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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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The profound review of Fenton process:What’s the next step? 被引量:5
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作者 Yimin Lin Junlian Qiao +1 位作者 Yuankui Sun Hongyu Dong 《Journal of Environmental Sciences》 2025年第1期114-130,共17页
Fenton and Fenton-like processes,which could produce highly reactive species to degrade organic contaminants,have been widely used in the field of wastewater treatment.Therein,the chemistry of Fenton process including... Fenton and Fenton-like processes,which could produce highly reactive species to degrade organic contaminants,have been widely used in the field of wastewater treatment.Therein,the chemistry of Fenton process including the nature of active oxidants,the complicated reactions involved,and the behind reason for its strongly pH-dependent performance,is the basis for the application of Fenton and Fenton-like processes in wastewater treatment.Nevertheless,the conflicting views still exist about the mechanism of the Fenton process.For instance,reaching a unanimous consensus on the nature of active oxidants(hydroxyl radical or tetravalent iron)in this process remains challenging.This review comprehensively examined the mechanism of the Fenton process including the debate on the nature of active oxidants,reactions involved in the Fenton process,and the behind reason for the pH-dependent degradation of contaminants in the Fenton process.Then,we summarized several strategies that promote the Fe(Ⅱ)/Fe(Ⅲ)cycle,reduce the competitive consumption of active oxidants by side reactions,and replace the Fenton reagent,thus improving the performance of the Fenton process.Furthermore,advances for the future were proposed including the demand for the high-accuracy identification of active oxidants and taking advantages of the characteristic of target contaminants during the degradation of contaminants by the Fenton process. 展开更多
关键词 Advanced oxidation process feNTON Hydroxyl radical fe(iv) Wastewater treatment
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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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[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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Spectrophotometric Investigation of Complex Formation of Ge(IV) with Bis(2,3,4-Trigidroksifenilazo) Benzidine in the Presence of Cationic Surfactants Active Substances
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作者 Mardanova Samira Rafiq Alieva Rafiqa Alirza +1 位作者 Bahmanova Fidan Nariman Chyragov Famil Musa 《Journal of Chemistry and Chemical Engineering》 2014年第1期21-24,共4页
It is investigated the interaction of Ge(IV) with bis(2,3,4-trigodroksifenolazo) benzidine (R) in the presence of KSAS (cationic surface active substances)-CPCl (cetylpyridinium chloride), CPBr (cetylpyridi... It is investigated the interaction of Ge(IV) with bis(2,3,4-trigodroksifenolazo) benzidine (R) in the presence of KSAS (cationic surface active substances)-CPCl (cetylpyridinium chloride), CPBr (cetylpyridinium bromide) and CTMABr (cetyltrimethylammonium bromide). It is studied the effect pH, time on the formation of ternary complexes. It is determinated of molar absorption coefficients and stability constants of germanium. Binary (Ge-R) and triple (Ge-R-CPCI, Ge-R-CPBr, Ge-R-CTMaBr) complex form at pH 4 and pH 1, respectively. The composition proportion of binar system is 1:2 and the composition proportion triple complex is 1:1:2. The concentration interval of germanium which obeying beer low in the Ge-R 0.12-2.92 mkq/mL, in the Ge-R-CPCI is 0.04-1.46 mkq/mL, in the Ge-R-CPBr is 0.00-1.00 mkq/mL and in the Ge-R-CTMaBr is 0.00-1.00 mkq/mL. Molar absorbtivities of complexes are 45,000, 57,000, 59,000 and 60,000, respectively. The effect of interfering ions and masking agents has been learned. Stability constants of complexes have been determined: lgKl = 7.21 + 0.06 (Ge-R),' lgK1 = 12.08 _+ 0.05 (Ge-R-CPCI), lgK1 = 12.12 + 0.07 (Ge-R-CPBr) and lgK1 = 12.85 + 0.06 (Ge-R-CTMaBr). It is developed highly selective method of photometric determination of trace amounts of Ge(IV) in petroleum coke. 展开更多
关键词 Ge(iv temary complexes Ge(iv photometric determination of Ge(iv).
