Biomedical subjects

D E Demco

Publications and source records attributed to D E Demco.

13 recordsLinked to original sources

PubMed2001

Double-quantum-filtered NMR signals in inhomogeneous magnetic fields.

The possibility of exciting and detecting proton NMR double-quantum coherences in inhomogeneous static and radiofrequency magnetic fields was investigated. For this purpose specialized pulse sequences which partially refocus the strongly inhomogeneous evolution of the spin system and generate double-quantum buildup and decay curves were implemented on the NMR MOUSE (mobile universal surface explorer). The theoretical justification of the method was developed for the simple two-spin-1/2 system. The performances of the same pulse sequences were also tested on a solid-state high-field NMR spectrometer. It was shown that DQ decay curves have a better signal-to-noise ratio in the initial time regime than DQ buildup curves. The double-quantum buildup and decay curves were recorded for a series of cross-linked natural rubber samples. These curves give access to quantitative values of the ratio of proton total residual dipolar couplings which are in good agreement with those measured in homogeneous fields. A linear dependence of these ratios on the sulfur-accelerator content was found.

Journal Article↗

PubMed2001

Dipolar and J encoded DQ MAS spectra under rotational resonance.

A two-dimensional (2D) double-quantum (DQ) experiment under rotational resonance (R(2)) conditions is introduced for evaluating dipolar couplings in rotating solids. The contributions from the R(2)-recoupled dipolar interaction and the J coupling can be conveniently separated in the resulting 2D R(2)-DQ spectrum, so that the unknown dipolar coupling can readily be extracted, provided that the values of the involved J coupling constants are known. Since the measured parameters are integral intensity ratios between suitably chosen absorption peaks in the 2D spectrum, the proposed method is characterized by a reduced sensitivity to relaxation parameters. The effect of rotor-modulated terms, including chemical shift anisotropy, is efficiently averaged out by synchronizing the excitation/reconversion time with the rotor period. All of these features are demonstrated theoretically by the example of two model systems, namely, isolated spin-pairs and a three-spin system. The results of the theoretical models are applied to both (13)C and (1)H nuclei to extract dipolar couplings in uniformly (13)C labeled L-alanine and a crosslinked natural rubber.

Journal Article↗

PubMed1999

Heteronuclear double-quantum MAS NMR spectroscopy in dipolar solids.

A new pulse sequence for high-resolution solid-state heteronuclear double-quantum MAS NMR spectroscopy of dipolar-coupled spin-12 nuclei is introduced. It is based on the five-pulse sequence known from solution-state NMR, which is here applied synchronously to both spin species. The heteronuclear double-quantum (HeDQ) spinning-sideband patterns produced by this experiment are shown to be sensitive to the heteronuclear distance, as well as the relative orientations of the chemical-shift and dipolar tensors. In particular, it is shown that the HeDQ patterns exhibit an enhanced sensitivity to the chemical shielding tensors as compared with the single-quantum spinning-sideband patterns. The detection of HeDQ patterns via the I and S spins is discussed. The isolated (13)C-(1)H spin pair in deuterated ammonium formate with (13)C in natural abundance was chosen as a model system, and the perturbing influence of dipolar couplings to surrounding protons on the (13)C-(1)H DQ coherence is discussed. The pulse sequence can also be used as a heteronuclear double-quantum filter, hence providing information about heteronuclear couplings, and thus allowing the differentiation of quaternary and CH(n) bonded carbons. The elucidation of (13)C-(1)H dipolar proximities is presented for a sample of bisphenol A polycarbonate with (13)C in natural abundance, recorded with a broadband version of the synchronized five-pulse sequence.

Magnetic Resonance Spectroscopy↗

PubMed1999

1H NMR imaging of residual dipolar couplings in cross-linked elastomers: dipolar-encoded longitudinal magnetization, double-quantum, and triple-quantum filters.

