Hydrogen Donor Research Articles

The adsorption mechanism and optimal dosage of walnut shell biochar for chloramphenicol

Biochar derived from biomass pyrolysis has proven to be an excellent material for pesticide adsorption and can be used as soil amendment for pesticide non-point pollution. However, the adsorption and desorption mechanisms for certain biochar and pesticide are still unclear. In this study, we investigated the properties of biochar derived from walnut (Juglans regia L.) shell (WSB), and used batch equilibrium method to investigate the adsorption and desorption behavior for chlorantraniliprole (CAP). The physical-chemical analysis showed that there were mainly lignin charcoal of alkyl carbon, methoxyl carbon, aromatic carbon, and carboayl carbon as the primary carbon compounds of WSB. The π - π electron donor acceptor interaction, electrostatic interaction, and hydrogen bond were the primary adsorption mechanisms of the WSB adsorption. Batch equilibrium study under 298 K showed that WSB application in the soil significantly improved the adsorption ability for CAP, and the adsorption behavior was a mono-layer adsorption process as Langmuir model fitted the adsorption isotherm data better than the Freundlich model. While Freundlich model analysis showed that WSB addition to the soil changed the isothermal adsorption line from the S style to the L style. The spontaneous degree reaction of sorbents from strong to weak was in the following order: 5%-WSB >7%-WSB >10%-WSB >1%-WSB >3%-WSB > soil > WSB, and the maximum application effect was achieved at 5 % (m/m) WSB dosage mixed with the soil. Therefore, we considered that WSB addition in soil increased its CAP adsorption capacity, and 5 % (m/m) WSB application was the best choice for CAP pollution control. These data will contribute to the adsorption mechanism and the optimal use dosage of WSB for CAP pollution control.

Novel ternary deep eutectic solvents pretreatment of corn stalk to realize high-value utilization

The high-valued utilization of biomass components through pretreatment technology can effectively alleviate the pressure of energy and environment. In this study, a ternary deep eutectic solvent (TDES) was prepared by using glycolic acid (GA) and ethylene glycol (EG) as double hydrogen donors and benzyl trimethyl ammonium chloride (TMBAC) as hydrogen acceptor. The corn stalk was separated by TDES to obtain cellulose-rich solid residue and low-condensed lignin. Moreover, the solid residue was converted into bio-oil by rapid pyrolysis, and the low-condensed lignin was converted into fluorescent lignin by grafting luminol for information encryption. The results showed that under the pretreatment condition of 150℃ for 3 h, TDES with the molar ratio of 1:1:2 had a lignin removal ratio of 90.60 %, and the yield of levoglucosan obtained from solid residue pyrolysis bio-oil reached 36.38 %. Furthermore, TDES prevented lignin from forming a C-C polycondensation structure and endowed it with polyhydroxy properties, which was beneficial to graft luminolto enhance the fluorescence intensity efficiently. The high-intensity fluorescent grafted lignin was used for information encryption of various materials. The mechanism of TDES pretreatment and luminol grafting were explored, and the mass balance of corn stalk during pretreatment was described. This study provides a green, environmentally friendly, and efficient pretreatment process for the high-value utilization of biomass.

Novel Ketone Derivatives Involving Triphenylamine Electron‐Donating Group as Low Migration Photoinitiators for Visible Light Radical Polymerization and 3D Printing

AbstractGiven the ongoing advancements in photopolymerization technology, there is an imperative need to develop novel free radical photoinitiators (PIs) with long‐wavelength absorbance and low migration. To meet the demand for visible light photopolymerization, four novel ketone derivatives photoinitiators (PHMOs) were synthesized in this study via a one‐step reaction. By constructing the push‐pull structure, the maximum absorption wavelength of the new PIs was red‐shifted to the vicinity of 400 nm, satisfying the requirement of visible excitation. The one‐component photoinitiation effect of PHMOs under visible light was comparable to that of Irgacure 1173, among which the photopolymerisation performance of PHMO‐2 was significantly superior to that of 1173. The photopolymerization effect of the two‐component photoinitiaton system composed by the addition of hydrogen donor was significantly improved. PHMO‐1 was successfully used in 3D printing to produce well‐defined printed products. The photolysis mechanism of PHMOs was investigated by steady‐state photolysis and electron spin resonance test. In addition, PHMOs had good solubility, thermal stability and good biosafety. Attributed to the presence of double bonds, PHMOs had low migration. These excellent properties indicated that PHMOs had desirable potential applications in the field of visible light polymerization.

