High-resolution Solid-state Nuclear Magnetic Resonance Research Articles

Extraction of In-Cell β-Amyloid Fibrillar Aggregates for Studying Molecular-Level Structural Propagations Using Solid-State NMR Spectroscopy.

Molecular-level structural polymorphisms of β-amyloid (Aβ) fibrils have recently been recognized as pathologically significant. High-resolution solid-state nuclear magnetic resonance (ssNMR) spectroscopy has been utilized to study these structural polymorphisms, particularly in ex-vivo fibrils seeded from amyloid extracts of post-mortem brain tissues of Alzheimer's disease (AD) patients. One unaddressed question in current ex-vivo seeding protocol is whether fibrillation from exogenous monomeric Aβ peptides, added to the extracted seeds, can be quantitatively suppressed. Addressing this issue is critical because uncontrolled fibrillation could introduce biased molecular structural polymorphisms in the resulting fibrils. Here, we present a workflow to optimize the key parameters of ex-vivo seeding protocols, focusing on the quantification of amyloid extraction and the selection of exogenous monomeric Aβ concentrations to minimize nonseeded fibrillation. We validate this workflow using three structurally different 40-residue Aβ (Aβ40) fibrillar seeds, demonstrating their ability to propagate their structural features to exogenous wild-type Aβ40.

Molecular structure and evolution mechanism of shale kerogen: Insights from thermal simulation and spectroscopic analysis

During thermal evolution, the kerogen in shale formation undergoes significant chemical, structural and compositional changes, continuously influencing the shale storage capacity, hydrocarbon generation potential, and gas occurrence state. This study systematically examines the chemical structural changes during the thermal evolution of Longmaxi shale kerogen using hydrothermal laboratory experiments from 420 to 850 °C. Additionally, a range of characterization techniques, including Fourier Transform Infrared (FTIR) spectroscopy, Raman spectroscopy, High-Resolution Transmission Electron Microscopy (HRTEM), X-ray Diffraction (XRD), and Solid-state 13C Nuclear Magnetic Resonance (13C NMR), were employed to systematically investigate the kerogen structure and its evolution patterns. Results indicate that Longmaxi Formation kerogen comprises a large molecular carbon framework with aromatic structures, long-chain aliphatic components, and oxygen-containing functional groups. As thermal maturity reaches 2.6 %, the alignment of aromatic fringes gradually increased, with over 60 % aligning in the main direction. Throughout thermal evolution (1.9–3.2 %), fringes in the 5–10 Å range within aromatic structures peak at over 20.45 %, with fringes over 50 Å rapidly increasing from 3 % to over 15 %. Early in the thermal evolution, the long-chain aliphatic component of the kerogen decreases rapidly and part of the structure forms small aromatic rings through aromatisation. The mature to over-mature stage can be divided into three phases: 1) 1.7–2.4 % (loss of oxygen-containing functional groups), 2) 2.4–3.5 % (formation of larger aromatic structures via condensation reactions), 3) over 3.5 % (continued aggregation of aromatic rings, resulting in an increase in the length of aromatic fringes). At a macroscopic level, this induces changes in kerogen pore structure and carbonization features. This study thus provides new insights into the thermal evolution of shale kerogen, which in turn improve understanding of shale reservoirs for hydrocarbon exploitation.

Structural Characterization and Electrochemical Performance of Spinel Oxide Cathodes for High Voltage Mg-Ion Batteries

Non-aqueous Mg-ion batteries are a class of next generation batteries that promise high energy densities as an alternative to Li-ion batteries. Materials discovery and development is therefore required to fulfill this promise. MgCrMnO4 solid-solution oxide spinel with suitable redox voltages and facile Mg2+ mobility has been identified as a promising candidate for practical, high voltage cathodes in Mg-ion batteries. Here, we discuss the development of this solid-solution spinel oxide class as a cathode material, novel synthesis methods of these oxide spinels, as well as their electrochemical performance. Mg-Cr-Mn spinel oxides with varying Cr and Mn content were synthesized via conventional sol-gel methods, urea co-precipitation, and layered double hydroxide precursors. High-resolution synchrotron XRD and solid-state nuclear magnetic resonance (NMR) spectroscopy characterization along with electron microscopy indicated that different synthetic routes resulted in structural and morphological differences. This in turn lead to differences in electrochemical performance: overpotentials on charge or discharge, reversibility, and deliverable capacity. Electrochemical results in Mg-ion full cells indicate improved performance (lower overpotentials, higher reversibility, and increased capacity) for MgCrxMn2-xO4 cathodes synthesized via urea co-precipitation. To the best of our knowledge, full cells testing these Mg-Cr-Mn spinel oxide cathodes have not been previously reported.

