Reaction Conditions Research Articles

Tailored pore-confined single-site iron(III) catalyst for selective CH4 oxidation to CH3OH or CH3CO2H using O2.

Direct oxidation of methane to valuable oxygenates like alcohols and acetic acid under mild conditions poses a significant challenge due to high C‒H bond dissociation energy, facile overoxidation to CO and CO2 and the intricacy of C-H activation/C-C coupling. In this work, we develop a multifunctional iron(III) dihydroxyl catalytic species immobilized within a metal-organic framework (MOF) for selective methane oxidation into methanol or acetic acid at different reaction conditions using O2. The active-site isolation of monomeric FeIII(OH)2 species at the MOF nodes, their confinement within the porous framework, and their electron-deficient nature facilitate chemoselective C‒H oxidation, yielding methanol or acetic acid with high productivities of and , respectively. Experiments and theoretical calculations suggest that methanol formation occurs via a FeIII-FeI-FeIII catalytic cycle, whereas CH3CO2H is produced via hydrocarboxylation of in-situ generated CH3OH with CO2 and H2, and direct CH4 carboxylation with CO2.

C–H Trifluoromethylthiolation of aldehyde hydrazones

The selective C–H trifluoromethylthiolation of aldehyde hydrazones afforded interesting fluorinated building blocks, which could be used as a synthetic platform. Starting from readily available (hetero)aromatic and aliphatic hydrazones, the formation of a C–SCF3 bond was achieved under oxidative and mild reaction conditions in the presence of the readily available AgSCF3 salt via a one-pot sequential process (28 examples, up to 91% yield). Mechanistic investigations revealed that AgSCF3 was the active species in the transformation.

Insights into Target Gas-Oxygen Interactions in Highly Sensitive Gas Sensors Using Data-Driven Methods.

In the gas-sensing mechanism of a metal-oxide-semiconductor (n-type) gas sensor, oxygen adsorption or desorption on the oxide surface leads to an increase or decrease in the resistance of the gas sensor system. Additionally, oxygen can be adsorbed again at the location where initially adsorbed oxygen reacted with the target gas. Thus, the adsorption-desorption equilibrium of the reducing gas on the oxide surface is a significant factor in determining the sensitivity and reaction rate. In particular, for ultralow-concentration gas measurements, the relative concentration of oxygen was very high. To design an ultrasensitive gas sensor, not only the reaction of the target gas but also the competing reaction between the target gas and oxygen must be considered. Although qualitative investigations of these complex relationships have been performed according to the gas concentration and flow rate, reliable quantitative results are limited. In this study, a quantitative approach was used to understand the correlation between oxygen and a target gas by applying data analysis methods. We investigated the behavior of oxygen and the target molecules depending on the gas concentration and flow rate using the parts per billion level of the acetone gas sensor. Initial response data according to various detection conditions were processed using principal component analysis and K-means clustering; as a result, four types of reaction behaviors were inferred for 15 types of reaction conditions. Furthermore, the response time, depending on the detection conditions, can be distinguished using the suggested categorization. Our investigation suggests a possibility beyond simple optimization through the data analysis of the gas-sensing results.

Synthesis of Homoallylamine Covalent Organic Frameworks Via Hosomi-Sakurai Reaction Under Mild Conditions.

One-pot multicomponent reactions (MCRs) are a valuable strategy to synthesize functional covalent organic frameworks (COFs) in a single step. Most reported COF syntheses involve solvothermal processes, and because of the harsh reaction conditions, such as high temperature or high pressure, large-scale production of COFs has been limited. The synthesis of homoallylamine substituted COFs via a one-pot Hosomi-Sakurai reaction is reported. At room temperature the reaction of allyltriethylgermane with either terephthalaldehyde or [1,1'-biphenyl]-4,4'-dicarbaldehyde, and 1,3,5-tris(4-aminophenyl)benzene (TAPB) is catalyzed by Sc(OTf)3 to produce two COFs: TAPB-1P-Allyl COF and TAPB-BP-Allyl COF. The allyl functionalized COFs shows high crystallinity, with micropores ranging from 3.2 to 3.9nm, for TAPB-1P-Allyl COF and TAPB-BP-Allyl COF respectively, and both COFs are hydrolytically stable at different pH levels. Post-synthetic modification of these COFs with iodomethane produces methylated cationic COFs that demonstrates >98% adsorption efficiencies below the detection limit of perfluorooctanoic acid (PFOA) and perfluorodecanoic acid (PFDA) from aqueous solutions. After four cycles adsorption efficiency remains high with concentrations of PFOA below the detection limit.

