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The effect of iron-containing substances with different forms on the properties of carbon-black filled natural rubber compound is discussed. The ionic iron substances (Fe[Cl.sub.2], Fe[Cl.sub.3], Fe[(SA).sub.3]) have a detrimental effect on the rubber. Based on the oxidation induction temperature values, the relative deteriorating effects of ionic iron substances on the rubber are in the order: Fe[(SA).sub.3] > Fe[Cl.sub.3] [approximately equal to] Fe[Cl.sub.2]. Not only are the metal ions ([Fe.sup.2+], [Fe.sup.3+]) with adjacent stable oxidation states catalytically active in degrading rubber, but also the counterions have an influence on the effect of oxidation, particularly the stearic anion. Ionic iron materials can decrease the molecular weight, especially for the case of Fe[(SA).sub.3] as measured by gel permeation chromatography. Due to the degrading effect on the rubber molecules, Fe[(SA).sub.3] brings about a torque decrease in moving die rheometer and evident decrease of the Mooney viscosity at 100[degrees]C, which is different from the effects of [Fe.sub.2][O.sub.3] and 304L-Fe. The insoluble iron substances behave more like hard fillers. Additionally, Fe[(SA).sub.3] remarkably alters the bound rubber content and the tensile properties after aging via two different process (scission and crosslinking). Overall, this work has a thorough comparison of effect of iron-containing materials on rubber aging and provides useful inspiration to protect the rubber from deterioration by foreign reagents and regulating the rubber stability and degradation rate via introducing degradative metal ions. KEYWORDS aging, GPC, ionic iron substances, natural rubber, OIT, 1 | INTRODUCTION Investigation of mechanism on rubber autoxidation (degradation) is important in maintaining the lifetime/stability of rubber materials and developing the easy-degradable polymer material. Rubber degradation involves chain initiation, [...]

Nonfullerene electron acceptors (NFAs) improve the photoelectrical conversion efficiency of organic solar cells (OSCs), but they suffer from high synthetic cost and time‐consuming thermal annealing treatment. Nevertheless, low‐cost NFAs and simple device fabrication are still crucial issues to boosting the commercial application of OSCs. Herein, one kind of low‐cost pentacyclic NFAs based on benzothiadiazole and thiophene derivatives named L1‐EH and L1‐BO with different substitutions is successfully synthesized and characterized. The optimized OSCs based on PM6:L1‐BO (2‐butyloctyl side chain) display an outstanding power conversion efficiency of 13.15%. Moreover, OSC devices based on these acceptors operate in thermal annealing‐free conditions. Further studies manifest that the proper side chains in NFAs can induce more favorable face‐on molecule orientation, enhance carrier mobility, balance charge transport, and reduce recombination losses. This research demonstrates that these types of low‐cost NFAs are promising active layer candidates of high‐efficiency organic solar cells featuring simple device manufacture. [ABSTRACT FROM AUTHOR]

Objective. Endometriosis, which is a common disease affecting approximately 10% of women of reproductive age, usually causes dysmenorrhea and infertility, thus seriously harming the patients' physical and mental health. However, there is a mean delay of 6.7 years between the onset of the symptoms and the surgical diagnosis of endometriosis. There is an increasing amount of evidence that suggests that epigenetic aberrations, including deoxyribonucleic acid (DNA) methylation, play a definite role in the pathogenesis of endometriosis. This study aimed to explore the noninvasive or minimally invasive biomarkers of this disease. Materials and Methods. Six patients with surgically confirmed ovarian endometriosis and six patients who received IUD implantation for contraception without endometriosis were recruited in the East Hospital of Tongji University in 2018. The genome methylation profiling of the eutopic and ectopic endometrium of ovarian endometriosis patients and normal endometrial specimens from healthy women was determined using a methylation microarray test. The test screened methylation-differentiated 5′–C–phosphate–G–3′ (CpG) sites and then located the target genes affected by these sites following sequence alignment. Then, an additional 22 patients and 26 healthy controls were enrolled to further verify the difference in the selected genes between endometriosis patients and healthy women. The differential DNA methylation of the selected genes was validated via direct bisulfite sequencing and analysis of their messenger ribonucleic acid (mRNA) levels using quantitative reverse transcription polymerase chain reaction (qRT-PCR). Results. Fifteen differentially methylated CpG sites were found among the patients and healthy women, and five CpG sites were mapped to the introns of the human leukocyte antigen-C (HLA-C) gene; these were highly polymorphic between different HLA-C alleles and were HLA-C ∗ 07 specific. The results indicated that the HLA-C ∗ 07 carrier patients exhibited significantly higher DNA methylation levels at the intron VII of HLA-C compared to the HLA-C ∗ 07 carrier healthy controls. High HLA-C ∗ 07 mRNA levels were also observed using qRT-PCR with HLA-C ∗ 07-specific primers, which indicated that the hypermethylation of CpG in intron VII might suppress a silencer that regulates HLA-C ∗ 07 expressions. Conclusion. Deoxyribonucleic acid hypermethylation in the intron VII of the HLA-C ∗ 07 gene appears to regulate the expression of HLA-C ∗ 07. The aberrant DNA methylation in this region was positively correlated with the occurrence of endometriosis. [ABSTRACT FROM AUTHOR]

