ZEITSCHRIFT FUR KRISTALLOGRAPHIE-NEW CRYSTAL STRUCTURES
·
2022
·Vol. 238
·期 1
·13-14
·
IF 0.365
Zhihong Zhu,Lilei Zhang
C 14 H 12 BrClN 2 O, monoclinic, P 2 1 / c (no. 14), a = 13.4072(6) Å, b = 8.6103(5) Å, c = 12.3824(6) Å, β = 100.475(4), V = 1405.60(12) Å 3 , Z = 4, R gt
( F ) = 0.0499, wR ref
( F
2 ) = 0.1215, T = 173 K.
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高影响因子
PEST MANAGEMENT SCIENCE
·
2020
·Vol. 76
·期 9
·2978-2985
·
IF 3.75
Xianfei Zhang,Jiuyong Xu,Solange Muhayimana,Hui Xiong,Xuefeng Liu,Qingchun Huang
BACKGROUND Sclerotinia stem rot (SSR) caused by Sclerotinia sclerotiorum threatens oilseed rape cultivation, and the emergence of fungicide-resistant strains has led to control failures worldwide. Identifying novel chemical alternatives with different modes of action and high antifungal activities is thus crucial. Herein we evaluated the antifungal effects of 3-(2-pyridyl)methyl-2-(4-chlorphenyl)imino- thiazolidine (PMAS) on S. sclerotiorum to determine its efficacy for SSR management. RESULTS PMAS had an inhibitory effect on mycelial growth; the EC 50 values were 17.83 and 21.15 μg mL −1 for the carbendazim-susceptible strain Ss01 and carbendazim-resistant strain Hm25, respectively. PMAS treatment changed the color of inhibited mycelia to green, and the hyphae were sustained in the undifferentiated stage. Cysteine supplementation made this green color disappear, whereas methionine enhanced the color. Moreover, PMAS treatment markedly inhibited oxalic acid biogenesis, increased free thiol content in mycelia, and weakened the activities of oxaloacetase and malate dehydrogenase, but had little effect on the activity of glyoxylate dehydrogenase. Cysteine could reverse the inhibitory effects of PMAS on mycelial morphogenesis and biochemical constituents, except thiol production. In the pot-culture experiment, PMAS showed a good protective effect, with the control efficacy being >91% on SSR. CONCLUSION PMAS appears to be an effective fungicide for SSR management. © 2020 Society of Chemical Industry
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PubMed
高影响因子
SYNTHESIS-STUTTGART
·
2020
·Vol. 53
·期 07
·1341-1348
·
IF 2.675
Xinxin Zhao,Lin Guo,Chao Yang,Wujiong Xia
A highly regioselective [3+2] cyclization of alkenes with 2-iodoanilines under the irradiation of UV light is described. This general, metal-free strategy facilitates the direct preparation of 2-mono-/disubstituted indolines as well as spiroindolines through alkene carboamination in one step. Mechanistic studies suggested that the photochemical protocol proceeded via a radical pathway.
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TETRAHEDRON
·
2026
·
IF 2.1
Jiahui Ma,Yiming Ma,Huida Qian,Yu Wang,Zhongxue Fang
A silver-catalyzed [3 + 2] cycloaddition of imines with isocyanoacetates was developed. This reaction represents a novel protocol for the efficient and practical synthesis of polysubstituted imidazolines bearing a broad range of substituents with good to excellent yields under mild conditions. The practicality of this cycloaddition was shown by a gram-scale synthesis.
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高影响因子
CHINESE SCIENCE BULLETIN
·
2013
·Vol. 59
·期 2
·147-153
·
IF 1.319
Wang Wei,Yan Xiao Li,Zhan Lei,Leng Fei,Yang Xiao Xi,Huang Cheng Zhi
A new type of highly selective aptamer-labeled fluorescent silica nanoparticles [Apt-tris(2,2′-bipyridyl)ruthenium(II)@SiO 2 NPs] were prepared through the reverse microemulsion method by using prolonged fluorescence lifetime ruthenium complexes of tris(2,2′-bipyridyl)ruthenium(II) (Ru(bpy)
2+ 3
) as the source of the fluorescence for cellular prion protein imaging. Investigations showed that the newly prepared Ru(bpy)
2+ 3
@SiO 2 NPs possessed superior advantages of strong fluorescence, low toxicity, and easy surface modification for bioconjugation. Cell imaging experiments indicated that Apt-Ru(bpy)
2+ 3
@SiO 2 NPs had great tendency to human bone marrow neuroblastoma cells (SK-N-SH cells), since they can express large amount of prion protein on the surface of the cell, while in HeLa cells this phenomenon disappeared for the reason that HeLa cells cannot express prion proteins.