Benzoic Acid Serves as Precursor of Catalytic HAT Reagent in a Two-Molecule Photoredox System.

The photoinduced regioselective HAT reactions of acetals, ethers, and alcohols using benzoic acids in a two-molecule photoredox system led to the formation of new C-C bonds with alkenes under mild conditions. Aryl carboxy radicals generated from benzoic acids in a two-molecule photoredox system can function as catalytic HAT reagents, even though an excess amount of a hydrogen donor substrate is required. Various acetals, ethers, alcohols, and alkenes can be employed in the photoreaction to provide both high yields of adducts and high recoveries of benzoic acids.

Air-Stable Triazole-Based Ru(II) Complexes Catalyzed Transfer Hydrogenation of Ketones and Aldehydes Using Ethanol as a Solvent and a Hydrogen Donor

Abstract. The synthesis and characterization of two air-stable ruthenium (II) complexes from readily available triazole-based ligands are described. Both ruthenium complexes, one bearing a bidentate ligand (C-1) and the other a tridentate ligand (C-2), were tested as catalysts in the transfer hydrogenation of ketones and aldehydes using ethanol as a sustainable hydrogen source under aerobic conditions. Notably, the C-2 complex displayed exceptional efficiency under relatively mild conditions, demonstrating a wide substrate tolerance encompassing both alkyl and aryl ketones, as well as aryl aldehydes. Furthermore, our findings highlight the potential of Ru(II) complexes as effective catalysts for the hydrogenation of carbonyl bonds using ethanol, representing a green and sustainable approach without the necessity for an inert gas. Resumen. En este trabajo se describe la síntesis y caracterización de dos complejos de rutenio(II) estables al aire con ligantes basados en triazoles. En general, los triazoles pueden obtenerse fácilmente a través de reacciones simples utilizando reactivos comercialmente disponibles. Ambos complejos de rutenio, uno con un ligante bidentado (C-1) y el otro con un ligando tridentado (C-2), se probaron como catalizadores en reacciones de hidrogenación por transferencia de cetonas y aldehídos, utilizando etanol como fuente sostenible de hidrógeno en condiciones aeróbicas. En particular, el complejo C-2 mostró una eficiencia excepcional en condiciones relativamente suaves, demostrando una amplia tolerancia tanto con cetonas alquílicas como aromáticas, además de hidrogenar eficientemente aldehídos aromáticos. Estos resultados ponen de manifiesto el potencial de los complejos de Ru(II) como catalizadores eficaces para la hidrogenación de enlaces carbonilo utilizando etanol, lo que representa un enfoque ecológico y sostenible sin necesidad de un gas inerte.

Advances in Sustainable γ-Valerolactone (GVL) Production via Catalytic Transfer Hydrogenation of Levulinic Acid and Its Esters.

γ-Valerolactone (GVL) is a versatile chemical derived from biomass, known for its uses such as a sustainable and environmentally friendly solvent, a fuel additive, and a building block for renewable polymers and fuels. Researchers are keenly interested in the catalytic transfer hydrogenation of levulinic acid and its esters as a method to produce GVL. This approach eliminates the need for H2 pressure and costly metal catalysts, improving the safety, cost effectiveness and environmental sustainability of the process. Our Perspective highlights recent advancements in this field, particularly with respect to catalyst development, categorizing them according to catalyst types, including zirconia-based, zeolites, precious metals, and nonprecious metal catalysts. We discuss factors such as reaction conditions, catalyst characteristics, and hydrogen donors and outline challenges and future research directions in this popular area of research.