Immunotherapy begins to be widely used due to the increasing exploration and gratifying effects in multiple cancers. Chordoma, as a rare bone malignant tumor, often recurs and metastasizes after undergoing surgery and radiotherapy. Therefore, immunotherapy can be explored as an emerging, potentially effective treatment to improve the survival rate and clinical benefit of patients. However, a variety of immune-related adverse events (irAEs) cannot be avoided completely. And the immunotherapy-induced myocarditis, as a rare but fatal irAE, has been increasingly reported. Understanding the mechanism involved in irAEs can inform best practices for side effects management. Here, we firstly reported a case of immune myocarditis and subsequent myasthenia gravis (MG) following anti-PD-1 treatment for chordoma. [ABSTRACT FROM AUTHOR]

Herein, a multi-functional nanoplatform (PDA-DTC/Cu–MnO2) was established, which has been employed for MR imaging-guided multi-therapy (CDT, PTT and chemotherapy) for cancer treatment. The in vitro and in vivo results confirmed that the biocompatible nanoplatform could significantly induce tumor cell death and inhibit tumor growth. [ABSTRACT FROM AUTHOR]

Despite drug delivery nanoplatforms receiving extensive attention, development of a simple, effective, and multifunctional theranostics nanoplatform still remains a challenge. Herein, a versatile nanoplatform based on a zirconium framework (UiO‐66‐N3) was synthesized, which demonstrated a combined photodynamic therapy (PDT), photothermal therapy (PTT), and chemotherapy (CT) for cancer treatment. A RuII polypyridyl alkyne complex (Ra) as a photosensitizer was modified into a nanoplatform by click reactions for the first time. When exposed to suitable light irradiation, the as‐prepared multifunctional nanoplatform (UiO‐Ra‐DOX‐CuS) not only demonstrated efficient 1O2 generation, but also exhibited excellent photothermal conversion ability. In particular, the nanotherapeutic agent presented a dual‐stimuli response; either acidic environment or NIR laser irradiation would trigger the drug release. The synergetic efficacy of UiO‐Ra‐DOX‐CuS combined PDT, PTT, and CT, which was evaluated by cell experiments. Moreover, the design could promote the development of RuII polypyridyl alkyne complexes based multifunctional nanoparticles and multimodal cancer treatment. [ABSTRACT FROM AUTHOR]

