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Severe fever with thrombocytopenia syndrome virus (SFTSV) nonstructural protein (NSs) is an important viral virulence factor that sequesters multiple antiviral proteins into inclusion bodies to escape the antiviral innate immune response. However, the mechanism of the NSs restricting host innate immunity remains largely elusive. Here, we found that the NSs induced complete macroautophagy/autophagy by interacting with the CCD domain of BECN1, thereby promoting the formation of a BECN1-dependent autophagy initiation complex. Importantly, our data showed that the NSs sequestered antiviral proteins such as TBK1 into autophagic vesicles, and therefore promoted the degradation of TBK1 and other antiviral proteins. In addition, the 8A mutant of NSs reduced the induction of BECN1-dependent autophagy flux and degradation of antiviral immune proteins. In conclusion, our results indicated that SFTSV NSs sequesters antiviral proteins into autophagic vesicles for degradation and to escape antiviral immune responses. [ABSTRACT FROM AUTHOR]

The research investigated the influences of international students' perceived online learning environments, self-efficacy, and online interaction on their online learning achievement, as measured by these students' self-reported development of generic skills, research capacities, and Chinese proficiency and global abilities. Data were generated by a nationwide survey involving 1,010 international students across disciplines at 41 universities in China. The SEM analysis showed that among all factors directly and positively supporting international students' learning achievement, the two online environmental factors, i.e. accessibility to online learning resources and opportunities for knowledge acquisition, presented the strongest effects. The mediation analysis showed that through interaction, environmental interactivity had significant and positive indirect influences on learning achievement; and through self-efficacy, knowledge acquisition had significant and positive indirect influences on learning achievement. The SEM analysis also revealed a significant negative influence of environmental flexibility on international students' generic skill development. Possible explanations for the results were proposed. Implications of the results were discussed to support the sustainable development of online international education. [ABSTRACT FROM AUTHOR]

In the event of a large-scale radiological accident, rapid and high-throughput biodosimetry is the most vital basis in medical resource allocation for the prompt treatment of victims. However, the current biodosimeter is yet to be rapid and high-throughput. Studies have shown that ionizing radiation modulates expressions of circular RNAs (circRNAs) in healthy human cell lines and tumor tissue. circRNA expressions can be quantified rapidly and high-throughput. However, whether circRNAs are suitable for early radiation dose classification remains unclear. We employed transcriptome sequencing and bioinformatics analysis to screen for radiation-differentially expressed circRNAs in the human lymphoblastoid cell line AHH-1 at 4 h following exposure to 0, 2, and 5 Gy 60Co γ-rays. The dose–response relationships between differentially expressed circRNA expressions and absorbed doses were investigated using real-time polymerase chain reaction and linear regression analysis at 4 h, 24 h, and 48 h post-exposure to 0, 2, 4, 6, and 8 Gy. Six distinct dose classification models of circRNA panels were established and validated by receiver operating characteristic (ROC) curve analysis. A total of 11 radiation-differentially expressed circRNAs were identified and validated. Based on dose–response effects, those circRNAs changed in a dose-responsive or dose-dependent manner were combined into panels A through F at 4 h, 24 h, and 48 h post-irradiation. ROC curve analysis showed that panels A through C had the potential to effectively classify exposed and non-exposed conditions, which area under the curve (AUC) of these three panels were all 1.000, and the associate p values were.009. Panels D through F excellently distinguished between different dose groups (AUC = 0.963–1.000, p <.05). The validation assay showed that panels A through F demonstrated consistent excellence in sensitivity and specificity in dose classification. Ionizing radiation can indeed modulate the circRNA expression profile in the human lymphoblastoid cell line AHH-1. The differentially expressed circRNAs exhibit the potential for rapid and high-throughput dose classification. [ABSTRACT FROM AUTHOR]

With mandelic acid (MA) as the chiral core, two series of non-symmetric liquid crystal (LC) dimers have been synthesised by changing the rigidity of the side-arms, namely the DBM-nC2B series and the DBBM-nC2B series. In the DBM-nC2B series, one side-arm is the same, while the length of the flexible tail of the other side-arm increases from 0 to 4. The same is true of the DBBM-nC2B series. Chemical structures and LC properties of the two series LC dimers were characterised by FT-IR, 1H NMR, 13C NMR, DSC, TGA and POM. The results show that the DBM-nC2B series LC dimers display the nematic phase (N), and the DBBM-nC2B series LC dimers exhibit the chiral nematic phase (N*). It shows that the side-arm should have sufficient rigidity for MA to induce the N* phase. In the same series, when the length of the flexible tails of the side-arm increases from 0 to 4, it does not change the mesophase, while it has some effect on the melting temperature (Tm), the clearing temperature (TN(*)I), and mesophase range of the dimers. The molecular length-width ratio (l/w) and dipole moment (μ) were used to explain the variation of Tm and (TN(*)I) of LC dimer. [ABSTRACT FROM AUTHOR]

In this paper, we have synthesised cholesteryl 4-allyloxybenzoate (MB), crosslinking agent dodecane-1,12-diyl bis(undec-10-enoate) (MG), and A'BGF series liquid crystalline elastomer (LCE) films which take polymethylhydrosiloxane (A') as the backbone, MB as the cholesteric liquid crystal (LC) monomer, and MG and bis-vinyl silicone oil (MF) with different reactivities as cross-linking agent for exploring the effect of the change of MF content on the properties of the elastomeric films. The experimental results show that the synthesised MB, MG, and the LCE films are all consistent with the molecular design; MB is an enantiotropic cholesteric LC. The synthesised LCE films are cholesteric LCs, have certain selective reflection characteristic, higher thermal stability, and their Tg decreased down to 3.9°C as MF increasing. During the heating and cooling, the liquid crystalline properties of the LCE films have a good reversibility. Among the synthesised LCE films, A'BGF-2 has stretching radio of 264.8% at room temperature, with the best elastic properties. By adjusting the ratio of MF, the content of small-molecule MB remained in the films can be changed, which will affect the optical properties and elasticity of the LCE films. The experiments provide a method for the preparation of highly elastic side chain LCE film. [ABSTRACT FROM AUTHOR]

The use of lipid-lowering drugs is still highly controversial in patients with amyotrophic lateral sclerosis (ALS). We performed a drug-target Mendelian randomization (MR) analysis to investigate the effect of targeted lipid-lowering drugs on the risk of ALS. First, we evaluated the causal relationship between HMG-CoA (3-hydroxy-3-methylglutaryl coenzyme A) reductase (HMGCR) inhibitors-taking trait and ALS using a bidirectional two-sample MR study. Second, we investigated the causal relationship between lipid-lowering drugs and ALS through a drug-target MR approach. The summary data for HMGCR inhibitors-taking traits were extracted from a genome-wide association study (GWAS) of medication use and associated disease in the UK Biobank. The summary data for low-density lipoprotein cholesterol and apolipoprotein B (apoB) were extracted from a meta-analysis of GWAS in individuals of European ancestry in the UKB. The GWAS summary data of ALS were obtained from the Project MinE. Our bidirectional two-sample MR showed that genetically determined increased HMGCR inhibitors-taking trait was an independent risk factor for ALS (odds ratio [OR] = 1.090, 95% confidence interval [CI] = 1.035–1.150, p = 0.001). The results of drug-target MR showed that the increased expression of the HMGCR gene in blood with the higher risk of ALS (OR = 1.21, 95% CI = 1.01–1.46; p = 0.042) through SMR method and the apoB level mediated by the APOB gene increased the risk of ALS (OR = 1.15; 95% CI =1.05–1.25; p = 0.001) through inverse-variance weighted MR method. This present study provides genetic support for a positive causal effect of HMGCR inhibitors-taking trait and ALS. The reason for this may be due to the underlying disease condition behind the medication, rather than the medication itself. Our findings also suggested that HMGCR and apoB inhibitors may have potential protective effects on ALS. [ABSTRACT FROM AUTHOR]

