Phenyl Amino Research Articles

Selective Detection of Cyanide Ion Using Mechno-Chemical Synthesized Fluorophore: 3-(4-(diphenylamino)phenyl)-1-(phenyl)prop-2-en-1-one

A novel probe has been developed to find the cyanide ion pollutant in our environment. A new chalcone analog (E)-3-(4- (diphenyl amino) phenyl)-1-(phenyl) prop-2-en-1-one was synthesized by solvents free mechano-chemical method. To detect numerous anions (CN−, F−, Cl−, Br−, NO3−, SO42−, PO43−, OH−, OAc−) in the DMSO medium, the probe's sensing capabilities were tested using UV-Vis absorption and fluorescence spectroscopy methods. The probe exhibited selectivity and sensitivity towards cyanide ions (CN−) in the presence of the various analytes. The interaction energies with the same anions and their sensing behavior through density functional theory (DFT) calculations were reported. The chalcone derivatives' higher electron affinity accelerates, which can also boost the compound's reactivity to cyanide anions following the intramolecular charge transfer (ICT) mechanism.

Shining light on green chemistry: BODIPY-infused porphyrin nanocomposite-enzymatic photocatalyst boosts selective aldehydes hydrogenation and organic transformation under solar spectrum

Photo-bio enzyme coupled biotransformation solar radiation driven processes grasp promising in the production of solar driven organic chemicals. Here we reported the synthesis and development of (NH2)4TPP@BODIPY photocatalyst, which was constructed from 5,10,15,20 tetrakis (4 amino phenyl) porphyrin and BODIPY {5,5-difluoro-3,7-bis((E)-4-nitrobenzylidene)-10-(4-nitrophenyl)-5,7-dihydro-3H-4l4,5l4-dipyrrolo[1,2-c:2′,1′-f][1,3,2]diazaborinine} molecule through poly-condensation mechanism resulting in the composite formation which manifest excellent light harvesting properties and photocatalytic reactions with suitable satisfactory band gap and formation of huge electrons channels which bears the organic transformation (98 %) and photo-regeneration of NADH (66.92 %) in 60 min which further enhances reduction of aldehyde resulting alcohol production. The highly selective aldehyde hydrogenation process is proposed via coordination of alcohol dehydrogenase with (NH2)4TPP@BODIPY assistant reduces from the coupling process; regeneration of nicotinamide adenine dinucleotide (NADH). Our results show an excellent benchmark for the NAD+ co-factor coupled solar-driven alcohol production via (NH2)4TPP@BODIPY photocatalyst.

Synthesis and Characterization of Ester Derivatives of N-Phenylanthranilic Acid

N-Phenylanthranilic acid (fenamic acid) serves as the fundamental structure for synthesizing several non-steroidal anti-inflammatory drugs, antibacterial drugs and also functions as a modulator of membrane transport. To reduce the dose-related side effects of existing drugs, research is focussing to improve fenamic acid derivative solubility and bioavailability. A series of ester derivatives of N-phenylanthranilic acid (MB-1 to MB-5) viz. 2-(phenyl amino)methyl benzoate, 2-(phenyl amino)ethyl benzoate, 2-(phenyl amino)isopropyl benzoate,2-(phenyl amino)butyl benzoate and 2-(phenyl amino)phenyl benzoate were synthesized. The chemical structures and functional groups of these derivatives were confirmed using elemental analysis and spectral data. Furthermore, the derived compounds were evaluated for their antibacterial activity against Escherichia coli (Gram-negative) and Staphylococcus aureus (Gram-positive) strains using the agar-well diffusion method followed by molecular docking studies to predict binding interactions of the synthesized compounds with DNA gyrase.

