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D Massiot

Publications and source records attributed to D Massiot.

18 recordsLinked to original sources
PubMed2006

19F high magnetic field NMR study of beta-ZrF4 and CeF4: from spectra reconstruction to correlation between fluorine sites and 19F isotropic chemical shifts.

High magnetic field and high spinning frequency one- and two-dimensional one-pulse MAS 19F NMR spectra of beta-ZrF4 and CeF4 were recorded and reconstructed allowing the accurate determination of the 19F chemical shift tensor parameters for the seven different crystallographic fluorine sites of each compound. The attributions of the NMR resonances are performed using the superposition model for 19F isotropic chemical shift calculation initially proposed by Bureau et al. (Bureau, B.; Silly, G.; Emery, J.; Buzaré, J.-Y. Chem. Phys. 1999, 249, 85-104). A satisfactory reliability is reached with a root-mean-square (rms) deviation between calculated and measured isotropic chemical shift values equal to 1.5 and 3.5 ppm for beta-ZrF4 and CeF4, respectively.

Journal Article↗
PubMed2005

Application of the MAS-J-HMQC experiment to a new pair of nuclei {29Si,31P}: Si5O(PO4)6 and SiP2O7 polymorphs.

We report the results of the two-dimensional MAS-J-HMQC experiment providing scalar correlations between 29Si and 31P nuclei in solid state NMR, and we give the first evaluation of the 2JSi-O-P coupling constants (approximately 15 Hz) for a crystalline silicophosphate phase Si5O(PO4)6. The experiment is applied to the characterization of complex mixtures of SiP2O7 phases, through editing of 31P spin pairs by the heteronuclear 2JP-O-Si interaction.

Journal Article↗
PubMed2003

77Se and 87Rb Solid state NMR study of the structure of Rb2[Pd(Se4)2].Se8.

The structure of Rb(2)[Pd(Se(4))(2)].Se(8) has been investigated using (87)Rb magic angle spinning and static NMR and (77)Se magic angle spinning NMR. The number and the integrated intensities of the (87)Rb and (77)Se resonances are in full agreement with the crystallographic structure of the compound. The (87)Rb and (77)Se nuclear spin interaction parameters have been used to characterize the main structural units of the compound: infinite [Rb(Se(8))](x)(x+) columns and polymeric [Pd(Se(4))(2)](x)(2x-) sheet anions.

Journal Article↗
PubMed2003

Solid-state 1H and 27Al NMR studies of amorphous aluminum hydroxides.

Two kinds of amorphous aluminum hydroxides, a sample precipitated from admixing AlCl3 and NaOH aqueous solutions and the commercial product, were measured by 27Al and 1H solid-state NMR spectroscopy. Pentahedral and tetrahedral coordinations, as well as octahedral coordination of oxygen atoms for aluminum, are observed in 27Al magic angle spinning (MAS) spectra of both amorphous samples. In contrast, octahedral coordination is only observed in gibbsite, bayerite, and boehmite. According to 1H MAS-NMR spectra under conditions of high spinning rate (35 kHz) and high field (14.09 T), free waters and OH groups coupled with aluminum for amorphous samples are observed at approximately 5 and approximately 4.5 ppm, respectively, the latter peak being broader. This is consistent with the differential spectra between spin echo and transfer of populations in double resonance. We conclude that the subunits of AlO4, AlO5, and AlO6 in amorphous aluminum hydroxides are bound through hydrogen bonds with a wide distribution of bonding strength.

Journal Article↗
PubMed2001

New pillared layered gallium phosphonates in the gallium/1,2-ethylenediphosphonic acid system.

1,2-Ethylenediphosphonic acid reacts with gallium nitrate in water to give new pillared layered gallium phosphonates, the structure of which depends on the experimental conditions used for their preparation. Thus, Ga(4)(O(3)PC(2)H(4)PO(3))(3) (1) and Ga(2)(OH)(2)(O(3)PC(2)H(4)PO(3)) (2) were isolated and the structure of 1 was solved by single-crystal X-ray diffraction, while 2 was shown to have the same metal/PO(3) arrangement as the previously described Ga(OH)(O(3)PCH(3)). Ga(4)(O(3)PC(2)H(4)PO(3))(3) (1) is triclinic, with space group P1 with Z = 2, a = 5.1480(4), b = 8.0354(7), and c = 12.383(1) A; alpha = 91.34(1), beta = 101.40(1), and gamma = 90.86(1) degrees; V = 501.9(1) A(3). The structure of 1 is unusual with (i) mixed GaO(4) and GaO(5) sites while a 6-fold coordination is observed for gallium in (2) and (ii) the presence of the organic moiety within both the layers and the interlayer space. The two compounds were fully characterized using (31)P and (71)Ga solid-state NMR.

