.44 h-1, and a production rate of 52.83 μL h-1, highlighting the effective catalytic activity of the (corrolato)(oxo)antimony(V) dimer in hydrogen evolution.

Chromatographic Determination of Permeability-Relevant Lipophilicity Facilitates Rapid Analysis of Macrocyclic Peptide Scaffolds.

Hydrocarbon-determined shake-flask measurements have demonstrated great utility for optimizing lipophilicity during early drug discovery. Alternatively, chromatographic methods confer reduced experimental error and improved handling of complex mixtures. In this study, we developed a chromatographic approach for estimating hydrocarbon-water shake-flask partition coefficients for a variety of macrocyclic peptides and other bRo5 molecules including PROTACs. The model accurately predicts experimental shake-flask measurements with high reproducibility across a wide range of lipophilicities. The chromatographic retention times revealed subtle conformational effects and correlated with the ability to sequester hydrogen bond donors in low dielectric media. Estimations of shake-flask lipophilicity from our model also accurately predicted trends in MDCK passive cell permeability for a variety of thioether-cyclized decapeptides. This method provides a convenient, high-throughput approach for measuring lipophilic permeability efficiency and predicting passive cell permeability in bRo5 compounds that is suitable for multiplexing pure compounds or investigating the properties of complex library mixtures.

Design of Eutectic Solvents with Specified Extraction Properties Based on Intermolecular Interaction Energy.

A new approach to managing the extraction properties of eutectic solvents based on aliphatic alcohols is proposed. Aliphatic alcohols, when functioning as hydrogen bond donors within a eutectic solvent, significantly enhance the solvent's efficiency in extracting metal ions. Conversely, when the alcohol acts as a hydrogen bond acceptor, its extraction properties diminish. Molecular modelling reveals that the extraction efficiency of these alcohols is directly proportional to the intermolecular interaction energy between the components of the eutectic solvent.

Synthesis of new 1,4-dihydropyridine derivative, anti-cancer, bacterial activity, molecular docking and adsorption, distribution, metabolism and excretion analysis.

Aim: The amination and cyclization method developed a new strategy for designing and assembling new 1,4-dihydropyridine derivatives of compounds 3a-g and 4a-g.Methods & materials: Newly prepared pyridine compounds are more economical, and reduce the reaction time. FT-IR, 1H-NMR, 13C-NMR, mass spectroscopy and elemental analyses elucidated the synthesized derivatives. All the derivatives are subjected to in vitro assay against MCF-7 (breast) and anti-bacterial activity.Results: In the anti-bacterial activity compound 3c is moderately active against Escherichia coli (6.0g/ml), and 4c is extremely active against Lactiplantibacillus plantarum (10.0g/ml) compared with standard Erythromycin. In cytotoxic activity, the compound 3g (lC50 24.5μM) is slightly active against standard doxorubicin. We also present the outcome of a molecular docking study connecting the methoxsalen (Protein Data Bank, PDB ID: 1Z11). Compound 3g shows a higher binding affinity (-7.7Kcal/mol) matching up with doxorubicin(-9.0Kcal/mol). The synthesized analogs were predicted for their adsorption, distribution, metabolism and excretion profiles and pharmacokinetics. The compound 3g has three rotatable bonds (NROB≤10), five hydrogen bond acceptors (HBA≤10) and four hydrogen bond donors (HBD≤5). All the compounds follow Lipinski's rule.Conclusion: Therefore, the compounds 3c and 3g are used as cytotoxic and anti-bacterial drugs in feature.