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Pb(Ⅱ)配合物的晶体结构及其对Al^(3+)、Fe^(3+)的荧光检测性质
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作者 宋合兴 江旭滢 +3 位作者 任娜娜 丁要蝶 王雅茹 孙赞 《化学研究与应用》 北大核心 2025年第7期1887-1894,共8页
在水热条件下,以硝酸铅为金属源,1-萘甲酸(Hna)、4,4′-二甲基-2,2′-联吡啶(Dmbpy)为配体合成了一例双核铅配合物[Pb_(2)(na)_(4)(Hna)_(2)(Dmbpy)_(2)],并通过元素分析(EA)、X-射线单晶衍射(SXRD)、X-射线粉末衍射(PXRD)、红外光谱(IR... 在水热条件下,以硝酸铅为金属源,1-萘甲酸(Hna)、4,4′-二甲基-2,2′-联吡啶(Dmbpy)为配体合成了一例双核铅配合物[Pb_(2)(na)_(4)(Hna)_(2)(Dmbpy)_(2)],并通过元素分析(EA)、X-射线单晶衍射(SXRD)、X-射线粉末衍射(PXRD)、红外光谱(IR)和热重分析(TGA)进行表征。单晶X-射线衍射结果表明:该配合物属三斜晶系P1空间群,中心金属Pb(Ⅱ)位于七配位的畸形五角双锥构型中,结构单元通过分子间C—H…O氢键、π…π堆积作用以及C—H…π作用形成二维超分子结构。固态荧光测试发现该配合物在334 nm的激发波长下,最大发射波长为380 nm。金属离子荧光传感与抗干扰实验表明,该配合物不仅具备良好的抗干扰能力,Al^(3+)能增强该配合物的荧光且增强常数为6.34×10^(4) M^(-1),检出限为0.09μM;Fe^(3+)能淬灭该配合物的荧光且淬灭常数为2.42×10^(4) M^(-1),检出限为0.24μM,同时探讨了该配合物的荧光增强/淬灭机理。 展开更多
关键词 铅配合物 晶体结构 固态发射 荧光识别 Al^(3+) fe^(3+)
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Dissolved Organic Matter-Complexed Iron in Two Rivers with Different Types of Soils in Watershed Area
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作者 Kunio Moroi Nobuyoshi Isamoto Akira Watanabe 《International Journal of Geosciences》 2012年第4期710-718,共9页
Concentrations of dissolved organic matter (DOM), dissolved humic substances (DHS), and DOM-complexed Fe (DOM-Fe) in Yamakuni and Oita Rivers, Japan, of which headstream is near in location, flow pass length is simila... Concentrations of dissolved organic matter (DOM), dissolved humic substances (DHS), and DOM-complexed Fe (DOM-Fe) in Yamakuni and Oita Rivers, Japan, of which headstream is near in location, flow pass length is similar, but watershed soil type differs, were investigated. Soil organic matter level was higher in black Andosols distributing 67% of the watershed area of the Oita River than in Cambisols covering 90% of the watershed area of Yamakuni River. However, the DOM concentration in the Yamakuni River (0.44 - 1.62 mg·C·L-1) tended to be higher than that in the Oita River (0.13 - 1.37 mg·C·L-1). DHS accounted for 49% - 80% of DOM in both rivers. Fe and DOM-Fe concentrations showed a trend to increase toward downstream but decrease at the estuary in both rivers. DOM-Fe accounted for 26% - 90% and 55% - 93% of dissolved Fe in the Yamakuni and Oita Rivers, respectively. Correlation analysis suggested that the DOM-Fe concentration in the river water was controlled by the capacity for supplying Fe ions rather than that for supplying DOM. Although the ability to form a complex with Fe was suggested to be greater in the DOM in the Oita River than that in the Yamakuni River, the DOM-Fe concentration at the estuary was similar in the two rivers. Thus, the effect of soil organic matter level in the watershed area on the supply of Fe or DOM-Fe to the estuarine ecosystem was not significant. 展开更多
