High Yield Research Articles

Chitosan/poly-γ-glutamic acid crosslinked hydrogels: Characterization and application as bio-glues

Ecofriendly hydrogels were prepared using chitosan (CH, 285 kDa) and two fractions of low molecular weight microbial poly-γ-glutamic acid (γ-PGA) (R1 and R2 of 59 kDa and 20 kDa, respectively). The hydrogels were synthesized through sustainable physical blending, employing three CH/γ-PGA mass ratios (1/9, 2/8, and 3/7), resulting in the formation of physically crosslinked materials. The six resulting CH/R1 and CH/R2 hydrogels were physico-chemically characterized and the ones with the highest yields (CH/R1 and CH/R2 ratio of 3/7), analyzed for rheological and morphological properties, showed to act as bio-glues on wood and aluminum compared to commercial vinyl- (V1) and acetovinyl (V2) glues. Lap shear analyses of CH/R1 and CH/R2 blends exhibited adhesive strength on wood, as well as adhesive/cohesive failure like that of V1 and V2. Conversely, CH/R2 had higher adhesive strength and adhesive/cohesive failure on aluminum, while CH/R1 showed an adhesion strength with adhesive failure on the metal similar to that of V1 and V2. Scanning electron microscopy revealed the formation of strong physical bonds between the hydrogels and both substrates. Beyond their use as bio-adhesives, the unique properties of the resulting crosslinked materials make them potentially suitable for various applications in paint, coatings, heritage preservation, and medical sector.

Novel triphenylamine-pyrene-based AIEgens: Specific detection and imaging of H2O2 in aqueous solution and cells

H2O2 plays a key regulatory role as a bioendogenous reactive oxygen species in cells and organisms. However, excessive production or accumulation of H2O2 during mitochondrial oxidative stress may lead to oxidative damage of cellular proteins and trigger rheumatic diseases, cancers, and a variety of neurodegenerative disorders such as Alzheimer's disease and Parkinson's disease. In addition, H2O2 is a very useful chemical widely employed in the textile and chemical industries, and its excessive emission not only pollutes the environment but also jeopardizes human health. Therefore, the sensitive and specific detection and removal of H2O2 is important for early diagnosis of diseases, treatment prognosis and environmental pollution monitoring. We have designed two novel triphenylamine-based AIEgens MOTPP and MOTPP-B, which each have a high solid-state fluorescence quantum yield and excellent aggregation-induced emission properties. MOTPP-B has high selectivity and anti-interference ability toward H2O2, a wide pH tolerance range, a sensing process that is complete in under 40 min, and a low detection limit of 120.77 nM. It has been successfully applied for the detection of low concentrations of H2O2 in the environment and to dual-channel imaging of low concentrations of exogenous H2O2 in living cells.

A bright Ce-based downshifting luminescence nanoprobe for NIR-IIb vessel imaging

Nanomaterials with unique emission in the second near-infrared window (NIR-II, 1000–1700 nm) are regarded as the promising probes for visualization of tumor vessels and cerebrovascular architecture, because of their superior features such as deep tissue penetration and large imaging resolution. Herein, the new Ce-based fluoride nanoparticles (NPs) with high-efficiency NIR-IIb emission were explored for high-resolution vascular imaging and tumor associated vessel detection. Under the same synthesis conditions, the Ce-based fluoride present the preferential formation CeF3 host and low upconversion (UC) emission, but possess more strong (1.45 times) NIR-IIb downconversion (DC) emission centered at 1525 nm under the irradiation of a 980 nm laser, which is significantly different from the traditional NaYF4:Yb/Er host. Through the efficient cross relaxation between Ce3+ and Er3+, intense NIR-IIb luminescence from Er3+ with high quantum yields were achieved, which make sure the entire mouse body and brain blood vessel imaging with supernal resolution (47.6 μm) were demonstrated. Moreover, the optical imaging in NIR-IIb region guided tumorous vascular visualization was successfully achieved. Therefore, the explored CeF3 NPs with boosting NIR-IIb emission can be employed as new diagnostic bio-probes used in high spatial resolution tumorous vessel detection.

