Two-dimensional Heteronuclear Correlation Research Articles

Ionic salt cocrystals studied via multinuclear solid-state magnetic resonance: a case study of lithium 4-methoxybenzoate:L-proline polymorphs

Lithium salts continue to find pharmaceutical applications, particularly as psychiatric medications. As with any active pharmaceutical ingredient, structural polymorphism is an important concern for lithium-based medications that can influence solubility and other physicochemical properties. Here we report a 13C, 1H, and 7Li magic-angle spinning solid-state nuclear magnetic resonance (MAS SSNMR) study of two 1:1 polymorphic ionic cocrystals of lithium 4-methoxybenzoate and L-proline (L4MPRO(α) and L4MPRO(β)). One-dimensional 13C cross-polarization MAS and two-dimensional heteronuclear correlation NMR spectra hint at differential mobilities of the proline and benzoate moieties for the two polymorphs. Five key resonances differ in 13C chemical shift by more than 1 ppm between the two polymorphs, clearly distinguishing between them. Gauge-including projector-augmented-wave density functional theory calculations of 13C and 1H magnetic shielding constants correlate strongly with the experimental chemical shifts for both polymorphs. R2 and root-mean-square deviation metrics are shown to be insufficient in the case of 13C, but sufficient in the case of 1H, for differentiating between the polymorphs. 7Li satellite-transition MAS NMR of both polymorphs are identical, as are the computed lithium magnetic shielding constants, demonstrating the insensitivity of 7Li NMR to polymorphism in these samples. This work highlights the utility of solid-state NMR spectroscopy for examining ionic salt cocrystals and also highlights some caveats in this regard.

Effective conversion of corn stalk into ethyl levulinate and crude lignin catalyzed by ionic liquids

The chemical transformation of lignocellulosic biomass into platform chemicals is one of the most efficient utilization methods for agricultural wastes. In this work, a one-pot strategy for the conversion of corn stalk to ethyl levulinate and further extraction of valorizable lignin catalyzed by ILs was proposed. With the optimized catalyst of [C3H6SO3Hmim]HSO4, corn stalk of 92.45% was transformed into ethyl levulinate with a favorable yield of 24.72% at 200 °C for 90 min. Furthermore, the lignin extraction was substantially influenced by co-solution system. A high lignin yield of 79.94% was achieved with ethanol content of 75% (v/v) in the ethanol-water system. The analysis on morphology, thermal stability and functional group showed that condensation of lignin occurred during the liquefaction process, the two-dimensional heteronuclear single quantum correlation (2D-HSQC) investigation demonstrated that the stable structure of lignin provides a favorable foundation for its valorization. Overall, this work proposed a feasible biorefinery strategy for effective conversion and utilization of lignocellulosic biomass.

Enhanced catalytic cleavage of C-O and C-C bonds of raw biomass into lignin monomers and glucose

Reductive catalytic fractionation (RCF) of lignocellulose has been considered to be a promising strategy for the separation and subsequent upgradation of biomass constituents. However, the recalcitrant C-C bonds in lignin were the major limitation to produce aromatic monomers in high yield for the hydrogenolysis of lignocellulosic biomass under mild conditions. Herein, an efficient approach was developed to catalytic in-situ hydrogenolysis of solid biomass into lignin monomers and glucose using Ni-Al catalyst with Ni2Al3 alloy phase. 62.9 wt% of aromatic monomers yield was achieved with the degree of delignification up to 89.8 %. Two-dimensional heteronuclear single quantum correlation nuclear magnetic resonance (2D HSQC NMR) spectrum emerged that the C-O and C-C bonds involving β-O-4, β-β and β-5 linkages were all catalytically broken. Moreover, the cellulose was recovered with the cellulose retention and purity of 80.1 % and 88.2 %, respectively, which was further enzymatically hydrolyzed to glucose with the yield of 92 %. Overall, the efficient fractionation and transformation of biomass constituents were realized simultaneously.

NMR Titration Studies in Z-DNA Dynamics.

Chemical shift perturbation (CSP) is a simple NMR technique for studying the DNA binding of proteins. Titration of the unlabeled DNA into the 15N-labeled protein is monitored by acquiring a two-dimensional (2D) heteronuclear single-quantum correlation (HSQC) spectrum at each step of the titration. CSP can also provide information on the DNA-binding dynamics of proteins, as well as protein-induced conformational changes in DNA. Here, we describe the titration of DNA for the 15N-labeled Z-DNA-binding protein, monitored via 2D HSQC spectra. NMR titration data can be analyzed with the active B-Z transition model to provide the protein-induced B-Z transition dynamics of DNA.

