Coordination Polymers from Biphenyl-Dicarboxylate Linkers: Synthesis, Structural Diversity, Interpenetration, and Catalytic Properties.

Inorg Chem

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.

Published: August 2022

AI Article Synopsis

Article Abstract

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.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9775469PMC
http://dx.doi.org/10.1021/acs.inorgchem.2c01488DOI Listing

Publication Analysis

Top Keywords

biphenyl-dicarboxylate linkers
12
coordination polymers
8
properties work
8
polymers biphenyl-dicarboxylate
4
linkers synthesis
4
structural
4
synthesis structural
4
structural diversity
4
diversity interpenetration
4
interpenetration catalytic
4

Similar Publications

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 PDF

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 PDF

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 PDF

Coordination Polymers from Biphenyl-Dicarboxylate Linkers: Synthesis, Structural Diversity, Interpenetration, and Catalytic Properties.

Inorg 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 PDF

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.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!