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Adsorption Properties of CS/PAM/Fe(Ⅲ)Complex for Phosphate Removal from Water
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作者 CAO Tian LI Wei +7 位作者 REN Lin SONG Tao SONG Jie LIN Jiacheng YANG Li LIU Wenxiu WANG Ping FENG Shaojie 《Journal of Wuhan University of Technology(Materials Science)》 2025年第2期382-388,共7页
The adsorption of phosphate was conducted by the complex of chitosan/polyacrylamide/ferric(CS/PAM/Fe(Ⅲ))prepared.The SEM images and XPS spectra confirmed the successful adsorption of phosphate.The adsorption process ... The adsorption of phosphate was conducted by the complex of chitosan/polyacrylamide/ferric(CS/PAM/Fe(Ⅲ))prepared.The SEM images and XPS spectra confirmed the successful adsorption of phosphate.The adsorption process was studied by varying the influencing aspects like pH,co-existing ions,contact time,and initial phosphate concentration.The experimental results indicate that the adsorptive capacity decreases with the increase of pH.However,it is commendable that there is still a adsorption capacity of more than 5 mg/g when the pH is 8-11.The adsorption kinetics can be accurately described by the pseudo-second-order model and is controlled by both chemisorption and surface diffusion.The adsorption process is a single layer adsorption.This paper proposed that the adsorption mechanism of CS/PAM/Fe(Ⅲ)complex is the joint action of electrostatic attraction and ligand exchange. 展开更多
关键词 CS/PAM/fe(Ⅲ) complex PHOSPHATE ADSORPTION MECHANISM
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β-二亚胺Cr、Fe配合物的合成及结构研究
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作者 王斌 何逸飞 《化学研究与应用》 北大核心 2025年第9期2588-2595,共8页
过渡金属配合物因其独特的电子结构和化学性质,在催化、发光、材料等领域展现出独特的优势和广泛的应用潜力,本论文参考文献通过C-C偶联反应合成了一例大位阻的β-二亚胺配体PhC(PhCNDip)_(2)H 1,对其锂化后分别与CrCl_(2)和FeCl_(2)反... 过渡金属配合物因其独特的电子结构和化学性质,在催化、发光、材料等领域展现出独特的优势和广泛的应用潜力,本论文参考文献通过C-C偶联反应合成了一例大位阻的β-二亚胺配体PhC(PhCNDip)_(2)H 1,对其锂化后分别与CrCl_(2)和FeCl_(2)反应,得到β-二亚胺Cr和Fe的配合物PhC(PhCNDip)_(2)MCl(M=Cr,2;Fe,3)。再使用强还原剂KC_8对配合物3进行还原,得到配合物4。利用X-射线单晶衍射对配合物2~4的结构进行了表征。结果显示:配合物2为β-二亚胺CrCl的二聚体,配合物3为β-二亚胺FeCl单体,而配合物4的中心骨架为线形Fe-O-Fe构型。同时,利用理论计算进一步优化了配合物2和4,对其成键进行了详细分析。本项工作为开发新的过渡金属有机配合物提供了重要依据。 展开更多
关键词 β-二亚胺 过渡金属 线性构型 Cr、fe配合物
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钯基催化剂还原Fe(Ⅱ)EDTA-NO络合脱硝液
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作者 任晓聪 胡紫瑞 张光旭 《华中师范大学学报(自然科学版)》 北大核心 2025年第2期237-246,共10页
Fe(Ⅱ)EDTA络合脱硝法对一氧化氮(NO)具有良好的吸收效果,是脱硝技术重点研究方向,但Fe(Ⅱ)EDTA-NO络合液再生困难限制了它的发展.为达到Fe(II)EDTA络合液循环使用的目的,以阴离子交换树脂IRA900为载体,通过浸渍法负载钯前驱体,经硼氢... Fe(Ⅱ)EDTA络合脱硝法对一氧化氮(NO)具有良好的吸收效果,是脱硝技术重点研究方向,但Fe(Ⅱ)EDTA-NO络合液再生困难限制了它的发展.为达到Fe(II)EDTA络合液循环使用的目的,以阴离子交换树脂IRA900为载体,通过浸渍法负载钯前驱体,经硼氢化钠还原后制备出了Pd/IRA900催化剂.通过X射线衍射、X射线光电子能谱图、透射电子显微镜、热重分析等表征表明,Pd/IRA900催化剂中钯纳米微团的平均粒径为2.14nm,Pd0含量为84%(质量分数),对还原Fe(II)EDTA-NO有着良好的催化活性.搭建一套可持续运转的流化床试验装置,评价结果如下:在气相的条件为总流量200L·h^(-1)、NO含量为0.07%(体积分数)、含氧量10%,络合液再生条件为初始浓度0.05mol·L^(-1)、温度60℃、pH=5、液气比6的最佳工艺条件下,可以维持脱硝率90%以上稳定运行300min. 展开更多
关键词 fe(Ⅱ)EDTA-NO 脱硝 络合液 催化剂 阴离子交换树脂
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Heterogeneous Fenton degradation of azodyes catalyzed by modified polyacrylonitrile fiber Fe complexes: QSPR (quantitative structure peorperty relationship) study 被引量:4
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作者 Bing Li Yongchun Dong Zhizhong Ding 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2013年第7期1469-1476,共8页