Two series of symmetric liquid crystal dimers, namely 1F and 3F, have been synthesised by varying the length of the flexible odd spacer. The melting temperatures and clear points of the 3F series are higher than those of the 1F series. The 1F series only exhibits nematic phase, while the 3F series displays both smectic A and nematic phases. As the length of the flexible spacer increases, the dominance of the smectic phase becomes more pronounced. This phenomenon may be attributed to the combined effect by the polar end group CF3 and the long flexible spacer on the molecular conformation. [ABSTRACT FROM AUTHOR]

In this article, we designed and synthesized two novel swallow-tailed liquid crystal monomers (M1 and M2) with different chain lengths and rigidities centered on 3,4,5-trihydroxybenzoic acid and two series of side-chain liquid crystals polymers PN1 and PN2. All liquid crystal monomers and polymers were conformed to the molecular designs by FT-IR and NMR. The liquid crystal properties were tested by DSC and POM, and the results showed that M1 and M2 were thermotropic enantiotropic nematic liquid crystals and the side-chain liquid crystal polymers PN1 and PN2 series were typical amorphous liquid crystal polymers. With the increase of monomer content, the glass transition temperatures and clearing points of PN1 and PN2 series enhanced. With the increase of the number of mesogens in the liquid crystal monomer, the rigidity was enhanced, and the liquid crystal performance of the polymer was better. [ABSTRACT FROM AUTHOR]

Ionizing radiation (IR)-induced transcriptional changes are considered a potential biodosimetry for dose evaluation and health risk monitoring of acute or chronic radiation exposure. It is crucial to understand the impact of confounding factors on the radiation-responsive gene expressions for accurate and reproducible dose assessment. This study aims to explore the potential influence of exposures to chemotherapeutic agents such as cyclophosphamide (CP) and mitomycin C (MMC) on IR-induced transcriptional biomarkers. The human B lymphoblastoid cells (AHH-1) were exposed to 0, 20, 50, 100, 200 and 500 μg/ml CP or 0, 0.025, 0.05, 0.1 and 1 μg/ml MMC, respectively. The appropriate concentrations of CP and MMC were added for 1 h before irradiation with 0, 2, 4 and 6 Gy of 60Co γ-rays at a dose rate of 1 Gy/min. Cell viability was evaluated by CCK-8 assay. The gene expression responses of 18 radiation-induced transcriptional biomarkers were examined at 24 h after exposures to CP and MMC, respectively. The expression levels of five crucial DNA interstrand crosslinks (ICLs) repair genes were also evaluated. The biodosimetry models were established based on the specific radiation-responsive gene combinations. The baseline transcriptional levels of the 18 selected genes were slightly affected by CP treatment in the absence of IR, while the transcript responses to IR could be inhibited as the concentration of CP up to 50 μg/ml. MMC treatment up-regulated the background levels in most radiation-responsive gene expressions. Of 18 genes, only the relative mRNA expression levels of CDKN1A and BBC3 were repressed after treatment with IR and MMC in combination. The relative mRNA level of RAD51 was significantly up-regulated after exposure to CP, while the expression of FANCD2, RAD51 and BLM showed an overall increase in response to MMC treatment. After irradiation, the relative mRNA expression levels of FANCD2, BRCA2 and RAD51 exhibited dose-dependent increases in IR alone and MMC treatment groups. In addition, the biodosimetry models were established using 2-4 radiation-responsive genes based on different radiation exposure scenarios. Our findings suggested that IR-induced gene expression changes were slightly affected after exposure to a relatively low concentration of CP and MMC. Gene expression combinations might improve the broad applicability of transcriptional biodosimetry across diverse radiation exposures. [ABSTRACT FROM AUTHOR]

Two series of chiral liquid crystal compounds were synthesised from benzoic acid containing cholesterol with different carbon-chain lengths and bisphenol monoester containing camphoric acid with different carbon-chain lengths, named BCP-C and DCP-C. The structure of the monomers is characterised by IR, 1H NMR and 13C NMR, which indicate that the synthesised molecule conforms to the molecular design. The textures of monomers were characterised by POM, and their selective reflection was studied. It was found that the synthesised liquid crystal compounds exhibited good liquid crystal and optical properties. The phase transition behaviour was characterised using DSC, and the results were consistent with those observed by POM. TGA showed that they had good thermal stability. [ABSTRACT FROM AUTHOR]

In this paper, a series of novel liquid crystal units (ASE-n, n = 4, 6, 8) of azo Schiff bases with sulphonic acid (-SO3H) as terminal substituents and different alkyl chain lengths were designed and synthesised. Nine star-shaped liquid crystal macromolecules with different central groups (ASE-P-n, ASE-T-n, ASE-G-n, n = 4, 6, 8) were synthesised by esterification of three novel azo Schiff base liquid crystal units (ASE-n, n = 4, 6, 8) with phloroglucinol, pentaerythritol and glucose. The structure of the synthesised compounds were analysed by infrared spectroscopy and 1H NMR. The results showed that all the compounds were consistent with the molecular structure design. The properties of liquid crystal such as phase transition temperature and liquid crystal mesophase range were characterised by POM and DSC. The effects of alkyl chain length and branched degree on the properties of liquid crystal were studied. The maximum absorption spectrum of the compound was determined by UV-Vis spectrophotometry. The photoisomerisation reaction of the compound was also studied. Under ultraviolet light (λ = 365 nm) irradiation, the effect of different duration on the cis-absorption percentage of azo (-N=N-) bond in the compound was studied. [ABSTRACT FROM AUTHOR]

In this study, two novel aromatic ester multi-arm liquid crystal monomers M1 and M2 with different terminal substituents centred on 3,4,5-trihydroxybenzoic acid, and a rod-shaped chiral liquid crystal monomer N were designed and synthesised. The synthesised liquid crystal monomers M and N were grafted and copolymerised with polymethylhydrosiloxane (PMHS). The structural characterisation of the synthesised liquid crystal compounds was carried out by FT-IR and 1H-NMR. The mesomorphic properties of the synthesised liquid crystal compounds were characterised by POM and DSC, and the results showed that the multi-arm liquid crystal monomers M1 and M2 are typical enantiotropic nematic liquid crystal compounds and N is typical thermotropic enantiotropic cholesteric liquid crystal. Polymers P1 and P2 are both cholesteric liquid crystal polymers. The glass transition temperatures and liquid crystal isotropic transition temperatures of polymers P1 and P2 series both tend to increase with the increase of multi-arm liquid crystal monomer M. [ABSTRACT FROM AUTHOR]