Design of some phthalazine molecules as novel VEGFR-2 target inhibitors through 3D-QSAR modeling, molecular docking and dynamic simulation and pharmacokinetics profiling

AbstractBreast cancer is one of the dominant cause of cancer-related mortality in females, with an incidence of approximately 1.3 million cases annually, necessitating the development of effective therapeutic strategies. In this study, 3D-QSAR models were reported based on Phthalazine derivatives as VEGFR-2 inhibitors. The activities of these derivatives were correlated with the steric (S), electrostatic (E), hydrogen bond acceptor (A), and donor (D), and hydrophobic (H) fields, which served as critical parameters in model development. Statistical studies of these models showed that the best models are; CoMFA_S (Q2 = 0.623, R2 = 0.941), and CoMSIA_E + D (Q2 = 0.615, R2 = 0.977). Based on the insights from the model fields and docking simulation of the template (compound 17), twelve molecules were designed. These novel molecules exhibited stronger potency compared to the template and the standard, Sorafenib. Compound 17A emerged as the most potent, with pIC50 = 5.98, for CoMFA_S and 5.85, for CoMSIA_E + D, and a strong docking affinity of − 97.271 kcal/mol, therefore subjected to a 100-ns MD simulation. Results indicate better interaction and stabilizing potential over Sorafenib, due to the lower RMSD, RMSF, Rg, values and favorable hydrogen bond analyses. These conclusions were validated by Gibbs free energy analysis and MM-GBSA calculations, revealing a more favorable interaction free energy of − 18.48 kcal/mol related to Sorafenib. Furthermore, these designed compounds demonstrated promising pharmacokinetic profiles.

Ligand-based pharmacophore modeling targeting the fluoroquinolone antibiotics to identify potential antimicrobial compounds

Antibiotic resistance presents a serious challenge to global healthcare, making the discovery of new therapeutic agents crucial. In this study, we used pharmacophore modeling and virtual screening to identify potential lead compounds against drug-resistant bacteria. We developed a shared feature pharmacophore (SFP) map using four antibiotics—Ciprofloxacin, Delafloxacin, Levofloxacin, and Ofloxacin—and generated a drug library of 160,000 compounds from ZINCPharmer based on these features, which included hydrophobic areas, hydrogen bond acceptors (HBA), hydrogen bond donors (HBD), and aromatic moieties (Ar). Through virtual screening, we identified 25 potential drug compounds as hits, with fit scores ranging from 97.85 to 116 and RMSD values from 0.28 to 0.63. These hits were then subjected to molecular docking against the DNA gyrase subunit A protein (PDB ID: 4DDQ), with ciprofloxacin as a control. The top five compounds—ZINC09133461, ZINC03791737, ZINC21983587, ZINC26469742, and ZINC26740199—achieved the highest docking scores, ranging from − 7.3 to − 7.4 kcal/mol and ciprofloxacin − 7.3 kcal/mol. After evaluating the drug-likeness of these compounds using Lipinski’s rule and analyzing their physicochemical properties, ZINC26740199 emerged as the most promising lead, offering hope in the fight against antibiotic resistance. Furthermore, molecular scaffold analysis revealed key similarities between ZINC26740199 and Ciprofloxacin, particularly in aromatic rings, hydrophobic regions, and hydrogen bond acceptors. These features suggest its potential as an effective antimicrobial agent, though further laboratory studies are needed to confirm its efficacy.

Diethylene glycol-zinc chloride based deep eutectic solvent for green extraction of bixin compound

Deep eutectic solvents (DESs) are ionic liquid alternatives that replace volatile and flammable organic solvents. DESs are formed by hydrogen bond interaction between the hydrogen bond donor (HBD) and the hydrogen bond acceptor (HBA). We prepared DES using zinc chloride (ZnCl2) as HBA and diethylene glycol (DEG) as HBD. Formed DES was applied to extract the bixin contained in annatto seeds. The homogenous liquid mixtures were analysed for their pH, viscosity, density, conductivity, thermal properties, and solubility in various solvents. Bixin extracted using DES was identified by thin-layer chromatography (TLC), UV–Vis spectrophotometer, Fourier Transform Infra-Red (FTIR), and Proton Nuclear Magnetic Resonance (1HNMR). The mixtures with a mole fraction of ZnCl2 0.1 (DES1), 0.2 (DES2), and 0.3 (DES3) are liquid at room temperature. The analysis results prove that bixin has been successfully extracted using DES, where DES1 was better for bixin extraction than DES2 and DES3, with extracted bixin levels of 32.42, 28.84, and 0.46 mg g-1 by dry seeds mass, respectively. In this case, DES1, DES2, and DES3 could extract 62.17, 55.31, and 0.88 % of bixin from the entire total bixin contained in annatto seeds. The DES can be used for bixin extraction using a relatively simple method based on the results obtained.

