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Nature Communications · 2024 ·Vol. 15 ·期 1 ·1-12 · IF 14.7

Concentrated solar CO2 reduction in H2O vapour with >1% energy conversion efficiency

Ren Yuqi,Fu Yiwei,Li Naixu,You Changjun,Huang Jie,Huang Kai,Sun Zhenkun,Zhou Jiancheng,Si Yitao,Zhu Yuanhao,Chen Wenshuai,Duan Lunbo,Liu Maochang

H 2 O dissociation plays a crucial role in solar-driven catalytic CO 2 methanation, demanding high temperature even for solar-to-chemical conversion efficiencies <1% with modest product selectivity. Herein, we report an oxygen-vacancy (V o ) rich CeO 2 catalyst with single-atom Ni anchored around its surface V o sites by replacing Ce atoms to promote H 2 O dissociation and achieve effective photothermal CO 2 reduction under concentrated light irradiation. The high photon flux reduces the apparent activation energy for CH 4 production and prevents V o from depletion. The defects coordinated with single-atom Ni, significantly promote the capture of charges and local phonons at the Ni d -impurity orbitals, thereby inducing more effective H 2 O activation. The catalyst presents a CH 4 yield of 192.75 µmol/cm 2 /h, with a solar-to-chemical efficiency of 1.14% and a selectivity ~100%. The mechanistic insights uncovered in this study should help further the development of H 2 O-activating catalysts for CO 2 reduction and thereby expedite the practical utilization of solar-to-chemical technologies.

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INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE · 2025 ·Vol. 55 ·期 3 ·1-14 · IF 5.8

Aquaporin‑1 regulates microglial polarization and inflammatory response in traumatic brain injury

Yixuan Ma,Yimin Huang,Xuyang Liu,Liwu Jiao,Hongtao Zhu,Zhiye Chen,Zhuojin Wu,Yuanzhong Shen,Kehan Lin,Feng Hu,Kai Shu

The present study investigated the mechanisms by which aquaporin 1 (AQP1) influences microglial polarization and neuroinflammatory processes in traumatic brain injury (TBI). A model of TBI was generated in AQP1‑knockout mice to assess the impact of AQP1 deletion on inflammatory cytokine release, neuronal damage and cognitive function. Immunofluorescence, reverse transcription‑quantitative PCR, western blotting and enzyme‑linked immunosorbent assay were employed to evaluate pro‑inflammatory and anti‑inflammatory markers. Behavioral assessments, including the Barnes maze, were performed to determine cognitive outcomes. Moreover, AQP1 knockout inhibited the activation of inflammation‑related signaling pathways, including nuclear factor‑κB, Janus kinase/signal transducer and activator of transcription, phosphoinositide 3‑kinase/protein kinase B and extracellular signal‑regulated kinase/mitogen‑activated protein kinase pathways. Further studies indicated that the AQP1 inhibitor m‑phenylenediacrylic acid demonstrated significant neuroprotective effects in a mouse model of TBI. These findings suggested that AQP1 may be essential in post‑TBI inflammatory responses and neuronal injury, establishing a theoretical foundation for future therapies aimed at AQP1.

CAS / MDL: 314-13-6
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JOURNAL OF NEUROCHEMISTRY · 2015 ·Vol. 134 ·期 5 ·904-914 · IF 4.281

Allosteric modulation of sigma-1 receptors by SKF83959 inhibits microglia-mediated inflammation

