Cross-polarization Magic Angle Spinning Research Articles

Inclusion Polymerization of Pyrrole and Ethylenedioxythiophene in Assembled Triphenylamine Bis-Urea Macrocycles

Herein, two different monomers, pyrrole (Py) and ethylenedioxythiophene (EDOT), are loaded into a self-assembled bis-urea host 1 and oxidatively polymerized within its nanochannels, dramatically changing the properties of the crystalline complexes. Molecular dynamics (MD) simulation of both monomers within the channel demonstrates that they diffuse through the confinement upon applying thermal energy, which may facilitate the polymerization reaction. The structures of these host–guest complexes are characterized before and after polymerization using solid-state and photophysical measurements. The host maintains its columnar morphology during polymerization at 90 °C using iodine as an oxidizing agent. Intriguingly, upon dissolution of the host and recovery by filtration, the polymers exhibit memory of their nanoreactor environment, displaying unusual order by scanning electron microscopy, powder X-ray diffraction, and small- and wide-angle X-ray analysis. Solid-state 13C cross-polarized magic angle spinning NMR suggests that polypyrrole (PPy) exhibits primarily α,α′ linkages with some contributions from the quinoid form. Similarly, poly(ethylenedioxythiophene) (PEDOT) also exhibits formation of primarily α,α′ linkages with minor quinoid contributions. Both the 1·PPy and 1·PEDOT crystals show a 103-fold increase in conductivity to ∼10–6 S/cm versus host 1 crystals, which are nonconductive ∼10–9 S/cm. Overall, supramolecular polymerization strategies have the potential to readily modulate the properties of nanostructured materials.

Routes to improve the strengthening of paper with aminoalkylalkoxysilanes

Aminoalkylalkoxysilane copolymers (co-AAAS) have the ability to simultaneously deacidify and strengthen paper documents. Nevertheless, despite enhancing the tensile strength, they generally fail to improve the folding endurance of the degraded groundwood pulp-rich papers. Focusing on that specific type of papers, several ways to overcome their lack of reinforcement were investigated. Promoting the polymerization of AAAS using catalysts and thermal steps was one of them. A monitoring with FTIR spectroscopy showed that the thermal step was the most efficient in speeding up the hydrolysis and polycondensation of 3-aminopropylmethyldiethoxysilane (AM) monomer in aqueous solutions. The progress of the two-steps reaction in terms of degree of polymerization of AAAS polymers was then studied in-situ after heating the paper, using Cross Polarization—Magic Angle Spinning 29Si solid-state NMR, and was shown to be enhanced as well. The other optimization route explored was to stabilize the paper before treatment. Our previous research had shown that the presence of oxidized groups in paper hampered the strengthening. Sodium borohydride, a known bleaching agent in paper conservation, was used prior to the AAASs treatment to decrease the amount of carbonyls in paper. The reduction and the thermal step were compared in terms of the mechanical properties (folding endurance and tensile strength) upon AAASs treatment of several lignocellulosic papers, including three newsprints dated 1911–1923. The use of sodium borohydride led to a significant improvement of the folding endurance of the samples, an unprecedented result. It enabled at the same time to counteract the yellowing induced by the AAAS and to build a larger alkaline reserve.

Circular adsorptive utilization of benzalkonium chloride via construction of ionic microenvironment in dopamine quinone-functionalized acrylic fiber surface