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高影响因子
JOURNAL OF ORGANIC CHEMISTRY
·
2019
·
IF 4.745
Erbao Zhao,Feilong Zhou,Yujun Zhao
Syntheses of isoxazolidines through the carbonyl imine intermediates are currently limited to monosubstituted olefin substrates. Herein, we reported syntheses of novel bicyclic isoxazolidine-containing compounds through 1,3-dipolar cycloaddition reactions using cyclic allylic alcohols as substrates, which proved challenging in previous reports. Generally, the reaction yields range from good to high, and the reaction substrates tolerate various functional groups, including the cyclopropyl and amine groups. Mechanistic studies suggest that an allylic cation and a carbonyl imine intermediate are involved and responsible for the observed stereochemistry and diastereoselectivity.
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PubMed
高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2025
·
IF 8.3
Hengyi Wang,Yong-Fei Li,Xueli Niu,Peiyun Dai,Mingyu Dou,Guang Yang,Fatao Gong,Hongjie Zhu,Hua Yang,Jianmin Dou
Due to the consumption of traditional fossil fuels, human society faces global energy shortages and increasing environmental pollution problems. To address water pollution caused by the abuse of antibiotics and to promote green hydrogen production. In this paper, a Bi 2 WO 6 /CdS S-scheme heterojunction was prepared to realize the photocatalytic levofloxacin (LEV) degradation coupled with hydrogen production reaction. Under the introduction of [Co(bpy) 3 Cl 2 ] (CoBpy) as a molecular photosensitizer, the hydrogen production activity of Bi 2 WO 6 /CdS increased remarkably to 5395.9 μmol g −1 h −1 , meanwhile, the degradation rate of LEV could reach 87.5 %, which was much higher than that of the pure phase material and exhibited excellent stability over five cycles. The enhanced photocatalytic activity originates from the S-scheme heterojunction mechanism that enables the oxidizing and reducing abilities of the material to be fully exploited, meanwhile the sensitization of CoBpy further optimizes the charge transfer pathway, which realizes the combination of visible-light-driven wastewater treatment and green hydrogen production. Our findings provide an efficient and safe approach to environmental remediation and green energy production for a sustainable energy future.
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高影响因子
JOURNAL OF MEMBRANE SCIENCE
·
2025
·
IF 9
Qianqian Zhao,Haiqi Jia,Wenxiong Shi,Shaolu Li,Xiaohui Yi,Siqi Yin,Genghao Gong,Yunxia Hu
Aromatic polyamide (PA) reverse osmosis (RO) membrane has gained widespread usage in desalination and water production. Nevertheless, their surfaces are prone to fouling during practical applications stemming from their inherent physicochemical properties. Therefore, conducting research on enhancing the antifouling properties of PA membranes through surface modification is of significant importance. In this work, high-flux and superior antifouling RO membranes were fabricated via surface grafting and self-crossing of [3-(2-aminoethyl) aminopropyl] triethoxysilane (AEAPTES) on the pristine PA membrane surface. Benefiting from solvent activation by n-hexane/n-decane and the strong hydrophilicity of AEAPTES, the modified membranes showed a significant enhancement in water permeance by approximately 73 % (reaching up to 4.10 LMH/bar) compared to unmodified PA membrane, while maintaining NaCl rejection above 98.67 %. Additionally, the modified membrane exhibited outstanding stability. Dynamic fouling experiments with charged model foulants of varying molecular sizes, supported by molecular dynamics simulation analysis, demonstrated that the surface charge plays a crucial role in resisting small-molecule foulants, while hydrophilicity is more effective against macromolecule foulants. Although AEAPTES incorporation did not improve the antifouling performance to negatively charged sodium dodecyl sulfate (SDS), it significantly improved resistance to positively charged dodecyl trimethyl ammonium bromide (DTAB) and charged protein model foulants, including lysozyme (LYZ) and bovine serum albumin (BSA). These improvements are attributed to the creation of a thick hydration layer, as well as the electrostatic interactions and steric hindrance effects provided by the AEAPTES modified layer. This research offers new perspectives on the antifouling mechanisms of PA membranes modified by organoalkoxysilane molecules.