Opportunities and Challenges in Applying Solid-State NMR Spectroscopy in Organic Mechanochemistry.

In recent years it is shown that mechanochemical strategies can be beneficial in directed conversions of organic compounds. Finding new reactions proved difficult, and due to the lack of mechanistic understanding of mechanochemical reaction events, respective efforts have mostly remained empirical. Spectroscopic techniques are crucial in shedding light on these questions. In this overview, the opportunities and challenges of solid-state nuclear magnetic resonance (NMR) spectroscopy in the field of organic mechanochemistry are discussed. After a brief discussion of the basics of high-resolution solid-state NMR under magic-angle spinning (MAS) conditions, seven opportunities for solid-state NMR in the field of organic mechanochemistry are presented, ranging from ex situ approaches to structurally elucidated reaction products obtained by milling to the potential and limitations of in situ solid-state NMR approaches. Particular strengths of solid-state NMR, for instance in differentiating polymorphs, in NMR-crystallographic structure-determination protocols, or in detecting weak noncovalent interactions in molecular-recognition events employing proton-detected solid-state NMR experiments at fast MAS frequencies, are discussed.

Lithium Self-Diffusion in a Polymer Electrolyte for Solid-State Batteries: ToF-SIMS/ssNMR Correlative Characterization and Modeling Based on Lithium Isotopic Labeling.

Manufacturers aim to commercialize efficient and safe batteries by finding new strategies. Solid-state electrolytes can be seen as an opportunity to develop batteries with a high energy density. They allow the use of lithium foil as the anode, increasing the energy density. Also, they are composed of nonflammable materials making them safer than liquid electrolytes. However, to enhance the electrochemical performances of forthcoming solid-state lithium metal batteries, phenomena governing ionic conductivity have yet to be mastered in such devices. Lithium isotopic tracing was successfully used in previous works to further understand lithium ion transport mechanisms in batteries. Time-of-flight secondary ion mass spectrometry (ToF-SIMS) and 6/7Li high-resolution solid-state nuclear magnetic resonance (ssNMR) spectroscopy are two complementary techniques probing local and global scale, respectively. Both techniques can distinguish lithium isotopes. Here, four polymer membranes were elaborated with the same lithium concentration, but with various isotopic enrichments from 7.6 to 95.4% of 6Li. The selected material was a poly(ethylene oxide) (PEO) membrane containing lithium bis(trifluoromethylsulfonyl)imide (LiTFSI) as lithium salt. They are widely studied in the lithium battery field. First, reliable ToF-SIMS and ssNMR methodologies were validated in light of the converging results. They led to accurate determination of lithium isotopic abundance of polymer membranes with a 1 or a 2% uncertainty, respectively. Then, the developed methodologies were applied to characterize lithium self-diffusion in a polymer membrane. Furthermore, numerical simulations based on a two-dimensional diffusion model compared with ToF-SIMS analyses allowed us to extract a lithium self-diffusion coefficient of 1.6 × 10-12 m2·s-1 at 60 °C, which complements other published values. The robust methodologies described in this work can be extended to various applications and materials. They stand as powerful strategies to better understand lithium ionic transport, especially in multiphase materials, for example, in hybrid solid-state electrolytes.

High resolution solid-state NMR on the desktop

High-resolution low-field nuclear magnetic resonance (NMR) spectroscopy has found wide application for characterization of liquid compounds because of the low maintenance cost of modern permanent magnets. Solid-state NMR so far is limited to low-resolution measurements of static powders, because of the limited space available in this type of magnet. Magic-angle sample spinning and low-magnetic fields are an attractive combination to achieve high spectral resolution especially for paramagnetic solids. Here we show that magic angle spinning modules can be miniaturized using 3D printing techniques so that high-resolution solid-state NMR in permanent magnets becomes possible. The suggested conical rotor design was developed using finite element calculations and provides sample spinning frequencies higher than 20 kHz. The setup was tested on various diamagnetic and paramagnetic compounds including paramagnetic battery materials. The only comparable experiments in low-cost magnets known so far, had been done in the early times of magic angle spinning using electromagnets at much lower sample spinning frequency. Our results demonstrate that high-resolution low-field magic-angle-spinning NMR does not require expensive superconducting magnets and that high-resolution solid-state NMR spectra of paramagnetic compounds are feasible. Generally, this could introduce low-field solid-state NMR for abundant nuclei standard as a routine analytical tool.