Synthesis of N-substituted 4-phenyl-2-aminothiazole derivatives and investigation of their inhibition properties against hCA I, II, and AChE enzymes

In this study, thiazole derivatives containing sulphonamide, amide, and phenyl amino groups were synthesized to protect the free amino groups of 5-methyl-4-phenyl-2-aminothiazole and 4-phenyl-2-aminothiazole. Halogenated reactions of N-protected thiazole derivatives have been investigated. LCMS, FT-IR, 1H NMR, and 13C NMR spectroscopy techniques were used to elucidate the structures of the synthesized compounds. Inhibition effects of the N-protected thiazole derivatives against human carbonic anhydrase I, II (hCA I, hCA II), and acetylcholinesterase (AChE) were investigated. The best results among the synthesized N-protected thiazole derivatives showed Ki values in the range of 46.85–587.53 nM against hCA I, 35.01–578.06 nM against hCA II, and in the range of 19.58–226.18 nM against AChE. Furthermore, in silico studies with the target enzyme of the thiazole derivatives (9 and 11), which showed the best results experimentally, have examined the binding interactions of the related compounds at the enzyme active site.

Synthesis, characterization and bioactive evaluation of cobalt(II) and copper(II) complexes of {4-[5-(5-sulfanylidene-2,5-dihydro-1H-1,2,4-triazol-3-yl) furan-2-yl] phenyl} acetic acid

A new triazole derivative was synthesized by three steps. The first step involve adding 2-carboxyaledhyed furan to the 4-amino phenyl acetic acid after converting the substituted aromatic amine to the diazanium salt. In the first stage, [4-(5-formylfuran-2-yl) phenyl] acetic acid is the title of product. The second step is adding the thiosemicarbazide to the [4-(5-formylfuran-2-yl) phenyl] acetic acid which it gives the (4-{5-[(2-carbamothioylhydrazinylidene) methyl] furan-2-yl} phenyl) acetic acid. A final compound with the title {4-[5-(15-sulfanylidene-2,5-dihydro-1H-1,32,4-triazol-3-yl) furan-22-yl] phenyl} acetic acid was produced as a result of adding sodium acetate and chloro ethyl acetate to the product from the second step in the presence of triethyl amine which is used as a ligand to prepare cobalt(II) and copper(II) complexes. The structures of synthesized compounds were identified through the utilization of diverse measures, these measurements were (UV-Vis spectrum, LC-MS technique, FT-IR spectrophotometer, conductivity measurements, GC-mass spectra and atomic absorption) and melting point measurement. The results confirmed that the complexes have octahedral geometry. The biological activity data for the synthesized compounds revealed that the ligand and its complexes had antibacterial activity. KEY WORDS: Synthesis, Triazole derivatives, Cobalt(II) complex, Copper(II) complex, Biological evaluation Bull. Chem. Soc. Ethiop. 2024, 38(6), 1595-1607. DOI: https://dx.doi.org/10.4314/bcse.v38i6.8

Zein spray-dried microparticles loaded with chemically modified curcumin for active wound healing

Wound healing is a delicate process comprising various phases, of which inflammation constitutes the most critical one, as some wounds fail to evolve from this state due to pre-existing pathologies or medical conditions, becoming chronic and causing pain and serious consequences for the patients. Given this context, innovative strategies able to support the body in the transition through the inflammatory and the proliferative phases are needed. Here, we propose to deliver to the wound zein microparticles (ZμP) loaded with chemically modified curcumin (mCUR), a novel bioactive molecule with strong antioxidant properties. Derived from the classic curcumin, mCUR chemical structure has been modified with an amino phenyl carbonyl group on C4 to overcome the poor bioavailability in the human body and to reach stronger inhibition of inflammatory markers thanks to a higher in vitro efficacy (lower IC50). ZμP were fabricated via spray drying starting from various zein/mCUR ratios. An exhaustive characterization of the physico-chemical properties of ZμP, either empty or loaded, has been carried out, alongside with bioactivity assessments via human keratinocytes and Escherichia coli cultures. All the formulations presented average diameters of 1 μm, resulted biocompatible, and led to an encapsulation efficiency in the range of 78.1–83.0 %. Finally, antioxidant properties of loaded microparticles were assessed via DCFH-DA assay, where a fluorescence decrease proportional to mCUR concentration was clearly visible (down to 41.7 %). These promising results highlight our formulations’ ability to reduce oxidative stress inside the cells, representing a promising strategy to address the problem of chronic wounds, supporting the body in overcoming the inflammatory stage.

