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J P Amoureux

Publications and source records attributed to J P Amoureux.

At least 19 recordsLinked to original sources

HMQC and refocused-INEPT experiments involving half-integer quadrupolar nuclei in solids.

Hetero-nuclear coherence transfers in HMQC and refocused-INEPT experiments involving half-integer quadrupolar nuclei in solids are analyzed. 1D and 2D schemes are considered under MAS for the general case of multi-spin systems SI(n) (n4), where S is an observed nucleus. These results are also discussed in the context of high-resolution schemes featuring MQMAS or STMAS. The theoretical predictions are verified experimentally in a series of 1D and 2D experiments performed at 9.4 and 18.8T.

Algorithms↗

Homogeneous broadenings in 2D solid-state NMR of half-integer quadrupolar nuclei.

The question of the homogeneous broadening that occurs in 2D solid-state NMR experiments is examined. This homogeneous broadening is mathematically introduced in a simple way, versus the irreversible decay rates related to the coherences that are involved during t1 and t2. We give the pulse sequences and coherence transfer pathways that are used to measure these decay rates. On AlPO4 berlinite, we have measured the 27Al echo-type relaxation times of the central and satellite transitions on 1Q levels, so that of coherences that are situated on 2Q, 3Q, and 5Q levels. We compare the broadenings that can be deduced from these relaxation times to those directly observed on the isotropic projection of berlinite with multiple-quantum magic-angle spinning (MAS), or satellite-transition MAS. We show that the choice of the high-resolution method, should be done according to the spin value and the corresponding homogeneous broadening.

Journal Article↗

Increasing the sensitivity of 2D high-resolution NMR methods applied to quadrupolar nuclei.

Gan and Kwak recently proposed a soft-pulse added mixing (SPAM) idea in the classical two-pulse multiple-quantum magic-angle spinning scheme. In the SPAM method, a soft pi/2 pulse is added after the second hard-pulse (conversion pulse) and all coherence orders in between them are constructively used to obtain the signal. We, here, further extend this idea to distributed samples where the signal mainly results from echo pathways and that from anti-echo pathways dies out after a few t1 increments. We show that, with a combination of SPAM and collection of fewer anti-echoes, an enhancement of the signal to noise ratio by a factor of ca. 3 may be obtained over the z-filtered version. This may prove to be useful even for samples with long T2' relaxation times.

Journal Article↗

Implementing SPAM into STMAS: a net sensitivity improvement in high-resolution NMR of quadrupolar nuclei.

Gan and Kwak recently introduced two new tools for high-resolution 2D NMR methods applied to quadrupolar nuclei: double-quantum filtering in STMAS (DQF-STMAS) and the soft-pulse added mixing (SPAM) idea. Double-quantum filtering suppresses all undesired signals in the STMAS method with limited loss in sensitivity. With SPAM, all pathways are added constructively after the second hard-pulse instead of using a single pathway as previously. Here, the sensitivity, advantages and drawbacks of DQF-STMAS are compared to 3QMAS. Additionally, SPAM can be included into DQF-STMAS method, resulting in a net sensitivity gain with respect to 3QMAS of ca. 10-15.

Journal Article↗

Location of protons in anhydrous Keggin heteropolyacids H(3)PMo(12)O(40) and H(3)PW(12)O(40) by (1)H[(31)P]/(31)P[(1)H] REDOR NMR and DFT quantum chemical calculations.

HeteroPolyAcids (HPA's) are a class of solid acids that have broad applications in many fields of science and technology, including catalysis and chemical engineering. The proton locations within the thermally stable and commonly known Keggin unit, which is the primary structure building unit/block, has remained undetermined in anhydrous HPAs, despite numerous theoretical and experimental efforts. However, Rotational Echo DOuble Resonance (REDOR) NMR and Density Functional Theory (DFT) quantum chemical calculations offer a new opportunity to determine the exact locations of protons within the Keggin unit. The crucial experimental evidence is provided for the basic and very extensively studied acidic form of H(8-n)X(n+)M(12)O(40), X = Si, P and M = Mo, W, belonging to the Keggin structure. While showing that the acidic protons are located in the bridging oxygen positions (R(P-H) = 520 +/- 20 pm) in H(3)PMo(12)O(40) and in the terminal oxygen positions (R(P-H) = 570 +/- 20 pm) in H(3)PW(12)O(40), REDOR measurements also provide for the first time the structural basis to consistently rank the acid strength for the important class of Keggin solid catalysts.