Study on thermal decomposition and enrichment quality of coal from Mogoin gol deposit in Mongolia

The main purpose of this study is to investigate the thermal stability and the mechanism of thermal decomposition of Mogoin gol coal, the possibility of liquefaction by pyrolysis and thermolysis, and the possibility of enriching by heavy liquids to reduce the mineral content of coal and improve its quality. Under this purpose, The Mogoin gol coal was characterized by proximate and ultimate analysis, thermogravimetry, and investigated its thermal decomposition (thermolysis and pyrolysis). Thermogravimetric analysis was performed using Japanese HITACHI TG/DTA7300 instrument and pyrolysis investigation was carried out at different heating temperatures 200–700 °C with constant heating rate 20 °C/min for 80 min. On the basis of proximate and elemental analysis results, it has been indicated that the Mogoin gol coal is high-rank coking coal. The pyrolysis of Mogoin gol coal was studied by SNOL furnace at different heating temperatures and obtained from pyrolysis products such as hard residue, tar, pyrolytic water, and gas. From pyrolysis, the yield of pyrolysis tar (6.28%) was highest at 700 °C. The experiment of thermal decomposition (thermolysis) was carried out in air closed autoclave at 350–450 °C and using hydrogen donor solvent (tetraline) with different mass ratios of coal and solvent (1:1.75; 1:1.5). In the thermolysis experiment, the yield of liquid product is highest with the coal: solvent ratio of 1:1.5 at 450 °C.

Iron-Catalyzed Transfer Hydrogenation of Allylic Alcohols with Isopropanol.

Herein, we report an iron-catalyzed transfer hydrogenation of allylic alcohols. The operationally simple protocol employs a well-defined bench stable (cyclopentadienone)iron(0) carbonyl complex as a precatalyst in combination with K2CO3 (4 mol %) and isopropanol as the hydrogen donor. A diverse range of allylic alcohols undergo transfer hydrogenation to form the corresponding alcohols in good yields (33 examples, ≤83% isolated yield). The scope and limitations of the method have been investigated, and experiments that shed light on the reaction mechanism have been conducted.

Achieving the Birefringence Optimization by Methyl Modulation in Organic Nonlinear Optical Crystals

AbstractNon‐centrosymmetric organics are promising nonlinear optical (NLO) candidates, which always exhibit a short UV absorption cutoff edge, and a strong second harmonic generation (SHG) response, but an overlarge birefringence. Here, in order to optimize the birefringence, the methyl modulation of π‐conjugated organic planar units is proposed and implemented with the urea structure as a template. Thus, N‐methylurea and N,N'‐dimethylurea crystals are obtained by partially replacing hydrogen atoms with methyl groups. This replacement reduces hydrogen donors and weakens interchain hydrogen bonds, which facilitates the decreasing density and the parallel arrangement of π‐conjugated planar units. Hence, both N‐methylurea and N,N'‐dimethylurea crystals exhibit not only an optimized birefringence (N‐methylurea ≈0.099 and N,N'‐dimethylurea ≈0.072 at 546 nm) but also an enhanced SHG response (N‐methylurea ≈1.2 × β‐BaB2O4 and N,N'‐dimethylurea ≈1.9 × β‐BaB2O4), while maintaining a short UV absorption cutoff edge. Therefore, this work provides a novel strategy for the structural design and performance modulation of organic NLO crystals.

Effects of Ultrasonic Treatment and Hydrogen Donor Addition on the Viscosity of Iraqi Heavy Crude Oil

