The syntheses, structural characterization, and magnetic behavior of four new copper(II) complexes derived from tert-butylphosphonic acid and di-2-pyridyl ketone with formulae [Cu{(py)(2)C(OH)(2)}](C(4)H(9)PO(3)H)(2).(H(2)O)(2) (1), [Cu(2)(mu(2)-C(4)H(9)PO(3)H){(py)(2)C(OCH(2)CH(3))O}(mu(2)-NO(3))(NO(3))(H(2)O)](n).(H(2)O)(n) (2), [Cu(4)(mu(2)-C(4)H(9)PO(3)H)(2)(mu(4)-C(4)H(9)PO(3))(2){(py)(2)C(OCH(3))O}(2)].2H(2)O (3) and Na[Cu(6)(mu(3)-C(4)H(9)PO(3))(3){(py)(2)C(OCH(3))O}(3)(mu(6)-NO(3))(NO(3))(3)] (4) (C(4)H(9)PO(3)H(2) = tert-butylphosphonic acid, (py)(2)C(OH)(2) = bis(2-pyridyl)methanediol, {(py)(2)C(OCH(2)CH(3))O}(-) = bis(2-pyridyl)ethoxymethanolato {(py)(2)C(OCH(3))O}(-) = bis(2-pyridyl)methoxymethanolato, are reported. 1 is a mononuclear compound, with tert-butylhydrogenphosphonate in the anionic form. 2 is a nitrate bridged monodimensional compound with 2.110 tert-butylhydrogenphosphonate bridging ligands. 3 is a tetranuclear compound with 2.110 tert-butylhydrogenphosphonate and 3.111 tert-butylphosphonate bridging ligands and 4 is a hexanuclear compound with 3.111 tert-butylphosphonate bridging ligands. The magnetic properties of 2-4 are reported.
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http://dx.doi.org/10.1039/b925793d | DOI Listing |
Phys Chem Chem Phys
May 2022
Institute of Chemistry, St. Petersburg State University, Russia.
The structure of intermolecular hydrogen-bonded complexes formed between -butylphosphonic acid and trimethylpyridine molecules has been experimentally studied as the simplest model system of the structural motifs in blend proton-conducting polymer membranes based on phosphonic acid residues. The stoichiometry of the formed complexes and proton positions in OHO and OHN hydrogen bonds were established by the H/D isotope effects and temperature dependences of the signals in H and P NMR spectra. Two structural motifs, namely, 1 : 2 and 2 : 2 acid-base complexes, were identified at the low temperature in a polar aprotic environment.
View Article and Find Full Text PDFRSC Adv
February 2020
Department of Molecular Sciences, Swedish University of Agricultural Sciences Box 7015 750 07 Uppsala Sweden
Titanium (oxo-) alkoxide phosphonate complexes were synthesized using different titanium precursors and -butylphosphonic acid (BPA) as molecular models for interaction between phosphonates and titania surfaces and to investigate the solution stability of these species. Reflux of titanium(iv) ethoxide or titanium(iv)(diisopropoxide)bis(2,4-pentadionate) with -butylphosphonic acid in toluene-ethanol mixture or acetone yielded seven titanium alkoxide phosphonate complexes; [Ti(μ-O)(μ-O)(μ-HOEt)(μ-OEt)(μ-OEt)(μ-BPA)(μ-HBPA)(μ-BPA)(μ-HBPA)]·3EtOH, 1, [TiO(μ-OEt)(μ-OEt)(μ-BPA)], 2, [Ti(μ-O)(μ-OEt)(μ-HOEt)(μ-PBA)(μ-HPBA)]·4EtOH, 3, [Ti(μ-O)(μ-OEt)(μ-HOEt)(μ-PBA)(μ-HPBA)]·2EtOH, 4, [Ti(μ-O)(μ-O)(μ-OEt)(μ-OEt)(μ-BPA)(μ-HBPA)], 5, [Ti(μ-OPr)(acac)(μ-BPA)], 6 and [Ti(μ-O)(μ-O)(μ-OEt)(μ-OEt)(μ-HOEt)(μ-BPA)], 7. The binding mode of BPA to the titanium oxo-core were either double or triple bridging or a combination of the two.
View Article and Find Full Text PDFInorg Chem
January 2019
State Key Laboratory of Materials Processing and Die & Mould Technology, School of Materials Science and Engineering , Huazhong University of Science and Technology, Wuhan 430074 , China.
tert-Butylphosphonic acid and rare-earth precursors are employed to construct four trinuclear rare-earth phosphonate clusters, RE( BuPO)(hfac)(CHOH)]·2CHOH (RE = Eu, Y, Pr, and Sm; hfac = hexafluoroacetylacetonate), which are composed of three RE ions alternately bridged by two phosphonates. With the introduction of bismuth oxido diketonate, [BiO(hfac)], three different types of rare-earth/bismuth phosphonate clusters, BiRE (RE = Pr and Sm), BiEu, and BiY, are successfully obtained via variation of the reaction conditions, and they are the first reported examples of bismuth-oxo clusters encapsulated by cyclic rare-earth-oxo or rare-earth/bismuth-oxo phosphonate clusters, respectively. These clusters show obvious absorption in the UV region, and the Eu-containing clusters exhibit bright-red fluorescence.
View Article and Find Full Text PDFChemistry
May 2018
Department of Chemistry and Center of Novel Functional Molecules, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong SAR, P.R. China.
tert-Butylphosphonic acid and lanthanide precursors were employed to construct two high-nuclearity hybrid silver(I)-ytterbium(III) phosphonate clusters: compound 1 consists of a Ag ethynide cluster fused with a trinuclear hydroxoytterbium phosphonate cluster, whereas compound 2 is composed of two Ag ethynide clusters bridged by a hexanuclear oxo/hydroxoytterbium phosphonate cluster. Using transition-metal-substituted lacunary polyoxotungstates in place of the lanthanide reactant, new phosphonate-functionalized silver(I)-copper(II) ethynide clusters [Ag Cu (3) and Ag Cu (4)] and silver(I) ethynide clusters [Ag (5) and Ag (6)] were obtained. The structures of complexes 3-6 feature core-shell arrangements, in which silver(I)-copper(II) or silver(I) ethynide cluster shells stabilized by peripheral phosphonate ligands enclose different kinds of tungstate core templates.
View Article and Find Full Text PDFInorg Chem
November 2017
Department of Chemistry, Indian Institute of Technology Bombay, Powai, Mumbai 400076, India.
[Ti(acac)(OPr)] reacts with tert-butylphosphonic acid to yield a series of titanium organophosphonates such as tetranuclear [Ti(acac)(μ-O)(μ-BuPO)(μ-BuPOH)]·2CHCN (1), pentanuclear [Ti(acac)(μ-O)(OPr)(μ-BuPO)(μ-BuPOH)] (2), hexanuclear [Ti(acac)(μ-O)(OPr)(μ-BuPO)] (3), or [Ti(acac)(μ-O)(OPr)(μ-BuPO)(μ-BuPOH)]·2CHCN (4). The isolation of each of these products in pure form depends on the molar ratio of the reactants or the solvent medium. Among these, 3 is obtained as the only product when the reaction is conducted in CHCl.
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