Revealing Reaction Conditions to Drive the Oxidation Reaction of Hydroxyacetone to Lactic Acid on Cu/ZrO2 Catalyst

Revealing Reaction Conditions to Drive the Oxidation Reaction of Hydroxyacetone to Lactic Acid on Cu/ZrO2 Catalyst

Triflyl [18F]Fluoride as a Solution for Base-sensitive Late-stage Nucleophilic Aromatic 18F-Fluorination Reactions.

Fluorine-18 is the predominant radionuclide used to label Positron Emission Tomography (PET) tracers. One outstanding challenge in nucleophilic aromatic radiofluorination reactions is the sensitivity of precursors and catalysts for basic reaction conditions, which are necessary for the work-up of [18F]fluoride, resulting in limited reproducibility. Triflyl [18F]fluoride is a new [18F]fluoride source that allows freedom in choice of type and amounts of base and cryptand. The aim of the current work is to explore the scope and limitations of triflyl [18F]fluoride in the late-stage nucleophilic aromatic 18F-fluorination of various functionalized precursors, exploring reduced amounts of base and cryptand. The assessment allowed for the application of this new nucleophilic [18F]fluoride reagent to the successful radiosynthesis of boron, stannane, hypervalent iodonium ylide and phenol substrates bearing electron-deficient, -neutral and -rich functional groups as well as the clinically relevant PET tracers [18F]FPEB, [18F]mFBG and [18F]SynVesT-1.

Uncommon Phosphonylation of Pyrazine‐2,3‐dicarbonitrile Derivatives via C(sp2)‐CN Bond Cleavage

A direct phosphonylation of the sp2C−CN bond under mild catalytic and non‐catalytic reaction conditions is disclosed. Pyrazine‐2,3‐dicarbonitriles are readily coupled with HPO(OEt)2 to produce the corresponding dialkoxyphosphoryl‐substituted pyrazines. The phosphonylation reaction occurs in the presence of a base (Et3N, Cs2CO3) as nucleophilic substitution of the CN groups. The yield of target diphosphonates depends on the nature of substituents in the 5,6‐positions of the pyrazine ring: it exceeds 90% for di‐5,6‐aryl‐substituted pyrazines and is significantly lower when electron‐donating alkyl (n‐propyl) groups are attached to the 5,6‐positions. It should be noted that for pyrazine‐2,3‐dicarbonitriles bearing vicinal 4‐bromophenyl groups, the nucleophilic phosphonylation leading to C‐‐CN/P‐‐H coupling in the pyrazine ring is predominant over Pd‐catalyzed Hirao’s C‐‐Br/P‐‐H coupling reaction in phenyl rings. Detailed structural characterization, both in solution by means of 1H, 13C and 31P NMR spectroscopy and in the solid state by single crystal X‐ray diffraction, of a series of newly synthesized pyrazine phosphonates is reported.

Establishment and application of a duplex fluorescent quantitative PCR assay for H9N2 subtype avian influenza virus and infectious bronchitis virus.

The H9N2 subtype of avian influenza virus (AIV) and infectious bronchitis virus (IBV) are important avian viruses that cause respiratory symptoms in poultry, and can form mixed infections. In this study, primers and probes were designed based on the HA gene of H9N2 and the 5' noncoding region of IBV, respectively, and a fluorescent quantitative RT-PCR assay was established for simultaneous detection of these two pathogens. The reaction system and conditions were optimized. The method only detected AIV subtype H9N2 and IBV and no other viruses, confirming its high specificity. The assay detected 13.5 copies/μL and 1.66 copies/μL of H9N2 and IBV in clinical samples, respectively. The coefficients of variation for intra- and interassay repeatability were < 3%. The established method was used to analyze 254 clinical samples (oropharyngeal and cloacal swabs) from Hubei Province, China; 98.82% were positive for both pathogens. In summary, a duplex fluorescent quantitative RT-PCR method capable of simultaneously detecting AIV subtype H9N2 and IBV was established. It is specific, sensitive, and reproducible, and can be used for diagnosis of a variety of clinical samples. It provides a technological means for the rapid and simultaneous detection of both pathogens, and thus can facilitate clinical diagnosis and epidemiological investigations.