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SYNLETT
·
2018
·Vol. 29
·期 09
·1244-1248
·
IF 2.369
Xiangwen Kong,Lihua Liu,Siqin Luo,Shilu Fan,Haisheng Qian,Hua Xiao
A triphenylphosphine-promoted [3+2] cycloaddition of α,γ-bis-substituted allenoates and N-tosylaldimines followed by alkene isomerization was disclosed, affording a series of functionalized 2-pyrroline derivatives in moderate chemical yields with random diastereoselectivities.
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高影响因子
JOURNAL OF MATERIALS SCIENCE
·
2022
·Vol. 57
·期 45
·21009-21019
·
IF 4.682
Lin Lingyin,Zhou Yanfang,Chen Piaoyi,Xiao Qinglin,Ye Guodong
Transcatheter arterial embolization is an established treatment for hepatocellular carcinoma (HCC). However, the existing embolic materials still have some shortcomings, e.g., particle clumping can cause catheter occlusion. In this study, after the synthesis of monomer glyceryl triallyl ether monomer (GE), amorphous embolic agent (PGE) was synthesized by photopolymerization in the presence of GE and photoinitiator. Combined with RT-IR, TG and GPC, we verified that the polymerization followed a photo-driven radical-mediated [3 + 2] cyclopolymerization mechanism (PRMC) through experimental and modeled NMR. The macromolecular properties such as polymerization profile and morphology were studied by TG and SEM–EDS. Finally, the degradation, swelling and migration behavior of PGE were characterized, which indicated that PGE could embolize HCC by blocking the blood supply. In this study, PRMC prevented GE polymerization from degradative chain transfer with 70% yield in an hour, and 200–350 µm PGE was synthesized using this mechanism suitable for clinical use. Graphical abstract
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高影响因子
NEW JOURNAL OF CHEMISTRY
·
2023
·Vol. 47
·期 26
·12296-12303
·
IF 3.3
Wen-Hui Zhang,Zi-Yue Chen,Ren-Ming Liu,Xiong-Wei Liu,Bo-Wen Pan,Jian Zhou,Ying Zhou,You-Ping Tian,Xiong-Li Liu
Herein, previously unreported trimethylindolenines serving as useful C–N synthons in [3+2] cycloaddition reactions of donor–acceptor 3-isothiocyanato oxindoles to build a library of spiro[oxindole-thioxoimidazolidine-indoline] hybrids are described. A wide range of intriguing and complex products bearing three pharmacophores and three adjacent quaternary stereocentres were smoothly afforded in up to 92% yield, >20 : 1 dr, under catalyst-free conditions. Moreover, this strategy further expands the skeletal diversity of polyheterocycles, which will aid the search for new bioactive molecules.
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高影响因子
SYNTHETIC COMMUNICATIONS
·
2019
·
IF 1.439
Shuang Chen,Jing Yue,Xiong-Li Liu,Jun-Xin Wang,Xiong Zuo,Yu Cao
A new method was developed for the facile one-pot multicomponent construction of heterocycle-fused spiro compounds containing chromanone and pyrrolidinyl spirooxindoles, two potential pharmacophores, in one molecule through a decarboxylative 1,3-dipolar [3 + 2] cycloaddition reaction of carboxylic acid group-activated chromones 1 with isatin-derivated azomethine ylides based on molecular hybridization strategy. A wide variety of products with three contiguous stereocenters including a spiro quaternary stereocenter were smoothly prepared with high efficiency (up to 87% yield and 20:1 diastereomeric ratio). This method could offer libraries of architecturally diverse and multiple pharmacore collections, potentially useful in medicinal chemistry.
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