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This study elucidates the impact of surface chemistry on solvent spin relaxation rates via time-domain nuclear magnetic resonance (TD-NMR). Suspensions of polymer particles of known surface chemistry were prepared in water and n -decane. Trends in solvent transverse relaxation rates demonstrated that surface polar functional groups induce stronger interactions with water with the opposite effect for n -decane. NMR surface relaxivities (ρ 2 ) calculated for the solid-fluid pairs ranged from 0.4 to 8.0 μm s -1 and 0.3 to 5.4 μm s -1 for water and n -decane, respectively. The values of ρ 2 for water displayed an inverse relationship to contact angle measurements on surfaces of similar composition, supporting the correlation of the TD-NMR output with polymer wettability. Surface composition, i.e., H/C ratios and heteroatom content, mainly contributed to the observed surface relaxivities compared to polymer % crystallinity and mean particle sizes via multiple linear regression. Ultimately, these findings emphasize the significance of surface chemistry in TD-NMR measurements and provide a quantitative foundation for future research involving TD-NMR investigations of wetted surface area and fluid-surface interactions. A comprehensive understanding of the factors influencing solvent relaxation in porous media can aid the optimization of industrial processes and the design of materials with enhanced performance., Competing Interests: The authors declare no competing financial interest., (© 2023 The Authors. Published by American Chemical Society.)

Nitrile hydrogenation via the in situ-generated PNP-Fe II (H) 2 CO ( 1 ) catalyst leads to a previously inexplicable loss of mass balance. Reaction kinetics, reaction progress analysis, in situ pressure nuclear magnetic resonance, and X-ray diffraction analyses reveal a mechanism comprising reversible imine self-condensation and amine-imine condensation cascades that yield >95% primary amine. Imine self-condensation has never been reported in a nitrile hydrogenation mechanism. The reaction is first order in catalyst and hydrogen and zero order in benzonitrile when using 2-propanol as the solvent. Variable-temperature analysis revealed values for Δ G 298 K ⧧ (79.6 ± 26.8 kJ mol -1 ), Δ H ⧧ (90.7 ± 9.7 kJ mol -1 ), and Δ S ⧧ (37 ± 28 J mol -1 K -1 ), consistent with a solvent-mediated proton-shuttled dissociative transition state. This work provides a basis for future catalyst optimization and essential data for the design of continuous reactors with earth-abundant catalysts.

Enzymatic processes, particularly those capable of performing redox reactions, have recently been of growing research interest. Substrate specificity, optimal activity at mild temperatures, high selectivity, and yield are among the desirable characteristics of these oxidoreductase catalyzed reactions. Nicotinamide adenine dinucleotide (phosphate) or NAD(P)H-dependent oxidoreductases have been extensively studied for their potential applications like biosynthesis of chiral organic compounds, construction of biosensors, and pollutant degradation. One of the main challenges associated with making these processes commercially viable is the regeneration of the expensive cofactors required by the enzymes. Numerous efforts have pursued enzymatic regeneration of NAD(P)H by coupling a substrate reduction with a complementary enzyme catalyzed oxidation of a co-substrate. While offering excellent selectivity and high total turnover numbers, such processes involve complicated downstream product separation of a primary product from the coproducts and impurities. Alternative methods comprising chemical, electrochemical, and photochemical regeneration have been developed with the goal of enhanced efficiency and operational simplicity compared to enzymatic regeneration. Despite the goal, however, the literature rarely offers a meaningful comparison of the total turnover numbers for various regeneration methodologies. This comprehensive Review systematically discusses various methods of NAD(P)H cofactor regeneration and quantitatively compares performance across the numerous methods. Further, fundamental barriers to enhanced cofactor regeneration in the various methods are identified, and future opportunities are highlighted for improving the efficiency and sustainability of commercially viable oxidoreductase processes for practical implementation., (© 2022 Wiley-VCH GmbH.)

