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Background: In China, individuals diagnosed with esophageal cancer are confronted with an elevated risk of nutritional inadequacy or malnutrition throughout the course of their disease, a condition that contributes to various adverse clinical outcomes. A vast corpus of data are burgeoning at an unprecedented rate, primarily due to the revolutionary growth of digitalization technologies and artificial intelligence, notably within the domains of health care and medicine. The purpose of this investigation is to initiate the development of a nutritional screening and assessment indicator framework for patients with esophageal cancer within the Chinese context. We seek to furnish an instrumental reference to facilitate preparations for the forthcoming era of advanced, "deep," evidence‐based medicine. Methods: An integrative methodology was employed to forge the preliminary draft of the nutritional screening and assessment indicator system for preoperative patients with esophageal cancer. This encompassed a rigorous literature survey, in‐depth clinical practice investigation, and the facilitation of expert panel discussions. Thereafter, two iterative consultation phases were conducted using the Delphi method in China. The analytic hierarchy process was deployed to ascertain the weighting of each index within the definitive evaluation indicator system. Results: The effective response rates for the dual rounds of expert consultation were 91.7% and 86.4%, with commensurate authority coefficients of 0.97 and 0.91. The Kendall harmony coefficients were ascertained to be 0.19 and 0.14 (p < 0.01), respectively. The culminating nutritional screening and assessment indicator system for patients with esophageal cancer comprised 5 primary‐level indicators and 38 secondary‐level indicators. Conclusions: The nutritional screening and assessment indicator system contrived for patients with esophageal cancer is underpinned by cogent theoretical principles, leverages an astute research methodology, and manifests dependable outcomes. This system may be appositely utilized as a meaningful reference for the nutritional screening and assessment process in patients afflicted with esophageal cancer. [ABSTRACT FROM AUTHOR]

Transition‐metal‐catalyzed acceptorless dehydrogenative coupling (ADC) has emerged as a sustainable synthetic strategy for the construction of N‐heteroaromatics. Herein, a series of water‐soluble amidato Ru catalysts were designed, synthesized, and utilized in the selective synthesis of 2‐substituted benzimidazoles from the aromatic diamines and primary alcohols, as well as 2‐substituted quinolines from the substituted 2‐aminobenzyl alcohols and acetophenones via the ADC strategy in water. Catalyst 1 d bearing a strong electron‐donating hydroxyl group on the ligand exhibited the best catalytic activity. The catalytic system demonstrated remarkable efficiency and versatility, allowing for the application of over 40 substrates in two ADC reactions with good to high yields. Based on control experiments and density functional theory (DFT) calculations, a plausible mechanism was proposed, highlighting the significant role of functionalized amidato Ru complexes in catalyzing alcohol dehydrogenation via an outer‐sphere pathway. [ABSTRACT FROM AUTHOR]

Background: In Parkinson's disease (PD), inflammation may lead to the degeneration of dopaminergic (DAergic) neurons. Previous studies showed that inflammatory mediators mainly contributed to this phenomenon. On the other hand, invasive neuromodulation methods such as deep brain stimulation (DBS) have better therapeutic effects for PD. One possibility is that DBS improves PD by influencing inflammation. Therefore, we further explored the mechanisms underlying inflammatory mediators and DBS in the pathogenesis of PD. Methods: We measured serum levels of two inflammatory markers, namely RANTES (regulated on activation, normal T cell expressed and secreted) and tumor necrosis factor‐alpha (TNF‐α), using Luminex assays in 109 preoperative DBS PD patients, 49 postoperative DBS PD patients, and 113 age‐ and sex‐matched controls. The plasma protein data of the different groups were then statistically analyzed. Results: RANTES (p < 0.001) and TNF‐α (p = 0.005) levels differed significantly between the three groups. A strong and significant correlation between RANTES levels and Hoehn‐Yahr (H‐Y) stage was observed in preoperative PD patients (rs = 0.567, p < 0.001). Significant correlations between RANTES levels and Unified Parkinson's Disease Rating Scale III (UPDRS III) score (rs1 = 0.644, p = 0.033 and rs2 = 0.620, p = 0.042) were observed in matched patients. No correlation was observed for TNF‐α levels. Conclusion: The results of this study indicate that PD patients have a persistent inflammatory profile, possibly via recruitment of activated monocytes, macrophages, and T lymphocytes to the central nervous system (CNS). DBS was shown to have a significant therapeutic effect on PD, which may arise by improving the inflammatory environment of the central nervous system. [ABSTRACT FROM AUTHOR]

The sialidases, which catalyze the hydrolysis of sialic acid from extracellular glycoconjugates, are a group of major virulence factors in various pathogenic bacteria. In Porphyromonas gingivalis, which causes human periodontal disease, sialidase contributes to bacterial pathogenesis via promoting the formation of biofilms and capsules, reducing the ability for macrophage clearance, and providing nutrients for bacterial colonization. Here, the crystal structure of the P. gingivalis sialidase SiaPG is reported at 2.1 Å resolution, revealing an N‐terminal carbohydrate‐binding domain followed by a canonical C‐terminal catalytic domain. Simulation of the product sialic acid in the active‐site pocket together with functional analysis enables clear identification of the key residues that are required for substrate binding and catalysis. Moreover, structural comparison with other sialidases reveals distinct features of the active‐site pocket which might confer substrate specificity. These findings provide the structural basis for the further design and optimization of effective inhibitors to target SiaPG to fight against P. gingivalis‐derived oral diseases. [ABSTRACT FROM AUTHOR]

BACKGROUND: The application of curcumin (CUR) in the food industry is limited by its instability, hydrophobicity and low bioavailability. Yeast cell protein (YCP) is a by‐product of spent brewer's yeast, which has the potential to deliver bioactive substances. However, the environmental stresses such as pH, salt and heat treatment has restricted its application in the food industry. Maillard reaction as a non‐enzymatic browning reaction can improve protein stability under environmental stress. RESULTS: The CUR was successfully encapsulated into the hydrophobic core of YCP/glycated YCP (GYCP) and enhanced by hydrogen bonding, resulting in static fluorescence quenching of YCP/GYCP. The average diameter and dispersibility of GYPC−CUR nanocomplex were significantly improved after glucose glycation (121.40 nm versus 139.70 nm). Moreover, the encapsulation capacity of CUR was not influenced by glucose glycation. The oxidative stability and bioaccessibility of CUR in nanocomplexes were increased compared with free CUR, especially complexed with GYCP conjugates. CONCLUSION: Steric hindrance provided by glucose conjugation improved the enviriomental stability, oxidative activity and bioaccessibility of CUR in nanocomplexes. Thus, glucose‐glycated YCP has potential application as a delivery carrier for hydrophobic compounds in functional foods. © 2022 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