关键词 Dissolved Organic Matter (DOM) Dissolved HUMIC Substances (DHS) DOM-complexed fe (DOM-fe) WATERSHED Area
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单宁酸-Fe(Ⅲ)络合物作涂层的pH响应智能控释体系的构建
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作者 张凤芬 陈华丹 +1 位作者 谢春玲 李昭汪 《广州化工》 2025年第10期89-93,共5页
为优化药物控释体系性能,抑制药物的初期快速释放并实现环境响应性释放,本研究采用滴涂法在二氧化钛纳米管阵列/介孔二氧化硅复合材料表面构建单宁酸-Fe3+配合物涂层,制备p H智能控制药物释放体系。实验结果显示,该涂层可有效抑制药物... 为优化药物控释体系性能,抑制药物的初期快速释放并实现环境响应性释放,本研究采用滴涂法在二氧化钛纳米管阵列/介孔二氧化硅复合材料表面构建单宁酸-Fe3+配合物涂层,制备p H智能控制药物释放体系。实验结果显示,该涂层可有效抑制药物初期高剂量释放(24 h累计释放量降低至25.8%),且体系能根据不同p H环境响应:在正常骨骼组织中性生理环境(p H=7.4)下保持稳定以抑制药物释放,在炎症酸性微环境中触发药物释放,实现药物载量提升与释放行为精准调控的协同优化。该体系在骨科等领域的炎症治疗上中展现出良好的应用潜力。 展开更多
关键词 单宁酸-fe(Ⅲ)络合物 涂层 PH响应 释药 二氧化钛纳米管阵列 介孔二氧化硅
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Fe(Ⅲ)-XG配合物选择性絮凝微细粒赤铁矿与石英及其机理研究 被引量:5
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作者 韩英棋 杨志超 +4 位作者 滕青 张郭阳 方淑华 张素红 刘生玉 《有色金属(选矿部分)》 CAS 2024年第1期116-125,共10页
基于金属离子配位理论,将FeCl_(3)·6H_(2)O与黄原胶(XG)按一定比例混合制备Fe(Ⅲ)-XG配合物,用于改善微细粒赤铁矿难沉降、回收效果差的问题。采用沉降实验研究了不同条件下Fe(Ⅲ)-XG对微细粒赤铁矿和石英的选择性絮凝行为,结合动... 基于金属离子配位理论,将FeCl_(3)·6H_(2)O与黄原胶(XG)按一定比例混合制备Fe(Ⅲ)-XG配合物,用于改善微细粒赤铁矿难沉降、回收效果差的问题。采用沉降实验研究了不同条件下Fe(Ⅲ)-XG对微细粒赤铁矿和石英的选择性絮凝行为,结合动电位、红外光谱和显微镜分析,揭示Fe(Ⅲ)-XG对赤铁矿的絮凝作用机理。矿物絮凝沉降试验结果表明:以黄原胶和Fe(Ⅲ)为絮凝剂,无法实现赤铁矿与石英的选择性絮凝,而黄原胶与FeCl_(3)·6H_(2)O质量比为1︰9时生成的Fe(Ⅲ)-XG配位絮凝剂,对赤铁矿和石英表现出较强的选择性絮凝作用,pH值为6时两者沉降率差异最大,分别为91.50%和39.96%。显微镜观察结果证实,Fe(Ⅲ)-XG作用下,赤铁矿颗粒形成块状絮体,且絮体密实程度更大,而石英颗粒间未发生团聚作用,处于相对分散的状态。Zeta电位、溶液化学计算、吸附量实验与红外光谱分析结果表明:黄原胶主要通过羧酸基团的羰基C=O与Fe^(3+)发生配位作用形成Fe(Ⅲ)-XG配合物,Fe(Ⅲ)-XG在石英和赤铁矿表面吸附方式不同,因而在两种矿物表面吸附量不同。Fe(Ⅲ)-XG中的羟基氧和赤铁矿表面的铁元素发生化学键合特异性吸附在赤铁矿表面,而在石英表面只有微弱的氢键吸附。通过FeCl_(3)·6H_(2)O与黄原胶配位组装可显著提升微细粒赤铁矿选择性絮凝分离效果,为赤铁矿选择性絮凝分选提供新的策略和理论指导。 展开更多
关键词 fe(Ⅲ)-XG配合物 赤铁矿 石英 絮凝剂 选择性絮凝 微细粒
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Antituberculosis and cytotoxic activities of triorganotin(Ⅳ) complexes 被引量:1
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作者 Hidayat Hussain NaziaBibi +4 位作者 Ahmed Al-Harrasi Salman Siddiqi Shahana U. Kazmi Ying Zhang Amin Badshah 《Chinese Chemical Letters》 SCIE CAS CSCD 2012年第6期731-735,共5页
