13C Solid-state Nuclear Magnetic Resonance Spectrum Research Articles

Catalytic Upgrading of Acetaldehyde to Acetoin Using a Supported N-Heterocyclic Carbene Catalyst.

We report the catalytic synthesis of 3-hydroxy-2-butanon (acetoin) from acetaldehyde as a key step in the synthesis of C4-molecules from ethanol. Facile C-C bond formation at the α-carbon of the C2 building block is achieved using an N-heterocyclic carbene (NHC) catalyst. The immobilization of the catalyst on a Merrifield's peptide resin and its spectroscopic characterisation using solid-state Nuclear Magnetic Resonance (NMR) is described herein. The immobilization of the NHC catalyst allows for process intensification steps and the reported catalytic system was subjected to batch recycling as well as continuous flow experiments. The robustness of the catalytic system was shown over a maximum of 10 h time-on-stream. Overall, high selectivity S>90 % was observed. The observed deactivation of the catalyst with increasing time-on-stream is explained by ex-situ 1H solution-state, as well as 13C and 15N solid-state NMR spectra allowing us to develop a deeper understanding of the underlying decomposition mechanism of the catalyst.

Formylation of Recombinant Spider Silk in Formic Acid and Wet Spinning Studied Using Nuclear Magnetic Resonance and Infrared Spectroscopies.

We reported wet spinning of recombinant spider silk protein (RSSP) and formylation of RSSP in formic acid (FA). First, FA was selected as the spinning solvent and the detailed spinning condition was determined. Next, the mechanical property was compared between the RSSP fiber spun after allowing the spinning solution dissolved in FA to stand for 2 days and the fiber spun immediately after being dissolved in FA for 4 h. The tensile strength of the former fiber was lower than the strength of the latter fiber. This difference can be explained by the difference in the degree of formylation as follows. FA is a known formylating agent, although most researchers who prepared silk fiber by wet spinning with FA have not pointed out about formylation. The formylation of the Ser OH group was confirmed by 13C solution nuclear magnetic resonance (NMR), and the time course of formylation of the RSSP film prepared from the FA solution was tracked by Fourier transform infrared spectroscopy. The 13C solid-state NMR spectra were also compared between two kinds of the formylated RSSP fibers and indicated that the packing state was tighter for the latter fiber than the former one, which could explain higher tensile strength of the latter fiber in the dry state. The sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis indicated that the RSSP sample decomposed gradually with storage time in FA and the decomposition has begun partly even at 2 h after dissolution in FA. The decomposition by formylation seems to have no significant effect on the backbone structure of the RSSP fiber, although the packing of the fiber becomes loose as a whole. Finally, preliminary trial of deformylation of the formylated RSSP fiber was performed.

The Boltzmann-Monte-Carlo-Percolation (BMCP) model on pyrolysis of coal: The quantitative correction on CP/MAS 13C solid-state NMR spectra and insight on structural evolution during coalification

Because of the Nuclear Overhauser Effect (NOE), the quantitative bonds’ population can hardly be obtained directly from Cross-polarization Magic Angle Spinning (CP/MAS) 13C solid-state Nuclear Magnetic Resonance (NMR) spectra. Thus, correction must be carried out to obtain the bonds’ population with high precision. In this work, the correction factor was derived from Solomon equation, and the previously developed Boltzmann-Monte-Carlo-Percolation (BMCP) model was employed reversely to the calculate correction factor from the tar yields of coal pyrolysis. The results showed that correction on the bonds’ population from tar yields improved the prediction results both on the bonds’ population and product distribution; the correction factor showed an abrupt trend corresponding to coalification jumps. Furthermore, an empirical equation for calculating the correction factor was obtained. The success of the correction indicates that the pyrolysis behaviors of coals under moderate conditions are governed by the bonds’ population, and BMCP model is a proper way to describe the structure–activity relationship quantitatively.

Selective One-Dimensional 13C-13C Spin-Diffusion Solid-State Nuclear Magnetic Resonance Methods to Probe Spatial Arrangements in Biopolymers Including Plant Cell Walls, Peptides, and Spider Silk.