In this paper, first series of liquid crystal polymers (PF) synthesised by hydrosilylation of monomer containing furan group (MA), monomer containing cholesterol group (MB), monomer containing D (+)-camphoric acid group (MC) and monomer containing cyano-group (MD), catalysed by platinum catalyst. Another series of liquid crystal polymers (EF) is synthesised by the Dies-Alder reaction of the former series and cross-linker containing bismaleimide group. The results of Fourier transform infrared spectroscopy (FT-IR) and proton nuclear magnetic resonance(1H NMR) showed the successful preparation of various monomers as well as polymers. The thermal properties of two series were characterised by differential scanning calorimetry (DSC) and thermogravimetry analysis (TGA). We observed dramatic colour changes and Grand-jean textures of polymers using polarised optical macroscope (POM). The results of POM and selective reflection showed that both series of polymers are cholesteric liquid crystals. In the latter series, crosslinking by Diels-Alder reaction can make the liquid crystal better oriented, which can maintain their wonderful liquid crystal (LC) texture and selective reflection, and at the same time, it has a certain regulation effect on the appearance of cholesteric Grand-jean blue texture. The results of X-ray diffraction (XRD) further proved the two series of polymers are cholesteric liquid crystals. [ABSTRACT FROM AUTHOR]

In this paper, two novel aromatic ester swallow-tailed liquid crystal monomers M1 and M2 and a straight chain cholesteric liquid crystal monomer M3 were designed and synthesised. Two series of liquid crystal polymers, P1 series and P2 series, were graft-copolymerised with M and polymethylhydrosiloxane (PHMS). All the synthesised liquid crystal monomers and polymers were characterised by IR and 1H NMR and confirmed to the predicted molecular structure. The liquid crystal and thermal properties of the synthesised compounds were tested by DSC, POM, TGA and optical rotation. The results show that the monomer M1 is a monotropic nematic liquid crystal, and the Schlieren texture appears during the cooling process. M2 is an enantiotropic nematic liquid crystal with filamentous and schlieren texture. M3 is a thermotropic enantiotropic cholesteric phase with oily streak and focal cone texture. Both polymers P1 and P2 show typical Grand-Jean texture, and with the increase of monomer M3 content, the polymer clearing point temperature Ti increases continuously, the liquid crystal mesophase range widens, and the specific rotation value increases. [ABSTRACT FROM AUTHOR]

In this paper, we designed and synthesised three Schiff base mesogenic units X-YP and six Y-shaped liquid crystal oligomers X-AYP and X-BYP (×= -CH3O, -CH3, -Cl). Molecular structures of the prepared compounds were confirmed via FT-IR, 1H NMR and elemental analysis. The mesomorphic properties were investigated by differential scanning calorimetry (DSC) and polarised light microscopy (POM). The photochemical properties of Y-shaped liquid crystal oligomers were preliminarily studied by UV-Vis spectrum. The results indicated that X-YP containing OCH3 and Cl substituents exhibited mesophase, while X-YP with CH3 substituent was non-mesogenic. The synthesized Y-shaped liquid crystals X-AYP and X-BYP both had liquid crystal properties and exhibited nematic phase during heating and cooling, which belonged to thermotropic enantiotropic nematic liquid crystals. The polarity of the terminal groups and the number of mesogenic units had a significant effect on the mesophase behaviour of Y-shaped liquid crystals. The absorption intensities of X-AYP and X-BYP in the UV spectra were affected by the terminal substituents. [ABSTRACT FROM AUTHOR]

A series of liquid crystal elastomer films (the PBC series) have been synthesized by grafting liquid crystal (LC) monomer 4-allyloxybenzoic acid cholesteryl ester (MB) and crosslinking agent [1,1'-biphenyl]-4,4'-diyl bis(undec-10-enoate) (MC) onto polymethylhydrosiloxane catalyzed by hexachloroplatinic acid at 60 °C. The PBC series are cholesteric liquid crystal elastomers (LCEs). The glass transition temperatures (Tg) of the PBC series are between 23-33 °C, and the LC range is above 200 °C. The temperatures of 5% weight loss of the PBC series are above 300 °C, which shows good thermal stability. The PBC series display good orientation. PB3C3 shows a good ability of shape recovery above Tg. [ABSTRACT FROM AUTHOR]

In this paper, we designed and synthesised three H-shaped liquid crystal monomers ABOP-n (n = 4,6,8) and a straight-chain liquid crystal monomer M. Then, we used three H-shaped liquid crystal monomers as crosslinking agents, which were graft-copolymerised with M and polymethylhydrosiloxane (PMHS), respectively, to synthesise three series of liquid crystal elastomers P1–P3. The products were structurally well characterised by elemental analysis, 1HNMR, and FT-IR. The phase behaviours were investigated using the polarising microscope (POM) and differential scanning calorimetry (DSC). The results showed that ABOP-8, ABOP-6, ABOP-4 and M were thermotropic enantiotropic nematic liquid crystals, exhibiting schlieren texture during heating, and spherulite texture and schlieren texture during cooling. The photochemical properties of H-shaped liquid crystal monomers were preliminarily studied by UV-Vis spectra, and it was found that they have good photosensitivity. Both the P1–P3 series were typical non-crystalline polymers with anisotropic coloured textures. With the increase of crosslinking monomer content, the glass transition temperature of the P1–P3 series both increased, while the isotropic temperature showed a trend of first decreasing and then increasing. [ABSTRACT FROM AUTHOR]

In this paper, we designed and synthesised two azo liquid crystal monomers (M1 and M2) and a chiral liquid crystal monomer N, followed by side-chain graft copolymerisation with polymethylhydrosiloxane (PMHS) to synthesize comb-like liquid crystalline polymers PN1 and PN2. The structures of all liquid crystal monomers and polymers conform to the molecular designs by FT-IR and 1H NMR. The liquid crystal properties were tested by DSC and POM, and the results showed that M1 and M2 were thermotropic enantiotropic nematic liquid crystals and N was a thermotropic enantiotropic cholesteric liquid crystal. Both the PN1 and PN2 series were amorphous polymers. The PN1 and PN2 series exhibited a typical Grand-jean texture. The glass transition temperature and isotropic temperature of the PN1 and PN2 series decreased first and then increased with the increase of azo monomer M content. And the glass transition temperature and isotropic temperature of the PN1 series were higher than the PN2 series. Both the PN1 and PN2 series had good thermal stability. The mesophase range of the PN1 series was 173.5°C~181.5°C, and the PN2 series was 162.5°C~172.9°C. [ABSTRACT FROM AUTHOR]

Three series of new branched liquid crystal oligomers with 4-hydroxybenzoic acid, 3,5-dihydroxybenzoic acid, 3,4,5-trihydroxybenzoic acid as the centre and cholesterol as the chiral group were designed and synthesised (Dn, Fn and Hn, n = 4,6,8). DSC and POM results showed that their liquid crystal phase behaviour was closely related to the number of mesogenic unit and the rigidity and flexibility of the structure. They were all cholesteric liquid crystals. In the same series, as the value of n increased, the mesophase ranges became narrower. When the value of n was the same in different series, as the degree of branching increased, the mesophase ranges became narrower. [ABSTRACT FROM AUTHOR]