Photothermal-enabled metal-free polyfuran photocatalysts for efficient solar-to-hydrogen peroxide energy conversion from seawater

Solar-driven H2O2 photosynthesis from inexhaustible seawater is promising for alleviating increasingly-serious energy/environmental crises. Herein, a new metal-free photothermal-assisted photocatalyst containing strong π-stacked polyfuran D-A couples is synthesized by employing 5-hydroxymethylfurfural as precursor, which enables the highly-efficient H2O2 photosynthesis from seawater without any sacrificial agent. Its unique aromatic and quinoid furan alternating structure promotes the photogenerated charge transfer and the activation of oxygen molecules, thus remarkedly boosting H2O2 production rate. Furthermore, its localized photothermal and “electron bridge” effects can enhance the kinetic process of this reaction and accelerate the charge transfer, respectively, resulting in a high H2O2 yield of 1883.81 μmol g−1 h−1 with a high solar-to-chemical conversion efficiency of 0.48 % in seawater under simulated-sunlight irradiation. Impressively, it can achieve a high H2O2 concentration of 1867.81 μmol L−1 in natural seawater in one day under natural-sunlight irradiation, representing the first successful application of metal-free polyfuran photocatalysts for the photothermal-assisted H2O2 photosynthesis from natural seawater.

Practical synthesis of chenodeoxycholic acid from phocaecholic acid

In this study, we developed an effective method for the large-scale synthesis of chenodeoxycholic acid (CDCA) from phocaecholic acid (PhCA). A high total yield of up to 72 % was obtained via five steps including methyl esterification, Ts-protection, bromination, reduction, and hydrolysis. The structures of the intermediates were confirmed by 1H NMR (Nuclear Magnetic Resonance), 13C NMR, HRMS (High Resolution Mass Spectrometry), and IR (Infrared Spectroscopy) spectroscopies. This method offers a new and practical approach to the synthesizing of CDCA.

In-situ passivation and anchoring of perovskite quantum dots on KSF:Mn phosphor for liquid crystal display

Perovskite quantum dots (PQDs) hold immense potential for application in backlight liquid crystal display (LCD) owing to their narrow emission spectra, tunable luminous wavelength along with high photoluminescence quantum yield. However, their poor stability severely impedes the practical application of PQDs in optoelectronic devices. Here, we prepare KSF@PQDs composites by in-situ generation of green-emitting MAPbBr3 PQDs on the surface of treated KSF:Mn red phosphors. The surface treatments on KSF:Mn are employed for realization of in-situ passivation and anchoring of MAPbBr3 through chemical interaction between the NH2 group on KSF:Mn and Pb2+ on PQDs, which enables high luminescence intensity, narrow spectral width and simultaneously high photostability of PQDs. Moreover, the ratio of green-to-red emission intensity in KSF@PQDs can be easily modulated by changing APTES content during the surface treatment of KSF:Mn. Further, white light-emitting diode devices consisting of InGaN chip and KSF@PQDs composite achieve luminous efficiency of 41.6lm·W-1, as well as wide color gamut of 116.6% for National Television Systems Council standard and 87.2% for Rec.2020 standard, which paves the way for the application of high stability PQDs in wide color gamut LCD.

Novel LaCl3:Yb2+ crystal scintillator for X-ray spectrometer

This work investigated the growth, optical properties, and scintillation performance of a LaCl3 single crystal doped with Yb2+ ions. The crystal was grown using the vertical Bridgman method. The photoluminescence spectrum resembled the X-ray induced luminescence spectrum, indicating emission from the 5d→4f transition of Yb2+. LaCl3:Yb2+ exhibited an energy resolution of 14.3% and a light output of 24,940 ph/MeV under 662 keV γ-ray excitation. Additionally, the scintillation decay profiles were measured using alpha particles and gamma rays from 241Am and 137Cs sources, respectively. These results suggest that Yb2+ could be a promising luminescence center for high light yield scintillation detectors.