Zhuang Wu,Linlang Li,Long-Tai Zheng,Zhihong Xu,Lin Guo,Xuechu Zhen

Recent studies have shown that sigma-1 receptor orthodox agonists can inhibit neuroinflammation. SKF83959 (3-methyl-6-chloro-7,8-hydroxy-1-[3-methylphenyl]-2,3,4,5-tetrahydro-1H-3-benzazepine), an atypical dopamine receptor-1 agonist, has been recently identified as a potent allosteric modulator of sigma-1 receptor. Here, we investigated the anti-inflammatory effects of SKF83959 in lipopolysaccharide (LPS)-stimulated BV2 microglia. Our results indicated that SKF83959 significantly suppressed the expression/release of the pro-inflammatory mediators, such as tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), inducible nitric oxide synthase (iNOS), and inhibited the generation of reactive oxygen species. All of these responses were blocked by selective sigma-1 receptor antagonists (BD1047 or BD1063) and by ketoconazole (an inhibitor of enzyme cytochrome c 17 to inhibit the synthesis of endogenous dehydroepiandrosterone, DHEA). Additionally, we found that SKF83959 promoted the binding activity of DHEA with sigma-1 receptors, and enhanced the inhibitory effects of DHEA on LPS-induced microglia activation in a synergic manner. Furthermore, in a microglia-conditioned media system, SKF83959 inhibited the cytotoxicity of conditioned medium generated by LPS-activated microglia toward HT-22 neuroblastoma cells. Taken together, our study provides the first evidence that allosteric modulation of sigma-1 receptors by SKF83959 inhibits microglia-mediated inflammation. SKF83959 is a potent allosteric modulator of sigma-1 receptor. Our results indicated that SKF83959 enhanced the activity of endogenous dehydroepiandrosterone (DHEA) in a synergic manner, and inhibited the activation of BV2 microglia and the expression/release of the pro-inflammatory mediators, such as tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), inducible nitric oxide synthase (iNOS).

CAS / MDL: 53-43-0
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CHINESE JOURNAL OF CATALYSIS · 2015 · IF 1.964

Rh-PPh3-polymer@mesosilica composite catalyst for the hydroformylation of 1-octene

Xiaoming Zhang,Shengmei Lu,Mingmei Zhong,Yaopeng Zhao,Qihua Yang

Rh-PPh 3 -polymer@mesosilica composites were prepared by the polymerization of mixtures of divinylbenzene (DVB) and 4-vinyl-triphenylphosphine monomer in the nanopores of mesoporous silicas followed by coordination with Rh(acac)(CO) 2 (acac =acetylacetonate). These catalysts were characterized by XRD, N 2 sorption , TEM, FT-IR, and TG, and could efficiently catalyze the hydroformylation of 1-octene with higher activity than a pure polymer catalyst because of their high surface area and large pore volume, which were beneficial for the exposure of active sites and mass transport. Through the control of pore size and pore connectivity by using different mesoporous silica (MCM-41, SBA-15, and FDU-12), the activity and selectivity can be controlled. Rh-PPh 3 -polymer@FDU-12 with a cage-like mesostrucuture showed lower activity but slightly higher selectivity than the catalyst with a 2-D hexagonal mesostructure (Rh-PPh 3 -polymer@SBA-15 or Rh-PPh 3 -polymer@MCM-41). By varying the polymer content in the nanopores of the mesosilica, the activity and selectivity (92%–96%) can also be tuned. The solid composite catalyst can be recycled without loss of activity, but a decrease in selectivity was observed.

CAS / MDL: 1321-74-0
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RSC Advances · 2016 ·Vol. 6 ·期 113 ·112445-112450 · IF 3.289

Building a chimera of aptamer–antisense oligonucleotide for silencing galectin-1 gene

Shanni Hong,Na Sun,Min Liu,Jine Wang,Renjun Pei

Galectin-1 is closely related with immune systems, and its overexpression may cause tumor metastasis. Owing to the better stability of antisense oligonucleotides than siRNA, we constructed a chimera of aptamer–antisense oligonucleotide (Apt–AS) for silencing the galectin-1 gene specifically. For studying the endocytosis pathways of Apt–AS by aptamer targeted delivery, we marked the 3′ terminus of Apt–AS with Alexa Flour 488 (Apt–AS488) so as to trace the pathways through the confocal microscope. Furthermore, Apt–AS was used to silence the expression of galectin-1. The results showed Apt–AS entered cells by a caveolae mediated endocytosis pathway, and the aptamer–antisense chimeras did not impair the antisense gene silencing efficiency. Moreover Apt–AS could improve the cellular uptake and selectively entered cells.

