Cross-polarization Nuclear Magnetic Resonance Research Articles

Properties of humin isolated from Polish arable soils: The most recalcitrant fraction of soil organic matter that prevent soil degradation

AbstractThe purpose of the research was to determine the molecular properties of humin (HUM) determined by elemental composition, as well as spectroscopic 13C Magic Angle Splitting Cross Polarisation Nuclear Magnetic Resonance (13C MAS CP NMR), Fourier transformed infrared, electron paramagnetic resonance and scanning electron microscope energy‐dispersive x‐ray (SEM–EDX) techniques. Soil samples were isolated from the mollic horizon of Phaeozem and Chernozem arable soils derived from different parent materials in Poland. The HUM was isolated as the fraction that was remined after exhaustive extraction of the humic and fulvic acids by NaOH and was followed by removal of the mineral fraction with HF/HCl treatment. The results obtained indicated that the HUM structures isolated by the adopted method are a chemically heterogeneous conglomerate, composed of a complex of many strongly combined units of organic substances. This fraction indicated a highly condensed structure with a predominance of aromatic components (predominating over chain forms ranging from 7.05% to 10.32%) and hydrophobic reactive moieties. The share of hydrophobic forms ranges from 77.41% to 80.83%. The ash content, ranging from 22.89% to 54.50%, as well as SEM–EDX used indicated that the HUM isolated with the adopted procedure is strongly associated with the mineral components of the soil. The aromatic part of HUM is strongly associated with the mineral components of the soil, what provides their stability in the environment. These observations confirm the high resistance of HUM to decomposition and indicate the great importance of this fraction in carbon sequestration and preventing soil degradation.

On the use of cross polarization in solid-state NMR: 1H spin-lock versus adiabatic demagnetization in the rotating frame

Cross polarization (CP) is a widely used solid-state nuclear magnetic resonance (NMR) technique for enhancing the polarization of dilute S spins from much larger polarization of abundant I spins such as 1H. To achieve such a polarization transfer, the I spin should either be spin-locked or be converted to the dipolar ordered state through adiabatic demagnetization in the rotating frame. In this work, we analyze the spin dynamics of the Hartmann-Hahn CP (HHCP) utilizing the 1H spin-locking, and the dipolar-order CP (DOCP) having the 1H adiabatic demagnetization. We further propose an adiabatic demagnetization CP (ADCP) where a constant radio-frequency pulse is applied on the S spin while 1H is adiabatically demagnetized. Our analyses indicate that ADCP utilizes the adiabatic passage to effectively achieve the polarization transfer from the 1H to S spins. In addition, the dipolar ordered state generated during the 1H demagnetization process could also be converted into the observable S polarization through DOCP, further enhancing the polarized signals. It is shown by both static and magic-angle-spinning (MAS) NMR experiments that ADCP has dramatically broadened the CP matching condition over the other CP schemes. Various samples have been used to demonstrate the polarization transfer efficiency of this newly proposed ADCP scheme.

Study of metakaolins with different amorphities and particle sizes activated by KOH and K2SiO3

The study of alkaline activated materials is very promising regarding the production of materials with high durability. The particle size and the content of reactive silica e alumina (amorphous) influence the performance of the geopolymer as well as the type of activator. In this study, geopolymers are produced using metakaolin precursors with similar chemical composition and different amorphities and particle sizes. KOH and K2SiO3 are used as activators, therefore, potassium solutions provide a lower viscosity of the pastes, better workability with a lower liquid to solids ratio and, consequently, better mechanical strength, denser and exhibited low porosity than sodium solutions. Produced precursors and pastes were characterized in the solid state by fluorescence X-ray spectroscopy, X-ray diffraction, infrared spectroscopy, nuclear magnetic resonance single pulse and nuclear magnetic resonance cross-polarization. The pastes were also evaluated for compressive strength, bulk density and water absorption. The results indicate that geopolymers can be obtained from metakaolins of incomplete calcination and with average grain diameter of 23.5 µm and 12.0 µm. Despite having similar bulk density and a slight difference in water absorption, the mechanical strength of the paste produced with coarser and more amorphous metakaolin at 28 days is 50 MPa, while the other paste reaches 22 MPa. The difference in mechanical strength is likely due to the greater extent of geopolymerization indicated by the NMR. The difference in the precursors and consequently in the pastes impacts on the expected durability.

