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Synthesis, Crystal Structure and DNA-binding Property of Bismuth(Ⅲ) Complex with p-Hydroxy-phenylacetic Acid
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作者 陈小菊 胡未极 +1 位作者 秦毅 赵国良 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2013年第4期509-514,共6页
A bismuth(Ⅲ) complex 1 (H2-4,4'-bipy)[Bi(HPPA)5](H2PPA).4H2O (H2PPA = p- hydroxy- phenylacetic acid, 4,4'-bipy = 4,4"-bipyridyl) was hydrothermally synthesized from p-hydroxy-phenylacetic acid (H2PPA),... A bismuth(Ⅲ) complex 1 (H2-4,4'-bipy)[Bi(HPPA)5](H2PPA).4H2O (H2PPA = p- hydroxy- phenylacetic acid, 4,4'-bipy = 4,4"-bipyridyl) was hydrothermally synthesized from p-hydroxy-phenylacetic acid (H2PPA), Bi(NO3)3"6H20 and 4,4'-bipyridyl, and characterized by elemental analysis, IR, molar conductivity and TG. The single-crystal X-ray diffraction studies demonstrated that the complex is of monoclinic system, space group P21 with a = 10.928(7), b = 22.558(7), c = 11.313(7) A, β = 91.864(4)°, V = 2787.7(4) A3, Z = 2, C58H61BiN2O22, Mr = 1347.07, F(000) = 1364, Dc= 1.605 g/cm-3, p(MoKa) = 3.247 mm-1, the final R = 0.0269 and wR = 0.0540 for 9776 observed reflections with I 〉 2or(I). The bismuth(I/I) is seven-coordinated with O atoms, forming a monocapped octahedral geometry. Complex 1 further forms a 3D supramolecular architecture by hydrogen bonds and π-π stacking interactions. Moreover, the interaction between the complex and DNA was studied by EtBr fluoescent probe. 展开更多
关键词 bismuth(ⅲ) complex p-hydroxy-phenylaeetie acid 4 4"-bipyridyl crystal structure DNA-BINDING
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Synthesis,Structure and Dielectric Properties of a Novel 1D Chain Bismuth(Ⅲ) Complex[(C_6H_6NO_2)_2·(BiCl_5)·2H_2O]_n 被引量:3
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作者 陈立庄 高延敏 +1 位作者 邹俊 黄美娜 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2011年第2期284-288,共5页
Under hydrothermal conditions,isonicotinic acid reacted with BiCl 3 to give 1D zigzag chain complex [(C 6 H 6 NO 2) 2 ·(BiCl 5)·2H 2 O] n (1).Single-crystal X-ray determination shows that compound 1 cr... Under hydrothermal conditions,isonicotinic acid reacted with BiCl 3 to give 1D zigzag chain complex [(C 6 H 6 NO 2) 2 ·(BiCl 5)·2H 2 O] n (1).Single-crystal X-ray determination shows that compound 1 crystal-lizes in the monoclinic system,space group C2/c with a=13.115(3),b=19.957(4),c=7.9374(16),β=97.45(3)°,Z=4,V=2060.0(8) 3,C 12 H 16 BiCl 5 N 2 O 6,D c=2.162 g/cm 3,M r=670.50,λ(MoKa)=0.71073,μ=9.237 mm-1,F(000)=1272,R=0.0208 and wR=0.0503.Dielectric constant of compound 1 was measured at different conditions.Measurements on the dielectric properties of 1 showed that the 1D chain coordination polymer exhibited a dipolar chain relaxation process and a relatively high dielectric constant. 展开更多
关键词 1D chain bismuth complex HYDROTHERMAL PERMITTIVITY
