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1H spin-lattice Nuclear Magnetic Resonance relaxometry experiments have been performed for collagen and collagen-based artificial tissues in the frequency range of 10 kHz–20 MHz. The studies were performed for non-hydrated and hydrated materials. The relaxation data have been interpreted as including relaxation contributions originating from 1H–1H and 1H–14N dipole–dipole interactions, the latter leading to Quadrupole Relaxation Enhancement effects. The 1H–1H relaxation contributions have been decomposed into terms associated with dynamical processes on different time scales. A comparison of the parameters for the non-hydrated and hydrated systems has shown that hydration leads to a decrease in the dipolar relaxation constants without significantly affecting the dynamical processes. In the next step, the relaxation data for the hydrated systems were interpreted in terms of a model assuming two-dimensional translational diffusion of water molecules in the vicinity of the macromolecular surfaces and a sub-diffusive motion leading to a power law of the frequency dependencies of the relaxation rates. It was found that the water diffusion process is slowed down by at least two orders of magnitude compared to bulk water diffusion. The frequency dependencies of the relaxation rates in hydrated tissues and hydrated collagen are characterized by different power laws ( ω H − β , where ωH denotes the 1H resonance frequency): the first of about 0.4 and the second close to unity. [ABSTRACT FROM AUTHOR]

1H spin-lattice relaxation studies have been performed for binary systems, including glycerol as the first component and alanine, glycine, and aspartic acid (with different levels of deuteration) as the second one. The relaxation studies have been performed in the frequency range from 10 kHz to 10 MHz vs temperature. A theoretical framework, including all relevant 1H–1H and 1H–2H relaxation pathways, has been formulated. The theory has been exploited for a thorough interpretation of a large set of the experimental data. The importance of the 1H–2H relaxation contributions has been discussed, and the possibility of revealing dynamical properties of individual liquid components in binary liquids has been carefully investigated. As far as the dynamical properties of the specific binary liquids, chosen as an example, are considered, it has been shown that in the presence of the second component (alanine, glycine, and aspartic acid), both molecular fractions undergo dynamics similar to that of glycerol in bulk. [ABSTRACT FROM AUTHOR]

1H spin–lattice relaxation experiments have been performed for gels based on fish collagen in order to analyze water dynamics. The covered frequency range ranges from 10 kHz to 10 MHz; in some cases, the temperature has varied as well. The relaxation data have been reproduced in terms of two models of water motion—a model including two relaxation contributions associated with the diffusion of water molecules on the macromolecular surfaces and a second model being just a phenomenological power law. The concept of surface diffusion has led to a very good agreement with the experimental data and a consistent set of parameters, with the diffusion coefficients being about five orders of magnitude slower compared to bulk water for one of the pools and considerably faster for the second one (smaller by factors between 2 and 20 compared to bulk water). In some cases, the attempt to reproduce the data in terms of a power law has led to a good agreement with the experimental data (the power law factor varying between 0.41 and 0.57); however, in other cases, the discrepancies are significant. This outcome favors the concept of surface diffusion. [ABSTRACT FROM AUTHOR]

1H fast field-cycling and time-domain nuclear magnetic resonance relaxometry studies have been performed for 15 samples of sugar of different kinds and origins (brown, white, cane, beet sugar). The extensive data set, including results for crystal sugar and sugar/water mixtures, has been thoroughly analyzed, with a focus on identifying relaxation contributions associated with the solid and liquid fractions of the systems and non-exponentiality of the relaxation processes. It has been observed that 1H spin–lattice relaxation rates for crystal sugar (solid) vary between 0.45 s−1 and 0.59 s−1, and the relaxation process shows only small deviations from exponentiality (a quantitative measure of the exponentiality has been provided). The 1H spin–lattice relaxation process for sugar/water mixtures has turned out to be bi-exponential, with the relaxation rates varying between about 13 s−1–17 s−1 (for the faster component) and about 2.1 s−1–3.5 s−1 (for the slower component), with the ratio between the amplitudes of the relaxation contributions ranging between 2.8 and 4.2. The narrow ranges in which the parameters vary make them a promising marker of the quality and authenticity of sugar. [ABSTRACT FROM AUTHOR]

Magnetic Resonance Imaging (MRI) is one of the most powerful diagnostic tools providing maps of 1H relaxation times of human bodies. The method needs, however, a contrast mechanism to enlarge the difference in the relaxation times between healthy and pathological tissues. In this work, we discuss the potential of a novel contrast mechanism for MRI based on Quadrupole Relaxation Enhancement (QRE) and estimate the achievable value of QRE under the most favorable conditions. It has turned out that the theoretically possible enhancement factors are smaller than those of typical paramagnetic contrast agents, but in turn, the field-selectivity of QRE-based agents makes them extremely sensitive to subtle changes of the electric field gradient in the tissue. So far, QRE has been observed for solids (in most cases for 14N) as a result of very slow dynamics and anisotropic spin interactions, believed to be necessary for QRE to appear. We show the first evidence that QRE can be achieved in solutions of compounds containing a high spin nucleus (209Bi) as the quadrupole element. The finding of QRE in a liquid state is explained in terms of spin relaxation theory based on the stochastic Liouville equation. The results confirm the relaxation theory and motivate further exploration of the potential of QRE for MRI. [ABSTRACT FROM AUTHOR]

The aim of this work is to analyze in detail the effect of the alkyl chain length on the dynamics of glass-forming propylene carbonate (PC) derivatives. Examined samples are low-molecular weight derivatives of the PC structure, i.e., the 4-alkyl-1,3-dioxolan-2-one series, modified by changing the alkyl substituent from methyl to hexyl. The molecular dynamics (MD) has been analyzed based on experimental data collected from differential scanning calorimetry, broadband dielectric spectroscopy (BDS), X-ray diffraction (XRD), and nuclear magnetic resonance relaxometry measurements as well as MD simulations. The dielectric results show in samples with the propyl- or longer carbon chain the presence of slow Debye-like relaxation with features similar to those found in associative materials. Both XRD and MD reveal differences in the intermolecular structure between PC and 4-butyl-1,3-dioxolan-2-one liquids. Moreover, MD shows that the probability of finding one terminal carbon atom of the side chain of BPC in the vicinity of another carbon atom of the same type is much higher than in the case of PC. It suggests that there is a preference for longer hydrocarbon chains to set themselves close to each other. Consequently, the observed slow-mode peak may be caused by movement of aggregates maintained by van der Waals interactions. Reported herein, findings provide a new insight into the molecular origin of Debye-like relaxation. [ABSTRACT FROM AUTHOR]