Solid state nuclear magnetic resonance of polymers

The development of Solid-State Nuclear Magnetic Resonance (SSNMR) in Argentina took a great buster at the beginning of the 1990s along with the acquisition of many “state-of-the-art” high-field NMR spectrometers, two of them multipurpose solid-liquid spectrometers. From then to nowadays, the study of solid samples, including polymers, has been a current topic at the NMR group of the Facultad de Matemática, Astronomía, Física y Computación of Universidad Nacional de Córdoba, in Argentina. In this work, we propose a review approach of several research works on solid polymers performed in our group, covering low-field relaxation studies and high-resolution SSNMR.

Quasi-Solid Polymer Electrolyte with Multiple Lithium-Ion Transport Pathways by In Situ Thermal-Initiating Polymerization.

Solid polymer electrolytes (SPEs) are considered to be attractive candidates for rechargeable batteries on account of their high safety and flexible processability. However, the restricted polymer segmental dynamics limit the Li+ conduction of SPEs. Herein, a composite electrolyte membrane was prepared via in situ thermal-initiating polymerization of diethylene glycol diacrylate (DEGDA) in a poly(vinylidene fluoride) frameworks (PVDF FMs) electrospun in advance. As a quasi-solid polymer electrolyte (QSPE), it provides multiple transport highways for Li+ built by the C═O or C-O or C═O/C-O groups in poly(diethylene glycol) diacrylate (PDEGDA), respectively, proved by density functional theory calculations together with the high-resolution 7Li solid-state nuclear magnetic resonance spectra. Since the interaction between Li+ and C═O is weaker than that between Li+ and C-O, Li+ tends to move along C═O dominating paths in PDEGDA/PVDF FMs QSPEs, even skipping back to C═O nodes from the original C-O dominating way. Multiple transport patterns facilitate Li+ migration within PDEGDA/PVDF FMs QSPEs, contributing to the ionic conductivity of 1.41 × 10-4 S cm-1 at 25 °C and the Li+ transference number of 0.454. Ascribing to the wetting capability of the monomer to the electrodes in use, compatible electrolyte/electrode interfaces with low interface resistance and compact cells were acquired by the in situ polymerization. Protective lithiated oligomers (RCOOLi) and LiF are enriched at the Li anode surface, promoting a lasting stable Li plating/stripping over 2000 h. By applying the QSPEs in LiFePO4 cell, a capacity of 157.7 mAh g-1 with almost 100% coulombic efficiency during 200 cycles is achieved at 25 °C.

Probing microstructure of solid-state synthesized LiCoO2 with MAS NMR spectroscopy

LiCoO2 is an important category of active cathode materials in lithium-ion batteries due to its high compacted electrode density, good thermal stability, and stable voltage platform. Recent works on LiCoO2 have focused on the realization of higher charging voltages to fully utilize its high theoretical capacity. However, an unambiguous atomic-level local probe is essential for the understanding of structure-function correlation. Here we employ high-resolution solid-state nuclear magnetic resonance (NMR) spectroscopy to study the local atomic environments in LiCoO2 synthesized with three common sintering methods. While one-dimensional 7Li NMR shows distinct linewidth and subtle dependence on lithium over-stoichiometry, both 7Li and 59Co relaxation times are highly dependent on the sintering method. We prove that the two-step sintering method favors the elimination of unreacted Co3O4, thereby enabling the best discharge capacity in all-solid-state lithium batteries assembled with LiCoO2/LGPS/LiIn, which is in accordance with its narrowest 7Li linewidth and the longest 7Li/59Co T1.

Hydration of Wheat Flour Water-Unextractable Cell Wall Material Enables Structural Analysis of Its Arabinoxylan by High-Resolution Solid-State 13C MAS NMR Spectroscopy.

