Dynamic Exchange Research Articles

Comparing Surface and Bulk Curing Processes of an Epoxy Vitrimer.

We used atomic force microscopy-based infrared spectroscopy (AFM-IR) and nanomechanical mapping (AFM-NM) to image the surface of a vitrimer, specifically dicarboxylic acid-cured diglycidyl ether of bisphenol A (DGEBA), to assess the curing process of a surface layer and compared this to the process in the bulk. We identified the β-hydroxy esters with various functionalities that are the key to form the cross-links for a system, including difunctional DGEBA and carboxylic acids. The IR peaks of the carbonyl group in generated ester groups are distinguished clearly from those in acids, allowing us to quantitatively assess the curing process at the surface and in the bulk. The initial curing at the surface exhibits a gradual cross-linking and is found to be lower than a rapid cross-linking in the bulk due to a relatively lower concentration of the β-hydroxy esters with high functionalities. This curing process leads to a smaller chemically and mechanically heterogeneous nanostructure at the surface relative to the bulk. After multiple reprocessings, a substantial number of esters lacking dynamic exchange capability form in the bulk, which decrease the flowability and reprocessability of the vitrimers and therefore the mechanical properties.

Effects of Revetments on Nitrification and Denitrification Potentials in the Urban River–Riparian Interface

River–riparian interfaces (RRIs) are not only an important type of urban land but also a key area for mitigating and controlling urban river nitrogen pollution. However, the material and energy exchange dynamics in the natural interaction between rivers and RRIs undergo changes due to the introduction of recently constructed revetments, affecting the nitrogen cycling of the RRI, and the impact of revetments on the control and mitigation of river nitrogen pollution in an RRI is unknown. Therefore, RRI soil properties, nitrification potentials (NPs), and denitrification potentials (DPs) were measured in natural, permeable, and impervious revetments in this study. Furthermore, structural equation models were developed to investigate the potential mechanism of the revetment’s impact on RRI NPs and DPs. The NPs of the natural revetment (NR) (7.22 mg/(kg·d)) were 2.20 and 2.16 times that of the impervious revetment (IR) and permeable revetments (PRs), respectively. The most important influencing factors of NPs were the aboveground biomass (AB) and available nitrogen. Similarly, the denitrification potential (DP) of the PR was 3.41 and 2.03 times that of the NR (22.44 mg/(kg·d)) followed by the IR (37.59 mg/(kg·d)). Furthermore, the AB had the greatest direct and total benefit on the DP, and nitrate may be a factor limiting the denitrification process. A revetment primarily disturbs the anaerobic environment and soil properties at RRIs, as well as changing the nitrification and denitrification potentials via soil erosion, solute exchange, and dry–wet alternation. These research results furnish a theoretical foundation for the restoration of urban rivers’ ecology and additionally provide benchmarks for sustainable development in urban areas.

How transcription factor binding controls transcriptional bursting dynamics: A single-molecule view

In this issue, Pomp etal.1 simultaneously tracked transcriptional bursts of yeast gene GAL10 and transient binding of transcription factor Gal4 at the gene using novel methods. Dynamic exchange and infrequent long binding of Gal4 together enable prolonged transcriptional bursts of GAL10.

Front Cover

The cover image by Simon van Hurne depicts the formation of a dynamic covalent boronate‐TetraAzaADamantane bond, which could be integrated in a covalent adaptable network. As a result of the on‐going dynamic bond exchange reactions within this network, the material could undergo stress relaxation. At the same time, the more robust triple bonding motif allowed for stronger materials compared to their conventional boronate ester‐based counterparts. DOI: 10.1002/pol.20230446 image

Ligand Relay Catalysis Enables Asymmetric Migratory Hydroarylation for the Concise Synthesis of Chiral α-(Hetero)Aryl-Substituted Amines.

