207Pb Nuclear Magnetic Resonance Research Articles

Characterization of the Pb Coordination Environment and Its Connectivity in Lead Silicate Glasses: Results from 2D 207Pb NMR Spectroscopy.

The Pb-O coordination environment in binary (PbO)x(SiO2)100-x glasses with 30 ≤ x ≤ 70 is probed by using two-dimensional 207Pb nuclear magnetic resonance (NMR) isotropic-anisotropic correlation spectroscopy. The isotropic 207Pb NMR spectra show little composition-dependent evolution of the Pb-O nearest-neighbor coordination environment. The systematic variation of the chemical shift tensor parameters offers a unique insight into their local site symmetry and suggests the presence of pyramidal PbO3 and PbO4 sites with sterically active electron lone pairs and with Pb-O bond lengths ranging between 0.23 and 0.25 nm. The PbO3/PbO4 ratio shows a small but monotonic increase from ∼70:30 to 80:20 as the PbO content increases from 30 to 70 mol %. When taken together, the isotropic and anisotropic 207Pb NMR spectra suggest that the majority of the PbOn (3 ≤ n ≤ 4) pyramids in these glasses are connected to the SiO4 tetrahedra via Pb-O-Si linkages. A significant fraction of Pb-O-Pb linkages, where the oxygen is linked only to Pb atoms, appears only in glasses with PbO ≥ 60 mol %. These oxygen atoms appear to be corner-shared between the PbOn pyramids in the structure, and no evidence for edge-sharing between these pyramids is observed in this composition range. We hypothesize that a substantial fraction of the constituent PbOn pyramids start to participate in edge-sharing only at higher PbO contents (>70 mol %), which diminishes the glass-forming ability of the network. This work illustrates the potential of isotropic-anisotropic correlation NMR spectroscopy in structural studies involving nuclides with large chemical shift ranges and anisotropy.

Benchmark Study on the Calculation of 207Pb NMR Chemical Shifts.

A benchmark set for the computation of 207Pb nuclear magnetic resonance (NMR) chemical shifts is presented. The PbS50 set includes conformer ensembles of 50 lead-containing molecular compounds and their experimentally measured 207Pb NMR chemical shifts. Various bonding motifs at the Pb center with up to seven bonding partners are included. Six different solvents were used in the measurements. The respective shifts lie in the range between +10745 and -5030 ppm. Several calculation settings are assessed by evaluating computed 207Pb NMR shifts for the use with different density functional approximations (DFAs), relativistic approaches, treatment of the conformational space, and levels for geometry optimization. Relativistic effects were included explicitly with the zeroth order regular approximation (ZORA), for which only the spin-orbit variant was able to yield reliable results. In total, seven GGAs and three hybrid DFAs were tested. Hybrid DFAs significantly outperform GGAs. The most accurate DFAs are mPW1PW with a mean absolute deviation (MAD) of 429 ppm and PBE0 with an MAD of 446 ppm. Conformational influences are small as most compounds are rigid, but more flexible structures still benefit from Boltzmann averaging. Including explicit relativistic treatments such as SO-ZORA in the geometry optimization does not show any significant improvement over the use of effective core potentials (ECPs).

Composition‐dependent structural role of lead in aluminoborate and galloborate glasses: A solid‐state NMR study

AbstractInvestigations on binary lead‐bearing glass systems have shown that Pb2+ functions as a charge compensator at low concentrations and can participate in network formation at higher loadings. We use multinuclear magnetic resonance spectroscopy to investigate the mechanism underlying this dual‐role nature of Pb2+ in ternary lead‐borate glasses containing aluminum or gallium. 207Pb nuclear magnetic resonance (NMR) spectra—in conjunction with charge‐balance calculations, bond‐valence principles, and precedents from crystalline lead‐borates—are interpreted in terms of high‐ and low‐coordinate Pb2+ species, representing charge‐compensating “network modifier” sites and covalently‐bound “network forming” sites, respectively. Both high‐field 27Al and 71Ga magic‐angle spinning NMR spectra indicate the presence of substantial fractions of four, five, and six‐fold coordinated Al/Ga, reinforcing the isostructural nature of these elements. However, systematic differences in the boron speciation in Al‐ and Ga‐bearing glasses reveal that their size difference has a measurable effect on the short‐range structure in these glasses.

