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Synthesizing medium
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In this study, the hn gene coding for the HN antigen of NDV genotype VIII was artificially synthesized, ligated into donor vector pFastBacHT A and integrated into the baculovirus genome for the purpose of HN expression in Spodoptera frugiperda 9 (Sf9) cells. The recombinant HN protein was successfully expressed in Sf9 cells in the SF900 III medium.
8p
dianmotminh02
03-05-2024
1
1
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In the present investigation, GNS have been prepared by an aqueous anodic exfoliation of pencil graphite in an acidic medium at different dc voltages (5 Ve12 V). The GNS prepared at optimum voltage were mixed with polyaniline (PANI) polymer and drop casted on an indium tin oxide (ITO)/Polyethylene terephthalate (PET) substrate to study the I-V characteristics and to measure the band gap of composites.
7p
viberbers
09-08-2023
4
3
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In this work, a functional nanocomposite consisting of silver nanoparticles and multiwalled carbon nanotubes (MWCNTs-Ag) was successfully synthesized using a two-step chemical process. The MWCNTsAg nanocomposite has been studied as a surface-enhanced Raman scattering (SERS) sensing platform for detection of methylene blue (MB) dye in an aqueous medium.
6p
viberbers
09-08-2023
6
4
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Synthesis of some new isoxazole compounds and their biological tyrosinase and antioxidant activities
In this study, 7 new isoxazole compounds (8-14) were synthesized from the cyclization of chalcone compounds (1-7) containing different functional groups with hydroxylamine hydrochloride in alkaline medium. Tyrosinase and antioxidant properties of 8-14 were investigated. IC50 values for the tyrosinase enzyme inhibition of compounds 8, 11, 12, and 13 were varied between 61.47 ± 3.46 and 188.52 ± 5.85, while compounds 9, 10 and 14 did not show any inhibition effect.
22p
lyhuyenthu
31-01-2023
4
2
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In this study, a new copolymer, which is a combination of two chemical structure (9,10-di(furan-2-yl)anthracene and 3,4-ethylenedioxythiophene was synthesized via electrochemical synthesis methods in the electrolyte medium of 0.1 M TBAPF6 / ACN solution. PEDOT homopolymer was also electrosynthesized for comparator experiments of the polymer formations in the same medium. The characterizations of polymers were achieved with general optical and electrochemical characterization techniques.
10p
lyhuyenthu
31-01-2023
7
2
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Known 1,6-di(thiophen-2-yl)hexane-1,6-dione (2) and novel 1,7-di(thiophen-2-yl)heptane-1,7-dione (4) were obtained from the reactions of thiophene with the corresponding diacyl chlorides. Furthermore, compounds with furan and pyrrole units in place of thiophene units in compound 2 were obtained in the same way. Bromination of 2 and 4 gave bromides regioselectively. The reaction of each of the compounds 2 and 4 in HOAc medium yielded cyclocondensation products. In total, four known and eleven novel compounds were synthesized.
15p
lyhuyenthu
31-01-2023
3
2
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A new electrochromic copolymer based on 4,7-di(thiophen-2-yl)benzo[c] [1,2,5]thiadiazole and 3,4-ethylenedioxythiophene was successfully obtained via the electrochemical polymerization method in the medium of electrolyte solution, which consists of 0.1 M tetrabutylammonium hexafluorophosphate and dichloromethane. Then, electrochemical and spectroelectrochemical characterizations of electrochemically synthesized polymers and copolymers were performed.
9p
lyhuyenthu
31-01-2023
7
2
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A quaternized derivative of chitosan, namely N-(2-hydroxy)-propyl-3-trimethylammonium chitosan chloride (QCh), was synthesized by reacting glycidyltrimethylammonium chloride (GTMAC) and chitosan (Ch)in acid medium under microwave irradiation.
10p
vihermione
06-01-2023
5
2
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Modafinil is a drug used in the treatment of narcolepsy, approved by the FDA in 1998. In previous studies, modafinil was easily synthesized through three stages, in the Bunte salt medium, the overall yield of 74,56 %. The quality of the modafinil was evaluated following USP 41. The results have shown that the synthesized modafinil satisfied quality requirements in pharmacopoeia.
6p
vikissinger
03-03-2022
11
1
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One-pot syntheses of the value-added heterocyclic compounds 3-methylpyridine and pyridine using a renewable chemical, glycerol, were achieved in acidic medium by thermal conversion reactions. Condensation/cyclization reactions of the thermal degradation products of glycerol were investigated in situ using different ammonia and acidic moiety producing inorganic ammonium salts under pyrolysis or microwave heating conditions.
10p
langthannam
29-12-2021
21
0
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A green light emitting polymer in a PMMA matrix: oligo(azomethine-ether) with benzothiazole moieties
This study aimed to synthesize an oligo(azomethine-ether) with benzothiazole moiety in organic medium by means of chemical oxidative polycondensation (OP). Optical properties were examined by photoluminescence (PL) and UV-Vis measurements both in solutions and solid film involved a poly (methyl methacrylate) (PMMA) matrix. Oligomer film in the PMMA matrix emitted a fine green light with a fluorescence quantum yield (QY) of 3.30%. Spectral and thermal observations showed a high rate of C–O–C coupling (cross-linking) for the oligomer.