A series of multi-arm liquid crystals (2T series) containing trifluoromethyl terminal group were synthesised, with chenodeoxycholic acid (CDCA) as the first core; 10-oxo-10-(4'-((4-(trifluoromethyl)benzoyl)oxy)-[11'−biphenyl]-4-yl)oxy)decanoic acid (TA) as the liquid crystal arms; and (R,S)-1,2-propanediol (PD), 44'-biphenyldiol (BD), isosorbide (IB) and p-dihydroxybenzene (DHB) as the second cores, respectively. CDCA2TA is the intermediate product obtained by introducing liquid crystal arm TA into CDCA. 2T-PD, 2T-IB, 2T-DHB and 2T-BD are multi-armed liquid crystals obtained by introducing CDCA2TA into the second cores PD, IB, DHB and BD, respectively. The IR results of CDCA2TA in solid and CCl4 solutions indicate the presence of hydrogen bonds involving C-F, OH, C=O and Ar-H in the CDCA2TA molecules. When CDCA2TA of chiral smectic A (SmA*) phase is introduced into the second cores, the multi-arm LCs show different LC phases under the influence of the second cores. 2T-PD shows the SmX* phase. 2T-DHB shows cholesteric (Ch) and nematic (N) phases. 2T-BD and 2T-IB show Ch phase. The rigidity of the second cores plays an important role in displaying cholesteric phase for the multi-arm LCs. The second cores also play an important influence on the thermal performance by influencing the conformation of the multi-arm LCs. [ABSTRACT FROM AUTHOR]

Ionizing radiation (IR) can induce autophagy and premature senescence; however, the link between them has not been clarified. Our research has shown that X-ray irradiation induces premature senescence in lung adenocarcinoma cells, and its occurrence partially depends on the signal transducer and activator of transcription 3 (STAT3). STAT3 can bind to the promoter region of Beclin1 and regulate its expression. Therefore, it is speculated that there may be a close link between premature senescence and autophagy induced by ionizing radiation in lung adenocarcinoma cells. p62 plays a regulatory role in both autophagy and premature senescence, and it is also an irreplaceable molecule that causes the senescence -associated secretory phenotype (SASP) and a substrate for selective autophagy. This study focused on STAT3, Beclin1 and p62 to clarify the regulatory relationship between IR-induced autophagy and premature senescence. After exposure to 4 Gy X-rays, a β-galactosidase staining kit was used to detect the positive rate of premature senescence. STAT3 was overexpressed by pcDNA3.0-STAT3 transfection, and was inhibited by AG490 and rapamycin. Lung adenocarcinoma cells were transduced with the adenovirus vector GV119-Beclin1 to knockdown the expression of Beclin1, or treated with ATM and ATR inhibitors to inhibit premature senescence. Western blotting was used to examine alterations in the radiation response proteins STAT3 and p-STAT3, senescence-related proteins p62 and GATA4, autophagy-related proteins Beclin1, and LC3-II/LC3-I. The mRNA expression levels of SASP factors, including IL-6 and IL-8, were examined by real-time polymerase chain reaction. The activity of SA-β-gal increased significantly (p <.05), and the expression of p62 decreased significantly at 72 h after 4 Gy X-ray irradiation, accompanied by the increased expression of STAT3, p-STAT3, Beclin1, and the LC3-II/LC3-I ratio. Up- or down-regulation of STAT3 expression was followed by an increase or decrease in Beclin1 expression. After treatment with ATM and ATR inhibitors, there were no significant changes in Beclin1 expression or LC3-II/LC3-I ratio in A549 cells after 4 Gy X-ray irradiation. The p62 expression, the percentage of the SA-β-gal-positive staining cells, and the expression of IL-6 and IL-8 mRNA in cells transduced with GV119-Beclin1 were also decreased significantly after 4 Gy X-ray irradiation compared with that of the 0 Gy group. Radiation induces premature senescence and autophagy in lung adenocarcinoma cells. Autophagy regulates X-ray radiation-induced premature senescence through the STAT3-Beclin1-p62 pathway in lung adenocarcinoma cells. [ABSTRACT FROM AUTHOR]

In the event of radiological accidents and cancer radiotherapies in the clinic, the gastrointestinal (GI) system is vulnerable to ionizing radiation and shows GI injury. Accessible biomarkers may provide means to predict, evaluate, and treat GI tissue damage. The current study investigated radiation GI injury biomarkers in rat plasma. High-coverage targeted lipidomics was employed to profile lipidome perturbations at 72 h after 0, 1, 2, 3, 5, and 8 Gy (60Co γ-rays at 1 Gy/min) total-body irradiation in male rat jejunum. The results were correlated with previous plasma screening outcomes. In total, 93 differential metabolites and 28 linear dose-responsive metabolites were screened in the jejunum. Moreover, 52 lipid species with significant differences both in jejunum and plasma were obtained. Three lipid species with linear dose-response relationship both in jejunum and plasma were put forth, which exhibited good to excellent sensitivity and specificity in triaging different exposure levels. The linear dose-effect relationship of lipid metabolites in the jejunum and the triage performance of radiation GI injury biomarkers in plasma were studied for the first time. The present study can provide insights into expanded biomarkers of IR-mediated GI injury and minimally invasive assays for evaluation. [ABSTRACT FROM AUTHOR]

Design and synthesis a series of azo multi-arm liquid crystal monomers (M1-M3) with cholic acid as the chiral core, followed by side chain graft copolymerisation with polymethylhydrosiloxane (PMHS) to synthesise the liquid crystal polymer PM series. All liquid crystal monomers and polymers were conformed to the molecular design in structure by FT-IR and NMR. The liquid crystal performance was tested by DSC and POM, and the results revealed that M1 and M2 were thermotropic enantiotropic cholesteric phase liquid crystals. Liquid crystal monomer M3 has no liquid crystal behaviour in both the up and down temperature processes. Polymers of the PM series exhibited different liquid crystal phases depending on the monomer content, with Grand-Jean texture at lower percentage and oil filament texture at higher percentage. The glass transition temperature and melting temperature decrease progressively with the increase in the liquid crystal monomer content, as opposed to the isotropic temperature. [ABSTRACT FROM AUTHOR]

Two series of symmetric LC dimers with the same rigid group and different fluorine terminal group (F and F3C) have been synthesised by varying the length of flexible spacers, termed 1 F series (1 F-4, 1 F-6, 1 F-8) and 3 F series (3 F-4, 3 F-6, 3 F-8). Chemical structures and LC properties of the six symmetric LC dimers were characterised by Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance hydrogen spectrometer (1H NMR), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and polarised optical microscopy (POM). The 1 F series dimers only show nematic phase. While for 3 F series, smectic phase appeared, and with the increase of flexible spacers, the smectic phase is dominant. For the formation of smectic phase of 3 F series, the larger intermolecular transverse force coming from CF3 may be the driving force, and the long flexible spacer makes it possible. The melting temperatures of the 1 F series and 3 F series gradually decrease as the length of the flexible spacer increases, respectively, indicating that molecular rigidity has a greater influence on the melting temperatures. The melting temperatures of the 3 F series dimers decrease faster, which may attribute to the influence of CF3 on the conformation of the dimers. [ABSTRACT FROM AUTHOR]

Using tartaric acid as the core, six azo H-shaped liquid crystal compounds M1-M6 with different terminal substituents were synthesised. All products were structurally well characterised by elemental analysis, 1HNMR, and FT-IR. The phase behaviours were investigated by means of polarised optical microscopy and differential scanning calorimetry. M1-M6 were thermotropic enantiotropic nematic liquid crystals. They all showed schlieren texture in the process of heating up, and exhibited spherulite texture in the process of cooling down. M1 and M4 whose terminal substitution was nitro had the widest liquid crystal range in the same series of liquid crystal compounds, which were 135.1°C and 96.1°C, respectively, under heating cycle and 167.4°C and 112.7°C, respectively, under cooling cycle. The results show that the terminal substituents and flexible chain have important influence on the mesogenic phase and range. With the increase of flexibility, the mesogenic range of liquid crystal compounds becomes smaller when the end groups are the same. And when the flexible chain is the same, the greater the induced and polarised force of the terminal substituents, the better the mesogenic properties of the liquid crystal compounds. [ABSTRACT FROM AUTHOR]