(Invited) Advances in Photon-Harvesting Technologies for Perovskite Absorbers and Water Splitting Reactions

Hybrid halide perovskites have made significant progress in power conversion efficiencies (> 25 %) and high stability achieved through chemical engineering of the AMX3 composition. Compositional engineering of perovskite precursor inks minimizes batch-to-batch variations and fluctuation in PCE values, however the understanding of perovskite inks and solution behavior remains a key step towards the exploitation of solution-processed perovskite devices. Herein, a comprehensive 207Pb nuclear magnetic resonance spectroscopy (NMR) study performed on various lead perovskite precursor inks will be presented. The NMR data provide fresh insights in identifying molecular species that are invariably and predominantly formed in precursor mixtures to coexist with larger networks and colloids. The solution chemistry of PbI2+I- is dominated by the type of connectivity as edge- face- and corner-sharing (PbI6)-octahedra and their dimensionality. The trends in the 207Pb chemical shifts revealed dynamic equilibria in the inks that can be controlled by stoichiometry, nature of the solvents and temperature. Furthermore, perovskite precursor ink development can be applied to fabricate devices beyond the planar device structures, such as direct electrospinning of the three major perovskite solar cell components, namely, photo absorber, hole, and electron transport materials, as continuous single triaxial fibers of μm radial dimensions. These perovskite fibers lay the foundation of materials engineering for fabricating tiny solar cells, which can either be woven into fabrics or incorporated as single fibers to power wearables and a variety of devices or sensors, forming the internet of things. They are also suited for tandem PV-PEC set-up for solar-assisted photoelectrochemical production of hydrogen by water-splitting reactions.

Pascoite Minerals and Potential Application of NMR Spectroscopy

The 20 minerals encompassing the pascoite family of decavanadate isopolyanion-containing [V10O28]6− minerals include a few minerals, such as rakovanite, that have been described as containing a protonated decavanadate anion. Rakovanite was originally assigned the formula Na3[H3V10O28]•15H2O and now is redefined with an ideal formula (NH4)3Na3[V10O28]•12H2O. Nuclear magnetic resonance (NMR) and particularly 51V NMR spectroscopy is an informative method used to describe the protonation state and speciation in both solid and solution states of materials in the chemical and life sciences. However, 51V NMR spectroscopy has not yet been used experimentally to distinguish the protonation state of the decavanadate ion of leaching solutions and thus contributing to the discussion regarding the controversial protonation states of decavanadate ions in gunterite, rakovanite, and nashite. In contrast, the morphology and crystal structure for apatites, vanadinite, pyromorphite, and mimetite was related to 207Pb NMR chemical shifts, assisting in describing the local environments of these minerals. NMR spectroscopy could be a useful method if used in the future for decavanadate-containing minerals. Currently, partial reduction of two Pascoite minerals (caseyite and nashite) is proposed and accordingly could now effectively be investigated using a different magnetic resonance technique, EPR spectroscopy.

Untying the Cesium "Not": Cesium-Iodoplumbate Complexation in Perovskite Solution-Processing Inks Has Implications for Crystallization.

We illustrate the critical importance of the energetics of cation-solvent versus cation-iodoplumbate interactions in determining the stability of ABX3 perovskite precursors in a dimethylformamide (DMF) solvent medium. We have shown, through a complementary suite of nuclear magnetic resonance (NMR) and computational studies, that Cs+ exhibits significantly different solvent vs iodoplumbate interactions compared to organic A+-site cations such as CH3NH3+ (MA+). Two NMR studies were conducted: 133Cs NMR analysis shows that Cs+ and MA+ compete for coordination with PbI3- in DMF. 207Pb NMR studies of PbI2 with cationic iodides show that perovskite-forming Cs+ (and, somewhat, Rb+) do not comport with the 207Pb chemical shift trend found for Li+, Na+, and K+. Three independent computational approaches (density functional theory (DFT), ab initio Molecular Dynamics (AIMD), and a polarizable force field within Molecular Dynamics) yielded strikingly similar results: Cs+ interacts more strongly with the PbI3- iodoplumbate than does MA+ in a polar solvent environment like DMF. The stronger energy preference for PbI3- coordination of Cs+ vs MA+ in DMF demonstrates that Cs+ is not simply a postcrystallization cation "fit" for the perovskite A+-site. Instead, it may facilitate preorganization of the framework precursor that eventually transforms into the crystalline perovskite structure.

