Local and medium range order in the glass system 50Ag2O-50[(B2O3)x-(P2O5)(1-x)] (x=0, 0.1, 0.2, 0.3, 0.4, 0.5, and 0.6) have been investigated by high-resolution solid state nuclear magnetic resonance (NMR) techniques. The detailed local site distribution has been derived from deconvolution analysis of the 11B and 31P magic-angle spinning (MAS) NMR signals. Quantitative information regarding the extent of boron-oxygen-phosphorus connectivity has been obtained on the basis of 11B[31P} and 31P{11B} rotational echo double resonance experiments. Incorporation of borate into silver metaphosphate glasses produces four-coordinate BO4/2- sites, which crosslink the metaphosphate chains, resulting in a significant increase in the glass transition temperature. Furthermore, the presence of borate favors the disproportionation of P(2) chain-like units into P(1) and P(3) sites, an effect not observed in binary alkali phosphate glasses. Finally, borate incorporation beyond x=0.3 results in the formation of neutral BO3/2 units, indicating some net charge transfer from the borate to the phosphate network former species. This latter result corresponds to the general metal ion scavenging effect observed for phosphate species in other mixed network former glass systems. In the present system, the effect is relatively moderate, however, suggesting that anionic BO4/2- groups are stabilized by the interaction with the phosphate groups.
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http://dx.doi.org/10.1016/j.ssnmr.2004.08.007 | DOI Listing |
J Mater Chem B
February 2020
Institut für Materialchemie, Technische Universität Wien, Getreidemarkt 9/BC/02, 1060 Wien, Austria.
B2O3 doped (0.5-15 mol%) ordered mesoporous bioactive glasses (MBG) with the composition 80% SiO2-15% CaO-5% P2O5 were synthesized via a sol-gel based evaporation-induced self-assembly process using the block-copolymer P123 as a structure directing agent and characterized by biokinetic, mechanical and structural investigations. Nitrogen physisorption isotherms and electron microscopy indicate no detrimental effect of B2O3 on the ordered hexagonal pore structure.
View Article and Find Full Text PDFSolid State Nucl Magn Reson
October 2018
Univ. Lille, CNRS-8181, UCCS-Unit of Catalysis and Chemistry of Solids, F-59000, Lille, France; Institut Universitaire de France, 1 rue Descartes, F-75231, Paris, France. Electronic address:
We introduce a novel heteronuclear dipolar recoupling based on the R2 symmetry, which uses the tanh/tan (tt) shaped pulse as a basic inversion element and is denoted R2(tt). Using first-order average Hamiltonian theory, we show that this sequence is non-γ-encoded and that it reintroduces the |m| = 1 spatial component of the Chemical Shift Anisotropy (CSA) of the irradiated isotope and its heteronuclear dipolar interactions. Using numerical simulations and one-dimensional (1D) Al-{P} through-space D-HMQC (Dipolar Heteronuclear Multiple-Quantum Correlation) experiments on VPI-5, we compare the performances of this recoupling to those of other non-γ-encoded |m| = 1 heteronuclear recoupling schemes: REDOR (Rotational-Echo DOuble Resonance), SFAM (Simultaneous Frequency and Amplitude Modulation) and R4(tt).
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September 2018
Institut für Physikalische Chemie, Westfälische Wilhelms-Universität Münster, Corrensstraße 30, D 48149 Münster, Germany; Instituto de Física em São Carlos, Universidade de São Paulo, CEP 369, São Carlos 13566-590, Brazil. Electronic address:
The case of rotational echo double resonance (REDOR) experiments on the observe nuclei B and P interacting with multiple I=1 quadrupolar nuclei is analyzed in detail by SIMPSON simulations and experimental studies. The simulations define the region within the parameter space spanned by nutation frequency, quadrupolar coupling constant and spinning frequency where the parabolic analysis of the initial REDOR curve in terms of dipolar second moments has validity. The predictions are tested by experimental studies on the crystalline model compounds lithium diborate and lithium pyrophosphate, which are subsequently extended to measure dipolar second moments M(B{Li}) and M(P{Li}) in three borophosphate glasses.
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March 2015
Institut für Physikalische Chemie and Graduate School of Chemistry, WWU Münster, Corrensstrasse 30, D 48149 Münster, Germany. Electronic address:
By N,N addition of NO to the norbonane annulated borane-phosphane Frustrated Lewis pair (FLP) 1 a five-membered heterocyclic persistent aminoxyl radical 2 and its diamagnetic hydroxylamine reduction product 3 are prepared, and the comprehensive multinuclear solid state NMR characterization ((1)H, (11)B, (19)F, (31)P) of these FLP adducts is reported. Signal quantification experiments using a standard addition method reveal that the (11)B and (31)P NMR signals observed in 2 actually arise from molecular impurities of 3 embedded in the paramagnetic crystal. In contrast analogous quantification experiments reveal that the (1)H and (19)F MAS-NMR spectra originate from spin-carrying molecules.
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March 2015
Institut für Physikalische Chemie and Graduate School of Chemistry, WWU Münster, Corrensstrasse 30, D 48149 Münster, Germany. Electronic address:
A solid state NMR method is described for measuring the angle Θ specifying the orientation of the principal component of the (11)B electric field gradient tensor relative to the (11)B(…31)P internuclear vector of (11)B-(31)P spin pairs. It is based on the anisotropic dephasing of (11)B spins in the dipolar field of (31)P nuclei via (11)B{(31)P} Rotational Echo DOuble Resonance (REDOR) experiments. The method is applied to four solid borane-phosphane compounds related to Frustrated Lewis Pair (FLP) chemistry.
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