Enhanced production of sugars and UV-shielded lignin/PAN fiber mats from chemi-mechanical pulps

This study investigated poplar pretreatments by chemi-mechanical pulping (CMP) under different beating degrees and alkali concentrations. The enzyme-mediated hydrolysis of pretreated poplar was enhanced by deacetylation and delignification. Meanwhile, the remaining lignin residues were used to produce lignin/polyacrylonitrile (PAN) fiber mats by electrospinning. These mats exhibited excellent mechanical and UV-blocking performance when the lignin was obtained from pulps under milder alkali concentrations (5 g/L). 31P nuclear magnetic resonance (31P NMR) and two-dimensional heteronuclear single-quantum correlation nuclear magnetic resonance (2D HSQC NMR) data revealed that increasing the beating degree at low alkali concentration during the CMP process led to the cleavage of β-O-4′ interunit linkages and re-condensation in lignin, releasing several phenolic groups. Lignin with more linear β-O-4′ interunit linkages and lesser phenolic groups, obtained from treatment of CMP with lower alkali concentration (5 g/L) and beating degree (20°SR), resulted in the corresponding lignin/PAN fiber mats exhibiting better mechanical performance. Further, lignin, along with the increased phenolic-OH and COOH, and p-hydroxybenzoate (PB) units with a more extended conjugate structure, derived from CMP under lower alkali concentration (5 g/L) and higher beating degree (45°SR), led to a stronger ultraviolet (UV) absorption in the corresponding lignin/PAN mats. To summarize, this study reports a mild and low-pollution biomass pretreatment method (CMP) that can efficiently regulate the lignin structure and exhibit efficient anti-ultraviolet properties. The corresponding UV-blocking fiber mats can be potentially used as materials for wearable fabrics.

Enzymatic Conversion of Hydrolysis Lignin—A Potential Biorefinery Approach

Lignin is an abundant and renewable source capable of replacing different raw materials in the chemical industry. It can be obtained from lignocellulosic biomass (LCB) via different pretreatment methods. In the present study, hydrolysis lignin (HL) from the SunburstTM pretreatment technology was utilized to investigate its enzymatic conversion. At first, soluble HL fractions were obtained via alkali solubilization followed by acid precipitation, referred to as acid precipitated lignin (APL). Furthermore, the APL was tested with three different bacterial laccases to identify the optimal conditions for its conversion into small molecular weight fractions. Among the tested laccases, Streptomyces coelicolor A3(2) (ScLac) displayed the highest rate of APL conversion with a high lignin dosage and under extremely alkaline conditions, i.e., 50 g/L in 0.25 M NaOH solution, resulting in higher molecular weight fractions. The increase in the molecular weight and quantitative linkages before and after the enzymatic oxidation of the APL were characterized by size exclusion chromatography (SEC), Fourier-transform infrared spectroscopy (FT-IR), and two-dimensional heteronuclear single quantum correlation nuclear magnetic resonance (2D HSQC NMR) methods.

Understanding the impact of steam pretreatment severity on cellulose ultrastructure, recalcitrance, and hydrolyzability of Norway spruce

The efficient use of softwood in biorefineries requires harsh pretreatment conditions to overcome biomass recalcitrance. Following harsh pretreatments, the hemicellulose is solubilized. Here, we studied the material characteristics of Norway spruce following steam pretreatment at six different severities, relating chemical and structural information to the enzymatic hydrolyzability. Steam pretreatment conditions were defined by two different temperatures (180 °C and 210 °C), with and without the addition of various acids (CH3COOH, H3PO4, H2SO4, SO2). Structural knowledge of the streams is a cornerstone for developing an efficient saccharification process.This study combines advanced structural characterizations to gain fundamental understanding of the influence of severity of pretreatment on spruce. Structural knowledge is a cornerstone in developing an effective saccharification process by modulating pretreatment conditions and enzymes employed.Overall structural properties were assessed by scanning electron microscopy. The effect of stream pretreatment severity on lignin and lignin-carbohydrate bonds was investigated by two-dimensional heteronuclear single quantum correlation nuclear magnetic resonance. Finally, cellulose ultrastructure was studied by applying small/wide-angle X-ray scattering. The structural characteristics of the six pretreated softwood substrates were related to the enzymatic hydrolyzability.With increasing pretreatment severity, surface defibrillation, and lignin depolymeryzation were observed. Further, lignin-carbohydrate complexes signals were detected. Cellulose analysis revealed the rearrangement of microfibrils leading to the formation of larger microfibril aggregates. This microfibril rearrangement likely contributed to the observed increase in enzymatic hydrolysis yields as better enzyme accessibility resulted.

