Characterization of Mammea A/AA in solution and in interaction with β-cyclodextrin: UV–visible spectroscopy, cyclic voltammetry and DFT-TDDFT/MD study

2016 ◽  
Vol 213 ◽  
pp. 294-303 ◽  
Author(s):  
Baruch A. Ateba ◽  
Daniel Lissouck ◽  
Anatole Azébazé ◽  
Christophe Thiery Ebelle ◽  
Achille Nassi ◽  
...  
2019 ◽  
Vol 824 ◽  
pp. 163-167
Author(s):  
Pema Dechen ◽  
Ekasith Somsook

In this report, synthesis and characterization of gold nanoparticles (AuNPs) from gold leaf by electrolysis in two different media (gel and paper) in presence of sodium chloride (NaCl), glucose (C6H12O6) and polyvinyl pyrrolidone (PVP) at room temperature were investigated. Graphite was used as two electrodes, NaCl was used as an electrolyte, C6H12O6 was used as reducing agent and PVP was used as stabilizer to control the aggregation of the nanoparticles. UV-Visible spectroscopy (UV-Vis) and scanning electron microscopy (SEM) were used to confirm the characteristics and morphologies of the synthesized AuNPs.


2012 ◽  
Vol 557-559 ◽  
pp. 371-374
Author(s):  
Lian Liu ◽  
Teng Yu ◽  
Pei Wang ◽  
Guang Shuo Wang

Nanocomposites of poly(ε-caprolactone) (PCL) and layered double hydroxide (LDH) were prepared by in situ polymerization at low LDHs loadings in this work. The resultants were characterized by FTIR spectroscopy, X-ray diffraction (XRD), differential scanning calorimeter (DSC) and UV-visible spectroscopy (UV-vis). FTIR showed that the PCL/LDHs nanocomposites were prepared successfully by in situ polymerization and XRD spectra showed that the crystal structure did not change greatly in the presence of LDHS. DSC results confirmed that LDHs could act as nucleating agents. UV-vis spectra showed that LDHs had stronger absorbance peak than LDH. Moreover, the PCL/LDHs nanocomposites had strong anti-ultraviolet effect by introduction of LDHs into polymer matrix.


2005 ◽  
Vol 58 (7) ◽  
pp. 517 ◽  
Author(s):  
Yannick Teral ◽  
Gabriel Roubaud ◽  
Claude Aubert ◽  
Robert Faure ◽  
Mylène Campredon

The synthesis of some new fluoro-2H-1-benzopyran derivatives utilizing a reaction between titanium phenolates and β-phenylcinnamaldehydes in toluene is reported. These compounds were characterized by NMR and UV/visible spectroscopy as well as mass spectrometry. In solution all the compounds are photochromic. Complete assignment of the 1H and 13C resonances was achieved by concerted application of homonuclear (gs-COSY), proton-detected (C, H) one-bond (gs-HMQC), and long-range (gs-HMBC) heteronuclear two-dimensional chemical shift correlation experiments using a 500 MHz NMR spectrometer equipped with a cryoplatform and a 5 mm cryoprobe. The mass spectra of the different compounds were characterized by intense molecular and high fragment ions. The introduction of an atom of fluorine as a molecular probe is of interest in determining the mechanistic aspects of the photochemical process.


Complex iron(III) salicylaldehyde thiosemicarbazone with a formula Na[Fe(STSC)2] have been synthesized. Ligand, salicylaldehyde thiosemicarbazone (SCT) was prepared through the condensation reaction of salycilaldehide with thiosemicarbazide. Na[Fe(STSC)2] has been synthesized by reacting FeCl3 with thiosemicarbazide based ligand bearing ONS donor atoms. Complex has been formulated and characterized by mass spectrometry, infrared and UV/visible spectroscopy. The facts showed the formation of a complex in metal:ligand stoichiometric ratio 1:2. The ligand is coordinated as an ONS tridentate dianion via oxygen atom after the deprotonation of the phenolic OH-group, azomethine nitrogen and sulphur in thiol form of the deprotonated thiosemicarbazide residue. Antioxidant activity was determined, where ligand showed significant activity, while complex, at low concentration, exhibited almost no activity.


Crystals ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 1144
Author(s):  
Konda Shireesha ◽  
Thida Rakesh Kumar ◽  
Tumarada Rajani ◽  
Chidurala Shilpa Chakra ◽  
Murikinati Mamatha Kumari ◽  
...  

This paper describes the synthesis and characterization of NiMgOH-rGO nanocomposites made using a chemical co-precipitation technique with various reducing agents (e.g., NaOH and NH4OH) and reduced graphene oxide at 0.5, 1, and 1.5 percent by weight. UV-visible spectroscopy, Fourier-transform infrared spectroscopy, X-ray diffraction, a particle size analyzer, and cyclic voltammetry were used to characterize the composite materials. The formation of the NiMgOH-rGO nanocomposite with crystallite sizes in the range of 10–40 nm was inferred by X-ray diffraction patterns of materials, which suggested interlayers of Ni(OH)2 and Mg(OH)2. The interactions between the molecules were detected using Fourier-transform infrared spectroscopy, while optical properties were studied using UV-visible spectroscopy. A uniform average particle size distribution in the range of 1–100 nm was confirmed by the particle size analyzer. Using cyclic voltammetry and galvanostatic charge/discharge measurements in a 6 M KOH solution, the electrochemical execution of NiMgOH-rGO nanocomposites was investigated. At a 1 A/g current density, the NiMgOH-rGO nanocomposites prepared with NH4OH as a reducing agent had a higher specific capacitance of 1977 F/g. The electrochemical studies confirmed that combining rGO with NiMgOH increased conductivity.


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