Advances and Challenges in the Creation of Porous Metal Phosphonates

Total Page:16

File Type:pdf, Size:1020Kb

Advances and Challenges in the Creation of Porous Metal Phosphonates Supplementary information Advances and Challenges in the Creation of Porous Metal Phosphonates Bharadwaj Mysore Ramesha * and Vera Meynen Laboratory for Adsorption and Catalysis (LADCA), Department of Chemistry, University of Antwerp, Universiteitsplein 1, 2610 Wilrijk, Belgium; [email protected] * Correspondence: [email protected]; Tel.: +32-(0)3-265-23-53 Received: 26 October 2020; Accepted: 24 November 2020; Published: 26 November 2020 Table S1. Synthesis Protocol for Porous Metal Phosphonates. Metal Precursor Phosphonic Linker Synthesis Method Final Morphology References Mono-alkyl Direct precipitation phosphonic acids Lamellar hexagonal ZrOCl2 in HF (aqueous [1] and their dialkyl particles (10–100 μm) media) ester Direct precipitation Th(NO3)4 Mono-terphenyl and in HF Lamellar particles [2] ZrOCl2 bis-terphenylene PA (dioxane/water) α,ω-bis(phosphonic Direct precipitation ZrOCl2 acid) alkyl or aryl Lamellar thin films [3] in HF linker Butane DPA, benzene DPA,bis(phosphono Direct precipitation Lamellar structure ZrOCl2 [4] methyl) DPA, in HF (DMSO/water) with mesoporosity diphenyl DPA with H3PO4 Lamellar structure Zr (IV) fluoro Direct precipitation 3,3’, 5,5’-TMBPDA with inter-layer [5] complexes in HF microporosity Phenyl-DPA Co-condensation in ZnCl2 Lamellar structure [6] Biphenylyl-DPA water Co-condensation in CuSO4 5H2O & Phenyl-DPA and water under reflux or Lamellar structure [7] CuNO3 2.5H2O Biphenylyl-DPA hydrothermal conditions Ethylene-DPA and Co-condensation in CuSO4 5H2O & ZnCl2 Lamellar structure [8] Propylene-DPA water Lamellar particles Benzene DPA + Direct precipitation ZrOCl2 with [9] H3PO4 in HF micro/mesoporosity Bis(methylene) Co-condensation in Zn(NO3)2 & Cd(NO3) Lamellar structure [10] phenyl-PA water Phenyl DPA with Hydrothermal in Lamellar with slit- ZnCl2 [11] H3PO4 water shape pores 6.6 nm Lamellar structure Hydrothermal in with Mn(ac)2 & Zn(ac)2 NMIB-DPA [12] EtOH/water 3D porous framework Co-condensation & 1D polymeric Co(ac)2 Octyl DPA Hydrothermal in network and [13] water (HF) Layered structure Micro and SnCl4 Phenyl PA Hydrothermal in HF [14] mesoporous Hydrothermal in 3D non-porous Sn(CO2)2 Phenyl DPA [15] water layered structure Materials 2020, 13, 5366; doi: 10.3390/ma13235366 www.mdpi.com/journal/materials Materials 2020, 13, 5366 2 of 7 Layered spherical Phenyl PA SnCl4 Hydrothermal in HF globules with [16] Methyl PA micro/mesoporosity Direct precipitation Supermicroporous SnCl4 PPPA followed by [17] layered particles hydrothermal in HF Layered micro and SnCl4 PPPA Direct precipitation mesoporous [18] ZrOCl2 PPA in HF structure Layered nano-sized Phenyl-PA SnCl4 Hydrothermal in HF particles with [19] Biphenyl-PA micro/mesoporosity Small nanoparticles SnCl4 bpyBPAE + Methyl Hydrothermal in (<15 nm) with [20] ZrOCl2 PA DMSO (HF) micro/mesoporosity Abbreviations: PA = Phosphonic acid; DPA = Diphosphonic acid; 3,3’,5,5’-TMBDPA = Tetramethylbiphenyldiphosphonic acid; NMIB = N-methyliminobis(methylenephosphonic acid); PPPA = 4-(4’- phosphonophenoxy)phenyl phosphonic acid; PPA = Phenylphosphonic acid; and bpyBPAE = Tetraethyl 2,2’- bipyridinediyl-5,5’-bis(phosphonate). Table S2. Phosphonate—MOFs. Metal Precursor Phosphonic Linker Synthesis Method Final Morphology References 3D framework with Hydrothermal in Hydrous TiO2 Methylene DPA layered structure— [21] HF/water Non-porous Hexagonal array of CoCl2 & Co(ac)2 Hydrothermal in N,N’-PBMDPA channels with 10 Å [22] NiCl2 & Ni(ac)2 water pores Hydrous TiO2 Hydrothermal in 3D framework with N,N’-PBMDPA [23] AlCl3 HF/water microporosity Co-condensation in 3D porous structure Zn(ClO4)2 DHBP water & reflux with with microporosity [24] DMF (10 Å pores) Open-framework Pb(ac)2 Hydrothermal in EDTP with tunnels & [25] ZnCl2 