Structural Evolution of Lanthanum Hydroxides during Long-Term Phosphate Mitigation: Effect of Nanoconfinement.

Lanthanum (La)-based materials are effective in removing phosphate (P) from water to prevent eutrophication. Compared to their bulky analogues, La(OH)3 nanoparticles exhibit a higher P removal efficiency and a more stable P removal ability when spatially confined inside the host. Consequently, the understanding of the nanoconfinement effects on the long-term evolution of La-P structures is crucial for their practical use in P sequestration and recycle, which, however, is still missing. Here, we describe an attempt to explore the evolution of La-P structures, the P environment, and the status of La(OH)3 nanoparticles confined in the nanopores of the D201 resin, compared to a nonconfined analogue, over a P adsorption period of 25 days in both simulated wastewater and the real bioeffluent. A combinative use of X-ray diffraction (XRD), cross-polarization nuclear magnetic resonance (CP-NMR), and X-ray photoelectron spectroscopy (XPS) techniques confirms the transition from La-P inner-sphere complexation to the formation of LaPO4·xH2O and finally to LaPO4 in both samples. Interestingly, the rate of structural transformation in the real bioeffluent is substantially reduced. Nevertheless, in both conditions, nanoconfinement results in a much faster rate and larger extent of the structural transition. Moreover, nanoconfinement also facilitates the reverse transformation of stable LaPO4 back to La(OH)3. Our work provides the scientific basis of nanoconfinement for the preferable use of La-based nanocomposites in P mitigation, immobilization, and recycle application.

Chirality-Induced Electron Spin Polarization and Enantiospecific Response in Solid-State Cross-Polarization Nuclear Magnetic Resonance.

NMR-based techniques are supposed to be incapable of distinguishing pure crystalline chemical enantiomers. However, through systematic studies of cross-polarization magic angle spinning (CP-MAS) NMR in a series of amino acids, we have found a rather unexpected behavior in the intensity pattern of optical isomers in hydrogen/nitrogen nuclear polarization transfer that would allow the use of CP NMR as a nondestructive enantioselective detection technique. In all molecules considered, the d isomer yields higher intensity than the l form, while the chemical shift for all nuclei involved remains unchanged. We attribute this striking result to the onset of electron spin polarization, accompanying bond charge polarization through a chiral center, a secondary mechanism for polarization transfer that is triggered only in the CP experimental setup. Electron spin polarization is due to the chiral-induced spin selectivity effect (CISS), which creates an enantioselective response, analogous to the one involved in molecular recognition and enantiospecific separation with achiral magnetic substrates. This polarization influences the molecular magnetic environment, modifying the longitudinal relaxation time T1 of 1H, and ultimately provoking the observed asymmetry in the enantiomeric response.

Structural Elucidation of Amorphous Photocatalytic Polymers from Dynamic Nuclear Polarization Enhanced Solid State NMR

Dynamic nuclear polarization (DNP) solid-state nuclear magnetic resonance (NMR) offers a recent approach to dramatically enhance NMR signals and has enabled detailed structural information to be obtained in a series of amorphous photocatalytic copolymers of alternating pyrene and benzene monomer units, the structures of which cannot be reliably established by other spectroscopic or analytical techniques. Large 13C cross-polarization (CP) magic angle spinning (MAS) signal enhancements were obtained at high magnetic fields (9.4–14.1 T) and low temperature (110–120 K), permitting the acquisition of a 13C INADEQUATE spectrum at natural abundance and facilitating complete spectral assignments, including when small amounts of specific monomers are present. The high 13C signal-to-noise ratios obtained are harnessed to record quantitative multiple contact CP NMR data, used to determine the polymers’ composition. This correlates well with the putative pyrene:benzene stoichiometry from the monomer feed ratio, enabl...

Selective observation of charge storing ions in supercapacitor electrode materials

Nuclear magnetic resonance (NMR) spectroscopy has emerged as a useful technique for probing the structure and dynamics of the electrode-electrolyte interface in supercapacitors, as ions inside the pores of the carbon electrodes can be studied separately from bulk electrolyte. However, in some cases spectral resolution can limit the information that can be obtained. In this study we address this issue by showing how cross polarisation (CP) NMR experiments can be used to selectively observe the in-pore ions in supercapacitor electrode materials. We do this by transferring magnetisation from 13C nuclei in porous carbons to nearby nuclei in the cations (1H) or anions (19F) of an ionic liquid. Two-dimensional NMR experiments and CP kinetics measurements confirm that in-pore ions are located within Ångströms of sp2-hybridised carbon surfaces. Multinuclear NMR experiments hold promise for future NMR studies of supercapacitor systems where spectral resolution is limited.

