scholarly journals One-pot green synthesis of antimicrobial chitosan derivative nanocomposites to control foodborne pathogens

RSC Advances ◽  
2022 ◽  
Vol 12 (2) ◽  
pp. 1095-1104
Author(s):  
Mahmoud H. Abu Elella ◽  
Ahmed Esmail Shalan ◽  
Magdy W. Sabaa ◽  
Riham R. Mohamed

This study aimed to show the efficacy of the one-pot green biosynthesis of nanocomposites as effective antimicrobial agents based on a water-soluble biodegradable polysaccharide and silver nitrate (AgNO3).

2016 ◽  
Vol 4 (16) ◽  
pp. 3540-3545 ◽  
Author(s):  
Guomei Zhang ◽  
Ting Xu ◽  
Huizhi Du ◽  
Yunyun Qiao ◽  
Xiaohong Guo ◽  
...  

A one-pot “green” synthesis of water soluble and pH-responsive natural silk fibroin (SF)-stabilized fluorescent copper nanoclusters (CuNCs) was reported without using any additional reducing agents.


2021 ◽  
Author(s):  
Lamiaa Reda Ahmed ◽  
Ahmed F. M. EL-Mahdy ◽  
Cheng-Tang Pan ◽  
Shiao-Wei Kuo

In this paper, we describe the construction of a new fluorescent hydroxyl- and hydrazone-based covalent organic framework (TFPB-DHTH COF) through the one-pot polycondensation of 1,3,5-tris(4-formylphenyl)benzene (TFPB) and 2,5-dihydroxyterephthalohydrazide (DHTH) under...


2021 ◽  
Author(s):  
Yi-Nan Zhang ◽  
Zheng Li ◽  
Suriguga Meng ◽  
Alideertu Dong ◽  
Ying-Wei Yang

Carboxylated leaning tower[6]arene sodium salts are used as an efficient stabiliser for the one-pot synthesis of silver nanoparticles. The resulting hybrid material with good dispersion, excellent stability and narrow size...


Molecules ◽  
2018 ◽  
Vol 23 (12) ◽  
pp. 3363 ◽  
Author(s):  
Aitor Arlegui ◽  
Zoubir El-Hachemi ◽  
Joaquim Crusats ◽  
Albert Moyano

A convenient protocol for the preparation of 5-phenyl-10,15,20-tris(4-sulfonatophenyl)porphyrin, a water-soluble porphyrin with unique aggregation properties, is described. The procedure relies on the one-pot reductive deamination of 5-(4-aminophenyl)-10,15,20-tris(4-sulfonatophenyl)porphyrin, that can be in turn easily obtained from 5,10,15,20-tetraphenylporphyrin by a known three-step sequence involving mononitration, nitro to amine reduction and sulfonation of the phenyl groups. This method provides the title porphyrin in gram scale, and compares very favorably with the up to now only described procedure based on the partial sulfonation of TPP, that involves a long and tedious chromatographic enrichment of the final compound. This has allowed us to study for the first time both the use of its zwitterionic aggregate as a supramolecular catalyst of the aqueous Diels–Alder reaction, and the morphology of the aggregates obtained under optimized experimental conditions by atomic force microscopy and also by transmission electron cryomicroscopy.


Molecules ◽  
2020 ◽  
Vol 25 (22) ◽  
pp. 5479
Author(s):  
Abdallah Mahmoud ◽  
Piotr Smoleński ◽  
M. Guedes da Silva ◽  
Armando Pombeiro

The 3,7-diacetyl-1,3,7-triaza-5-phosphabicyclo[3.3.1]nonane (DAPTA) derivatives, viz. the already reported 3,7-diacetyl-1,3,7-triaza-5-phosphabicyclo[3.3.1]nonane 5-oxide (DAPTA=O, 1), the novel 3,7-diacetyl-1,3,7-triaza-5-phosphabicyclo[3.3.1]nonane-5-sulfide (DAPTA=S, 2), and 3,7-diacetyl-1,3,7-triaza-5-phosphabicyclo[3.3.1]nonane-5-selenide (DAPTA=Se, 3), have been synthesized under mild conditions. They are soluble in water and most common organic solvents and have been characterized using 1H and 31P NMR spectroscopy and, for 2 and 3, also by single crystal X-ray diffraction. The effect of O, S, or Se at the phosphorus atom on the structural features of the compounds has been investigated, also through the analyses of Hirshfeld surfaces. The presence of 1–3 enhances the activity of copper for the catalytic azide-alkyne cycloaddition reaction in an aqueous medium. The combination of cheaply available copper (II) acetate and compound 1 has been used as a catalyst for the one-pot and 1,4-regioselective procedure to obtain 1,2,3-triazoles with high yields and according to ‘click rules’.