Journal Article↗

On the conversion of triple- to single-quantum coherences in MQMAS NMR.

A systematic experimental and numerical evaluation of several basic approaches to multiple-quantum magic angle spinning (MQMAS) NMR is presented for spin-32 nuclei. The approaches use identical MQ excitation, via a single RF pulse of high power, and three types of methods for conversion to observable coherence: (a) nutation by strong continuous wave pulse; (b) rotation-induced adiabatic coherence transfer (RIACT), and (c) fast amplitude modulation (FAM-1). The optimization strategies and maximum achievable MQMAS efficiencies of (87)Rb in RbNO(3) and LiRbSO(4) are investigated using several coherence transfer schemes under a wide range of experimental parameters. These parameters include the strength of the RF magnetic field nu(RF), the sample rotation speed nu(R), the length of the conversion period, and the modulation frequency in FAM-1. The data provide new insights into the spin dynamics involved in these techniques and the experimental guidelines for achieving the best sensitivity. The RF requirements for maximum efficiency of conversion depend on the method to be used. In general, FAM-1 performs better than the nutation and RIACT methods in terms of efficiency and off-resonance behavior, especially when nu(RF) is small compared to the quadrupole frequency nu(Q). The experiments performed using nutation, RIACT, and FAM-1 methods yield similar resolution in the isotropic dimension, regardless of nu(RF).

Magnetic Resonance Spectroscopy↗

Very fast MAS and MQMAS NMR studies of the spectroscopically challenging minerals kyanite and andalusite on 400, 500, and 800 MHz spectrometers.

The well-characterized minerals kyanite and andalusite have long presented great challenges in using solid state 27Al NMR to determine the isotropic chemical shift deltaCS, quadrupole coupling constant e2qQ/h, and asymmetry parameter eta for each of the inequivalent aluminum sites in these minerals. Indeed, these minerals have frequently been used to test advances in instrumentation. Recent advances in magnet technology (up to 18.8 T = 800 MHz 1H) and in MAS probe technology (spinning up to 35 kHz and considerably stronger rf) and refinements of the two-dimensional, multiple quantum magic angle spinning (MQMAS) technique suggested that these developments could be profitably used to study kyanite and andalusite by solid state 27Al NMR. The benefit of being able to study kyanite both by MAS and MQMAS techniques on 400, 500, and 800 MHz spectrometers is demonstrated. The two octahedral aluminum sites with the largest (and nearly equal) e2qQ/h values give overlapping 1D MAS or 2D 3QMAS signals at all three field strengths. Nevertheless, quantitatively accurate 3Q signal intensities at 9.4 T for all four octahedral aluminum sites (with e2qQ/h values up to 10 MHz) allow more detailed analysis. Even if the 3Q signal intensities are not quantitative, their isotropic shifts provide an approach (if accurate e2qQ/h and eta values are available) other than deconvolution of the MAS spectrum for calculating deltaCS values. For andalusite, 34 kHz MAS on the 800 MHz spectrometer significantly narrows the extremely broad signal for the octahedral aluminum, and only slight difficulties are encountered in quantitating the relative amounts of AlO5 and AlO6 present. Even with e2qQ/h = 15.3 MHz, the octahedral aluminum in andalusite gives a signal in a MQMAS experiment, albeit of reduced intensity. As appropriate, we discuss some of the benefits and limitations of these advances in instrumentation and of different experimental approaches for studying non-integral spin quadrupolar nuclei in solids.

Aluminum Silicates↗

Evaluation of human recombinant bone morphogenetic protein-2-loaded tricalcium phosphate implants in rabbits' bone defects.

Porous beta-tricalcium phosphate (betaTCP) has osteoconductive properties. The adsorption of human recombinant bone morphogenetic protein-2 (rhBMP-2) onto TCP could realize an osteoinductive bone substitute. We evaluated it on an animal model using dual-energy X-ray absorptiometry (DEXA) and solid-state 31P nuclear magnetic resonance (NMR) spectroscopy. BetaTCP cylinders loaded with rhBMP-2 were implanted into rabbits' femoral condyle bone defects, and betaTCP alone as control into the contralateral femur. We studied two different doses of rhBMP-2 (10 and 40 microg) on two groups of four animals. Evaluation consisted in radiography, histology, and histomorphometry, DEXA, and NMR spectroscopy using an original method of quantification. With both doses of rhBMP-2, we observed on radiographs an increase of trabecular bone around implants. Histology showed resorption of the ceramic, trabecular bone with osteoblasts and osteoid substance around the implants, and colonization inside the porous betaTCP by new bone formed. Histomorphometry showed that the osteoid surface (OS/BS) was greatest with the high dose of rhBMP-2. The difference was slight between the low dose of rhBMP-2 and control. DEXA showed a dose-dependent increase of bone mineral density of rhBMP-2-loaded betaTCP vs. control. NMR spectroscopy confirmed that the amount of new bone formed in betaTCP was greater when betaTCP carried rhBMP-2, and increased with the dose of rhBMP-2 used. We showed that betaTCP was a good matrix for rhBMP-2, which gave it osteoinductive properties in an orthotopic site, in a dose-dependent manner. Thus, such composite biomaterial seems to be of great interest in reconstructive bone surgery. Further studies are needed in clinical practice to determine optimal doses.