A novel dopamine quinone-functionalized acrylic fiber (PANdpqF) was successfully synthesized, which adsorbed the disinfectant dodecyl dimethyl benzyl ammonium chloride (DDBAC) to in-situ construct a highly efficient catalyst (DDBAC@PANdpqF) for the cyclization of CO2 with epoxide. The successful preparation of PANdpqF was proved by 13C Cross Polarization-Magic Angle Spinning nuclear magnetic resonance, X-ray photoelectron spectroscopy, Fourier transform infrared, and scanning electron microscopy. High adsorption capacity of DDBAC on PANdpqF has been demonstrated by ultraviolet analysis, and the theoretical maximum adsorption capacity was calculated as 666.67 mg/g. Based on comprehensive analysis, the corresponding adsorption mechanism is proposed in which chloride ion of DDBAC is added to o-quinone moiety through Michael addition, followed by the formation of phenoxy and quaternary ammonium ion pair. DDBAC@PANdpqF was well applicable to catalyze the cyclization of CO2, and the yield could reach 93.7% even with a low catalyst loading. The possible cooperatively catalytic mechanism was proposed correspondingly, in which phenolic hydroxyl helps to activate CO2 and epoxide, phenoxy anion attacks CO2 as a nucleophile, and quaternary ammonium cation stabilizes the anionic intermediates. Overall, the functionalized acrylic fiber adsorbed environmentally harmful disinfectant DDBAC to furnish a highly active catalyst for the transformation of greenhouse gas CO2 into useful carbonates, which provides a new method for advanced environmental pollution control.

Supercritical CO2 impregnation process applied to polymer samples preparation for dynamic nuclear polarization solid-state NMR.

In this study, supercritical CO2 (scCO2 ) was used to impregnate polymers with paramagnetic polarizing agents to prepare samples for dynamic nuclear polarization (DNP) solid-state NMR (ssNMR) experiments. As a proof of concept, we impregnated polystyrene samples with bTbK, which stands for bis-TEMPO-bisketal where TEMPO is 2,2,6,6-tetra-methylpiperindin-1-oxyl. Substantial DNP signal enhancements could be measured on DNP-enhanced 1 H → 13 C cross-polarization (CP) magic-angle spinning (MAS) spectra recorded at 9.4T and ~100 K, reaching a maximum value of 8 in the most favorable case, which appeared comparable or even higher than what is typically obtained on similar systems for former sample preparation methods. These results highlight the potential of scCO2 impregnation as an efficient and possibly versatile methodology to prepare polymer samples for DNP ssNMR investigations.

The Photodegradation of Lignin Methoxyl C Promotes Fungal Decomposition of Lignin Aromatic C Measured with 13C-CPMAS NMR.

Solar radiation has been regarded as a driver of litter decomposition in arid and semiarid ecosystems. Photodegradation of litter organic carbon (C) depends on chemical composition and water availability. However, the chemical changes in organic C that respond to solar radiation interacting with water pulses remain unknown. To explain changes in the chemical components of litter organic C exposed to UV-B, UV-A, and photosynthetically active radiation (PAR) mediated by water pulses, we measured the chemistry of marcescent Lindera glauca leaf litter by solid-state 13C cross-polarization magic angle spinning (CPMAS) nuclear magnetic resonance (NMR) over 494 days of litter decomposition with a microcosm experiment. Abiotic and biotic factors regulated litter decomposition via three pathways: first, photochemical mineralization of lignin methoxyl C rather than aromatic C exposed to UV radiation; second, the biological oxidation and leaching of cellulose O-alkyl C exposed to PAR and UV radiation interacts with water pulses; and third, the photopriming effect of UV radiation on lignin aromatic C rather than cellulose O-alkyl C under the interaction between radiation and water pulses. The robust decomposition index that explained the changes in the mass loss was the ratio of aromatic C to O-alkyl C (AR/OA) under radiation, but the ratio of hydrophobic to hydrophilic C (hydrophobicity), the carbohydrate C to methoxyl C ratio (CC/MC), and the alkyl C to O-alkyl C ratio (A/OA) under radiation were mediated by water pulses. Moreover, the photopriming effect and water availability promoted the potential activities of peroxidase and phenol oxidase associated with lignin degradation secreted by fungi. Our results suggest that direct photodegradation of lignin methoxyl C increases microbial accessibility to lignin aromatic C. Photo-oxidized compounds might be an additional C pool to regulate the stability of the soil C pool derived from plant litter by degrading lignin methoxyl and aromatic C.