CAS / MDL: 22144-77-0
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JOURNAL OF MOLECULAR LIQUIDS · 2015 · IF 2.515

Densities and conductivities of seven 1-allyl-3-methylimidazolium carboxylate ionic liquids

Airong Xu,Yajuan Zhang,Zhiyong Li,Jianji Wang

In the present work, seven 1-allyl-3-methylimizodalium carboxylate ionic liquids (ILs), including 1-allyl-3-methylimizodalium formate [Amim][HCOO], acetate [Amim][CH 3 COO], propionate [Amim][CH 3 CH 2 COO], butyrate [Amim][CH 3 (CH 2 ) 2 COO], glycollate [Amim][HOCH 2 COO], lactate [Amim][CH 3 CHOHCOO]) and benzoate [Amim][C 6 H 5 COO], have been synthesized and characterized. Density ( ρ ) and conductivity ( σ ) have been determined experimentally for these ILs at 298.15   K and atmospheric pressure. Then molar volume ( V m ), standard entropy ( S °), lattice energy ( U POT ) and molar conductivity ( Λ ) of the ILs have been derived from the density and conductivity data. Ionicity of the ILs has been estimated using the Walden plot. Meanwhile, how anionic structure of the ILs affects the volumetric and conductivity properties of 1-allyl-3-methylimidazolium carboxylate ILs has been discussed from the analysis of structure–property relationship.

CAS / MDL: 107-05-1 107-92-6
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CHEMICAL ENGINEERING JOURNAL · 2014 · IF 4.058

Synthesis of TS-1 on porous glass beads for catalytic oxidative desulfurization

C. Shen,Y.J. Wang,J.H. Xu,G.S. Luo

Porous glass supported with titanium silicalite (TS-1) particles were successfully prepared and used for oxidative desulfurization (ODS) of dibenzothiophene (DBT) and 4,6-dimethyldibenzothiophene (4,6-DMDBT). Uniform-sized TS-1 particles were homogeneously dispersed on the surface of the porous glass beads. Effects of reaction duration, catalyst content, initial concentration, oxidant amount, and temperature on conversions were investigated. The prepared catalysts showed excellent catalytic performance. The optimal mole ratio of oxidant-to-DBT was 10 or 15. Complete conversion was obtained within 3   min at 343   K using catalyst with Ti content of 0.507   wt.%. Compared with other studies, the space–time yield was increased by one order of magnitude without any addition of solvent or metal nanoparticles. Experimental results and computer simulations revealed that the coordinated state of Ti species has a key role in the catalytic activity. Spent catalyst would be regenerated by heating at high temperature, no decrease was observed in catalytic activity after three cycles.

CAS / MDL: 4499-86-9
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RESEARCH ON CHEMICAL INTERMEDIATES · 2017 ·Vol. 43 ·期 8 ·4697-4710 · IF 1.369

Impact of acidic properties of HBEA zeolite on isomerization of 1-methylnaphthalene

Sun Hao,Huang Xin,Wang Fang,Gu Zhenggui

Selective isomerization of 1-methylnaphthalene was carried out in a fixed-bed reactor over HBEA catalysts modified by acid and tetraethoxysilane treatments, respectively. Catalysts were characterized by X-ray diffraction, NH 3 temperature-programmed desorption, N 2 physisorption, inductively coupled plasma analysis, thermogravimetric analysis and Fourier transform infrared spectrometry after adsorption of pyridine. The results demonstrated that tetraethoxysilane treatment successfully passivated external active sites of the zeolite, but had little effect on the selectivity of isomerization reaction and catalytic stability. Dealumination of HBEA zeolite by treatment with oxalic and hydrochloric acids can lead to higher surface area and pore volume. Sufficiently strong Brönsted acidic sites were found to be responsible for the isomerization activity. Furthermore, a decrease in the number of Lewis acidic sites in acid-modified zeolites were advantageous to suppress the hydride transfer and subsequent side reactions that form coke, leading to higher 2-methylnaphthalene selectivity and longer catalytic life.

CAS / MDL: 90-12-0
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Nano Life · 2015 · IF 0

Removal of Azo Dyes from Aqueous Solution by Composite HKUST-1/GO

Qiong Yi,Ling Li,Lu Fan,Keke Sun,Lebao Mao,Keke Liang,Li Liu

The adsorption of three kinds of azo dyes from aqueous solution on HKUST-1/graphene oxide (GO) composite was studied in view of the removal efficiency, adsorption isotherm, and regenerate of the sorbent. HKUST-1/GO was found to be with higher dyes removal efficiency than HKUST-1. All the adsorption isotherms of azo dyes on HKUST-1/GO composite followed Freundlich isotherm. The adsorbed azo dyes on HKUST-1/GO could be eluted by acetone, so HKUST-1/GO can also be used for enrichment of azo dyes as adsorbent.

