JOURNAL OF MATERIALS SCIENCE
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2018
·Vol. 53
·期 24
·16263-16275
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IF 2.993
Li Jiali,Kong Xianggui,Jiang Meihong,Lei Xiaodong
Up to now, although tremendous effort has been made in exploring Pd-based catalysts for the Suzuki–Miyaura coupling reactions, there is still much room to enhance its catalytic performance by synthesis catalyst with define-designed and tailored structure. Herein, a new kind of Pd-based structured catalyst with hierarchical hollow structure (Pd/Co(OH) 2 /Cu(OH) 2 /copper foam) has been successfully synthesized by three facile steps. As framework, the hierarchical hollow nanoarray structure of Co(OH) 2 /Cu(OH) 2 /copper foam is fabricated by immersion and electrolytic deposition methods. Uniformly dispersed Pd nanoparticles with a narrow size distribution (1.5 ± 0.2 nm) are anchored on the surface of the hierarchical nanotube array through an in situ spontaneous redox reaction between Co(OH) 2 and PdCl 4 2− without any surfactant at room temperature. Compared with other synthesis approaches, it just takes less than 1 h for the whole fabrication process in our strategy, exhibiting very high efficiency. In order to evaluate the catalytic performance of the as-prepared structured catalyst, 16 kinds of reagents were chosen as substrates for Suzuki–Miyaura coupling reaction, exhibiting excellent activity and reusability under mild conditions. We hope this simple and efficient method will open a new strategy to design and prepare structured catalysts.
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NEW JOURNAL OF CHEMISTRY
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2018
·Vol. 42
·期 12
·9702-9708
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IF 3.201
Hengchang Ma,Yucheng Ma,Lei Lei,Manyi Yang,Yanfang Qin,Ziqiang Lei,Lu Chang,Tao Wang,Yuan Yang,Xiaoqiang Yao
A set of multiple cation-doped linear polymers (abbreviated as OPY-1,2-BE, OPY-1,4-BB, OPY-1,8-BO, OPY-1,4-OBB) synthesized from a dipyridine derivative (OPY) and dibrominated compounds were employed as fluorescent probes for adenosine triphosphate (ATP) sensing. Among them, OPY-1,8-BO is particularly able to recognize ATP over its related compounds adenosine diphosphate (ADP), adenosine monophosphate (AMP), and other phosphate anions, with very desirable switch off–on performances. The interesting phenomenon of aggregate-induced emission (AIE) is proposed as the main reason for the ATP sensing, which is due to the ATP being more negative than the polymers and therefore there is more opportunity for connections with the multiple cation doped polymers through electrostatic attractions. Cell imaging measurements were carried out and demonstrated that even though these probes bear the same OPY core and only slightly different linkers, they are able to image different cell environments. The controlled cell imaging verified that the OPY-1,8-BO probe has ATP-specific recognition in living cells.
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
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2018
·
IF 3.141
Maiping Yang,Weiqu Liu,Chi Jiang,Chunhua Liu,Sha He,Yankun Xie,Zhengfang Wang
A facile and mild dip-coating method of fabricating superhydrophobic coating for cotton textiles was proposed. Cotton fabric was treated with TiO2 sol prepared under mild conditions and subsequently dip-coated by fluoropolymer (PHM). The PHM was synthesized by copolymerization of hexafluorobutyl methacrylate (HFBMA) and 3-methacryloxypropyltrimethoxysilane (MPS) to replace long-chain fluoroalkylsilanes, which are costly and potentially harmful. The coated textile displayed wonderful superhydrophobicity with a water contact angle of 153.5°. Additionally, the stability of the coated textile was tested by placement in acidic and alkali solutions, ultrasonic processing, and washing, during which it exhibited desirable durability. Furthermore, the surface showed an excellent biomimetic self-cleaning effect of removing both liquid pollutant and solid powder stains. Importantly, the prepared textile exhibited efficient oil–water separation for its superhydrophobicity and superoleophilicity. These advantages make it an ideal material for large-scale industrial applications under various conditions.
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JOURNAL OF SEPARATION SCIENCE
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2015
·Vol. 38
·期 16
·2880-2886
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IF 2.737
Xi Zhang,Xiaohuan Zang,Guijiang Zhang,Chun Wang,Zhi Wang
A mesoporous carbon was fabricated using MCM-41 as a template and sucrose as a carbon source. The carbon material was coated on stainless-steel wires by using the sol–gel technique. The prepared solid-phase microextraction fiber was used for the extraction of five volatile aromatic compounds (chlorobenzene, ethylbenzene, o -xylene, bromobenzene, and 4-chlorotoluene) from tea beverage samples (red tea and green tea) prior to gas chromatography with mass spectrometric detection. The main experimental parameters affecting the extraction of the volatile aromatic compounds by the fiber, including the extraction time, sample volume, extraction temperature, salt addition, and desorption conditions, were investigated. The linearity was observed in the range from 0.1 to 10.0 μg/L with the correlation coefficients ( r ) ranging from 0.9923 to 0.9982 and the limits of detection were less than 10.0 ng/L. The recoveries of the volatile aromatic compounds by the method from tea beverage samples at spiking levels of 1.0 and 10.0 μg/L ranged from 73.1 to 99.1%.
