Gallium and indium compounds of sulphur donor ligands: Pyridine-2-thiolates and diphenylthiophosphinates

Polyhedron ◽  
1996 ◽  
Vol 15 (3) ◽  
pp. 391-402 ◽  
Author(s):  
Christopher C. Landry ◽  
Alan Hynes ◽  
Andrew R. Barron ◽  
Ionel Haiduc ◽  
Crisian Silvestru
2014 ◽  
Vol 70 (a1) ◽  
pp. C1227-C1227
Author(s):  
Lina Aguirre-Diaz ◽  
Marta Iglesias ◽  
Natalia Snejko ◽  
Enrique Gutierrez-Puebla ◽  
Maria Monge

Generally, group IIIA metal-based polycarboxylates are less studied, compared with those of transition or rare earth metals. However, In-MOFs have received recently much attention due to their interesting network topologies, which are mainly owing to the variety of coordination modes (6, 7 or 8) in indium MOFs with O- and N-donor ligands. [1]. Some of In-MOFs exhibit an exceptional gas absorption, fluorescent, ion-exchange properties, and can be used as heterogeneous Lewis acid catalysts in various organic transformations. The high relevance of Indium materials in catalytic studies for important organic reactions led to development of indium MOFs. [2-3] Here we report the solvothermal synthesis, structural characterization, topological analysis and catalytic studies of six new indium-based MOFs using 5-(4-carboxy-2-nitrophenoxy)isophtalic acid (H3popha) together with N-donor ancillary ligands (Figure 1). The three indium compounds showing 3D networks are the following: [In8(OH)6(popha)6(H2O)4]·xH2O (1), [In2(popha)2(4,4-bipy)2] (2) and [In3(OH)3(popha)2(4,4'-bipy)2]·xH2O (3). Meanwhile, compounds with a 2D network have a composition [In(popha)(1,10-phen)]·xH2O (4), [In(popha)(1,10-phen)]·xH2O (5) and [In(popha)(2,2'-bipy)]·xH2O (6). The catalytic study performed using indium compounds 1-6 as catalysts in a Lewis acidity promoted organic reaction, allows for establishing a connection between the corresponding MOF network dimensionality and its catalytic behavior.


2018 ◽  
Author(s):  
Katherine Marczenko ◽  
James Goettel ◽  
Gary Schrobilgen

Oxygen coordination to the Xe(VI) atom of XeO<sub>3</sub> was observed in its adducts with triphenylphosphine oxide, dimethylsulfoxide, pyridine-N-oxide, and acetone. The crystalline adducts were characterized by low-temperature, single-crystal X-ray diffraction and Raman spectroscopy. Unlike solid XeO<sub>3</sub>, which detonates when mechanically or thermally shocked, the solid [(C<sub>6</sub>H<sub>5</sub>)<sub>3</sub>PO]<sub>2</sub>XeO<sub>3</sub>, [(CH<sub>3</sub>)<sub>2</sub>SO]<sub>3</sub>(XeO<sub>3</sub>)<sub>2</sub>,<sub> </sub>and (C<sub>5</sub>H<sub>5</sub>NO)<sub>3</sub>(XeO<sub>3</sub>)<sub>2</sub> adducts are insensitive to mechanical shock, but undergo rapid deflagration when ignited by a flame. Both [(C<sub>6</sub>H<sub>5</sub>)<sub>3</sub>PO]<sub>2</sub>XeO<sub>3 </sub>and (C<sub>5</sub>H<sub>5</sub>NO)<sub>3</sub>(XeO<sub>3</sub>)<sub>2</sub> are air-stable whereas [(CH<sub>3</sub>)<sub>2</sub>SO]<sub>3</sub>(XeO<sub>3</sub>)<sub>2</sub> slowly decomposes over several days and [(CH<sub>3</sub>)<sub>2</sub>CO]<sub>3</sub>XeO<sub>3</sub> undergoes adduct dissociation at room temperature. The xenon coordination sphere of [(C<sub>6</sub>H<sub>5</sub>)<sub>3</sub>PO]<sub>2</sub>XeO<sub>3</sub> is a distorted square pyramid which provides the first example of a five-coordinate XeO<sub>3</sub> adduct. The xenon coordination spheres of the remaining adducts are distorted octahedra comprised of three Xe---O secondary contacts that are approximately trans to the primary Xe–O bonds of XeO<sub>3</sub>. Quantum-chemical calculations were used to assess the Xe---O adduct bonds, which are predominantly electrostatic σ-hole bonds between the nucleophilic oxygen atoms of the bases and the σ-holes of the xenon atoms.


2020 ◽  
Vol 18 (1) ◽  
pp. 391-398
Author(s):  
Shao-Hsuan Wu ◽  
Jun-Hui Huang

AbstractTwo novel mixed-ligand coordination polymers, {[Co(tdc)(btrp)]·0.67DMF}n (1) and {[Zn2(bimb)2(tdc)2]·2H2O}n (2) involving 2,5-thiophenedicarboxylate (H2tdc), and bitopic flexible N-donor ligands, 1,3-bis(1,2,4-triazol-1-yl)propane (btrp) and 1,4-bis((1H-benzo[d]imidazol-1-yl)methyl)benzene (bimb), have been synthesized by the hydrothermal method and characterized via IR, elemental analysis, thermal analysis, and powder X-ray diffraction. The biological functional studies were performed; the treatment activity of the compounds on periodontitis and the specific mechanism was explored. First, the real-time RT-PCR was carried out to determine the inflammatory genes nf-κb and p53 relative expression in periodontal mucosal cells after treating with compounds 1 and 2. Then, the level of the inflammatory cytokine in the gingival crevicular fluid after treating with compounds was also determined by the ELISA detection kit.


2021 ◽  
Author(s):  
Plinio Cantero-López ◽  
Yoan Hidalgo-Rosa ◽  
Zoraida Sandoval-Olivares ◽  
Julián Santoyo-Flores ◽  
Pablo Mella ◽  
...  

Rhenium tricarbonyl complexes are one of the most important classes of coordination compounds in inorganic chemistry. Exploring their luminescent excited states, lowest singlet (S1), and the lowest triplet (T1), is...


Author(s):  
hua yang ◽  
Huiying Li ◽  
Ling Yue ◽  
Xi Chen ◽  
Dongdong Song ◽  
...  

A series of four-coordinated PtII(C^N)(N-donor ligand)Cl-type complexes have been synthesized through combination between C^N-type and N-donor ligands with different size. Photophysical features, electrochemical behaviors and electroluminescent (EL) performances have been...


RSC Advances ◽  
2021 ◽  
Vol 11 (39) ◽  
pp. 23975-23984
Author(s):  
Xue Yang ◽  
Yixia Ren ◽  
Hongmei Chai ◽  
Xiufang Hou ◽  
Zhixiang Wang ◽  
...  

Four fluorescent 2D Zn-MOFs based on a flexible triangular ligand and linear N-donor ligands are hydrothermally prepared and used to detect nitrobenzene in aqueous solution with high sensitivity, demonstrating their potential as fluorescent sensors.


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