Keyword search (4,163 papers available)

"Forgione P" Authored Publications:

Title Authors PubMed ID
1 Regioselective Stepwise Synthesis of Unsymmetrical 1,2,5-Triarylpyrroles via Palladium-Catalyzed Decarboxylative Cross-Coupling and C-H Arylation Buonomano C; Patterson S; Ngou JS; Messina C; Taylor S; Bilodeau F; Forgione P; 41900086
CHEMBIOCHEM
2 A Modular and Regioselective Synthesis of Di- and Triarylated Thiophenes: Strategies for Accessing Challenging Isomeric Motifs Messina C; McKibbon K; Wong KS; Prevost P; Petkov V; Forgione P; 41160050
CONCORDIA
3 In vitro evaluation of isatin-pyridine oxime hybrids as potential acetylcholinesterase inhibitors for nerve agent prophylaxis Silva MCJD; Pinto AMV; Balthar MA; Correa ABA; Bhattacharyya D; Simas ABC; Kuca K; Forgione P; França TCC; Cavalcante SFA; Kitagawa DAS; 40516590
CHEMBIOCHEM
4 A Modular and Catalytic Methodology To Access 2,5-Furan-Based Phenylene/Thiophene Oligomers through a One-Pot Decarboxylative Cross-Coupling from 5-Bromofurfural Cigana B; Lapointe V; Majewski MB; Forgione P; 38808994
CHEMBIOCHEM
5 Sterically-Hindered Molecular p-Dopants Promote Integer Charge Transfer in Organic Semiconductors Charoughchi S; Liu JT; Berteau-Rainville M; Hase H; Askari MS; Bhagat S; Forgione P; Salzmann I; 37220083
CHEMBIOCHEM
6 Diverse Applications of Biomass-Derived 5-Hydroxymethylfurfural and Derivatives as Renewable Starting Materials Chacón-Huete F; Messina C; Cigana B; Forgione P; 35652539
CHEMBIOCHEM
7 Solvent-free synthesis of 3,5-isoxazoles via 1,3-dipolar cycloaddition of terminal alkynes and hydroxyimidoyl chlorides over Cu/Al2O3 surface under ball-milling conditions Hernandez R RA; Burchell-Reyes K; Braga APCA; Lopez JK; Forgione P; 35424611
CHEMBIOCHEM
8 Characterization of a recently synthesized microtubule-targeting compound that disrupts mitotic spindle poles in human cells Jaunky DB; Larocque K; Husser MC; Liu JT; Forgione P; Piekny A; 34880347
BIOLOGY
9 Programmed Synthesis of Tetra-Aryl Thiophenes with Stepwise, Ester-Controlled Regioselectivity Messina C; Ottenwaelder X; Forgione P; 34506149
CHEMBIOCHEM
10 Design, structure-activity relationship study and biological evaluation of the thieno[3,2-c]isoquinoline scaffold as a potential anti-cancer agent Liu JT; Jaunky DB; Larocque K; Chen F; Mckibbon K; Sirouspour M; Taylor S; Shafeii A; Campbell D; Braga H; Piekny A; Forgione P; 34416378
BIOLOGY
11 Synthesis of 2,5-Diaryl Nonsymmetric Furans C6-Platform Chemicals via Catalytic Conversion of Biomass and the Formal Synthesis of Dantrolene. Chacón-Huete F, Lasso JD, Szavay P, Covone J, Forgione P 33253575
CHEMBIOCHEM
12 Approaching the Integer-Charge Transfer Regime in Molecularly Doped Oligothiophenes by Efficient Decarboxylative Cross-Coupling Liu JT; Hase H; Taylor S; Salzmann I; Forgione P; 31961982
CHEMBIOCHEM
13 Facile Aqueous-Phase Synthesis of an Ultrasmall Bismuth Nanocatalyst for the Reduction of 4-Nitrophenol. Liang Y, Manioudakis J, Macairan JR, Askari MS, Forgione P, Naccache R 31552336
CHEMBIOCHEM
14 Virtual screening, docking, and dynamics of potential new inhibitors of dihydrofolate reductase from Yersinia pestis. Bastos Lda C, de Souza FR, Guimarães AP, Sirouspour M, Cuya Guizado TR, Forgione P, Ramalho TC, França TC 26494420
CHEMISTRY
15 Analysis of Coxiela burnetti dihydrofolate reductase via in silico docking with inhibitors and molecular dynamics simulation. de Souza FR, Guimarães AP, Cuya T, de Freitas MP, Gonçalves ADS, Forgione P, Costa França TC 27726597
CHEMBIOCHEM
16 Investigating the selectivity of potential new inhibitors of dihydrofolate reductase from Yersinia pestis designed by molecular modeling. Bastos LDC, de Souza FR, Pereira Souza LM, Forgione P, Cuya T, de Alencastro RB, Pimentel AS, Celmar Costa França T 29542379
CHEMBIOCHEM

 

Title:Facile Aqueous-Phase Synthesis of an Ultrasmall Bismuth Nanocatalyst for the Reduction of 4-Nitrophenol.
Authors:Liang YManioudakis JMacairan JRAskari MSForgione PNaccache R
Link:https://www.ncbi.nlm.nih.gov/pubmed/31552336?dopt=Abstract
DOI:10.1021/acsomega.9b01736
Publication:ACS omega
Keywords:
PMID:31552336 Category:ACS Omega Date Added:2019-09-26
Dept Affiliation: CHEMBIOCHEM
1 Department of Chemistry and Biochemistry, Center for NanoScience Research, and Quebec Centre for Advanced Materials, Concordia University, Montreal, Quebec H4B 1R6, Canada.
2 Centre for Green Chemistry and Catalysis, Montreal, Quebec H4B 1R6, Canada.

Description:

Facile Aqueous-Phase Synthesis of an Ultrasmall Bismuth Nanocatalyst for the Reduction of 4-Nitrophenol.

ACS Omega. 2019 Sep 17;4(12):14955-14961

Authors: Liang Y, Manioudakis J, Macairan JR, Askari MS, Forgione P, Naccache R

Abstract

Bismuth metallic nanoparticles have evoked considerable interest in catalysis owing to their small size, high surface area-to-volume ratio, and low toxicity. However, the need for toxic reductants and organic solvents in their synthesis often limits their desirability for application development. Here, we describe a green strategy to synthesize bismuth nanodots via the redox reactions between bismuth nitrate and d-glucose, in the presence of poly(vinylpyrrolidone) in the basic aqueous phase. Both reagents play a crucial role in the formation of monodisperse bismuth nanodots acting as mild reducing and capping agents, respectively. We further demonstrate that the catalytic activity of these dots via the successful reduction of the environmental contaminant 4-nitrophenol to its useful 4-aminophenol analogue requiring only 36 µg/mL nanocatalyst for 20 mM of the substrate. Moreover, they can be recovered and recycled in multiple reactions before the onset of an appreciable loss of catalytic activity. The proposed facile synthetic route and inexpensive matrix materials lead the way to access bismuth nanodots for both the fundamental study of reactions and their industrial catalysis applications.

PMID: 31552336 [PubMed]





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