Novel thio-kaolinite nanohybrid materials and their application as heavy metal adsorbents in wastewater

A new clay nanohybrid adsorbent material was obtained by grafting the compound 3,6-dithia-1,8-octanediol (HO(CH2)2S(CH2)2S(CH2)2OH) onto the internal aluminol surfaces of both the urea- and dimethylsulfoxide (DMSO) precursors of two kaolinite clay minerals: the Source clay KGa-1b and a Portuguese clay sample collected from the Clays of Taveiro formation. All samples were characterised by X-ray diffraction and solid-state 13C cross-polarisation nuclear magnetic resonance (CP-MAS NMR) spectroscopy. Initial materials and final products were also characterised by thermal gravimetric analysis (TGA) and Fourier-Transform infrared (FTIR) spectroscopy. The results describe nanohybrid materials that are resistant to hydrolysis and exhibit different grafting fashions.The potential application of these materials as a heavy metal adsorbents was tested in ZnCl2 solutions as well as in zinc-spiked raw wastewater. The first assessment of the zinc adsorption capacity of the Source clay KGa-1b was made. Zinc concentrations were analysed concomitant with other metal species by inductively coupled plasma mass spectrometry (ICP-MS), demonstrating variable adsorption capacities of the different clay samples, and a consistently greater zinc removal in the wastewater system compared to simple zinc solutions. Measured concentrations of concomitantly analysed metals reveal a potentially worrying release of certain heavy metal species from some of the clay samples as a result of zinc adsorption.

Proton Environments in Biomimetic Calcium Phosphates Formed from Mesoporous Bioactive CaO-SiO2-P2O5 Glasses in Vitro: Insights from Solid-State NMR.

When exposed to body fluids, mesoporous bioactive glasses (MBGs) of the CaO–SiO2–P2O5 system develop a bone-bonding surface layer that initially consists of amorphous calcium phosphate (ACP), which transforms into hydroxy-carbonate apatite (HCA) with a very similar composition as bone/dentin mineral. Information from various 1H-based solid-state nuclear magnetic resonance (NMR) experiments was combined to elucidate the evolution of the proton speciations both at the MBG surface and within each ACP/HCA constituent of the biomimetic phosphate layer formed when each of three MBGs with distinct Ca, Si, and P contents was immersed in a simulated body fluid (SBF) for variable periods between 15 min and 30 days. Directly excited magic-angle-spinning (MAS) 1H NMR spectra mainly reflect the MBG component, whose surface is rich in water and silanol (SiOH) moieties. Double-quantum–single-quantum correlation 1H NMR experimentation at fast MAS revealed their interatomic proximities. The comparatively minor H species of each ACP and HCA component were probed selectively by heteronuclear 1H–31P NMR experimentation. The initially prevailing ACP phase comprises H2O and “nonapatitic” HPO42–/PO43– groups, whereas for prolonged MBG soaking over days, a well-progressed ACP → HCA transformation was evidenced by a dominating O1H resonance from HCA. We show that 1H-detected 1H → 31P cross-polarization NMR is markedly more sensitive than utilizing powder X-ray diffraction or 31P NMR for detecting the onset of HCA formation, notably so for P-bearing (M)BGs. In relation to the long-standing controversy as to whether bone mineral comprises ACP and/or forms via an ACP precursor, we discuss a recently accepted structural core–shell picture of both synthetic and biological HCA, highlighting the close relationship between the disordered surface layer and ACP.

Apoptotic Bax at Oxidatively Stressed Mitochondrial Membranes: Lipid Dynamics and Permeabilization