Fluorescent and colorimetric dual-mode chemosensor for easy detection of Cu2+: Practical and smartphone-based application to test strip and water sample

A fluorescent and colorimetric dual-mode chemosensor HNHQ, based on the julolidine and naphthol moieties, was synthesized. Compound HNHQ exhibited unique photophysical properties of an intense fluorescence with a high quantum yield (Φ = 0.363) and a light yellow color through the ICT mechanism. HNHQ could detect Cu2+ through both a fluorescence turn-off and a colorimetry variation of light yellow to yellowish brown. HNHQ reacted with Cu2+ with a binding ratio of 1:1. The detection limit for Cu2+ was analyzed to be 1.60 μM for fluorescence and 1.32 μM for UV–vis, considerably below the safe value of 31.5 μM established by the World Health Organization (WHO). HNHQ analyzed Cu2+ in the pH range of 6–8 and reversibly identified Cu2+ by using ethylenediaminetetraacetic acid (EDTA). Moreover, HNHQ could effectively detect Cu2+ in mineral and tap water samples, in addition to test strips through fluorescent and colorimetric changes. As a portable probe, HNHQ was successfully applied to a smartphone-based RGB analysis for the quantitative examination of Cu2+. The detection mechanism of HNHQ for Cu2+ was illustrated by 1H NMR titration, ESI-MS analysis, and density functional theory (DFT) calculations.

Insight in NO synthesis in a gliding arc plasma via gas temperature and density mapping by laser-induced fluorescence

A gliding arc (GA) plasma, operating at atmospheric pressure in a gas mixture of 50% N2 and 50% O2, is studied using laser-induced fluorescence spectroscopy. The main goal is to determine the two-dimensional distribution of both the gas temperature and the NO ground state density in the afterglow. As GA plasma discharges at atmospheric pressure normally produce rather high NO x densities, the high concentration of relevant absorbers, such as NO, may impose essential restrictions for the use of ‘classical’ laser-induced fluorescence methods (dealing with excitation in the bandhead vicinity), as the laser beam would be strongly absorbed along its propagation in the afterglow. Since this was indeed the case for the studied discharge, an approach dealing with laser-based excitation of separate rotational lines is proposed. In this case, due to a non-saturated absorption regime, simultaneous and reliable measurements of both the NO density and the gas temperature (using a reference fitting spectrum) are possible. The proposed method is applied to provide a two-dimensional map for both the NO density and the gas temperature at different plasma conditions. The results show that the input gas flow rate strongly alters the plasma shape, which appears as an elongated column at low input gas flow rate and spreads laterally as the flow rate increases. Finally, based on temperature map analysis, a clear correlation between the gas temperature and NO concentration is found. The proposed method may be interesting for the plasma-chemical analysis of discharges with high molecular production yields, where knowledge of both molecular concentration and gas temperature is required.

Biorefinery of red seaweed Palmaria palmata for production of bio-based chemicals and biofuels

The seaweed Palmaria palmata was used as feedstock for production of chemical/fuel precursors (acetone, butanol, ethanol) and biogas. Palmaria palmata consists of xylan as major cell wall polysaccharide, as well as galactan and glucan. First, the biomass was subjected to acid hydrolysis at laboratory scale to solubilise fermentable sugars using acetic or hydrochloric acid as catalysts. Differences were observed in composition and amenability to hydrolysis of seaweeds from different harvests. Highest saccharification yields were obtained using HCl (pH 1.7, 120 °C, up to 80 % of xylose). Hydrolysates were fermented to acetone-butanol-ethanol by Clostridium beijerinckii reaching yields of 0.28 g products/g consumed sugars. The process by-products (solids after acetic acid hydrolysis and spent fermentation broth) were used as feedstocks for anaerobic digestion showing biogas yields between 310 and 650 L/kg dry organic material when mixed in different ratios with sugar beet pulp. Subsequently, the hydrolysis and fermentation processes were upscaled up to a 100-L pilot volume where nanofiltration was implemented to increase sugar concentration and remove salts. While high monomeric sugar yields were replicated during upscaling, fermentation inhibition was observed in the upscaled process. This paper shows Palmaria palmata to be a suitable feedstock for the co-production of bio-butanol and biogas and highlights process development needs to desalt and detoxify seaweed hydrolysates prior to fermentation.

