Metal Phosphates and Phosphonates

A special issue of Inorganics (ISSN 2304-6740). This special issue belongs to the section "Inorganic Solid-State Chemistry".

Deadline for manuscript submissions: closed (31 May 2019) | Viewed by 12980

Special Issue Editors


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Guest Editor
Department of Chemistry, Texas A and M University, 400 Bizzell St, College Station, TX 77843, USA
Interests: solid-state chemistry; layered materials; crystallography; metal phosphonate chemistry

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Guest Editor
Polymer Program, Institute of Materials Science and Department of Chemical & Biomolecular Engineering, University of Connecticut, Storrs, CT 06269, USA
Interests: solid state chemistry; layered compounds; clays; hydrates; polymers; composites; green science
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Special Issue Information

Dear Colleagues,

It has been surprising over the last few years that there has been an increase in high-level and diverse papers based on metal phosphate and phosphonate chemistry. A survey of these papers has shown significant progress in the areas of catalysis, magnetic cages, combinations with MOFs, drug delivery, and polymer composites. These compounds exhibit fascinating structures (of all types), including amorphous materials. Because of their structural differences, they exhibit extraordinary properties with a great variety of potential uses. Among these, we can include energy storage, sensors, biosensors, flame retardants, and many more. 

Because of the great potential of these metal phosphates and phosphonates, we would like to bring together a variety of areas of research of these compounds. Therefore, we are proposing the formation of a Special Issue that will publish the very best recent papers on metal phosphates and phosphonates, along the lines of the areas of interest that are listed below:

  • Catalysis
  • MOFs
  • Polymers
  • Layered Materials
  • Magnetic Materials
Prof. Dr. Abraham Clearfield
Prof. Dr. Luyi Sun

Guest Editors

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Keywords

  • Catalysis
  • MOFs
  • Polymers
  • Layered Materials
  • Magnetic Materials

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Published Papers (3 papers)