water/EtOH microporous Hydrothermal in 3D supramolecular Pb(NO3)2 N,N’-PBMDPA [26] water framework Co- condenastion/Precipi ZrOCl2 PBMPA Layered framework [27] tation in water (NH4F or HF) Co-condensation 3D network with Zn(NO3)2 BDPEt [28] (THF/water) channels of ~4.5A° Layered pillar BDPEt Co-condensation CuCl2 structure with VdW [29] BDPMe (EtOH/water) interaction Pillared interlayer BDPA Co-condensation CuCO3·Cu(OH)2 architecture with [30] Amino triazole (MeOH/water) apparent pores Hydrothermal in 3D frameworks with Ni(ac)2 N,N’-PBMDPA [31] water 0.9 nm pores 3D honeycomb Hydrothermal in Co(ac)2 N,N’-BPBMDPA architecture with [32] water pores of 1.8 nm Octaethyl pyrene- 3D framework made Hydrothermal in BaBr2·2H2O 1,3,6,8- up by crosslink of 1D [33] EtOH/water tetraphosphonate chains Hydrothermal in Amorphous SnCl4 BTBP [34] MeOH microporous (~8.5 Å) CuSO4, NiO, NiSO4, BTTMT Hydrothermal in 2D double-layered [35] & MnSO4 TMB-BTTMT water structure with 1D Materials 2020, 13, 5366 3 of 7 tunnel with aperture of 3.5 Å × 7.0 Å ZrOCl2 BTBP Direct precipitation Non-porous [36] in HF honeycomb-like motif ZrOCl2 TTBMP Direct precipitation Permanent [37] in HF microporosity & channels of (~5–10 Å) Al2(SO4)3 TMB-TTMT Hydro(solvo)thermal 3D framework with [38] in EtOH/water hexagonal channels (1.2 nm width) ZrCl4 BTBP Direct precipitation 3D amorphous and [39] & Hydrothermal semi-crystalline (HF) framework with microporosity (10 Å pores) ZrOCl2 TTBMP Direct precipitation 2D layered structure [40] in HF with no porosity Abbreviations: DPA = Diphosphonic acid; N,N’-PBMDPA = N,N’-piperazine bis(methylenephosphonic acid); DHBP = 1,4-dihydroxy-2,5-benzenediphosphonate; EDTP = N,N,N’,N’- ethylenediaminetetrakis(methylenephosphonic acid); PBMPA = Piperazine-N,N’-bis(methylenephosphonic acid); BDPEt = 1,4-benzenediphosphonate bis(monoethyl ester); BDPMe = 1,4-benzenediphosphonate bis(monomethyl ester); BDPA = Benzene-1,4-diphosphonic acid; BTTMT = Benzene-1,3,5- triyltris(methylene)triphosphonic acid; TMB-BTTMT = (2,4,6-trimethylbenzene-1,3,5- triyl)tris(methylene)triphosphonic acid; BTBP = 1,3,5-tris(4-phosphonophenyl) benzene; TTBMP = 2,4,6-tris(4- (phosphonomethyl)phenyl)-1,3,5-triazine; and TMB-TTMT = 2,4,6-trimethylbenzene-1,3,5-triyl- tris(methylene)triphosphonic acid. Table S3. Mesoporous Metal Phosphonates—Templated. Metal Phosphonic Template Synthesis Method Final Morphology References Precursor Acid Amorphous, Co-condensation at Al(OiPr)3 MDPA ODTMACl Mesoporous (1.8 [41] RT in water nm pores) Amorphous, Atrane route, Co- Al(OsBu)3 EDPA CTAB Mesoporous [42] precipitation in water (hexagonal) Brij-56/58 Co-condensation in Amorphous AlCl3 MDPA F68, F127 EtOH/water followed [43] Mesoporous (p6m) P123 by EISA MDPA Co-condensation in Al(OiPr)3 Amorphous with EDPA CTAB water and [44] AlCl3 Mesoporosity PDPA EtOH/water Semi-crystalline, SnCl4 PPA SDS Hydrothermal Micro and [45] mesoporous Amorphous, Inter- Hydrothermal in ZrOCl2 PPA - particle [46] water mesoporosity Atrane route, Co- Amorphous with Al(OsBu)3 H3PMP CTAB [47] precipitation in water mesoporosity Amorphous with Non-hydrolytic Ti(OiPr)4 TPPhA - inter-particle [48] condensation in THF porosity Non-hydrolytic Amorphous with V(O)(OiPr)3 TPPhA - condensation in inter-particle [49] DMSO porosity Materials 2020, 13, 5366 4 of 7 Amorphous, Inter- HEDP Hydrothermal in particle Ti(OBu)4 PS beads [50] (β-CD) EtOH/water mesoporosity & macroporous Amorphous, plate- like particles & slit HEDP Hydrothermal in Ti(OBu)4 - shaped inter- [51] EDTMP EtOH/water particle mesoporosity Co-condensation in Amorphous, Inter- F127 Ti(OBu)4 HEDP EtOH followed by particle [52] P123 EISA mesoporosity Cryogenic condensation in EtOH Amorphous, p6mm TiCl4 EDTMP Brij-56 [53] followed by Mesophase hydrothermal and EISA Cryogenic condensation in Amorphous, la3d TiCl4 HEDP CTAB EtOH followed by [54] cubic mesophase hydrothermal treatment Amorphous