Two-dimensional (2D) and 3D through-space 13C-13C homonuclear spin-diffusion techniques are powerful solid-state nuclear magnetic resonance (NMR) tools for extracting structural information from 13C-enriched biomolecules, but necessarily long acquisition times restrict their applications. In this work, we explore the broad utility and underutilized power of a chemical shift-selective one-dimensional (1D) version of a 2D 13C-13C spin-diffusion solid-state NMR technique. The method, which is called 1D dipolar-assisted rotational resonance (DARR) difference, is applied to a variety of biomaterials including lignocellulosic plant cell walls, microcrystalline peptide fMLF, and black widow dragline spider silk. 1D 13C-13C spin-diffusion methods described here apply in select cases in which the 1D 13C solid-state NMR spectrum displays chemical shift-resolved moieties. This is analogous to the selective 1D nuclear Overhauser effect spectroscopy (NOESY) experiment utilized in liquid-state NMR as a faster (1D instead of 2D) and often less ambiguous (direct sampling of the time domain data, coupled with increased signal averaging) alternative to 2D NOESY. Selective 1D 13C-13C spin-diffusion methods are more time-efficient than their 2D counterparts such as proton-driven spin diffusion (PDSD) and dipolar-assisted rotational resonance. The additional time gained enables measurements of 13C-13C spin-diffusion buildup curves and extraction of spin-diffusion time constants TSD, yielding detailed structural information. Specifically, selective 1D DARR difference buildup curves applied to 13C-enriched hybrid poplar woody stems confirm strong spatial interaction between lignin and acetylated xylan polymers within poplar plant secondary cell walls, and an interpolymer distance of ∼0.45-0.5 nm was estimated. Additionally, Tyr/Gly long-range correlations were observed on isotopically enriched black widow spider dragline silks.

Boosting CO2 Conversion with Terminal Alkynes by Molecular Architecture of Graphene Oxide-Supported Ag Nanoparticles

Summary Carboxylation of terminal alkynes with CO2 via direct C–H bond activation is a highly appealing way to capture and convert CO2 but faces great challenges and difficulty. Here, we report an efficient catalyst that is prepared simply through introduction of p-tert-butylaniline into graphite oxide powders followed by localized growth of Ag nanoparticles (NPs). The bulky nature of p-tert-butylaniline facilitates the powder exfoliation, giving rise to mass production of uniform modified graphene oxide (tert-GO) nanosheets of 4 nm in thickness. Notably, Ag/tert-GO shows excellent catalytic activity for converting alkynes regardless of containing electron-donating or electron-withdrawing groups under mild reaction conditions. The synergy of the amide linkages on tert-GO nanosheets and the supported small-sized Ag NPs is recognized as the vital role in promoting adsorption of CO2 and subsequent conversion.

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.

Solid-State NMR Characterization of the Structure of Self-Assembled Ile–Phe–OH

Solid-state nuclear magnetic resonance (NMR) spectroscopy provides significant structural information regarding the conformation and dynamics of a variety of solid samples. In this study, we recorded the 13C and 15N solid-state NMR spectra of a self-assembled isoleucine-phenylalanine (Ile–Phe–OH) dipeptide. Immediately after the addition of hexane to a solution of concentrated peptide in ethyl acetate, the peptide visually aggregated into a nanofiber. Then, we obtained well-resolved 13C and 15N NMR signals of the natural, isotopic-abundant Ile–Phe–OH peptide in the nanofiber. Furthermore, we calculated the chemical shift values of the reported crystal structure of the Ile–Phe dipeptide via the density functional theory (DFT) calculation and compared these results with the experimental values. Notably, the two sets of values were in good agreement with each other, which indicated that the self-assembled structure closely reflected the crystal structure. Therefore, herein, we demonstrated that solid-state NMR characterization combined with DFT calculations is a powerful method for the investigation of molecular structures in self-assembled short peptides.

X-ray Absorption and Solid-State NMR Spectroscopy of Fluorinated Proton Conducting Polymers

19F and 13C solid-state nuclear magnetic resonance (SSNMR) spectra and near edge X-ray absorption fine structure (NEXAFS) spectra at the S 2p, C 1s, O 1s, and F 1s edges of three different types of perfluorosulfonic acid (PFSA) proton conducting polymers are reported. The NEXAFS spectra were recorded in a scanning transmission X-ray microscope (STXM). They are reported on quantitative intensity scales, suitable for use as reference standards for analytical spectromicroscopy studies. The NEXAFS spectral features are assigned using comparisons to the corresponding spectra of small molecule and polymer analogues, including C 1s and F 1s spectra of polytetrafluoroethylene (PTFE) recorded using STXM. The 19F and 13C SSNMR spectra are reported and analyzed. Within each type of spectroscopy, the spectra of the three types of PFSA are very similar. However, small but statistically significant differences were identified which give insights into how minor molecular structure differences are reflected in the SSNMR ...

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.