An investigation of quantum dot theranostic probes for prostate and leukemia cancer cells using a CdZnSeS QD-based nanoformulation

Anticancer theranostic nanocarriers have the potential to enhance the efficacy of pharmaceutical evaluation of drugs. Semiconductor nanocrystals, also known as quantum dots (QDs), are particularly promising components of drug carrier systems due to their small sizes and robust photoluminescence properties. Herein, bright CdZnSeS quantum dots were synthesized in a single step via the hot injection method. The particles have a quasi-core/shell structure as evident from the high quantum yield (85 %), which decreased to 41 % after water solubilization. These water solubilized QDs were encapsulated into gallic acid / alginate (GA-Alg) matrices to fabricate imaging QDs@mod-PAA/GA-Alg particles with enhanced stability in aqueous media. Cell viability assessments demonstrated that these nanocarriers exhibited viability ranging from 63 % to 83 % across all tested cell lines. Furthermore, the QDs@mod-PAA/GA-Alg particles were loaded with betulinic acid (BA) and ceranib-2 (C2) for in vitro drug release studies against HL-60 leukemia and PC-3 prostate cancer cells. The BA loaded QDs@mod-PAA/GA-Alg had a half-maximal inhibitory concentration (IC50) of 8.76 μg/mL against HL-60 leukemia cells, which is 3-fold lower than that of free BA (IC50 = 26.55 μg/mL). Similar enhancements were observed with nanocarriers loaded with C2 and simultaneously with both BA and C2. Additionally, BA:C2 loaded QDs@mod-PAA/GA-Alg nanocarriers displayed a similar enhancement (IC50 = 3.37 μg/mL compared against IC50 = 11.68 μg/mL for free BA:C2). The C2 loaded QDs@mod-PAA/GA-Alg nanocarriers had an IC50 = 2.24 μg/mL against HL-60 cells. C2 and BA loaded QDs@mod-PAA/GA-Alg NCr had IC50 values of 7.37 μg/mL and 24.55 μg/mL against PC-3 cells, respectively.

How Photosynthetic Performance Impacts Agricultural Productivity in Hybrid Cotton Offspring

Currently, heterosis is an effective method for achieving high crop quality and yield worldwide. Owing to the challenges of breeding and the high cost of the F1 generation, the F2 generation is considered the more desirable hybrid offspring for agricultural production. The use of OJIP fluorescence provides rapid insights into various photosynthetic mechanisms. However, OJIP fluorescence has not been previously studied as an indicator of the rate of heterosis. Consequently, we investigated the relationship between photosynthetic characteristics and growth and developmental parameters in hybrid cotton cultivars. The findings showed a gradual decline in the photosynthetic performance of hybrid cotton as the number of generations increased. In comparison to the F3 generation, both the F1 and F2 generations showed minimal variations in parameters, thus maintaining hybrid dominant and emphasizing the agricultural production potential of the F2 generation. The JIP-test revealed significant differences in the relationship between ψEo and φEo parameters, as well as variations in the connections between the photo-response center and electron transfer efficiency, and between cotton yield and fiber quality in the hybrid progeny. These variations can serve as indicators for predicting the extent of hybrid dominance in cotton. The results indicated significant differences in the light and dark responses of the hybrid offspring. By using parents with similar photosynthetic performance as genetic resources for crossbreeding, the photosynthetic capacity of the hybrid progeny can be enhanced to facilitate the efficient absorption and conversion of light energy in crops.