with HEDP Hydrothermal in hierarchical Ti(OBu)4 - [55] EDTMP EtOH/water meso/macroporosit y Crystalline (anatase domains) with EDTMP Hydrothermal in phosphonate cap Ti(OBu)4 - [56] DTPMP EtOH/water and hierarchical meso/macroporosit y Amorphous, Cubic Co-condensation in AlCl3 BDPA F127 mesoporous [57] EtOH/water (Im3m) DEPT Amorphous, Co-condensation in AlCl3 DPAEP F127 mesoporous thin [58] EtOH/water DPEP film Anatase Non-hydrolytic sol crosslinked bBzP Ti(OiPr)4 - gel hydrothermal in bisphosphonates [59] bPyP toluene with inter-crystal mesopores Abbreviations: MDPA = Methylenediphosphonic acid; EDPA = Ethylenediphosphonic acid; PDPA = Propylenediphosphonic acid; PPA = Phenylposphonic acid; H3PMP = 1-phosphonomethylproline; TPPhA = Tetrakis-1,3,5,7-(4-diethylphosphonatophenyl) adamantane; HEDP = 1-hydroxyethane 1,1-diphosphonic acid; EDTMP = Ethylenediamine tetra(methylene phosphonic acid); DTPMP = Diethylenetriamine penta(methylene phosphonic acid); BDPA = 1,4-phenylene diphosphonic acid; DEPT = 2,5-bis(diethoxyphosphoryl) thiophene; DPAEP = Diethyl (N-diethylphosphonomethylcarbonyl)aminoethyl phosphonate; DPEP = Diethyl 2-(2’- diethylphosphonoethoxy)ethylphosphonate; bBzP = 4,4’-bis(diethylphosphonomethyl)biphenyl; and bByP = tetraethyl 2,2’-bipyridine-5,5’-bisphosphonate. Materials 2020, 13, 5366 5 of 7 References 1. Dines, M.B.; Digiacomo, P.M. Derivatized lamellar phosphates and phosphonates of M (IV) ions. Inorg. Chem. 1981, 20, 92–97, doi:10.1021/ic50215a022. 2. Dines, M.B.; Griffith, P.C. Synthesis and characterization of layered tetravalent metal terphenyl mono- and bis-phosphonates. Polyhedron 1983, 2, 607–611, doi:10.1016/s0277-5387(00)81519-3. 3. Cao, G.; Hong, H.G.; Mallouk, T.E. Layered metal phosphates and phosphonates: from crystals to monolayers. Accounts Chem. Res. 1992, 25, 420–427, doi:10.1021/ar00021a007. 4. Alberti, G.;
Recommended publications
  • Synthetic Routes to Bromo-Terminated Phosphonate Films and Alkynyl Pyridine Compounds for Click Coupling
    University of Mary Washington Eagle Scholar Student Research Submissions Spring 5-7-2018 Synthetic Routes to Bromo-Terminated Phosphonate Films and Alkynyl Pyridine Compounds for Click Coupling Poornima Sunder Follow this and additional works at: https://scholar.umw.edu/student_research Part of the Biochemistry Commons Recommended Citation Sunder, Poornima, "Synthetic Routes to Bromo-Terminated Phosphonate Films and Alkynyl Pyridine Compounds for Click Coupling" (2018). Student Research Submissions. 226. https://scholar.umw.edu/student_research/226 This Honors Project is brought to you for free and open access by Eagle Scholar. It has been accepted for inclusion in Student Research Submissions by an authorized administrator of Eagle Scholar. For more information, please contact [email protected]. Synthetic Routes to Bromo-Terminated Phosphonate Films and Alkynyl Pyridine Compounds for Click Coupling Poornima Rachel Sunder Thesis submitted to the faculty of University of Mary Washington in partial fulfillment of the requirements for graduation with Honors in Chemistry (2018) ABSTRACT Click reactions are a highly versatile class of reactions that produce a diverse range of products. Copper-catalyzed azide-alkyne cycloaddition (CuAAC) click reactions require an azide and a terminal alkyne and produce a coupled product that is “clicked” through a triazole ring that can have a variety of substituents. In this work, bromo-terminated phosphonate films on copper oxide surfaces were explored as the platform for click coupling, as the terminal azide needed for the reaction can be generated through an in situ SN2 reaction with a terminal bromo group. The reactions were characterized using model reactions in solution before being conducted on modified copper oxide surfaces.
    [Show full text]
  • H-Phosphonates: Versatile Synthetic Precursors to Biologically Active Phosphorus Compounds*