Summary: Antarctic krill oil (AKO) and fish oil (FO) were microencapsulated by a pilot‐scale spray dryer in this study. The effect of lipid class compositions on the encapsulation properties of the obtained microcapsules was investigated. The particle size distribution of both microcapsules ranged from 29.23 ± 2.20 to 36.79 ± 3.45 μm, and the moisture content and water activity (aw) also indicated that both AKO and FO microcapsules were suitable for long‐term storage. Interestingly, differences in lipid composition affected the microstructure of the microcapsules formed, thereby affecting their oxidative stability and digestive behaviour. Compared with FO microcapsules, the surface microstructure of PLs‐enriched microcapsules (AKO microcapsules) was smoother, endowing it better oxidative stability and higher DHA (72.13 ± 2.32% vs. 63.08 ± 2.98%) and EPA (75.94 ± 1.43% vs. 68.26 ± 2.98%) bioaccessibility. These findings may have important implications for the development of microcapsules formulated with different lipid classes in the food industry. [ABSTRACT FROM AUTHOR]

The olive genus Olea includes c. 30–40 taxa in three subgenera (Olea, Tetrapilus, and Paniculatae) within the family Oleaceae. Historically, the Olea genus was classified into four groups that were overall well supported by reconstructed phylogenies, despite incomplete sampling of subgenus Tetrapilus and poor resolution within clades. These analyses also showed that the genus was not monophyletic. Reliable identification of Olea species is important for both their conservation and utilization of this economically important genus. In this study, we used phylogenomic data from genome skimming to resolve relationships within Olea and to identify molecular markers for species identification. We assembled the complete plastomes, and nrDNA of 26 individuals representing 13 species using next‐generation sequencing and added 18 publicly available accessions of Olea. We also developed nuclear SNPs using the genome skimming data to infer the phylogenetic relationships of Olea. Large‐scale phylogenomic analyses of 138 samples of tribe Oleeae supported the polyphyly of Olea, with Olea caudatilimba and Olea subgenus Tetrapilus not sharing their most recent common ancestor with the main Olea clade (subgenus Paniculatae and subgenus Olea). The interspecific phylogenetic resolution was poor owing to a possible rapid radiation. By comparing with the plastome data, we identified the markers ycf1b and psbE‐petL as the best Olea‐specific chloroplast DNA barcodes. Compared with universal barcodes, specific DNA barcodes and super‐barcode exhibited higher discriminatory power. Our results demonstrated the power of phylogenomics to improve phylogenetic relationships of intricate groups and provided new insights into barcodes that allow for accurate identification of Olea species. Highlights: Genus Olea was a polyphyletic group and had undergone rapid radiation.ycf1b and psbE‐petL were two Olea‐specific chloroplast DNA barcodes.Plastome sequence data had effective power to improve phylogenetic resolution and species discrimination. [ABSTRACT FROM AUTHOR]

Objective: To determine whether robot‐assisted laparoscopic partial nephrectomy (RALPN) can benefit patients in terms of functional recovery in the treatment of renal hilar tumors compared to conventional laparoscopic partial nephrectomy (CLPN). Methods: Between January 2019 and July 2021, patients with hilar tumors who underwent partial nephrectomy (PN) were acquired at our center and were classified into RALPN and CLPN groups. Ipsilateral parenchymal volume (IPV) and glomerular filtration rate (GFR) were determined independently 3–5 days before and 3 months after PN using contrast‐enhanced computed tomography and nuclear renal scans. Pearson correlation was used to determine the link between ipsilateral GFR preservation and IPV preserved. Concurrently, multivariable analysis was employed to determine characteristics associated with functional recovery. Results: A total of 96 patients with hilar tumors were studied, of which 41 received RALPN and 55 received CLPN. Excisional parenchymal volume was 27 and 37 cm3 (p = 0.005) in RALPN and CLPN groups, respectively, and IPV preserved was 77% and 68% (p < 0.001). Furthermore, the ipsilateral GFR preserved was 77.7% and 75.3%, respectively (p = 0.003). On Pearson correlation, ipsilateral GFR preservation was linked with IPV preserved (r = 0.36, p < 0.001). According to a multivariate study, baseline GFR, IPV preserved, and surgical procedures (RALPN vs. CLPN) were significant factors influencing functional recovery. Conclusion: Our study suggests that RALPN, rather than CLPN, can achieve better functional recovery in the treatment of hilar tumors due to its ability to win more IPV preserved. RALPN should be recommended as the first‐line treatment for hilar tumors, but randomized controlled trials are required to validate our findings. [ABSTRACT FROM AUTHOR]

Summary: Bovine serum albumin (BSA) and BSA‐glucose Maillard conjugate with different degree of glycation (GBSAI and GBSAII) were used as emulsifiers to stabilised curcumin (CUR)‐loaded oil‐in‐water nanoemulsions. Nanoemulsions were stabilised by BSA with greater degree of glycation (BSA < GBSAI < GBSAII) resulting in smaller Z‐average diameter, higher zeta potential and higher encapsulation efficiency. The GBSA (especially GBSAII) conjugates significantly improved the environmental stability of nanoemulsions and enhanced the CUR retention rate during long‐time storage at 4 and 25 °C. Furthermore, BSA with a higher degree of glycation (GBSAII) was more efficiently promoted the formation of mixed micelles, thereby improving the stability and bioaccessibility of encapsulated CUR during in vitro digestion. The advantages of GBSAII‐stabilised nanoemulsions may provide a better option for efficient protection and delivery of hydrophobic ingredients. [ABSTRACT FROM AUTHOR]