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有机膦酸改性碳纳米管/硫化铋复合材料的设计合成及其对Au(Ⅲ)的吸附性能研究
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作者 张万松 宋雨桐 +5 位作者 徐彦宾 王峰 张少华 王颖 杨正龙 殷平 《鲁东大学学报(自然科学版)》 2024年第2期159-169,共11页
本研究设计合成新型高效重金属吸附材料有机膦酸羧酸改性多壁碳纳米管/硫化铋(PBTCA-MWCNTs/Bi_(2)S_(3)),对材料进行了傅里叶红外光谱(FT-IR)、扫描电镜(SEM)、能谱(EDX)和X射线光电子能谱(XPS)等表征,并研究其对重金属离子的吸附性能... 本研究设计合成新型高效重金属吸附材料有机膦酸羧酸改性多壁碳纳米管/硫化铋(PBTCA-MWCNTs/Bi_(2)S_(3)),对材料进行了傅里叶红外光谱(FT-IR)、扫描电镜(SEM)、能谱(EDX)和X射线光电子能谱(XPS)等表征,并研究其对重金属离子的吸附性能。结果发现:PBTCA-MWCNTs/Bi_(2)S_(3)有优良的Au(Ⅲ)吸附性能;Langmuir模型拟合结果显示,材料在25℃时吸附容量达到1655.50 mg·g^(-1)。对该材料吸附热力学、吸附动力学和吸附选择性等方面的研究为Au(Ⅲ)回收提供了有效的技术支持。 展开更多
关键词 水处理 Au()吸附 碳纳米管 膦酸 硫化铋
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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
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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()-XG配合物 赤铁矿 石英 絮凝剂 选择性絮凝 微细粒
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Synthesis and Crystal Structure of Novel Dimer of Bismuth(Ⅲ) Complex with Dithiotetrahydropyrrolocarbamate: [Bi(S_2CNC_4H_8)_2(NO_3)]_2
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作者 YINHan-dong WANGChuan-hua MAChun-lin 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2004年第5期565-567,共3页
A novel dimer of the bismuth(Ⅲ) complex with dithiotetrahydropyrrolocarbamate, [Bi(S_2CNC_4H_8)_2·(NO_3)]_2, was synthesized and the crystal structure was determined by X-ray single crystal diffraction. The crys... A novel dimer of the bismuth(Ⅲ) complex with dithiotetrahydropyrrolocarbamate, [Bi(S_2CNC_4H_8)_2·(NO_3)]_2, was synthesized and the crystal structure was determined by X-ray single crystal diffraction. The crystal belongs to a monoclinic system with space group P2_1/n, a=0.64718(13) nm, b=2.6738(6) nm, c=1.0423(2) nm, β=106.384(3)°, Z=4, V=1.730(3) nm^3, D_c=2.163 g/cm^3, μ=10.682 mm^(-1), F(000)=1072, R=0.0329, wR=0.0659. The structure shows a distorted pentagonal bipyramidal configuration with the seven-coordinated central Bi atom. In the crystal, the molecular packing in the unit cell reveals that the two adjacent molecules are symmetrically linked each other in the dimer by virtue of a couple of Bi-S interaction. 展开更多
关键词 bismuth() complex Dithiotetrahydropyrrolocarbamate DIMMER Crystal structure
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Bismuth-Complex-Incorporated Nanocellulose Sheet for Biomedical Application:A Review on New Nanocellulose Composites
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作者 Kirubanandan Shanmugam P Dhanasekaran +2 位作者 Deepa Priya R Narendhar Chandrasekar Ramachandran Balaji 《Journal of Clinical and Nursing Research》 2023年第6期193-206,共14页
