A non-conventional methodology has been utilized for the synthesis of a series of 1,2,4-triazolo-quinazoline-thiones (2a-l). Here the reaction was carried out between 1,2,4-triazolo-quinazolinones (1a-l), in the presence of 1,4-dioxane. The mixture was irradiated under microwave (100W) for 7min to obtain targeted molecules (2a-l). All the synthesized molecules were confirmed by (1)H, (13)C NMR and HRMS. The solvatochromic property (absorption spectra) of compounds (2a-l) in solvents of different polarities was studied. The compounds (2a-l) were further subjected for their in vitro free radical screening using 2,2-diphenyl-1-picrylhydrazyl (DPPH) method and also screened for their in vitro anti-fungal property against Aspergillus flavus (A. flavus) and Aspergillus niger (A. niger). The results from free radical scavenging assay showed promising activity for compounds 2a, e-i, whereas compound 2d showed significant antioxidant activity when compared to ascorbic acid. In vitro anti-fungal study showed that the 1,2,4-triazolo-quinazoline-thiones (2a-l) had significant activity against A. flavus and A. niger compared with widely used antifungal agent Fluconazole.

Mohana Roopan S

Department of Chemistry

School of Advanced Sciences

Vellore Campus

Suthindhiran K

Department of Bio-Medical Sciences

School of Bio Sciences and Technology

Sompalle R

Al-Dhabi N.A

Sarkar G

Arasu M.V.

Vellore Institute of Technology (VIT) is a private university located in&nbsp;Tamil Nadu, India. Founded in 1984, as Vellore Engineering College, the institution offers 20 undergraduate, 34 postgraduate, four integrated and four research programs. It has campuses in Vellore, Amravati, Bhopal and Chennai.

VIT is one of the top ranked private universities in India according to NIRF, THE and QS Rankings.&nbsp;Govt. of India has recognized&nbsp;VIT, Vellore as an&nbsp;Institution of Eminence. This has allowed VIT to take independent quality initiatives and move up in world ranking.

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VIT University

Journal of Photochemistry and Photobiology B: Biology

Zinc oxide (ZnO) nanoparticles (NPs) were synthesized by a conventional method using Pithecellobium dulce peel extract. The phytochemicals present in the peel act as stabilizing agents. The ZnO NPs were characterized by UV–vis spectroscopy, X-ray diffraction (XRD), scanning electron microscopy and transmission electron microscopy. The XRD pattern confirmed the formation of crystals, which exactly matched with JCPDS card no.36–1451. The nondestructive XRD pattern showed a hexagonal crystalline nature and scanning electron microscopy revealed a spherical shape. Further, the ZnO NPs exhibited excellent photodegradation efficiency with regard to the dye methyleneblue (MB), a major water pollutant released by the textile industry. A kinetic study of photodegradation of MB showed 63{\%} degradation and a rate constant of 0.00812 min−1. The antifungal activity of the ZnO NPs resulted in 37.81{\%} and 63.57{\%} inhibition of the growth of Aspergillus flavus and 40.21{\%} and 43.04{\%} of growth inhibition of Aspergillus niger at 500 and 1000 ppm of ZnO NPs, respectively.

Journal of Physics and Chemistry of Solids

Green synthesis, characterization and antifungal and photocatalytic activity of Pithecellobium dulce peel–mediated ZnO nanoparticles

AbstractNature and nanotechnology have not yet achieved a lucid correlation in the field of science but together they have exhibited immense potential towards the advancement and modification in future science and technology. Due to the unique properties of nanomaterials like nanoparticles gained considerable importance. Among all the nanoparticles, zinc oxide (ZnO NPs) are greatly utilized in sensors, catalysis, bioscience, etc. Antimicrobial activity by ZnO NPs had more attention by the implementation of nanotechnology for the preparation of ZnO NPs. At present, antimicrobial activity of ZnO NPs using Aegle marmelos (A. marmelos) leaves extract was done. The ZnO NPs subjected to UV-Vis, FT-IR, XRD, SEM and TEM analysis. The presence of phenolic group in extract has the capacity to form ZnO NPs and act as stabilizing agent. Every 5 min interval ZnO NPs was formed which recorded by UV-Vis spectrophotometer. The SEM analysis displayed a fine spherical ZnO NPs and EDAX report showed that the existence of zinc and oxygen in the ratio of 30.51% and 69.49%. The antimicrobial activity of ZnO NPs has high percentage inhibition against A. niger at 1000 ppm. Till now, no research carryout on A. marmelos mediated ZnO NPs and applications towards antimicrobial activity.

Fulltext

Green Processing and Synthesis

Aegle marmelos phytochemical stabilized synthesis and characterization of ZnO nanoparticles and their role against agriculture and food pathogen

The photochemical preparation of benzo[4,5]imidazo[2,1-b]quinazoline was assessed under the illumination of UV wavelength (&gt;360 nm). The compound 3,4-dihydronaphthalen-1(2H)-one 1 with 1H-benzo[d]imidazol-2-amine 2 in the existence of KOH/DMF which lead to the aromatized compound 3. The notable remark of this reaction is that the UV irradiation (312 nm) plays a vital part in the formation of compound, 3 in shorter duration (2 h) which resulted in higher yield of 96%. Compound 3 was analyzed by H1, C13 NMR, and HRMS. Solvatochromism impacts of the compound 3 was computed with different solvents (DCM

UV-light intervened synthesis of imidazo fused quinazoline and its solvatochromism, antioxidant, antifungal and luminescence properties

A new and highly efficient microwave promoted N-alkylation of triazolo-quinazolinones was developed by treating various phenyl-substituted heterocyclic amines with benzyl chloride using K2CO3 as a base in the presence of DMF. Also the heterocyclic amines were synthesized by condensing the 3-amino-1,2,4-triazole substituted benzaldehydes and 1,3-cyclohexanedione in the presence of microwave irradiation under solvent free condition. The synthesized heterocycles 4a–o and 6a–o were further confirmed by using different spectroscopic techniques such as NMR and HRMS. The compounds 6a–o was studied for their solvatochromic property with increasing polarity of solvents. The determinations of 2,2-diphenyl-1-picrylhydrazyl radical (DPPH) scavenging effect of the scaffolds 6a–o were carried out by UV–Vis spectrometer. In terms of IC50 all the compounds have shown remarkable antioxidant property compared with Ascorbic acid. © 2016 Elsevier B.V.