A series of star-shaped liquid crystal (LC), respectively, based on phloroglucinol, pentaerythritol and glucose as cores, rod-shaped molecules (MeOSBAA, MeSBAA and ClSBAA) containing a schiff base as mesogenic mesogen were synthesised. The molecular structures were confirmed by FT-IR and 1H-NMR techniques. The LC textures and thermal phase behaviours were investigated by polarising optical microscopy and differential scanning calorimetry. The results showed that MeOSBAA and ClSBAA were thermally enantiotropic liquid crystals. Three-arm star LC macromolecules X-SBA3E and four-arm star LC macromolecules X-SBA4E were found to display enantiotropic nematic liquid crystals behaviour. While the five-arm star-shaped chiral LC molecules X-SBA5E exhibited enantiotropic chiral nematic phase. [ABSTRACT FROM AUTHOR]

The objective of this research was to explore the dose-effect relationships of dicentric plus ring (dic + r), micronucleus (MN) and nucleoplasmic bridges (NPB) induced by carbon ions in human lymphocytes. Venous blood samples were collected from three healthy donors. 12C6+ ions beam was used to irradiate the blood samples at the energy of 330 MeV and linear energy transfer (LET) of 50 keV/μm with a dose rate of 1 Gy/min in the spread-out Bragg peak. The irradiated doses were 0 (sham irradiation), 1, 2, 3, 4, 5 and 6 Gy. Dic + r chromosomes aberrations were scored in metaphases. The cytokinesis-block micronucleus cytome (CBMN) was conducted to analyze MN and NPB. The maximum low-dose relative biological effectiveness (RBEM) values of the induction of dic + r, MN and NPB in human lymphocytes for 12C6+ ions irradiation was calculated relative to 60Co γ-rays. The frequencies of dic + r, MN and NPB showed significantly increases in a dose-depended manner after exposure to 12C6+ ions. The distributions of dic + r and MN exhibited overdispersion, while the distribution of NPB agreed with Poisson distribution at all doses. Linear-quadratic equations were established based on the frequencies of dic + r and MN. The dose-response curves of NPB frequencies followed a linear model. The derived RBEM values for dic + r, MN and NPB in human lymphocytes irradiated with 12C6+ ions were 8.07 ± 2.73, 2.69 ± 0.20 and 4.00 ± 2.69 in comparison with 60Co γ-rays. The dose-response curves of carbon ions-induced dic + r, MN and NPB were constructed. These results could be helpful to improve radiation risk assessment and dose estimation after exposed to carbon ions irradiation. [ABSTRACT FROM AUTHOR]

Leptinotarsa decemlineata Say 1824, an invasive and globally devastating beetle, inflicts great damage to potato crops worldwide. The complete mitogenome of L. decemlineata is described in this study. It is a 16,741 bp long circular DNA molecule with a high A + T content of 76.9%, containing a typical 37 gene pattern. All PCGs (protein-coding genes) initiate with typical ATN codons. Most PCGs use TAN as a stop codon, whereas ND4 and COX3 use the incomplete codon TA as the stop codon. The lengths of rrnL and rrnS genes are 1,337 bp and 811 bp, respectively. All 22 tRNAs ranged from 62 to 77 bp. Phylogenetic analysis of Chrysomelidae indicated that L. decemlineata clusteres with three other Chrysomelinae species, which is consistent with previous analyses. [ABSTRACT FROM AUTHOR]

Five non-symmetric three-arm liquid crystals (LCs) based on chenodeoxycholic acid (CDCA), termed as EFSD, EFSL, EFXD, EFXL and EFDZ, were synthesised. EF, which is a chiral smectic A (SmA*) LC, was synthesised by using CDCA as the chiral core and introducing fluorinated LC arm, 4ʹ-((10-chloro-10-oxodecanoyl)oxy)-[1,1ʹ- biphenyl]-4-yl 4-(trifluoromethyl)benzoate, into the hydroxyl of CDCA. The third side arm with different rigidity and the length of the terminal chain was introduced into the carboxyl group of CDCA to prepare the non-symmetric three-arm LCs. The results indicate that the proper increase of the third side arm's rigidity can stabilise the LC phases and widen LC ranges. In addition, the structure of the third side arm also had an influence on the LC phase type. EFSD, EFXD, EFXL and EFDZ display cholesteric (Ch) phases, while EFSL exhibits chiral smectic C (SmC*) phase. The longer alkyl terminal chain of the third side arm can lead to the appearance of lamellar phase. For this type LCs, it is beneficial to the formation of Ch phase LCs to adopt short alkyl terminal chain. That EFDZ displays Ch phase may be due to the increase of molecular biaxiality of EFDZ due to the biaxiality of cholesterol. 궜 [ABSTRACT FROM AUTHOR]

Purpose: Simple, rapid and high-throughput dose assessment is critical for clinical diagnosis, treatment and emergency intervention in a large-scale radiological accident. The goal of this study is to screen and identify new ionizing radiation-responsive protein biomarkers in rat plasma. Materials and methods: Sprague-Dawley rats were exposed to single doses of 0, 1, 3, 5 Gy of Cobalt-60 γ-rays total body irradiation at a dose rate of 1 Gy/min. The tandem mass tag labeling (TMT) combined with liquid chromatography mass spectrometry (LC-MS/MS) approach was used to screen the differentially expressed proteins in rat plasma collected at 1, 3, 5 and 7 days post-irradiation. Bioinformatics analysis was conducted to explore the biological functions of these proteins. The expression levels of candidate radiation-sensitive protein biomarkers were confirmed using enzyme-linked immune-sorbent assay (ELISA). Results: A total of 503 differentially expressed proteins were identified. Most of these proteins were implicated in immune response, phagocytosis and signal transduction following ionizing radiation. Five up-regulated proteins including alpha-2-macroglobulin (A2m), chromogranin-A (CHGA), glutathione pertidase 3 (GPX3), clusterin (Clu) and ceruloplasmin (Cp) were selected for ELISA analysis. It was found that the expression levels of A2m, CHGA and GPX3 protein were increased in a dose-dependent manner at 1, 3 and 5 days after irradiation. Conclusion: Proteomics analysis revealed radiation-induced differentially expressed proteins in rat plasma. Our results suggested that A2m, CHGA, GPX3 protein expressions alterations in rat plasma may have potential as biomarkers to evaluate radiation exposure. [ABSTRACT FROM AUTHOR]