Triphenyllead Hydroperoxide: A 1D Coordination Peroxo Polymer, Single-Crystal-to-Single-Crystal Disproportionation to a Superoxo/Hydroxo Complex, and Application in Catalysis.

The synthesis, transformation, and application in catalysis of triphenyllead hydroperoxide, the first dioxygen lead complex, are described. Triphenyllead hydroperoxide is characterized by 207Pb nuclear magnetic resonance (NMR), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, and single-crystal X-ray diffraction, revealing the first one-dimensional (1D) coordination peroxo polymer. Photolytic isomorphous transformation of Ph3PbOOH yields a mixed hydroxo/superoxo crystalline structure, the first nonalkali superoxo crystalline metal salt, which is stable up to 100 °C. Upon further photolysis, another isomorphous transformation of the superoxide to hydroxide is observed. These are the first single-crystal-to-single-crystal hydroperoxide-to-superoxide and then to hydroxide transformations reported to date. Photolysis of triphenyllead hydroperoxide yields two forms of superoxide-doped crystalline structures that are distinguished by widely different characteristic relaxation times. The use of Ph3PbOOH as an easy-to-handle solid two-electron oxidant for the highly enantioselective epoxidation of olefins is described.

In situ NMR Investigation of the Photoresponse of Perovskite Crystal

Summary Hybrid perovskites are outstanding candidates for use in optoelectronic devices. Nonetheless, hybrid perovskites present numerous fundamental issues that are not yet fully understood. This study seeks to address this problem by reporting on the occurrence of ultraslow dynamic orientation changes in the methylammonium (MA) cations and the corresponding changes in the inorganic lattice of MAPbI3 perovskite crystals occurring over a time scale of 100 s under continuous illumination based on in situ single-crystal 2H nuclear magnetic resonance and in situ X-ray diffraction results. The demonstrated ultraslow dynamic changes in MAPbI3 are far slower than elementary molecular motions typically having time scales of femtoseconds and picoseconds and have never been reported previously. The ultraslow dynamic changes have been correlated with the reduction of band gap and the increase of absorption coefficient of MAPbI3, providing the molecular origins of the stabilization process in the photoresponse of the MAPbI3 device.

Relationship between 207Pb NMR chemical shift and the morphology and crystal structure for the apatites Pb5(AO4)3Cl, vanadinite (A = V), pyromorphite (A = P), and mimetite (A = As)

Abstract In this paper, we discuss information on crystal structure and morphology available from nuclear magnetic resonance (NMR) spectroscopy of 207Pb for the mineral family [Pb(4f)]2[Pb(6h)]3(AO4)3Cl with A = V (vanadinite), P (pyromorphite), and As (mimetite). The isotropic chemical shift of the 207Pb atoms at Wyckoff positions 4f and 6h was (re-)determined from either static single-crystal or magic angle spinning NMR experiments. This isotropic shift can be linearly correlated to the unit-cell volume within the mineral family, and in the wider context of lead-bearing minerals, to the shortest Pb-O distance for position 4f, in which 207Pb is solely coordinated by oxygen. By evaluating the number of resonances and their respective line widths in the 207Pb-NMR spectra of these three naturally grown minerals, it could be established that vanadinite forms single-domain macroscopic crystals with very small mosaicity, whereas pyromorphite crystals show NMR characteristics, which can be interpreted as being caused by significant mosaicity. In some instances, this mosaic spread could be quantitatively approximated by a Gaussian distribution with a standard deviation angle of σ = 5°. In contrast, our mimetite specimen was composed of multiple sub-crystals with a very high variability of orientations, going beyond mere mosaicity effects. By extending the NMR methodology presented here to other minerals, it may be possible to gain new insights about structure-property relationships and the morphology of natural grown minerals.

Lead‐207 NMR spectroscopy at 1.4 T: Application of benchtop instrumentation to a challenging I = ½ nucleus

The practicality of obtaining liquid- and solid-state 207 Pb nuclear magnetic resonance (NMR) spectra with a low permanent-field magnet is investigated. Obtaining 207 Pb NMR spectra of salts in solution is shown to be viable for samples as dilute as 0.05 M. The concentration dependence of the 207 Pb chemical shifts for lead nitrate was investigated; the results are comparable with those obtained with high-field instruments. Likewise, the isotope effect of substituting D2 O for H2 O as the solvent was investigated and found to be comparable with those reported previously. Obtaining solid-state 207 Pb NMR spectra is challenging, but we demonstrate the ability to obtain such spectra for three unique solid samples. An axially symmetric 207 Pb powder pattern for lead nitrate and the powder pattern expected for lead chloride reveal linewidths dominated by shielding anisotropy, while 207 Pb-35/37 Cl J-coupling dominates in the methylammonium lead chloride perovskite material. Finally, recent innovations and the future potential of the instruments are considered.