يختبر البحث الحالي التأثيرات المشتركة للإشعاع بالموجات فوق الصوتية والمادة المانحة للهيدروجين على لزوجة النفط الخام الثقيل. تمت دراسة تأثير زمن التعرض للموجات فوق الصوتية والطاقة ودورة التشغيل ودرجة الحرارة على لزوجة النفط الخام العراقي الثقيل الذي يملك قيمة .20.32 = API كما تم فحص لزوجة عينات النفط الخام التي تم خلطها بمانح الهيدروجين (Decalin) وإخضاعها للمعالجة بالموجات فوق الصوتية في ظل الظروف المثالية، لتقييم التأثير المشترك للإشعاع بالموجات فوق الصوتية والمانح للهيدروجين على لزوجة النفط الخام. شهدت اللزوجة انخفاضًا بنسبة 52.34 % بعد دقيقتين من التعرض للموجات فوق الصوتية، عند طاقة 360 W ، دورة تشغيل 0.8، 35 درجة مئوية، وأضافه %8 نسبة حجمية من Decalin. للتحقق من صحة نتائج التجارب، تم إجراء فحص محتوى الأسفلتين، محتوى الكبريت، API، واختبار التقطير على كل من العينة الاولية و النهائية (في ظل الظروف المثلى). وأظهرت تراكيز الأسفلتين والكبريت انخفاضا قدره37.51 % و%35.04 على التوالي. تشير النتائج إلى أن ظاهرة التجويف وظاهرة الحرارة والتأثير الميكانيكي للموجات فوق الصوتية قد تساهم في تكسير سلاسل الكربون الممتدة وتقليل حجم الإسفلتين المتجمع مما يؤدي إلى انخفاض لزوجة النفط الخام. علاوة على ذلك، أظهرت النتائج أن التطبيق المتزامن للموجات فوق الصوتية والمادة المانحة للهيدروجين أدى إلى انخفاض كبير في لزوجة النفط الخام عند مقارنته بالنفط الخام غير المعالج أو المعالج بالموجات فوق الصوتية فقط.

Mechanism of coal pitch pre-hydrogenation catalyzed by metal-free catalytic system and preparation of mesophase pitch

Coal pitch (CP) molecules have high aromaticity, planarity and condensation degree, usually requiring hydrogenation to prepare high-quality mesophase pitch (MP). However, current hydrogenation methods often face challenges such as harsh conditions, residual ash or insufficient hydrogenation. Here, with 5 wt% tetrahydronaphthalene (THN) as the hydrogen donor, hydrogenated CP (HCP) with low ash content and high H/C was prepared at low temperature and pressure via a metal-free catalytic system with boron trifluoride ether (BF3·Et2O) as catalyst and p-toluenesulfonic acid (TsOH) as co-catalyst and 5 wt%. Subsequently, MP was prepared from the HCP, and the mechanisms of catalytic hydrogenation and the formation of mesophase macromolecules were elucidated. The characterization results indicated that CP achieved optimal hydrogenation when the molar ratio of BF3 to TsOH was 1:1. The HCP obtained under this condition can further prepare a wide-area streamlined MP. During the hydrogenation process, TsOH provided proton hydrogen to BF3, forming a complex acid that facilitated carbocation reactions between THN and CP molecules, thereby enhancing hydrogenation efficiency. However, when the molar amount of TsOH exceeded that of BF3, it would catalyze the polymerization of HCP molecules to a certain extent, reducing the hydrogenation effect. Meanwhile, it could introduce more sulfonic acid groups into the molecular structure, causing cross-linking of polycyclic aromatic hydrocarbons and excessive system viscosity during the preparation of the MP, resulting in a mosaic optical texture. This work is of significant importance for promoting the efficient hydrogenation of CP and the preparation of high-quality MP.

Investigating the antioxidant potential and mechanism of a hydrazide bioactive component of garlic: insights from density functional theory calculations, drug-likeness and molecular docking studies.

Glutathione remains one of the most efficient antioxidant compounds in living systems, and the biological abilities of hydrazides have been well documented in literature. This study highlights the phytochemical constituents of garlic and the separation of the bioactive benzoic acid, 4-chloro- 1-(4-methoxyphenyl) hydrazide (BA4C) using gas chromatography-mass spectroscopy (GC-MS) technique. Preliminary phytochemical screening reveals the presence of alkaloids, saponins, flavonoids, tannins, terpenoids, steroids and phenols. Computationally, compound BA4C was optimized using the B3LYP/aug-cc-PVDZ DFT method. Spectroscopic studies of the compound involved analysis of the vibrational FT-IR frequencies and the modes of vibrations. Frontier molecular orbitals analysis records an energy gap of 4.3391eV; NBO studies reveal that the compound has strong perturbation energies of 246kcal/mol and 269kcal/mol among its intramolecular interactions such as *C12 - C13 to *C14 - C15 and *C11 - C16 to *C14 - C15, respectively. According to the visualization of non-covalent interactions, steric repulsions were observed at the core of the phenyl and benzene rings. However, other regions of the compound depict a significant balance of forces between steric repulsions and van der Waals forces. To significantly deduce the reducing power of compound BA4C, electrons were found to be highly localized at the methoxy and hydrazide moieties significantly implying their propensity to donate electrons to oxidized systems. Furthermore, ADMET analysis reveals that the compound has two hydrogen donors. Most significantly, the compound binds to NADPH dehydrogenase (5V4P) and glutathione reductase (1XAN) with binding energies of - 6.0kcal/mol and - 8.0kcal/mol showing considerable favourable binding feasibility as well as forming plural hydrogen bonds with the amino acid residues. Notably, BA4C was bonded at the active site of 1XAN, which implies the ability of the compound for the reduction of oxidized glutathione.