To enable its structural characterization by nuclear magnetic resonance (NMR) spectroscopy, the native structure of cereal water-unextractable arabinoxylan (WU-AX) is typically disrupted by alkali or enzymatic treatments. Here, WU-AX in the wheat flour unextractable cell wall material (UCWM) containing 40.9% ± 1.5 arabinoxylan with an arabinose-to-xylose ratio of 0.62 ± 0.04 was characterized by high-resolution solid-state NMR without disrupting its native structure. Hydration of the UCWM (1.7 mg H2O/mg UCWM) in combination with specific optimizations in the NMR methodology enabled analysis by solid-state 13C NMR with magic angle spinning and 1H high-power decoupling (13C HPDEC MAS NMR) which provided sufficiently high resolution to allow for carbon atom assignments. Spectral resonances of C-1 from arabinose and xylose residues of WU-AX were here assigned to the solid state. The proportions of un-, mono-, and di-substituted xyloses were 59.2, 19.5, and 21.2%, respectively. 13C HPDEC MAS NMR showed the presence of solid-state fractions with different mobilities in the UCWM. This study presents the first solid-state NMR spectrum of wheat WU-AX with sufficient resolution to enable assignment without prior WU-AX solubilization.

Conformational Selection in Biocatalytic Plastic Degradation by PETase

Due to the steric effects imposed by bulky polymers, the formation of catalytically competent enzyme and substrate conformations is critical in the biodegradation of plastics. In poly(ethylene terephthalate) (PET), the backbone adopts different conformations, gauche and trans, coexisting to different extents in amorphous and crystalline regions. However, which conformation is susceptible to biodegradation and the extent of enzyme and substrate conformational changes required for expedient catalysis remain poorly understood. To overcome this obstacle, we utilized molecular dynamics simulations, docking, and enzyme engineering in concert with high-resolution microscopy imaging and solid-state nuclear magnetic resonance (NMR) to demonstrate the importance of conformational selection in biocatalytic plastic hydrolysis. Our results demonstrate how single-amino acid substitutions in Ideonella sakaiensis PETase can alter its conformational landscape, significantly affecting the relative abundance of productive ground-state structures ready to bind discrete substrate conformers. We experimentally show how an enzyme binds to plastic and provide a model for key residues involved in the recognition of gauche and trans conformations supported by in silico simulations. We demonstrate how enzyme engineering can be used to create a trans-selective variant, resulting in higher activity when combined with an all-trans PET-derived oligomeric substrate, stemming from both increased accessibility and conformational preference. Our work cements the importance of matching enzyme and substrate conformations in plastic hydrolysis, and we show that also the noncanonical trans conformation in PET is conducive for degradation. Understanding the contribution of enzyme and substrate conformations to biocatalytic plastic degradation could facilitate the generation of designer enzymes with increased performance.

The chemical evolution of solid electrolyte interface in sodium metal batteries.

The solid electrolyte interface (SEI) formed on the anode is one of the key factors that determine the life span of sodium metal batteries (SMBs). However, the continuous evolution of SEI during charging/discharging processes complicates the fundamental understanding of its chemistry and structure. In this work, we studied the underlying mechanisms of the protection effect offered by the SEI derived from sodium difluoro(oxalato)borate (NaDFOB). In situ nuclear magnetic resonance (NMR) shows that the prior reduction of DFOB anion contributes to the SEI formation, and it suppresses the decomposition of carbonate solvents. Depth-profiling x-ray photoelectron spectroscopy and high-resolution solid-state NMR reveal that the DFOB anion is gradually turned into borate and fluoride-rich SEI with cycling. The protection effect of SEI reaches the optimum at 50 cycles, which triples the life span of SMB. The detailed investigations provide valuable guidelines for the SEI engineering.

Solid-state NMR analysis of unlabeled fungal cell walls from Aspergillus and Candida species

Fungal infections cause high mortality in immunocompromised individuals, which has emerged as a significant threat to human health. The efforts devoted to the development of antifungal agents targeting the cell wall polysaccharides have been hindered by our incomplete picture of the assembly and remodeling of fungal cell walls. High-resolution solid-state nuclear magnetic resonance (ss NMR) studies have substantially revised our understanding of the polymorphic structure of polysaccharides and the nanoscale organization of cell walls in Aspergillus fumigatus and multiple other fungi. However, this approach requires 13C/15N-enrichment of the sample being studied, severely restricting its application. Here we employ the dynamic nuclear polarization (DNP) technique to compare the unlabeled cell wall materials of A. fumigatus and C. albicans prepared using both liquid and solid media. For each fungus, we have identified a highly conserved carbohydrate core for the cell walls of conidia and mycelia, and from liquid and solid cultures. Using samples prepared in different media, the recently identified function of α-glucan, which packs with chitin to form the mechanical centers, has been confirmed through conventional ss NMR measurements of polymer dynamics. These timely efforts not only validate the structural principles recently discovered for A. fumigatus cell walls in different morphological stages, but also open up the possibility of extending the current investigation to other fungal materials and cellular systems that are challenging to label.