Contrastfilters for NMR imaging of residual 1H dipolar couplings of elastomers are introduced based on dipolar-encoded longitudinal magnetization, as well as double- and triple-quantum coherences. The spin response is discussed in the initial excitation time regime for methylene, methyl, and methine protons applicable to poly(isoprene) and other elastomers, taking into account the hierarchy of dipolar couplings and the associated editing features of multiple-quantum experiments. The efficiency of these filters is investigated for a series of cross-linked poly(isoprene) samples. Spatially resolved dipolar-encoded longitudinal magnetization decays and double-quantum and triple-quantum buildup curves are presented for a phantom made of poly(isoprene) with different cross-link densities. Two-dimensional images representing residual dipolar couplings are presented using dipolar-encoded longitudinal magnetization, double-quantum, and triple-quantum contrast filters. Images from dipolar-encoded longitudinal magnetization and triple-quantum coherences show the highest resolution and contrast, respectively.

Algorithms↗

PubMed1999

Proton residual dipolar couplings by NMR magnetization exchange in cross-linked elastomers: determination and imaging.

Proton nuclear magnetic resonance (NMR) magnetization exchange is used to investigate residual dipolar couplings in a series of cross-linked poly(styrene-cobutadiene) elastomers. A new model for the dipolar unit is used for the evaluation of the signal decay in magnetization exchange experiments. It takes into account an extended residual dipolar coupling network along the polymer chain. It is shown that in the regime of short mixing times, information about the residual dipolar coupling between methine and methylene protons can be obtained which is not affected by other inter- and intramolecular dipolar couplings. The dynamic order parameter of methine-methylene protons is measured and correlated with cross-link density. This study certifies the quality of a filter for magnetization from residual dipolar couplings which exploit magnetization exchange. The filter can be used to generate contrast in NMR images of heterogeneous elastomers. The first proton NMR parameter image of a dynamic order parameter is presented for a phantom made from poly(styrene-cobutadiene) samples with different cross-link densities.

Algorithms↗

PubMed1998

Resolution enhancement in multiple-quantum MAS NMR spectroscopy.

Two techniques for resolution and sensitivity enhancement are introduced in multiple-quantum (MQ) MAS spectroscopy of rigid solids. The first makes use of ultrafast MAS with spinning frequencies of up to 35 kHz, while the second combines MAS at moderately fast spinning frequencies of about 13 kHz with multiple-pulse (MP) dipolar decoupling. For the latter approach, a semiwindowless WHH-4 sequence is applied during the MQ evolution period (MQ dimension) and/or detection period (single-quantum dimension). In the MQ dimension, the MP sequence has to be supplemented by two bracketing pulses in order to preserve the order and the intensities of the evolving MQ coherences. Double-quantum 1H NMR spectra of l-alanine recorded using both decoupling techniques are shown and compared to each other. Triple-quantum 1H NMR spectra under ultrafast MAS conditions are also presented.

Alanine↗

PubMed1998

Selective residual dipolar couplings in cross-linked elastomers by 1H double-quantum NMR spectroscopy.

1H double-quantum (DQ) solid-state NMR spectroscopy under fast magic-angle spinning (MAS) is introduced as a new spectroscopic tool for the investigation of the structure and local chain dynamics of elastomers. Dipolar connectivities between the protons of the various functional groups can be directly established from the highly resolved DQ solid-state NMR spectra as is shown for a series of cross-linked poly(styrene-co-butadiene). More quantitatively, residual dipolar couplings within and between the functional groups are evaluated selectively from the build-up curves of the double-quantum signals in the limit of the spin-pair approximation. In particular, the CH-CH and the CH2-CH couplings of butadiene, which both act predominantly along the chain-segment direction, have been measured relative to the CH2 coupling. The total build-up intensity is correlated with the cross-link density.

Cross-Linking Reagents↗

PubMed1997

Multiple nonlinear stimulated echoes.

Three-pulse sequences in the presence of magnetic field gradients at high magnetic fields produce multiple nonlinear stimulated echoes (NOSE) at times ntau1 after the third pulse, where n is an integer and tau1 the interval between the first two pulses. These phenomena are due to the demagnetizing field produced by the spatial modulation of the nuclear magnetization arising in the sample after the first two pulses. The theory is presented and compared with experiments. The dependence of the NOSE amplitudes on the flip angles and on the pulse intervals is described. Implications for multidimensional NMR experiments based on sequences of three or more pulses in the presence of field gradients are discussed.

