The present work explores two biphenyl-dicarboxylate linkers, 3,3'-dihydroxy-(1,1'-biphenyl)-4,4'-dicarboxylic (HL) and 4,4'-dihydroxy-(1,1'-biphenyl)-3,3'-dicarboxylic (HL) acids, in hydrothermal generation of nine new compounds formulated as [Co(μ-HL)(phen)(HO)] (), [Mn(μ-HL)(phen)]·4HO (), [Zn(μ-HL)(2,2'-bipy)(HO)] (), [Cd(μ-HL) (2,2'-bipy)(HO)] (), [Mn(μ-HL)(μ-HL)(μ-4,4'-bipy)]·4HO (), [Zn(μ-HL)(μ-4,4'-bipy)] (), [Zn(μ-HL)(phen)] (), [Cd(μ-HL)(phen)] (), and [Cu(μ-HL) (μ-4,4'-bipy)(HO)] (). These coordination polymers (CPs) were generated by reacting a metal(II) chloride, a HL or HL linker, and a crystallization mediator such as 2,2'-bipy (2,2'-bipyridine), 4,4'-bipy (4,4'-bipyridine), or phen (1,10-phenanthroline). The structural types of - range from molecular dimers () to one-dimensional (, , ) and two-dimensional (, ) CPs as well as three-dimensional metal-organic frameworks (, , ). Their structural, topological, and interpenetration features were underlined, including an identification of unique two- and fivefold 3D + 3D interpenetrated nets in and . Phase purity, thermal and luminescence behavior, as well as catalytic activity of the synthesized products were investigated. Particularly, a Zn(II)-based CP acts as an effective and recyclable heterogeneous catalyst for Henry reaction between a model substrate (4-nitrobenzaldehyde) and nitroethane to give β-nitro alcohol products. For this reaction, various parameters were optimized, followed by the investigation of the substrate scope. By reporting nine new compounds and their structural traits and functional properties, the present work further outspreads a family of CPs constructed from the biphenyl-dicarboxylate HL and HL linkers.
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http://dx.doi.org/10.1021/acs.inorgchem.2c01488 | DOI Listing |
Dalton Trans
September 2024
Department of Chemistry - Ångström Laboratory, Uppsala University, Box 523, 751 20 Uppsala, Sweden.
The postsynthetic metalation (PSM) of metal-organic frameworks (MOFs) with intrinsic metal binding sites is an intriguing strategy to introduce catalytic function into MOFs. The spatial distribution of the catalytic sites within the MOF crystal will affect the efficiency of the material, but the factors that govern depth distribution of the introduced metal sites are often not well understood. Herein, we employ Rutherford backscattering spectrometry (RBS) to investigate the metal distribution in a series of post-synthetically metalated mixed linker bpdc/BPY UiO-67 (UiO = Universitet i Oslo, bpdc = biphenyl-dicarboxylate, BPY = 2,2'-bipyridine-5,5'-dicarboxylate) single crystals as a function of linker ratio and metalation time.
View Article and Find Full Text PDFRSC Adv
May 2023
Ho Chi Minh City University of Technology (HCMUT) 268 Ly Thuong Kiet Street, District 10 Ho Chi Minh City Vietnam
CO capture is a crucial strategy to mitigate global warming and protect a sustainable environment. Metal-organic frameworks with large surface area, high flexibility, and reversible adsorption and desorption of gases are good candidates for CO capture. Among the synthesized metal-organic frameworks, the MIL-88 series has attracted our attention due to their excellent stability.
View Article and Find Full Text PDFChemSusChem
March 2023
Department of Physics and Astronomy, Purdue University, West Lafayette, 47907, USA.
Artificial photosynthesis strives to convert the energy of sunlight into sustainable, eco-friendly solar fuels. However, systems with light-driven water oxidation reaction (WOR) at pH=1 are rare. Broadly used [Ru(bpy) ] (bpy=2,2'-bipyridine) photosensitizer has a fixed +1.
View Article and Find Full Text PDFInorg Chem
August 2022
Centro de Química Estrutural, Institute of Molecular Sciences, Departamento de Engenharia Química, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, Lisbon 1049-001, Portugal.
The present work explores two biphenyl-dicarboxylate linkers, 3,3'-dihydroxy-(1,1'-biphenyl)-4,4'-dicarboxylic (HL) and 4,4'-dihydroxy-(1,1'-biphenyl)-3,3'-dicarboxylic (HL) acids, in hydrothermal generation of nine new compounds formulated as [Co(μ-HL)(phen)(HO)] (), [Mn(μ-HL)(phen)]·4HO (), [Zn(μ-HL)(2,2'-bipy)(HO)] (), [Cd(μ-HL) (2,2'-bipy)(HO)] (), [Mn(μ-HL)(μ-HL)(μ-4,4'-bipy)]·4HO (), [Zn(μ-HL)(μ-4,4'-bipy)] (), [Zn(μ-HL)(phen)] (), [Cd(μ-HL)(phen)] (), and [Cu(μ-HL) (μ-4,4'-bipy)(HO)] (). These coordination polymers (CPs) were generated by reacting a metal(II) chloride, a HL or HL linker, and a crystallization mediator such as 2,2'-bipy (2,2'-bipyridine), 4,4'-bipy (4,4'-bipyridine), or phen (1,10-phenanthroline). The structural types of - range from molecular dimers () to one-dimensional (, , ) and two-dimensional (, ) CPs as well as three-dimensional metal-organic frameworks (, , ).
View Article and Find Full Text PDFJ Am Chem Soc
March 2021
Wolfson Catalysis Centre, Department of Chemistry, University of Oxford, Oxford OX1 3QR, U.K.
Understanding structural responses of metal-organic frameworks (MOFs) to external stimuli such as the inclusion of guest molecules and temperature/pressure has gained increasing attention in many applications, for example, manipulation and manifesto smart materials for gas storage, energy storage, controlled drug delivery, tunable mechanical properties, and molecular sensing, to name but a few. Herein, neutron and synchrotron diffractions along with Rietveld refinement and density functional theory calculations have been used to elucidate the responsive adsorption behaviors of defect-rich Zr-based MOFs upon the progressive incorporation of ammonia (NH) and variable temperature. UiO-67 and UiO-bpydc containing biphenyl dicarboxylate and bipyridine dicarboxylate linkers, respectively, were selected, and the results establish the paramount influence of the functional linkers on their NH affinity, which leads to stimulus-tailoring properties such as gate-controlled porosity by dynamic linker flipping, disorder, and structural rigidity.
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