Jacob Schaefer III

Jacob Schaefer III, 83, died June 27 in Saint Louis, Missouri. “Jake published the first 13 C NMR spectra of synthetic copolymers, the first magic-angle spinning 13 C NMR spectrum of a solid polymer, and the first cross-polarization magic angle spinning (CPMAS) 13 C NMR spectra of polymers. His laboratory produced monumental NMR tools including CPMAS, rotational-echo, double-resonance (REDOR), and multichannel transmission line probes. Today, these tools are so widely used that they are simply referenced by their acronyms, and their impact on medicine, biochemistry, and materials science has been profound. Jake himself applied these techniques to important studies that led to advanced understanding of proteins, living cell metabolism, and polymers.”—Lee G. Sobotka, Lynette Cegelski, Richard Loomis, and Karen Wooley, colleagues Most recent title: Charles Allen Thomas Emeritus Professor of Chemistry, Washington University in St. Louis Education: BS, chemistry, Carnegie Institute of Technology, 1960; PhD, chemistry, University of Minnesota, 1964

Organic amendments and gypsum reduce dispersion and increase aggregation of two sodic Vertisols

Sodic soils are widespread in semi-arid and arid regions of the world, with agricultural production on these soils constrained due to structural instability resulting from high concentration of exchangeable sodium (Na). The structural instability results in clay dispersion, reduced infiltration, crust formation and poor seed germination. One way to decrease undesirable effects of Na on soil structure is to apply gypsum (G) and organic amendments. We evaluated the effect of G and four organic amendments [polyacrylamide (PAM), feedlot manure (FLM), chicken manure (CM), and lucerne pellets (LP)] on two sodic soils. These amendments differed in their chemical nature as assessed by 13C cross-polarisation magic angle spinning nuclear magnetic resonance (13C CPMAS NMR) spectroscopy after amended soils were incubated for 60 d at field water capacity. Gypsum reduced dispersion but had no effect on macroaggregates or aggregate mean weight diameter (MWD). Using principal component analysis, we found that aryl C and O-aryl C functional groups were positively correlated with microaggregates and the silt + clay fraction, and O-alkyl C and di-O alkyl C were positively correlated with soil dispersion after 1 d of soil incubation. The CM reduced dispersion more than FLM, LP, or PAM, although LP increased the proportion of large macroaggregates and MWD. We also found that large macroaggregates and MWD were positively correlated with microbial respiration and dissolved organic carbon. Except for the G + LP amendment, G had no synergistic effect with other organic amendments on macroaggregates and MWD of the two sodic soils. This study demonstrates that the functional groups of organic amendments and microbial activity play important roles in aggregation and dispersion of sodic soils. This study also demonstrates that a combination of gypsum and organic amendments will be a better option to ameliorate sodic soils by decreasing dispersion and increasing aggregate formation.

Controlling the Nucleation Process to Prepare a Family of Crystalline Tribenzimidazole-Based Covalent Organic Frameworks

Covalent organic frameworks (COFs) are at the forefront of porous material research due to their crystallinity and topological diversity. However, most COFs are connected by reversible chemical bonds, which limit their applications under harsh conditions. Herein, we develop a novel synthetic method to lock the imine bond using amino groups via a precursor-involved cascade reaction. We experimentally demonstrated that the nucleation process of COFs can be controlled by precursor hydrolysis. A family of crystalline two-dimensional tribenzimidazole-based COFs (2D BI-COFs) was prepared by the condensation of o-phenylenediamine derivative and aryl aldehydes. Their structures were confirmed by powder X-ray diffraction, Fourier-transform infrared spectroscopy, and solid-state 13C cross-polarization magic angle spinning nuclear magnetic resonance (CP/MAS NMR) spectroscopy. They showed high surface areas, good CO2 uptake capacities, excellent CO2/N2 selectivities, and high chemical stabilities. Of these materials, BI-COF-1 was an efficient photocatalyst for the visible-light-driven photocatalytic oxidation of sulfides, which displayed high conversion (∼100%) and excellent selectivity (>90%). We believe that our study can provide new insights into the synthesis of 2D chemical-stable COFs.