The amidoximated polyacrylonitrile (PAN) fiber Fe complexeswere prepared and used as the heterogeneous Fenton catalysts for thedegradation of28 anionicwater soluble azodyes inwater under visible irradiation. The mul... The amidoximated polyacrylonitrile (PAN) fiber Fe complexeswere prepared and used as the heterogeneous Fenton catalysts for thedegradation of28 anionicwater soluble azodyes inwater under visible irradiation. The multiple linear regression (MLR) methodwas employed todevelop the quantitative structure property relationship (QSPR) model equations for thedecoloration and mineralization of azodyes. Moreover, the predictive ability of the QSPR model equationswas assessed using Leave-one-out (LOO) and cross-validation (CV) methods. Additionally, the effect of Fe content of catalyst and the sodium chloride inwater on QSPR model equationswere also investigated. The results indicated that the heterogeneous photo-Fentondegradation of the azodyeswithdifferent structureswas conducted in the presence of the amidoximated PAN fiber Fe complex. The QSPR model equations for thedyedecoloration and mineralizationwere successfullydeveloped using MLR technique. MW/S (molecularweightdivided by the number of sulphonate groups) and N N=N (the number of azo linkage) are considered as the most importantdetermining factor for thedyedegradation and mineralization, and there is a significant negative correlation between MW/S or N N=N anddegradation percentage or total organic carbon (TOC) removal. Moreover, LOO and CV analysis suggested that the obtained QSPR model equations have the better prediction ability. The variation in Fe content of catalyst and the addition of sodium chloridedid not alter the nature of the QSPR model equations. 展开更多
关键词 AZODYE heterogeneous fentondegradation quantitative structure property relationship polyacrylonitrile fiber fe complex
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Dual-functional Se/Fe complex facilitates TRAIL treatment against resistant tumor cells via modulating cellular endoplasmic reticulum stress 被引量:2
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作者 Yahui Yang Yifan Wang +1 位作者 Ligeng Xu Tianfeng Chen 《Chinese Chemical Letters》 SCIE CAS CSCD 2020年第7期1801-1806,共6页
Tumor cell resistance is one of the big hurdles limiting the therapeutic efficacy of tumor necrosis factorrelated apoptosis-inducing ligand(TRAIL)-based cancer treatment.Therefore,the development of a sa fe and effect... Tumor cell resistance is one of the big hurdles limiting the therapeutic efficacy of tumor necrosis factorrelated apoptosis-inducing ligand(TRAIL)-based cancer treatment.Therefore,the development of a sa fe and effective sensitizer agent is greatly desired for optimizing TRAIL therapy.Herein,we successfully developed a Se/Fe complex with low toxicity to highly effectively inhibit tumor cells proliferation and migration capabilities through down-regulating ER stress related selenoproteins.Furthermore,it could more efficiently damage tumor spheroids with good penetration capability.More importantly,it could synergize with TRAIL treatment to induce the robust generation of reactive oxygen species(ROS),downregulating ER stress related selenoproteins for triggering tumor cells apoptosis in extrinsic and intrinsic signaling pathways.Taken together,this study provides a potential chemo-drug and sensitizer agent to improve the therapeutic efficacy of TRAIL-based cancer treatment. 展开更多
关键词 Se/fe complex TRAIL ER stress ROS Cancer treatment
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Degradation of Azo Dyes by Photocatalysis of Fe(Ⅲ)-oxalate Complexes/H_2O_2 in Aqueous Non-ionic Surfactant Triton X-100 Solution 被引量:1
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作者 董永春 王秋芳 +2 位作者 刘春燕 潘巧斌 徐天标 《Journal of Donghua University(English Edition)》 EI CAS 2010年第4期535-543,共9页