Graphical abstract Abstract Covalent grafting and electrostatic-driven assembly have been two strategies in constructing well-defined polyoxometalate (POM) assemblies to produce specific morphologies and desirable properties. The modification of anionic counter-ions of amphiphilic compounds in POM-surfactant hybrid systems is still unexploited. Herein, we report the co-assembly of a synthetic double-tailed magnetic surfactant (MagSurf), (C 18) 2 C 2 N+[FeCl 4 ]−, and POM, {Mo 72 Fe 30 }. The magnetic aggregate (POM/MagSurf) results from the building up hierarchical structures at a time-dependent interface. In this construct, both the MagSurfs and {Mo 72 Fe 30 } POMs contribute to and mutually strengthen the magnetization of the designed magnetic assembles. Interestingly, the POM/MagSurf aggregates are compatible with aqueous mixtures and successfully employed to serve as magnetic transporting vehicles to anchor and deliver a protein molecule, myoglobin (Mb). Upon applying a magnetic field (0.3 T), the magnetic aggregates induced a directional migration and enrichment of the Mb protein (71–90%). During this process, the protein/POM/MagSurf complexes exhibited strong interactions facilitating stable anchoring and efficient enrichment of the Mb. [ABSTRACT FROM AUTHOR]

DNA microgels of oligonucleotides and polymers were constructed via a combination of DNA complementarity and photo-initiated free radical polymerization. The DNA microgels did not feature the conventional core–shell structure but were instead based on the copolymers of N-isopropylacrylamide and acrylamide and DNA crosslinks. By incorporating the aptamer-functionalized moieties, the AptMG–Dox system was demonstrated to possess excellent biocompatibility and highly selective killing efficacy for target cancer cells via stimuli-responsiveness, which could provide immense potential as an intelligent drug delivery carrier for targeted cancer therapy. [ABSTRACT FROM AUTHOR]

Metal–organic gels (MOGs) of three-dimensional (3D) networks comprising nanosheets of ∼30 nm thickness and square-micrometer in size were easily produced via coordination interactions of iron (Fe3+) and 1,4-naphthalenedicarboxylic acid (NDC). Such MOGs exhibit ultrahigh removal of arsenic(v) in water, with the adsorption capacity of 144 mg g−1, dramatically superior to those of the recently reported Fe-based inorganic and organic adsorbents. [ABSTRACT FROM AUTHOR]

A multiresponsivehydrogel material consisting of a commercialcationic surfactant and an azobenzene derivative functionalized withfour carboxylic acid groups was constructed. The achiral azobenzenemolecule as a gelator produces chirality at the supramolecular levelin the presence of H+. The acid-induced gelation and morphologychange of supramolecular gels were investigated in detail by cryogenictransmission electron microscopy (cryo-TEM), rheological measurements,circular dichroism (CD), and 1H NMR spectra. Based on theresults, a mechanism of the intermolecular H-bond-directed gelationand supramolecular chirality was proposed. Other than the pH sensitivity,the microstructure and the chirality of the hydrogel demonstrate reversibleswitching behavior in response to photoirradiation, on account ofthe photoisomerization of the azobenzene derivative. Accordingly,a chiroptical switch comprising four different states in responseto pH and light stimuli is strategically constructed. Not only doesthe present system provide a good opportunity for investigating thegelation-induced supramolecular chirality by symmetry breaking totallybased on achiral molecules, but it also proposes a new strategy tobuild multiresponsive supramolecular switches as particularly attractivefor the future development of functional materials. [ABSTRACT FROM AUTHOR]

We report a new, simple strategy to apply honeycomb films for the patterning of colloidal particles. By combination of a 'bottom-up' breath figure method and the electrochemical properties of the honeycomb films of ferrocenyl-based oligomers, highly ordered hybrid membranes coated with ring-like patterning of 0D- and 1D-Ag nanoparticles (NPs) have been fabricated. One interesting phenomenon is that the nucleation and adsorption of Ag dots occurred preferentially at the edges of the micropores. The hybrid membranes exhibited richly electrochemical activities towards reduction of iodate and enhanced effectively catalytic reduction of organic dyes. We believe that this method can be used to decorate and/or assemble functional metal NPs such as Au, Pd, and Cu on honeycomb-patterned materials for the further applications of photonics, sensors, and catalysis. [ABSTRACT FROM AUTHOR]

