Co-sorption of metal ions and inorganic anions/organic ligands on environmental minerals: A review

Author(s):  
Yupeng Yan ◽  
Biao Wan ◽  
Muammar Mansor ◽  
Xiaoming Wang ◽  
Qin Zhang ◽  
...  
1999 ◽  
Vol 382 (3) ◽  
pp. 291-299 ◽  
Author(s):  
Maria Concetta Bruzzoniti ◽  
Edoardo Mentasti ◽  
Corrado Sarzanini

2013 ◽  
Vol 2013 (21) ◽  
pp. 3632-3640 ◽  
Author(s):  
Jing-Xu Hu ◽  
Ying-Feng Hu ◽  
Xin Xiao ◽  
Yun-Qian Zhang ◽  
Zhu Tao ◽  
...  

2019 ◽  
Vol 48 (27) ◽  
pp. 10011-10022 ◽  
Author(s):  
Hui-Sheng Wang ◽  
Cheng-Ling Yin ◽  
Zhao-Bo Hu ◽  
Yong Chen ◽  
Zhi-Quan Pan ◽  
...  

Two [MIII2DyIII2] complexes (M = Fe for 1 and Co for 2) with mixed organic ligands were obtained. Complex 2 exhibits single molecule magnet behavior with Ueff = 64.0(9) K.


2019 ◽  
Vol 970 ◽  
pp. 290-296
Author(s):  
Nadezhda V. Saranchina ◽  
Eldar V. Urazov ◽  
Maria M. Gavrilenko ◽  
Nataliya A. Gavrilenko

A new automated smartphone-based assay for metals ions determination based on the color reaction with organic ligands was developed. Quantification was performed by measuring the color of the polymer optode. This offers a smartphone-based alternative to the colorimeric method for signal treatment usually employed in automatic methods. The technique enabled linear calibration within the range 1–500 ppb of metals ions. The sampling time used for this concentration range was 15 min. The method was also tested for the quantification of metals ions in water samples, followed by digital image treatment of the optode. The automated detection metals ions approach was demonstrated by applying smartphone to the analysis of metals ions. Relative recoveries of the analytes ranged from 87 % to 105 %. The described procedure has the potential to be a fully automated online smartphone platform for the purpose of routine onsite water analysis.


2000 ◽  
Vol 381 (2) ◽  
pp. 127-133 ◽  
Author(s):  
Jewad Shneine ◽  
Marc Voswinkel ◽  
Matthias Federwisch ◽  
Axel Wollmer

Abstract Structurally, the T→R transition of insulin mainly consists of a rearrangement of the N-terminal B-chain (residues B1–B8) from extended to helical in one or both of the trimers of the hexamer. The dependence of the transition on the nature of the ligands inducing it, such as inorganic anions or phenolic compounds, as well as of the metal ions complexing the hexamer, has been the subject of extensive investigations. This study explores the effect of helix-enhancing modifications of the N-terminal B-chain sequence where the transition actually occurs, with special emphasis on N-capping. In total 15 different analogues were prepared by semisynthesis. 80% of the hexamers of the most successful analogues with zinc were found to adopt the T3R3 state in the absence of any transforming ligands, as compared to only 4% of wild-type insulin. Transformation with SCN− ions can exceed the T3R3 state where it stops in the case of wild-type insulin. Full transformation to the R6 state can be achieved by only one-tenth the phenol concentration required for wild-type insulin, i. e. almost at the stoichiometric ratio of 6 phenols per hexamer.


2016 ◽  
Vol 62 ◽  
pp. 541-570 ◽  
Author(s):  
H. A. O. Hill ◽  
A. J. Thomson

Robert J. P. Williams was a pioneer in advancing our understanding of the roles of chemical elements, especially the metals, in biology and in biological evolution. During the first half of his career of more than 60 years at Oxford University he studied the thermodynamic stabilities of transition-metal complexes with organic ligands, their redox properties, magnetism and colour, to understand their biological function. In parallel he collaborated with biologists and biophysicists, for example with Bert Vallee, studying zinc in proteins. Williams was the first to describe how proton gradients could be used to drive the formation of the universal biological fuel, ATP (adenosine triphosphate), a fundamental step in biological energetics. From the late 1960s he studied many proteins that use metal ions for catalysis, for electron transfer and cellular regulation. A leading figure in the establishment of the Oxford Enzyme Group, Williams developed high-field nuclear magnetic resonance (NMR) to study the mobility and dynamics of many protein structures, leading to a deeper understanding of protein function. He held the Royal Society Napier Research Professorship from 1974 until his retirement in 1991. Subsequently he published several books setting out his understanding of the roles of metal ions in biology, and their wider significance in evolution. Bob Williams's deep insights across many disciplines made him a charismatic teacher. His lateral style of thinking never failed to inspire. His legacy lies in the successful careers of his many students and collaborators worldwide and the vigour of the new discipline of bioinorganic chemistry that he helped to establish.


Talanta ◽  
2013 ◽  
Vol 110 ◽  
pp. 202-228 ◽  
Author(s):  
K. Pytlakowska ◽  
V. Kozik ◽  
M. Dabioch

1990 ◽  
Vol 99 (1-2) ◽  
pp. 93-103 ◽  
Author(s):  
Susumu Osaki ◽  
Yasuhiro Kuroki ◽  
Shinji Sugihara ◽  
Yoshimasa Takashima

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