Absorptiometry, Photon↗

Triple, quintuple and higher order multiple quantum MAS NMR of quadrupolar nuclei.

The optimization of the coherence transfers involved in five, seven and nine-quantum versions of the recently discovered MQMAS technique, is analysed numerically. Data reported in this paper may serve as starting parameters for the experiment set up. An analysis of the intensity and resolution given by each type of experiment is performed, which confirms the need to use very high rf fields for MQ transfers. It follows that five-quantum is achievable rather easily but the use of seven and nine-quantum MAS experiments becomes increasingly difficult due to the demand for high rf power and decreasing sensitivity. The advantages of using the z-filter MQMAS method with respect to a two-pulse sequence are analysed. The method for qualitatively and quantitatively interpret the MQMAS spectra is described. The nature of the spinning side bands along the multiple quantum dimension is explained. It is shown that the rotor synchronization can be conveniently used to eliminate these side bands, but only for 3QMAS experiments. The use of the multiple-quantum method in combination with static samples and VAS, DAS and DOR techniques is finally discussed.

Magnetic Resonance Spectroscopy↗

Quantitative study of the short range order in B2O3 and B2S3 by MAS and two-dimensional triple-quantum MAS 11B NMR.

Two-dimensional multiple-quantum magic angle spinning (MQMAS) NMR and MAS NMR of 11B at various magnetic fields, were applied to elucidate the structure of vitreous (glassy) boron trioxide (v-B2O3), vitreous boron trisulfide (v-B2S3) and crystalline boron trisulfide (c-B2S3). These techniques, when combined with computer simulations of the resulting spectra, provide the isotropic chemical shifts and the quadrupole parameters, as well as a quantitative measure of the intensities of various boron resonances. The MAS NMR of v-B2O3 produced overlapping anisotropic lineshapes corresponding to the -1/2<-->1/2 transition in two distinct types of BO3 units with 3(+/-0.08):] intensity ratio. A combination of MAS and the multiple-quantum method resulted in a better resolved, isotropic 11B spectrum of v-B2O3. A remarkable enhancement of resolution of the MQMAS NMR proved instrumental in finding and identifying various impurities present in v-B2S3 and c-B2S3. In addition to the resonances from boron in two types of BS3 groups, four other structural units, BOS2, BO2S, BO3 and BS4, were elucidated from the spectra of vitreous and crystalline samples. The effects of various experimental parameters, such as the magnitude of the B0 and B1 fields, on the resolution of the MAS and MQMAS techniques are also shown.

Algorithms↗

Multiple-quantum magic-angle spinning NMR with cross-polarization: spectral editing of high-resolution spectra of quadrupolar nuclei.

An experiment is presented that combines the multiple-quantum magic-angle spinning (MQMAS) technique with cross-polarization (CP). As a preliminary test of this new method, we measured and compared the 27Al 3QMAS and 19F-->27Al CP 3QMAS spectra of a fluorinated AlPO4 aluminophosphate. Complete discrimination between the fluorinated and nonfluorinated Al sites was easily achieved, which demonstrates the usefulness of CP MQMAS for spectral editing. Future applications of this experiment will include other spin pairs and heteronuclear correlation NMR spectroscopy.

Magnetic Resonance Spectroscopy↗

Solid-state NMR studies of interstitial phosphorus atoms in rhodium carbonyl clusters.

Pure samples and as-prepared mixtures of Rh9 and Rh10 carbonyl clusters with interstitial P atoms have been studied quantitatively by 31P MAS and 1H-31P CP/MAS NMR. Information on the 31P chemical shift tensor of the Rh9 and Rh10 clusters has been derived from spinning sideband simulations. The chemical shift anisotropy is slightly larger in the Rh10 clusters (340-400 ppm) than in the Rh9 clusters (230-300 ppm), while the asymmetry parameters are similar (eta = 0.1-0.4). The results contribute to the understanding of the relationship between the shielding anisotropy and the structure of the cluster cavity.