Biorefinery of red seaweed Palmaria palmata for production of bio-based chemicals and biofuels

The seaweed Palmaria palmata was used as feedstock for production of chemical/fuel precursors (acetone, butanol, ethanol) and biogas. Palmaria palmata consists of xylan as major cell wall polysaccharide, as well as galactan and glucan. First, the biomass was subjected to acid hydrolysis at laboratory scale to solubilise fermentable sugars using acetic or hydrochloric acid as catalysts. Differences were observed in composition and amenability to hydrolysis of seaweeds from different harvests. Highest saccharification yields were obtained using HCl (pH 1.7, 120 °C, up to 80 % of xylose). Hydrolysates were fermented to acetone-butanol-ethanol by Clostridium beijerinckii reaching yields of 0.28 g products/g consumed sugars. The process by-products (solids after acetic acid hydrolysis and spent fermentation broth) were used as feedstocks for anaerobic digestion showing biogas yields between 310 and 650 L/kg dry organic material when mixed in different ratios with sugar beet pulp. Subsequently, the hydrolysis and fermentation processes were upscaled up to a 100-L pilot volume where nanofiltration was implemented to increase sugar concentration and remove salts. While high monomeric sugar yields were replicated during upscaling, fermentation inhibition was observed in the upscaled process. This paper shows Palmaria palmata to be a suitable feedstock for the co-production of bio-butanol and biogas and highlights process development needs to desalt and detoxify seaweed hydrolysates prior to fermentation.

Anticancer activity of synthesized 5-benzyl juglone on selected human cancer cell lines.

Cancer is a malignant disease that causes millions of deaths each year worldwide. As one of the cancer therapeutic strategies, chemotherapy is a means to destroy rapidly dividing cells. The main problem with cancer chemotherapy is the lack of selectivity of conventional chemotherapeutic drugs, leading to toxicity towards normal cells. Therefore, the discovery of anticancer agents with selectivity for fast-growing cancer cells was desirable. In this study, we report the synthesis and identification of the novel 5-benzyl juglone as a potential anticancer agent with selectivity toward certain cancer cell lines. An efficient synthetic method for 5-benzyl juglone has been established. The proliferation of cancer cell lines and a normal cell line treated by the target compound were studied using an MTT assay. In addition, the cell cycle arrest and apoptosis were determined by flow cytometry. Based on the Diels-Alder (D-A) reaction between 3,6-dimethoxy benzyne intermediate with furan, further acid-catalyzed intramolecular rearrangement and CAN-mediated oxidation, a convenient synthesis of 5-benzyl juglone has been achieved with high overall yield. The results from in vitro biological evaluation indicated that the juglone derivative exhibited potent antiproliferative activity against HCT-15 human colorectal cancer cells with an IC50 value of 12.27 μM. It exerted high inhibitory activity toward MCF-7 human breast cancer cells and, to a much lesser extent, to corresponding MCF-10A human breast epithelial normal cells with the IC50 ratio (IC50 in MCF-7 divided by IC50 in MCF-10A) of 0.62. The mechanistic investigations indicated that 5-benzyl juglone could induce cell cycle arrest at the G0/G1 phase and promote apoptosis of HCT-15 cells. The apoptotic effects possibly also contributed to its higher selectivity toward cancer cells than normal cell lines.