Journal Article↗
PubMed2000

Pure absorption-mode spectra using a modulated RF mixing period in MQMAS experiments.

Different approaches to obtain pure absorption-mode lineshapes in MQMAS experiments employing a train of 180 degrees phase-alternating pulses for the multiple-quantum to single-quantum mixing period are investigated. Four pulse sequences, which achieve this by using either the shifted-echo approach or the hypercomplex approach with symmetric coherence transfer pathways, are presented and their improved lineshape- and sensitivity-performance is experimentally demonstrated by (87)Rb MQMAS of RbNO(3). Compared to the original modulated-rf mixing sequence, sensitivity enhancements by factors up to 1.3 are obtained with the sequences described here.

Magnetic Resonance Spectroscopy↗
PubMed2000

Characterization of an Al-, Ga-based catalyst by Ga NMR and XAS.

Both Nuclear Magnetic Resonance (NMR) and X-Ray absorption spectroscopies characterize local order around the observed nuclei. With the recent progresses of 71Ga solid state NMR, it has become possible to take advantage of the complementary information that can be obtained using these two methods. This opens the possibility of a more thorough description of the first coordination shells of Ga in oxide. We present and discuss the example of an Al-, Ga-based catalyst.

Aluminum↗
PubMed1999

Chemical bonding of lead in glasses through isotropic vs anisotropic correlation: PASS shifted echo.

When observing spin I = (1/2) nuclei with important chemical shift anisotropy in disordered materials, the distribution of isotropic shift can become so large that no accessible spinning rate is able to provide a resolved spectrum. This is the case of 207Pb in glasses where static and high-speed MAS spectra are nearly identical. It is still possible in such a case to rebuild a spinning sideband free spectrum using a shifted echo modified PASS sequence. This makes it possible to discuss isotropic and anisotropic chemical shifts of lead in phosphate glasses, to characterize its structural role and its chemical bonding state.

Anisotropy↗
PubMed1999

From crystalline to glassy gallium fluoride materials: an NMR study of 69Ga and 71Ga quadrupolar nuclei.

Owing to the implementation of acquisition techniques specific for nuclei with very large quadrupolar interaction (full shifted echo and variable offset cumulative spectra (VOCS)), NMR spectra of 69Ga and 71Ga are obtained in crystallised (PbGaF5, Pb3Ga2F12, Pb9Ga2F24 and CsZnGaF6) and glassy (PbF2-ZnF2-GaF3) gallium fluorides. Simulations of both static (full echo or VOCS) and 15 kHz MAS spectra allow to obtain consistent determinations of isotropic chemical shifts and very large quadrupolar parameters (nu(Q) up to 14 MHz). In the crystalline compounds whose structures are unknown, the number and the local symmetry of the different gallium sites are tentatively worked out. For the glassy systems, a continuous Czjzek's distribution of the NMR quadrupolar parameters accounts for the particular shape of the NMR spectrum.

Chemical Phenomena↗
PubMed1999

71Ga NMR of reference GaIV, GaV, and GaVI compounds by MAS and QPASS, extension of gallium/aluminum NMR parameter correlation.

We report new measurements of NMR parameters for 71Ga in gallium bearing oxide reference compounds, ranging from perfectly ordered systems to disordered crystalline structures and their aluminate counterparts. Static, MAS, and QPASS spectra are obtained at magnetic fields ranging from 7.0 to 18.8 T. With these results we enhance the previously established correlation between isotropic chemical shifts of 71Ga and 27Al and propose a correlation between gallium and aluminum electric field gradients (EFG). This correlation shows that the EFG at 71Ga sites are generally three times greater than those at equivalent 27Al sites.

Aluminum Oxide↗
PubMed1999

From crystalline to glassy gallium fluoride materials: an NMR study of 69Ga and 71Ga quadrupolar nuclei.