Computer-aided molecular modeling and design studies of some N-(4-(dimethyl amino) phenyl)-4-methoxy-3-propionamidobenzamide derivatives as NS5B polymerase inhibitors

Hepatitis C Virus (HCV) is a stealthy ailment, and most people are unaware they have it in the early stages. Insilco modeling was used to develop a model with high predictive power for N-(4-(dimethyl amino) phenyl)-4-methoxy-3-propionamidobenzamide inhibitors. The inhibitors were optimized using Density Functional Theory (DFT) based on a notion of B3LYP/6–31 G* levels. The genetic function algorithm (GFA) was utilized to create the QSAR models. The best model was chosen based on its statistical fitness using the subsequent measurement parameters: R2trng = 0.828181, R2adj = 0.800468, Q2cv = 0.734795, R2test = 0.7028, and LOF = 0.613985, led to its selection and publication. The model underwent additional assessments, including the Y-scrambling test, and applicability domain, and was considered to have statistical significance. The docking results demonstrate that compound 17 has the greatest inhibitory effect on NS5B-polymerase of any drug in the dataset. Using this compound as a template, novel anti-hepatitis C compounds were developed by including a few beneficial substituents. The docking results of the proposed compounds yielded a high MolDock score (−152.12), indicating effective binding to the target's active sites. Two comparable compounds (SBD4 and SBD3) were shown to be superior to the food drug administration (FDA) approved medication, revibirin/pegylated interferon. The chemicals were determined to be orally accessible after passing Lipinski's criteria, a drug similarity test. Furthermore, the synthesized compounds were found to have favorable pharmacokinetic (absorption, distribution, metabolism, excretion, and toxicity) properties. In conclusion, using the QSAR model, a model with excellent prediction power for certain Biaryl amide inhibitors was constructed. The model was validated and determined to have good internal and external assessment criteria. According to the docking results, compound 17 inhibits NS5B-polymerase the most out of the compounds in the dataset. Furthermore, the compounds' oral bioavailability met drug-like standards. The ultimate goal of this research is to contribute to the development of new therapeutic agents for the treatment of HCV infections, addressing the pressing need for effective antiviral medications.

Pseudo-Jahn-Teller effect in deprotonated dimethyl amino phenyl substituted phthalocyanine

Geometries of dimethyl amino phenyl substituted phtalocyanine deprotonated at two nitrogen atoms [dmaphPc]q, q = -2, -1 and 0, were optimized within the D4h symmetry group and its subgroups. Their excited states were evaluated using the TD-DFT treatment. Using an epikernel principle method based on the symmetries of the imaginary vibrations of the optimized geometries and the symmetries of the corresponding excited states, the symmetry descent paths D4h → D4 for [dmaphPc]2-, D4h → D2 for [dmaphPc]−, and D4h → C2 for [dmaphPc]0 were explained as a consequence of the pseudo-Jahn-Teller effect.

Pre-clinical evaluation of 99mTc-labeled chalcone derivative for amyloid-β imaging post-head trauma.

Aβ42 plaque formation is one of the preliminary pathologic events that occur post traumatic brain injury (TBI) which is also among the most noteworthy hallmarks of AD. Their pre symptomatic detection is therefore vital for better disease management. Chalcone-picolinic acid chelator derivative, 6-({[(6-carboxypyridin-2-yl)methyl](2-{4-[(2E)-3-[4-(dimethyl amino)phenyl]prop-2-enoyl]phenoxy}ethyl)amino}methyl)pyridine-2-carboxylic acid, Py-chal was synthesized to selectively identify amyloid plaques formed post head trauma using SPECT imaging by stable complexation to 99mTc with > 97% efficiency without compromising amyloid specificity. The binding potential of the Py-chal ligand to amyloid plaques remained high as confirmed by in vitro binding assay and photophysical spectra. Further, the Py-chal complex stained amyloid aggregates in the brain sections of rmTBI mice model. In vivo scintigraphy in TBI mice model displayed high uptake followed by high retention while the healthy rabbits displayed higher brain uptake followed by a rapid washout attributed to absence of amyloid plaques. Higher uptake in brain of TBI model was also confirmed by ex vivo biodistribution analysis wherein brain uptake of 3.38 ± 0.2% ID/g at 2min p.i. was observed for TBI mice model. This was followed by prolonged retention and more than twofold higher activity as compared to sham mice brain. This preliminary data suggests the specificity of the radiotracer for amyloid detection post head trauma and applicability of 99mTc labeled Py-chal complex for TBI-induced β-amyloid SPECT imaging.