Biosensor Based on ZIF-67-HRP and MWCNTs Nanocomposite Modified Glass Carbon Electrode for the Detection of Luteolin in Vegetables.

Luteolin has various pharmacological properties, including anti-inflammatory, antioxidant, and antitumor characteristics. Due to its potential value in drugs and functional foods, it is important to develop an efficient method for detecting luteolin. In this work, the poor selectivity of existing luteolin nonenzymatic sensors was solved by translating the enzyme-catalyzed reaction from bulk solution to the surface of a horseradish peroxidase (HRP) modified electrode through an electrocatalytic oxidation process. Here, we modified the surface of a glassy carbon electrode (GCE) with metal-organic frameworks (MOFs; ZIF-67 here, abbreviated as ZIF), functional nanomaterials, and HRP and finally covered it with Nafion (NF). In this case, luteolin acts as a hydrogen donor, and the electrode acts as a hydrogen acceptor; the oxidation reaction occurs on the electrode surface. The use of ZIF-67 ensured the conformational stability of HRP to ensure the selectivity and anti-interference property, and SDS-dispersed multiwalled carbon nanotubes (MWCNTs) enhanced the electrode conductivity. The use of NF avoids shedding of the electrode material during the testing process. A UV-vis spectrophotometer was used to study the selectivity of luteolin by HRP and the compatibility between HRP and ZIF. The materials were characterized and analyzed by scanning electron microscopy and transmission electron microscopy. Due to the synergistic effect of these nanomaterials, the linear range of NF/ZIF-HRP/MWCNTs-SDS/GCE was 1.0 × 10-2 to 6.0 μM, with detection limits of 25.3 nM (S/N = 3). The biosensor showed long-term stability and reproducibility, with a relative standard deviation of 4.2% for the peak current (n = 5). Finally, the biosensor was successfully used to detect luteolin in carrots, celery, and cauliflower.

New ruthenium(II) isocyanide catalysts for the transfer hydrogenation of ethyl levulinate to γ-valerolactone in C2-C6 alcohols

Transfer hydrogenation (TH) processes are receiving great attention for biomass valorization and ruthenium(II) complexes are renowned TH catalysts both on laboratory and industrial scale. Only a few homogeneous catalytic precursors are available in the literature for the TH of ethyl levulinate (EL) to γ-valerolactone (GVL). Herein, starting from simple, commercially available isocyanides, two classes of air-stable ruthenium(II) complexes were synthesized and tested as catalytic precursors. First, an optimized preparation of Ru(II) p-cymene isocyanide complexes was developed. Then, the thermally induced p-cymene/DMSO substitution gave access to unprecedented ruthenium isocyanide-DMSO complexes. All the complexes were characterized and tested in TH of EL to GVL showing promising performances, adopting 2-propanol as hydrogen donor, a low catalyst (Ru) and co-catalyst (KOH) amount, working under microwave heating for 1 h at 150 °C. The most selective systems were also successfully tested with different biomass-derived alcohols, including 2-butanol. Finally, the recycling of the best catalyst was also investigated, thus improving the efficiency of the entire process.