Complementary to the design of a single structurally complex chiral ligand to promote each step in transition-metal catalysis, multiligand relay catalysis through dynamic ligand exchange with each step in the catalytic cycle promoted by its best ligand provides an attractive approach to enhance the whole reaction reactivity and selectivity. Herein, a regio- and enantioselective NiH-catalyzed migratory hydroarylation process with a simple combination of a chain-walking ligand and an asymmetric arylation ligand, producing high-value chiral α-(hetero)aryl-substituted amines and their derivatives under mild conditions, is reported. The potential synthetic applications of this transformation are demonstrated by the concise synthesis of (S)-nicotine and a CDK8 inhibitor.

Temporal and Spatial Assessment of Carbon Flux Dynamics: Evaluating Emissions and Sequestration in the Three Northern Protection Forest Project Areas Supported by Google Earth Engine

Contemporary research on terrestrial carbon exchange processes is paramount for a nuanced comprehension of global and local climatic fluctuations and their interaction with anthropogenic activities. This study delves into the spatiotemporal dynamics of vegetation carbon exchanges within the Three Northern Protection Forest Project Area, leveraging two decades of MODIS NPP data and an innovative NEP estimation model. Our analysis highlights a generally increasing trend in Net Ecosystem Productivity (NEP) from 2000 to 2020, with significant growth in approximately 32.97% of the study area and slight increases in 24.18%. Notably, lower NEP values were found in desert and arid zones, whereas higher values were observed in more vegetated regions like Ningxia, Hebei, Inner Mongolia, and the northeast. The study also assesses the impact of climate variables and land-use changes on NEP, identifying both negative and positive correlations in specific regions. Despite the overall positive trend towards ecological restoration and enhancement, significant uncertainties remain, emphasizing the urgent need for further research to support ecosystem resilience and sustainable management practices.

The α-crystallin Chaperones Undergo a Quasi-ordered Co-aggregation Process in Response to Saturating Client Interaction

Small heat shock proteins (sHSPs) are ATP-independent chaperones vital to cellular proteostasis, preventing protein aggregation events linked to various human diseases including cataract. The α-crystallins, αA-crystallin (αAc) and αB-crystallin (αBc), represent archetypal sHSPs that exhibit complex polydispersed oligomeric assemblies and rapid subunit exchange dynamics. Yet, our understanding of how this plasticity contributes to chaperone function remains poorly understood. Using biochemical and biophysical analyses combined with single-particle electron microscopy (EM), we examined structural changes in αAc, αBc and native heteromeric lens α-crystallins (αLc) in their apo-states and at varying degree of chaperone saturation leading to co-aggregation, using lysozyme and insulin as model clients. Quantitative single-particle analysis unveiled a continuous spectrum of oligomeric states formed during the co-aggregation process, marked by significant client-triggered expansion and quasi-ordered elongation of the sHSP oligomeric scaffold, whereby the native cage-like sHSP assembly displays a directional growth to accommodate saturating conditions of client sequestration. These structural modifications culminated in an apparent amorphous collapse of chaperone-client complexes, resulting in the creation of co-aggregates capable of scattering visible light. Intriguingly, these co-aggregates maintain internal morphological features of highly elongated sHSP oligomers with striking resemblance to polymeric α-crystallin species isolated from aged lens tissue. This mechanism appears consistent across αAc, αBc and αLc, albeit with varying degrees of susceptibility to client-induced co-aggregation. Importantly, our findings suggest that client-induced co-aggregation follows a distinctive mechanistic and quasi-ordered trajectory, distinct from a purely amorphous process. These insights reshape our understanding of the physiological and pathophysiological co-aggregation processes of α-crystallins, carrying potential implications for a pathway toward cataract formation.