Five triorganotin(IV) (1-5) complexes of cinnamic acid, (Z)-2-acetamido-3-phenylacrylic acid, 3-methylbut-2-enoic acid, and 2,2-diphenylacetic acid have been synthesized and characterized by IH-13C-119Sn NMR, UV... Five triorganotin(IV) (1-5) complexes of cinnamic acid, (Z)-2-acetamido-3-phenylacrylic acid, 3-methylbut-2-enoic acid, and 2,2-diphenylacetic acid have been synthesized and characterized by IH-13C-119Sn NMR, UV, and IR. The spectroscopic investigation demonstrated that the carboxylate group acts as a monodentate ligand in triorganotin(IV) compounds. Five triorganotin(IV) complexes were screened against the log phase culture of Mycobacterium tuberculosis H37Rv by colorimetric method using XTT dye as growth indicator. The MICs were found to he 0.08 and 1.25μg/mL. 展开更多
关键词 Triorganotin(iv complexes Antituberculosis activity MICS CYTOTOXICITY
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SYNTHESES,CHARACTERIZATION AND ETHYLENE POLYMERIZATION OF HALF-SANDWICH GROUP IV METAL COMPLEXES WITH TRIDENTATE [O,N,S] LIGANDS 被引量:1
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作者 Ya-lin Qiao Ping Hu 金国新 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2013年第5期760-768,共9页
A series of half-sandwich group IV metal complexes with tridentate monoanionic phenoxy-imine arylsulfide [O-NS] ligand [2-Bu^t4-Me-6-((2-(SC6H5)C6H4N = CHC6H2O)]- (La) and dianionic phenoxy-amine arylsulfide [O... A series of half-sandwich group IV metal complexes with tridentate monoanionic phenoxy-imine arylsulfide [O-NS] ligand [2-Bu^t4-Me-6-((2-(SC6H5)C6H4N = CHC6H2O)]- (La) and dianionic phenoxy-amine arylsulfide [O-N-S] ligand [2-Bu^t4-Me-6-((2-(SC6H5)C6H4N-CH2C6H2O)]2- (Lb) have been synthesized and characterized. Lb was obtained easily in high yield by reduction of ligand La with excess LiAlH4 in cool diethyl ether. Half-sandwich Group Ⅳ metal complexes CpTi[O-NS]Cl2 (1a), CpZr[O-NS]Cl2 (1b), CpTi[O-N-S]Cl (2a), CpZr[O-N-S]Cl (2b) and CpZr[O-N-S]Cl (2c) were synthesized by the reactions of La and Lb with CpTiCl3, CpZrCl3 and Cp ZrCl3, and characterized by IR, ^1H-NMR, ^13C-NMR and elemental analysis. In addition, an X-ray structure analysis was performed on ligand Lb. The title Group IV half-sandwich bearing tridentate [O,N,S] ligands show good catalytic activities for ethylene polymerization in the presence of methylaluminoxane (MAO) as co-catalyst up to 1.58 × 10^7 g-PE.mol-Zr-1.h-1. The good catalytic activities can be maintained even at high temperatures such as 100 ℃ exhibiting the excellent thermal stability for these half-sandwich metal pre-catalysts. 展开更多