Reduction of Nitroarenes to Anilines Using H2S as a Hydrogen Donor by a Ceria-Supported Iron Composite

Reduction of Nitroarenes to Anilines Using H2S as a Hydrogen Donor by a Ceria-Supported Iron Composite

Stage of lactation, parity, breed, milk composition and minerals affect the non-enzymatic antioxidant activity of sheep milk

The aims of this study were to i) characterize sheep milk for non-enzymatic antioxidant activity via 2 different assays, namely the ferric reducing antioxidant power (FRAP) and the 2-diphenyl-1-picryl-hydrazyl-hydrate (DPPH), and ii) investigate the effect of milk composition and animal-related parameters on these 2 assays by using Generalized Additive Mixed Model (GAMM) approach. A total of 740 ewes belonging to Massese and Comisana breeds were sampled once during the morning milking across 11 sampling sessions. All milk samples were analyzed for fat, protein, casein, and lactose, somatic cell score (SCS) and minerals (Ca, Mg, Na and Cl). The FRAP and DPPH assays were tested to measure the non-enzymatic antioxidant activity of milk, expressed as μM eq. ascorbic acid/mL of milk and % of inhibition, respectively. The GAMM model included the effect of parity and breed as parametric terms, and the effect of days in milk (DIM), milk yield and the interactions protein × fat, casein × SCS, Ca × Mg and Na × Cl as smooth terms. The sampling day was included in the model as random effect. Results revealed that the non-enzymatic antioxidant capacity of sheep milk, expressed as FRAP, was affected by DIM, potentially because of changes in milk composition over time. Conversely, parity and breed of ewes affected DPPH, suggesting that age- and breed-specific factors are related to specific components in milk acting as hydrogen donors. Milk fat and high casein percentages were found to significantly affect FRAP, while protein content was crucial for high DPPH levels. Additionally, Ca and Mg emerged as important non-enzymatic antioxidants for both FRAP and DPPH, highlighting their important role in antioxidant activity of sheep milk. On the other side, combinations of Na and Cl were particularly influential for FRAP, revealing the complex relationship between these minerals and non-enzymatic antioxidant activity of milk. These findings offer valuable insights into the factors affecting the antioxidative properties of sheep milk, highlighting the need for further exploration of other non-enzymatic antioxidants and their contribution to the total antioxidant activity.

Pyrolysis behaviour and synergistic effect in co-pyrolysis of wheat straw and polyethylene terephthalate: A study on product distribution and oil characterization

Renewable lignocellulosic biomass is a favorable energy resource since its co-pyrolysis with hydrogen-rich plastics can produce high-yield and high-quality biofuel. In contrast to earlier co-pyrolysis research that concentrated on increasing product yield, this study comprehends the synergistic effects of two distinct feedstocks that were not considered earlier. This work focuses on co-pyrolyzing wheat straw (WS) with non-reusable polyethylene terephthalate (PET) for the production of pyrolysis oil. WS and PET were blended in different ratios (100/0, 80/20, 60/40, 40/60, 20/80, and 0/100), and pyrolysis experiments were conducted in a fixed-bed reactor under different temperatures to assess their synergistic effect on oil yield. Synergy rates of up to 7.78 % were achieved on yield for the blends of plastic and biomass at a temperature of 500 °C. In comparison to individual biomass or plastics, co-pyrolyzing PET-biomass blends demonstrated good process interaction and promoted the yields of value-added products. The heating value of the pyrolysis oils was in the range of 16.45–28.64 MJ/kg, which depends on the amount of plastic present in the feedstock. The physical analysis of the oils shows that they can be used for heat production by direct combustion in boilers or furnaces. The correlation between WS and PET was validated with the aid of Fourier transform infrared spectroscopy (FT-IR) and gas chromatography-mass spectrometry (GC-MS) analysis. The GC-MS result demonstrated the presence of different compounds such as O-H compounds, esters, carbonyl group elements, acids, hydrocarbons, aromatics, and nitrogenated compounds in the pyrolysis oil, which differed based on the proportions of PET in the feedstock. The increased hydrocarbon and reduced oxygen percentages in the pyrolysis oil were implicitly caused by enhanced hydrocarbon pool mechanisms, in which the breakdown of PET may be supplied as a hydrogen donor. Overall, waste lignocellulosic biomass and plastics can be used to produce biofuels, which helps reduce the amount of solid waste that ends up in landfills. This study also revealed that future research should be focused on the reaction mechanisms of WS and PET co-pyrolysis in order to examine the synergistic interactions.