Dimethylpolysiloxanes↗

PubMed1996

Spectral parameters for quantitative mobility contrast in NMR imaging of solid polymers.

Different procedures based on parameters of the wideline NMR absorption spectrum are presented to obtain localized molecular mobility contrast for imaging of solid polymers. For this purpose a 1H-NMR imaging technique with magic sandwich echoes is used for acquiring localized wideline spectra. With samples composed of polystyrene and high impact strength polystyrene, and polycarbonate and low density polyethylene a spatial difference in NMR absorption spectrum lineshape and linewidth is displayed. Furthermore, the spatial distribution of rigid and mobile domains in a heterogeneous polymer can be derived from the NMR spectral components. It is demonstrated that a van Vleck moment analysis can be performed from spatially resolved magic echo decays. The second (M2) and fourth (M4) moments of the rigid components show considerable variation with the spatial composition of the investigated samples.

Chemical Phenomena↗

PubMed1996

The influence of molecular motion on cross-polarization in cross-linked elastomers.

The effect of molecular motion on the heteronuclear cross-polarization rate for the case of the spin-lock procedure was investigated. In applying heteronuclear solid state NMR techniques to mobile elastomer systems the influence of molecular motion cannot be neglected. Starting in the slow motion regime a strong collision model was used for predicting changes of the cross-polarization rate in the dipolar spectral density function of abundant spins. The dipolar correlation time and hence the cross-polarization rate is found to scale with the inverse of the correlation time of the molecular motion. The same behavior is obtained using a second approach valid in the intermediate molecular motion regime. This is based on the effect of the motion on the homonuclear and heteronuclear van-Vleck moments and leads to a linear dependence of the cross-polarization rate on the correlation time of molecular motion. This dependence was verified experimentally by 1H-13C high-resolution cross-polarization measurements on sulfur cross-linked elastomer systems. 13C rotating frame spin-lattice relaxation rate measurements were used to corroborate these data and the approximations used to evaluate the influence of molecular motion on cross-polarization rates. The dependence of these rates on the cross-link density of the elastomer network is analyzed and it is shown that they scale with the cross-link density. The correlation of the 1H-13C cross-polarization rates with the dynamic storage moduli was demonstrated.

Chemical Phenomena↗

PubMed1996

Magic echoes and NMR imaging of solids.

Solid state NMR imaging techniques based on magic echoes are reviewed. The theoretical background of magic echoes in general and their spatial encoding in particular is treated. The magic-echo imaging pulse sequences presently in use are described and discussed. Particular emphasis is devoted to those techniques, which allow the incorporation of spectroscopic or parameter-selective information. The applicability of these methods for the investigation of materials is demonstrated and perspectives for materials science are outlined.

Image Enhancement↗

PubMed1995

Proton spin diffusion for spatial heterogeneity and morphology investigations of polymers.

The diffusion of Zeeman spin order in the laboratory frame for a system with microscopic spatial heterogeneity, due to either molecular mobility or chemical heterogeneity, has been analysed by solving the diffusion equation in the limit of two different models. By simulation of proton spin diffusion nuclear magnetic resonance (NMR) spectral areas for poly(ethylene oxide) we have demonstrated, for both models, the sensitivity of these observables to phase domain size and to the dimensionality of the diffusion process. The possibility to obtain information about the morphology is analysed. Results from calculations based on the two models are compared with experimental spin diffusion results from 1H NMR spectra of poly(ethylene oxide). Two methods for filtering the z-magnetization from the different phase domains in a solid are discussed. The efficiency of a magnetization dipolar filter based on magic and polarization echoes is presented.

Magnetic Resonance Spectroscopy↗

PubMedDate not supplied

The NMR-MOUSE: quality control of elastomers.

New applications of the NMR-MOUSE (mobile universal surface explorer) to non-destructive quality control of elastomers are reported. One example concern the thermal aging of fast clutches which was probed by measurements of 1H transverse relaxation time. Novel methodological developments show that 1H double-quantum filtered NMR signals can be generated in the inhomogeneous fields of the NMR-MOUSE for characterization of residual dipolar couplings. This technique was applied to characterize reference natural rubber samples with different crosslink density and carbon black and silica fillers.

Elastomers↗