Routes to new mixed-divalent metal phosphonate materials by Bouzid Menaa

Cover of: Routes to new mixed-divalent metal phosphonate materials | Bouzid Menaa

Published by University of Birmingham in Birmingham .

Written in English

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Edition Notes

Thesis (Ph.D.) - University of Birmingham, School of Chemical Sciences, 2003.

Book details

Statementby Bouzid Menaa.
The Physical Object
Pagination265 p. :
Number of Pages265
ID Numbers
Open LibraryOL15987947M

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Metal phosphate- and phosphonate-based nanoarchitectured materials offer a unique opportunity to design hierarchically porous nanomaterials consisting of interconnected micropores, mesopores, and macropores. Due to their strong affinity toward the metal centers, the phosphate and phosphonate moieties act as ligand sites/linkers to form a wide spectrum of nanoarchitectured by: Routes to new mixed-divalent metal phosphonate materials Author: Menaa, Bouzid.

ISNI: Awarding Body: University of Birmingham Current Institution: University of Birmingham Date of Award: Availability of Full Text: Full text unavailable from EThOS. Currently there is no other book on the topic and this book fills the gap in the literature by summarising in a concise way the latest developments in the field.

Metal phosphonate chemistry has seen impressive growth in the last years Routes to new mixed-divalent metal phosphonate materials book there is a. Layered mixed divalent metal phosphonates Mg1 − xZnx(O3PR)H2O [with R = CH3, C2H3, C6H5] and Ni1 − xZnx(O3PR)H2O [with R = CH3, C2H3, C6H5, (CH2)2COOH] have been prepared by heating, respectively, mixed divalent magnesium–zinc hydroxides and nickel–zinc hydroxides above the melting point of the phosphonicCited by: Metal phosphonate chemistry is a highly interdisciplinary field, as it encompasses several other areas, such as materials chemistry, gas storage, pharmaceutics, corrosion control, classical.

Titania–phosphonate hybrid porous materials: preparation, photocatalytic activity and heavy metal ion adsorption. Journal of Materials Chemistry18 (17), Metal phosphonates (MPs) are a class of inorganic–organic hybrid polymeric materials built by the coordination of phosphonate ligands to metal ions, forming extended structures of various dimensionalities [].The field of MPs chemistry has seen steady growth over the last few decades, which has been driven by the interest for applications in areas such as ion exchange [], intercalation.

The discovery of new compounds in unknown reaction systems is often a time consuming and tedious task. The first example on the use of HT methods presented here, involves the rapid investigation of crystalline metal phosphonates based on the functionalized diphosphonic acid (H 2 O 3 PCH 2) 2 N-CH 2 C 6 H 4 COOH (H 5 L).

Any time a new ligand is applied in the synthesis of inorganic-organic. Application of Host-Guest Reactions to Synthesis of New Materials: The Case of S.T.A.

Project in Japan p Layered and Pillared Zirconium Phosphates with α- and γ-Structures p Hydrothermal Synthesis of New Oxide Materials Using the Tetramethyl Ammonium Ion Synthesis of Novel Metal Phosphonate Complex Structures through Soft Chemistry.

The wide-angle powder X-ray diffraction (XRD) patterns for two metal phosphonate materials were measured using a Rigaku RINT × diffractometer with monochromated Cu Kα radiation (40 kV, 40 mA) at a ° min −1 scan rate.

All FT-IR spectra were obtained using a Thermo Scientific Nicolet spectrometer, where a KBr pellet was used as a. In the expansive world of porous hybrid materials, a category of materials that has been rather less explored than others and is gaining attention in development is the porous metal phosphonates.

They offer promising features towards applications which demand control over the inorganic–organic network and interface, which is critical for adsorption, catalysis and functional devices and. X‐ray diffractometry, transmission electron microscopy, N 2 sorption, and thermogravimetry measurements confirm that the obtained metal phosphonates possess a hierarchically porous structure with pore sizes of – nm and – nm for mesopores and micropores, respectively, and the metal phosphonate materials are thermally stable up.

phosphonate ester not previously attainable under standard conditions. Isotopic labelling experiments provided additional mechanistic insight suggesting a probable carbocation process. The mild and facile reaction conditions and the good yields of diverse, complex phosphonate products emphasize the broad applicability of this protocol.

The first route to highly stable crystalline microporous zirconium phosphonate metal–organic frameworks by: Marco, Taddei Published: () Synthesis, breathing, and gas sorption study of the first isoreticular mixed-linker phosphonate based metal–organic frameworks by:.