Multifunctional Dual Nano-MOF-Modified Decellularized Small Intestinal Submucosa Membrane Accelerates Healing of Infected Wound.

The treatment of complex or chronic skin wounds caused by burns, trauma, surgery, and genetic disorders has been a worldwide challenge. Small intestinal submucosa (SIS) is a biological material that is widely used in wound healing. How to further expand the wound healing application of SIS, especially in repairing infected wounds, remains a hot research topic for many tissue engineering and biomaterial scholars focusing on skin regeneration. This study uses nanometal-organic frameworks (nano-MOFs), which have not been applied to modify the SIS membrane before, to construct multifunctional dual nano-MOFs @ SIS membrane (dnMOF@SISm). Nano-MOFs are functionalized onto the nanofiber of SIS via in situ self-assembly under mild reaction conditions without any toxic reagent or complex instruments. The dnMOF@SISm can release Co2+, Zn2+, and bioactive factors, participating in the whole stage of the repair of infected wounds. In vitro, it can regulate the biological activities of various functional cells such as fibroblasts, endothelial cells, and macrophages and shows good antibacterial ability. In the infected full-thickness skin defect rat model, dnMOF@SISm can release metal ions and ligands, killing pathogenic bacteria colonized on the wound surface at the first stage, and then trigger and accelerate the skin repair process via angiogenesis, immune regulation, and collagen deposition. Above all, an efficient, nontoxic, mild self-assembly strategy realizes the functionalization of dual nano-MOFs on the nanofiber of SIS to expand its clinical application scenarios, especially in infected wounds.

A Novel 2-Methylimidazole Promoted Oxyacyloxylation of α-Hydroxy Ketones and Anhydrides: An Easy Access to α-Acyloxy Ketones

An efficient and operationally simple method for the synthesis of α-acyloxy ketones through the readily available 2-methylimidazole-promoted reaction of α-hydroxy ketones and anhydrides is developed. In the reaction, the anhydrides act as both a substrate and a solvent. The new method features good substrate tolerance, mild reaction conditions, readily accessible starting materials, and excellent yields, providing facile and green access to the targets. Importantly, the reaction also avoids the use of reagents with pungent odors, such as pyridine, in traditional esterification, which may promote the development of organocatalysis using nitrogen-containing heterocyclic compounds as catalysts.

Femtosecond Laser-Induced Recrystallized Nanotexturing for Identity Document Security With Physical Unclonable Functions.

Counterfeit identity (ID) documents pose a serious threat to personal credit and national security. As a promising candidate, optical physical unclonable functions (PUFs) offer a robust defense mechanism against counterfeits. Despite the innovations in chemically synthesized PUFs, challenges persist, including harmful chemical treatments, low yields, and incompatibility of reaction conditions with the ID document materials. More notably, surface relief nanostructures for PUFs, such as wrinkles, are still at risk of being replicated through scanning lithography or nanoimprint. Here, a femtosecond laser-induced recrystallized silicon nanotexture is reported as latent PUF nanofingerprint for document anti-counterfeiting. With femtosecond laser irradiation, nanotextures spontaneously emerge within 100ms of exposure. By introducing a low-absorption metal layer, surface plasmon polariton waves are excited on the silicon-metal multilayer nanofilms with long-range boosting, ensuring the uniqueness and non-replicability of the final nanotextures. Furthermore, the femtosecond laser induces a phase transition in the latent nanotexture from amorphous to polycrystalline state, rather than creating replicable relief wrinkles. The random nanotextures are easily identifiable through optical microscopy and Raman imaging, yet they remain undetectable by surface characterization methods such as scanning electron and atomic force microscopies. This property significantly hinders counterfeiting efforts, as it prevents the precise replication of these nanostructures.

Pd-Catalyzed Site-Selective Defluorinative Etherification between Unactivated Perfluoroarenes and Hydrobenzoxazoles.