Multifunctional polyphosphazene grafted with triphenylamine and aminostilbene chromophore for electrochromic and sensor application

In this paper, a sequence of polyphosphazenes (PPZs) as electrochromic (EC) and sensor materials have been designed and synthesized by introducing chromophores, (4-(diphenyl amino)phenyl) methanol (CH1) for PPZ1, 3-(4-(dimethyl amino) phenyl)-2-(4hydroxyphenyl) acrylonitrile (CH2) for PPZ2, and CH1 and CH2 for PPZ3 into the main chain. In terms of EC performance, PPZ1 shows the best EC performance among the three PPZs which can achieve 60 % optical contrast at 690 nm with good cyclic stability within 1000 s and fast switching response time (tcolor/tbleach = 1.2 s/0.6 s). Compared to PPZ1, the oxidation potential of PPZ3 is reduced compared to PPZ1. PPZ2 and PPZ3 as sensors are more sensitive for the detection of 2,4,6-trinitrophenol (TNP) and trifluoroacetic acid (TFA) compared to PPZ1. What's more, PPZs can be used in memory devices with non-volatile flash memory performance and switching current ratios of 103:102.4:1, 104.7:101.3:1 and 103.5.:100.6:1 respectively. Therefore, PPZs have the promising prospect in optoelectronic field.

Phytochemical analysis of root extracts of Rhynchostylis retusa (L.) Blume from the Eastern Ghats of India

Rhynchostylis retusa (Orchidaceae) is an important ethnomedicinal herb in Indian systems of medicine. Tribal healers commonly employ the roots of this epiphytic orchid to treat various ailments. In the present study, the shade-dried root powder of R. retusa was subjected to cold extraction with four solvents, such as n-hexane, acetone, ethyl acetate, and methanol. The crude root extracts were then taken for qualitative phytochemical screening. Furthermore, GC-MS analysis of ethyl acetate and methanol root extracts was carried out. The methanol root extract of R. retusa showed a positive result for all the phytochemicals tested except for saponins. GC-MS analysis of R. retusa methanol root extract revealed the presence of 16 phytoconstituents. Major phytoconstituents such as 9-Hexadecenoic acid, methyl ester, [Z] Heptadecanoic acid, 16-methyl-, methyl ester, Ethanone,1-[4-(4-morpholyl benzylidene amino)phenyl]-, are recorded in the methanol root extract. In the present study, both methanol and ethyl acetate root extracts showed the presence of9-Hexadecenoic acid, methyl ester, [Z] as the major phytocompound. The phytocompounds identified in methanol and ethyl acetate root extracts exhibit various biological activities, including anti-inflammatory, antibacterial, antifungal, antioxidant, and anticancer properties. Based on the findings of the current study, it can be inferred that the roots of R. retusa contain diverse bioactive compounds with medicinal properties. Further investigation of these R. retusa root extracts holds the potential for the discovery and development of innovative pharmaceuticals.

Synthesis of New Bismaleimide Homopolymer and Copolymers Derived from 4, 4ˉ-Bis[4-(N-maleimidyl) Phenyl Schiff Base] Tolidine

Polyimides are widely used in high-temperature plastics, adhesives, dielectrics, photoresists, nonlinear optical materials, separation membrane materials, and Langmuir-Blodgett (LB) films. They are commonly regarded as the most heat-resistant polymers. This work involved the synthesis of a new bismaleimide homopolymer and copolymer by performing many steps. The synthesis of compound (1) (bis [4-(amino phenyl) Schiff base] tolidine) via condensation of o-tolidine with two moles of 4-aminoacetophenone. Secondly, compound (1) was combined with maleic anhydride to form compound (2) (4, 4ˉ-bis[4-(N-maleamic acid) phenyl Schiff base] toluidine). Thirdly, a dehydration reaction was carried out affording compound (3) (4,4ˉ-bis [4-(N-maleimidyl) phenyl Schiff base] toluidine). Compound (3) represents the new vinylic monomer, which was successfully introduced in addition to homopolymerization and copolymerization with selected vinylic monomers, affording homopolymer (4) and copolymers (5, 6), respectively. The new homopolymer and copolymers showed good fusibility and solubility in many organic solvents, leading to easy processing and expected to serve a broad spectrum of applications.