    Pure Appl. Chem., Vol. 79, No. 12, pp. 2217–2227, 2007. doi:10.1351/pac200779122217 © 2007 IUPAC H-Phosphonates: Versatile synthetic precursors to biologically active phosphorus compounds* Adam Kraszewski1,‡ and Jacek Stawinski1,2,‡ 1Institute of Bioorganic Chemistry, Polish Academy of Sciences, Noskowskiego 12/14, 61-704 Poznan, Poland; 2Department of Organic Chemistry, Arrhenius Laboratory, Stockholm University, S-10691 Stockholm, Sweden Abstract: In this review, a short account of H-phosphonate chemistry and its application to the synthesis of biologically important phosphates and their analogs is given. Keywords: H-phosphonates; phosphate analogs; biological activity; nucleic acids; drugs. INTRODUCTION Located at the crossroad of various bioinformation exchange pathways, phosphorus-containing com- pounds play a key role in living organisms as carriers of genetic information and important signalling, regulatory, energy transfer, and structural compounds [1]. Due to this pivotal role, biologically impor- tant phosphorus compounds have become therapeutic targets in various modern medicinal techniques, such as antisense [2] and antigene [3] approaches to modulation gene expression, or a gene silencing technique using short interfering RNA (siRNA) [4]. To maximize the desired biological effect and to minimize cytotoxicity, a biologically active com- pound has to have very precisely adjusted chemical and pharmacokinetic properties. This can be achieved by, e.g., changing pKa values of the ionizeable functions, changing electronegativity of the substituents, their size, hydrophobicity, etc. These features can also influence transport of a drug across cell membranes, its preferential degradation in normal or activation in the neoplastic or virus-infected cells, and can contribute to the overall efficiency of the drug. A prominent example here are antiviral pronucleotides in which the phosphate moiety is masked with alkyl or aryl groups that are removed chemically and enzymatically in cells to produce an active antiviral nucleotide [5].
    [Show full text]
  • The Hydrolysis of Phosphinates and Phosphonates: a Review
    molecules Review The Hydrolysis of Phosphinates and Phosphonates: A Review Nikoletta Harsági and György Keglevich * Department of Organic Chemistry and Technology, Budapest University of Technology and Economics, 1521 Budapest, Hungary; [email protected] * Correspondence: [email protected]; Tel.: +36-1-463-1111 (ext. 5883) Abstract: Phosphinic and phosphonic acids are useful intermediates and biologically active com- pounds which may be prepared from their esters, phosphinates and phosphonates, respectively, by hydrolysis or dealkylation. The hydrolysis may take place both under acidic and basic conditions, but the C-O bond may also be cleaved by trimethylsilyl halides. The hydrolysis of P-esters is a challenging task because, in most cases, the optimized reaction conditions have not yet been explored. Despite the importance of the hydrolysis of P-esters, this field has not yet been fully surveyed. In order to fill this gap, examples of acidic and alkaline hydrolysis, as well as the dealkylation of phosphinates and phosphonates, are summarized in this review. Keywords: hydrolysis; dealkylation; phosphinates; phosphonates; P-acids 1. Introduction Phosphinic and phosphonic acids are of great importance due to their biological activity (Figure1)[ 1]. Most of them are known as antibacterial agents [2,3]. Multidrug- resistant (MDR) and extensively drug-resistant (XDR) pathogens may cause major problems Citation: Harsági, N.; Keglevich, G. in the treatment of bacterial infections. However, Fosfomycin has remained active against The Hydrolysis of Phosphinates and both Gram-positive and Gram-negative MDR and XDR bacteria [2]. Acyclic nucleoside Phosphonates: A Review. Molecules phosphonic derivatives like Cidofovir, Adefovir and Tenofovir play an important role 2021, 26, 2840.