Polyfluoroaryl ethers represent an important framework of biologically active molecules and materials. Owing to the strong bond dissociation energy of C-F bond, selectivity and other issues, transition metal-catalyzed synthesis of polyfluoroaryl ethers from perfluoroarenes via the activation of C-F bond is challenging and underdeveloped, as compared to the well-documented C-O bond formation starting from aryl iodides, aryl bromides or aryl chlorides. Herein, an unprecedented Pd-catalyzed defluorinative etherification for the synthesis of polyfluoroaryl ether skeletons using hydrobenzoxazoles as phenol surrogate, has been reported. The substrate scope for this protocol is broad, with respect to hydrobenzoxazoles and perfluoroarenes, under mild reaction conditions. More importantly, challenging alkenyl and alkynyl substituted polyfluoroarenes could be successfully used as the coupling component for Pd-catalyzed etherification reaction. Density functional theory (DFT) calculations were employed to investigate the reaction mechanism, which suggested that oxidative addition between polyfluorobenzene and Pd(0) constituted the ratedetermining step.

EPCO-19. MULTIOMIC PROFILING OF EPIGENETIC HETEROGENEITY IN GLIOBLASTOMA AT SINGLE-CELL RESOLUTION USING MULTIOMIC SINGLE-CELL CUT&amp;TAG

Abstract INTRODUCTION Recent evidence suggests epigenetic heterogeneity may be the primary driver of cell phenotype and treatment resistance in glioblastoma (GBM). Epigenetic heterogeneity is defined by alterations of chromatin histone modifications with activating marks such as H3K27 acetylation and repressive marks such as H3K27 trimethylation. Combinations of these histone marks govern the activity of functional genomic elements such as enhancers or promoters. Single-cell (“sc-”) technologies have only recently been adapted to the study of epigenetic cell states and significant technical challenges have limited their widespread adoption, especially in complex tissues. Here, we report the development of an optimized method for performing tissue processing and simultaneous single-cell epigenetic and transcriptomic analyses in flash frozen GBM samples. METHODS Building on our prior work, we developed a new protocol, multiomic single-cell cleavage-under-targets and tagmentation, or “mscCUT&amp;TAG”. We optimized nuclei isolation, cleanup and permeabilization from flash frozen GBM and reaction conditions for the scCUT&amp;TAG portion of the assay. Critically, these changes maintained high-quality, intact nuclei in suspension while limiting well-described technical issues such as nuclei clumping and sample loss. Furthermore, we incorporated the ability to multiplex both patient samples and histone marks. RESULTS We applied 10X scRNA-seq, 10X Multiome (RNA+ATAC-seq), and mscCUT&amp;TAG for five histone marks to the same GBM sample, enabling an integrated evaluation of the tumor’s transcriptome, chromatin accessibility and epigenetic regulation at single-cell resolution. mscCUT&amp;TAG enabled the first assessment of single-cell genome segmentation in GBM. We integrated across modalities to identify specific tumor cell populations, cell-type specific coordinated changes in epigenetics and transcriptome, and define functional regulatory elements. CONCLUSIONS We developed a novel multiomic protocol, mscCUT&amp;TAG, that allows for a comprehensive analysis of epigenetic heterogeneity in GBM. We anticipate this protocol will enhance our understanding of fundamental biology and potential therapeutic avenues in GBM.

Efficient Hydroboration of Ketones and Imines Using Amidophosphine‐Borane Under Catalyst‐Free Conditions

AbstractWe report here the use of amidophosphine borane {(BH₃)₂(PPh)₂N(CH₂)C₆H₅} as a competent reducing agent for the hydroboration of ketones and imines under mild and catalyst‐free reaction conditions yielding the corresponding secondary alcohols and secondary amines after aqueous work. Solid amidophosphine boranes, which are easy to synthesize, and easy to handle demonstrated excellent reactivity and functional group tolerance toward a wide variety of ketones and imines, including aromatic, heteroaromatic, and aliphatic derivatives with electron‐withdrawing and electron‐donating substitutions, thus showing excellent chemoselectivity.

Simplification of solvation shell with water clusters in the simulation of electrochemical nitrogen reduction reaction.

Electrochemical methods for nitrogen reduction have received extensive attention due to the mild reaction conditions. In order to gain an insight into the mechanism of the electrochemical nitrogen reduction process, theoretical simulations are necessary. However, current simulation studies contain many imprecise approximations that may hinder the real recognition of the reaction process. Although solvation methods have recently been developed to provide efficient descriptions, their further applications are hindered by controversy over modeling of solvents and the enormous computational effort required. In this work, we simplify the solvation conditions by using water clusters and compare them with an accurate water layer model. The results demonstrate that the simplified water clusters can effectively capture protons, simulate the surface electric environment, and enable the calculation of the activation energy of the reaction. This method offers an affordable approach for simulating the surface potentials and solvents and provides a new reference for the theoretical study of the electrochemical nitrogen reduction reaction.