Phase Evolution in Methylammonium Tin Halide Perovskites with Variable Temperature Solid-State 119Sn NMR Spectroscopy

Hybrid organic–inorganic metal-halide perovskite materials are an emerging class of materials that could profoundly change the optoelectronic and solar absorber research fields and have far-reaching applications. Unfortunately, the leading solar-absorbing candidates are lead-containing materials and suffer from chemical instability, eventually decomposing, resulting in detrimental long-term environmental concerns. A series of nontoxic group 14 Sn(II)-based hybrid organic–inorganic metal-halide perovskites is investigated using variable-temperature solid-state nuclear magnetic resonance (NMR) spectroscopy to examine their unique phases that appear between 150 and 540 K. Each phase of the MASnX3 (MA+ = CH3NH3+ and X– = Cl–, Br–, or I–) series is identified and compared to results from quantum chemical calculations of anionic polyhedron clusters. The analysis of the polyhedra about the Sn center is further related to the measured chemical shift anisotropy present when Sn deviates from octahedral symmetry. We also discuss the rapid degradation of pristine MASnI3 over 2 days studied using in situ 119Sn NMR spectroscopy. Finally, we report on the 1H, 13C, 119Sn, and 207Pb NMR structural properties of a Sn/Pb mixed B-site (MASn0.5Pb0.5I3) perovskite, demonstrating the sensitivity of the chemical shift to B-site substitution.

Lead-Halide Scalar Couplings in 207Pb NMR of APbX3 Perovskites (A\u2009=\u2009Cs, Methylammonium, Formamidinium; X\u2009=\u2009Cl, Br, I)

Understanding the structure and dynamics of newcomer optoelectronic materials - lead halide perovskites APbX3 [A = Cs, methylammonium (CH3NH3+, MA), formamidinium (CH(NH2)2+, FA); X = Cl, Br, I] - has been a major research thrust. In this work, new insights could be gained by using 207Pb solid-state nuclear magnetic resonance (NMR) spectroscopy at variable temperatures between 100 and 300 K. The existence of scalar couplings 1JPb-Cl of ca. 400 Hz and 1JPb-Br of ca. 2.3 kHz could be confirmed for MAPbX3 and CsPbX3. Diverse and fast structure dynamics, including rotations of A-cations, harmonic and anharmonic vibrations of the lead-halide framework and ionic mobility, affect the resolution of the coupling pattern. 207Pb NMR can therefore be used to detect the structural disorder and phase transitions. Furthermore, by comparing bulk and nanocrystalline CsPbBr3 a greater structural disorder of the PbBr6-octahedra had been confirmed in a nanoscale counterpart, not readily captured by diffraction-based techniques.

13C and 207Pb NMR Chemical Shifts of Dirhodio- and Dilithioplumbole Complexes: A Quantum Chemical Assessment.

Density functional theory (DFT) and zeroth-order regular approximation DFT calculations were performed to investigate the electronic structures and 13C and 207Pb nuclear magnetic resonance (NMR) chemical shifts of metal-coordinated plumboles, namely, monorhodioplumbole ([Rh-plumbole]-), dirhodioplumbole (Rh2-plumbole), and dilithioplumbole (Li2-plumbole), which have a five-membered ring containing lead. The molecular orbital correlation diagram and extended transition state-natural orbitals for chemical valence analysis of the [Rh-plumbole]- and Rh2-plumbole complexes showed that the plumbole is primarily a π-donor, with π-donation being dominant in the Rh2-plumbole complex. The present calculations show that the Pb-Cα internuclear distances are longer in the Rh2-plumbole complex than in [Rh-plumbole]- because of the combined effect of strong π-donation and weak π-back-donation in the Rh2-plumbole complex. The calculated 207Pb and 13Cα NMR chemical shifts agree with the experimental trends reasonably well. The influences of the relativistic effect, role of the functional, effect of the solvent, and dependence of the exact exchange admixture on the calculated 207Pb and 13Cα NMR chemical shifts were investigated. The NMR chemical shift trend of the 207Pb atom in the complexes originates from the paramagnetic and spin-orbit contributions. NMR component analysis revealed that the upfield shift of the 13Cα atoms of the [Rh-plumbole]- and Rh2-plumbole complexes compared to that of the Li2-plumbole complex is mainly due to the decrease in the paramagnetic term.