Engineering the Distinct Structure Interface of Subnano-alumina Domains on Silica for Acidic Amorphous Silica-Alumina toward Biorefining.

Amorphous silica–aluminas (ASAs) are important solid catalysts and supports for many industrially essential and sustainable processes, such as hydrocarbon transformation and biorefining. However, the wide distribution of acid strength on ASAs often results in undesired side reactions, lowering the product selectivity. Here we developed a strategy for the synthesis of a unique class of ASAs with unvarying strength of Brønsted acid sites (BAS) and Lewis acid sites (LAS) using double-flame-spray pyrolysis. Structural characterization using high-resolution transmission electron microscopy (TEM) and solid-state nuclear magnetic resonance (NMR) spectroscopy showed that the uniform acidity is due to a distinct nanostructure, characterized by a uniform interface of silica–alumina and homogeneously dispersed alumina domains. The BAS population density of as-prepared ASAs is up to 6 times higher than that obtained by classical methods. The BAS/LAS ratio, as well as the population densities of BAS and LAS of these ASAs, could be tuned in a broad range. In cyclohexanol dehydration, the uniform Brønsted acid strength provides a high selectivity to cyclohexene and a nearly linear correlation between acid site densities and cyclohexanol conversion. Moreover, the concerted action of these BAS and LAS leads to an excellent bifunctional Brønsted–Lewis acid catalyst for glucose dehydration, affording a superior 5-hydroxymethylfurfural yield.

Microscopic (Dis)order and Dynamics of Cations in Mixed FA/MA Lead Halide Perovskites.

Recent developments in the field of high efficiency perovskite solar cells are based on stabilization of the perovskite crystal structure of FAPbI3 while preserving its excellent optoelectronic properties. Compositional engineering of, for example, MA or Br mixed into FAPbI3 results in the desired effects, but detailed knowledge of local structural features, such as local (dis)order or cation interactions of formamidinium (FA) and methylammonium (MA), is still limited. This knowledge is, however, crucial for their further development. Here, we shed light on the microscopic distribution of MA and FA in mixed perovskites MA1–xFAxPbI3 and MA0.15FA0.85PbI2.55Br0.45 by combining high-resolution double-quantum 1H solid-state nuclear magnetic resonance (NMR) spectroscopy with state-of-the-art near-first-principles accuracy molecular dynamics (MD) simulations using machine-learning force-fields (MLFFs). We show that on a small local scale, partial MA and FA clustering takes place over the whole MA/FA compositional range. A reasonable driving force for the clustering might be an increase of the dynamical freedom of FA cations in FA-rich regions. While MA0.15FA0.85PbI2.55Br0.45 displays similar MA and FA ordering as the MA1–xFAxPbI3 systems, the average cation–cation interaction strength increased significantly in this double mixed material, indicating a restriction of the space accessible to the cations or their partial immobilization upon Br– incorporation. Our results shed light on the heterogeneities in cation composition of mixed halide perovskites, helping to exploit their full optoelectronic potential.

Solid-state NMR spectroscopy.

Solid-state nuclear magnetic resonance (NMR) spectroscopy is an atomic-level method used to determine the chemical structure, three-dimensional structure, and dynamics of solids and semi-solids. This Primer summarizes the basic principles of NMR as applied to the wide range of solid systems. The fundamental nuclear spin interactions and the effects of magnetic fields and radiofrequency pulses on nuclear spins are the same as in liquid-state NMR. However, because of the anisotropy of the interactions in the solid state, the majority of high-resolution solid-state NMR spectra is measured under magic-angle spinning (MAS), which has profound effects on the types of radiofrequency pulse sequences required to extract structural and dynamical information. We describe the most common MAS NMR experiments and data analysis approaches for investigating biological macromolecules, organic materials, and inorganic solids. Continuing development of sensitivity-enhancement approaches, including 1H-detected fast MAS experiments, dynamic nuclear polarization, and experiments tailored to ultrahigh magnetic fields, is described. We highlight recent applications of solid-state NMR to biological and materials chemistry. The Primer ends with a discussion of current limitations of NMR to study solids, and points to future avenues of development to further enhance the capabilities of this sophisticated spectroscopy for new applications.