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ACS Applied Materials & Interfaces · 2024 · IF 8.3

Hydrogel-Composited Laminate for Islet Immune-Isolation to Treat Type 1 Diabetes

Yi Wang,Kai Wang,Xi Wang,Ying Luo,Haifeng Chen

Challenges remain to be solved for the clinical translation of β-cell encapsulation technology in the treatment of type 1 diabetes (T1D). Successful delivery of β cells urgently needs the development of an encapsulation device with a thin dimension and rapid mass transport that offers stable immune isolation and complete retrieval. In this study, we focus on a laminate in which an islet-embedding alginate hydrogel layer (Alg) is sandwiched between two polymer layers (polyether sulfone, PES). Mechanical support by the PES layer protects the alginate from disintegrating after implantation and allows complete retrieval. The multilayered device has a thin membrane configuration (∼1 mm), and the edge of the laminate and the gaps between Alg and PES offer a semiopen structure that could be more permeable to molecules compared with the closed pocket of conventional macroencapsulation. Islets are suspended in the alginate solution and then encapsulated in the hydrogel layer in the middle of the laminate after gelation. Encapsulating syngeneic or xenogeneic islets in the laminate device corrected chemically induced T1D in mice for over 90 days in both the intraperitoneal space and the epididymal fat pad. The multilayered membrane system may therefore provide a translatable solution in β cell-transplantation therapy in T1D.

CAS / MDL: 39346-81-1
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BIOORGANIC & MEDICINAL CHEMISTRY · 2024 · IF 3.3

Design of a novel long-acting dual GLP-1/GIP receptor agonist

Yuanzhen Dong,Jinhua Zhang,Hongjiang Xu,Hengqiao Shen,Qin Lu,Jun Feng,Zhengyan Cai

Tirzepatide , the first approved dual GLP-1/GIP receptor agonist (RA), has achieved better clinical outcomes than other GLP-1RAs. However, it is an imbalanced dual GIP/GLP-1 RA, and it remains unclear whether the degree of imbalance is optimal. Here, we present a novel long-acting dual GLP-1/GIP RA that exhibits better activity than tirzepatide toward GLP-1R. A candidate conjugate, D314, identified via peptide design, synthesis, conjugation, and experimentation, was evaluated using chronic studies in db/db and diet induced obese (DIO) mice. D314 achieved favorable blood glucose and body weight-lowering effects, equal to those of tirzepatide. Its half-life in dogs (T 1/2 : 78.3 ± 14.01 h) reveals its suitability for once-weekly administration in humans . This preclinical study suggests the potential role of D314 as an effective agent for treating T2DM and obesity.

CAS / MDL: 2592-95-2 15307-86-5
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JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY · 2010 ·Vol. 48 ·期 24 ·5679-5692 · IF 3.971

Luminescent mesogen jacketed poly(1-alkyne) bearing lateral terphenyl with hexyloxy tail

Hongxia Peng,Yiwang Chen,Lie Chen,Xiaohui He,Fan Li

Mesogen jacketed liquid crystalline poly(1-alkyne) and poly(1-phenyl-1-alkyne) linked pendants of terphenyl mesogens with hexyloxy tails at the waist position (  {RCC  [(CH 2 ) 3 OOC-terpheyl-(OC 6 H 13 ) 2 ]} n  , where RH, PHATP(OC6)2 ; RC 6 H 5 , PPATP(OC6)2 ) were synthesized. The influences of structural variations on the thermal, mesomorphic, and luminescent properties were investigated. Polymerizations of all monomers are carried out by WCl 6 -Ph 4 Sn catalysts successfully. The polymers are stable ( T d ≥ 340 °C) and soluble in common solvents. The monomers and polymers show enantiotropic SmA phases in the heating and cooling processes, and the lateral side chains of the mesogenic units are perpendicular to the main chain. The “jacket effect” of chromophoric terphenyl core “shell” around the main chain also contributes to polymers with high photoluminescence, and the pendant-to-backbone energy transfer path is involved in the luminescence process of this polymers. In comparison with monosubstituted polyacetylene PHATP(OC6)2 , the disubstituted polyacetylene PPATP(OC6)2 shows better photoluminescence in both THF solution and film, and exhibited about 40 nm red-shifted than PHATP(OC6)2 , indicating that the “jacket effect” of terphenyl mesogens forces poly(1-phenyl-1-alkyne) backbone to extend in a more planar conformation with a better conjugation. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010

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