CP-MAS and Solution NMR Studies of Allosteric Communication in CA-assemblies of HIV-1

Solution and solid-state NMR spectroscopy are highly complementary techniques for studying structure and dynamics in very high molecular weight systems. Here we have analysed the dynamics of HIV-1 capsid (CA) assemblies in presence of the cofactors IP6 and ATPγS and the host-factor CPSF6 using a combination of solution state and cross polarisation magic angle spinning (CP-MAS) solid-state NMR. In particular, dynamical effects on ns to µs and µs to ms timescales are observed revealing diverse motions in assembled CA.Using CP-MAS NMR, we exploited the sensitivity of the amide/Cα-Cβ backbone chemical shifts in DARR and NCA spectra to observe the plasticity of the HIV-1 CA tubular assemblies and also map the binding of cofactors and the dynamics of cofactor-CA complexes. In solution, we measured how the addition of host- and co-factors to CA -hexamers perturbed the chemical shifts and relaxation properties of CA-Ile and -Met methyl groups using transverse-relaxation-optimized NMR spectroscopy to exploit the sensitivity of methyl groups as probes in high-molecular weight proteins. These data show how dynamics of the CA protein assembly over a range of spatial and temporal scales play a critical role in CA function. Moreover, we show that binding of IP6, ATPγS and CPSF6 results in local chemical shift as well as dynamic changes for a significant, contiguous portion of CA, highlighting how allosteric pathways communicate ligand interactions between adjacent CA protomers.

Effects of whole-tree and stem-only clearcutting on forest floor and soil carbon and nutrients in a balsam fir (Abies balsamea (L.) Mill.) and red spruce (Picea rubens Sarg.) dominated ecosystem

Intensive harvesting of forest biomass for bioenergy has the potential to degrade forest soils and productivity if ecosystem carbon and other nutrients are depleted faster than replenished naturally or by management inputs. Climate change mitigation potential associated with bioenergy may be threatened if forest management operations reduce soil carbon stocks. Research reported here was initiated in 1979 to determine the effects of whole-tree harvesting on long-term site productivity and ecosystem carbon and nutrient pools and fluxes in a northeastern North American temperate balsam fir-red spruce forest. A sequence of harvesting and silvicultural treatments were applied from 1981 to 1993 using a paired-watershed experimental design. Treatments included whole-tree clearcutting, stem-only harvesting, simulated by return of chipped or lopped delimbing residue, conifer release by applying herbicide, and pre-commercial thinning and fertilizer application. Quantitative samples of the forest floor were excavated in 2016. Quantitative soil pits were sampled in 2017 to a depth of 50 cm below the forest floor, where possible; the basal till subsoil was sampled to a depth of 100 cm with an auger. Forest floor samples were analyzed for total carbon, nitrogen, phosphorus, potassium, calcium, magnesium and aluminum. Organic and mineral soil layer samples from the quantitative pits were analyzed for pH, short and long-lived soil carbon via 13C cross polarization magic angle spinning (CP-MAS) nuclear magnetic resonance (NMR), total carbon and nitrogen and extractable phosphorus, potassium, calcium, magnesium and aluminum. Forest floor carbon and nitrogen on whole-tree harvested plots 35 years after harvest were about 50% of the amount on the unharvested watershed. Stem-only harvesting partially mitigated the reduction, and gross losses were apparently offset by increases in the mineral soil solum to depth 50 cm, suggesting that downward translocation of soil organic matter was a significant ecosystem process during the 35 years since harvest. Accumulated forest floor and mineral soil stock of total carbon and nitrogen and extractable nutrients to depth 100 cm did not differ significantly between the harvested and unharvested watershed. A corresponding similarity in mineral soil pools of extractable phosphorus and non-acid cations in the two watersheds suggests that inputs from atmospheric deposition, primary and secondary mineral weathering, organic matter mineralization and litterfall balanced exports including leaching and plant uptake. Ecosystem stocks of extractable phosphorus, base cations, and total organic carbon and nitrogen were maintained 35 years after whole-tree harvesting of a primary spruce-fir forest.