Metal phosphonate chemistry is going through a renaissance in the last decade. Synthetic chemists, chemical engineers, pharmacists, medical doctors, water technologists, and other application scientists have been involved in this exciting area of chemistry and technology from different perspectives.

Metal phosphonate chemistry has found. Synthesis and characterization of new layered mixed metal phosphonate materials magnesium–zinc phosphonates Mg1 – xZnx(O3PR)H2O and nickel–zinc phosphonates Ni1 – xZnx(O3PR)H2O using.

“Metal-Organic Frameworks: A New Class of Crystalline Porous Materials” published by Lambert Academic Publishing,is a book written by Dr Behnam Seyyedi on the emerging porous materials of metal-organic frameworks (MOFs).

The term MOF was coined by Omar Yaghi in (1). MOFs consist of both organic and inorganic building entities, where the organic ligands, i.e.

spacers, are. AbstractDivalent metal phosphonates are promising hybrid materials with a broad field of application. The rich coordination chemistry of the phosphonate linkers enables the formation of structures with different dimensionalities ranging from isolated complexes and layered structures to porous frameworks incorporating various functionalities through the choice of the building blocks.

“Synthesis and characterization of new layered mixed metal phosphonate materials magnesium-zinc phosphonates Mg 1-x Zn x (O 3 PR).H 2 O, and nickel-zinc phosphonates Ni 1-x Zn x (O 3 PR).H 2 O using mixed divalent magnesium-zinc and nickel-zinc hydroxides”, B.

Menaa, I. Shannon. Mater. Chem., 12 (),   Metal phosphonate chemistry is an interdisciplinary field encompassing materials chemistry, gas storage, pharmaceutics, corrosion control, classical chemical synthesis, crystallography, etc.

It has acquired additional significance due to "Metal-Organic Frameworks", as evidenced by the hundreds of papers published each : Gebundenes Buch.

a wide variety of materials properties.'*' Recently it was shown that surface-bound multilayer metal phosphonate structures, analogous to Langmuir-Blodgett films, can be grown through stepwise absorption of metal ions and bisphosphonic acid on metal substrates., Earlier work on metal phosphonates concen.

Title: Organophosphorus Supramolecular Chemistry. Part 2. Organophosphorus Receptors. VOLUME: 11 ISSUE: 18 Author(s):Pawel Kafarski, Piotr Mlynarz, Ewa Rudzinska and Lukasz Berlicki Affiliation:Department of Bioorganic Chemistry, Faculty of Chemistry, Wroclaw University of Technology,Wybrzeze Wyspianski Wroclaw, Poland.

Title: A New, Efficient Entry to Non-Lipophilic H-Phosphonate Monoesters – Preparation of Anti-HIV Nucleotide Analogues VOLUME: 6 ISSUE: 6 Author(s):Joanna Romanowska, Agnieszka Szymanska-Michalak, Malgorzata Pietkiewicz, Michal Sobkowski, Jerzy Boryski, Jacek Stawinski and Adam Kraszewski Affiliation:Institute of Bioorganic Chemistry, Polish Academy of Sciences, Noskowskiego.

New layered mixed Ba2+/Ti4+ metal phosphonates, BaTi(O3PC6H5)3 and SrTi(O3PC6H5)3, have been prepared via a hydrothermal route, in which mixed metal oxides, BaTiO3 and SrTiO3, were reacted with phenyl phosphonic acid. The mixed-metal phosphonates were combined with polystyrene (PS) via a solution route and cast as thin films for dielectric permittivity measurements.

Soft chemistry routes to new materials: chimie douce: proceedings of the international symposium held in Nantes, France, SeptemberBook, Internet Resource: All Authors / Contributors: Using the Tetramethyl Ammonium IonA Pillared Rectorite Clay with Highly Stable SupergalleriesSynthesis of Novel Metal Phosphonate Complex.

Bring your club to Amazon Book Clubs, start a new book club and invite your friends to join, or find a club that’s right for you for free. Explore Amazon Book Clubs Hardcover. #7, in Materials Science (Books) #24, in Industrial Manufacturing Systems #1, in Textbooks; Tell the Publisher.

I'd like to read this book on Kindle. As seen in Figure 5, both the tin phosphonate and zirconium phosphonate materials have a first peak at (°, Å) corresponding to the distance between the layers which is crosslinked by the phosphonate pillar (O 3PC 6H 4PO 3).