A scalable solid-state nanoporous network with atomic-level interaction design for carbon dioxide capture.

Carbon capture and sequestration reduces carbon dioxide emissions and is critical in accomplishing carbon neutrality targets. Here, we demonstrate new sustainable, solid-state, polyamine-appended, cyanuric acid–stabilized melamine nanoporous networks (MNNs) via dynamic combinatorial chemistry (DCC) at the kilogram scale toward effective and high-capacity carbon dioxide capture. Polyamine-appended MNNs reaction mechanisms with carbon dioxide were elucidated with double-level DCC where two-dimensional heteronuclear chemical shift correlation nuclear magnetic resonance spectroscopy was performed to demonstrate the interatomic interactions. We distinguished ammonium carbamate pairs and a mix of ammonium carbamate and carbamic acid during carbon dioxide chemisorption. The coordination of polyamine and cyanuric acid modification endows MNNs with high adsorption capacity (1.82 millimoles per gram at 1 bar), fast adsorption time (less than 1 minute), low price, and extraordinary stability to cycling by flue gas. This work creates a general industrialization method toward carbon dioxide capture via DCC atomic-level design strategies.

Exploring correlations between MS and NMR for compound identification using essential oils: A pilot study.

In this era of 'omics' technology in natural products studies, the complementary aspects of mass spectrometry (MS)- and nuclear magnetic resonance (NMR)-based techniques must be taken into consideration. The advantages of using both analytical platforms are reflected in a higher confidence of results especially when using replicated samples where correlation approaches can be used to statistically link results from MS to NMR. Demonstrate the use of Statistical Total Correlation (STOCSY) for linking results from MS and NMR data to reach higher confidence in compound identification. Essential oil samples of Melaleuca alternifolia and M. rhaphiophylla (Myrtaceae) were used as test objects. Aliquots of 10 samples were collected for GC-MS and NMR data acquisition [proton (1 H)-NMR, and carbon-13 (13 C)-NMR as well as two-dimensional (2D) heteronuclear single quantum correlation (HSQC), heteronuclear multiple-bond correlation (HMBC), and HSQC-total correlated spectroscopy (TOCSY) NMR]. The processed data was imported to Matlab where STOCSY was applied. STOCSY calculations led to the confirmation of the four main constituents of the sample-set. The identification of each was accomplished using; MS spectra, retention time comparison, 13 C-NMR data, and scalar correlations of the 2D NMR spectra. This study provides a pipeline for high confidence in compound identification using a set of essential oils samples as test objects for demonstration.

5-(R)BENZYLIDENE-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONES IN SYNTHESIS OF AROMATIC OXIMES, THIOSEMICARBAZONES AND HYDRAZONES