Crystal and molecular structures of fac-[Re(Bid)(PPh3)(CO)3] [Bid is tropolone (TropH) and tribromotropolone (TropBr3H)

Two rhenium complexes, namely, fac-tricarbonyl(triphenylphosphane-κP)(tropolonato-κ2O,O')rhenium(I), [Re(C7H5O2)(C18H15P)(CO)3] or fac-[Re(Trop)(PPh3)(CO)3] (1), and fac-tricarbonyl(3,5,7-tribromotropolonato-κ2O,O')(triphenylphosphane-κP)rhenium(I), [Re(C7H2Br3O2)(C18H15P)(CO)3] or fac-[Re(TropBr3)(PPh3)(CO)3] (2) (TropH is tropolone and and TropBr3H is tribromotropolone), were synthesized and their crystal and molecular structures confirmed by single-crystal X-ray diffraction. Both crystallized in the space group P-1 and display an array of inter- and intramolecular interactions which were confirmed by solid-state 13C NMR spectroscopy using cross polarization magic angle spinning (CPMAS) techniques, as well as Hirshfeld surface analysis. The slightly longer Re-P distance of 1 [2.4987 (5) versus 2.4799 (11) Å for 1 and 2, respectively] suggests stronger back donation from the carbonyl groups in the former case, possibly due to the stronger electron-donating ability of the unsubstituted tropolonate ring system. However, this is not supported in the Re-CO bond distances of 1 and 2.

Study of microheterogeneity of silatrane-based silica surface bonding chemistry and its optimization for the synthesis of chiral stationary phases for enantioselective liquid chromatography

The present work systematically investigates the chemical microheterogeneity as part of the optimization of a single-step surface bonding chemistry of 3-mercaptopropylsilatrane (MPS) on mesoporous silica gel in comparison to the state-of-the-art silane chemistry with 3-mercaptopropyltrimethoxysilane (MPTMS). MPS functionalization turns out to be a favourable chemistry for the further use in thiol-ene click reactions such as the immobilization of chiral selectors, herein tert-butylcarbamoylquinine (tBuCQN), for the synthesis of chiral stationary phases (CSPs). MPS has higher reactivity than MPTMS and prefers the formation of trifunctional siloxane bondings unlike MPTMS which favours difunctional siloxane bonds to silica, as investigated by solid-state cross-polarization/magic angle spinning (CP/MAS) NMR (29Si and 13C nuclei). Reaction conditions (ternary mixtures of methanol, water and toluene; with and without acid; prewetting of silica; HCl pretreatment of silica) were evaluated with the aim to find conditions which promote the formation of a horizontal siloxane polymer layer on top of the silica surface. Silanization reaction times could be reduced to 2 h. The 29Si NMR signal corresponding to trifunctional siloxane bonding could be increased to 60% with no T1 signal that refers to monofunctional siloxane bonding in spite of water in the ternary reaction mixture. Furthermore, no significant disulfide bridges were formed in this approach, leading to high selector loadings. The thiol and selector coverage reached up to 4.6 and 1.4 µmol/m2, respectively. With the preferred CSP, the enantioselectivity could be increased for a chiral probe (FMOC-Phe) and the mass transfer resistance (C-term) bisected compared to the corresponding CSP prepared from benchmark MPTMS-modified silica (2.54 vs 5.72 ms). It is demonstrated that the fine-tuning of the microstructure on the silica surface can have a significant influence on enantioselectivity and mass transfer kinetics of the resultant CSPs.