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Research

14 pages, 3105 KiB  
Article
High-Throughput Synthesis of Pillared-Layered Magnesium Tetraphosphonate Coordination Polymers: Framework Interconversions and Proton Conductivity Studies
by Rosario M.P. Colodrero, Inés R. Salcedo, Montse Bazaga-García, Eleni Barouda, Maria Papadaki, Konstantinos E. Papathanasiou, Daniel Hernández-Alonso, Jordi Rius, Miguel A.G. Aranda, Enrique R. Losilla, Pascual Olivera-Pastor, Konstantinos D. Demadis and Aurelio Cabeza
Inorganics 2018, 6(3), 96; https://doi.org/10.3390/inorganics6030096 - 11 Sep 2018
Cited by 5 | Viewed by 4407
Abstract
Novel pillared-layered framework materials were synthesized by high-throughput or microwave-assisted methodology that contain Mg2+ and the zwitterionic linker HDTMP (hexamethylenediamine-N,N,N′,N′-tetrakis(methylenephosphonic acid)). Three compounds were structurally characterized by X-ray powder diffraction. In the compound {Mg[(HO3PCH [...] Read more.
Novel pillared-layered framework materials were synthesized by high-throughput or microwave-assisted methodology that contain Mg2+ and the zwitterionic linker HDTMP (hexamethylenediamine-N,N,N′,N′-tetrakis(methylenephosphonic acid)). Three compounds were structurally characterized by X-ray powder diffraction. In the compound {Mg[(HO3PCH2)2N(CH2)6N(CH2PO3H2)2]·(H2O)}n(1), obtained at 140 °C by hydrothermal or microwave-assisted reaction, the layers are built by isolated Mg2+ octahedra coordinated by oxygen atoms from six different zwitterionic HDTMP ligands. Each amino-bis(methylenephosphonate) moiety links three Mg2+ ions, bridging two of them through one phosphonate group and connecting the third polyhedron in a monodentate fashion. In Compound 2, {Mg[(HO3PCH2)2N(CH2)6N(CH2PO3H2)2]}n, hydrothermally synthesized at 180 °C, the layers are composed of bidentate amino-bis(methylenephosphonate) moieties connected to three Mg2+ ions, with one of the phosphonate groups acting as a bridging ligand. Various subtle structural changes are noted for the other two compounds. Thermodiffraction of 1 reveals that a crystalline-to-crystalline phase transformation occurs concomitantly with its dehydration, leading to a new anhydrous phase, namely, {Mg[(HO3PCH2)2N(CH2)6N(CH2PO3H2)2]}n(1deh). This process is fully reversible upon equilibrating the solid at room temperature. The reported compounds can adsorb ammonia and CO2. Compound 1 exhibits a moderate proton conductivity, ~1.5 × 10−5 S·cm−1 at 80 °C and 95% RH, that increases a half order of magnitude after experiencing a complete dehydration/rehydration process, 11deh1. Full article
(This article belongs to the Special Issue Metal Phosphates and Phosphonates)
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11 pages, 4305 KiB  
Article
One-Dimensional Fluorene-Based Co(II) Phosphonate Co(H2O)2PO3C–C12H9·H2O: Structure and Magnetism
by Clarisse Bloyet, Jean-Michel Rueff, Olivier Perez, Alain Pautrat, Vincent Caignaert, Bernard Raveau, Guillaume Rogez and Paul-Alain Jaffrès
Inorganics 2018, 6(3), 93; https://doi.org/10.3390/inorganics6030093 - 5 Sep 2018
Cited by 2 | Viewed by 4270
Abstract
A new Co(II) phosphonate, Co(H2O)2PO3C–C12H9·H2O, has been synthesized under hydrothermal conditions. The monoclinic P21/c structure of this organic–inorganic hybrid consists of isolated perovskite-type chains of corner-shared CoO [...] Read more.
A new Co(II) phosphonate, Co(H2O)2PO3C–C12H9·H2O, has been synthesized under hydrothermal conditions. The monoclinic P21/c structure of this organic–inorganic hybrid consists of isolated perovskite-type chains of corner-shared CoO4(H2O)2 octahedra interconnected via phosphonate groups. The unique one-dimensional structure of this phase is closely related to the single-chain magnet (SCM) phosphonate Co(H2L)(H2O), with L = 4-Me-C6H4-CH2N(CPO3H2)2, that contains isolated chains of CoO5N octahedra. Like the latter, this hybrid exhibits 1D antiferromagnetic interactions and the possibility of an effective pseudo spin contribution due to spin canting at low temperature, but, in contrast, is not an SCM. This different magnetic behavior is explained by the different geometry of the octahedral chains and by the possible existence of weak antiferromagnetic interactions between the chains. This opens the route to the investigation of a large series of compounds by tuning the chemical composition and structure of the phosphonic acid used as organic precursor of hybrid materials. Full article
(This article belongs to the Special Issue Metal Phosphates and Phosphonates)
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11 pages, 3792 KiB  
Article
Manganese Fluorene Phosphonates: Formation of Isolated Chains
by Clarisse Bloyet, Jean-Michel Rueff, Vincent Caignaert, Bernard Raveau, Jean-François Lohier, Mélissa Roger, Guillaume Rogez and Paul-Alain Jaffrès
Inorganics 2018, 6(3), 92; https://doi.org/10.3390/inorganics6030092 - 5 Sep 2018
Cited by 2 | Viewed by 3630
Abstract
9,9-dimethylfluorenyl-2-phosphonic acid 1 was reacted with manganese nitrate tetrahydrate to produce under hydrothermal conditions the crystalline manganese phosphonate Mn(H2O)2[O2(OH)PC15H13]2·2H2O which crystallize in the P21/c space [...] Read more.
9,9-dimethylfluorenyl-2-phosphonic acid 1 was reacted with manganese nitrate tetrahydrate to produce under hydrothermal conditions the crystalline manganese phosphonate Mn(H2O)2[O2(OH)PC15H13]2·2H2O which crystallize in the P21/c space group. This compound is a rare example of Mn-phosphonate material featuring isolated chains. The interactions between these chains containing the 9,9-dimethylfluorenyl moieties, result from Van der Waals interactions involving the fluorene ligands and C···H–C hydrogen bonds as revealed by Hirshfeld Surfaces. This material features antiferromagnetic exchange interactions as revealed by the magnetic susceptibility as a function of the temperature. Full article
(This article belongs to the Special Issue Metal Phosphates and Phosphonates)
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