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PubMed
高影响因子
JOURNAL OF STRUCTURAL CHEMISTRY
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2015
·Vol. 56
·期 3
·458-462
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IF 0.508
Huang Q. -W.,Liu S. -G.,Li G. -B.,Wang S. -X.,Su W. -Y.,Liang D. -M.,Mao S. -Q.
A new complex Cu(bpbp)Cl 2 ·DMF·H 2 O is synthesized by treatment of CuCl 2 with 2,6-bis(1-phenylbenzimidazol-2-yl)pyidine in DMF. Its structure is characterized by elemental, IR, UV, and single crystal X-ray structure analyses. For the complex: crystal system, triclinic, space group \(P\bar 1\) , a = 1.0537(1) nm, b = 1.1735(1) nm, c = 1.3749(2) nm, α = 112.275(2)°, β = 91.531(2)°, γ = 97.700(2)°, V = 1.553(4) nm 3 , Z = 2. In a distorted trigonal bipyramidal geometry the Cu(II) ion is coordinated by three nitrogen atoms from 2,6-bis(1-phenylbenzimidazol-2-yl)pyridine and two chloride ions. The antiproliferative activities of the complex are screened by MTT assay against HepG2, Huh7, Eca109, and Eca9706 cancer cells. The complex exhibits specific inhibition on Eca9706 cancer cells with the IC 50 value of 28 μM after 48 h treatment. CCDC: 968927.
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CHINESE JOURNAL OF CATALYSIS
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2016
·
IF 2.628
Zhifeng Dai,Fang Chen,Qi Sun,Yanyan Ji,Liang Wang,Xiangju Meng,Feng-Shou Xiao
An efficient catalyst system based on a Pd-metalated porous organic polymer bearing phenanthroline ligands was designed and synthesized. This catalyst was applied to various C–C bond-forming reactions, including the Suzuki, Heck and Sonogashira couplings, and afforded the corresponding products while exhibiting excellent activities and selectivities. More importantly, this catalyst can be readily recycled. These features show that such catalysts have significant potential applications in the future.
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RSC Advances
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2014
·Vol. 4
·期 58
·30914-30922
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IF 3.708
Mingxi Chen,Zhe Zhang,Lingzhi Li,Yu Liu,Wei Wang,Jianping Gao
Ultrafine Ag–Pd bimetallic nanoparticles homogeneously distributed on reduced graphene oxide (rGO) were prepared by redox reactions between Pd2+, Ag+ and GO. This method is simple, and the use of rGO as a support facilitated the separation and reuse of the Ag–Pd@rGO catalyst. The Ag–Pd@rGO bimetallic nanoparticles were characterized by ultraviolet-visible spectroscopy, Raman spectroscopy, thermogravimetric analysis, X-ray diffraction analysis, and X-ray photoelectron spectroscopy. The microstructure of the Ag–Pd@rGO was investigated with scanning electron microscopy and transmission electron microscopy. The Ag–Pd@rGO catalyst exhibited high catalytic activities in the Suzuki-Miyaura carbon coupling reaction and the Sonogashira carbon coupling (SCC) reaction. These reactions used mild, efficient, ligand-free and heterogeneous conditions. Interestingly, the presence or absence of oxygen in the SCC catalytic system resulted in two different products, in which oxygen can be used as “switch” to control different products.
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RSC Advances
·
2014
·Vol. 4
·期 51
·26804-26809
·
IF 3.708
Liang Ren,Fan Yang,Yongfeng Li,Ting Liu,Liqiang Zhang,Guoqing Ning,Zhichang Liu,Jinsen Gao,Chunming Xu
We report an environmentally-friendly approach to the synthesis of hybrids based on porous graphene and metal nanoparticles. The nitrogen-doped porous graphene (N-PG) and Pd nanoparticles decorated N-PG (Pd/N-PG) was synthesized by a plasma method. The N-PG was characterized by X-ray photoelectron spectroscopy and Raman spectroscopy, and the results clearly indicate that the amount of nitrogen doping was 6.65 wt%. The synthesized Pd/N-PG hybrid materials were confirmed by transmission electron microscopy, X-ray diffraction and energy-dispersive X-ray spectroscopy mapping. The hybrid material based on Pd/N-PG as a new catalyst was applied in Suzuki reaction. This catalyst offers a number of advantages such as high stability, easy removal from the reaction mixture and reusability with minimal loss of activity, showing better performance than the well-known commercial Pd/C catalyst.