DENSITY FUNCTIONAL THEORY, DOCKING, SYNTHESIS AND BIOLOGICAL EVALUATION OF SOME 2-(2-ARYL AMINO) PHENYL ACETAMIDE DERIVATIVES

A series of new 2-(2-aryl amino) phenyl acetamide derivatives were synthesized and their chemical structures were identified using spectroscopic techniques (UV-VIS, FTIR, 1HNMR, and MS). Computational studies have been carried out for prediction reactivity and density function theory (DFT) calculations for the acetamide derivatives, as well as the spatial electron distribution of the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) were computed. The docking study against prostaglandin synthetase-2 (COX-II coenzyme) was computed, and four compounds (D, F, H, and L) gave high scores (Kcal/mol). Some of these synthetic compounds were evaluated for their biological activities in vitro (antimicrobial, antioxidant, anticancer, and anti-inflammatory). Finally, the compounds B, D, F, and K have a good correlation between theoretical and experimental studies as cyclooxygenase inhibitors and weak to moderate antimicrobial, antioxidant, and cancer activities

Expeditious Microwave-assisted Synthesis of 1,3-Benzoxazoles Incorporating Substituted Thiazolidinone Moieties

The rapid synthesis of 3-[4-(1,3-benzoxazol-2-yl)phenyl]-2-aryl-1,3-thiazolidin-4-one 4(a-h) was achieved through microwave-assisted methods. This involved the reaction of Schiff bases derived from 2-(4-amino phenyl) benzoxazole 3(a-h) with ethanol, SHCH2COOH (thioglycolic acid) (1 mol, 0.92 mL), and ZnCl2 (5 mol%) under microwave irradiation (400W, 146°C) for 3 to 4 minutes, resulting in excellent yields. Compound precursors 3(a-h) were prepared from aromatic aldehydes and 2-(4-amino phenyl) benzoxazole in ethanol, followed by microwave irradiation for 1 to 2 minutes, with reaction progress monitored via TLC. The expeditious reaction time is a notable advantage of this protocol. Comprehensive structural elucidation of the synthesized compounds involved elemental analysis, IR, NMR, 13C-NMR, and mass spectroscopy. These newly synthesized compounds, 4(a-h), were subjected to in-vitro antimicrobial screening against Staphylococcus aureus, Escherichia coli, and antifungal screening against Aspergillus niger. The zone of inhibition in millimeters was measured using the cup plate method. Several compounds within the series exhibited substantial activity when compared to the standard drugs streptomycin and fluconazole.

Design, spectral, molecular modeling, antimitotic, analytical and mechanism studies of phenyl isothiocyanate Girard's T derived metal complexes