Structure of type A CAI-like melts: A view from multi-nuclear NMR study of melilite (Ca2Al2SiO7-Ca2MgSi2O7) glasses

Exploring the polymerization and structural disorder of Ca-Al-rich inclusion (CAI)-like melts is a key question in cosmochemistry due to strong implications for macroscopic properties of melts (i.e., viscosity and diffusivity). Here, we report experimental results showing the effect of composition on the structure of melilite glasses and melts [åkermanite (Åk, Ca2MgSi2O7) - gehlenite (Gh, Ca2Al2SiO7)] in type A CAIs with varying composition using high-resolution solid-state nuclear magnetic resonance (NMR). The 27Al magic angle spinning (MAS) and 3Q (triple quantum) MAS NMR spectra of melilite glasses show predominant [4]Al. A non-negligible fraction of [5]Al is observed in Åk50Gh50 and Åk72Gh28 glasses and it slightly increases with increasing åkermanite content. The 17O 3QMAS NMR spectra of melilite glasses show that bridging oxygens (BOs, Si–O–Si, Al–O–Al, and Si–O–Al) and non-bridging oxygens (NBOs, Ca–O-Si, Ca-O-Al, and mixed {Ca, Mg}–NBO) are partially resolved. Despite the strong preference of Si over Al for NBOs, for the first time, Ca-O-Al is observed in natural melts (i.e., gehlenite and Åk25Gh75 glasses and melts). The results show that Al-NBO (~150 ppm in MAS dimension) can be distinguished from Si-NBO (~110 ppm) in melilite glasses and melts. The fraction of NBO increases with increasing åkermanite content. The experimental results suggest that composition-induced structural changes should be considered to interpret the melt viscosity, diffusivity, and oxygen isotopic composition of CAI-like melts in the early Solar System.

Dynamics and Proton Transport in Imidazole-Doped Nanocrystalline Cellulose Revealed by High-Resolution Solid-State Nuclear Magnetic Resonance Spectroscopy

CNC-Im is a new proton conductor based on imidazole-functionalized nanocrystalline cellulose with a conductivity of about 10-1 S/m at 160 0C. Its conductivity is possible due to the transport of pr...

Structure and Dynamics of Perylene Bisimide Pigments for “Cool” Organic Coatings by Solid-State NMR: A Combined Experimental and DFT Study

In this work, a combination of high-resolution solid-state nuclear magnetic resonance (SSNMR) experiments and density functional theory calculations has been exploited for obtaining a detailed characterization of the structural and dynamic properties of the perylene bisimide derivative (PBI) Paliogen Black L0086 (P-black). This “cool” organic pigment is characterized by unusual transparent, reflective, and cooling features in the near-infrared (NIR) spectrum. A full assignment of the 13C SSNMR spectrum was achieved, highlighting correlations between 13C isotropic chemical shifts and specific supramolecular features. The π-flip motion of the phenyl rings of the methoxybenzyl side groups bonded to the imide nitrogen atoms was characterized in the 310–386 K temperature range, determining activation energy and correlation times. This motion showed a strong dependence on the supramolecular order of P-black and the length of the alkyl linker between the side group and the perylene bisimide core. The results obtained in this work open the way to investigations on similar PBI pigments, aiming at achieving a collection of molecular, supramolecular, and NIR data that could allow the identification of the main factors determining the NIR performance.

Water-lipid interactions in native bone by high-resolution solid-state NMR spectroscopy

The study of structural and dynamical properties of lipid and its associated interaction with different components of bone is essential to understand its role at a different level of bone homeostasis such as bone mineralization and bone metabolism. In this article, we present water-dependent dynamical changes observed in lipids (triglycerides) in its absolute native environment inside bone by high-resolution 1H solid-state nuclear magnetic resonance spectroscopy (ssNMR). Relaxation measurement (T2 measurement) ssNMR experiments were performed at different levels of water network induced by dehydration and H/D exchange in native bone. Our measurements reflect the changes in the local environment and dynamical properties of triglyceride due to different hydration levels. The present study explains the role of water in stabilizing the structural properties of triglycerides in bone hence will help understand its pathological role associated with bone physiology and bone disorders.