    [Show full text]
  • Discovery of Phosphonic Acid Natural Products by Mining the Genomes of 10,000 Actinomycetes
    Discovery of phosphonic acid natural products by mining the genomes of 10,000 actinomycetes Kou-San Jua, Jiangtao Gaoa, James R. Doroghazia, Kwo-Kwang A. Wanga, Christopher J. Thibodeauxa, Steven Lia, Emily Metzgera, John Fudalaa, Joleen Sua, Jun Kai Zhanga,b, Jaeheon Leea, Joel P. Cionia,b, Bradley S. Evansa, Ryuichi Hirotaa,c, David P. Labedad, Wilfred A. van der Donka,e,1, and William W. Metcalfa,b,1 aCarl R. Woese Institute for Genomic Biology, University of Illinois, Urbana, IL 61801; bDepartment of Microbiology, University of Illinois, Urbana, IL 61801; cDepartment of Molecular Biotechnology, Graduate School of Advanced Sciences of Matter, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima, Hiroshima 739-8530, Japan; dBacterial Foodborne Pathogens and Mycology Research, US Department of Agriculture, Agricultural Research Service, National Center for Agricultural Utilization Research, Peoria, IL 61604; and eDepartment of Chemistry and Howard Hughes Medical Institute, University of Illinois, Urbana, IL 61081 Edited by Jerrold Meinwald, Cornell University, Ithaca, NY, and approved July 31, 2015 (received for review January 14, 2015) Although natural products have been a particularly rich source of generally adopted. If we hope to revitalize the use of natural human medicines, activity-based screening results in a very high products in the pharmaceutical industry, genome mining must be rate of rediscovery of known molecules. Based on the large number shown to be a high-throughput discovery process complementary of natural product biosynthetic genes in microbial genomes, many or superior to existing methods (13, 14). Here, we demonstrate the have proposed “genome mining” as an alternative approach for feasibility of this approach in a campaign to identify the full ge- discovery efforts; however, this idea has yet to be performed ex- netic repertoire of phosphonic acid natural products encoded by a perimentally on a large scale.
    [Show full text]
  • Addition of A-Lithioalkane Phosphonates to Nitriles, Synthesis of ;3-Keto Phosphonate and Enamine Phosphonates
    Communications to the Editor Bull. Korean Chem. Soc., Vol. 10, No. 6, 1989 613 Addition of a-Lithioalkane Phosphonates to Nitriles, Synthesis of ;3-Keto Phosphonate and Enamine Phosphonates Kilsung Lee and Dong Young Oh * Department of Chemistry, Korea Advanced Institute of Science and Technology, Seoul 130-650 Received August 28, 1989 ^-Keto phosphonates bearing a a -hydrogen are in­ 0 0 N" 0 NH teresting for the conversion under Wittig-Horner condition (EtO)J다% .1,叶如닌T (EtO)5PCH--CPh 二二 (EtO)?PCH-CPh into the corresponding ff,/3-unsaturated ketones.1 fi-Keto £ S 2. PhCN £ c phosphonates fully substituted at the a-carbon do not find 4 5 such frequent use as synthetic intermediates, but because the geometry and spatial demands of phosphorus group are comparable to those of quaternary carbon, the isosteric re­ placement of carbon with phosphorus has been studied in biologically active molecules.2 In marked contrast to a number of investigations that in­ corporate phosphonate reagents or focus on the biological ac­ tivities of phosphonates, r이atively little work has appeared describing general new synthesis of this functionality (par­ ticularly in case of fully substituted /9-keto phosphonate).3 Recently developed reaction of dialkyl phosphoro chloridites with a -hydroxy carbonyl compounds in the presence of a a-hydrogen dimerized products were obtained as side pro­ Lewis acid is a good candidate for fully substituted g-ket。 ducts, as previously reported by G. Sumrell.5*2 In the case of phosphonates.4 However, its process is limited due primary an phenyl or thiophenyl substituent on the carbon to the to the availability of starting material.