In the past century, ferroelectrics are well known in electroceramics and microelectronics for their unique ferroelectric, piezoelectric, pyroelectric, and photovoltaic effects. Nowadays, the advances in understanding and tuning of these properties have greatly promoted a broader application potential especially in energy and environmental fields, by harvesting solar, mechanical, and heat energies. For example, high piezoelectricity and high pyroelectricity can be designed by defect or microstructure engineering for piezo‐ and pyro‐catalyst, respectively. Moreover, highly piezoelectric and broadband (UV–Vis–NIR) light‐responsive ferroelectrics can be designed via defect engineering, giving rise to a new concept of photoferroelectrics for efficient photocatalysis, piezocatalysis, pyrocatalysis, and related cocatalysis. This article first summarizes the recent developments in ferroelectrics in terms of piezoelectricity, pyroelectricity, and photovoltaic effects based on defect and microstructure engineering. Then, the potential applications in energy generation (i.e., photovoltaic effect, H2 generation, and self‐powered multisource energy harvesting and signal sensing) and environmental protection (i.e., photo‐piezo‐pyro‐ cocatalytic dye degradation and CO2 reduction) are reviewed. Finally, the outlook and challenges are discussed. This article not only covers an overview of the state‐of‐art advances of ferroelectrics, but also prospects their applications in coping with energy crisis and environmental pollution. [ABSTRACT FROM AUTHOR]

The surface of gold nanorods is chemically charged by ascorbic acid; the charging effect results in not only the blue shift on their surface plasmon bands, but also the change of the deposition rate of silver on their surfaces. The rate was prominently accelerated at room temperature, but slightly slowed down at higher temperature. The shape of gold‐silver core‐shell nanoparticles could not be obviously affected. The Fermi level of gold nanorods begins to increase under the action of charging and alters the electrical double‐layer structure of gold nanorods, resulting in the different deposition rate of silver on gold. [ABSTRACT FROM AUTHOR]

Summary: Mimicry is the phenomenon in which one species (the mimic) closely resembles another (the model), enhancing its own fitness by deceiving a third party into interacting with it as if it were the model. In plants, mimicry is used primarily to gain fitness by withholding rewards from mutualists or deterring herbivores cost‐effectively. While extensive work has been documented on putative defence mimicry, limited investigation has been conducted in the field of chemical mimicry.In this study, we used field experiments, chemical analyses, behavioural assays, and electrophysiology, to test the hypothesis that the birthwort Aristolochia delavayi employs chemical mimicry by releasing leaf scent that closely resembles stink bug defensive compounds and repels vertebrate herbivores.We show that A. delavayi leaf scent is chemically and functionally similar to the generalized defensive volatiles of stink bugs and that the scent effectively deters vertebrate herbivores, likely through the activation of TRPA1 channels via (E)‐2‐alkenal compounds.This study provides an unequivocal example of chemical mimicry in plants, revealing intricate dynamics between plants and vertebrate herbivores. Our study underscores the potency of chemical volatiles in countering vertebrate herbivory, urging further research to uncover their potentially underestimated importance. [ABSTRACT FROM AUTHOR]

The vision Transformer structure performs better in salient object detection than the convolutional neural network (CNN)‐based approach. Vision Transformer predicts saliency by modelling long‐range dependencies from sequence to sequence with convolution‐free. It is challenging to distinguish the salient objects' location and obtain structural details for the influence of extracting irrelevant contextual information. A novel saliency sparse Transformer network is proposed to exploit sparse attention to guide saliency prediction. The convolution‐like with dilation in the token to token (T2T) module is replaced to achieve relationships in larger regions and to improve contextual information fusion. An adaptive position bias module is designed for the Vision Transformer to make position bias suitable for variable‐sized RGB images. A saliency sparse Transformer module is designed to improve the concentration of attention on the global context by selecting the Top‐k of the most relevant segments to improve the detection results further. Besides, cross‐modality to exploit the complementary RGB and depth modality fusion module (CMF) is used to take advantage of the complementary RGB image features and spatial depth information to enhance the feature fusion performance. Extensive experiments on multiple benchmark datasets demonstrate this method's effectiveness and superiority that it is suitable for saliency prediction comparable to state‐of‐the‐art RGB and RGB‐D saliency methods. [ABSTRACT FROM AUTHOR]

Summary: Oestrogens play an important role in the development and progression of papillary thyroid carcinoma (PTC) through oestrogen receptor (ER)‐α and ‐β, which may exert different or even opposing actions in PTC. The roles of ERβ in ERα‐negative PTC are still not clear. This study investigated the expression dynamics of ERβ1 (wild‐type ERβ) and its clinical significance in female ERα‐negative PTC patients. ERβ1 expression was detected in thyroid tissues of 136 female patients diagnosed with PTC. The relationships between ERβ1 expression and clinicopathological/biological factors were also analysed in female ERα‐negative PTC patients. The total score for ERβ1 was significantly lower in female ERα‐negative PTC patients with LNM or ETE when compared to those without LNM or ETE (Z = −2.923, P = 0.003 and Z = −3.441, P = 0.001). Accordingly, the total score for ERβ1 was significantly higher in ERα‐negative PTC patients expressing E‐cadherin compared to patients negative for E‐cadherin expression (Z = −2.636, P = 0.008). The total score was lower in ERα‐negative PTC patients positive for VEGF expression compared to those negative for VEGF expression (Z = −1.914, P = 0.056). This preliminary study indicates that reduced expression of ERβ1 in female ERα‐negative PTC patients is associated with greater progression of the disease. This may provide insights into the underlying molecular mechanisms of ERβ1 and could help design targeted approaches for treating or even preventing this disease. [ABSTRACT FROM AUTHOR]

A series of homo- and hetero-trinuclear cobalt(II) complexes [Co3(L)(OAc)2(CH3CH2OH)(H2O)] (1), [Co2Ba(L)(OAc)2] (2) and [Co2Ca(L)(OAc)2]·CHCl3 (3), containing an acyclic naphthalenediol-based ligand H4L were synthesized. All the three complexes were characterized by elemental analyses, IR, UV–vis spectra and single crystal X-ray diffraction analyses. Comparative studies of the structures and spectroscopic properties are carried out on these complexes. All of the complexes show catechol oxidase activities in MeCN. Using UV–vis spectroscopy, we monitored the aerial oxidation of 3,5-di-tert-butylcatechol (3,5-DTBCH2) to 3,5-di-tert-butylquinone (3,5-DTBQ), which confirms the essential role of these complexes in enhancing the catalytic reaction. [ABSTRACT FROM AUTHOR]