Two azo dyes,C.I.Reactive Red 195(RR195)and C.I.Acid Black 234(AB234)were degraded by photocatalysis of Fe(Ⅲ)-oxalate complexes/H2O2 in aqueous non-ionic surfactant,Triton X-100(TX-100)solution.Some factors affecting... Two azo dyes,C.I.Reactive Red 195(RR195)and C.I.Acid Black 234(AB234)were degraded by photocatalysis of Fe(Ⅲ)-oxalate complexes/H2O2 in aqueous non-ionic surfactant,Triton X-100(TX-100)solution.Some factors affecting the dye degradation such as TX-100 concentration,irradiation intensity,and sodium chloride were investigated.The interaction and competition between dye and TX-100 during the degradation were also examined using spectrophotometry and maximum bubble pressure method,respectively.The results indicated that TX-100 showed a significant reduction effect on degradation of two azo dyes,but which was largely confined to TX-100 concentration below the Critical Micellar Concentration(CMC).And the reduction was considerably decreased above the CMC,especially in the case of AB234.Moreover,the reducing effect of TX-100 on dye degradation almost did not vary with irradiation intensity.And the impact of sodium chloride on dye degradation was limited by the addition of TX-100. 展开更多
关键词 azo dyes Triton X-100 DEGRADATION fe(Ⅲ)-oxalate complexes H2O2
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Species distribution of polymeric aluminium ferrum——timed complexation colorimetric analysis method of Al-Fe-Ferron 被引量:8
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作者 Hu, YY Tu, CQ Wu, HH 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2001年第4期418-421,共4页
The effects of the calorimetric buffer solutions were investigated while the two colorimetric reactions of AI-ferron complex and Fe-ferron complex occurred individually, and the effects of the testing wavelength and t... The effects of the calorimetric buffer solutions were investigated while the two colorimetric reactions of AI-ferron complex and Fe-ferron complex occurred individually, and the effects of the testing wavelength and the pH of the solutions were also investigated. A timed complexatian colorimetric analysis method of Al-Fe-ferron in view of the total concentration of {AI + Fe} was then established to determine the species distribution of polymeric Al-Fe. The testing wavelength was recommended at 362 net and the testing pH value was 5. With a comparison of the ratios of n(Al)/n(Fe), the standard adsorption curves of the polymeric Al-Fe solutions were derived from the experimental results. Furthermore, the solutions' composition were carious in both the molar n(Al)/n(Fe) ratios, i.e. 0/0, 5/5, 9/1 and 0/10, and the concentrations associated with the total ( Al + Fe which ranged from 10(-5) to 10(-4) mol/L.. 展开更多
关键词 polymeric aluminum-ferrum species distribution timed complexation colarimetric analysis method Al-fe-ferron
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Synthesis of novel 1:2 Fe-complexed dye containing polyamine groups 被引量:1
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作者 Lei Yun Zhou Bing Tao Tang Shu Fen Zhang Jin Zong Yang 《Chinese Chemical Letters》 SCIE CAS CSCD 2009年第11期1296-1298,共3页
A Fe-complexed dye containing crosslinkable polyamine groups was synthesized through diazotization and coupling reaction, chlorination, amination and metallization. The structure of the Fe-complexed crosslinking dye w... A Fe-complexed dye containing crosslinkable polyamine groups was synthesized through diazotization and coupling reaction, chlorination, amination and metallization. The structure of the Fe-complexed crosslinking dye was characterized by FT-IR and Atomic Absorption Spectroscopic techniques. The dyeing and light fastness properties of the Fe-complex on silk and wool were tested, and the results showed that the novel Fe-complex exhibited both high fixation and good light fastness. 展开更多
关键词 Crosslinking dye fe-complexed dye Polyamine groups Light fastness
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Photodegradation of bisphenol A in Fe(Ⅲ)-oxalate complexes solution
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作者 ZHAN Man-jun YANG Xi +1 位作者 XIAN Qi-ming KONG Ling-ren 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2006年第4期771-776,共6页
