scholarly journals The effect of pH and transition metal ions on cysteine-assisted gold aggregation for a distinct colorimetric response

RSC Advances ◽  
2021 ◽  
Vol 11 (16) ◽  
pp. 9664-9674
Author(s):  
Trang Thi Thuy Nguyen ◽  
Olivia A. Han ◽  
Eun Bi Lim ◽  
Seungjoo Haam ◽  
Joon-Seo Park ◽  
...  

Divalent transition metal ions facilitated the aggregation of gold nanoparticles: Fe2+ < Ni2+ < Zn2+ < Co2+ ≪ Mn2+ < Cu2+ at pH 7. The optimized AuNPs-Cu2+ system produced the progressive color change upon the addition of cysteine (0.2–2.0 μM).

RSC Advances ◽  
2021 ◽  
Vol 11 (19) ◽  
pp. 11255-11255
Author(s):  
Trang Thi Thuy Nguyen ◽  
Olivia A. Han ◽  
Eun Bi Lim ◽  
Seungjoo Haam ◽  
Joon-Seo Park ◽  
...  

Correction for ‘The effect of pH and transition metal ions on cysteine-assisted gold aggregation for a distinct colorimetric response’ by Trang Thi Thuy Nguyen et al., RSC Adv., 2021, 11, 9664–9674, DOI: 10.1039/D1RA00013F.


Molecules ◽  
2020 ◽  
Vol 25 (3) ◽  
pp. 612 ◽  
Author(s):  
Shufang Zhu ◽  
Lilin Lu

Detection of biologically important transition metal ions such as copper by using a simple method is desirable and of great importance. In this work, we firstly reported that water-soluble thiacalix[4]arene tetrasulfonate (TCAS) exhibited selective chromogenic recognition towards copper(II) ion over other transition metal ions. Color change from colorless to salmon pink was observed in TCAS solution, weak bathochromic shift was induced in UV absorption spectrum of TCAS upon addition of copper(II) ion, and the absorbance of characteristic absorption band at 312 nm increased linearly with copper(II) ion concentration. The recognition mechanism of TCAS to copper(II) ion was investigated by a comparative study with calix[4]arene tetrasulfonate (CAS) and time-dependent density functional theory(TD-DFT) study, and the absorption bands were assigned based on transition orbital analysis.


Author(s):  
R. Ai ◽  
H.-J. Fan ◽  
L. D. Marks

It has been known for a long time that electron irradiation induces damage in maximal valence transition metal oxides such as TiO2, V2O5, and WO3, of which transition metal ions have an empty d-shell. This type of damage is excited by electronic transition and can be explained by the Knoteck-Feibelman mechanism (K-F mechanism). Although the K-F mechanism predicts that no damage should occur in transition metal oxides of which the transition metal ions have a partially filled d-shell, namely submaximal valence transition metal oxides, our recent study on ReO3 shows that submaximal valence transition metal oxides undergo damage during electron irradiation.ReO3 has a nearly cubic structure and contains a single unit in its cell: a = 3.73 Å, and α = 89°34'. TEM specimens were prepared by depositing dry powders onto a holey carbon film supported on a copper grid. Specimens were examined in Hitachi H-9000 and UHV H-9000 electron microscopes both operated at 300 keV accelerating voltage. The electron beam flux was maintained at about 10 A/cm2 during the observation.


Author(s):  
Mohammed Al-Amery1 ◽  
Ashraf Saad Rasheed ◽  
Dina A. Najeeb

Five new mixed ligand metal complexes have been synthesized by the reaction of divalent transition metal ions (Hg, Ni, Zn, Cu and Cd) with 2-(naphthalen-l-ylamino)-2-phenylacetonitrile (L1 ) and 1,10-phenanthroline (L2). The coordination likelihood of the two ligands toward metal ions has been suggested in the light of elemental analysis, UV-Vis spectra, FTIR, 1H-NMR, flam atomic absorption, molar conductance and magnetic studies. Results data suggest that the octahedral geometry for all the prepared complexes. Antibacterial examination of synthesized complexes in vitro was performed against four bacterias. Firstly, Gram-negative bacteria namely, Pseudomonas aerugin and Escherichia. Secondly, Gram-positive bacteria namely, Bacillus subtilis, Staphylococcuaurouss. Results data exhibit that the synthesized complexes exhibited more biological activity than tetracycline pharmaceutical.


Author(s):  
Olivier Charles Gagné ◽  
Frank Christopher Hawthorne

Bond-length distributions are examined for thirty-three configurations of the metalloid ions and fifty-six configurations of the post-transition-metal ions bonded to oxygen. Lone-pair stereoactivity is discussed.


Author(s):  
Olivier Charles Gagné ◽  
Frank Christopher Hawthorne

Bond-length distributions are examined for thirty-three configurations of the metalloid ions and fifty-six configurations of the post-transition-metal ions bonded to oxygen. Lone-pair stereoactivity is discussed.


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