In recent years, a methodology merging photoredox catalysis with organocatalysis termed 'photoredox organocatalysis' has emerged to allow the direct, selective and efficient functionalization of the α/ β-C of carbonyl compounds under mild reaction condition. In this review, photophysics background of photoredox catalysis is introduced, followed by a report on recent advances in direct α- and β-functionalization of carbonyls with photoredox organocatalysis methodology. With this different reaction modes, valuable synthetic targets including different α/ β-functionalized carbonyls are accessible. [ABSTRACT FROM AUTHOR]

Two trinuclear CoII and ZnII complexes, [(CoL)2(OAc)2Co] and [(ZnL)2(OAc)2Zn], with an asymmetric Salen-type bisoxime ligand [H2L = 4-( N, N-diethylamine)-2,2′-[ethylenediyldioxybis(nitrilomethylidyne)]diphenol] were synthesized and characterized by elemental analyses, IR, UV/Vis, and fluorescent spectroscopy. The crystal structures of the CoII and ZnII complexes were determined by single-crystal X-ray diffraction methods. The CoII atom is pentacoodinated by N2O2 donor atoms from the (L)2- unit and one oxygen atom from the coordinated acetate ion, resulting in a trigonal bipyramid arrangement. With the help of intermolecular hydrogen bonding C-H ···O and C-H ···π interactions, a self-assembled continual zigzag chain-like supramolecular structure is formed. The ZnII atom is pentacoodinated by N2O2 donor atoms from the (L)2- unit and one oxygen atom from the coordinated acetate ion, resulting in an almost regular trigonal bipyramid arrangement. A self-assembled continual 1D supramolecular chain-like structure is formed by intermolecular hydrogen bonding C-H ···O and C-H ···π interactions. Additionally, the photophysical properties of the CoII and ZnII complexes were discussed. [ABSTRACT FROM AUTHOR]

Mononuclear copper(II) and trinuclear cobalt(II) complexes, namely [Cu(L1)]2 ·CH2Cl2 and [{Co(L2)(EtOH)}2Co(H2O)] ·EtOH {H2L1 = 4,6-dichloro-6′-methyoxy-2,2′-[1,1′-(ethylenedioxydinitrilo)dimethylidyne]diphenol and H3L2 = 6-ethyoxy-6′-hydroxy-2,2′-[1,1′-(ethylenedioxydinitrilo)dimethylidyne]diphenol}, were synthesized and characterized by elemental analyses, IR and UV/Vis spectroscopy, and single-crystal X-ray diffraction. In the CuII complex, the CuII atom is four-coordinate, with a N2O2 coordination sphere, and has a slightly distorted square-planar arrangement. Interestingly, the obtained trinuclear CoII complex is different from the common reported 2:3 (L:CoII) salamo-type CoII complexes. Infinite 2D layer supramolecular structures are formed via abundant intermolecular hydrogen bonding and π ···π stacking interactions in the CuII and CoII complexes. [ABSTRACT FROM AUTHOR]

Large‐scale multi‐heterostructure and optimal band alignment are significantly challenging but vital for photoelectrochemical (PEC)‐type photodetector and water splitting. Herein, the centimeter‐scale bismuth chalcogenides‐based cascade heterostructure is successfully synthesized by a sequential vapor phase deposition method. The multi‐staggered band alignment of Bi2Te3/Bi2Se3/Bi2S3 is optimized and verified by X‐ray photoelectron spectroscopy. The PEC photodetectors based on these cascade heterostructures demonstrate the highest photoresponsivity (103 mA W−1 at −0.1 V and 3.5 mAW−1 at 0 V under 475 nm light excitation) among the previous reports based on two‐dimensional materials and related heterostructures. Furthermore, the photodetectors display a fast response (≈8 ms), a high detectivity (8.96 × 109 Jones), a high external quantum efficiency (26.17%), and a high incident photon‐to‐current efficiency (27.04%) at 475 nm. Due to the rapid charge transport and efficient light absorption, the Bi2Te3/Bi2Se3/Bi2S3 cascade heterostructure demonstrates a highly efficient hydrogen production rate (≈0.416 mmol cm−2 h−1 and ≈14.320 µmol cm−2 h−1 with or without sacrificial agent, respectively), which is far superior to those of pure bismuth chalcogenides and its type‐II heterostructures. The large‐scale cascade heterostructure offers an innovative method to improve the performance of optoelectronic devices in the future. [ABSTRACT FROM AUTHOR]

A Salamo-type ligand 6,6′-diethoxy-2,2′-[1,1′-(ethylenedioxydinitrilo)dimethylidyne]diphenol (H2L) and its pentacoordinate copper(II) complex [CuL(H2O)] were synthesized and structurally characterized. The molecule of H2L is located in a crystallographic inversion center and adopts E configuration with respect to the C=N bond. In the complex [CuL(H2O)], the CuII atom has a tetragonally elongated square-pyramidal configuration with donor atoms N2O2 forming a perfect basal plane. And an infinite 2D layer supramolecular structure is formed through intermolecular C1-H1A ···O5 and C2-H2A ···O3 hydrogen bonding interactions. [ABSTRACT FROM AUTHOR]

Nelumbonaceae is a morphologically unique family of angiosperms and was traditionally placed in Nymphaeales; more recently, it was placed in Proteales based on molecular data, or in an order of its own, Nelumbonales. To determine the systematic position of the family and to date the divergence time of the family and the divergence time of its two intercontinentally disjunct species, we sequenced the entire chloroplast genome of Nelumbo lutea and most of the chloroplast genes of N. nucifera. We carried out phylogenetic and molecular dating analyses of the two species and representatives of 47 other plant families, representing the major lineages of angiosperms, using 83 plastid genes. The N. lutea genome was 163 510 bp long, with a total of 130 coding genes and an overall GC content of 38%. No significant structural differences among the genomes of N. lutea, Nymphaea alba, and Platanus occidentalis were observed. The phylogenetic relationships based on the 83 plastid genes revealed a close relationship between Nelumbonaceae and Platanaceae. The divergence times were estimated to be 109 Ma between the two families and 1.5 Ma between the two Nelumbo species. The estimated time was only slightly longer than the age of known Nelumbo fossils, suggesting morphological stasis within Nelumbonaceae. We conclude that Nelumbonaceae holds a position in or close to Proteales. We further conclude that the two species of Nelumbo diverged recently from a common ancestor and do not represent ancient relicts on different continents. [ABSTRACT FROM AUTHOR]