The aqueous photodegradation of bisphenol A (BPA) in the presence of Fe(Ⅲ)-oxalate complexes (Fe(Ⅲ)-Ox), which are common compositions of natural water, was investigated in this study. BPA underwent rapid in... The aqueous photodegradation of bisphenol A (BPA) in the presence of Fe(Ⅲ)-oxalate complexes (Fe(Ⅲ)-Ox), which are common compositions of natural water, was investigated in this study. BPA underwent rapid indirect photolysis in Fe(Ⅲ)-Ox solution under simulated solar irradiation, proceeding pseudo-first-order kinetics. The photolysis rate increased with decreasing pH or initial BPA level and increasing Fe(Ⅲ)/oxalate concentration ratio. Hydroxyl radicals (·OH), which were generated from the photochemical processes of Fe(Ⅲ)-Ox complexes and contributed to the photooxidation of BPA, were determined by molecular probe and electron spin resonance (ESR) methods with the steady-state concentration of 2.56 × 10^-14 mol/L. Superoxide anion radical (O2^·-) was considered as the precursor of. OH and qualitatively determined by adding nitro blue tetrazolium as well as ESR experiments. Based on the structural analysis of the intermediate photoproducts of BPA in Fe(Ⅲ)-Ox complexes solution, the possible degradation pathways of BPA were proposed, involving ·OH addition, alkyl scission and alky oxidation. The results indicate that the photochemical reactivity of Fe(Ⅲ) may affect the environmental fate of BPA in natural water significantly. 展开更多
关键词 bisphenol A fe(Ⅲ)-oxalate complexes PHOTOOXIDATION reactive oxygen species
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Syntheses, Structural Characterization of Fe and Ni Complexes with Polypyrazolyl Borate Ligand: Fe[HB(pz)_3]_2 and Ni[HB(pz)_3]_2
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作者 XINGYong-heng KatsuyukiAoki BAIFeng-ying 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2005年第4期396-400,共5页
Fe(Ⅱ) complex Fe[HB(pz)_3]_2(compound 1, pz=pyrazole) and Ni(Ⅱ) complex Ni[HB(pz)_3]_2(compound 2) have been obtained by the reaction of MCI_2(M=Fe and Ni) with NaHB(pz)_3 in MeOH. The two complexes(compounds 1 and ... Fe(Ⅱ) complex Fe[HB(pz)_3]_2(compound 1, pz=pyrazole) and Ni(Ⅱ) complex Ni[HB(pz)_3]_2(compound 2) have been obtained by the reaction of MCI_2(M=Fe and Ni) with NaHB(pz)_3 in MeOH. The two complexes(compounds 1 and 2) were characterized by IR, NMR, elemental analysis and X-ray diffraction. Compound 1 crystallizes in space group P2_1/c with a=1.224(3) nm, b=1.161(2) nm, c=1.648(3) nm, β=107.62(15)°, V=2.233(8) nm3, Z=2. Compound 2 crystallizes in space group P2_1/c with a=0.97926(18) nm, b= 1.7423(3) nm, c=1.3156(2) nm, β=97.055(16)°, V=2.2277(7) nm3, Z=4. The results of X-ray structural analyses show that both compounds 1 and 2 are monomeric neutral, possessing a similar coordination mode and a similar structure around the metal centers. The related spectral characterizations, steric effects and binding properties are discussed. 展开更多
关键词 Polypyrazolylborate fe and Ni complexes Crystal structure
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FERROMAGNETICALLY COUPLED BINUCLEAR Fe(Ⅲ) COMPLEXES THROUGH ISOPHTHALATO-BRIDGE
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作者 Yan Tuan LI Dai Zheng LUO +1 位作者 Zong Hui JIANG Geng Lin WANG(Department of Chemistry, Nankai University, Tianjin, 300O71.) 《Chinese Chemical Letters》 SCIE CAS CSCD 1994年第9期799-802,共4页