Anisotropy↗

Triple-quantum MAS-NMR of quadrupolar nuclei.

From two-dimensional multiquantum NMR spectra of quadrupolar nuclei, it is now possible to obtain much greater resolution than in a classical single-quantum magic-angle spinning or variable-angle spinning spectrum. We describe here a very simple pulse scheme which efficiently excites the desired multiquantum NMR coherence and a new acquisition procedure which yields to pure-absorption mode 2D spectra. Experimental spectra for 87Rb in polycrystalline rubidium nitrate illustrate the method.

Magnetic Resonance Spectroscopy↗

Characterisation of sodium cations in dehydrated zeolite NaX by 23Na NMR spectroscopy.

23Na MAS, 2D nutation MAS, and DOR NMR spectroscopy has been applied to characterise the location of sodium cations in dehydrated zeolite NaX (Si/Al = 1.23). The 23Na MAS NMR spectra recorded at three different magnetic field strengths were decomposed by computer simulation into five lines, which were attributed to five crystallographically distinct cation sites known from X-ray diffraction studies. The assignments of the lines follow from electric field gradient calculations at the 23Na nuclei applying a simple point charge model based on crystal structure data. A weak Gaussian line at low field (delta iso = -6 ppm) is assigned to sodium cations at site I, two broad quadrupole patterns at the high-field side of the spectra are attributed to site I' (delta iso = -19 ppm, QCC = 5.2 MHz, eta = 0) and site II cations (delta iso = -15 ppm, QCC = 4.6 MHz, eta = 0), and two quadrupolar lines dominating the central region of the spectra originate from Na+ at two different III' sites (delta iso = -13 and -29 ppm, QCC = 2.6 and 1.6 MHz, eta = 0.7 and 0.9, respectively). Na+ ions located on a second I' site could be identified from the DOR NMR spectra. The line assignment is further corroborated by the reasonable agreement of the site occupancies estimated from the line intensities with those determined by X-ray diffraction. In addition, sodium site populations of five dehydrated zeolites NaX and NaY with Si/Al ratios between 1.09 and 4.0 were derived from the 23Na MAS NMR spectra.

Cations↗

Variable-angle double rotation technique: a new two-dimensional high-resolution technique for quadrupolar nuclei.

We describe a new two-dimensional high-resolution technique for nuclei with semi-integer spins subjected to strong quadrupole interactions. This variable-angle double rotation (VADOR) technique separates anisotropic spectral patterns according to the isotropic shift of each species. No sudden sample reorientation is needed for VADOR which can consequently be used regardless of the "relaxation times". This technique can also be utilized to characterize slow molecular reorientations in two- or three-dimensional experiments. We also propose a new geometry for DOR probes (theta e = 70.124 degrees, theta i = 54.736 degrees) which suppresses first-order interactions (chemical shift anisotropy and dipolar) more efficiently than the geometry (theta e = 54.736 degrees, theta i = 30.556 degrees) presently employed.

Magnetic Resonance Spectroscopy↗

Refinement of solid-state MAS NMR spectra of quadrupolar nuclei: application to the analysis of some 51V compounds.

Magic angle solid-state 51V NMR spectra of several vanadium powder compounds have been recorded. A refinement of these spectra using theoretical simulations of the powder spectra have been performed assuming the simultaneous anisotropic effects of electric field gradients (EFG) and of electronic shielding. It is shown that the relative orientation of the principal axes of the two tensors have to be considered.

Anisotropy↗

Determination of 51V quadrupole and chemical shift tensor orientations in V2O5 by analysis of magic-angle spinning nuclear magnetic resonance spectra.

Magic-angle spinning (MAS) 51V nuclear magnetic resonance (NMR) spectra of V2O5 have been recorded at various fields to evidence the relative effects of the quadrupole interaction and electronic shielding at the nucleus. A refinement of the spectra using theoretical simulations has been performed assuming a simultaneous existence of these two anisotropic interactions. The relative orientation of the principal axes for both tensors has been obtained. The results agree with previous single-crystal studies. Reliability of the results is discussed. A fundamental indetermination of the actual relative tensor orientations remains, owing to the powder nature of the sample.

Anisotropy↗