A method to quantify composition, purity, and cross-link density of the active polyamide layer in reverse osmosis composite membranes using 13C cross polarization magic angle spinning nuclear magnetic resonance spectroscopy

A method for harvesting and purifying the thin polyamide (PA) active layer from thin-film composite (TFC) reverse osmosis (RO) membranes was developed, enabling quantitative nuclear magnetic resonance (NMR) measurements of the composition and cross-linking in the PA layer that can be directly related to membrane performance. Using our chemical separation process, we report on four trimesoyl chloride (TMC)/isophthaloyl chloride (IPC)/ m -phenylene diamine (MPD)-based TFC membranes in which the cross-link density was intentionally reduced by replacing trifunctional cross-linking TMC monomers with their linear IPC difunctional analog. While the NMR results show a two-fold decrease in cross-linking that causes a 30% increase in salt passage, the addition of the difunctional analog leads to increased polar amine groups that reduce water permeance due to tighter binding of water in the PA membrane. Our results demonstrate that 13 C cross polarization magic angle spinning (CPMAS) is a powerful method for quantitatively monitoring the purity, cross-linking, and chemical composition in PA membranes and will be an essential tool in ascertaining atomistic models of PA structure. • A method for purifying the polyamide layer from TFC RO membranes was developed. • 13 C CPMAS quantifies composition and crosslinking in harvested polyamide TFC RO films. • Crosslinking is controlled by IPC/TMC ratio. • With a two-fold decrease in crosslinking, a 30% increase in salt passage. • With a two-fold increase of amine content, a 30% decrease in water permeance.

Thermo-Reversible Cellulose Micro Phase-Separation in Mixtures of Methyltributylphosphonium Acetate and γ-Valerolactone or DMSO.

We have identified cellulose solvents, comprised of binary mixtures of molecular solvents and ionic liquids that rapidly dissolve cellulose to high concentration and show upper‐critical solution temperature (UCST)‐like thermodynamic behaviour ‐ upon cooling and micro phase‐separation to roughly spherical microparticle particle‐gel mixtures. This is a result of an entropy‐dominant process, controllable by changing temperature, with an overall exothermic regeneration step. However, the initial dissolution of cellulose in this system, from the majority cellulose I allomorph upon increasing temperature, is also exothermic. The mixtures essentially act as ‘thermo‐switchable’ gels. Upon initial dissolution and cooling, micro‐scaled spherical particles are formed, the formation onset and size of which are dependent on the presence of traces of water. Wide‐angle X‐ray scattering (WAXS) and 13C cross‐polarisation magic‐angle spinning (CP‐MAS) NMR spectroscopy have identified that the cellulose micro phase‐separates with no remaining cellulose I allomorph and eventually forms a proportion of the cellulose II allomorph after water washing and drying. The rheological properties of these solutions demonstrate the possibility of a new type of cellulose processing, whereby morphology can be influenced by changing temperature.

Assessing Factors Controlling Structural Changes of Humic Acids in Soils Amended with Organic Materials to Improve Soil Functionality