Self-aggregation and microhydration mechanisms of monoethanolamine: Far-infrared identification of large-amplitude hydrogen bond libration.

The strong tendency for self-aggregation together with an intriguing mechanism for the microhydration of monoethanolamine (MEA) have been explored by low-temperature far-infrared cluster spectroscopy in doped neon "quantum" matrices at 4K complemented by high-level quantum chemical modeling. In addition to the assignment of new mid-infrared perturbed intramolecular transitions, a distinct far-infrared transition is unambiguously assigned to the concerted large-amplitude hydrogen bond librational motion of the MEA homodimer. This observation confirms a global "head-to-head" intermolecular potential energy minimum associated with the formation of a compact doubly intermolecular OH⋯N hydrogen-bonded cyclic structure, where both monomeric intramolecular OH⋯N hydrogen bonds are broken upon complexation. By means of relative mixing ratio dependencies, dedicated annealing procedures, and selective complexation between MEA and isotopic H216O and H218O samples, distinct far-infrared transitions associated with large-amplitude intra-molecular hindered OH torsional motion and inter-molecular H2O librational (hindered c-type overall rotational) motion of the MEA monohydrate are furthermore assigned unambiguously for the first time. These spectroscopic observations reveal an intriguing metastable conformation, where H2O acts as a OH⋯O hydrogen bond donor to the hydroxy group instead of the amino group of MEA upon microhydration in the cryogenic neon environment, where the microhydration strengthens the intramolecular OH⋯N hydrogen bond of MEA due to hydrogen bond cooperativity.

Optimization of White Tea Flavanol Extraction Process by the Ultrasonic‐Assisted Deep Eutectic Solvent Method and Determination of the Antioxidant and Antibacterial Activity

ABSTRACTFlavanols have a variety of health benefits and biological activities and become the hotspot of the food development and research. In this research, flavanols were extracted from white tea by ultrasonic‐assisted deep eutectic solvent (DES) method. High‐performance liquid chromatography was used to determine the content of flavanols. The influence of four factors on the flavanol extraction yield was analyzed by single factor experiments, including deep eutectic solvent mole ratio (the mole of hydrogen bond acceptors: the mole of hydrogen bond donors), solid–liquid ratio (white tea sample weight/g: the volume of DES/mL), extraction time and extraction temperature. On the basis of single factor experiments, the factors which had significant effects on the flavanol extraction yield were further optimized by the response surface test. The results showed that the optimized extraction conditions were as follows: the mole ratio of DES 1: 4 (choline chloride: 1,2‐propanediol), the solid–liquid ratio 1:30, the extraction temperature 56°C, the extraction time 53 min, and the ultrasonic power 341 W. Under the above parameters, the extraction yield of white tea flavanols was 9.63 mg/g. After purification with macroporous resin, antioxidation and antibacterial experiments were carried out. The results showed that the antioxidant and antibacterial effects of white tea flavanols were remarkable. The antibacterial effects performed best on Escherichia coli, followed by Bacillus subtilis and Staphylococcus aureus. The maximum diameter of the antibacterial zone on Escherichia coli was 0.95 ± 0.11 mm. The best radical scavenging rates of OH, ABTS+ and DPPH were 97.1%, 97.5%, and 88.4%, respectively, when the flavanol concentration was 9.5 mg/mL. The conclusions of this research can provide theoretical foundation for the further study of white tea flavanols.