Mechanism of Nanoparticle Formation from Ternary Coground Phenytoin and Its Derivatives

The mechanism of drug nanoparticle formation of phenytoin (DPH) and its derivatives monomethylphenytoin (MDPH) and dimethylphenytoin (DMDPH) was investigated. The drug, polyvinylpyrrolidone K17 (PVP), and sodium dodecyl sulfate were coground to obtain the ground mixture (GM). The DPH GM was amorphous; however, MDPH and DMDPH GMs contained drug crystals. Spectral changes in infrared and (13)C solid-state nuclear magnetic resonance were observed in the DPH GM, partially observed in the MDPH GM, and hardly observed in the DMDPH GM. Mean particle sizes of the DPH, MDPH, and DMDPH GM nanosuspension were almost the same; however, stability after storage differed in the order of DPH > MDPH > DMDPH. The intermolecular interaction between the drug and PVP reflected not only the crystallinity of the drug in the GM but also the stability of the GM suspension. The size and stiffness of drug nanoparticles were evaluated using atomic force microscopy. Crystallization of the amorphous GM and agglomeration of the primary nanocrystals were observed in the DPH GM suspension. In contrast, primary nanocrystals were observed in the DMDPH GM suspension. The size of the drug nanocrystals formed from the different molecular states of the drug in the GM reflects the agglomerated states in water and stability.

The α-Helical C-Terminal Domain of Full-Length Recombinant PrP Converts to an In-Register Parallel β-Sheet Structure in PrP Fibrils: Evidence from Solid State Nuclear Magnetic Resonance

We report the results of solid state nuclear magnetic resonance (NMR) measurements on amyloid fibrils formed by the full-length prion protein PrP (residues 23−231, Syrian hamster sequence). Measurements of intermolecular 13C−13C dipole−dipole couplings in selectively carbonyl-labeled samples indicate that β-sheets in these fibrils have an in-register parallel structure, as previously observed in amyloid fibrils associated with Alzheimer’s disease and type 2 diabetes and in yeast prion fibrils. Two-dimensional 13C−13C and 15N−13C solid state NMR spectra of a uniformly 15N- and 13C-labeled sample indicate that a relatively small fraction of the full sequence, localized to the C-terminal end, forms the structurally ordered, immobilized core. Although unique site-specific assignments of the solid state NMR signals cannot be obtained from these spectra, analysis with a Monte Carlo/simulated annealing algorithm suggests that the core is comprised primarily of residues in the 173−224 range. These results are consistent with earlier electron paramagnetic resonance studies of fibrils formed by residues 90−231 of the human PrP sequence, formed under somewhat different conditions [Cobb, N. J., Sonnichsen, F. D., McHaourab, H., and Surewicz, W. K. (2007) Proc. Natl. Acad. Sci. U.S.A. 104, 18946−18951], suggesting that an in-register parallel β-sheet structure formed by the C-terminal end may be a general feature of PrP fibrils prepared in vitro.

Variable-temperature 13C solid-state NMR study of the molecular structure of honeybee wax and silk

To elucidate the native-state crystal structure of beeswax from the Japanese bee, Apis cerana japonica, we determined the relationship between temperature and the 13C solid-state nuclear magnetic resonance (NMR) chemical shift of methylene carbon of beeswax, with comparison to n-alkanes and polyethylene in the orthorhombic, monoclinic, or triclinic crystal form. Variable-temperature 13C solid-state NMR observations of n-alkanes and polyethylene revealed that the chemical shifts of methylene carbon in the orthorhombic crystal form increased linearly with increasing temperature, that of the triclinic form decreased, and that of the monoclinic form was unaltered. These relations were compared with results of variable-temperature 13C solid-state NMR observation of beeswax. Results clarified that the two crystal forms comprising the beeswax in the native state are orthorhombic and monoclinic. The variable-temperature 13C solid-state NMR observations were also applied to interpret the differential scanning calorimetry (DSC) curve of beeswax. They were used to clarify the structural changes of beeswax for widely various temperatures. For beeswax secreted by the Japanese bee, the transition from the orthorhombic form to the rotator phase occurred at 36 °C, that is from the crystalline to the intermediate state at 45 °C. Moreover, the variable-temperature 13C solid-state NMR spectrum of honeybee silk in the native state was observed. Results demonstrated that the secondary structures of honeybee silk proteins in the native state comprised coexisting α-helix and β-sheet conformations and that the amount of α-helices was greater. The α-helix content of honeybee silk was compared with that of hornet silk produced by Vespa larvae.

Comparisons of the Structural and Chemical Properties of Melanosomes Isolated from Retinal Pigment Epithelium, Iris and Choroid of Newborn and Mature Bovine Eyes¶

Melanosomes were isolated from the retinal pigment epithelium (RPE), iris and choroid of mature (age >2 years) and newborn (age <1 week) bovine eyes. Scanning electron microscopy was utilized to analyze the morphology of the melanosomes, which were found to vary among different tissues and different ages. While the total content of amino acids differs slightly (ranging from 9% to 15% by mass), the distributions of the amino acids are similar. The pheomelanin content is low in the choroid and the RPE (0.1-0.5%), and moderate in the iris (<2%); therefore, the major melanin component of bovine eye melanosomes is eumelanin, independent of the shape of the melanosomes. The yields of pyrrole-2,3,5-tricarboxylic acid from melanosomes decrease in the following order: choroid > iris > RPE, and exhibit decreasing yields with age. 13C solid-state nuclear magnetic resonance (NMR) spectroscopic analysis of iris and choroid melanosomes indicates the same trends. These observations suggest that the 5,6-dihydroxyindole-2-carboxylic acid contents decrease in the following order: choroid > iris > RPE, and decrease with age. Moreover, the 13C solid-state NMR spectra show (1) for the same age samples, the CH:Cq ratio for choroid is larger than that for iris melanosomes; and (2) an increase in the concentration of carbonyl groups with age within each type of melanosome.

