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2. Understanding Soap Formation in Paint Films by 207Pb, 119Sn, and 13C Solid-State NMR

   Catalano, J. ; Yao, Y. ; Murphy, A. ; Zumbulyadis, N. ; Centeno, S.A. ; Dybowski, C. ( October 2014 , Materials science and technology)

   The formation of lead carboxylates (lead soaps) has been identified as the cause of deterioration of hundreds of oil paintings. Soaps form when heavy metal-containing pigments, for example lead white and lead-tin yellow, react with saturated fatty acids in the oil medium. Understanding the mechanism of the reactions requires chemical information, which can be obtained with solid-state ²⁰⁷Pb, ¹¹⁹Sn and ¹³C NMR spectroscopy. Using the chemical-shift tensors determined by solid-state NMR we can gain structural insights on the coordination environment of the lead carboxylates and identify and quantify components in a paint film mixture. We have examined the spectroscopy of lead-containing pigments, lead carboxylates, and model paint films that were subjected to accelerated aging. We have also begun to investigate the dynamics of soap formation by ¹³C NMR spectroscopy. The NMR methods applied to the model paint systems could also be applied to other lead-containing materials. 

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4. Revealing the Surface Structure of CdSe Nanocrystals by Dynamic Nuclear Polarization-Enhanced 77 Se and 113 Cd Solid-State NMR Spectroscopy

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5. Enhancing the resolution of 1 H and 13 C solid-state NMR spectra by reduction of anisotropic bulk magnetic susceptibility broadening

   https://doi.org/10.1039/C7CP04223J  

   Hanrahan, Michael P. ; Venkatesh, Amrit ; Carnahan, Scott L. ; Calahan, Julie L. ; Lubach, Joseph W. ; Munson, Eric J. ; Rossini, Aaron J. ( January 2017 , Phys. Chem. Chem. Phys.)

   We demonstrate that natural isotopic abundance 2D heteronuclear correlation (HETCOR) solid-state NMR spectra can be used to significantly reduce or eliminate the broadening of 1 H and 13 C solid-state NMR spectra of organic solids due to anisotropic bulk magnetic susceptibility (ABMS). ABMS often manifests in solids with aromatic groups, such as active pharmaceutical ingredients (APIs), and inhomogeneously broadens the NMR peaks of all nuclei in the sample. Inhomogeneous peaks with full widths at half maximum (FWHM) of ∼1 ppm typically result from ABMS broadening and the low spectral resolution impedes the analysis of solid-state NMR spectra. ABMS broadening of solid-state NMR spectra has previously been eliminated using 2D multiple-quantum correlation experiments, or by performing NMR experiments on diluted materials or single crystals. However, these experiments are often infeasible due to their poor sensitivity and/or provide limited gains in resolution. 2D 1 H– 13 C HETCOR experiments have previously been applied to reduce susceptibility broadening in paramagnetic solids and we show that this strategy can significantly reduce ABMS broadening in diamagnetic organic solids. Comparisons of 1D solid-state NMR spectra and 1 H and 13 C solid-state NMR spectra obtained from 2D 1 H– 13 C HETCOR NMR spectra show that the HETCOR spectrum directly increases resolution by a factor of 1.5 to 8. The direct gain in resolution is determined by the ratio of the inhomogeneous 13 C/ 1 H linewidth to the homogeneous 1 H linewidth, with the former depending on the magnitude of the ABMS broadening and the strength of the applied field and the latter on the efficiency of homonuclear decoupling. The direct gains in resolution obtained using the 2D HETCOR experiments are better than that obtained by dilution. For solids with long proton longitudinal relaxation times, dynamic nuclear polarization (DNP) was applied to enhance sensitivity and enable the acquisition of 2D 1 H– 13 C HETCOR NMR spectra. 2D 1 H– 13 C HETCOR experiments were applied to resolve and partially assign the NMR signals of the form I and form II polymorphs of aspirin in a sample containing both forms. These findings have important implications for ultra-high field NMR experiments, optimization of decoupling schemes and assessment of the fundamental limits on the resolution of solid-state NMR spectra. 

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