Approximately half of all vaccines produced annually are wasted because effectivity is dependent on protein structure and heat exposure disrupts the intermolecular interactions needed to maintain the structure. Thus, most vaccines require a temperature-controlled supply chain to minimize waste. A more sustainable technology was developed via the adsorption of invasion plasmid antigen D (IpaD) onto mesoporous silica, improving the thermal stability of this protein-based therapeutic. Seven silicas were characterized to determine the effects of pore diameter, pore volume, and surface area on protein adsorption. The silica-IpaD complex was then heated above the IpaD denaturing temperature and N , N -dimethyldodecylamine N -oxide was used to remove IpaD from the silica. Circular dichroism confirmed that the adsorbed IpaD after the heat treatment maintained a native secondary structure rich in α-helix content. In contrast, the unprotected IpaD after heat treatment lost its secondary structure. Isotherms using Langmuir, Freundlich, and Temkin models demonstrated that the adsorption of IpaD onto silicas is best fit by the Langmuir model. If pores are less than 15 nm, adsorption is negligible. If the pores are between 15 and 25 nm, then monolayer coverage is achieved and IpaD is protected from thermal denaturing. If pores are larger than 25 nm, the adsorption is a multilayer coverage and it is easier to remove the protein from the silica because of a less-developed hydrogen bond network. This case study provides strong evidence that IpaD is thermally stabilized via adsorption on mesoporous silica with the proper range of pore sizes.

Hollow silica particles (HSPs) have become the focus of interest in many laboratories recently, because of their versatility, stemming from the ability to control their size and shape, as well as surface functionalization. Determining the mechanical stability of hollow particles is essential for their use, both in applications in which they need to retain their structure, as well as those in which they need to break down. We have synthesized a series of HSPs (inner diameter of 231 nm) with increasing wall thickness (7-25 nm), using a template approach. Their mechanical stability was measured using mercury intrusion porosimetry (MIP), which represents the novel application of the technique for these materials. The samples with complete shells break at progressively higher pressures, and samples with wall thickness ≥21 nm remain stable to the highest pressure applied (414 MPa). Other characterization methods, namely microscopy, gas adsorption, and small-angle X-ray scattering, shed light on the size parameters of the particles, as well as the porosity of the silica walls. By varying the amount of silica precursor used in the template coating step, we were able to produce hollow silicas with variable stability, thereby allowing for control of their mechanical properties.

Chemoselective reduction of nitro groups in the presence of activated heteroaryl halides was achieved via catalytic hydrogenation with a commercially available sulfided platinum catalyst. The optimized conditions employ low temperature, pressure, and catalyst loading (<0.1 mol % Pt) to afford heteroaromatic amines with minimal hydrodehalogenation byproducts., (© 2011 American Chemical Society)

Intracellular levels of the hypoxia-inducible transcription factor (HIF) are regulated under normoxic conditions by prolyl hydroxylases (PHD1, 2, and 3). Treatment of cells with PHD inhibitors stabilizes HIF-1α, eliciting an artificial hypoxic response that includes the transcription of genes involved in erythropoiesis, angiogenesis, and glycolysis. The different in vivo roles of the three PHD isoforms are not yet known, making a PHD-selective inhibitor useful as a biological tool. Although several chemical series of PHD inhibitors have been described, significant isoform selectivity has not been reported. Here we report the synthesis and activity of dipeptidyl analogues derived from a potent but non-selective quinolone scaffold. The compounds were prepared by Pd-catalyzed reductive carbonylation of the 6-iodoquinolone derivative to form the aldehyde directly, which was then attached to a solid support via reductive amination. Amino acids were coupled, and the resulting dipeptidyl-quinolone derivatives were screened, revealing retention of PHD inhibitory activity but an altered PHD1, 2, and 3 selectivity profile. The compounds were found to be ∼10-fold more potent against PHD1 and PHD3 than against PHD2, whereas the specific parent compound had shown no appreciable selectivity among the different PHD isoforms.

The title copolymerization catalyzed by BnCOCo(CO)4 affords poly-beta-alanoids in excellent yields and selectivity. The poly-beta-alanoids have narrow molecular weight distributions, controllable molecular weights, and definite end groups.

Changing the oxidation state of redox-active ligands is a powerful method for electrochemically controlling the reactivity and selectivity of bound transition metals (see drawing on the right). In some cases reaction rates can be increased by many orders of magnitude simply by removing an electron from a metal-ligand complex. In the case of polymeric redox-active ligands, a continuous range of properties can be achieved for the transition metal complex., (© 1998 WILEY-VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany.)