Abstract: Dysregulated Skp2 function promotes cell proliferation, which is consistent with observations of Skp2 over-expression in many types of human cancers, including cervical carcinoma (CC). However, the molecular mechanisms underlying elevated Skp2 expression have not been fully explored. Interleukin-6 (IL-6) induced Stat3 activation is viewed as crucial for multiple tumor growth and metastasis. Here, we demonstrate that Skp2 is a direct transcriptional target of Stat3 in the human cervical carcinoma cells. Our data show that IL-6 administration or transfection of a constitutively activated Stat3 in HeLa cells activates Skp2 mRNA transcription. Using luciferase reporter and ChIP assays, we show that Stat3 binds to the promoter region of Skp2 and promotes its activity through recruiting P300. As a result of the increase of Skp2 expression, endogenous p27 protein levels are markedly decreased. Thus, our results suggest a previously unknown Stat3–Skp2 molecular network controlling cervical carcinoma development. [Copyright &y& Elsevier]

Objective: Polyunsaturated fatty acids (PUFAs) have attracted increasing attention for their role in liver cancer development. The objective of this study is to develop a prognosis prediction model for patients with liver cancer based on PUFA-related metabolic gene characteristics., Method: Transcriptome data and clinical data were obtained from public databases, while gene sets related to PUFAs were acquired from the gene set enrichment analysis (GSEA) database. Univariate Cox analysis was conducted on the training set, followed by LASSO logistic regression and multivariate Cox analysis on genes with p < .05. Subsequently, the stepwise Akaike information criterion method was employed to construct the model. The high- and low-risk groups were divided based on the median score, and the model's survival prediction ability, diagnostic efficiency, and risk score distribution of clinical features were validated. The above procedures were also validated in the validation set. Immune infiltration levels were evaluated using four algorithms, and the immunotherapeutic potential of different groups was explored. Significant enrichment pathways among different groups were selected based on the GSEA algorithm, and mutation analyses were conducted. Nomogram prognostic models were constructed by incorporating clinical factors and risk scores using univariate and multivariate Cox regression analysis, validated through calibration curves and clinical decision curves. Additionally, sensitivity analysis of drugs was performed to screen potential targeted drugs., Results: We constructed a prognostic model comprising eight genes (PLA2G12A, CYP2C8, ABCCI, CD74, CCR7, P2RY4, P2RY6, and YY1). Validation across multiple datasets indicated the model's favorable prognostic prediction ability and diagnostic efficiency, with poorer grading and staging observed in the high-risk group. Variations in mutation status and pathway enrichment were noted among different groups. Incorporating Stage, Grade, T.Stage, and RiskScore into the nomogram prognostic model demonstrated good accuracy and clinical decision benefits. Multiple immune analyses suggested greater benefits from immunotherapy in the low-risk group. We predicted multiple targeted drugs, providing a basis for drug development., Conclusion: Our study's multifactorial prognostic model across multiple datasets demonstrates good applicability, offering a reliable tool for personalized therapy. Immunological and mutation-related analyses provide theoretical foundations for further research. Drug predictions offer important insights for future drug development and treatment strategies. Overall, this study provides comprehensive insights into tumor prognosis assessment and personalized treatment planning., (© 2024 Wiley Periodicals LLC.)