Antibiotic resistance is one of the major issues in the medical field and a potential threat to human health.However,newly emerging antimicrobial compounds failed to combat antimicrobial resistance developed by bacter... Antibiotic resistance is one of the major issues in the medical field and a potential threat to human health.However,newly emerging antimicrobial compounds failed to combat antimicrobial resistance developed by bacterial pathogens.Recently,a bismuth-based complex has been developed to eradicate antimicrobial-resistant microorganism infections.The complex is known as organobismuth(III)phosphinate,which is said to be a potential broad-spectrum antimicrobial agent.This complex has been incorporated into the nanocellulose suspension to fabricate a biomedical composite for various applications.The composite can be fabricated by two methods namely vacuum filtration and spray coating.In this paper,the surface and topography of the composite are investigated and discussed in terms of SEM micrographs and their antimicrobial potential.This review focuses on the organo-bismuth nanocellulose composite and its biomedical application in the future. 展开更多
关键词 bismuth complex NANOCELLULOSE NANOCOMPOSITE Spray coating Vacuum filtration Antimicrobial activity Antifungal activity
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Syntheses, Crystal Structures and Anticancer Activities of Dithiocarbamate Bismuth(Ⅲ) Complexes
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作者 郭应臣 马勤阁 +2 位作者 陈书阳 冯玉全 孙汝中 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2015年第7期1028-1034,共7页
Two novel complexes, [Bi(III)(S2CNBn Et)3] 1 and [Bi(III)(S2CNPPPy-2)3] 2, were synthesized and characterized by elemental analysis, IR, ^1H NMR, ^13C NMR, TG-DTG and X-ray single-crystal diffraction. The stru... Two novel complexes, [Bi(III)(S2CNBn Et)3] 1 and [Bi(III)(S2CNPPPy-2)3] 2, were synthesized and characterized by elemental analysis, IR, ^1H NMR, ^13C NMR, TG-DTG and X-ray single-crystal diffraction. The structure reveals that complex 1 belongs to the monoclinic system, space group P21/c with a = 11.457(5), b = 17.437(8), c = 33.439(14), β= 98.499(8)o, Z = 4, V = 6607(5)3, Dc = 1.689 g·cm^-3, F(000) = 3328, μ= 5.742 mm^-1, the final R = 0.0906, w R = 0.1678 and S = 1.032. The structure indicates that complex 2 belongs to the triclinic system, space group P1 with a = 12.608(9), b = 12.622(8), c = 12.49(6), α = 102.652(15), β = 103.013(14), γ = 109.698(10)o, Z = 1, V = 1762.3(19)3, Dc = 1.741 g·cm^-3, F(000) = 916, μ = 5.395 mm^-1, the final R = 0.048 2, w R = 0.1206 and S =1.046. In the two complexes, each six-coordinated Bi(III) atom adopts a pentagonal pyramidal configuration with six sulfur atoms from three ligands, and the dimmer structures are formed by weak interactions of Bi···S between two molecules. The anticancer activities of the two complexes were studied by evaluating their cytotoxicities against several human cancer cell lines using the MTT assay. Results indicated complex 2 showed moderate cytotoxic effects on the selected cancer cells. 展开更多