Four new binuclear Fe(Ⅲ) complexes containing the diboon of isophthallc acid as bridge have been synthesized, namely [Fe2(IPHTA)(L)4](ClO4)4[L denotes 2, 2'-bipyridyl (bpy); 1,10-phenanthroline (phen); 4, 4'-... Four new binuclear Fe(Ⅲ) complexes containing the diboon of isophthallc acid as bridge have been synthesized, namely [Fe2(IPHTA)(L)4](ClO4)4[L denotes 2, 2'-bipyridyl (bpy); 1,10-phenanthroline (phen); 4, 4'-dimethyl-2, 2'-bipyridyl (Me2bpy ) and 5-nitro-1, 10-phenanthroline (NO2-phen), respectively], where IPHTA represents the isophthalate dianion. The complex [Fe2(IPHTA)(phen)4](CIO4)4 was characterized with variable temperature magnetic susceptibility (4-300K). The exchange integral J was found to be 9. 96cm(-1), indicating that weakly ferromagnetic spin-exchange interaction operates between Fe(Ⅲ) and Fe(Ⅲ) ions. 展开更多
关键词 fe BINUCLEAR BRIDGE complexES COUPLED feRROMAGNETICALLY
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REACTION OF FERROCENOYL CHLORIDE WITH [Et_(?)NH] [μ-CO)(μ-RS)Fe_2(CO)_6]COMPLEXES SYNTHESIS AND STRUCTURE OF Fe_2(CO)_6COMPLEXES WITH BRIDGING FERROCENOYL LIGAND
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作者 Jin Ting LIU Xin SHENG Xia ZHONG Department of Chemistry, Shandong University, Jinan, 250100 《Chinese Chemical Letters》 SCIE CAS CSCD 1993年第11期1025-1028,共4页
Reaction of ferrocenoyl chloride with [Et;NH] [(μ-CO)(μ-RS) Fe;=(CO);] complexes gave bridging ferrocenoyl complexes(μ-FcCO)(μ-RS)Fe;(CO);(Fc=ferrocenyl, R=Et, i-Pr, n-Bu, t-Bu, Ph).The structures of all... Reaction of ferrocenoyl chloride with [Et;NH] [(μ-CO)(μ-RS) Fe;=(CO);] complexes gave bridging ferrocenoyl complexes(μ-FcCO)(μ-RS)Fe;(CO);(Fc=ferrocenyl, R=Et, i-Pr, n-Bu, t-Bu, Ph).The structures of all new complexes were characterised by;HNMR, IR and MS. 展开更多
关键词 fe complexES SYNTHESIS AND STRUCTURE OF fe2 RS)fe2 Et REACTION OF feRROCENOYL CHLORIDE WITH NH
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Preparation and Characterization of Ferromagnetic Calcium Alginate Complex Gel
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作者 萧聪明 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2009年第1期65-67,共3页
Fe3O4 suspension, derived from chemical coprecipitation and subsequent ultrasonic treatment, was embedded into calcium alginate to form complex gel. Both gel beads and injectable gel floc were obtained by slightly tai... Fe3O4 suspension, derived from chemical coprecipitation and subsequent ultrasonic treatment, was embedded into calcium alginate to form complex gel. Both gel beads and injectable gel floc were obtained by slightly tailoring the preparation condition. SEM analysis showed that the iron oxide was dispersed homogenously in nanometer. TGA profiles revealed that the content of Fe3O4 in beads was about 7.2%. 展开更多
关键词 calcium alginate fe3O4 complex GEL PREPARATION
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CRYSTAL STRUCTURE OF A 2D SHEET-LIKE μ-CYANIDO-OXAMIDATO BRIDGED Fe(III)-Cu(II) HETERNUCLEAR COMPLEX
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作者 Nei Fang Wu Zhong Ning CHEN Jun QIU and Wen Xia TANG (State Key Laboratory of Coordination Chemistry,Nanjing University, Manjing 210093)Jing Ling WANG and Fang Ming NIAO(Department of Chemistry, Tianjin Normal University, Tianjin 300074) 《Chinese Chemical Letters》 SCIE CAS CSCD 1994年第8期713-714,共2页
The synthesis is and crystal structure are reported for the sheet-like compourd [CU2(oxpn)Fe(CN )5(NO)]. there oxpn is the dianion of M, M'-bis(3-aminopropyl)oxamide. This compound crustallizes in the orthogonal s... The synthesis is and crystal structure are reported for the sheet-like compourd [CU2(oxpn)Fe(CN )5(NO)]. there oxpn is the dianion of M, M'-bis(3-aminopropyl)oxamide. This compound crustallizes in the orthogonal space group Puma. with a=11 .413(4), b=22.242(5), c=7.736(2) A, and Z=4.The structure was refined to conventionat discrepancy factors R=0.047 and Pw=0.054. The Cu(II ) and Fe(III)centers are bridged by oxpn and cyanide, the formal behaves as a his-terdentate tigand bound to cooper(II)ion to form (II) dimers. whereas the latter bridges Cu(II) and Fe(III) centers in both symmetric and asymetric end- to-end bis-monodentate fashions, spreading out along be plane to form a 20 network. The Structure is made up of CuFe unit with Cu(II) and Fe(III) ions locating in a distorted square-based pyramid and a compressed octahedron, respectively. 展开更多