Two nickel(II) complexes, namely {[NiL(MeOH)(μ-OAc)]2Ni} ·2CH2Cl2 ·2MeOH ( 1) and {[NiL(EtOH)(μ-OAc)]2Ni} ·2EtOH ( 2) {H2L = 5, 5′-dimethoxy-2, 2′-[(ethylene)dioxybis(nitrilomethylidyne)]diphenol}, were synthesized and structurally characterized. Two trinuclear NiII complexes are both hexacoordinate around the central NiII atoms, showing octahedral coordination arrangements, and each complex comprises three divalent NiII atoms, two deprotonated L2- ligands, in which four μ-phenoxo oxygen atoms forming two [NiL( X)] ( X = MeOH or EtOH) units, and coordinated and non-coordinated solvent molecules. Complex 1 exhibits a 2D supramolecular network through intermolecular O-H ···O, C-H ···O and C-H ···π interactions, whereas complex 2 forms an infinite 1D chain by intermolecular C-H ···O hydrogen bonding interactions. [ABSTRACT FROM AUTHOR]

With 1 figure and 1 table Abstract Public sequence databases provide a convenient and inexpensive resource for the rapid development of microsatellite markers. We analysed 3406 publically available expressed sequence tags (ESTs) from caespitose bamboo species ( Bambusa edulis and B. oldhamii) and found 245 non-redundant simple sequence repeats (SSRs) in 205 EST contigs that were used to develop 15 EST-SSR markers. The transferability of the markers was 59.6% among 14 additional caespitose bamboo species (4 within the same genus and 10 in other genera) and Phyllostachys pubescens. The successfully transferred markers showed 51.4% polymorphism. Markers BOM01 and BOM02 transferred successfully to most of the caespitose bamboo species showed rich polymorphism, and are therefore potentially valuable as species-specific alleles for the identification of caespitose bamboo interspecies hybrids. [ABSTRACT FROM AUTHOR]

We have generated a series of chicken skeletal muscle troponin C mutants to study the conformation of the regulatory domain in the N-terminal half of the molecule. These mutants each contained a single Trp at position 22 (helix A), 52 (linker of helices B and C), or 90 (central helix). Some of these mutants also contained additional mutations to introduce a single Cys at a desired position. The mutants were characterized by molecular graphics and CD and found to have a minimum of structural perturbations when compared with the native structure. They also retained the ability to regulate myofibrillar ATPase activity. The fluorescence of Trp22 was sensitive to Ca2+ binding only to the regulatory sites, whereas Trp52 and Trp90 responded to Ca2+ binding to both the regulatory and the Ca2+/Mg2+ sites. The tryptophan quantum yield (Q) of all Trp22-containing mutants was very high (0.33) in the absence of bound Ca2+, compared to that of L-tryptophan in aqueous solution (0.14). Q decreased 25 % upon binding of Ca2+ to the regulatory sites. The quantum yields of Trp52 and Trp90 in apo mutants were close to 0.14. In the presence of bound Ca2+ at the regulatory sites, the quantum yield of Trp52 decreased 16 %, whereas that of Trp90 increased 25 %. Results from acrylamide quenching of the fluorescence of the three Trp residues indicated that Trp22 was the least exposed and Trp52 was the most exposed, consistent with other spectral data that Trp22 was in a relatively nonpolar environment and Trp52 was in a highly polar environment. The ability of Trp52 and Trp90 to sense Ca2+ binding to sites located at both domains suggests inter-domain communication in the protein. These single Trp TnC mutants provide specific signals for probing Ca2+-induced conformational changes in the regulatory domain. [ABSTRACT FROM AUTHOR]

The title compound, C23H15F6NS2 is a new non-symmetric photochromic dithienylethene. The mol­ecule adopts a photoactive anti­parallel conformation, the distance between the two reactive C atoms being 3.552 (6) Å. The dihedral angles between the cyclo­pentene ring and the two thio­phene rings are 44.0 (5) and 45.8 (5)°. [ABSTRACT FROM AUTHOR]

Efficiently constructing structures with high thermal stability is a key objective in the development of energetic compounds. However, the existing synthesis processes for heat‐resistant energetic materials are frequently hampered by their complexity and low yields. This study presents a significant breakthrough in addressing these challenges. It successfully synthesizes 4‐amino‐5‐(3‐amino‐1H‐pyrazole‐4‐yl)‐2,4‐dihydro‐3H‐1,2,4‐triazol‐3‐one (APTO) using a streamlined two‐step process, achieving an impressive high yield of 87.5 %. The structure was determined through X‐ray single crystal diffraction analysis, revealing a nearly planar intramolecular structure. Hirshfeld surface analysis, weak interaction analysis, and aromaticity analysis were conducted, illustrating a substantial presence of hydrogen bonds and π ‐ π stacking interactions within and between molecules. These interactions contribute significantly to exceptional thermal stability of ATPO. Furthermore, the thermal stability of ATPO was confirmed through DSC analysis, exhibiting a decomposition temperature as high as 365.2°C. This temperature surpasses that of the heat‐resistant explosive HNS (325°C), further validating its excellent thermal stability. The construction of this conjugated structure offers valuable guidance for the future structural design of heat‐resistant energetic materials. It opens up possibilities for the development of novel compounds with improved thermal stability based on similar conjugated architectures. [ABSTRACT FROM AUTHOR]

In this work, a series of N‐doped carbon supported FeCo bimetallic catalysts with plentiful FeCo alloy‐FeO interfaces, which are derived from metal‐organic frameworks (MOFs) ZIF‐67, are designed for the one‐pot direct conversion of methyl levulinate to 1,4‐pentanediol. The FeCo alloy‐FeO interfaces are precisely controlled via tuning the reduction temperatures and Fe/Co ratios. The optimal catalyst gives a high 1,4‐pentanediol yield of 90.5 % along with complete conversion of methyl levulinate. These catalysts are carefully characterized by multiple techniques, such as HRTEM, XRD, XPS, NH3−TPD, and Py−IR. It is found that Co presents in electron deficiency caused by the electron transference from Co to Fe in FeCo alloy, which in turn enhances the heterolysis of H2. In addition, plentiful Lewis acid sites derived from interfacial FeO species favour the re‐adsorption and the ring‐opening reaction of γ‐valerolactone. With the synergy between FeCo alloy and Lewis acid, the FeCo alloy‐FeO interfaces exhibit excellent catalytic activity for selective hydrogenation of methyl levulinate to 1,4‐pentanediol. [ABSTRACT FROM AUTHOR]