    [Show full text]
  • Cyclophostin, (±)-Cyclipostin P, Their Phosphonate Analogs and New
    University of Missouri, St. Louis IRL @ UMSL Dissertations UMSL Graduate Works 8-2-2011 Synthesis of (±)-Cyclophostin, (±)-Cyclipostin P, Their hoP sphonate Analogs and New Chemistry of Vinyl Phosphonates Raj Kumar Malla University of Missouri-St. Louis, [email protected] Follow this and additional works at: https://irl.umsl.edu/dissertation Part of the Chemistry Commons Recommended Citation Malla, Raj Kumar, "Synthesis of (±)-Cyclophostin, (±)-Cyclipostin P, Their hospP honate Analogs and New Chemistry of Vinyl Phosphonates" (2011). Dissertations. 416. https://irl.umsl.edu/dissertation/416 This Dissertation is brought to you for free and open access by the UMSL Graduate Works at IRL @ UMSL. It has been accepted for inclusion in Dissertations by an authorized administrator of IRL @ UMSL. For more information, please contact [email protected]. Synthesis of (±)-Cyclophostin, (±)-Cyclipostin P, Their Phosphonate Analogs and New Chemistry of Vinyl Phosphonates by Raj Kumar Malla A Dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy (Chemistry) University of Missouri-St. Louis August, 2011 Committee Prof. Christopher D. Spilling (Chair and Advisor) Prof. Alexei V. Demchenko Prof. Cynthia M. Dupureur Prof. Eike B. Bauer Abstract Synthesis of (±)-Cyclophostin, (±)-Cyclipostin P, Their Phosphonate Analogs and New Chemistry of Vinyl Phosphonates Raj Kumar Malla Doctor of Philosophy University of Missouri-St. Louis Prof. Christopher D. Spilling, Advisor This work is divided into 2 parts: a) total synthesis of (±)-cyclophostin, (±)-cyclipostin P and their monocyclic analogs b) development of a metathesis based methodology for transformation of vinyl phosphonates. Cyclophostin (1) and cyclipostins (2) are bioactive natural bicyclic organophosphates.
    [Show full text]
  • Wittig and Wittig-Horner Reactions Under Phase Transfer Catalysis
    CEJC 4(2003)491{542 Review article Wittigand Wittig-Horner reactions underphase transfer catalysis conditions AureliaPascariu, Gheorghe Ilia ¤,AlinaBora, Smaranda Iliescu, AdrianaPopa, Gheorghe Dehelean and Liliana Pacureanu Institute ofChemistry, Romanian A cademy, 24M. Viteazul Bv., R300223Timisoara, Romania Received 2April 2003;accepted 11August 2003 Abstract: Wittig andWittig-Horner reactions arefavorite tools in preparative organic chemistry.Theseole­ nation methodsenjoy widespread andrecognition becauseof their simplicity,convenience, ande¯ ciency.Phase transfer catalysis (PTC) is avery important methodin synthetic organicchemistry havingmany advantages over conventional, homogenous reaction procedures. Inthis paper, weattempt to summarizethe aspects concerningWittig andWittig-Horner reactions that take place under phasetransfer catalysis conditions. c Central EuropeanScience Journals. All rights reserved. ® Keywords: Wittig reactions, Wittig-Horner reactions, phasetr ansfercatalysis 1Introduction Thanks to numerous theoretical and practical implications,the modern chemistry of phosphorus draws increasing attention. Many scientists havededicated their work inves- tigating someof the unexplained aspects of organophosphorus compounds. They have synthesized new compounds and haveused them inthe new ¯eldof ¯ne organic synthesis or in order to clarifysome of the reaction mechanisms. Although vast literature concerning phase transfer catalysisis available, information concerning the Wittig and Wittig-Horner reactions are treated separately,not
    [Show full text]
  • Pyridine and Phosphonate Containing Ligands for Stable Lanthanide Complexation
    Pyridine and phosphonate containing ligands for stable lanthanide complexation. An experimental and theoretical study to assess the solution structure M. Mato-Iglesias, E. Balogh, C. Platas-Iglesias, É. Tóth, A. de Blas, T.R. Blas To cite this version: M. Mato-Iglesias, E. Balogh, C. Platas-Iglesias, É. Tóth, A. de Blas, et al.. Pyridine and phosphonate containing ligands for stable lanthanide complexation. An experimental and theoretical study to assess the solution structure. Dalton Transactions, Royal Society of Chemistry, 2006, 45, pp.5404- 5415. 10.1039/b611544f. hal-00512396 HAL Id: hal-00512396 https://hal.archives-ouvertes.fr/hal-00512396 Submitted on 30 Jun 2021 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Distributed under a Creative Commons Attribution| 4.0 International License Pyridine and phosphonate containing ligands for stable lanthanide complexation. An experimental and theoretical study to assess the solution structure† Marta Mato-Iglesias,a Edina Balogh,b Carlos Platas-Iglesias,*a Eva´ Toth,´ b,c Andres´ de Blas*a and Teresa Rodr´ıguez Blasa We report an experimental and theoretical study of the stability and solution structure of lanthanide complexes with two novel ligands 2 3 containing pyridine units and phosphonate pendant arms on either ethane-1,2-diamine (L ) or cyclohexane-1,2-diamine (L ) backbones.