Journal of Molecular Liquids

Conventional spectroscopic identification of N-alkylated triazolo-quinazolinones and its antioxidant, solvatochromism studies

A conventional approach has been used to synthesis Indole fused acridine, 4a–e. In this paper to achieve the target molecule, 4 the reaction was performed via two steps. In step 1, there was a reaction between Carbazolone, 1 and benzophenone, 2 to get dihydroindoloacridine, 3. In step 2, compound, 3 was treated with 5{\%} Palladium/Carbon in the presence of diphenyl ether for 5 h to give a dark brown product, 4. The column chromatography was used to purify final product, 4. All the synthesized compounds such as 3 and 4 were characterized by melting point, FTIR, 1H NMR and Mass spectra. Further to check the purity of the compounds it was subjected to CHN analyzer. The target molecules such as 3 and 4 were screened for antimicrobial studies against bacteria such as Bacillus subtilis (B. subtilis), Staphylococcus aureus (S. aureus), Klebsiella pneumonia (K. pneumonia), Salmonella typhi (S. typhi); and fungi like Aspergillus niger (A. niger), Aspergillus fumigatus (A. fumigatus). The obtained results clearly proves that the target molecules shown reasonable activity against K. pneumonia and A. niger. Further the compounds were screened for free radical scavenging activity using 2,2-diphenyl-1-picrylhydrazyl (DPPH). The free radical scavenging property was performed using UV–Visible spectroscopy. The results were compared with the standard BHT (Butylated Hydroxy Toluene). Compounds, 4a and 4e were shown higher percentage of inhibition when compare to the standard. The result confirms that further research on indoloacridine will leads effective drug to the market.

Application of UV–Vis spectrophotometric process for the assessment of indoloacridines as free radical scavenger

A series of 6,7-dihydro-[1,2,4]triazolo[5,1-b]quinazolin-8(5H)-ones, 4a–o were synthesized via a one-pot, multicomponent reaction in the presence of water as a solvent under microwave irradiation using ceric ammonium nitrate as an oxidizing agent. This techno-chemical method provides a rapid construction of higher molecules in short duration with high yield. The adopted method was carried out in the presence of water without catalyst and yielded the compounds without any side products, and thus further purification of compounds by column chromatography was not required. All the synthesized compounds, 4a–o were screened for their 2,2-diphenyl-1-picrylhydrazyl radical scavenging activity. All the compounds, 4a–o possessed moderate antioxidant activity when compared to their standard antioxidant (ascorbic acid). © 2015, Springer Science+Business Media Dordrecht.

Research on Chemical Intermediates

Microwave assisted synthesis of ring junction heterocyclic antioxidants

The present study investigates a simple method for the biosynthesis of silver chloride nanoparticles (AgCl-NPs) at 37 °C using Beta vulgaris peel extract. TEM morphology assessed that the diameter of stable AgCl-NPs was approximately 10 nm and EDAX spectrum confirmed the presence of silver ion, chloride ion and other elements in the plant metabolite. The photocatalytic activity of AgCl-NPs in the colour reduction of Methyl blue (MB) was evaluated by UV-vis spectrophotometer. These results showed that AgCl-NPs have significant catalytic activity of methylene blue. Also it showed good antioxidant activity as compared to standard ascorbic acid. © 2015 Elsevier B.V. All rights reserved.

Materials Letters

One step production of AgCl nanoparticles and its antioxidant and photo catalytic activity

The photochemical synthesis of a series of 2,3-dihydroquinazolin-4(1H)-ones were evaluated under the irradiation of visible light ({\textgreater}390 nm). The effect of the visible light mediated synthesis was carried out in the presence/absence of solvent. The effect of solvent plays a key role in the synthesis was evidenced through the formation of product in short duration. The solvatochromic effects of the fluorescent compounds (3a-k) were studied with respect to the solvents of increasing polarity (DCM {\textless} methanol {\textless} DMF {\textless} DMSO). The determination of in vitro anti-inflammatory activity of the compounds (3a-k) by the inhibition of bovine serum albumin (BSA) denaturation and 2,2-di(4-t-octylphenyl)-1-picrylhydrazyl (DOPPH•) radical scavenging consequence of the compounds (3a-k) were determined by spectroscopic technique. The compound 3j in DMSO exhibited extreme high quantum yield. The compound 3i was found to be superior both in the efficiency of the anti-inflammatory activity and radical scavenging ability.

2,3-Dihydroquinazolin-4(1H)-ones: Visible light mediated synthesis, solvatochromism and biological activity

We report an expeditious synthesis of selected indazolo-quinazolinone derivatives via an iodine-mediated multi-component reaction (MCR).

RSC Advances

Iodine-mediated synthesis of indazolo-quinazolinones via a multi-component reaction

An expedient method for the synthesis of 5,6-dihydrobenzo[h][1,2,4]triazolo[5,1-b]quinazolines by UV light has been developed.

Journal	Data powered by TypesetJournal of Photochemistry and Photobiology B: Biology
Publisher	Data powered by TypesetElsevier BV
ISSN	1011-1344
Open Access	No