Phytoalexins play a crucial role in plant immunity. However, the mechanism of how phytoalexin is primed by beneficial microorganisms against broad‐spectrum pathogens remains elusive. This study showed that Bacillus cereus AR156 could trigger ISR against broad‐spectrum disease. RNA‐sequencing and camalexin content assays showed that AR156‐triggered ISR can prime the accumulation of camalexin synthesis and secretion‐related genes. Moreover, it was found that AR156‐triggered ISR elevates camalexin accumulation by increasing the expression of camalexin synthesis genes upon pathogen infection. We observed that the priming of camalexin accumulation by AR156 was abolished in cyp71a13 and pad3 mutants. Further investigations reveal that in the wrky33 mutant, the ability of AR156 to prime camalexin accumulation is abolished, and the mediated ISR against the three pathogens is significantly compromised. Furthermore, PEN3 and PDR12, acting as camalexin transporters, participate in AR156‐induced ISR against broad‐spectrum pathogens differently. In addition, salicylic acid and JA/ET signalling pathways participate in AR156‐primed camalexin synthesis to resist pathogens in different forms depending on the pathogen. In summary, B. cereus AR156 triggers ISR against Botrytis cinerea, Pst DC3000 and Phytophthora capsici by priming camalexin synthesis. Our study provides deeper insights into the significant role of camalexin for AR156‐induced ISR against broad‐spectrum pathogens. Summary statement: Beneficial rhizobacterium AR156 triggered ISR by enhancing camalexin accumulation in Arabidopsis, with WRKY33 acting as a positive regulator. PEN3 and PDR12 are involved in AR156‐induced ISR. Salicylic acid and JA/ET signalling pathways participate in AR156‐primed camalexin synthesis to resist various pathogens. [ABSTRACT FROM AUTHOR]

Distant metastasis is the primary reason for treatment failure in patients with nasopharyngeal carcinoma (NPC). In this study, we investigated the effect of ulinastatin (UTI) on NPC metastasis and its underlying mechanism. Highly‐metastatic NPC cell lines S18 and 58F were treated with UTI and the effect on cell proliferation, migration, and invasion were determined by MTS and Transwell assays. S18 cells with luciferase‐expressing (S18–1C3) were injected into the left hind footpad of nude mice to establish a model of spontaneous metastasis from the footpad to popliteal lymph node (LN). The luciferase messenger RNA (mRNA) was measured by quantitative polymerase chain reaction (qPCR), and the metastasis inhibition rate was calculated. Key molecular members of the UTI‐related uPA, uPAR, and JAT/STAT3 signaling pathways were detected by qPCR and immunoblotting. UTI suppressed the migration and infiltration of S18 and 5‐8F cells and suppressed the metastasis of S18 cells in vivo without affecting cell proliferation. uPAR expression decreased from 24 to 48 h after UTI treatment. The antimetastatic effect of UTI is partly due to the suppression of uPA and uPAR. UTI partially suppresses NPC metastasis by downregulating the expression of uPA and uPAR. [ABSTRACT FROM AUTHOR]

Acetate‐bridged binuclear Co(II) and Ni(II) complexes, [Co2(L)(μ‐OAc)(EtOH)] (1) and [Ni2(L)(μ‐OAc)(EtOH)] (2) were synthesized via the reaction of a new bis(salamo)‐like ligand with two different metal(II) acetates. X‐ray single crystal diffraction analyses showed that two metal(II) ions (Co or Ni) occupy two sets of N2O2 cavities, respectively. The acetate group bridges the two metals, and the ethanol oxygen atom participates in the coordination. Furthermore, UV–vis titration experiments clearly indicated that the complexation between H3L and M(II) ions leads to the 1:2 complexes [(L)M2]+ through a highly synergistic process. Bond valence sum (BVS) calculations exhibited that the Co(II) and Ni(II) ions are divalent. Secondly, the ligand H3L highest occupied molecular orbital–lowest unoccupied molecular orbital (HOMO‐LUMO) gap analysis and surface electrostatic potential were theoretically analyzed by theoretical calculation (density functional theory), and the reactivity of M(II) ions and the ligand in the complex formation process was demonstrated. Finally, the microscopic properties of the complexes were deeply understood through the calculation of the weak intramolecular interactions and the unstressed regions outside the complexes. [ABSTRACT FROM AUTHOR]

Electrospun fibrous membranes have the potential to be effective wound dressings for promoting wound healing. However, the fabrication and application of the common electrospun fibrous wound dressings are usually complicated and separated. Here, electrospun zein/clove essential oil (CEO) fibrous membranes are fabricated and applied as a potential wound dressing through in situ electrospinning process by a portable electrospinning device. The in situ electrospinning process can directly electrospin zein/CEO membranes onto a wound site to cover the wound well and improve the convenience and comfort in use. The as‐spun zein/CEO membranes show a porous structure and exhibit higher gas permeability at 168.2 ± 43.3 mm s−1, with superhydrophilicity to absorb the wound exudate and good biocompatibility as well as antibacterial effects to protect from infection. Moreover, the mice wound model study suggests that in situ electrospun zein/CEO promotes the wound healing process. [ABSTRACT FROM AUTHOR]

Lanthanide coordination polymers (Ln‐CPs) are excellent candidates for designing white light materials due to their adjustable fluorescent characteristic by decorating organic ligands, changing metal centers and including guests. However, low quantum yield, weak blue emission, high prices and supply risks have hindered the application and developments of the pure Ln‐CPs materials. Herein, we have designed a new white color composite material capable of white light‐emission upon excitation at 338 nm, which fabricated by compositing a graphitic‐phase nitrogen carbon (g‐C3N4) treated with nitric acid and lanthanide‐based complexes, with the photoluminescencequantum yield (QY) in solid state reaching 11.7 %. WLEDs constructed by depositing the (g‐C3N4)0.783/Eu0.133/Tb0.083‐dbpt [dbpt = 3‐(3,5‐dicarboxylphenyl)‐5‐(pyrazinyl)‐1H‐1,2,4‐triazole] composites on a commercial UV LED chip feature a CIE chromaticity coordinate at (0.33, 0.33), high color rendering index (CRI) of 94.6. Compared to conventional white light‐emission Ln‐CPs materials of La0.928Eu0.045Tb0.027‐dbpt and La0.896Eu0.104‐dbpt reveals that (g‐C3N4)0.783/Eu0.133/Tb0.083‐dbpt composites have higher QY and CRI values. [ABSTRACT FROM AUTHOR]