Conductivity, DSC, and solid-state NMR studies of comb-like polymer electrolyte with a chelating functional group

The behavior of lithium ions in a comb-like polymer electrolyte with a chelating functional group has been characterized by differential scanning calorimetry (DSC), AC impedance, 13C and 7Li solid-state nuclear magnetic resonance (NMR) measurements. The comb-like copolymer is synthesized by poly(ethylene glycol) methyl ether methacrylate (PEGMEM) and (2-methylacrylic acid 3-(bis-carboxymethylamino)-2-hydroxy-propyl ester) (GMA–IDA). 7Li solid-state NMR spectra demonstrate the interactions of Li + ions with both the ether oxygen of the PEGMEM and the nitrogen atom of the GMA–IDA segments. Moreover, 7Li solid-state NMR shows that the lithium ions are preferentially coordinated to the GMA–IDA segment. Moreover, the 13C solid-state NMR spectra for the carbons attached to the ether oxygen atoms exhibited significant line broadening and a slight upfield chemical shift and short T CH when the dopant was added to the polymer. These findings indicate coordination between the Li cation and the ether oxygens in the PEG segment. T g increases for the copolymers doped with LiClO 4. These results indicate the interactions of Li + with both PEGMEM and GMA–IDA segments form transient cross-links. The Vogel–Tamman–Fulcher (VTF)-like behavior of conductivity implies the coupling of the charge carriers with the segmental motion of the polymer chains. The dependence of the maximum conductivity on the composition of the copolymers and the doping lithium ion concentration was determined. The GMA–IDA unit in the copolymer improves the dissociation of the lithium salt, the mechanical strength and the conductivity.

Nuclear magnetic resonance and infrared spectroscopic analysis of nedocromil hydrates.

Nedocromil sodium (NS), which is used in the treatment of reversible obstructive airway diseases, such as asthma, has been found to exist in the following solid phases: the heptahemihydrate, the trihydrate, a monohydrate, an amorphous phase, which contains variable amounts of water, and a recently discovered methanol + water (MW) solvate. Our aim was to apply 13C solid-state nuclear magnetic resonance (NMR) spectroscopy and solid-state Fourier transform infrared (FTIR) spectroscopy to the study of specific interactions in the various solid forms of NS. The 13C solid-state NMR and FTIR spectra of the various solid forms of NS were obtained and were related to the crystal structures of NS, the conformations of the nedocromil anion, and the interactions of the water molecules in these crystals. The 13C solid-state NMR spectrum is sensitive to the conformation of the nedocromil anion, while the solid-state FTIR spectrum is sensitive to interactions of water molecules in the solid state. In NS monohydrate, for which the crystal structure has not yet been solved, and in the amorphous phase, the information about the conformations of the nedocromil anion and the interactions of the water molecules are deduced from the 13C solid-state NMR spectra and solid-state FTIR spectra, respectively. 13C solid-state NMR spectroscopy and solid-state FTIR spectroscopy are shown to be powerful complementary tools for probing the chemical environment of molecules in the solid state, specifically the conformation of the nedocromil anion and the interactions of water-molecules, respectively.

Characterization of Silk Produced in Japan During the 12th Century

Abstract Nuclear magnetic resonance (NMR) has been widely accepted as an excellent characterization method in physics, chemistry, and biology as well as medical diagnosis. In this paper we show the applicability of NMR to archaeological polymer science. Mummies of three gentlemen are well preserved in Chusonji Temple in Northeastern Japan. They are Kiyohira Fujiwara, Motohira Fujiwara, and Hidehira Fujiwara, all belonging to the Fujiwara clans who governed Northeastern Japan in the 12th century. All of them were wound in silk. 13C solid-state high resolution NMR spectra were observed for these silks with the aid of the CP (cross polarization)/MAS (magic angle spinning) technique. For the convenience of comparison, SEM (scanning electron microscope) patterns were observed. From the former the fraction of Silk I1 (antiparallel β-sheet) structure was calculated, while from the latter the cross section and the circularity coefficient [l] of filament were determined. The fraction was defined by the ratio of in...