Mitochondria are crucial compartments of eukaryotic cells because they function as the cellular power plant and play a central role in the early stages of programmed cell death (apoptosis). To avoid undesired cell death, this apoptotic pathway is tightly regulated by members of the Bcl-2 protein family, which interact on the external surface of the mitochondria, i.e., the mitochondrial outer membrane (MOM), and modulate its permeability to apoptotic factors, controlling their release into the cytosol. A growing body of evidence suggests that the MOM lipids play active roles in this permeabilization process. In particular, oxidized phospholipids (OxPls) formed under intracellular stress seem to directly induce apoptotic activity at the MOM. Here we show that the process of MOM pore formation is sensitive to the type of OxPls species that are generated. We created MOM-mimicking liposome systems, which resemble the cellular situation before apoptosis and upon triggering of oxidative stress conditions. These vesicles were studied using 31P solid-state magic-angle-spinning nuclear magnetic resonance spectroscopy and differential scanning calorimetry, together with dye leakage assays. Direct polarization and cross-polarization nuclear magnetic resonance experiments enabled us to probe the heterogeneity of these membranes and their associated molecular dynamics. The addition of apoptotic Bax protein to OxPls-containing vesicles drastically changed the membranes’ dynamic behavior, almost completely negating the previously observed effect of temperature on the lipids’ molecular dynamics and inducing an ordering effect that led to more cooperative membrane melting. Our results support the hypothesis that the mitochondrion-specific lipid cardiolipin functions as a first contact site for Bax during its translocation to the MOM in the onset of apoptosis. In addition, dye leakage assays revealed that different OxPls species in the MOM-mimicking vesicles can have opposing effects on Bax pore formation.

Solid-state NMR studies for the development of non-woven biomaterials based on silk fibroin and polyurethane

Silk fibroin (SF) possesses several characteristics that are favorable for tissue engineering. However, the mechanical properties must be modified in some cases. For instance, soft tissues such as those of the circulatory system are more elastic than tissue-engineered materials. The development of polymer blends is a simple method with the potential to provide materials with extended useful properties. In this study, we developed a non-woven SF and thermoplastic polyurethane-blend sheet from a polymer solution. The structure and miscibility of the blend sheet was evaluated using solid-state nuclear magnetic resonance (NMR) methods. In the 13C cross-polarization and magic angle spinning NMR spectra, no peak shift was observed between the pure and blended samples. The miscibility of the sample was investigated using proton spin-lattice relaxation times in the laboratory frame (T1H). The T1H measurement clearly revealed that the molecular chains of SF and Pellethane exist in close proximity of several tens of nanometers. The development of polymer blends is a simple method with the potential to provide materials with extended useful properties. Here, the SF and Pellethane were observed to be highly miscible with each other even though SF maintained the strong β-sheet crystal structure. This result suggests that SF/Pellethane-blended sheets possess strength that is derived from SF and elasticity that is derived from Pellethane. Therefore, this blended sheet should be a good medical material for soft tissue engineering.

Quantitative 13C Solid-State NMR Spectra by Multiple-Contact Cross-polarization for Drug Delivery: From Active Principles to Excipients and Drug Carriers

In this contribution, we present an analysis of the main parameters influencing the efficiency of the 1H → 13C multiple-contact cross-polarization nuclear magnetic resonance (NMR) experiment in the context of solid pharmaceutical materials. Using the optimum experimental conditions, quantitative 13C NMR spectra are then obtained for porous metal–organic frameworks (potential drug carriers) and for components present in drug formulations (active principle ingredient and excipients, amorphous or crystalline). Finally, we show that mixtures of components can also be quantified with this method and, hence, that it represents an ideal tool for quantification of pharmaceutical formulations by 13C cross-polarization under magic-angle spinning NMR in the industry as it is robust and easy to set up, much faster than direct 13C polarization and is efficient for samples at natural abundance.

Nuclear magnetic resonance study of the ferroelastic phase transition of order-disorder type in [N(C2H5)4]2CdCl4

This study uses nuclear magnetic resonance (NMR) techniques to examine the detailed changes in [N(C2H5)4]2CdCl4 around its phase transition at the temperature TC = 284 K. The chemical shifts and spin-lattice relaxation times in the rotating frame (T1ρ) were determined from 1H magic angle spinning (MAS) NMR and 13C cross-polarization (CP)/MAS NMR spectra. The two sets of inequivalent 1H and 13C nuclei in CH3 and CH2 were distinguished. A ferroelastic phase transition was observed at TC, without structural symmetry change. The phase transition is mainly attributed to the orientational ordering of the [N(C2H5)4]+ cations, and the spectral splitting at low temperature is associated with different ferroelastic domains.