Binary and Ternary Deep Eutectic Solvents for Methylene Green Electropolymerization on Multiwalled Carbon Nanotubes: Optimization, Characterization and Application.

Choline chloride (ChCl) based binary and ternary deep eutectic solvents (DES) were evaluated for methylene green electropolymerization with oxalic acid (OA) and ethylene glycol (EG) as hydrogen bond donors. Binary DES ChCl : OA in molar ratios 1 : 1 and 2 : 1 and ChCl : EG 1 : 2 and ternary DES (tDES) in different molar ratios and percentages of water were evaluated. The highest polymer growth was in ChCl : OA : EG-tDES with 13% added water, that had a lower viscosity and higher ionic conductivity when associated with HCl as dopant. This enhanced the formation of more cation radicals and, consequently, more polymer formation. The PMG/MWCNT/GCE-tDES sensor was successfully applied to the simultaneous determination of 5-aminosalicylic acid (5-ASA) and acetaminophen (APAP) by differential pulse voltammetry in the concentration range 1 μM-200 μM, with detection limits of 0.37 μM and 0.49 μM for 5-ASA and APAP, respectively. The sensor demonstrated good repeatability, reproducibility and stability, and was successfully applied in pharmaceutical formulations.

Cobalt Tetracationic 3,4-Pyridinoporphyrazine for Direct CO2 to Methanol Conversion Escaping the CO Intermediate Pathway.

Molecular catalysts offer a unique opportunity to implement different chemical functionalities to steer the efficiency and selectivity for the CO2 reduction for instance. Metalloporphyrins and metallophthalocyanines are under high scrutiny since their most classic derivatives the tetraphenylporphyrin (TPP) and parent phthalocyanine (Pc), have been used as the molecular platform to install, hydrogen bonds donors, proton relays, cationic fragments, incorporation in MOFs and COFs, to enhance the catalytic power of these catalysts. Herein, we examine the electrocatalytic properties of the tetramethyl cobalt (II) tetrapyridinoporphyrazine (CoTmTPyPz) for the reduction of CO2 in heterogeneous medium when adsorbed on carbon nanotubes (CNT) at a carbon paper (CP) electrode. Unlike reported electrocatalysis with cobalt based phthalocyanine where CO was advocated as the two electron and two protons reduced intermediate on the way to the formation of methanol, we found here that CoTmTPyPz does not reduce CO to methanol. Henceforth, ruling out a mechanistic pathway where CO is a reaction intermediate.

Ring‐opening copolymerization of ε‐caprolactone and δ‐valerolactone to cyclic polyesters by a bimolecular system

AbstractBio‐based plastics have received much attraction because they are an alternative to petroleum‐based plastics in recent years. Among them, aliphatic polyesters have garnered the most attention due to their excellent properties. Polyester is primarily synthesized through ring opening polymerization of monomer, and the catalysts used are mostly synthesized through “click” reaction in the laboratory, which exhibits inferior activity and little commercial value. Herein, a facile approach was developed for the synthesis of high molecular‐weight cyclic aliphatic polyesters, specifically poly(valerolactone‐co‐caprolactone) with varying compositions. This involved the ring‐opening copolymerization of ε‐caprolactone (ε‐CL) and δ‐valerolactone (δ‐VL) in the absence of an initiator with commercial hydrogen bond donor triclorocarban and an organic base. The structure and properties of the prepared cyclic polyester were investigated using GPC, 13C NMR, 1H NMR, MALDI‐TOF mass spectrometry, TOF‐SIMS mass spectrometry, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and X‐ray diffraction (XRD) techniques. The results show that the molecular weight of cyclic polyester can rapidly exceed 40 kDa, with a PDI of approximately 1.10. In comparison to linear polyester, it has a higher melting point and superior thermodynamic properties, thus presenting greater application potential. Finally, based on nuclear magnetic resonance titration, the potential catalytic processes and mechanisms of bimolecular systems on monomers in different environments were discussed. This study not only offers new insights into the structure and properties of cyclic polyesters, but also presents novel bimolecular catalytic systems using commercial urea hydrogen bond donors for the synthesis of cyclic polymer polyesters.