Purpose: To clarify the necessity and effect of a single intraoperative instillation of chemotherapy during radical cystectomy. Methods: Patients who underwent radical cystectomy for bladder cancer between January 2013 and April 2019 were retrospectively evaluated and divided into a non‐instillation group and an instillation group according to the intraoperative instillation of chemotherapy. Univariate and multivariate Cox regression was used to determine the clinical predictors of overall survival and disease‐free survival. Kaplan–Meier analysis and log‐rank tests were performed to analyze overall survival and disease‐free survival. Results: Of the 320 patients who were enrolled in the study, 113 underwent radical cystectomy with intraoperative instillation of chemotherapy. Univariate Cox analysis showed that intraoperative instillation was not a risk factor for overall survival or disease‐free survival (HR: 1.04, 95% CI: 0.66–1.63, p = 0.864; HR: 1.11, 95% CI: 0.76–1.62, p = 0.602, respectively). As shown in the Kaplan–Meier analysis, no significant differences were noted in overall survival (p = 0.857) and disease‐free survival (p = 0.600) between the two groups. A subgroup analysis demonstrated that intraoperative instillation was not associated with a statistically better overall survival and disease‐free survival in the nonmuscle invasive (p = 0.852 and 0.836) and muscle‐invasive (p = 0.929 and 0.805) patients. Conclusion: A single intraoperative instillation of chemotherapy during radical cystectomy was not related to better disease‐free survival or overall survival. It is unnecessary to consider single instillation of chemotherapy as a regular procedure during radical cystectomy. [ABSTRACT FROM AUTHOR]

A water stable tetrazolate‐containing metal‐organic framework, [Cd2(L)(OH)(H2O)2]n (1) [H3L = 5‐(4‐(tetrazol‐5‐yl)phenyl)isophthalic acid], was synthesized under solvothermal conditions and structurally characterized. Compound 1 displays a three dimensional porous network with one dimensional tubular channels based on trinuclear cluster [Cd3(μ3‐OH)N4C] units. Notably, 1 exhibits highly sensitive response to Cu2+ and Cr2O72– through luminescence quenching effects with the detection limit of 0.666 ppm for Cu2+ and 0.846 ppm for Cr2O72–, respectively. The possible mechanism of the luminescence quenching was discussed in detail. [ABSTRACT FROM AUTHOR]

Objectives: To evaluate predictors of long‐term survival for patients with chronic kidney disease primarily due to surgery (CKD‐S). Patients with CKD‐S have generally good survival that approximates patients who do not have CKD even after renal cancer surgery (RCS), yet there may be heterogeneity within this cohort. Patients and Methods: From 1997 to 2008, 4 246 patients underwent RCS at our centre. The median (interquartile range [IQR]) follow‐up was 9.4 (7.3–11.0) years. New baseline glomerular filtration rate (GFR) was defined as highest GFR between nadir and 6 weeks after RCS. We retrospectively evaluated three cohorts: no‐CKD (new baseline GFR of ≥60 mL/min/1.73 m2); CKD‐S (new baseline GFR of <60 mL/min/1.73 m2 but preoperative GFR of ≥60 mL/min/1.73 m2); and CKD due to medical aetiologies who then require RCS (CKD‐M/S, preoperative and new baseline GFR both <60 mL/min/1.73 m2). Analysis focused primarily on non‐renal cancer‐related survival (NRCRS) for the CKD‐S cohort. Kaplan–Meier analysis assessed the longitudinal impact of new baseline GFR (45–60 mL/min/1.73 m2 vs <45 mL/min/1.73 m2) and Cox regression evaluated relative impact of preoperative GFR, new baseline GFR, and relevant demographics/comorbidities. Results: Of the 4 246 patients who underwent RCS, 931 had CKD‐S and 1 113 had CKD‐M/S, whilst 2 202 had no‐CKD even after RCS. Partial/radical nephrectomy (PN/RN) was performed in 54%/46% of the patients, respectively. For CKD‐S, 641 patients had a new baseline GFR of 45–60 mL/min/1.73 m2 and 290 had a new baseline GFR of <45 mL/min/1.73 m2. Kaplan–Meier analysis showed significantly reduced NRCRS for patients with CKD‐S with a GFR of <45 mL/min/1.73 m2 compared to those with no‐CKD or CKD‐S with a GFR of 45–60 mL/min/1.73 m2 (both P ≤ 0.004), and competing risk analysis confirmed this (P < 0.001). Age, gender, heart disease, and new baseline GFR were all associated independently with NRCRS for patients with CKD‐S (all P ≤ 0.02). Conclusion: Our data suggest that CKD‐S is heterogeneous, and patients with a reduced new baseline GFR have compromised survival, particularly if <45 mL/min/1.73 m2. Our findings may have implications regarding choice of PN/RN in patients at risk of developing CKD‐S. [ABSTRACT FROM AUTHOR]

as a direct entry to synthesize symmetrical biaryls (II) (11 examples) [ABSTRACT FROM AUTHOR]

The ligand-free reaction allows a simple and efficient access to various polyfluorinated biphenyl structures. [ABSTRACT FROM AUTHOR]

Two helical centrosymmetric homotetranuclear Cu (II) complexes, [Cu4(L)2(EtOH)2](ClO4)2·2EtOH·2CHCl3(1) and [{Cu4(L)2(EtOH)2}{Cu4(L)2(HNO3)2}](NO3)4·3EtOH·3MeOH (2), were synthesized by the reactions of a symmetric bis (salamo)‐based ligand H3L with Cu(ClO)2·6H2O and Cu(NO)3·3H2O, respectively, and certified by elemental analyses, UV–Visible absorption spectra, infrared spectra and single‐crystal X‐ray analysis techniques. X‐ray crystal structure analyses reveal that four Cu (II) atoms of complex 1 are attached to two deprotonated ligand (L)3− units with the help of two coordinated ethanol molecules, and then forming a helical centrosymmetric complex by H‐bonding and π⋯π interactions. While complex 2 unit cell contains two crystallographically independent but chemically identical homotetranuclear complexes (molecules A and B), eight Cu (II) atoms are coordinated by four deprotonated ligand (L)3− units. The coordination mode of four Cu (II) atoms from molecule A is the same as complex 1; at the same time, oxygen atoms on nitrates are involved in the coordination of another four Cu (II) atoms from molecule B. The short‐range interactions in complexes 1 and 2 were calculated by Hirshfeld surfaces analyses. The molecular orbital energy levels, molecular stabilities of complexes 1 and 2 were analyzed by DFT calculations. In addition, antibacterial assays were also investigated in detail. [ABSTRACT FROM AUTHOR]