Objective: Endometriosis, which is a common disease affecting approximately 10% of women of reproductive age, usually causes dysmenorrhea and infertility, thus seriously harming the patients' physical and mental health. However, there is a mean delay of 6.7 years between the onset of the symptoms and the surgical diagnosis of endometriosis. There is an increasing amount of evidence that suggests that epigenetic aberrations, including deoxyribonucleic acid (DNA) methylation, play a definite role in the pathogenesis of endometriosis. This study aimed to explore the noninvasive or minimally invasive biomarkers of this disease., Materials and Methods: Six patients with surgically confirmed ovarian endometriosis and six patients who received IUD implantation for contraception without endometriosis were recruited in the East Hospital of Tongji University in 2018. The genome methylation profiling of the eutopic and ectopic endometrium of ovarian endometriosis patients and normal endometrial specimens from healthy women was determined using a methylation microarray test. The test screened methylation-differentiated 5'-C-phosphate-G-3' (CpG) sites and then located the target genes affected by these sites following sequence alignment. Then, an additional 22 patients and 26 healthy controls were enrolled to further verify the difference in the selected genes between endometriosis patients and healthy women. The differential DNA methylation of the selected genes was validated via direct bisulfite sequencing and analysis of their messenger ribonucleic acid (mRNA) levels using quantitative reverse transcription polymerase chain reaction (qRT-PCR)., Results: Fifteen differentially methylated CpG sites were found among the patients and healthy women, and five CpG sites were mapped to the introns of the human leukocyte antigen-C (HLA-C) gene; these were highly polymorphic between different HLA-C alleles and were HLA-C ∗ 07 specific. The results indicated that the HLA-C ∗ 07 carrier patients exhibited significantly higher DNA methylation levels at the intron VII of HLA-C compared to the HLA-C ∗ 07 carrier healthy controls. High HLA-C ∗ 07 mRNA levels were also observed using qRT-PCR with HLA-C ∗ 07-specific primers, which indicated that the hypermethylation of CpG in intron VII might suppress a silencer that regulates HLA-C ∗ 07 expressions., Conclusion: Deoxyribonucleic acid hypermethylation in the intron VII of the HLA-C ∗ 07 gene appears to regulate the expression of HLA-C ∗ 07. The aberrant DNA methylation in this region was positively correlated with the occurrence of endometriosis., Competing Interests: The authors declare that they have no conflicts of interest., (Copyright © 2023 Wenrong Zhao et al.)

Herein, a multi-functional nanoplatform (PDA-DTC/Cu-MnO2) was established, which has been employed for MR imaging-guided multi-therapy (CDT, PTT and chemotherapy) for cancer treatment. The in vitro and in vivo results confirmed that the biocompatible nanoplatform could significantly induce tumor cell death and inhibit tumor growth.

Cationic magnetic Gemini surfactants (mag-G-surfs), [C 14 H 29 (CH 3 ) 2 N(CH 2 ) 2 N(CH 3 ) 2 C 14 H 29 ] 2+ ·2[XCl 3 Br] - (14-2-14·2X, X = Ce, Gd, or Ho), efficiently induce the aggregation of glutathione-protected Au nanoclusters (NCs) (GSH-Au NCs). These magnetic luminescent aggregates not only possess aggregation-induced emission (AIE) behavior but also display aggregation-induced magnetic enhancement. In particular, 14-2-14·2Ce and 14-2-14·2Gd have a better effect on boosting the luminescence intensity, quantum yield (QY), and luminescence lifetime (τ). The luminescent aggregates of GSH-Au NCs triggered by 14-2-14·2Gd or 14-2-14·2Ho exhibit more favorable paramagnetic behavior. Other Au NCs containing a Au(I)-thiolate complex shell also exhibit the obvious AIE phenomenon after introducing 14-2-14·2Gd, demonstrating the luminescence enhancement effect of mag-G-surfs. The luminescent aggregate 14-2-14·2Ce@GSH-Au NCs can serve as a "light up" fluorometric probe to detect cysteine selectively with the detection limit (DL) of 36 μM, and the magnetic luminescent aggregate 14-2-14·2Gd@GSH-Au NCs has the potential to be a novel contrast agent in T 1 -weighted magnetic resonance (MR) imaging due to its satisfactory contrasting ability.