Energy transfer characteristics in Tb(III)‒2,5-dihydroxybenzoic acid complex

Energy transfer through organic sensitization to ligand-centred Ln3+ ions is crucial for developing multifunctional materials with high brightness and good quantum yield from an application perspective. Gentisic acid (2, 5-Dihydroxybenzoic acid), as organic biomolecule is well known as the side minor metabolite of Salicylic acid/Aspirin and often used for palliative treatment. As fluorescence probes, significant optical absorption of 2, 5-DHBA in deep UV region fluoresce in near visible region and have also been employed to sensitize REs ions through metal-organic complexation. The present work emphasizes on the fluorescence assessment of DHBA, DHBA:Tb3+, PHEN:Tb3+, and DHBA/PHEN:Tb3+ complexes in PVA matrix as well as in aliphatic solvents. UV irradiation of DHBA embedded in PVA matrix or alcoholic solvent results in a vivid green emission of Tb3+via linker-to-metal energy transfer (5D4→7F0-6). Moreover, the addition of PHEN pairing with DHBA:Tb3+ doped PVA matrix culminated in a broadened stimulus region (deep UV harvesting) and proficient energy transfer. Quantum Yield assessment revealed about the efficacy of DHBA is approximately 59 %, whereas for the optimized DHBA:Tb3+ in PVA matrix is about the 22 %. Colour tunability with Tb3+ concentrations, as well as the consequence of PHEN's as extended energy harvesting possibility, make it suitable for potential applications in optoelectronic devices, green LEDs, security inks, and biomarkers, etc.

High-performance and low-cost electrochemical reactor for limestone decarbonation applied to clinker production – A validation at laboratory scale

Limestone decarbonation to obtain CaO (calcium oxide) and produce cement is an industrial activity with enormous CO2 emissions (CaCO3(s)→CaO(s)+CO2(g)), due to the intrinsic calcination reaction of CaCO3 (calcium carbonate), in addition to the use of fossil fuels. One of the most recent ideas to reduce CO2 emissions in this process has been the electrochemical decarbonation of limestone where Ca(OH)2 (calcium hydroxide) is obtained as an intermediate product that is then used as CaO precursor in clinker synthesis.This study shows the design of a low-cost electrochemical reactor and the optimization of the parameters to produce Ca(OH)2 with high purity and yield from the decarbonation processes of pure CaCO3 and limestone used in the cement industry. In addition, the remaining limestone sludge and electrolytic solutions were analyzed, and it was found that the sludge can be used as a correction material in clinker preparation, and it is also possible to reuse the electrolytic solution twice. Finally, the main finding is the proposal of a new clinker synthesis, which results in a cement with comparable characteristics to those of ordinary Portland cement, using Ca(OH)2 obtained from the electrochemical decarbonation of CaCO3, achieving a reduction in CO2 emissions of approximately 90% compared to the conventional method.

Lu, Sm, and Y-based double-decker phthalocyanines with enhanced photodynamic therapy performance

This paper focuses on the preparation of 3,5-di-tert-butylphenoxy substituted Lu, Sm, and Y-based double-decker phthalocyanines (Pcs), and investigation of their PDT properties. Briefly, 1,8,15,22-tetra-(3,5-di-tert-butylphenoxy) bisphthalocyanine derivatives (denoted LuPc2-3, SmPc2-4, YPc2-5) were synthesized by a two-step process. First, metal-free 1,8,15,22-tetra-(3,5-di-tert-butylphenoxy)phthalocyanine was prepared by tetramerization of 3,5-di-tert-butylphenoxy phthalonitrile, which is followed by reaction of different lanthanide salts with 1,8,15,22-tetra-(3,5-di-tert-butylphenoxy)bisphthalocyanine. The resultant double-decker Pcs were characterized in detail by UV–Vis, FT-IR, 1H NMR, fluorescence spectroscopy, MALDI-TOF MS, and elemental analysis. Strikingly, we report that double-decker phthalocyanines are not only photostable, but also exhibit relatively high singlet oxygen quantum yields of 0.96 (LuPc2-3), 0.91 (SmPc2-4) 0.87 (YPc2-5) and in THF.