18p
langthannam
29-12-2021
7
1
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Poly(N-isopropylacrylamide-co-allyl acetic acid) [p(NIPAM-co-AAAc)] microgels were synthesized in aqueous medium by free radical emulsion polymerization using N-isopropylacrylamide as monomer, allylacetic acid as comonomer, and N,N-methylene-bis-acrylamide as cross-linker. Silver nanoparticles were fabricated inside the microgels by in situ reduction of silver ions. Microgels were analyzed by UV-visible spectroscopy, FTIR, XRD, TEM, and DLS. The formation of silver nanoparticles was confirmed by UV-visible spectroscopy.
13p
langthannam
29-12-2021
8
0
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Synthesis of the magnesium type of the mineral boracite (Mg 3 B7 O13 Cl) was studied. Several parameters affecting boracite synthesis were investigated. The raw materials selected were magnesium chloride hexahydrate (MgCl 2 .6H2 O), magnesium oxide (MgO), and boron oxide (B2 O3). Reaction temperatures were selected between 600 ◦ C and 900 ◦ C. Moreover, three different reaction times of 4, 1, and 0.5 h were studied with the determined optimum molar ratio, reaction temperature, and reaction medium.
13p
langthannam
29-12-2021
12
1
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The monomers p-biphenyloxycarbonylphenyl acrylate (BPCPA) and p-biphenyloxycarbonylphenyl methacrylate (BPCPMA) were synthesized by the reaction of p-acryloyloxybenzoyl chloride and p-methacryloyloxybenzoyl chloride with 4-hydroxybiphenyl, respectively, and polymerized by bulk polymerization in vacuum by using dicumyl peroxide. The graft copolymerization of the monomers onto polypropylene were carried out by bulk melt polymerization at 170◦C with various concentration levels of the monomers and the initiator in reaction mixtures.
17p
langthannam
29-12-2021
4
0
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Polycarbazole/chitosan composite materials were synthesized electrochemically at various loadings of chitosan (Chi). Their electrochemical, structural, thermal, and morphological characterizations were investigated by cyclic voltammetry, chronoamperometry, electrochemical impedance spectroscopy, Fourier transform infrared spectroscopy, thermal gravimetry, and scanning electron microscopy. Further electrical conductivity was measured using a four-point probe technique.
10p
langthannam
29-12-2021
6
0
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Quaternary ammonium salts are a group of compounds with diverse biological properties, the most important of which are their antiviral, antibacterial, and antifungal activities. The quaternization reactions of 5'-O-tosyl derivatives of uridine and thymidine with triethylamine, trimethylamine, 4-(N ,N -dimethylamino)pyridine, 2-methylpyridine, and pyridine are described in this article.
15p
tudichquannguyet
29-11-2021
6
1
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Oleochemical-based long-chain diesters are potential organic phase change materials convenient for thermal energy storage. The development of efficient and green methods is an important requirement for the preparation of these environmentally friendly compounds, which also are finding wide industrial application. Thus, in the present work, a series of dibasic acid esters were synthesized through ionic liquid catalyzed scalable chemical esterification or transesterification reactions in a solvent-free medium.
7p
tudichquannguyet
29-11-2021
10
0
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The aim of this study is to synthesize novel piperazine-containing dihydrofuran compounds (3a-n)from radical additions and cyclizations of diacyl and alkyl-acyl piperazine derivatives (1a-h) with 1,3-dicarbonyl compounds (2a-c) mediated by Mn(OAc)3 for the first time. From the reactions of 1a-c with dimedone (2a);1a, 1c, and 1d with acetylacetone (2b); and 1a with ethylacetoacetate(2c) ,the dihydrofuran-piperazine compounds 3a-c, 3d-f, and 3g were obtained in medium to high yields (31%–81%), respectively.
30p
tudichquannguyet
29-11-2021
11
1
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A series of nine methyl sulphones (3a–3i) starting from the aldehydes (1a–1i) were synthesized in two consecutive steps. In the first step, preparation of allyl alcohols (2a–2i) from their corresponding aldehydes by the reaction of sodium borohydride in methanol at room temperature is reported. Finally, methyl sulphones are synthesized by condensing sodium methyl sulfinates with allyl alcohols in the presence of BF3 .Et2 O in acetic acid medium at room temperature for about 2–3 h. The reaction conditions are simple, yields are high (85%–95%), and the products were obtained with good purity.
9p
tudichquannguyet
29-11-2021
8
1
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The templated porous carbons were prepared from sucrose by one-pot method. In this method in which the pre-synthesis of the hard template is eliminated, the porous carbons were produced by organic-inorganic self-assembly of sucrose, tetraethyl ortosilicate (TEOS), Pluronic P123 and n-butanol in an acidic medium, and subsequent carbonization. The synthesis parameters such as sucrose amount, TEOS molar ratio and carbonization temperature were evaluated for describing their effects on the pore structures of the synthesized carbons.
13p
tudichquannguyet
29-11-2021
11
1
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