The requirements for the chemical to act as a primary explosive, its importance, and the hazards associated with heavy‐metal‐based primary explosives are all well‐stated in this review. In addition, it outlined the limitations of the heavy‐metal‐free primary explosives already in use. This analysis underlines the importance of green primary explosives with updated information. It summarizes the possible candidates of metal‐free new generation green primary explosives, including their preparation routes, energetic properties, applications, and comparisons to traditional primary explosives. Furthermore, this analysis also aims to discuss the necessity for metal‐free primary explosives as well as the significant problem of replacing traditional primary explosives. [ABSTRACT FROM AUTHOR]

Review: 39 refs. [ABSTRACT FROM AUTHOR]

By self-assembly of a Salamo-type ligand H2L [H2L = 1,2-bis(3-methoxysalicylideneaminooxy)ethane] with Ni(OAc)2·4H2O, Ce(NO3)3·6H2O, and H2bdc (H2bdc = terephthalic acid), a novel NiII-CeIII heterometallic complex, [{Ni(L)Ce(NO3)2(CH3OH) (DMF)}2(bdc)], was obtained. Two crystallographically equivalent [Ni(L)Ce(NO3)2(CH3OH)(DMF)] moieties lie in the inversion center, and are linked by one bdc2- ligand leading to a heterotetranuclear dimer, in which the carboxylato group bridges the NiII and CeIII atoms. Moreover, the photophysical properties of the NiII-CeIII complex were studied. [ABSTRACT FROM AUTHOR]

The facile synthesis of core-shell magnetic mesoporous silica nanoparticles (Fe3O4@mSiO2 NPs) was reported in aqueous phase using cetyltrimethylammonium bromide as a template under alcohol-free conditions. Compared to the conventional synthesis method for core-shell Fe3O4@mSiO2 NPs, the approach in this study is rapid (only 5-min reaction time), cheap (without using organic agents), and environmentally friendly (one-step synthesis in alcohol-free medium). Doxorubicin (DOX)-loaded Fe3O4@mSiO2 NPs exert extraordinarily high specificity for liver cancer cells, which was due to the pH-sensitive doxorubicin release, as well as higher endocytosis capacity in liver cancer cells rather than normal liver cells. The potential advantages of using such Fe3O4@mSiO2 NPs as the vehicle of anticancer drugs were that the Fe3O4@mSiO2 NPs exhibit good biocompatibility, high loading and protection of the guest molecules, selective killing effect, and efficient cellular uptake. The exciting pH-dependent release properties of doxorubicin-loaded Fe3O4@mSiO2 NPs make their use a promising strategy for enhancing efficient therapy toward tumors, while reducing the cytotoxicity of doxorubicin to human normal neutral tissue or cells. [ABSTRACT FROM AUTHOR]

In the title compound, C21H21ClN2O2, the pyrazole and chlorobenzene rings are coplanar and make a dihedral angle of 79.7 (2)° with the tert-butylbenzene ring. The crystal structure displays intermolecular O—H...O hydrogen bonding. [ABSTRACT FROM AUTHOR]

In the title compound, C19H18N2O2, the dihedral angles made by the central pyrazole ring with the benzyl and phenyl rings are 87.00 (9) and 15.23 (9)°, respectively. There is a short intermolecular interaction between a C—H bond and the benzyl ring. [ABSTRACT FROM AUTHOR]

In the structure of the title compound, C17H16O5, the dihydrofuran ring adopts an envelope conformation while the methylenedioxyphenyl ring system is essentially planar. The vinyl group is inclined to the dihydrofuran ring by 30.22 (12)°. The dihedral angle between the atoms defining the planar part of the dihydrofuran ring and the aryl ring is 19.12 (8)° [ABSTRACT FROM AUTHOR]

In the title structure, C23H25ClN2O2, there are weak intramolecular C—H...N and C—H...O hydrogen bonds. There is a C=O... Cg interaction ( Cg is the centroid of the pyrazole ring) and the distance between the centroids of the ring and the C=O bond is 3.017 (3) Å. The angle between the pyrazole ring and the chlorophenyl ring is 12.85 (13)°. The crystal packing is stabilized mainly by van der Waals forces. [ABSTRACT FROM AUTHOR]

In the title compound, C19H17ClN2O2, all non-H atoms except for the benzyl substituent are coplanar to within 0.044 Å. [ABSTRACT FROM AUTHOR]

In the structure of the title compound, [Fe(C5H5)(C13H14BrN2O2)], the two cyclopentadienyl (Cp) rings are in an eclipsed conformation and are parallel. The dihedral angle between the substituted Cp ring and the heterocyclic ring is 8.20°. [ABSTRACT FROM AUTHOR]

The integration of silver nanoparticles (Ag NPs) with mesoporous silica nanoparticles (MSNs) protects the former from aggregation and promotes the controlled release of silver ions, resulting in therapeutic significance on cancer and infection. The unique size, shape, pore structure and silver distribution of silver mesoporous silica nanoparticles (Ag‐MSNs) embellish them with the potential to perform combined imaging and therapeutic actions via modulating optical and drug release properties. Here, we comprehensively review the recent progress in the fabrication and application of Ag‐MSNs for combination therapies for cancer and infection. We first elaborate on the fabrication of star‐shaped structure, core‐shell structure, and Janus structure Ag‐MSNs. We then highlight Ag‐MSNs as a multifunctional nanoplatform to surface‐enhanced Raman scattering‐based detection, non‐photo‐based cancer theranostics and photo‐based cancer theranostics. In addition, we detail Ag‐MSNs for combined antibacterial therapy via drug delivery and phototherapy. Overall, we summarize the challenges and future perspectives of Ag‐MSNs that make them promising for diagnosis and therapy of cancer and infection. [ABSTRACT FROM AUTHOR]