A series of non-symmetric dimers with the same chiral core, mandelic acid (MA), have been synthesised by varying the terminal group and the rigidity of the molecules, termed QBBMA-3F3BT, QBMA-3F3BT, QBMA-3F2BT, 3F3BMA-BBCN, 3F2BMA-BBCN and 3F1BMA-BBCN. Chemical structures and liquid crystal (LC) properties of the dimers were characterised by Fourier transform infrared spectroscopy, 1H NMR, polarised optical microscopy (POM), differential scanning calorimetry (DSC), X-ray diffraction (XRD) and thermogravimetric analysis (TG). The six dimers displayed different optical activity (in THF). QBBMA-3F3BT and QBMA-3F3BT displayed enantiotropic chiral smectic A (SmA*) phase. QBMA-3F2BT displayed N phase. The Tm of QBMA-3F3BT is the highest among QBBMA-3F3BT, QBMA-3F3BT and QBMA-3F2BT, which indicated that molecular conformation played an important role on Tm besides molecular weight and molecular rigidity. 3F3BMA-BBCN and 3F2BMA-BBCN displayed chiral nematic (N*), which indicated that the mesogenic arm BBCN is beneficial to the formation of N* phase. The LC range of 3F2BMA-BBCN is wider, which may be due to that the similar length of the two LC arms is advantageous to the interaction between C≡N group and other molecules so as to stabilise the LC phase. [ABSTRACT FROM AUTHOR]

A series of symmetric liquid crystal (LC) dimers with the same chiral core (S)-1-phenylethane-1,2-diol ((S)-PE) have been synthesised, termed TBDA-(S)-PE, 3F3B-(S)-PE, 3F2B-(S)-PE, 1F3B-(S)-PE, 1F2B-(S)-PE, respectively. Chemical structures and LC properties of the five symmetric LC dimers were characterised by Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance hydrogen spectrometer (1H NMR), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), X-ray diffraction (XRD) and polarised optical microscopy (POM). TBDA-(S)-PE displayed enantiotropic chiral smectic A (SmA*) phase while 3F3B-(S)-PE, 3F2B-(S)-PE, 1F2B-(S)-PE all displayed enantiotropic chiral nematic (N*) phase and 1F3B-(S)-PE displayed monotropic N* phase. The results indicated that the removal of the flexible spacers between the rigid mesogenic arm and the chiral core facilitated the formation of the N* phase. When the rigid mesogenic units are connected to the chiral core directly, the structure of the terminal fluorine group and the rigidity of the mesogenic unit played certain influence on the thermal properties of the LC dimers, but did not change the type of mesomorphic phase. Compared to 3F3B-(S)-PE and 1F3B-(S)-PE, 3F2B-(S)-PE and 1F2B-(S)-PE displayed wider LC ranges, respectively, suggesting molecular regularity had greater influence on LC-isotropic (I) transition temperature. [ABSTRACT FROM AUTHOR]

This paper designed and synthesised a series of V-shaped liquid crystal molecules (X-SBAnE) with resorcinol as the core and Schiff base as the mesogenic arms (X-SBAAn). The effects of polarity of terminal groups (X=-CH3O,-CH3,-Cl) and length of flexible chain (n = 4,6,8) on mesogenic ranges were discussed. The chemical structure of X-SBAAn and X-SBAnE was studied using FT-IR and 1H-NMR while their thermal behaviour and mesogenic ranges were investigated via differential scanning calorimetry (DSC) and polarising optical microscopy (POM). The results indicated that X-SBAAn containing OCH3 and Cl substituents exhibited mesophase except for the analogue having CH3 substituent which was found to be non-mesogenic. All of the synthesised X-SBAnE had liquid crystal properties and exhibited nematic phases in heating and cooling. The length of the flexible spacers and terminal groups significantly influenced their mesogenic ranges. [ABSTRACT FROM AUTHOR]

Two series of novel four-arm azobenzene liquid crystal molecules were designed and synthesized, and their mesophase properties, photo-induced transition were studied. Two series of mesogenic arms were screened with different length of flexible chain (the carbon number n of flexible chain is 4, 6, 8, 10) using methoxy and nitro as terminal substituents R. The four-arm azobenzene LCs were synthesized by introducing the mesogenic arms into cholic acid. FACAE-O-n, FACAE-N-n all belonged to photosensitive thermotropic enantiotropicnematic LCs. For methoxyl series, melting transitions (Tm), liquid crystal-isotropic transitions (Ti) and mesogenic ranges decreased with the increase of carbon numbers in flexible chain both on heating and cooling. The mesophase performance of FACAE-O-4 was the most excellent. For nitro series, Tm and Ti on heating and cooling decreased with the increase of carbon numbers. Nevertheless, mesogenic ranges increased with the increase of carbon numbers only on heating. The cooling mesogenic ranges showed a trend of rising firstly and then falling, reaching the maximum 103.1oC (n=8). Under ultraviolet irradiation, there was no red shift. The intensity of maximum absorption has changed with the increase of ultraviolet irradiation time. After photo-induced, Tm and Ti on heating and cooling of the four-arm LCs decreased, and the mesogenic ranges became shorter. [ABSTRACT FROM AUTHOR]

Twenty novel azobenzene liquid crystal micromolecular compounds named ω-[4-(p-substituted azobenzeneoxy carbonyl]acid (X-ABCnA) have been designed and synthesised, followed by studies on the thermal performance and mesomorphic properties of the compounds. The liquid crystal compounds were divided into five homologous series based on the terminal substituents R (R = CH3O, CH3, H, Cl, NO2). In each series, the number of carbons on flexible chain was 4, 6, 8 and 10, respectively. Fourier-transform infrared, proton nuclear magnetic resonance and elementary analysis demonstrated that the structure of the synthesised azobenzene liquid crystal compounds was consistent with the molecular design. The mesomorphic properties were tested, analysed and characterised by using differential scanning calorimetry and polarised optical microscopy. The melting transition (Tm) of all the compounds in homologous series with different substituents appeared to decrease with the increase of carbon numbers on flexible chains. The same held true for the temperature of isotropic-mesophase/crystalline transition. The compounds with stronger polarity of terminal substituents were more likely to form broader mesogenic ranges. The liquid crystal compounds discussed in this work can be regarded as a reference for the synthesis of mesogenic arms participating in the synthesis of novel multi-arm liquid crystalline macromolecules and polymers. [ABSTRACT FROM AUTHOR]

We synthesized two series of cholesteric liquid-crystal elastomers by hydrosilylation among monomers MA containing a cholesteryl group, MB (MC) containing a phenolic hydroxyl group and MD as the crosslinker. The chemical structures of all the monomers and LCEs were confirmed by 1H NMR and FT-IR. We explored the mesomorphic properties and phase behaviours by TGA, DSC, POM, and XRD. All the LCEs presented elasticity, reversible phase transition, and high thermal stability. For two series of LCEs, the glass transition temperature increased slowly, and the isotropic transition temperature increased obviously. PA-I-PA-V and PB-I-PB-IV displayed selective reflection and colourful Grandjean texture, but PA-VI, PB-V, and PB-VI needed external pressure to show them. [ABSTRACT FROM AUTHOR]

With cholic acid as the core, five multi-arm ester liquid crystals were synthesised with different terminal substituents. B1–B5 were mesogenic arms which were linked to multifunctional chiral core cholic acid. The effect of electron-withdrawing and electron-donating groups on the mesogenic behaviour of the compounds was discussed. All products were structurally well characterised by elemental analysis, 1HNMR, and FT-IR. The phase behaviours were investigated by means of polarised optical microscopy and differential scanning calorimetry. B2, B4, B5 and C2, C4, C5 and D2, D4, D5 exhibited typical nematic texture and belonged to thermotropic enantiotropic nematic liquid crystals. B3, C3 and D3 also displayed typical nematic texture of thermotropic monotropic nematic liquid crystal. B1, C1 and D1 did not have mesogenic performance. Wider mesogenic range for 81.6°C of C5 whose terminal substituent is nitro on heating cycle while 121.1°C on cooling cycle. The results indicated that terminal substituents have a pretty important effect on the mesogenic phase and range of multi-arm liquid crystal compounds. The mesomorphic behaviour of compounds with polar groups terminally substituted performance much better than those without polar groups. In this ester multi-arm liquid crystal system, electron-withdrawing groups terminally substituted behave better than those electron-donating groups substituted. [ABSTRACT FROM AUTHOR]