The behavior of some derivatives of Meldrum's acid, namely, 5-(R)benzylidene-2,2-dimethyl-1,3-dioxane-4,6-diones (a well-known synthetic platform) was studied with mono- and biazanucleophiles (hydrochloric hydroxylamine, thiosemicarbazide, hydrazine hydrate). The reaction of the reagents was carried out in acetic acid in a 1:1 molar ratio at 75 °C for 6-8 h, which resulted in aromatic oximes, thiosemicarbazones and hydrazones. The synthesis of (E)-4-chlorobenzaldoxime, (E)-N-(4-nitrobenzylidene) hydroxylammonium chloride, (E)-2-(4-chloro)- and (E)-2-(4-nitrobenzylidene) hydrazine-1-carbothioamides is probably accompanied by the formation of the Michael β-adduct with the subsequent elimination of Meldrum's acid. The interaction of nitrobenzylidene dioxanedione with hydrazine hydrate occurs to form a mixture of (E)-N-(4-nitrobenzylidene) acetohydrazide, (E)-(4-nitrobenzylidene) hydrazine and acetate of the latter in a ratio of 17:3:1, found from the integral signal intensity in the 1Н NMR spectrum (the ratio of similar products was 6:2:1 for chlorobenzylidene dioxanedione). It has been shown that during the reaction the studied substrates are attacked by two hydrazine molecules at the arylidene fragment and the carboxyl group of the opened dioxane cycle of Meldrum's acid. Further, the intermediates are recondensed to form hydrazones and acetylhydrazides. The latters interact with the aromatic aldehydes arising under these conditions as a result of the Knoevenagel retro-reaction of the substrates, with the formation of major products, mixtures of (E)-N-(4-chloro)- or (E)-N-(4-nitrobenzylidene) acetohydrazides. Thus, under the selected conditions, in contrast to the common mechanism presented in the periodicals, no formation of N-heterocyclic systems is observed. The structure of the compounds obtained was confirmed on the basis of 1H, 13C NMR spectroscopy data, as well as elemental analysis. Methods of two-dimensional heteronuclear correlation spectroscopy (HSQC) were also used for more reliable identification of the signals of the products (the components of mixtures).

Stabilization mechanism of amorphous carbamazepine by transglycosylated rutin, a non-polymeric amorphous additive with a high glass transition temperature

α-Glycosyl rutin (Rutin-G), composed of a flavonol skeleton and sugar groups, is a promising non-polymeric additive for stabilizing amorphous drug formulations. In this study, the mechanism of the stabilization of the amorphous state of carbamazepine (CBZ) by Rutin-G was investigated. In comparison with hypromellose (HPMC), which is commonly used as a crystallization inhibitor for amorphous drugs, Rutin-G significantly stabilized amorphous CBZ. Moreover, the dissolution rate and the resultant supersaturation level of CBZ were significantly improved in the CBZ/Rutin-G spray-dried samples (SPDs) owing to the rapid dissolution property of Rutin-G. Differential scanning calorimetry measurement demonstrated a high glass transition temperature (Tg) of 186.4°C corresponding to Rutin-G. The CBZ/Rutin-G SPDs with CBZ weight ratios up to 80% showed single glass transitions, indicating the homogeneity of CBZ and Rutin-G. A solid-state NMR experiment using 13C- and 15N-labeled CBZ demonstrated the interaction between the flavonol skeleton of Rutin-G and the amide group of CBZ. A 1H-13C two-dimensional heteronuclear correlation NMR experiment and quantum mechanical calculations confirmed the presence of a possible hydrogen bond between the amino proton in CBZ and the carbonyl oxygen in the flavonol skeleton of Rutin-G. This specific hydrogen bond could contribute to the strong interaction between CBZ and Rutin-G, resulting in the high stability of amorphous CBZ in the CBZ/Rutin-G SPD. Hence, Rutin-G, a non-polymeric amorphous additive with high Tg, high miscibility with drugs, and rapid and pH-independent dissolution properties could be useful in the preparation of amorphous formulations.

Catalytic upgrading of tars generated in a 100 kWth low temperature circulating fluidized bed gasifier for production of liquid bio-fuels in a polygeneration scheme

Gasification of wheat straw, an agricultural residue with high ash content, was investigated in a low temperature circulating fluidized bed (LT-CFB) gasifier in combination with catalytic tar upgrading as a flexible process to co-produce high quality bio-oil, nutrient rich char, and utilize the producer gas for heat and power production. The change in product distribution and bio-oil quality was studied when conducting the catalytic treatment with HZSM-5/γ-Al2O3 and lower-cost γ-Al2O3. The fuel properties of the raw and upgraded bio-oils were analyzed by elemental composition, moisture, total acid number, size exclusion chromatography, basic nitrogen content, gas chromatography–mass spectrometry with flame ionization detection (GC–MS/FID), 1H nuclear magnetic resonance (NMR), 13C NMR, and two-dimensional heteronuclear single-quantum correlation (2D HSQC) NMR. The operating temperature of the LT-CFB pyrolysis chamber determined the tar yield and quality in the producer gas. With decrease in pyrolysis temperature from 690 to 570 °C, the tar concentration in the producer gas increased, while the higher heating value of the condensed oil phase decreased from ~35 to 30 MJ/kg and the oxygen content, moisture content, and acidity of the bio-oil increased. Both HZSM-5/γ-Al2O3 and γ-Al2O3 were effective catalysts as the tar treatment improved the bio-oil quality in terms of increased heating value and revaporization efficiency, and a reduction in oxygen content, moisture content, total acid number, and basic nitrogen content. Catalytic vapor treatment, e.g. using HZSM-5/γ-Al2O3 at 500 °C, decreased the energy content in the condensed bio-oil slightly from ~22% to ~20%. The oil quality improved significantly, as the oxygen content (water-free) and TAN of the bio-oil decreased from 13 wt% O and 34 mg KOH/g to 11 wt% O and 3 mg KOH/g, respectively. The catalytically treated bio-oils are thus better suited for further processing in existing oil refineries.