Despite drug delivery nanoplatforms receiving extensive attention, development of a simple, effective, and multifunctional theranostics nanoplatform still remains a challenge. Herein, a versatile nanoplatform based on a zirconium framework (UiO-66-N 3 ) was synthesized, which demonstrated a combined photodynamic therapy (PDT), photothermal therapy (PTT), and chemotherapy (CT) for cancer treatment. A Ru II polypyridyl alkyne complex (Ra) as a photosensitizer was modified into a nanoplatform by click reactions for the first time. When exposed to suitable light irradiation, the as-prepared multifunctional nanoplatform (UiO-Ra-DOX-CuS) not only demonstrated efficient 1 O 2 generation, but also exhibited excellent photothermal conversion ability. In particular, the nanotherapeutic agent presented a dual-stimuli response; either acidic environment or NIR laser irradiation would trigger the drug release. The synergetic efficacy of UiO-Ra-DOX-CuS combined PDT, PTT, and CT, which was evaluated by cell experiments. Moreover, the design could promote the development of Ru II polypyridyl alkyne complexes based multifunctional nanoparticles and multimodal cancer treatment., (© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Developing nontoxic artificial carriers for stimuli-responsive capture, transport, and delivery of biomolecules is of immense scientific interest. Herein, for the first time, we synthesize a double-tailed cationic surfactant, (C 16 H 33 ) 2 (CH 3 ) 2 N + [FeCl 3 Br] - , which possesses magnetic properties [magnetic surfactants (Mag-Surfs)]. The time-dependent formation of virus-shaped hybrid mixed assemblies of polyoxometalates (POMs) {Mo 72 Fe 30 }/Mag-Surf with hollow-shell structures is followed. These structures serve well as robust high-surface-area shuttles, which can be manipulated with applied magnetic fields. By using cationic Mag-Surfs, the anionic POMs and DNA can be complexed in these ternary mixtures. These virus-shaped complexes act as nanoanchors and nanomotors, which can be utilized for binding, anchoring, and delivery of biomolecules, such as DNA. It is found that they have a good absorption capacity for DNA and myoglobin over 24 h, after application of a magnetic field. The realization of magnetic virus-shaped {Mo 72 Fe 30 }/Mag-Surf spheres may open possibilities for designing other functional nanoparticles, allowing effective control over the delivery/separation of biomolecules.

Endometrial carcinoma is one of the most common gynecological malignant tumors. Recent evidence has demonstrated that miR-21 is involved in the proliferation and invasion of endometrial carcinoma. This study aims to explore the effect of biological behavior of miR-21 on endometrial carcinoma its relationship with PTEN. First, Collected endometrial carcinoma and adjacent non-tumor issues, the relative expression levels of miR-21 and PTEN mRNA were quantitated by real-time polymerase chain reaction (RT-PCR). Next, endometrial carcinoma cell line Ishikawa were transfected with miR-21 inhibitor. After transfection, real-time PCR was used to detect the expression levels of miR-21. Then, the cells proliferation, the apoptotic rates and the invasion rates were detected by MTT method, flow cytometry, and Transwell assay. The expression levels of p-PTEN and PTEN proteins were detected by western blot. The results showed that miR-21 was significantly up-regulation and PTEN was down-regulation in endometrial carcinoma tissues (P < 0.05). miR-21 inhibitor were successfully transfected into Ishikawa cell. The cell proliferation activity, and the number invasion cells in the miR-21 inhibitor group was obviously lower than the miR-21 NC group and Normal group (P < 0.05). The apoptosis rate in the miR-21 inhibitor group was significantly higher than the miR-21 NC group and Normal group (P < 0.05). The expression levels of p-PTEN in miR-21 inhibitor groups were significantly higher than miR-21 NC group and Normal group (P < 0.05). Therefore, we concluded that miR-21 could promote cell proliferation and invasion ability, and inhibite cell apoptosis in endometrial carcinoma partially by regulating its target gene PTEN on post-transcriptional level. In brief, miR-21 may be a new early diagnosis mark and therapy target in endometrial carcinoma., Competing Interests: None., (IJCEP Copyright © 2017.)

Bacillus-shaped bilayer vesicles of nanoscale size are very rare structures of stable surfactant self-assembly, because they are both thermodynamically and electrostatically unfavorable in solution. It is evidently demonstrated that appropriately aqueous mixtures of single-tailed cationic and anionic (catanionic) surfactants can produce rigidly bacillus-shaped bilayer vesicles with both flat parts and bent edges. The crucial requirement for forming bacillus-shaped bilayer vesicles is the use of cationic surfactants with relatively hydrophobic [FeCl 3 Br] - as counterions. [FeCl 3 Br] - can strongly associate with cationic surfactants to partition into the hydrophobic bilayer of bacillus-shaped bilayer vesicles, significantly increasing the edge energy of cationic surfactants to make them distribute in the low curvature part of bilayers. This causes the formation of bacillus-shaped bilayer vesicles, but not completely bent spherical vesicles, in the case of cationic surfactant excess. The specificity of hydrophobic counterions, [FeCl 3 Br] - , could also make the catanionic mixtures do not precipitate at the stoichiometric point. This new self-assembly on catanionic systems is culminated in the discovery of beautifully structured colloidal objects which are of practical use for molecular templating and controlled drug or DNA release.