One new indole diterpenoid, drechmerin I (1), was isolated from the fermentation broth of Drechmeria sp. isolated from the root of Panax notoginseng. Its structure was elucidated based on 1 D and 2 D nuclear magnetic resonance (NMR), high resolution electrospray ionization mass spectrum (HRESIMS), and electronic circular dichroism (ECD) spectroscopic analyses as well as TD DFT calculations of ECD spectra. Drechmerin I (1) was assayed for its antimicrobial activity against Candida albicans, Staphylococcus aureus, Bacillus cereus, B. subtillis, Pseudomonas aeruginosa, and Klebsiella pneumonia, respectively. Drechmerin I (1) showed antimicrobial activities against B. subtillis with an MIC value of 200 μg/mL. The interaction of S. aureus peptide deformylase with drechmerin I (1) was investigated by molecular docking. [ABSTRACT FROM AUTHOR]

Seven symmetric liquid crystal (LC) dimers containing different chiral cores and LC arms have been synthesised, termed EPDA-(R,S)PD, TFBDA-(R,S)PD, TFBA-(R,S)PD, TFBDA-(R)PD, TFBA-(R)PD, TFBDA-IB and TFBA-IB, respectively. TFBDA-(R,S)PD, TFBA-(R,S)PD, TFBDA-(R)PD and TFBDA-IB displayed chiral smectic A (SmA*) phase, while EPDA-(R,S)PD, TFBA-(R)PD and TFBA-IB exhibited chiral nematic (N*) phase. The effects of flexible spacer, structural type of LC arms and the chirality of the cores on the thermal properties of the dimers and the formation of N* phase have been studied. The results indicated that the chiral core was prone to induce the N* phase in LC dimer that contained nematic arms although the chirality of the core is very weak, while for the smectic LC arms containing CF3 terminal, the removal of the flexible spacer between chiral core and rigid LC units was conducive to the formation of N* phase. For example, TFBDA-(R)PD and TFBDA-IB displayed SmA* phase, while TFBA-(R)PD and TFBA-IB exhibited N* phase. However TFBA-(R,S)PD did not display N* phase, which reminded us that the chirality of the core and the conformation of the dimer also played an influence in the formation of the LC phase. [ABSTRACT FROM AUTHOR]

Six three-arm star-shaped liquid crystals (LCs) based on chenodeoxycholic acid (CDCA), termed as G-BH, G-YD, G-FD, G-DJ, G-DZ and G-BX, respectively, have been synthesised. CDCA was used as the chiral core and the nematic side arm, 6-(4-(ethylbenzoyloxy) phenoxy)-6-oxohexanoic acid, was chosen to be introduced into the two hydroxyl of CDCA to synthesise cholesteric LC (CDCA2EA) and different structures were introduced into the carboxyl group of CDCA to prepare the three-arm star-shaped LCs. Chemical structures and LC properties of the six three-arm LCs were characterised by FTIR, 1H-NMR, differential scanning calorimetry, thermogravimetric analysis, X-ray diffraction and polarised optical microscopy. G-BH and G-DJ displayed cholesteric phase with a long helical pitch; G-BX displayed nematic phase; and G-YD, G-FD and G-DZ displayed cholesteric phase on heating and on cooling. These results indicated that not only the chiral core CDCA but also the structures of the side arms played an important role in inducing the cholesteric phase of the CDCA-derived LCs. G-DZ displayed selective reflection, a wider ∆λ and red shift on cooling. [ABSTRACT FROM AUTHOR]

The first complete mitochondrial genome of the intertidal barnacle Fistulobalanus albicostatus Pilsbry, 1916 (Crustacea: Maxillopoda: Sessilia) is presented. The genome is a circular molecule of 15,665 bp, which encodes a set of 37 typical metazoan genes. All non-coding regions are 438 bp in length, with the longest one speculated as the control region (264 bp), which is located between srRNA and trnI. All protein-coding genes (PCGs) have an ATD (ATA, ATT, or ATG) start codon, except nad1, which is initiated with GTG. Remarkably, cox3, cob, nad1-5 have incomplete stop codons (T–– or TA–) and the remaining PCGs have the complete stop codon (TAA). Phylogenetic analysis based on 13 mitochondrial PCGs shows that the members of the Archaeobalanidae and Balanidae intermingle with species from Pyrgomatidae. The results supposed that Balanidae and Archaeobalanidae are non-monophyly. [ABSTRACT FROM AUTHOR]

Capitulum mitella (Crustacea: Cirripedia) is an important stalked barnacle. The first mitochondrial genome of C. mitella from China was presented, which is a circular molecule of 15,930 bp in length and AT content is 64.4%. It encodes 37 genes, including 13 PCGs, 22 tRNAs, and two rRNAs, which is consistent with most barnacles species reported. There are 15 genes encoded on the light strand and 22 genes encoded on the heavy strand. Identical to most barnacles species reported, srRNA and lrRNA genes are adjacent and separated only by trnV gene. Phylogenetic trees showed that C. mitella clustered with Pollicipes polymerus, indicating Pollicipedidae is monophyletic. However, Scalpelliformes was not monophyletic from the phylogenetic tree. From the level of order, the Lepadiformes was located at the base of the phylogenetic tree, indicating that its divergence time was earlier than Scalpelliformes. The results provided more insights into phylogenetic consideration at the genomic level within superorder Thoracica. [ABSTRACT FROM AUTHOR]

A new series of multi-arm liquid crystals (D1-D5) based on cholic acid as the chiral core and ω-[4-(p-substituted azobenzeneoxy carbonyl]valeric acid (B1-B5) as the mesogenic arms were designed and synthesised. All the mesogenic arms and the multi-arm liquid crystals were structurally well-characterised using elementary analysis (EA), 1H NMR and FT-IR. The photochemical properties were determined by UV spectra. The optical rotations were measured by Automatic Polarimeter. The phase behaviours were investigated by means of polarised optical microscopy, X-ray diffraction and differential scanning calorimetry, while the effect of the terminal groups of azobenzene on mesogenic and photochemical properties were discussed. The results demonstrated that the mesogenic arms exhibited nematic phase except B3. The multi-arm compounds showed chiral nematic except D3. Cholic acid played an important role in inducing chiral nematic of the multi-arm liquid crystals. Tm or Ti of B1-B5 and D1-D5 are influenced by the effect of electrical effects of the terminal groups and the molecular shapes. Furthermore, the multi-arm compounds exhibited well light sensitivity, owning the photoisomerisation of the tran-form azobenzene to the cis-form azobenzene. λmax of D1-D5 displayed blue shift first and then red shift with the different electrical effects of the terminal groups of mesogenic arms. [ABSTRACT FROM AUTHOR]