Tetrapropylammonium Occlusion in Nanoaggregates of Precursor of Silicalite-1 Zeolite Studied by 1H and 13C NMR

The dynamic behavior of tetrapropylammonium (TPA) cations in the clear precursor sols for silicalite synthesis has been investigated by 1H diffusion ordered spectroscopy (DOSY), T1, T2, and T1ρ 1H relaxation, as well as 1H→13C cross polarization (CP) nuclear magnetic resonance. The DOSY NMR experiments showed the presence of strong solute–solvent interactions in concentrated sols, which are decreasing upon dilution. Similarities in dependence of diffusion coefficients with fractional power of the viscosity constant observed for nanoparticles, TPA cations and water led to the conclusion that they aggregate as anisotropic silicate-TPA particles. Relaxation studies as well as 1H→13C CP experiments provide information on dynamic properties of ethanol, water and TPA cations, which are function of silicate aggregates. The general tendency showed that the presence of silicate as oligomers and particles decreases the relaxation times, in particular T2 and T1ρH, as a consequence of involvement of these latter in ion-pairing interactions with water-solvated TPA molecules slowing down their mobility. Furthermore, from the 1H→13C CP dynamics curve profiles a change in the CP transfer regime was observed from fast (TCH << T1ρH) for solutions without silicates to moderate (TCH~T1ρH) when silicates are interacting with the TPA cations that may reflect the occlusion of TPA into flexible silicate hydrate aggregates.

Study of the ferroelastic phase transition in the tetraethylammonium compound [N(C2H5)4]2ZnBr4 by magic-angle spinning and static NMR

The ferroelastic phase transition of tetraethylammonium compound [N(C2H5)4]2ZnBr4 at the phase transition temperature (TC) = 283 K was characterized by magic-angle spinning (MAS) and static nuclear magnetic resonance (NMR), and confirmed by optical polarizing spectroscopy. The structural geometry near TC was studied in terms of the chemical shifts and the spin-lattice relaxation times T1ρ in the rotating frame for 1H MAS NMR and 13C cross-polarization (CP)/MAS NMR. The two inequivalent ethyl groups were distinguishable in the 13C NMR spectrum, and the T1ρ results indicate that they undergo tumbling motion above TC in a coupled manner. From the 14N NMR results, the two nitrogen nuclei in the N(C2H5)4+ ions were distinguishable above TC, and the splitting in the spectra below TC was related to the ferroelastic domains with different orientations.

Secondary Structures in a Freeze-Dried Lignite Humic Acid Fraction Caused by Hydrogen-Bonding of Acidic Protons with Aromatic Rings.

A lignite humic acid (HA) was separated from inorganic and non-HA impurities (i.e., aluminosilicates, metals) and fractionated by a combination of dialysis and XAD-8 resin. Fractionation revealed a more homogeneous structure of lignite HA. New and more specific structural information on the main lignite HA fraction is obtained by solid-state nuclear magnetic resonance (NMR) spectroscopy. Quantitative (13)C multiple cross-polarization (multiCP) NMR indicated oxidized phenyl propane structures derived from lignin. MultiCP experiments, conducted on potassium HA salts titrated to pH 10 and pH 12, revealed shifts consistent with carboxylate and phenolate formation, but structural changes associated with enolate formation from aromatic beta keto acids were not detected. Two-dimensional (1)H-(13)C heteronuclear correlation (2D HETCOR) NMR indicated aryl-aliphatic ketones, aliphatic and aromatic carboxyl groups, phenol, and methoxy phenyl ethers. Acidic protons from carboxyl groups in both the lignite HA fraction and a synthetic HA-like polycondensate were found to be hydrogen-bonded with electron-rich aromatic rings. Our results coupled with published infrared spectra provide evidence for the preferential hydrogen bonding of acidic hydrogens with electron-rich aromatic rings rather than adjacent carbonyl groups. These hydrogen-bonding interactions likely result from stereochemical arrangements in primary structures and folding.

Solid state NMR studies of gels derived from low molecular mass gelators.

Since its invention more than six decades ago, nuclear magnetic resonance (NMR) spectroscopy has evolved as an inevitable part of chemical as well as structural analysis of small molecules, polymers, biomaterials and hybrid materials. In the solution state, due to the increased viscosity of complex viscoelastic fluids such as gels, liquid crystals and other soft materials, the rate of molecular tumbling is reduced, which in turn affects the chemical shift anisotropy, dipolar and quadrupolar interactions. As a consequence the solution state NMR spectra show broad lines, and therefore, extracting detailed structural information is a challenging task. In this context, solid state (SS) NMR has the ability to distinguish between a minute amount of polymorphic forms, conformational changes, and the number of non-equivalent molecules in an asymmetric unit of a crystal lattice, and to provide both qualitative as well as quantitative analytical data with a short-range order. Therefore, SS NMR has continued to evolve as an indispensable tool for structural analysis and gave birth to a new field called NMR crystallography. Solid state cross polarization (CP) and high resolution (HR) magic angle spinning (MAS) NMR spectroscopy has been used to study weak interactions in polymer gels. However, the application of SS NMR spectroscopy to study gels derived from low molecular weight gelators has been limited until recently. In this review, we will focus on the importance of solid state NMR spectroscopy in understanding and elucidating the structure of supramolecular gels derived from low molecular weight gelators with selected examples.