关键词 III OXAMIDATO complex CRYSTAL CYANIDO HETERNUCLEAR II LIKE OF BRIDGED fe Cu
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Preparation and Characterization of Magnetic Fe3O4-PAMAM-antibody Complex and Its Application in the Removal of Tetracycline from Wastewater
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作者 OU Min-Rui ZHANG Zi-Hui +3 位作者 CHEN Zhi-Hong WEN Yu-Kai YANG Huang-Hao XU Xiao-Ping 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2019年第7期1136-1145,共10页
Antigens and antibodies can bind specifically, so antibiotic antibody shows potential biological and environmental applications on the removal of antibiotic. In the present study, novel antibody complex was synthesize... Antigens and antibodies can bind specifically, so antibiotic antibody shows potential biological and environmental applications on the removal of antibiotic. In the present study, novel antibody complex was synthesized from polyamide-amine dendrimer immobilized tetracycline(TC) antibody with the encapsulation of magnetic Fe3O4 nanoparticles. As-prepared magnetic Fe3O4-PAMAM-antibody complexes were characterized by different techniques such as Fourier transform infrared(FT-IR), X-ray diffraction(XRD), Nuclear magnetic resonance(NMR)and ultraviolet(UV) analysis spectra. The prepared antibody complexes exhibited high adsorption properties for TC from aqueous solutions. These results suggest that the antibody complex expects to be a potential candidate for the wastewater treatment. 展开更多
关键词 PAMAM MAGNETIC fe3O4 ANTIBODY complex TETRACYCLINE
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SYNTHESIS AND CHARACTERIZATION OF A NOVEL BONDING TRINUCLEAR(Mo/Fe/Mo) COMPLEX (MoCl_4)_2·dppf
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作者 Zhen Feng XI Rui Na YANG +1 位作者 Dou Man JIN Jin Chun WU 《Chinese Chemical Letters》 SCIE CAS CSCD 1992年第10期809-810,共2页
By the reaction of bidentate ligand 1,1'-bis(diphenylphosphino)-ferrocene (dppf) with MoCl_4(CH_3CN)_2, a novel bonding type complex (MoCl_4)2_· (dppf) was synthesized and characterized by elemental analyses,... By the reaction of bidentate ligand 1,1'-bis(diphenylphosphino)-ferrocene (dppf) with MoCl_4(CH_3CN)_2, a novel bonding type complex (MoCl_4)2_· (dppf) was synthesized and characterized by elemental analyses, ^(31)p-NMR, IR and electronic spectra, TG and ICP-AES. Structure of the title complex was proposed. 展开更多
关键词 fe SYNTHESIS AND CHARACTERIZATION OF A NOVEL BONDING TRINUCLEAR DPPF MoCl4 complex
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Fe^(3+)配位调控分光光度法快速检测3,4-二羟基苯乙醇
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作者 周隽涵 郑建仙 孙璐 《食品与机械》 北大核心 2025年第9期42-51,共10页
[目的]解决在4-羟基苯乙醇(HPET)催化体系中快速检测3,4-二羟基苯乙醇(DHPET)因传统紫外分光光度法光谱重叠干扰受限问题。[方法]针对现有方法特异性不足的问题,提出基于Fe^(3+)配位调控的分光光度快速检测法,通过Fe^(3+)与DHPET邻苯二... [目的]解决在4-羟基苯乙醇(HPET)催化体系中快速检测3,4-二羟基苯乙醇(DHPET)因传统紫外分光光度法光谱重叠干扰受限问题。[方法]针对现有方法特异性不足的问题,提出基于Fe^(3+)配位调控的分光光度快速检测法,通过Fe^(3+)与DHPET邻苯二酚基团的双齿螯合作用,诱导特征吸收光谱红移至760 nm,显著区别于单酚化合物的弱配位响应。[结果]优化条件后,方法线性范围为3~100 mmol/L(R^(2)=0.998),检出限为0.709 mmol/L,精密度(RSD)<2%,满足工业催化体系实时监测需求。[结论]双齿配位增强选择性的分子机制在酶催化体系中具有实用性,可为DHPET工业化生产提供低成本、快速的分析工具。 展开更多
关键词 紫外—可见分光光度法 fe^(3+)配位 3 4-二羟基苯乙醇 选择性检测 金属—多酚络合
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STUDIES ON SCHIFF BASE COMPLEXES——Ⅳ. SYNTHESIS AND CRYSTAL STRUCTURE OF Fe (SALDPT) SAL
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作者 汪信 William T.Pennington James C.Fanning 《无机化学学报》 SCIE CAS CSCD 北大核心 1989年第3期46-53,共8页
制备了Fe(saldpt)sal单晶并作了晶体结构分析。晶体数据:单斜,空间群P2_1/C(#14),a=12.486(5),b=18.502(8),c=10.870(5)A,β=104.23(3)°,V=2434(2)A^3,Z=4,D_c=1.