Chemical exchange at the ferroelectric phase transition of lead germanate revealed by solid state 207Pb nuclear magnetic resonance.

The nature of the dynamics and structural changes that take place at the ferroelectric phase transition in lead oxides is a rich field of study. Solid-state nuclear magnetic resonance (NMR) of 207Pb is well suited to study the local structure and disorder in lead oxide ferroelectric transitions at the atomic level. However, very large 207Pb shielding anisotropy results in poor resolution in 1D static and magic angle spinning (MAS) NMR spectra. We address this problem by using short high-power adiabatic pulses (SHAPs) with magic-angle-turning sequences to correlate the isotropic and anisotropic parts of the 207Pb chemical shift tensor in a 2D NMR experiment, yielding resolved 207Pb NMR spectra of the nine distinct lead sites in uniaxial ferroelectric lead germanate (Pb5Ge3O11). Using this technique we detect the magnetic environments of displaced Pb2+ ions and unambiguously identify the nature of the phase transition as mixed displacive and order-disorder. We also observe that the atomic-level process responsible for the phase transition in ferroelectric lead germanate is chemical exchange on the kilohertz timescale. We derive an activation energy of 103.4 ± 1.7 kJ mol-1 and compare it to dielectric spectroscopy studies on similar materials. These results show that this method can be used to characterize ferroelectric phase transitions of complex materials with high resolution using nuclei that are typically inaccessible due to their large shielding anisotropy.

207Pb nuclear magnetic resonance study in PbWO4:Mn2+ and PbWO4:Dy3+ single crystals

207Pb nuclear magnetic resonance study in PbWO4:Mn2+ and PbWO4:Dy3+ single crystals

Fully gapped spin-singlet superconductivity in noncentrosymmetricPbTaSe2:Pb207nuclear magnetic resonance study

We report the $^{207}$Pb nuclear magnetic resonance (NMR) measurements on polycrystalline sample of PbTaSe$_2$ with noncentrosymmetric crystal structure and topological electronic band. The nuclear spin-lattice relaxation rate $1/T_1$ shows a suppressed coherence peak below the superconducting transition temperature $T_{\rm c}$ = 4.05 K and decreases as an exponential function of temperature. The penetration depth derived from the NMR spectrum is almost temperature independent below $T$ = 0.7 $T_{\rm c}$. The Knight shift $K$ decreases below $T_{\rm c}$. These results suggest spin-singlet superconductivity with a fully-opened gap $2\Delta = 3.5$ $k_{\rm B}T_{\rm c}$ in PbTaSe$_2$.

Methylammonium lead chloride: A sensitive sample for an accurate NMR thermometer

A new solid-state nuclear magnetic resonance (NMR) thermometry sample is proposed. The 207Pb NMR chemical shift of a lead halide perovskite, methylammonium lead chloride (MAPbCl3) is very sensitive to temperature, 0.905±0.010ppmK−1. The response to temperature is linear over a wide temperature range, from its tetragonal to cubic phase transition at 178K to >410K, making it an ideal standard for temperature calibrations in this range. Because the 207Pb NMR lineshape for MAPbCl3 appears symmetric, the sample is ideal for calibration of variable temperature NMR data acquired for spinning or non-spinning samples. A frequency-ratio method is proposed for referencing 207Pb chemical shifts, based on the 1H and 13C frequencies of the methylammonium cation, which are used asan internal standard. Finally, this new NMR thermometer has been used to measure the degree of frictional heating asa function of spinning frequency for a series of MAS rotors ranging in outer diameter from 1.3 to 7.0mm. As expected, the largest diameter rotors are more susceptible to frictional heating, but lower diameter rotors are subjected to higher frictional heating temperatures as they are typically spun at much higher spinning frequencies.

NMR absolute shielding scale and nuclear magnetic dipole moment of (207)Pb.