Integrating mitochondrial and nuclear genomic data to decipher the evolutionary history of Eubranchipus species in Japan

Understanding the genetic diversity and evolutionary history of species is crucial for their conservation and management. In this study, we investigated the genetic diversity and phylogenetic relationships among Eubranchipus species occurring in Japan. Phylogenetic analyses revealed that nuclear and mitochondrial data yield incompatible results. In E. uchidai, nuclear data support the monophyly of the Shimokita area, while mitochondrial data indicate a clustering of Higashidori2 individuals with Hokkaido (Ishikari and Wakkanai) E. uchidai. Similar incongruences were observed in E. hatanakai, where nuclear data favor the monophyly of the Chokai area, while mitochondrial data cluster some Chokai pool 3 individuals with Aizu individuals. These incompatibilities might be caused by mitochondrial gene flow. The findings emphasize the importance of considering both nuclear and mitochondrial data during phylogenetic studies and provide valuable insights into the complex dynamics of migration and genetic exchange in Eubranchipus species.

Drug-eluting stents for coronary artery disease in the perspective of bibliometric analysis.

Drug-eluting stents (DES) play a crucial role in treating coronary artery disease (CAD) by preventing restenosis. These stents are coated with drug carriers that release antiproliferative drugs within the vessel. Over the past two decades, DES have been employed in clinical practice using various materials, polymers, and drug types. Despite optimizations in their design and materials to enhance biocompatibility and antithrombotic properties, evaluating their long-term efficacy and safety necessitates improved clinical follow-up and monitoring. To delineate future research directions, this study employs a bibliometric analysis approach. We comprehensively surveyed two decades' worth of literature on DES for CAD using the Web of Science Core Collection (WOSCC). Out of 5,778 articles, we meticulously screened them based on predefined inclusion and exclusion criteria. Subsequently, we conducted an in-depth analysis encompassing annual publication trends, authorship affiliations, journal affiliations, keywords, and more. Employing tools such as Excel 2021, CiteSpace 6.2R3, VOSviewer 1.6.19, and Pajek 5.17, we harnessed bibliometric methods to derive insights from this corpus. Analysis of annual publication data indicates a recent stabilisation or even a downward trend in research output in this area. The United States emerged as the leading contributor, with Columbia University and CRF at the forefront in both publication output and citation impact. The most cited document pertained to standardized definitions for clinical endpoints in coronary stent trials. Our author analysis identifies Patrick W. Serruys as the most prolific contributor, underscoring a dynamic exchange of knowledge within the field.Moreover, the dual chart overlay illustrates a close interrelation between journals in the "Medicine," "Medical," and "Clinical" domains and those in "Health," "Nursing," and "Medicine." Frequently recurring keywords in this research landscape include DES coronary artery disease, percutaneous coronary intervention, implantation, and restenosis. This study presents a comprehensive panorama encompassing countries, research institutions, journals, keyword distributions, and contributions within the realm of DES therapy for CAD. By highlighting keywords exhibiting recent surges in frequency, we elucidate current research hotspots and frontiers, thereby furnishing novel insights to guide future researchers in this evolving field.

The Investigation of the Response Mechanism of SST and Chlorophyll to Super Typhoon “Rey” in the South China Sea

As one of the most significant disturbance sources in the upper marine environment of the South China Sea, tropical cyclones (typhoons) serve as a typical research subject for investigating the energy transfer process between the ocean and atmosphere. Utilizing satellite remote sensing data and focusing on Typhoon Rey No. 22’s transit event in 2021, this study quantitatively analyzes typhoon-induced energy input through heat pumping and cold suction at both surface and subsurface levels of the ocean. Additionally, it explores the response characteristics and feedback mechanisms of sea surface temperature (SST) and chlorophyll-a concentration (Chl-a) in the South China Sea to typhoon events. The research results show that the SST variation along the typhoon track displayed an asymmetric pattern, with a more pronounced warming on the right side and a cold anomaly lasting for 3–5 days on the left side. The subsurface warm anomaly dominated on the right side, showing a maximum temperature difference of 1.54 °C, whereas Ekman suction-induced upwelling led to cooling effects both at the subsurface and surface level on the left side, resulting in a maximum temperature difference of −3.28 °C. During the typhoon event, there was a significant decrease in sea surface heat flux, reaching 323.36 W/m2, accompanied by corresponding changes in SST due to processes such as upwelling, seawater mixing, and air–sea heat transfer dynamics where anomalies arising from oceanic dynamic processes and exchange through sea surface heat flux contributed equally. Furthermore, strong suction-induced upwelling during the typhoon influenced chlorophyll concentration within the central and western regions of the South China Sea (13.5° N–16.5° N, 111° E–112.5° E), resulting in significant enhancement and reaching its peak value at approximately 0.65 mg/L. The average chlorophyll concentration increased by approximately 0.31 mg/L.