Improving the value of planting and breeding waste compost in agricultural applications: A zucchini cultivation case and circular agricultural models analysis

An important way of utilizing agricultural wastes to improve soil quality is the use of planting and breeding waste compost (PBWC). However, the impact of compost on agricultural production systems is unclear. Therefore, in order to study the effect of PBWC on crop growth, soil environment, and circular agriculture, PBWC [sheep manure (SM): tail vegetable (TV): corn straw (CS) = 6: 3: 1] was used based on chemical fertilizer reduction for zucchini production. In zucchini production systems, R9 (chemical fertilizer reduction by 30 % + 9,000 kg ha−1 PBWC) treatment was most effective in improving the quality and yield of zucchini fruits, mainly by improving the soil microenvironment, manifested in (1) increasing soil alkali-hydrolyzable nitrogen (AN) available potassium(AK), and soil organic matter (SOM), reducing EC, and improving C/N. (2) Increasing the richness and metabolic capacity of bacterial community. (3) Increasing the abundance of Proteobacteria, a phylum with absolute dominance (up to 32.46 %). Then, an optimization model of “summer corn − greenhouse zucchini − fattened sheep” was constructed to analyze the effect of changes in fertilizer dosage usage on the whole model. Compared with the local traditional recycling model, the optimized system reduced the ratio of inorganic to organic nitrogen input from 2.8:1 to 1.4:1, increased the recycling rate of nitrogen (N), phosphorus (P), and potassium (K) by 31.28 %, 50.84 %, and 30.25 %, respectively, and the net energy yield ratio (EYR) increased by 1.04. The optimized recycling system had significant economic and environmental benefits, which would become the basis for moving towards more sustainable farming. Overall, the circular agriculture model with PBWC returning as the core achieves sustainable production by improving material recycling and soil microenvironment. Therefore, chemical fertilizer reduction by 30 % combined with 9000 kg ha−1 PBWC can be used in practical production to improve the productivity of the circular agriculture model and achieve high yield and high quality crops.

Synthesis of spiroindoline derivatives and biphenyl compounds in green solvent via a “capture–release” mechanism using modified polyacrylonitrile fiber as a catalyst

Green synthesis of critical bioactive molecules and fine chemicals is attracting increasing interest. This study investigates the use of two distinct functionalized polyacrylonitrile (PAN) fibers (PANEDBPF and PANEDBP-Pd0F) as effective catalysts in a green solvent comprising ethanol and water. Firstly, a PAN fiber was modified using 2-(diphenylphosphino) ethylamine, a strongly nucleophilic phosphine compound, to obtain PANEDBPF. Spiroindoline derivatives were obtained in 98 % yields when the reaction was conducted using 5 mol% of PANEDBPF as the catalyst at 70 °C for 30 min. Next, we loaded PdNPs onto PANEDBPF to obtain PANEDBP-Pd0F. When the Suzuki coupling reaction was conducted at room temperature (25 °C) using 0.5 mol% of PANEDBP-Pd0F, the products were obtained in an extremely high yield of 99 %. Additionally, the unique enrichment of the substrate by the functionalized fibers during the reaction and the subsequent release of the product from the microenvironment conform to the “capture–release” reaction mode of catalysis. Both PANEDBPF and PANEDBP-Pd0F demonstrated good gram-scale amplification, repeatability, catalytic activity, and stability. Hence, they are highly promising candidates for green chemistry applications.

Talc: A natural mineral base catalyst for the one pot synthesis of bis(pyrazolyl)methane derivatives under thermal and solvent-free conditions

In this work, we were decontaminated the ore to extract the talc, directly. Then, we used talc as a heterogeneous basic catalyst for one pot synthesis of bis(pyrazolyl)methane derivatives via the condensation of ethylacetoacetate, hydrazine hydrate and aromatic aldehyde derivatives under thermal and solvent-free conditions. This solid type of catalyst was identified by fourier transform infrared spectroscopy (FTIR), field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), thermogravimetric analysis (TGA), energy-dispersive X-ray spectroscopy (EDS), EDS mapping and Brunauer–Emmett–Teller (BET) theory. Heterogeneous and solvent-free conditions, catalyst recyclability, high yields of the products and short reaction times are some advantages of this method. The reusability of the catalyst was examined for five times and it was successfully used in each run without any significant decreasing in its activity.