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APPLIED CATALYSIS B-ENVIRONMENTAL
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2016
·
IF 8.328
Jiawei Xia,Yongsheng Fu,Guangyu He,Xiaoqiang Sun,Xin Wang
A magnetically separable core-shell-like catalyst Ni-Pd/CB is designed and synthesized via a facile sequential reduction strategy. It is found that the Pd nanocrystals with a thickness of ∼1.67 nm and a length of ∼7.92 nm are intimately coupled with the Ni cores and the formed core-shell-like Ni-Pd nanoparticles are well dispersed on the CB surface with much smaller particle size and narrower size distribution as compared with that of unsupported ones. The ligand-free Ni-Pd/CB nanocatalyst is evaluated for Suzuki-Miyaura coupling reaction and exhibits excellent catalytic activity under mild aerobic conditions without using toxic solvents and inert protective atmosphere, achieving green catalysis. The high catalytic performance of Ni-Pd/CB catalyst can be attributed to its unique core-shell-like nanostructure and the concerted effects between the individual components. The introduction of Ni not only makes the catalyst magnetically separable in a suspension system, but also significantly lowers the cost.
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MACROMOLECULES
·
2017
·
IF 5.835
Wen-Ming Wan,Shun-Shun Li,Dong-Ming Liu,Xin-Hu Lv,Xiao-Li Sun
Electron-deficient borinic acid monomers and corresponding polymers were synthesized with different substituents via a one-pot reaction of Grignard reagents with trimethoxyborane and reversible addition–fragmentation chain transfer polymerization, respectively. Further investigations of substituent effects of borinic acid polymers (PBAs) were carried out, indicating that the thermoresponsive properties of PBAs benefit from the increase of steric hindrance of PBA substituent, while the binding affinity of PBAs with Alizarin Red S, 8-hydroxyquinoline (HQ), and fluoride ion decreases with the increase of steric hindrance of substituent. Attributed to the strong dative N → B bond and the strongly luminescent boron quinolate, the application of phenyl PBA for fluorescence detection of HQ is realized with high sensitivity at the ppm level. These results therefore confirm that borinic acid-containing polymer is a new type of stimuli-responsive polymer in the field of thermoresponsiveness over a wide temperature range and chemical sensor for diol and electron-rich compounds.
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ACS Applied Materials & Interfaces
·
2017
·
IF 7.504
Qinrui Fu,Yuan Meng,Zilin Fang,Quanqin Hu,Liang Xu,Wenhua Gao,Xiaochun Huang,Qiao Xue,Ya-Ping Sun,Fushen Lu
Boron nitride nanosheets (BNNS) were used to anchor bimetallic Pd–Fe nanoparticles for Suzuki–Miyaura coupling catalysts. The bimetallic nanoparticles were found to be core–shell in structure, and their formation was likely facilitated by their interactions with the BNNS. The Pd–Fe/BNNS catalysts were highly effective in representative Suzuki–Miyaura reactions, with performances matching or exceeding those of the state-of-the-art methods. Specifically, the superior catalytic activities were characterized by generally shortened reaction times, minimal Pd usage, excellent reusability of the catalysts and high or nearly quantitative conversion yields in a benign solvent system without the need for any special conditions, such as ligands and surfactants or inert gas protection. The obvious advantages of the Pd–Fe/BNNS over similar catalysts based on other supports, such as reduced graphene oxide (rGO), suggest that BNNS may be developed into a versatile platform for many other important catalytic reactions.
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JOURNAL OF POWER SOURCES
·
2024
·
IF 8.1
Tingting Wu,Yue Liu,Jing Ye,Yi Chen,Gaole Dai,Xiaohong Zhang,Yu Zhao
Phenothiazine derivatives, as sustainable cathode materials for batteries , show significant promise for large-scale electrical energy storage applications. However, the irreversibility of the sulfur redox active center severely limits their energy density and discharge voltage in rechargeable organic batteries . This study concentrates on identifying the potential side reactions that contribute to the irreversibility of phenothiazine-based materials. We propose a molecular design strategy that synergistically blocks the active site and extends the conjugation, markedly improving the electrochemical reversibility of these materials. Our findings reveal that phenothiazine derivatives can undergo two successive, one-electron redox reactions without interference from chemical bond rearrangement and reactive radicals. The assembled cells, utilizing lithium (Li) and sodium (Na) as anodes, display two distinct discharge plateaus at 3.3/3.9 V vs. Li + /Li and 3.1/3.7 V vs. Na + /Na, respectively, with nearly identical contributions from the nitrogen (N) and sulfur (S) redox centers. The phenothiazine derivatives designed via this strategy rank among the few phenothiazine-based organic electrode materials capable of achieving highly reversible, two-electron transfer redox reactions in organic batteries.
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