A hybrid dynamic n-party quantum key exchange protocol based on three-particle GHZ states

A hybrid dynamic n-party quantum key exchange protocol based on three-particle GHZ states

High strength, self-healing and hydrophobic fully bio-based polybenzoxazine reinforced pine oleoresin-based vitrimer and its application in carbon fiber reinforced polymers

The traditional carbon fiber reinforced polymers (CFRPs) matrix is a permanent 3D cross-linked network that is difficult to degrade and reprocess. In order to solve the closed-loop recycling of carbon fibers (CFs) and develop green economy. We synthesized aldehyde-containing bio-based benzoxazine (VD) from vanillin and 1,10-diaminodecane, the epoxy resin vitrimer matrix (P-AE-MV) was prepared by curing acrylpimaric acid diglycidyl ester (AE) with a Schiff base (MV) formed by 1,8-menthane diamine (MDA) and VD. Under the double dynamic covalent bond of Schiff base and β-hydroxy ester, P-AE-MV has a very low dynamic bond exchange activation energy Ea = 48.1 kJ mol−1, which can realize the rapid topological rearrangement of polymer network, and give P-AE-MV excellent self-healing, shape memory, reprocessability and degradability. In addition, the introduction of polybenzoxazine (PBz) structure greatly improved the mechanical properties, thermal decomposition temperature, carbon yield and hydrophobicity of epoxy resin vitrimer, which is very suitable for CFRPs matrix. The CFRP (P-AE-MV-CF) prepared with P-AE-MV as matrix resin have good mechanical properties, reprocessability, shape memory and self-adhesion. Especially, it can be rapidly ammonolysis with n-butylamine under mild conditions (60 °C), achieving efficient and non-destructive recycling of CFs. This work provides an effective solution to promote the closed-loop recycling of CFs and the sustainable development of CFRPs using fully bio-based resources as raw materials.

Analysis of Social Interaction of Deaf Children in Special Schools


 
 
 
 Deaf is a term used to describe the symptoms and symptoms of someone who is hearing impaired or deaf. Deaf children interact through a variety of methods, including sign language, facial expressions, and body, as well as the use of hearing aid technology. They can also utilize visual communication approaches, peer support, and participation in group activities to strengthen social skills. Social interaction is a dynamic in which individuals or groups communicate, act, or influence each other in a particular environment or situation. Social interaction involves the exchange of information, emotions, ideas, or behaviors between individuals or groups. This research makes a valuable contribution to improving our understanding of the benefits of social interaction for deaf children in Special Schools, opening up opportunities for the development of more inclusive educational strategies and supporting their holistic development. This study aimed to analyze social interactions between deaf children. An observational approach and interview, this study explores the dynamics of communication, information exchange, and emotional understanding in interactions between both groups of children. Qualitative analysis methods are used to identify unique communication patterns and understand the challenges faced by deaf children in communicating. The subjects in this study were interviewing homeroom teachers and counseling teachers at the school, the number of subjects to be studied were children with deafness. The results highlight adaptation efforts and communication strategies developed by deaf children to interact. The results of these findings can provide valuable insights for educators, parents, and health practitioners in supporting the development of social skills of deaf children so that they can engage more effectively in society.
 