The subsequent peaks of the tin phosphonate occur at a higher 2θ angle as a result of the smaller size of the Sn4+. Academic Publishing,is a book written by Dr Behnam Seyyedi on the emerging porous materials of metal-organic frameworks (MOFs).

The term MOF was coined by Omar Yaghi in (1). MOFs consist of both organic and inorganic building entities, where the organic ligands, i.e. spacers, are coordinated to the metal ion clusters, i.e.

nodes, to. phosphonate-based frameworks. The first, by Chen and co-workers, provides an overview of metal−azolate frameworks, including MOFs constructed from imidazolate, pyrazolate, 1,2,4-triazolate, 1,2,3-triazolate, and tetrazolate.

In the article by Clearfield and co-workers, phosphonate. “The first route to highly stable crystalline microporous zirconium phosphonate metal–organic frameworks” Chem. Commun.50, (Ranked among the top 15 papers submitted for the PANalytical Award).

This technology is composed of mixed-metal phosphonates, which were synthesized from high dielectric oxides of the formula ABO3 and organophosphonic acids of the formula RPO3H2, where R = methyl, octyl, and phenyl.

These materials readily disperse into toluene, allowing easy fabrication of polystyrene-mixed-metal phosphonate nanocomposites. Final Report: Formation of Metal-Phosphonate Complexes and Their Subsequent Chemical Reactions with Mineral Surfaces EPA Grant Number: R Title: Formation of Metal-Phosphonate Complexes and Their Subsequent Chemical Reactions with Mineral Surfaces Investigators: Stone, Alan T.

Institution: The Johns Hopkins University EPA Project Officer: Chung, Serena. Historians have shown that technological advancements created new tools for agriculture and new weapons for armies. Explorers established trade routes to redistribute raw materials and finished products.

Modern culture is also influenced by the availability of new materials. In the 's. Upon disposal, metal-phosphonate complexes persist long enough to significantly alter toxic metal adsorption/desorption behavior. Ultimately, +II toxic metal ions are displaced from their phosphonate complexes by the dissolution of FeIII- and AlIII-containing minerals.

This project investigates the potential for toxic metal solubilization by. This book explores the limitless ability to design new materials by layering clay materials within organic compounds. Assembly, properties, characterization, and current and potential applications are offered to inspire the development of novel materials.

Coincides with the governments Materials Genome Initiative, to inspire the development of green, sustainable, robust materials that lead to. A deprotonative cross-coupling process (DCCP) enables a new synthetic route to access diarylmethyl phosphonates via introduction of aromatic groups on benzylic phosphonates.

A catalytic system based on Pd(OAc) 2 /CataCXium A allows a reaction between benzyl diisopropyl phosphonate derivatives and aryl bromides in very good isolated yields. Metal finishing is a primary example of the type of industry that has expanded on a worldwide basis.

This article details the impacts that metal finishing operations may have on the local water supplies and the types of treatment systems options available to make these discharges safe for the environment. Chemistry and Application of H-Phosphonates is an excellent source for those planning the synthesis of new phosphorus-containing compounds and in particular derivatives containing a phosphonate, phosphoramide or phosphonic acid diester group.

The rich chemistry, low cost and easy availability of diesters of H-phosphonic acid makes them an excellent choice as synthone in a number of practically.

Applications of organic–inorganic non-siliceous hybrid materials are emerging. But the developments of mesoporous hybrid materials lag far behind the achievements in syntheses. More strictly, there. In organic chemistry, phosphate or orthophosphate is an organophosphate, an ester of orthophosphoric acid of the form PO 4 RR′R″ where one or more hydrogen atoms are replaced by organic groups.

An example is trimethyl phosphate, (CH 3) 3 PO term also refers to the trivalent functional group OP(O-) 3 in such esters. Orthophosphates are especially important among the various. In the Reisner lab, we are interested in the synthesis of new materials and the factors that affect their formation from solution.

For the past several years, we have focused on the study of metal-organic frameworks based on both phosphonate, carboxylate and azolate linkers.Τμήμα Χημείας - Πανεπιστήμιο Κρήτης.Ester names are derived from the parent alcohol and the parent acid, where the latter may be organic or inorganic.

Esters derived from the simplest carboxylic acids are commonly named according to the more traditional, so-called "trivial names" e.g. as formate, acetate, propionate, and butyrate, as opposed to the IUPAC nomenclature methanoate, ethanoate, propanoate and butanoate.

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