The ligand N-{[(phenyl amino) thioxomethyl] hydrazino carbonyl methyl} trimethyl ammonium chloride (PTHAC) was prepared by the refluxing phenyl isothiocyanate and Girard-T (trimethyl ammonium-acethydrazide) in a molar ratio (1:1). The metal complexes derived from NiCl2.6H2O, CuCl2.2H2O and Co(CH3COO)2.6H2O were synthesized and purified. The PTHAC and its Cu(II), Co(II), and Ni(II) metal complexes(1–3) were characterized using a variety of various instrumental performances such as elemental analysis, magnetic moment, spectra (IR, UV–Vis, 1H NMR, mass) and thermal analysis (TGA and DTG).The results of element analysis, magnetic moment, spectra (IR, UV–Vis, 1H NMR, mass), and thermal (TGA and DTA) analyses provide the structures of the produced ligand and its (1–3) complexes. According to the spectroscopic results, PTHAC acts as an O, N and S tridentate donor, creating a mononuclear complex with copper(II), cobalt(II), and nickel(II) ions with an octahedral geometry. All of the atomic properties, including bond lengths, bond angles, HOMO, LUMO, dipole moments, and charges, have been determined. The cytotoxic activities of the PTHAC and the produced (1–3) complexes against breast carcinoma cells have been studied and correlated to the molecular modeling. When compared to the free ligand, CoII-L, and NiII-L, the CuII-L complex inhibits breast cancer cell growth more effectively. Furthermore, the PTHAC ligand was successfully applied for separation via flotation and spectrophotometric determination of Co(II) in several natural water, certified ore and pharmaceutical samples using oleic acid surfactant (HOL). At pH 6.5, PTHAC reacted with Co(II) to create a dark green (1:1) Co(II):PTHAC complex that was floated significantly using oleic acid (HOL) surfactant. The different experimental variable affecting the separation procedure e.g. pH, concentration of Co(II), HOL, PTHAC, temperature etc.…, were investigated. Co(II) had a linear range of (0.1–7.0) mgL−1. In the aqueous and scum layers, the molar absorptivities for the coloured complex are 0.14 × 104 and 0.16 × 105Lmol−1 cm−1, respectively. The LOD was 0.04 mgL−1, which is related to Sandell sensitivity of 3.7 × 10−3 µg cm−2 with a preconcentration factor of 200 and a RSD, % (n = 5) less than 4.2%. In addition, the mechanisms involved in the process of coordination of PTHAC with Cu(II), Co(II) and Ni(II) and the mechanism involved in the process of flotation of the PTHAC-Co(II) complex using HOL surfactant were elucidated.

On the Jahn-Teller Effect in Silver Complexes of Dimethyl Amino Phenyl Substituted Phthalocyanine.

The structures of Ag complexes with dimethyl amino phenyl substituted phthalocyanine m[dmaphPcAg]q of various charges q and in the two lowest spin states m were optimized using the B3LYP method within the D4h symmetry group and its subgroups. The most stable reaction intermediate in the supposed photoinitiation reaction is 3[dmaphPcAg]-. Group-theoretical analysis of the optimized structures and of their electron states reveals two symmetry-descent mechanisms. The stable structures of maximal symmetry of complexes 1[dmaphPcAg]+, 3[dmaphPcAg]+, 2[dmaphPcAg]0, and 4[dmaphPcAg]2- correspond to the D4 group as a consequence of the pseudo-Jahn-Teller effect within unstable D4h structure. Complexes 4[dmaphPcAg]0, 1[dmaphPcAg]-, 3[dmaphPcAg]-, and 2[dmaphPcAg]2- with double degenerate electron ground states in D4h symmetry structures undergo a symmetry descent to stable structures corresponding to maximal D2 symmetry, not because of a simple Jahn-Teller effect but due to a hidden pseudo-Jahn-Teller effect (strong vibronic interaction between excited electron states). The reduction of the neutral photoinitiator causes symmetry descent to its anionic intermediate because of vibronic interactions that must significantly affect the polymerization reactions.

One Pot Synthesis of 1-(phenyl)-1H Indoles, their Biological Screening and ADME Studies

This research aims to develop a novel way for synthesizing indole derivatives. 1-(phenyl)-1H-indole analogues were synthesized by cyclization of 1-phenyl-2-(phenyl amino)-ethane-1-one. Biological evaluation of title compounds and absorption, distribution, metabolism and excretion (ADME) studies were performed and title compounds had a higher affinity and created ample interactions with different proteins.

Efficient malachite green biodegradation by Pseudomonas plecoglossicide MG2: process optimization, application in bioreactors, and degradation pathway