 
 

A Water-Stable Boronate Ester Cage.

The reversible condensation of catechols and boronic acids to boronate esters is a paradigm reaction in dynamic covalent chemistry. However, facile backward hydrolysis is detrimental for stability and has so far prevented applications for boronate-based materials. Here, we introduce cubic boronate ester cages 6 derived from hexahydroxy tribenzotriquinacenes and phenylene diboronic acids with ortho-t-butyl substituents. Due to steric shielding, dynamic exchange at the Lewis acidic boron sites is feasible only under acid or base catalysis but fully prevented at neutral conditions. For the first time, boronate ester cages 6 tolerate substantial amounts of water or alcohols both in solution and solid state. The unprecedented applicability of these materials under ambient and aqueous conditions is showcased by efficient encapsulation and on-demand release of β-carotene dyes and heterogeneous water oxidation catalysis after the encapsulation of ruthenium catalysts.

Dynamic ion exchange engineering bismuth ferrite-derived Bi2O2CO3 for rapid piezo-photocatalytic degradation of tetracycline

Piezoelectric materials can generate the built-in electric field under ultrasound assistance, which is beneficial to the separation of the photogenerated electron-hole pairs in photocatalysis. Meanwhile, the ultrasound stress usually leads to accelerate electron transfer and enhance catalytic activity. Thus, piezo-photocatalysis technique is believed to be one of the effective techniques for organic pollutant degradation. In this work, a binary piezoelectric integrated piezo-photocatalytic Z-Scheme heterojunction with bismuth ferrite (BFO) and bismuth oxycarbonate (Bi2O2CO3, BOC) based on the in situ production of Bi2O2CO3 on Bi25FeO40 surface in dichloromethane, where Bi25FeO40 was employed as piezoelectric materials and Bi source, CO2 dissolved in dichloromethane was used as carbon source. Under 60 min ultrasound and visible light irradiation, the optimal BFO/BOC presented a higher piezo-photocatalytic tetracycline (TC) degradation rate (95 %) than Bi25FeO40 (30 %) and Bi2O2CO3 (17 %). Moreover, the optimal BFO/BOC illustrated higher piezo-photocatalytic TC degradation rate under ultrasound and visible light irradiation than that under visible light condition and ultrasound condition, respectively. These results strongly demonstrated the synergistically piezo-photocatalytic degradation of TC by BFO and BOC. This work not only provides a novel piezo-photocatalyst for pollutant degradation, but also provides a novel method to prepare Bi2O2CO3-based piezo-photocatalytic composite catalyst.

Facile Bond Exchanging Strategy for Engineering Wet Adhesion and Antioxidant/Antibacterial Thin Layer over a Dynamic Hydrogel via the Carbon Dots Derived from Tannic Acid/ε-Polylysine.

Adhesive hydrogels, playing an essential role in stretchable electronics, soft robotics, tissue engineering, and so forth, upon functioning often need to adhere to various substrates in wet conditions and simultaneously exhibit antibacterial/antioxidant properties while possessing the intrinsic stretchability and elasticity of the hydrogel network intact. Therefore, simple approaches to conveniently access adhesive hydrogels with multifunctional surfaces are being pursued. Herein, a facile strategy has been proposed to construct multifunctional adhesive hydrogels via surface engineering of a multifunctional carbon dot (CD)-decorated polymeric thin layer by dynamic bond exchange. By this strategy, a double cross-linked network hydrogel of polyacrylamide (PAM) and oxidized dextran (ODA) was engineered with a unique dense layer over the Schiff base hydrogel matrix by aqueous solution immersion of PA-120, versatile CDs derived from tannic acid (TA) and ε-polylysine (PL). Without any additional agents, the PA-120 CDs with residual polyphenolic/catechol and amine moieties were incorporated into the surface structure of the hydrogel network by the combined action of the Schiff base and hydrogen bonds to form a dense surface layer that can exhibit high wet adhesive performance via the amine-polyphenol/catechol pair. The armor-like dense architecture also endowed hydrogels with considerably enhanced tensile/compression properties and excellent antioxidant/antibacterial abilities. Besides, the single-sided modified Janus hydrogel and completely surface-modified hydrogel can be flexibly developed through this approach. This strategy will provide new insights into the preparation and application of surface-modified hydrogels featuring multiple functions and tunable interfacial properties.

