scholarly journals Heterogeneous catalitic activity of Novel Indium MOFs

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.

Polyhedron ◽  
1996 ◽  
Vol 15 (3) ◽  
pp. 391-402 ◽  
Author(s):  
Christopher C. Landry ◽  
Alan Hynes ◽  
Andrew R. Barron ◽  
Ionel Haiduc ◽  
Crisian Silvestru

2013 ◽  
Vol 91 (5) ◽  
pp. 338-347 ◽  
Author(s):  
Anthony F. Cozzolino ◽  
Philip J.W. Elder ◽  
Lucia Myongwon Lee ◽  
Ignacio Vargas-Baca

The secondary bonding interactions that link the supramolecular structures assembled by 1,2,5-chalcogenadiazoles were analyzed through explicit orthogonalization of molecular orbitals (NBO), topological analysis of the electron density (AIM), and the electron localization function (ELF). The results of these analyses are consistent with a bonding description that attributes important covalent and electrostatic character to these interactions. Application of these analyses to the individual molecules highlighted the structural features from which each of those contributions originates, namely the polarity and modest strength of the E–N bond. Both of these effects increase along the series S, Se, Te. Perturbations to the heterocycle electronic structure that result in a weaker and more polar E–N bond cause an increase in the Lewis acidity at the chalcogen centre, which in turn leads to stronger secondary bonding interactions with Lewis bases. Additionally, the contribution of dispersion forces is not negligible and is most important in the case of sulfur.


2019 ◽  
Vol 72 (5) ◽  
pp. 341 ◽  
Author(s):  
Yu-Ting Yang ◽  
Chang-Zheng Tu ◽  
Xiao-Lin Xu ◽  
Li-Li Xu ◽  
Bang-Ling Yan ◽  
...  

Solvothermal reactions of 3,3′,5,5′-biphenyltetracarboxylic acid (H4BPTC) and cobalt(ii) ions in the presence of two different flexible N-donor ancillary ligands afford two novel coordination polymers, {[Co(BPTC)0.5(bix)]·H2O}n (1), {[Co(BPTC)0.5(bpp)]·3H2O}n (2) (bix=1,4-bis(imidazol-1-ylmethyl)benzene; bpp=1,3-bis(4-pyridyl)propane). Their structures have been determined by elemental analyses, IR spectra, single-crystal X-ray diffraction analyses, and powder X-ray diffraction. The pillared layered framework of 1 can be simplified to a (4,6)-connected net with a Schläfli symbol of (44·62)(44·69·82). Complex 2 manifests a bilayered structure, and can be simplified to a (4,4)-connected net with a Schläfli symbol of (55·8)(54·62). The thermal stabilities of both complexes and the magnetic behaviours of 1 are also discussed.


2015 ◽  
Vol 6 (3) ◽  
pp. 2016-2021 ◽  
Author(s):  
Michael H. Holthausen ◽  
Rashi R. Hiranandani ◽  
Douglas W. Stephan

A series of electrophilic bis-fluorophosphonium dications dervied from diphosphines with naphthalene- and (oligo)methylene-linkers is presented. The resulting Lewis acidity is demonstrated to depend on the spatial proximity between the P moieties as evidenced in several Lewis acid catalyzed transformations.


2012 ◽  
Vol 11 (2) ◽  
pp. 1-16
Author(s):  
Sreejarani K Pillai ◽  
O Gheevarghese ◽  
I V Tleane

The present study has undertaken the Friedel-Crafts benzylation of aromatics over the V2O5/ZrO2 catalysts systems. Catalysts with different V2O5 content (0-15wt %) was prepared by wet impregnation method and characterized by XRD, BET surface area, FTIR and 5’V NMR techniques. The surface acidic properties were determined by temperature programmed desorption of NH3, cumene cracking and perylene adsorption. Under the optimized reaction conditions, these catalysts are found to be very effective and considerably more selective than the conventional homogeneous Lewis acid catalysts. The investigation of vanadia systems-catalyzed benzylation of o-xylene with benzyl chloride revealed that the catalytic activity and product selectivity are sensitive to the precise reaction parameters and can be related to the Lewis acidity of the systems. The reaction is found to be very clean and produces the desired monoalkylated product with high yield.


2007 ◽  
Vol 26 (4) ◽  
pp. 938-944 ◽  
Author(s):  
Vicki Hsieh ◽  
Antonio G. De Crisci ◽  
Alan J. Lough ◽  
Ulrich Fekl

2016 ◽  
Vol 40 (7) ◽  
pp. 5957-5965 ◽  
Author(s):  
Xiaobin Liu ◽  
Zhenyu Xiao ◽  
Ao Huang ◽  
Wen Wang ◽  
Liangliang Zhang ◽  
...  

Three new mixed-ligand coordination polymers have been synthesized based on 3,3′-(anthracene-9,10-diyl)diacrylate acid and different N-donor ligands. Complex 2 displays rapid and selective sensing of Fe3+.


2014 ◽  
Vol 38 (4) ◽  
pp. 1611-1626 ◽  
Author(s):  
Anna Świtlicka-Olszewska ◽  
Barbara Machura ◽  
Jerzy Mroziński ◽  
Bożena Kalińska ◽  
Rafał Kruszynski ◽  
...  

Through varying the auxiliary N-donor ligands nine new compounds have been synthesized and characterised structurally and spectroscopically. The magnetic properties of the complexes have been investigated and discussed in the context of their structures.


Sign in / Sign up

Export Citation Format

Share Document