2008 ◽  
Vol 8 (3) ◽  
pp. 1545-1550 ◽  
Author(s):  
Liling Zeng ◽  
Nancy Pattyn ◽  
Andrew R. Barron

Single-walled carbon nanotubes (SWNTs) were functionalized by direct fluorination and subsequent reaction with 6-aminohexanoic acid for water-soluble carboxylic acid functionalized SWNTs (AHA-SWNTs). Both of the compounds were used as precursors to attach SWNTs to APTES coated silicon surfaces. AHA-SWNTs in aqueous solution were reacted with APTES self-assembled monolayers (SAMs) with coupling reagents N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide (EDC) and N-hydroxysuccinimide (NHS). The surface coverage is a function of concentration of AHA-SWNTs, solvent and coupling method. While for the fluorinated SWNTs (F-SWNTs), direct addition of F-SWNTs to preformed APTES SAMs at 90 °C shows essentially no reaction, in contrast to the one-pot reaction of F-SWNTs with APTES molecules in the presence of SWNTs on a silicon substrate. This reaction route provides a convenient method to attach SWNTs to silicon surfaces.


RSC Advances ◽  
2015 ◽  
Vol 5 (9) ◽  
pp. 6578-6587 ◽  
Author(s):  
Balijapalli Umamahesh ◽  
Triveni Rajashekhar Mandlimath ◽  
Kulathu I. Sathiyanarayanan

The preparation of an eco-friendly, highly stable, reusable nano ZnAl2O4was used as an excellent catalyst for the pseudo four component synthesis of a library of fluorescent chromeno[2,3-d]pyrimidine derivatives.


RSC Advances ◽  
2021 ◽  
Vol 11 (55) ◽  
pp. 34589-34598
Author(s):  
Jae Hwan Jeong ◽  
Astrini Pradyast ◽  
Hyeonbo Shim ◽  
Hee-Chul Woo ◽  
Mun Ho Kim

A novel protocol for the one-pot, template/seed-free, and completely green synthesis of rose-shaped Au nanostructures with unique three-dimensional hierarchical structures was developed.


Molecules ◽  
2019 ◽  
Vol 24 (23) ◽  
pp. 4378 ◽  
Author(s):  
Juana Andrea Ibacache ◽  
Jaime A. Valderrama ◽  
Judith Faúndes ◽  
Alex Danimann ◽  
Francisco J. Recio ◽  
...  

In the search for new quinoid compounds endowed with potential anticancer activity, the synthesis of novel heterodimers containing the cytotoxic 7-phenylaminoisoquinolinequinone and 2-phenylaminonaphthoquinone pharmacophores, connected through methylene and ethylene spacers, is reported. The heterodimers were prepared from their respective isoquinoline and naphthoquinones and 4,4′-diaminodiphenyl alkenes. The access to the target heterodimers and their corresponding monomers was performed both through oxidative amination reactions assisted by ultrasound and CeCl3·7H2O catalysis “in water”. This eco-friendly procedure was successfully extended to the one-pot synthesis of homodimers derived from the 7-phenylaminoisoquinolinequinone pharmacophore. The electrochemical properties of the monomers and dimers were determined by cyclic and square wave voltammetry. The number of electrons transferred during the oxidation process, associated to the redox potential EI1/2, was determined by controlled potential coulometry.


2015 ◽  
Vol 7 (18) ◽  
pp. 7540-7547 ◽  
Author(s):  
Yan Liang ◽  
Hui Zhang ◽  
Yan Zhang ◽  
Fang Chen

The present article reports on the one-step rapid green synthesis of water-soluble, fluorescent carbon nanodots (C-dots) with a quantum yield of 8.9%.


Sign in / Sign up

Export Citation Format

Share Document