Enhanced Enzymatic Hydrolysis and Lignin Extraction of Wheat Straw by Triethylbenzyl Ammonium Chloride/Lactic Acid-Based Deep Eutectic Solvent Pretreatment.

Efficient and feasible pretreatment of lignocellulosic biomass waste is an important prerequisite step to promote subsequent enzymatic hydrolysis and enhance the economics of biofuels production. This study focuses on the pretreatment of wheat straw (WS) with triethylbenzyl ammonium chloride/lactic acid (TEBAC/LA)-based deep eutectic solvents to enhance biomass fractionation and lignin extraction. Effects of pretreatment time, temperature, and TEBAC/LA molar ratio on pretreatment were evaluated systematically. Results suggested that 89.06 ± 1.05% of cellulose and 71.00 ± 1.03% of xylan were hydrolyzed with enzyme loadings of 35 FPU cellulase and 82 CBU β-glucosidase (per gram of dry biomass) after pretreatment by TEBAC/LA (1:9) at 373 K for 10 h. A total monosaccharide yield of 0.550 g/g WS (91.27% of the theoretical yield) was achieved with 79.73 ± 0.93% of lignin removal. Furthermore, the 1H–13C two-dimensional heteronuclear single quantum correlation (2D-HSQC) NMR spectroscopy showed that the regenerated lignin (75.69 ± 1.32% purity) was mainly composed of the syringyl units and the guaiacyl units. Overall, the results in this study provide an effective and facile pretreatment method for lignocellulosic biomass waste to enhance enzymatic hydrolysis saccharification.

Catalytic deoxygenation of vapors obtained from ablative fast pyrolysis of wheat straw using mesoporous HZSM-5

Steam treated HZSM-5 with different Si/Al ratios were tested as catalysts for the upgrading of wheat straw pyrolysis vapors and their performance was compared to hierarchical counterparts, which were prepared by desilication followed by acid washing. Pyrolysis vapors were generated in an ablative system, hot gas filtered, and upgraded in an ex-situ catalyst bed to remove oxygen functionalities and reduce the oils' total acid number (TAN). Besides elemental analysis and TAN, the collected liquids were analyzed for water, chemical composition by gas chromatography mass spectrometry with flame ionization detection (GC–MS/FID), size exclusion chromatography (SEC), thermogravimetric analysis (TGA), and selectively by 1H nuclear magnetic resonance (NMR), 13C NMR, and two-dimensional heteronuclear single-quantum correlation (2D HSQC) NMR. Hierarchical and conventional catalysts were analyzed with X-ray fluorescence (XRF), ammonia temperature-programmed desorption (NH3-TPD) and ethylamine TPD, N2 and Ar-physisorption, transmission electron microscopy (TEM) and X-ray diffraction (XRD) to investigate changes induced by the desilication process. In addition, samples were analyzed after several reaction and regeneration cycles to investigate catalyst stability. The hierarchical samples showed an increased coking propensity compared to their parent version. The introduction of mesopores after desilication of HZSM-5 with molar Si/Al ratios of 29 and 39 lead to prolonged activity in deoxygenation and improved carbon recovery in the collected oil fractions compared to the parent counterparts. The results indicate that mild deoxygenation may be a viable way of pretreating pyrolysis oil before co-processing with fossil oil in refineries.