    [Show full text]
  • Synthesis and Mechanisms of Phosphoramidates
    Review Openingmolecules Up the Toolbox: Synthesis and Mechanisms of Phosphoramidates Emeka J.Review Itumoh 1,2,3, Shailja Data 1,3 and Erin M. Leitao 1,3,* 1 SchoolOpening of Chemical Sciences, up the The Toolbox:University of Auckland, Synthesis 23 Symonds and Street, Mechanisms Auckland 1010, Newof Zealand; Phosphoramidates [email protected] (E.J.I.); [email protected] (S.D.) 2 Department of Industrial Chemistry, Ebonyi State University, Abakaliki 480001, Ebonyi State, Nigeria 3 The MacDiarmidEmeka J. Itumoh Institute1,2,3 for, Shailja Advanced Data 1,3 Materialsand Erin and M. LeitaoNanotechnology,1,3,* Wellington 6140, New Zealand * Correspondence:1 School of Chemicalerin.leitao@ Sciences,auckland.ac.nz; The University Tel.: of Auckland, +64-9923-5567 23 Symonds Street, Auckland 1010, New Zealand; [email protected] (E.J.I.); [email protected] (S.D.) Academic Editor: Frederik Wurm 2 Department of Industrial Chemistry, Ebonyi State University, Abakaliki 480001, Ebonyi State, Nigeria 3 Received: 3 TheJuly MacDiarmid 2020; Accepted: Institute 11 for Augu Advancedst 2020; Materials Published: and Nanotechnology, 12 August 2020 Wellington 6140, New Zealand * Correspondence: [email protected]; Tel.: +64-9923-5567 Abstract:Academic This review Editor: Frederik covers Wurm the main synthetic routes to and the corresponding mechanisms of phosphoramidateReceived: 3 July formation. 2020; Accepted: The 11 August synthetic 2020; Published: routes 13can August be 2020separated into six categories: salt elimination,Abstract: oxidativeThis review cross-coupling, covers the main azide, synthetic reduction, routes to andhydrophosphinylation, the corresponding and phosphoramidate-aldehyde-dienophilemechanisms of phosphoramidate formation. (PAD). The Examples synthetic routesof some can be separatedimportant into compounds six synthesizedcategories: through salt elimination,these routes oxidative are provided.
    [Show full text]
  • United States Patent Office Patented Oct
    2,956,952 United States Patent Office Patented Oct. 18, 1960 2 reaction conditions, phosphonate polymers having mo 2,956,952 lecular weights in the range of about 1,000 to 3,500 or LUBRICATING OL COMPOSITIONS CONTAINING higher, preferably about 1,200 to 3,000 may be pre POLYMERS OF BIS-(BETA CHLOROETHYL) WIN pared. If desired, the polymerization reaction may be YL PHOSPHONATE carried out in the presence of an inert diluent or solvent William P. FitzGerald, Florham Park, Anthony H. such as, for example, highly refined mineral oils (e.g. Gleason, Westfield, Arnold J. Morway, Clark, and Al white oils), Xylene, cyclohexane, etc. fred H. Matuszak, Westfield, N.J., assignors to Esso Copolymers of bis-(beta chloroethyl) vinyl phos Research and Engineering Company, a corporation of phonate may be prepared employing generally the same reaction conditions as those set forth above for the phos Delaware 0. phonate polymers. The phosphonate monomer may be No Drawing. Filed Aug. 8, 1955, Ser. No. 527,174 copolymerized with the following monomers: ethylene, propylene, isobutylene, styrene, a-methylacrylamide, 7 Claims. (Cl. 252-49.9) acrylamide, a-methylacrylonitrile, acrylonitrile, isobutyl This invention relates to polymeric materials and a-methacrylate, isobutylacrylate, n-butyl a-methylacry more particularly relates to polymers and copolymers 5 late, n-butylacrylate, isopropyl a-methylacrylate, iso of bis-(beta chloroethyl) vinyl phosphonate, especially propylacrylate, n-propyl a-methylacrylate, n-propyl ac copolymers of ethylene and bis-(beta chloroethyl) vinyl rylate, ethyl a-methylacrylate, ethyl acrylate, methyl phosphonate. The invention also relates to methods of a-methylacrylate, methyl acrylate, a-methylacrylic acid, preparing such polymeric materials and to the uses of 20 acrylic acid, vinylidene chloride, vinyl chloride, vinyl such compounds, particularly as lubricant additives.