Precise control of phase structure transition for the synthesis of multi-dimensional soft materials is a fascinating target in amphiphilic molecule self-assembly. Here, we demonstrate a spontaneous formation of a closely packed lamellar phase consisting of uni- and multi-lamellar vesicles through the incorporation of a small amount of an extractant, di(2-ethylhexyl)phosphoric acid (DEHPA), into the highly swollen, planar lamellar phase of a non-ionic tetraethylene glycol monododecyl ether (C12EO4) surfactant in water. It is figured out that the introduction of negative membrane charges results in the electrostatic repulsion among the lamellae, which suppresses the Helfrich undulation and induces a phase structure transition from planar lamellae to closely packed vesicles. Our results provide important insight into amphiphilic molecule self-assembly, where additives and pH can satisfy the opportunities for the precise tuning of the lamellar structures, which makes a way for the development of lamellar soft materials.

For the first time, a new fabrication method for manipulating the ferromagnetic property of molecular magnets by forming wormlike micelles in magnetic-ionic-liquid (mag-IL) complexes is reported. The ferromagnetism of the mag-IL complexes was enhanced 4-fold because of the formation of wormlike micelles, presenting new evidence for the essence of magnetism generation at a molecular level. Characteristics such as morphology and magnetic properties of the wormlike micelle gel were investigated in detail by cryogenic transmission electron microscopy (Cryo-TEM), rheological measurements, circular dichroism (CD), FT-IR spectra, and the superconducting quantum interference device method (SQUID). An explanation of ferromagnetism elevation from the view of the molecular (ionic) distribution is also given. For the changes of magnetic properties (ferromagnetism elevation) in the wormlike micelle systems, the ability of CTAFe in magnetizing AzoNa4 (or AzoH4) can be ascribed to an interplay of the magnetic [FeCl3Br](-) ions both in the Stern layer and in the cores of the wormlike micelles. Formation of colloidal aggregates, i.e., wormlike micelles, provides a new strategy to tune the magnetic properties of novel molecular magnets.

We report a chiral gel of vesicles and disklike micelles that originated from achiral molecules. The supramolecular chirality was obtained via regulating pH, in which a sol-gel-sol transition in a colloidal system consisting of a gelator, 4,4-di(2,3-dicarboxylphenoxyl)azobenzene (AzoNa4), and a zwitterionic surfactant, tetradecyldimethylamine oxide (C14DMAO), happened. The supramolecular chirality was related to the state of aggregation, i.e., only the condensed gels show chiral sense and sols are chiral-silent. The coexistence of vesicles and disklike micelles was captured for the first time in supramolecular chiral hydrogels by cryo- and freeze-fracture transmission electron microscopy (cryo- and FF-TEM) observations. Ascribed to the photoisomerization of the azobenzene units, upon alternative UV/visible light irradiation, the gel chirality can be switched reversibly with the macroscopic changes between vesicles/disks and wormlike micelles. A pH- and light-dual-responsive chiroptical switch can be constructed, which may require understanding the regulating membrane permeability and reagent release of structural transformation through photoisomerization and also require understanding the origin of gelation-induced supramolecular chirality completely based on achiral molecules.

We report a new, simple strategy to apply honeycomb films for the patterning of colloidal particles. By combination of a "bottom-up" breath figure method and the electrochemical properties of the honeycomb films of ferrocenyl-based oligomers, highly ordered hybrid membranes coated with ring-like patterning of 0D- and 1D-Ag nanoparticles (NPs) have been fabricated. One interesting phenomenon is that the nucleation and adsorption of Ag dots occurred preferentially at the edges of the micropores. The hybrid membranes exhibited richly electrochemical activities towards reduction of iodate and enhanced effectively catalytic reduction of organic dyes. We believe that this method can be used to decorate and/or assemble functional metal NPs such as Au, Pd, and Cu on honeycomb-patterned materials for the further applications of photonics, sensors, and catalysis., (Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)