Deoxygenation of Wheat Straw Fast Pyrolysis Vapors using HZSM-5, Al2O3, HZSM-5/Al2O3 Extrudates, and Desilicated HZSM-5/Al2O3 Extrudates

HZSM-5 extrudates, its two constituents (HZSM-5 zeolite and alumina binder), and SiC for reference were tested after steam treatment for the upgrading of wheat straw fast pyrolysis (FP) vapors from an ablative bench scale system. In addition, mesoporosity was added to the HZSM-5 crystals of the zeolite/Al2O3 extrudates by desilication, which decreased the microporous volume and led to enhanced weak acidity and less strong acidity compared to the parent extrudates. For increasing biomass-to-catalyst ratios (w/w, B:C), oils were collected and analyzed for elemental composition, total acid number (TAN), moisture, molecular weight, evaporation characteristics, and chemical composition by gas chromatography–mass spectrometry with flame ionization detection (GC-MS/FID), 1H nuclear magnetic resonance (NMR), 13C NMR, and two-dimensional heteronuclear single-quantum correlation (2D HSQC) NMR. Compared to Al2O3, catalysts containing HZSM-5 promoted aromatization and limited the coke formation due to its shape selec...

Frequency selective coherence transfer NMR spectroscopy to study the structural dynamics of high molecular weight proteins.

Multidimensional nuclear magnetic resonance (NMR) spectroscopy has enabled detailed characterizations of protein structures and dynamics that are closely linked to functions. However, it leads to a large sensitivity loss in applications to high molecular weight proteins, which is caused by spin relaxation during the frequency discrimination period in the indirect dimension. Here, we describe a selective coherence transfer scheme, which enables us to selectively observe 1H nuclei bonded to 15N or 13C nuclei with specified resonance frequencies. By utilizing this scheme, we achieved a 2.5- to 6-fold increase in signal height per unit of time with this scheme by avoiding the relaxation loss in the indirect dimension, as compared to the conventional two-dimensional heteronuclear correlation spectroscopy. We also demonstrated the effectiveness of this approach with applications to the membrane protein KirBac1.1, and characterized the functionally relevant conformational exchange process in both detergent micelles and a reconstituted membrane environment, corresponding to the apparent molecular masses of 220 kDa and 300 kDa, respectively.

Evaluating the Effects of Fibrinogen αC Mutations on the Ability of Factor XIII to Crosslink the Reactive αC Glutamines (Q237, Q328, Q366).

Fibrinogen (Fbg) levels and extent of fibrin polymerization have been associated with various pathological conditions such as cardiovascular disease, arteriosclerosis, and coagulation disorders. Activated factor XIII (FXIIIa) introduces γ-glutamyl-ε-lysinyl isopeptide bonds between reactive glutamines and lysines in the fibrin network to form a blood clot resistant to fibrinolysis. FXIIIa crosslinks the γ-chains and at multiple sites in the αC region of Fbg. Fbg αC contains a FXIII binding site involving αC (389-402) that is located near three glutamines whose reactivities rank Q237 >> Q366 ≈ Q328. Mass spectrometry and two-dimensional heteronuclear single-quantum correlation nuclear magnetic resonance assays were used to probe the anchoring role that αC E396 may play in controlling FXIII function and characterize the effects of Q237 on the reactivities of Q328 and Q366. Studies with αC (233-425) revealed that the E396A mutation does not prevent the transglutaminase function of FXIII A2 or A2B2. Other residues must play a compensatory role in targeting FXIII to αC. Unlike full Fbg, Fbg αC (233-425) did not promote thrombin cleavage of FXIII, an event contributing to activation. With the αC (233-425) E396A mutant, Q237 exhibited slower reactivities compared with αC wild-type (WT) consistent with difficulties in directing this N-terminal segment toward an anchored FXIII interacting at a weaker binding region. Q328 and Q366 became less reactive when Q237 was replaced with inactive N237. Q237 crosslinking is proposed to promote targeting of Q328 and Q366 to the FXIII active site. FXIII thus uses Fbg αC anchoring sites and distinct Q environments to regulate substrate specificity.

Preparation of Lignin Nanoparticles from Wood Waste for Wood Surface Treatment.

