Search PubMed⌕ Search

PubMed · 8902956

Distortions in multiple-pulse solid state NMR imaging: gradient decoupling, time-sequenced second averaging, and over-sampling.

Abstract

Three approaches to reducing image artifacts are described that are specific to multiple-pulse line-narrowing methods of NMR imaging. Gradient decoupling avoids excess line broadening from off-resonance gradient phase evolution by restricting the gradient to selected windows in which the gradient Hamilton an commutes with the toggling frame state, and where the averaged Hamiltonian between gradient pulses is either cyclic or anti-cyclic. This forces the residual averaged dipolar Hamiltonian to be independent of the gradient evolution. Time-sequenced second averaging addresses the on-resonance broadening, where residual error terms dominate the spin dynamics (a lack of second averaging), by adding a second coherent averaging that retains part of the modulation associated with off-resonance terms, and thus smoothes out the line-narrowing efficiency with spatial offset. Over-sampling is useful to increase both the resolution and sensitivity of an image, but it introduces a sampling modulation that produces sidebands. These are eliminated by a series of prepulses in a fashion reminiscent of CYCLOPS phase cycling.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

D G Cory. 1996. Distortions in multiple-pulse solid state NMR imaging: gradient decoupling, time-sequenced second averaging, and over-sampling.. https://doi.org/10.1016/0926-2040(95)01206-0

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Structure of the alpha-homo-DNA:RNA duplex and the function of twist and slide to catalogue nucleic acid duplexes.

High-resolution NMR studies of an alpha-homo-DNA:RNA duplex reveal the formation of a right-handed parallel-oriented helix. It differs significantly from a standard A- or B-type helix by a small twist value (26.2 degrees ), which leads to a helical pitch of 13.7 base pairs per helical turn, a negative inclination (-1.78 Angstrom) and a large x displacement (5.90 Angstrom). The rise (3.4 Angstrom) is similar to that found in B-DNA. The solution of this new helix structure has stimulated us to develop a mathematical and geometrical model based on slide and twist parameters to describe nucleic acid duplexes. All existing duplexes can be positioned within this landscape, which can be used to understand the helicalization process.

Magnetic Resonance Spectroscopy↗

15N NMR study of substituted 2-(phenylamino)-5-phenyl-1,3,4-oxadiazoles.

Substituted 2-(phenylamino)-5-phenyl-1,3,4-oxadiazoles were studied by 15N NMR spectroscopy. All signals were assigned on the basis of HMQC and HMBC experiments. Chemical shifts values were correlated with empirical Hammett parameters as well as with calculated electron densities and chemical shieldings.

Magnetic Resonance Spectroscopy↗

Functionalization of titanium oxide surfaces by means of poly(alkyl-phosphonates).

The use of a multiple attachment sites strategy is considered in order to improve the stability of monomolecular adlayers. The hypothesis was tested in the case of PEG-ylated compounds carrying phosphonate groups, known for their affinity toward titanium oxide surfaces. As a result, a new class of co- and terpolymers were synthesized by free-radical polymerization of three different monomers: dialkyl(methacryloyloxyalkyl)phosphonates, PEG methyl ether methacrylate, and/or butyl methacrylate monomers. Adlayers were formed following a simple dip-and-rinse protocol using diluted aqueous polymer solutions and were characterized by evaluating their thicknesses with variable angle spectroscopic ellipsometry (VASE) and their elemental compositions with X-ray photoelectron spectroscopy (XPS). The same techniques were used to determine changes of the adlayer as a function of exposure to electrolytes at different pH values and to monitor nonspecific protein adsorption upon serum exposures. The results indicated that the poly(alkyl-phosphonate)-based adlayers combine multiple site attachment of phosphonic groups and presentation of PEG side chains to the aqueous environment, resulting in both improved stability over a wide pH range in comparison to the tested reference surfaces and excellent resistance to protein adsorption when exposed to full human serum.

Magnetic Resonance Spectroscopy↗