Owing to the implementation of acquisition techniques specific for nuclei with very large quadrupolar interaction (full shifted echo and variable offset cumulative spectra (VOCS)), NMR spectra of 69Ga and 71Ga are obtained in crystallised (PbGaF5, Pb3Ga2F12, Pb9Ga2F24 and CsZnGaF6) and glassy (PbF2-ZnF2-GaF3) gallium fluorides. Simulations of both static (full echo or VOCS) and 15 kHz MAS spectra allow to obtain consistent determinations of isotropic chemical shifts and very large quadrupolar parameters (nuQ up to 14 MHz). In the crystalline compounds whose structures are unknown, the number and the local symmetry of the different gallium sites are tentatively worked out. For the glassy systems, a continuous Czjzek's distribution of the NMR quadrupolar parameters accounts for the particular shape of the NMR spectrum.

Chemical Phenomena↗
PubMed1998

14N NMR in AlN and BN.

A characterisation by 14N NMR of the binary nitrides AlN and BN is presented. Both the static and magic angle spinning (MAS) lineshapes have been investigated in order to determine, or set upper limits on, the nuclear quadrupole coupling (Cq) at the nitrogen site. Additional data are given for the Cq values at the Al and B sites. A comparison is made with other similar (mainly wurtzite) binary compounds for which Cq is known at each atomic site.

Aluminum Compounds↗
PubMed1996

Two-dimensional magic-angle spinning isotropic reconstruction sequences for quadrupolar nuclei.

Two-dimensional magic-angle spinning (triple quantum, single quantum) correlation pulse sequences and phase cycles based on the technique of Frydman and Harwood for the reconstruction of the isotropic spectrum of half-integer spin quadrupolar nuclei broadened to second-order are described. These sequences provide pure absorption mode two-dimensional lineshapes and increased sensitivity. Experimental examples on spin I = 3/2 (87Rb in RbNO3) and I = 5/2 (27Al in NaSi3AlO8) are presented. The isotropic chemical shift and quadrupolar coupling parameters could be obtained from a simple analysis of the triple quantum filtered single quantum magic-angle spinning cross-sections.

Absorption↗
PubMed1995

71Ga and 69Ga nuclear magnetic resonance study of beta-Ga2O3: resolution of four- and six-fold coordinated Ga sites in static conditions.

71Ga and 69Ga nuclear magnetic resonance (NMR) spectra have been obtained for beta-Ga2O3 at magnetic fields of 11.7 and 7.0 T with a combination of static and spinning samples and using echo techniques. Isotropic chemical shifts and well constrained electric field gradient (EFG) tensors were measured for the GaIV and GaVI sites in beta-Ga2O3 and are reported for the first time. Due to its high quadrupolar coupling constant the GaIV site in beta-Ga2O3 is only resolved in static conditions. Analysis of spectral discontinuities obtained for different isotopes and magnetic field strengths and a method of readily obtaining very broad spectra without point by point acquisition demonstrate an approach that should be very useful in constraining the chemical shifts and quadrupole parameters involved in solid-state gallium NMR spectra.

Gallium↗
PubMed1995

Double rotation and magic-angle spinning nuclear magnetic resonance study of 27Al: reexamination of the aluminium borate 9Al2O3.2B2O3.

27Al nuclear magnetic resonance spectra of polycrystalline aluminium borate 9Al2O3.2B2O3 have been measured in double rotation at 11.7 and 7.0 T and high-speed magic-angle spinning at 7.0, 9.4, 11.7, 14.1 and 17.6 T. Spinning sidebands from the satellite transitions were observed at 7.0 and 14.1 T. Each of the four structural aluminium sites [Al(IV), Al(V)(1), Al(V)(2) and Al(VI)] are observed, characterised and assigned in the spectra. The obtained parameter set gives a fully consistent interpretation in agreement with the crystal structure of the compound.

Aluminum Compounds↗
PubMed1995

A time resolved 27Al NMR study of the cooling process of liquid alumina from 2450 degrees C to crystallisation.

Nuclear magnetic resonance is able to give insight into the structure and dynamics of liquids at very high temperature (T > 2000 degrees C). 27Al NMR spectra have been recorded every 25 ms during the cooling of an aerodynamically levitated liquid alumina droplet from 2450 degrees C to crystallisation in less than 3 s. The temperature is measured jointly by pyrometry and NMR, and this time resolved experiment provides a unique way of exploring the temperature dependence of both the structure (shift) and the dynamics (relaxation time of 27Al of the liquid and the supercooled liquid alumina until the crystallisation of alpha-Al2O3. The apparent Arrhenian activation energy of 130 kJ mol-1, derived from T1 measurement, is understood as the signature of the macroscopic viscosity in this high temperature liquid.

Aluminum Oxide↗