Lignin was isolated from wood wastes comprising Iroko sawdust (IR) and mixed sawdust from Iroko and Norway spruce (IRNS), furnished by a local wood houses producer. The respective acidolysis lignin fractions were structurally characterized using pyrolysis (Py)-GCMS, two-dimensional heteronuclear single quantum correlation nuclear magnetic resonance (2D HSQC NMR), Fourier-transform infrared FTIR and ultraviolet-visible (UV-VIS) spectroscopies, size exclusion chromatography, and standard wet-chemistry methods for Klason lignin and polysaccharides determination. The isolated lignin fractions were subsequently used for the preparation of lignin nanoparticles (LNPs) using a non-solvent method. LNPs were then used for wood surface treatment using a dip-coating technique. The coated wood samples were analyzed by colorimetry and scanning electron microscopy (SEM) before and after artificial weathering experiments in a UV chamber to investigate the UV protection potential of the LNPs coatings. Wood samples dip-coated with LNPs showed promising surface modifications resembling a sort of film of fused LNPs. Coatings made from IR-LNPs and IRNS-LNPs performed significantly better in artificial weathering experiments than uncoated reference samples.

Structural Elucidation of Cisplatin and Hydrated cis-Diammineplatinum(II) Complex Conjugated with Cyanocobalamin by Liquid Chromatography with Electrospray Ionization-Mass Spectrometry and Multistage Mass Spectrometry.

Pt(II)-based derivatives bearing a cyanocobalamin (CNCbl) unit were synthesized in aqueous solutions, and the reaction mixtures were examined by reversed-phase liquid chromatography with electrospray ionization and linear ion trap mass spectrometry (MS). Isotopic pattern analysis, multistage mass-spectra (MS/MS and MS3) interpretation, and differential isotopic labeling were used to establish the chemical composition and to suggest the chemical structures of reaction products. When cisplatin (cis-[PtCl2(NH3)2]) was used as a Pt(II) drug derivative, a coordination bond between diamminemonochloroplatinum(II) and the cyano group of CNCbl, in turn linked covalently to the vitamin Co(III) ion, occurred. The resulting conjugate with a CoIII–CN–PtII bridge was MS detected as a doubly positive charged ion with the prevailing isotopologue at m/z 810.26 (empirical formula [C63H95ClCoIIIN16O14PPt]2+). Likewise, a peak signal centered at m/z 811.26 was observed when 15N-labeled cisplatin cis-[PtCl2(15NH3)2] was used as Pt(II) complex, thus confirming the presence of both the cisplatin amino groups in the conjugate. A bifunctional conjugate was obtained between CNCbl and the cis-diamminediaquaplatinum(II), that is, cis-[Pt(NH3)2(H2O)2]2+; in this case, the planar coordination complex of Pt(II) was also involved in a covalent bond with the oxygen atom of one of the CNCbl amide moieties. The peak signal detected at m/z 792.26 (empirical formula [C63H94CoIIIN16O14PPt]2+) changed to m/z 793.26 when the labeled cis-[Pt(15NH3)2(H2O)2]2+ complex was adopted for conjugation. Comparison between MS/MS spectra allowed an extended structural characterization of both conjugates, as such or 15N-labeled. Two-dimensional heteronuclear (1H–15N) single quantum correlation NMR spectroscopy, applied to 15N-labeled conjugates, supported the hypotheses made on the Pt(II) coordination in both cases.

Application of High-Resolution NMR and GC-MS to Study Hydrocarbon Oils Derived from Noncatalytic Thermal Transformation of e-Waste Plastics.

The increases in the volumes of electronic waste have become an aggravating environmental, economic, and social health issue in recent times. This study investigates the conversion of e-waste plastics into hydrocarbon oils via noncatalytic thermal transformation followed by an in-depth characterization of these oils using diverse analytical techniques such as gas chromatography–mass spectrometry (GC–MS), Fourier transform infrared (FTIR) spectroscopy, and nuclear magnetic resonance (NMR) spectroscopy. In particular, NMR spectroscopy is a key analytical tool utilized in this study to gain a comprehensive insight into the chemical nature of the resultant oils along with a semiquantitative investigation of the changes in their composition over a temperature range of 800–1200 °C. The one-dimensional (1D) 1H and two-dimensional (2D) heteronuclear single-quantum correlation spectra were acquired for the oils, wherein the 2D NMR spectrum provided improved resolution of peaks to address the overlaps encountered in the 1D spectrum. The experimental results obtained from GC–MS, FTIR spectroscopy, and NMR spectroscopy were found to align well with each other. The oils produced in this study have a high calorific value of 38.27 MJ/kg and thus may find use in several applications. A detailed mechanism for the thermal degradation of styrene acrylonitrile plastics and the formation of major products is elucidated in this study.