Measuring Hydroxyl Exchange Rates in Glycans Using a Synergistic Combination of Saturation Transfer and Relaxation Dispersion NMR.

Molecular recognition events mediated by glycans play pivotal roles in controlling the fate of diverse biological processes such as cellular communication and the immune response. The affinity of glycans for their target receptors is governed primarily by the hydrogen bonds formed by hydroxyl groups decorating the glycan surface. Hydroxyl exchange rate constants are therefore vital parameters that report on glycan structure and dynamics. Here we present a strategy for characterizing hydroxyl hydrogen/deuterium (H/D) exchange in glycans that employs a synergistic combination of 13C chemical exchange saturation transfer (CEST) and Carr-Purcell-Meiboom-Gill relaxation dispersion (CPMG) NMR methods. We show that the combination of CEST and CPMG experiments facilitates the sensitive detection of the small (∼0.1 ppm) two-bond deuterium isotope shift on a 13C nucleus when the attached hydroxyl group fluctuates between protonated and deuterated states. This shift is leveraged for measuring site-specific kinetic H/D exchange rate constants as well as thermodynamic free energies of isotope fractionation. The CEST and CPMG modules are integrated with a selective J-cross-polarization scheme that provides the flexibility for rapid characterization of H/D exchange at a specific hydroxyl site. Moreover, our approach enables the precise isothermal measurement of hydroxyl exchange rate constants without the need for cumbersome isotope labeling. The H/D exchange rate constants of three different glycans assessed using this method highlight its potential for detecting transient intra- and intermolecular hydrogen bonds. In addition, the trends in H/D exchange rate constants establish site-specific steric accessibility as a key determinant of solvent exchange dynamics in glycans.

Educating dental students on social media ethics

Background: Ethics is essential in healthcare, including dentistry, to help dentists do the right things, build trust, and take good care of patients, but even though dentists learn about ethics, they still have some ethical problems, like sharing patient pictures without permission or criticizing other dentists on social media. Teaching ethics practically and interestingly could help them use ethical rules better in their work. Objective: To explain the better teaching mechanism about ethics to dental students, especially when using social media. Methods: Data was expected from dental medicine students at Airlangga University, who were taught ethics using four methods: conventional lectures, group discussions, paper assignments, and creating educational videos. Results: After completing the ethics class, students are expected to apply ethical principles as co-assistant doctors, extending to their use of social media. Conclusion: discussion-based classes significantly prepared dental medicine students for their roles as co-assistant doctors, fostering dynamic idea exchange, critical thinking, and practical application of ethical knowledge, especially when using social media.

How does perceived corporate social responsibility affect job performance during the COVID-19 pandemic? The roles of resilience and help exchange dynamics

How does perceived corporate social responsibility affect job performance during the COVID-19 pandemic? The roles of resilience and help exchange dynamics

Vitrimer Nanocomposites for Highly Thermal Conducting Materials with Sustainability.

Vitrimers, as dynamic covalent network polymers, represent a groundbreaking advancement in materials science. They excel in their applications, such as advanced thermal-conductivity composite materials, providing a sustainable alternative to traditional polymers. The incorporation of vitrimers into composite fillers enhances alignment and heat passway broadly, resulting in superior thermal conductivity compared to conventional thermosetting polymers. Their dynamic exchange reactions enable straightforward reprocessing, fostering the easy reuse of damaged composite materials and opening possibilities for recycling both matrix and filler components. We review an overview of the present advancements in utilizing vitrimers for highly thermally conductive composite materials.