Effect of lathyrane-type diterpenoids in neural stem cell physiology: Microbial transformations, molecular docking and dynamics studies

Promoting endogenous neurogenesis for brain repair is emerging as a promising strategy to mitigate the functional impairments associated with various neurological disorders characterized by neuronal death. Diterpenes featuring tigliane, ingenane, jatrophane and lathyrane skeletons, frequently found in Euphorbia plant species, are known protein kinase C (PKC) activators and exhibit a wide variety of pharmacological properties, including the stimulation of neurogenesis. Microbial transformation of these diterpenes represents a green and sustainable methodology that offers a hitherto little explored approach to obtaining novel derivatives and exploring structure–activity relationships. In the present study, we report the biotransformation of euphoboetirane A (4) and epoxyboetirane A (5), two lathyrane diterpenoids isolated from Euphorbia boetica, by Mucor circinelloides MC NRRL3631. Our findings revealed the production of nine biotransformation products (6–14), including jatrophane derivatives originated through an unprecedented rearrangement from the parent lathyranes. The chemical structures and absolute configurations of the new compounds were elucidated through comprehensive analysis using NMR and ECD spectroscopy, as well as MS. The study evaluated how principal metabolites and their derivatives affect TGFα and NRG1 release, as well as their potential to promote proliferation or differentiation in cultures of NSC isolated from the SVZ of adult mice. In order to shed some light on the mechanisms underlying the ability of 12 as a neurogenic compound, the interactions of selected compounds with PKC δ-C1B were analyzed through molecular docking and molecular dynamics. Based on these, it clearly appears that the ability of compound 12 to form both acceptor and donor hydrogen bonds with certain amino acid residues in the enzyme pocket leads to a higher affinity compound-PKC complex, which correlates with the observed biological activity.

Coupling aquathermolysis of water-heavy oil-methanol catalyzed by o-phenanthroline-Cu(II) complex at low temperature

In this study, a Cu(II) coordinated complex was synthesized using o-phenanthroline and copper chloride. The synthesized complex, serving as a aquathermolysis catalyst, significantly reduces heavy oil viscosity at lower temperatures. Studies indicate that at a reaction temperature of 200 °C, with a catalyst concentration of 0.1% and a reaction duration of 6 h, heavy oil viscosity significantly reduces. Heavy oil viscosity dropped from 392,000 mPa∙s to 63,000 mPa∙s, achieving an 83.93% reduction rate. This catalyst maintains superior catalytic performance at lower temperatures compared to other catalyst types. Using methanol as a hydrogen donor further enhances the catalyst’s effect, increasing the heavy oil viscosity reduction rate from 83.93% to 88.63%. Thermogravimetric, four-component, and elemental analyses reveal that aquathermolysis of heavy oil primarily occurs in its heavier components. Following the aquathermolysis reaction, there is an increase in light components and a decrease in impurity atoms in heavy oil, resulting in improved crude oil quality.

One-Pot Conversion of Biomass Saccharides to γ-Valerolactone over a Versatile Tin-Containing Material.

The synthesis of biofuel γ-valerolactone (GVL) from accessible biomass is an attractive and challenging goal. Here, we report an efficient, one-pot, and mild strategy for the efficient production of GVL from various biomass saccharides without using any homogeneous acid as a co-catalyst and molecular hydrogen as a hydrogen donor. A versatile porous tin-containing material (Sn(M)-S) was designed as an individual heterogeneous catalyst. As high as 68.4% yield of GVL form glucose was achieved in the presence of ammonia borane as a solid hydrogen donor under mild conditions, with GVL yields of 76.2%, 68.9%, 62.5%, and 52.2% being obtained from fructose, sucrose, cellobiose, and cellulose, respectively. The synergistic effect of Sn and sulfonic acid group in Sn(M)-S not only provides appropriate Lewis acid sites to promote the isomerization of glucose into fructose but also affords abundant Brønsted sites for the following conversion steps. Moreover, Sn(M)-S(1) showed good stability and reusability during consecutive recycles.