    [Show full text]
  • Functional Metal Phosphonates
    FUNCTIONAL METAL PHOSPHONATES A Dissertation by HOUSTON PHILLIPP PERRY 1 1 Submitted to the Office of Graduate Studies of Texas A&M University in partial fulfillment of the requirements for the degree of DOCTOR OF PHILOSOPHY 1 December 2011 Major Subject: Chemistry 2 2 2 Functional Metal Phosphonates Copyright 2011 Houston Phillipp Perry FUNCTIONAL METAL PHOSPHONATES A Dissertation by HOUSTON PHILLIPP PERRY Submitted to the Office of Graduate Studies of Texas A&M University in partial fulfillment of the requirements for the degree of 3 3 DOCTOR OF PHILOSOPHY Approved by: Chair of Committee, Abraham Clearfield Committee Members, Timothy Hughbanks Hongcai Zhou 3 Jaime Grunlan Head of Department, David Russell December 2011 Major Subject: Chemistry iii ABSTRACT Functional Metal Phosphonates. (December 2011) Houston Phillipp Perry, B.S., Texas A&M University Chair of Advisory Committee: Dr. Abraham Clearfield The primary goal of the work described in this dissertation was the incorporation of functionality into metal phosphonates. This was done in one of several ways. The first involved using phosphonate ligands that had covalently attached organic functional groups. In some cases, these ligands undergo reactions during the solvothermal syntheses which can impart new chemical reactivity. Another method used to introduce functionality was to iii iii partially or completely substitute metal atoms within phosphonate clusters to create materials which may have interesting magnetic properties. By controlling the way these clusters pack in the solids, their magnetic properties may be able to be augmented. The final method used to impart functionality to metal phosphonates was the incorporation of N- donor and bulky aryl groups into the phosphonate ligands.
    [Show full text]
  • 6004X0489.Pdf
    Pure & Appl. Chem., Vol. 60, No. 4, pp. 489493, 1988. Printed in Great Britain. @ 1988 IUPAC Kinetics and mechanism of the hydrolysis of functional groups in the side-chain of macrocyclic Cu2+-com piexes Daniel Tschudin and Thomas A. Kaden Institute of Inorganic Chemistry, Spitalstr.51, CH 4056 Basel, Switzerland Abstract- A series of functionalized tetraazamacrocycles 2-8 carrying in their pendant side-chain a group which can be hydrolyzed, have been synthesised and their Cu(I1) complexes prepared. The structure analysis of the Cu(I1) complex with 5 shows a pentacoordinate Cu(I1) surrounded by the four nitrogens of the macrocycle and the carbonyl oxygen of the ester group in a distorted square pyramidal geometry. Whereas the Cu(I1) complexes with the amide derivatives 7 and 8 do not react, the nitrile, the esters of the carbonic acids and of the phosphonate are hydrolyzed in alkaline solution. The kinetics of these reactions were measured and the rate constants determined. The pH-profiles log k/pH are linear with pH for the esters 3-5, whereas those of the nitrile 2 and the phosphonate ester 6 exhibit a plateau at high pH. This allows to state that the hydrolysis of these last two compounds proceeds through an internal OH- attack. For the mechanism of the carbonic acid ester hydrolysis several possibilities are discussed, but no definitive choice is yet possible. INTRODUCTION In several esterases and peptidases metal ions play an important role at the active site (ref.1). In general they are essential for activity and it is thought that the metal ion acts as a Lewis-acid and polarizes the bonds of the reactive group so that a nucleophilic attack is facilitated and thus hydrolysis takes place.
    [Show full text]