Humic acids (HAs) regulate soil chemical reactivity and improve many soil functions. The amendment of soil with organic materials increases soil organic matter (SOM) content and promotes the formation of HAs. However, the effect of the type, frequency and duration of amendment, and pedoclimatic conditions on SOM transformation and HA structural changes remains unclear. Herein, four experimental field sites (S1–4) with short-to-long-term organic fertilisation schemes were used to assess the effects of such factors, i.e., S1: loamy sand amended once with farmyard manure (FYM), brown coal waste (BCW), and biochar (BIO) for 0.5 and 1.5 years; S2: silt loam amended once with BIO for 8 years; S3: loamy sand amended every 5 years with FYM for 94 years; and S4: clayey silt amended every 2 years with FYM for 116 years. All HAs were extracted and analysed for structural differences by elemental analysis (EA), attenuated total reflectance–Fourier transform infrared spectroscopy (ATR-FTIR), solid-state cross polarisation magic angle spinning nuclear magnetic resonance spectroscopy (CP/MAS 13C-NMR), and differential scanning calorimetry (DSC). Results from EA, FTIR, and NMR showed that the long-term samples from S3 (treatments, T9–T10) and S4 (T11–T12) had the greatest aromatic characteristics, which increased with FYM amendment (T10 and T12). These agreed with DSC data, which indicated lower aliphatic contents compared with other samples. Samples from S2 (T7–T8), with receded amendment effects, had less aromatic and greater aliphatic characteristics compared with the short-term samples, S1 (T1–T6). In S1, structural changes were limited, but aromaticity increased with BIO (T3 and T6) compared with corresponding FYM (T1 and T4) and BCW (T2 and T5) amendments due to inherently high aromatic groups in the former. Overall, the results showed that the site (due to differences in pedoclimatic conditions), field age of OM, and amendment frequency were the main factors that influenced HA structure, and hence SOM transformation. Regular, long-term organic amendment increases the aromatic characteristics of HAs, which can improve soil functionality, but short-term structural improvements are achievable only when amending material is rich in aromatic compounds.

Assessment of halogen-bond induced cocrystallization of 1,3,5-trihalo-2,4,6-trifluorobenzenes with 2,3,5,6-Tetramethylpyrazine

Cocrystallization of each of 1,3,5-trichloro-2,4,6-trifluorobenzene, 1,3,5-tribromo-2,4,6-trifluorobenzene, and 1,3,5-triiodo-2,4,6-trifluorobenzene with 2,3,5,6-tetramethylpyrazine via selected mechanochemical and solution methods is assessed. In lieu of single crystals of suitable quality for structure determination via single-crystal X-ray diffraction, powder X-ray diffraction and 13C cross-polarization magic-angle spinning solid-state NMR spectroscopy are used to qualitatively assess halogen-bond induced cocrystal formation. The results suggest a rich polymorphic landscape worthy of further study.

Effect of cross polarization radiofrequency phases on signal phase

Utilizing phases of radio frequency (RF) pulses to manipulate spin dynamics is routine in NMR and MRI, leading to spectacular techniques like phase cycling. In a very different area, cross polarization (CP) also has a long history as part of a vast number of solid-state NMR pulse sequences. However, a detailed study devoted to the effect of CP RF phases on NMR signal, seems not to be readily available. From first principles, we arrive at a simple dependence of NMR signal on arbitrary CP RF phases, for static and MAS conditions, accompanied by experimental verification. In the process, the CP propagator emerges as a product of RF “pulses” and a period of “free precession”, conforming to coherence transfer pathway theory. The theoretical expressions may lend confidence for dealing with CP blocks with tunable phases in pulse sequences.

Trash into treasure: Converting waste polyester into C3N4-based intramolecular donor-acceptor conjugated copolymer for efficient visible-light photocatalysis

Carbon nitride (C3N4) is regarded as one of the most prospective photocatalysts for environmental remediation. The design of intramolecular donor-acceptor (D-A) conjugated structure has aroused particular interest for improving visible-light photocatalytic activity of C3N4, but remains a huge challenge. Herein, a novel C3N4-based D-A conjugated copolymer is synthesized by incorporating aromatic ring into the C3N4 skeleton by copolymerization of melamine with terephthalic acid from the in-situ controlled degradation of recycled poly(ethylene terephthalate) catalyzed by ZnO at 360 °C. The results of X-ray diffraction, solid-state 13C cross-polarization magic-angle spinning nuclear magnetic resonance, thermodynamics analysis, and X-ray photoelectron spectroscopy confirm the structure of C3N4-based D-A conjugated system, consisting of terminal amino group of the tri-s-triazine unit as electron-donating group and aromatic ring as acceptor. Notably, the C3N4-based D-A conjugated copolymer displays shorter lifetime of light-induced charge carriers, lower photoluminescence emission, and larger photocurrent response than pristine C3N4, certifying that the D-A conjugated system significantly promotes the separation efficiency of light-induced charge carriers. As such, the C3N4-based D-A conjugated copolymer displays high performance in the photocatalytic degradation of Amido black 10B upon visible light illumination, of which the kinetic constant is 101 times that of unmodified C3N4. Lastly, reactive oxygen species including ·OH, ·O2- and 1O2 are proved to be the main active sites. This work not only offers new insights into the synthesis of efficient C3N4-based D-A conjugated copolymers, but also will inspire new paradigms toward sustainable transformation of waste plastics into value-added products for environmental remediation.