Asymmetric Transfer Hydrogenation of 3‐Substituted 2H‐1,4‐Benzoxazines under Tethered Cp*Rh(III)‐Diamine Catalysis with Unexpected Reversal of Enantioselectivity

The asymmetric transfer hydrogenation of 3‐substituted 2H‐1,4‐benzoxazines with an azeotropic mixture of HCO2H/NEt3 (5/2) using tethered Cp*Rh(III)‐diamine catalysis has been realized. This process allows access to a broad range of chiral 3,4‐dihydro‐2H‐1,4‐benzoxazines in high yields with up to 99% ee, and tolerates a variety of functional groups. The enantiocontrol is achieved by the judicious choice of catalyst and hydrogen source. This reaction proceeds with unexpected reversal of enantioselectivity, which is attributed to the acidic reaction conditions and the hydrogen bond between the N−H of the rhodium species and the O atom in the substrate.

Enantioselective Electrocatalysis for Cross‐Dehydrogenative Heteroarylation with Indoles, Pyrroles, and Furans

AbstractOxidative cross‐dehydrogenative C−H/C−H functionalizations represent an exemplary approach for synthesizing carbonyl compounds via α‐heteroarylation. Here we present the development of a direct anodic oxidative coupling process between 2‐acylimidazoles and divergent heterocyclic systems including indole, pyrrole, and furan, facilitated by ferrocene‐assisted asymmetric nickel electrocatalysis with high levels of enantioselectivity. Mechanistic investigations indicate that the reaction initially involves the formation of a chiral Ni‐bound α‐carbonyl radical, which is then captured by the heteroarene radical cation via intermolecular stereoselective radical/radical cation coupling. The mild, scalable, and robust reaction conditions allow for a broad substrate scope and excellent functional group tolerance, enabling access to a wide range of chiral hetero‐compounds. The consequential α‐heteroaromatic carbonyl products can potentially be transformed into a plethora of synthetically valuable frameworks, as exemplified by their application in the asymmetric total synthesis of (−)‐COX‐2 inhibitor, (+)‐acremoauxin A, and (+)‐pemedolac.

Novel and efficient process for the synthesis of 1,3,4-oxadiazole containing MBX-4132 as antimicrobial agent in Neisseria gonorrhoeae

A novel and efficient approach to the synthesis of MBX-4132 has been reported. Having 1,3,4-oxadiazole-containing compound that inhibits trans translation process by binding to the bacterial ribosome and act as an antimicrobial agent. It involved the reaction of 5-(4-fluorophenyl)-1,3,4-oxadiazol-2-amine, with diphenyl carbonate to yield the corresponding carbamates, which in situ reacted with 1,2,3,4-tetrahydroisoquinoline to produce MBX-4132 with a comparatively higher yield (65%). The above process involves mild reaction conditions and uses nontoxic, non-hazardous, and cheaper reagents such as diphenyl carbonate as a carbonyl source thereby making the process economical and environment friendly.

Synthesis of 2‐Substituted‐4,5‐Dihydrothiazol‐4‐Ols by [3 + 2] Annulation of 1,4‐Dithiane‐2,5‐Diol with Thioamides

We developed a novel method for the synthesis of 2‐substituted‐4,5‐dihydrothiazol‐4‐ols compounds through cyclization of thioamides and 1,4‐dithiane‐2,5‐diol in the presence of Et3N. Stable hydroxy‐substituted thiazole compounds were isolated of substituted thioamides. The reaction conditions are simple, the substrate range is wide, and the target compounds were obtained in up to 82% yield.

Classification and Summary of Photocatalytic Chemical Reactions Driven by Triplet‐Triplet Annihilation Upconversion

AbstractTriplet‐triplet annihilation upconversion (TTA‐UC) technology could convert low‐energy light into high‐energy light, and it is a very promising one of the upconversion technologies due to its non‐coherent excitation light, low required excitation optical power density and sensitizer/annihilator flexible adjustability. The application of TTA‐UC into photocatalysis could not only broaden the range of solar energy spectrum utilization, but also bring mild reaction conditions and higher product yields via avoiding the side reaction. However, the detailed catalytic mechanism of TTA‐UC is unclear. Therefore, in this review, we summarized and classified TTA‐UC photocatalytic chemical reactions in terms of mechanism.