Microbial degradation of synthetic dyes is considered a promising green dye detoxification, cost-effective and eco-friendly approach. A detailed study on the decolorization and degradation of malachite green dye (MG) using a newly isolated Pseudomonas plecoglossicide MG2 was carried out. Optimization of MG biodegradation by the tested organism was investigated by using a UV–Vis spectrophotometer and the resultant degraded products were analyzed by liquid chromatography–mass spectrometry and FTIR. Also, the cytotoxicity of MG degraded products was studied on a human normal retina cell line. The optimum conditions for the significant maximum decolorization of MG dye (90–93%) by the tested organism were pH 6–7, inoculum size 4–6%, and incubation temperature 30–35 °C, under static and aerobic conditions. The performance of Pseudomonas plecoglossicide MG2 grown culture in the bioreactors using simulated wastewater was assessed. MG degradation (99% at 100 and 150 mg MG/l at an optimal pH) and COD removal (95.95%) by using Pseudomonas plecoglossicide MG2 culture were the best in the tested culture bioreactor in comparison with that in activated sludge or tested culture-activated sludge bioreactors.The FTIR spectrum of the biodegraded MG displayed significant spectral changes, especially in the fingerprint region 1500–500 as well as disappearance of some peaks and appearance of new peaks. Twelve degradation intermediates were identified by LC–MS. They were desmalachite green, didesmalachite green, tetradesmalachite green, 4-(diphenylmethyl)aniline, malachite green carbinol, bis[4-(dimethylamino)phenyl]methanone, [4-(dimethylamino)phenyl][4-(methyl-amino)phenyl]methanone, bis[4-(methylamino)phenyl]methanone, (4-amino- phenyl)[4-(methylamino)phenyl]methanone, bis(4-amino phenyl)methanone, (4-amino phenyl)methanone, and 4-(dimathylamino)benzaldehyde. According to LC–MS and FTIR data, two pathways for MG degradation by using Pseudomonas plecoglossicide MG2 were proposed. MG showed cytotoxicity to human normal retina cell line with LC50 of 28.9 µg/ml and LC90 at 79.7 µg/ml. On the other hand, MG bio-degraded products showed no toxicity to the tested cell line. Finally, this study proved that Pseudomonas plecoglossicide MG2 could be used as an efficient, renewable, eco-friendly, sustainable and cost-effective biotechnology tool for the treatment of dye wastewater effluent.

Synthesis and Anti-convulsant Activity of 1-[3-(4-Amin ophenyl)-3-Oxopropanoyl]- 5,5-Diphenyl imidazolidine -2,4-Dione and its Derivatives

Synthesis and Anti-convulsant Activity of 1-[3-(4-Amin ophenyl)-3-Oxopropanoyl]- 5,5-Diphenyl imidazolidine -2,4-Dione and its Derivatives

Derivatives of 2-Pyridone Exhibiting Hot-Exciton TADF for Sky-Blue and White OLEDs.

Development of emissive materials for utilization in organic light-emitting diodes (OLEDs) remains a highly relevant research field. One of the most important aspects in the development of efficient emitters for OLEDs is the efficiency of triplet-to-singlet exciton conversion. There are many concepts proposed for the transformation of triplet excitons to singlet excitons, among which thermally activated delayed fluorescence (TADF) is the most efficient and widespread. One of the variations of the TADF concept is the hot exciton approach according to which the process of exciton relaxation into the lowest energy electronic state (internal conversion as usual) is slower than intersystem crossing between high-lying singlets and triplets. In this paper, we present the donor-acceptor materials based on 2-pyridone acceptor coupled to the different donor moieties through the phenyl linker demonstrating good performance as components of sky-blue, green-yellow, and white OLEDs. Despite relatively low photoluminescence quantum yields, the compound containing 9,9-dimethyl-9,10-dihydroacridine donor demonstrated very good efficiency in sky-blue OLED with the single emissive layer, which showed an external quantum efficiency (EQE) of 3.7%. It also forms a green-yellow-emitting exciplex with 4,4',4″-tris[phenyl(m-tolyl)amino]triphenylamine. The corresponding OLED showed an EQE of 6.9%. The white OLED combining both exciplex and single emitter layers demonstrated an EQE of 9.8% together with excellent current and power efficiencies of 16.1 cd A-1 and 6.9 lm W-1, respectively. Quantum-chemical calculations together with the analysis of photoluminescence decay curves confirm the ability of all of the studied compounds to exhibit TADF through the hot exciton pathway, but the limiting factor reducing the efficiency of OLEDs is the low photoluminescence quantum yields caused mainly by nonradiative intersystem crossing dominating over the radiative fluorescence pathway.