Cobalt Tetracationic 3,4‐Pyridinoporphyrazine for Direct CO2 to Methanol Conversion Escaping the CO Intermediate Pathway

AbstractMolecular catalysts offer a unique opportunity to implement different chemical functionalities to steer the efficiency and selectivity for the CO2 reduction for instance. Metalloporphyrins and metallophthalocyanines are under high scrutiny since their most classic derivatives the tetraphenylporphyrin (TPP) and parent phthalocyanine (Pc), have been used as the molecular platform to install, hydrogen bonds donors, proton relays, cationic fragments, incorporation in MOFs and COFs, to enhance the catalytic power of these catalysts. Herein, we examine the electrocatalytic properties of the tetramethyl cobalt (II) tetrapyridinoporphyrazine (CoTmTPyPz) for the reduction of CO2 in heterogeneous medium when adsorbed on carbon nanotubes (CNT) at a carbon paper (CP) electrode. Unlike reported electrocatalysis with cobalt based phthalocyanine where CO was advocated as the two electron and two protons reduced intermediate on the way to the formation of methanol, we found here that CoTmTPyPz does not reduce CO to methanol. Henceforth, ruling out a mechanistic pathway where CO is a reaction intermediate.

Constructing Cyclic Hydrogen Bonding to Suppress Side Reactions and Dendrite Formation on Zinc Anodes.

The high electrochemical reactivity of H2O molecules and zinc metal results in severe side reactions and dendrite formation on zinc anodes. Here we demonstrate that these issues can be addressed by using N-hydroxymethylacetamide (NHA) as additives in 2 M ZnSO4 electrolytes. The addition of NHA molecules, acting as both a hydrogen bond donor and acceptor, enables the formation of cyclic hydrogen bonding with H2O molecules. This interaction disrupts the existing hydrogen bonding networks between H2O molecules, hindering proton transport, and containing H2O molecules within the cyclic hydrogen bonding structure to prevent deprotonation. Additionally, NHA molecules show a preference for adsorption on the (101) crystal surface of zinc metal. This preferential adsorption reduces the surface energy of the (101) plane, facilitating the homogeneous Zn deposition along the (101) direction. Thus, the NHA enables Zn||Zn symmetric cell with a cycle lifespan of 1100 hours at 5 mA cm-2 and Zn||Cu asymmetric cell with a high Coulombic efficiency over 99.5 %. Moreover, the NHA-modified Zn||AC zinc ion hybrid capacitor is capable of sustaining 15000 cycles at 2 A g-1. This electrolyte additive engineering presents a promising strategy to enhance the performance and broaden the application potential of zinc metal-based energy storage devices.

Structure Elucidation of Pharmaceutically Relevant Compounds Within Pyrene-Based Frameworks.

Single-crystal X-ray diffraction (SCXRD) is the preferred and most accurate technique for determining molecular structures. However, it can present challenges when dealing with specific small molecules and active pharmaceutical ingredients (APIs), as many do not form quality crystals without coformers or can be unstable. In this study, we introduce tetrakis(guanidinium) pyrenetetrasulfonate (G4PYR), a robust guanidinium-organosulfonate (GS) framework that efficiently encapsulates small molecules and APIs rich in functional groups. The hydrogen bonding frameworks formed by G4PYR display well-ordered structures with predictable pyrene-pyrene distances, making them ideally suited for targeting arene-based APIs with pendant groups. Successful encapsulation of various guests, including benzaldehyde, benzamide, and arenes containing multiple hydrogen bond donors and acceptors like uracil and thymine, was achieved. Furthermore, we successfully encapsulated important pharmaceutical and biologically relevant compounds, such as lidocaine, ropinirole, adenosine, thymidine, and others. Notably, we present a workflow for investigating host-guest complex formation using powder X-ray diffraction and high throughput experimentation.

