Two 2D sliver complexes with a symmetric and noncentrosymmetric architecture controlled by the metal–ligand ratio

CrystEngComm ◽  
2014 ◽  
Vol 16 (25) ◽  
pp. 5627-5632 ◽  
Author(s):  
Lin-Fei Wu ◽  
Zhao-Xi Wang ◽  
Chao-Chao Xue ◽  
Hong-Ping Xiao ◽  
Ming-Xing Li

By controlling the metal–ligand ratio, we obtained two 2D sliver complexes from a symmetric to noncentrosymmetric architecture based on 2,2′-phosphinico-dibenzoic acid (H3L). The four groups around the phosphorus atom of the L3− ligand connect the Ag(i) ions through different coordination modes to form a noncentrosymmetric complex 2.

2020 ◽  
Vol 49 (25) ◽  
pp. 8614-8624 ◽  
Author(s):  
Alberto Lopera ◽  
Ariadna Gil-Martínez ◽  
Javier Pitarch-Jarque ◽  
Begoña Verdejo ◽  
Salvador Blasco ◽  
...  

The great versatility of the pyrazole moiety combined with polyamines of different chain lengths gives rise to remarkable coordination features.


1988 ◽  
Vol 41 (9) ◽  
pp. 1347 ◽  
Author(s):  
D Baldwin ◽  
LF Lindoy ◽  
DP Graddon

The interaction of silver ion with a range of mixed-donor macrocyclic ligands incorporating nitrogen, oxygen and/or sulfur donors has been investigated. Complementary calorimetric and n.m.r. studies in acetonitrile (and its deuterated derivative) were used to investigate the nature of the equilibria present as the metal/ ligand ratio was varied. In all systems the formation of a 1 : 1 species was observed, with a 1:2 (metal/ ligand ) species also being formed in the presence of excess ligand in the majority of cases. Enthalpies of formation for the various complexes have been determined. Stepwise stability constants for the respective [ AgL ]+ + L ↔ [AgL2]+ equilibria have been estimated from the calorimetric titration data, and the factors promoting the formation of the 1:2 species are discussed. The studies confirm the enhanced affinity of AgI for thioether donors over ether donors.


2019 ◽  
Vol 55 (12) ◽  
pp. 1825-1828 ◽  
Author(s):  
Simran S. Saund ◽  
Samantha L. Goldschmid ◽  
Karina Ng ◽  
Veronica Stewart ◽  
Maxime A. Siegler ◽  
...  

A new strategy is reported for modifying the redox activity of diamidodipyrrins through coordination modes in the same metal–ligand platform.


1988 ◽  
Vol 17 (1) ◽  
pp. 69-83 ◽  
Author(s):  
Terézia Szabó-Plánka ◽  
Antal Rockenbauer ◽  
Miklós Györ ◽  
Ferenc Gaizer

2020 ◽  
Vol 502 ◽  
pp. 119387 ◽  
Author(s):  
Fang-Hua Zhao ◽  
Zhong-Lin Li ◽  
Yuan-Chun He ◽  
Mei Zhang ◽  
Jun Han ◽  
...  

2020 ◽  
Author(s):  
Victoria Bennett ◽  
Bamidele Amos-Tautua ◽  
Ayasen Kemeakegha

Abstract Chloroform solutions of 1-Phenyl-3-Methyl-4-Trichloroacetylpyrazolone-5 (HTCP) for the extraction of Uranium (VI) (UO22+) from various buffered solutions containing different SO42- ion concentrations was investigated. After extraction processes, colorimetric method was used to determine Uranium(VI) concentrations in aqueous media. Solutions of HTCP in chloroform did not extract U(VI) in buffered solutions containing SO42- ions between pH 0 – 2, which was attributed to the formation of unextractable Sulphate Uranyl (UO2)SO4 complex. However, there was extraction of U(VI) of 88,70 %, 76.84 % and 55.49 % between pH 2.96 – 3.21 for solutions containing 0.01 M, 0.1 M and 1 M SO42- ion respectively. An increase in SO42- ion concentration decreased the optimum extraction of U(VI). The presence of SO42- ion in buffered solutions had a masking effect on the extraction of U(VI). The metal ligand ratio was 1:1 and the adduct complex of the metal characterized as UO2(TCP) was extracted.


CrystEngComm ◽  
2012 ◽  
Vol 14 (13) ◽  
pp. 4478 ◽  
Author(s):  
Fanghua Zhao ◽  
Shuai Jing ◽  
Yunxia Che ◽  
Jimin Zheng

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