Vapor silylation of Ta-HMS mesoporous molecular sieve

Ta-HMS mesoporous molecular sieve was synthesized hydrothermally and vapor-silylated using hexamethyldisilazane. Two samples were characterized by Fourier transform infrared spectrometry, 29Si cross-polarization and magic angle spinning nuclear magnetic resonance, hydrophilicity–lipophilicity tests, X-ray diffraction, N2 adsorption, and diffuse reflectance ultraviolet–visible spectroscopy (DR UV–Vis), respectively. They were also evaluated by the epoxidation of cyclohexene using tert-butyl hydroperoxide as oxidant. Trimethylsilyl groups have been anchored on the surface of Ta-HMS after silylation treatment. The silylated Ta-HMS keeps a typical mesoporous structure, whereas it has a less pore diameter and a less specific area than Ta-HMS. On the other hand, the silylated Ta-HMS gives the less hydrophilicity and higher lipophilicity as well as the higher dispersity of Ta sites than Ta-HMS, and as a result, the silylated Ta-HMS exhibits the more excellent catalytic performance in epoxidation of cyclohexene than Ta-HMS. Ta-HMS mesoporous molecular sieve was synthesized hydrothermally and vapor-silylated using hexamethyldisilazane. Trimethylsilyl groups have been anchored on the surface of Ta-HMS after silylation treatment. The silylated Ta-HMS keeps the typical mesoporous structure, whereas it has the less pore diameter and specific area compared with Ta-HMS. On the other hand, the silylated Ta-HMS gives the less hydrophilicity and higher lipophilicity as well as the higher dispersity of Ta sites than Ta-HMS, and as a result, the silylated Ta-HMS exhibits more excellent catalytic performance in epoxidation of cyclohexene than Ta-HMS.

Evidence of the Influence of Hydrogen on the Magnetic Property of Polymerized Fullerene

We present experimental evidence for ferromagnetism in C60 polymerized under ultra-violet radiation in ambient hydrogen atmosphere. Polymerization was confirmed with measurements of the Raman peak for Ag(2) mode and of chemical shifts in 13C nuclear magnetic resonance (NMR) spectroscopy. 1H-13C cross polarization NMR spectra confirmed that some C were covalently bonded to hydrogen. This photopolymerized C60 partially bonded with H exhibited weak but discernible ferromagnetism, which may be explained with a spin-transfer mechanism.

Comparative study of the AT1 receptor prodrug antagonist candesartan cilexetil with other sartans on the interactions with membrane bilayers

Drug–membrane interactions of the candesartan cilexetil (TCV-116) have been studied on molecular basis by applying various complementary biophysical techniques namely differential scanning calorimetry (DSC), Raman spectroscopy, small and wide angle X-ray scattering (SAXS and WAXS), solution 1H and 13C nuclear magnetic resonance (NMR) and solid state 13C and 31P (NMR) spectroscopies. In addition, 31P cross polarization (CP) NMR broadline fitting methodology in combination with ab initio computations has been applied. Finally molecular dynamics (MD) was applied to find the low energy conformation and position of candesartan cilexetil in the bilayers. Thus, the experimental results complemented with in silico MD results provided information on the localization, orientation, and dynamic properties of TCV-116 in the lipidic environment. The effects of this prodrug have been compared with other AT1 receptor antagonists hitherto studied. The prodrug TCV-116 as other sartans has been found to be accommodated in the polar/apolar interface of the bilayer. In particular, it anchors in the mesophase region of the lipid bilayers with the tetrazole group oriented toward the polar headgroup spanning from water interface toward the mesophase and upper segment of the hydrophobic region. In spite of their localization identity, their thermal and dynamic effects are distinct pointing out that each sartan has its own fingerprint of action in the membrane bilayer, which is determined by the parameters derived from the above mentioned biophysical techniques.