Cellular Phosphate Sensing and Anion Binding by an Azacrown-Calixpyrrole Hybrid.

A hybrid receptor-sensor for anions originating from the merging of positively charged ammonium moieties for electrostatic attraction/stronger binding of azacrowns with directionality of calixpyrrole hydrogen bond donors for selectivity is investigated. As demonstrated this hybrid receptor-sensor shows a remarkable selectivity for orthophosphate even in the presence of other phosphates and anions found in cellular materials (Kassoc H2PO4 ->H2P2O7 2->AMP-≫ADP2- or ATP3- over halides, nitrate, or hydrogen sulfate; all Na+ salts in water) but also cellular polyphosphate or phospholipids. This selectivity is harnessed in a real-time monitoring of cell lysis by lysozyme, which releases orthophosphate and other phosphates and anions from the cells. This sensitive (LOD 0.4 μM) fluorescence-based microscale method compares favorably with the state-of-the-art techniques but can easily be practiced in a high-throughput screening (HTS) manner. The anion binding and selectivity in aqueous solutions were investigated by NMR and put in context with phosphate binding of the parent calix[4]pyrrole. The microscopic understanding of anion binding by the hybrid receptor was then obtained from a combination of density functional theory (DFT), classical molecular dynamics (MD) with explicit water solvation, and ab initio MD (AIMD) simulations. Correlating the NMR and fluorescence binding data with studies of solvation of the receptor, phosphate anion, and the resulting complex confirms the binding is largely driven by entropic component (TΔS) associated with receptor and anion desolvation.

A Novel Method to Incorporate 2,2-Difluoroethyl Group as a Lipophilic Hydrogen-Bond Donor

A Novel Method to Incorporate 2,2-Difluoroethyl Group as a Lipophilic Hydrogen-Bond Donor

Kinetic and mechanistic studies on the synthesis of dimethyl carbonate reaction using deep eutectic solvents as catalysts

Dimethyl carbonate (DMC) is extensively utilized in various industries due to its exceptional physical and chemical properties, functioning as an additive in gasoline and an electrolyte solvent in lithium batteries. Among several production methods, the transesterification of propylene carbonate (PC) with methanol (MeOH) is the most efficient and environmentally friendly. This study synthesized various deep eutectic solvents (DESs) using choline chloride (ChCl) as the hydrogen bond acceptor (HBA) and monoethanolamine (MEA) as the hydrogen bond donor (HBD) in molar ratios of 1: n (n = 5, 6, 7, 8). The DESs’ structures were analyzed using Fourier Transform Infrared (FT-IR) spectroscopy, and their melting points were determined via differential scanning calorimetry (DSC). The density, viscosity, and surface tension of the DESs were measured over a temperature range from 318.15 K to 358.15 K. The catalytic effects of four different DESs on PC transesterification with MeOH were investigated, revealing that ChCl-6MEA was the most effective catalyst, prompting its selection for further experiments. Subsequent investigations examined the effects of temperature, MeOH quantity, and catalyst dosage on PC conversion and DMC yield. Additionally, this study explored chemical equilibrium and reaction kinetics through experimental and theoretical approaches. Activity-based chemical equilibrium constants, derived from experimental data, and the van’t Hoff equation elucidated their temperature dependency. A pseudo-homogeneous (PH) model characterized the non-ideal thermodynamic behavior of the liquid phase in reaction kinetics analysis. The Arrhenius equation was employed to delineate the impact of temperature variations on reaction rate constants. Finally, the proposed reaction mechanism for ChCl-6MEA catalyzed transesterification was elucidated and verified through quantum chemistry (QC) calculations.