关键词 Half-sandwich group iv metal complexes Tridentate dianionic ligands Phenoxy-imine arylsulfide ligands Catalyst Ethylene polymerization
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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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Synthesis, Spectral and Antimicrobial Studies of Bis (Cyclopentadienyl) Titanium (IV) Bis (O,O’-Dialkyl and Alkylenedithiophosphate) Complexes 被引量:1
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作者 Adnan A. S. El Khaldy Florence Okafor Alaa M. Abu Shanab 《International Journal of Organic Chemistry》 2014年第5期339-346,共8页
A new complexes of Cp2Ti[S2P(OR)2]2 (where R = Et, Pr-n, Pr-i, Bu-i and Ph) and Cp2Ti[S2POGO]2 (where G = -CH2CMe2CH2-, -CH2CEt2CH2- and -CMe2CMe2-) were prepared by the dropwise addition of the appropriate O,O’-dial... A new complexes of Cp2Ti[S2P(OR)2]2 (where R = Et, Pr-n, Pr-i, Bu-i and Ph) and Cp2Ti[S2POGO]2 (where G = -CH2CMe2CH2-, -CH2CEt2CH2- and -CMe2CMe2-) were prepared by the dropwise addition of the appropriate O,O’-dialkyl or -alkylenedithiophosphoric acid to biscyclopentadienyl titanium dichloride in 1:2 molar ratio and refluxed in benzene solution. These novel deep red colored complexes were characterized by elemental analyses, molecular weight measurements and spectroscopic techniques (IR., NMR 1H, 13C and 31P NMR). These titanium (IV) dithio complexes have also been screened for their antibacterial activities. 展开更多
关键词 TITANIUM (iv) DIALKYL and Alkylenedithiophosphate complexES
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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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以泡沫镍为基底的Fe、Cu双金属复合电极对亚铁络合脱硝液的还原性能探究 被引量:1
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作者 梁越 丁静 童华 《环境工程学报》 CAS CSCD 北大核心 2024年第5期1395-1405,共11页
以EDTA为螯合剂的亚铁络合脱硝液能够快速吸收NO,但其面临着还原再生效率低下的问题。针对吸收产物Fe(Ⅱ)EDTA-NO(F-NO)和Fe(Ⅲ)EDTA的阴极催化电化学还原制备了一种以泡沫镍为基底的Fe、Cu双金属复合电极,通过SEM、XPS、XRD等材料表征... 以EDTA为螯合剂的亚铁络合脱硝液能够快速吸收NO,但其面临着还原再生效率低下的问题。针对吸收产物Fe(Ⅱ)EDTA-NO(F-NO)和Fe(Ⅲ)EDTA的阴极催化电化学还原制备了一种以泡沫镍为基底的Fe、Cu双金属复合电极,通过SEM、XPS、XRD等材料表征分析验证了此电极制备方法的可行性。电化学催化活性测试表明,还原FNO时设定阴极电位为-0.5 V(vs.SCE),pH为3~4之间,可以实现72.6%的F-NO还原率和83.19%的NH_(4)^(+)选择性;还原Fe3+时选定阴极电位为-1.2 V(vs.SCE),pH=2~3,此时还原产生Fe^(2+)的法拉第效率最高可以达到76.14%。此外,还考察了此电极连续工作10 h的还原效果,结果证明了其在实际运行中具有良好的稳定性。 展开更多
关键词 电催化还原 复合型电极 亚铁络合脱硝液 fe(Ⅱ)EDTA-NO fe(Ⅲ)EDTA
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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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