An absolute shielding scale is proposed for (207)Pb nuclear magnetic resonance (NMR) spectroscopy. It is based on ab initio calculations performed on an isolated tetramethyllead Pb(CH3)4 molecule and the assignment of the experimental resonance frequency from the gas-phase NMR spectra of Pb(CH3)4, extrapolated to zero density of the buffer gas to obtain the result for an isolated molecule. The computed (207)Pb shielding constant is 10 790 ppm for the isolated molecule, leading to a shielding of 10799.7 ppm for liquid Pb(CH3)4 which is the accepted reference standard for (207)Pb NMR spectra. The new experimental and theoretical data are used to determine μ((207)Pb), the nuclear magnetic dipole moment of (207)Pb, by applying the standard relationship between NMR frequencies, shielding constants and nuclear moments of two nuclei in the same external magnetic field. Using the gas-phase (207)Pb and (reference) proton results and the theoretical value of the Pb shielding in Pb(CH3)4, we find μ((207)Pb) = 0.59064 μN. The analysis of new experimental and theoretical data obtained for the Pb(2+) ion in water solutions provides similar values of μ((207)Pb), in the range of 0.59000-0.59131 μN.

Analysis of Lead Carboxylates and Lead-Containing Pigments in Oil Paintings by Solid- State Nuclear Magnetic Resonance

ABSTRACTSoap formation in traditional oil paintings occurs when heavy-metal-containing pigments, such as lead white, 2Pb(CO3)2·Pb(OH)2, and lead-tin yellow type I, Pb2SnO4, react with fatty acids in the binding medium. These soaps may form aggregates that can be 100-200 μm in diameter, which swell and protrude through the paint surface, resulting in the degradation of the paint film and damage to the integrity of the artwork. In addition, soap formation has been reported to play a role in the increased transparency of paint films that allows the painting support, the preparatory drawing, and the artists’ alterations to become visible to the naked eye. The factors that trigger soap formation and the mechanism(s) of the process are not yet well understood. To elucidate these issues, chemical and structural information is necessary which can be obtained by solid-state 207Pb, 119Sn, and 13C nuclear magnetic resonance (NMR). In the present study, a combination of 207Pb NMR pulse sequences was used to determine accurately the NMR parameters of lead-containing pigments and lead carboxylates known to be involved in soap formation, such as lead palmitate, lead stearate, and lead azelate. These results show that the local coordination environment of lead azelate is different from lead palmitate or lead stearate and therefore it is unlikely that lead azelate would be incorporated into an ordered structure containing lead palmitate and lead stearate. In addition, the chemical shifts of the pigments obtained are different from those of the soaps, demonstrating that 207Pb NMR is useful in characterizing the components when present in a mixture, such as a paint film. The NMR methods discussed can also be applied to other Pb-containing cultural heritage materials, electronic and optoelectronic materials, superconducting materials, and environmentally contaminated materials.

Nuclear Magnetic Resonance Spectra and 207Pb Chemical-Shift Tensors of Lead Carboxylates Relevant to Soap Formation in Oil Paintings

Soap formation in traditional oil paintings occurs when heavy-metal-containing pigments, such as lead white, 2PbCO3·Pb(OH)2, and lead tin yellow type I, Pb2SnO4, react with fatty acids in the binding medium. These soaps may form aggregates that can be 100-200 μm in diameter, which swell and protrude through the paint surface, resulting in the degradation of the paint film and damage to the integrity of the artwork. The factors that trigger soap formation and the mechanism(s) of the process are not yet well understood. To elucidate these issues, chemical and structural information is necessary, which can be obtained using solid-state (207)Pb and (13)C nuclear magnetic resonance (NMR). In this article, we report (207)Pb and (13)C solid-state NMR spectra and (207)Pb chemical-shift tensors of lead carboxylates implicated in soap formation: lead stearate, lead palmitate, and lead azelate, in addition to lead oleate and lead heptanoate for comparison. The (13)C cross polarization with magic-angle spinning (MAS) spectra of these lead carboxylates show resonance doubling for the carbons closest to the lead, indicating two different conformations of the fatty acid chains in the asymmetric unit. The (207)Pb NMR spectra, from which tensors were determined, were obtained with direct excitation and spin-temperature alternation, with and without MAS, and with the wide band uniform rate smooth truncation Carr-Purcell-Meiboom-Gill pulse sequence. The results of these experiments show that the local coordination environment of lead azelate is different from lead palmitate and lead stearate and could thus be distinguished from these in a paint film displaying soap formation. In addition, comparing the (207)Pb NMR chemical-shift tensors of the lead carboxylates studied shows that crystal packing of the acyl chains may be a factor in determining the coordination environment around the lead.