A 5-(2-Pyridyl)tetrazolate Complex of Molybdenum(VI), Its Structure, and Transformation to a Molybdenum Oxide-Based Hybrid Heterogeneous Catalyst for the Epoxidation of Olefins

There is a considerable practical interest in discovering new ways to obtain organomolybdenum heterogeneous catalysts for olefin epoxidation that are easier to recover and reuse and display enhanced productivity. In this study, the complex salt (H2pytz)[MoO2Cl2(pytz)] (1) (Hpytz = 5-(2-pyridyl)tetrazole) has been prepared, structurally characterized, and employed as a precursor for the hydrolysis-based synthesis of a microcrystalline molybdenum oxide/organic hybrid material formulated as [MoO3(Hpytz)] (2). In addition to single-crystal X-ray diffraction (for 1), compounds 1 and 2 were characterized by FT-IR and Raman spectroscopies, solid-state 13C{1H} cross-polarization (CP) magic-angle spinning (MAS) NMR, and scanning electron microscopy (SEM). Compounds 1 and 2 were evaluated as olefin epoxidation catalysts using the model reaction of cis-cyclooctene (Cy8) with tert-butyl hydroperoxide (TBHP), at 70 °C, which gave 100% epoxide selectivity up to 100% conversion. While 1 behaved as a homogeneous catalyst, hybrid 2 behaved as a heterogeneous catalyst and could be recovered for recycling without showing structural degradation or loss of catalytic performance over consecutive reaction cycles. The substrate scope was broadened to monoterpene DL-limonene (Lim) and biobased unsaturated fatty acid methyl esters, methyl oleate (MeOle), and methyl linoleate (MeLin), which gave predominantly epoxide products.

Solid-State NMR and Impedance Spectroscopy Study of Spin Dynamics in Proton-Conducting Polymers: An Application of Anisotropic Relaxing Model.

The 1H–13C cross-polarization (CP) kinetics in poly[2-(methacryloyloxy)ethyltrimethylammonium chloride] (PMETAC) was studied under moderate (10 kHz) magic-angle spinning (MAS). To elucidate the role of adsorbed water in spin diffusion and proton conductivity, PMETAC was degassed under vacuum. The CP MAS results were processed by applying the anisotropic Naito and McDowell spin dynamics model, which includes the complete scheme of the rotating frame spin–lattice relaxation pathways. Some earlier studied proton-conducting and nonconducting polymers were added to the analysis in order to prove the capability of the used approach and to get more general conclusions. The spin-diffusion rate constant, which describes the damping of the coherences, was found to be strongly depending on the dipolar I–S coupling constant (DIS). The spin diffusion, associated with the incoherent thermal equilibration with the bath, was found to be most probably independent of DIS. It was deduced that the drying scarcely influences the spin-diffusion rates; however, it significantly (1 order of magnitude) reduces the rotating frame spin–lattice relaxation times. The drying causes the polymer hardening that reflects the changes of the local order parameters. The impedance spectroscopy was applied to study proton conductivity. The activation energies for dielectric relaxation and proton conductivity were determined, and the vehicle-type conductivity mechanism was accepted. The spin-diffusion processes occur on the microsecond scale and are one order faster than the dielectric relaxation. The possibility to determine the proton location in the H-bonded structures in powders using CP MAS technique is discussed.