A series of non-symmetric liquid crystal (LC) dimers with the same chiral core 1,2-propanediol (PD) have been synthesised, termed as ABBA-PD-TFBA, PBBA-PD-TFBA, ABA-PD-TFBA, PBA-PD-TFBA and AA-PD-TFBA, respectively, in which one of the two mesogenic groups, the fluorinated mesogenic unit, was kept fix and the other arm was different. The intermediate compounds and LC dimers were characterised by FTIR, 1H NMR, differential scanning calorimetry, thermogravimetric analysis, polarised optical microscopy and X-ray diffractometer (XRD). The results of the measurements indicated that ABBA-PD-TFBA, PBBA-PD-TFBA and ABA-PD-TFBA displayed optical activity and enantiotropic chiral nematic phase, and PBA-PD-TFBA was an enantiotropic nematic LC while AA-PD-TFBA was a monotropic LC, displaying both nematic phase and smectic A phase on cooling. The results indicated that PD was able to induce the chiral nematic phase, nevertheless, the rigidity of the mesogenic arm, the flexibility of the terminal group and even the type of the terminal chemical bond played an important effect on the thermal properties of the dimers, and even on the formation of the chiral nematic phase. It is also worth noting that C=C at the terminal helped to stabilise the LC phase. [ABSTRACT FROM AUTHOR]

A new series of multi-arm chiral liquid crystals (LCs) D1-D3 were synthesised and characterised. Cholic acid was used as the core and ω-[4-(p-alkoxybenzoloxy)phenoxycarbonyl]valeric acid (B1-B3) was used as the mesogenic arms, containing different terminal substituent X (B1: X= -OCH3, B2:X= -CH3, B3: X= -Cl). Their structures and mesomorphic properties were investigated by Fourier-transform infrared spectroscopy, nuclear magnetic resonance hydrogen spectrometer, differential scanning calorimetry, polarised optical microscopy and X-ray diffraction, respectively. The mesogenic B1-B3 displayed smectic B phase. The multi-arm LC D1 displayed cholesteric, while D2 and D3 exhibited nematic phase. The formation of cholesteric phase of D1 was affected by both the chiral core - the bulky cholic acid and the polarity of the terminal substituent of the mesogenic arm. That D1 displayed cholesteric phase but D2-D3 did not indicated that the stronger polarity of the terminal group OCH3 of D1 played an important part in stabilising the cholesteric phase. The multi-arm LCs D1-D3 all showed ultraviolet activity. The wavelength of maximum absorption of D1-D3 was affected by the terminal substituent of the mesogenic arm. [ABSTRACT FROM AUTHOR]

Four non-symmetric dimers containing mandelic acid as the chiral core have been synthesised, termed as QBMA-B, QBMA-BCN, QBMA-BBCN and QBBMA-BBCN, respectively. Chemical structures and liquid crystal (LC) properties of the dimers were characterised by FTIR, 1H-NMR, differential scanning calorimetry (DSC), thermogravimetric analysis (TG) and polarised optical microscopy (POM). The results indicated that the rigidity and conformation of the molecules of the dimers played important effects on their mesophase properties. QBMA-B did not display any mesophase, QBMA-BCN and QBMA-BBCN exhibited nematic (N) phases, while QBBMA-BBCN displayed cholesteric (ch) phase, which indicated that chiral mandelic acid could induce cholesteric phase, but some attention should be paid to the molecular conformation to obtain cholesteric phase. For the four dimers, melting temperature (Tm) increased first and then decreased, inferring that molecular conformation played a more important effect besides molecular weight and rigidity. [ABSTRACT FROM AUTHOR]

The cholesteric polysiloxanes (PLQ series) were obtained by reacting cholesteric monomer and phenolic hydroxyl monomer in different ratios with polysiloxanes. The chiral azo-containing polysiloxanes liquid-crystalline elastomers (LCEs) were synthesised by esterifying PLQ series with acyl acid of azo diacid catalysed by 4-dimethylaminopyridine (DMAP). The chemical structures and mesomorphic properties of monomers and polymers were confirmed by conventional spectroscopic methods. The elastomers displayed elastic properties, reversible phase transition and high thermal stability. The Tg values changed irregularly and Ti values decreased at the beginning and then increased afterwards. The chiral azo-LCEs showed colourful textures and a Grandjean texture could be observed, which exhibited a red shift with increasing content of azo moiety. PLQ2-PLQ6 exhibited selective reflection in the visible light region, but PLZ1-PLZ4 can only observe selective reflection when appropriate mechanical pressure was imposed on the polymers. The PLZ series was carefully investigated by ultra violet-visible spectroscopy. [ABSTRACT FROM AUTHOR]

This study explores the challenges faced by young lecturers in managerial transformation in elite Chinese academic institutions which aim to develop into world-class universities. Drawing on data from in-depth interviews, the paper discusses how a group of lecturers on tenure-track contracts at a research university in China perceived the impacts of this managerial personnel reform. The study revealed intensified academic pressure and consequent feelings of insecurity, uncertainty and anxiety among the participants. Rigid tenure requirements pushed down research quality, and detracted from the efforts the participants could have devoted to teaching. Further negative impacts were strengthened power hierarchies and increasingly gendered nature of the academic culture. [ABSTRACT FROM PUBLISHER]

Background: Anxious distress in major depressive disorder (MDD) is common and associated with poor outcomes and management difficulties. Aims: This post hoc analysis aimed to examine the socio-demographic and clinical correlates of anxiety distress in Asian outpatients with MDD. Methods: Instead of two out of five specifiers defined by the Diagnostic and Statistical Manual Version-5, anxious distress defined in this study was operationalized as the presence of at least two out of four proxy items drawn from the 90-item Symptom Checklist, Revised (SCL-90-R). Other measures included the Montgomery--Asberg Depression Rating Scale (MADRS), the Fatigue Severity Scale, the Sheehan Disability Scale and the Multidimensional Scale of Perceived Social Support. Results: The data of 496 patients with MDD were included. Anxious distress was found in 371 participants (74.8%). The binary logistic regression analysis found that anxious distress was independently and significantly correlated with working status, higher MADRS scores, severe insomnia and functional impairment. Conclusions: Three-fourths of Asian patients with MDD in tertiary care settings may have DSM-5 anxious distress of at least moderate distress. Its prevalence may vary among working groups. The specifier was associated with greater depressive symptom severity, severe insomnia and functional impairment. [ABSTRACT FROM AUTHOR]

Four symmetric and non-symmetric chiral liquid crystal dimers containing trifluoromethyl groups, termed asTFBA-PD-TFBA, UEBBA-PD-TFBA, UEBA-PD-TFBAandUEA-PD-TFBA, respectively, have been synthesised and characterised.UEA-PD-TFBAexhibited chiral nematic phase, whereas the other three dimers displayed chiral smectic A phase. X-ray diffraction (XRD) has revealed the structure of the smectic A phase forTFBA-PD-TFBAto be intercalated, whereas that forUEBBA-PD-TFBAandUEBA-PD-TFBAto be monolayer and interdigitated, respectively. In addition, the weaker peak corresponding to a shorter layer spacing was observed forUEBBA-PD-TFBAandUEBA-PD-TFBA. Considering the results of XRD measurements and computer simulations, the structural model corresponding to the shorter layer spacing is assigned as horseshoe-like shape. The absence of smectic behaviour forUEA-PD-TFBAreveals that the weaker aromatic–aromatic interactions cannot stabilise the smectic A phase. [ABSTRACT FROM PUBLISHER]