关键词 铁配合物 Schiff合成 晶体结构
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Investigation on Molecular and Crystal Structures of Metal Complexes with Aminopolycarboxylic Acids(Ⅰ)─Synthesis and Structure of Na_2[Fe~Ⅲ(ida)2]2·3H_2O
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作者 Jun WANG Wei Qun ZHANG +4 位作者 Xi Ming SONG Xiang Dong ZHANG (Department of Chemistry, Liaoning University,Shenyang 110036)Yan XING Yong Hua LIN Heng Qing JIA Lei ZHANG(Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130024) 《Chinese Chemical Letters》 SCIE CAS CSCD 1997年第8期741-744,共4页
The crystal structure of the title complex salt has been determined by single-crystal X-ray structure analysis. The crystal data are as follows; Monoclinic, P21/c, a=15.6480(10)A,b=16.7870(10)A, c=10.347(2)A, β=90.79... The crystal structure of the title complex salt has been determined by single-crystal X-ray structure analysis. The crystal data are as follows; Monoclinic, P21/c, a=15.6480(10)A,b=16.7870(10)A, c=10.347(2)A, β=90.790(10), V=2717.7(6)A3, Z=3, and R=0.0333 for 4789 unique reflections. The complex anion has a pseudo-octahedral structure distorted more than the CrⅢand CoⅢ analogs, in which cach iminodiacetato ligand (ida2-) is coordinated in a facial fashion with the two N atoms in a cis configuration, resulting in an unsyin-fac structure. 展开更多
关键词 Na Synthesis and Structure of Na2[fe Investigation on Molecular and Crystal Structures of Metal complexes with Aminopolycarboxylic Acids ida)2]2
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[ONSN]-型Fe(Ⅲ)配合物催化环氧化物和酸酐的开环共聚反应
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作者 周永博 徐东晓 +3 位作者 赵晓静 李志彬 白世涛 刘宁 《有机化学》 北大核心 2025年第8期2854-2866,共13页
该工作合成了4种[ONSN]-型Fe(Ⅲ)配合物,并应用于环氧化物与酸酐的开环共聚(ROCOP)反应中.以环氧环己烷(CHO)与邻苯二甲酸酐(PA)为模型底物,对反应条件进行优化,发现在100℃条件下Fe配合物Cat 1和4-二甲氨基吡啶(DMAP)组成的二元催化体... 该工作合成了4种[ONSN]-型Fe(Ⅲ)配合物,并应用于环氧化物与酸酐的开环共聚(ROCOP)反应中.以环氧环己烷(CHO)与邻苯二甲酸酐(PA)为模型底物,对反应条件进行优化,发现在100℃条件下Fe配合物Cat 1和4-二甲氨基吡啶(DMAP)组成的二元催化体系具有较高的催化活性,在最优条件下其转化频率(TOF)值为99 h^(-1),所制备的聚酯数均分子量(M_(n))高达13.1 kg/mol,分子量分布(PDI)也仅为1.19.该催化体系适用于各类环氧化物与酸酐ROCOP反应,高收率地制备了一系列聚酯,且都具有较为理想的数均分子量(M_(n))和分子量分布(PDI).此外,该催化体系还适用于蓖麻油基环氧化物单体(OYU)与PA的ROCOP反应,所得聚合物数均分子量(M_(n))为16.5 kg/mol. 展开更多
关键词 fe配合物 开环共聚 聚酯 生物基高分子
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