关键词 N-ethyl-N-benzyl dithiocarbamate bismuth(III) complex 1-(2-pyrimidyl)piperazine dithiocarbamate bismuth(III) complex crystal str
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羟胺强化Fe(Ⅲ)-NTA络合物活化过二硫酸盐降解磺胺甲恶唑
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作者 王真然 彭藴斓 +1 位作者 刘义青 付永胜 《安全与环境学报》 CAS CSCD 北大核心 2024年第3期1163-1172,共10页
针对Fe(Ⅱ)/过二硫酸盐(Peroxydisulfate,PDS)高级氧化技术存在的pH值应用范围窄、铁泥产量大等缺陷,研究构建Fe(Ⅲ)-氨三乙酸(Nitrilotriacetic Acid,NTA)/羟胺(Hydroxylamine,HAm)/PDS体系,以在中性条件下高效降解水中新污染物磺胺甲... 针对Fe(Ⅱ)/过二硫酸盐(Peroxydisulfate,PDS)高级氧化技术存在的pH值应用范围窄、铁泥产量大等缺陷,研究构建Fe(Ⅲ)-氨三乙酸(Nitrilotriacetic Acid,NTA)/羟胺(Hydroxylamine,HAm)/PDS体系,以在中性条件下高效降解水中新污染物磺胺甲恶唑(Sulfamethoxazole,SMX)。研究结果显示,Fe(Ⅲ)-NTA/HAm/PDS体系在pH=7条件下对SMX的降解率可达91%,该体系降解SMX的主要活性物种为·SO_(4)^(-)和·OH。SMX在Fe(Ⅲ)-NTA/HAm/PDS体系中的降解效率随溶液pH值的升高而降低,且增加Fe(Ⅲ)、PDS的用量会加速SMX降解。NTA的引入可将Fe(Ⅱ)/PDS体系的pH值应用范围由酸性拓展至弱碱性,与此同时,向体系内加入HAm可有效减少铁泥的产量。根据检测到的降解产物,提出SMX在Fe(Ⅲ)-NTA/HAm/PDS体系中可能的降解途径包括断键反应、羟基化反应、氨基氧化反应。双酚AF、双氯芬酸、土霉素等其他新污染物也能在Fe(Ⅲ)-NTA/HAm/PDS体系中被高效去除,表明该体系在新污染物的降解领域有较大的应用潜力。 展开更多
关键词 环境工程学 磺胺甲恶唑 羟胺 Fe()-NTA络合物 过二硫酸盐
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Fe(Ⅲ)/2,6-吡啶二羧酸活化高碘酸盐强化染料脱色的效能与机制
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作者 陈文政 苏晗 +2 位作者 钟欣洋 牛丽君 冯明宝 《化学试剂》 CAS 2024年第4期59-64,共6页
有色染料是环境中非常重要的污染源之一,严重威胁着水生生态环境和人类健康。由于其难以被天然降解,且传统的污水处理工艺亦无法实现其高效去除,因此急需开发绿色、高效的水处理工艺进行有色染料污染控制。发现Fe(Ⅲ)/2,6-吡啶二羧酸(2,... 有色染料是环境中非常重要的污染源之一,严重威胁着水生生态环境和人类健康。由于其难以被天然降解,且传统的污水处理工艺亦无法实现其高效去除,因此急需开发绿色、高效的水处理工艺进行有色染料污染控制。发现Fe(Ⅲ)/2,6-吡啶二羧酸(2,6-PDA)可高效活化高碘酸盐(PI)实现亚甲基蓝(MB)这一典型染料的高效降解。实验结果表明,该体系在Fe(Ⅲ)浓度为10μmol/L、2,6-PDA浓度为10μmol/L和PI浓度为200μmol/L时,可在pH 3.0条件下使5 mg/L MB降解率在120 s内大于97%。该方法依托高级氧化原理和配位强化策略,利用PI对有色染料进行降解,为目前染料废水治理提供了新思路从而有效地修复了污染水体。 展开更多
关键词 亚甲基蓝 高碘酸盐 配位活化 Fe() 高级氧化
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Bismuth Ⅲ型肝门胆管癌的外科治疗 被引量:11
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作者 彭淑牖 牟一平 +6 位作者 蔡秀军 彭承宏 吴育连 曹利平 江献川 许元良 刘颖斌 《外科理论与实践》 2000年第4期228-230,共3页
目的:研究肝Bismuth Ⅲ型肝门胆管癌根治性切除时,需要伴同切除肝脏的范围。方法:对两家医院近两年半来收治的BismuthⅢ型肝门胆管癌31例进行分析。其中21例行根治性切除者,伴同左半肝切除11例,伴同右半肝切... 目的:研究肝Bismuth Ⅲ型肝门胆管癌根治性切除时,需要伴同切除肝脏的范围。方法:对两家医院近两年半来收治的BismuthⅢ型肝门胆管癌31例进行分析。其中21例行根治性切除者,伴同左半肝切除11例,伴同右半肝切除5例,伴同右三叶切除2例,伴同Ⅳ肝段切除3例。与上述各种肝切除合并作尾叶切除者9例。结果:全组无手术死亡,并发膈下脓肿2例,经穿刺置管引流治愈;并发肝衰腹水8例,其中右半肝切除后3例,左半肝切除后3例,右三叶切除后2例,均经强化护肝治疗、反复多次输注血浆和白蛋白治愈;并发胆漏3例,经保守引流而愈。施行Ⅳ肝段+尾叶切除的3例顺利恢复,无并发症。结论: BismuthⅢ型肝门胆管癌根治性切除伴同肝切除的范围应根据肿瘤所在的确切部位以及同侧门静脉有无受侵犯而定,尽量避免大范围的肝切除。 展开更多
关键词 肝门胆管癌 切除术 bismuth
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BismuthⅢ型肝门部胆管癌的肝切除范围问题
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作者 黄志勇 梁宾勇 《临床外科杂志》 2014年第3期149-150,共2页
肝门部胆管癌是指起源于左、右肝管及其汇合部胆管上皮的恶性肿瘤.因其解剖部位特殊,极易早期侵犯周围血管、肝脏、淋巴及神经组织.手术切除是治疗肝门部胆管癌的首选方法,R0切除是提高肝门部胆管癌患者长期生存率的关键.目前多采用Bism... 肝门部胆管癌是指起源于左、右肝管及其汇合部胆管上皮的恶性肿瘤.因其解剖部位特殊,极易早期侵犯周围血管、肝脏、淋巴及神经组织.手术切除是治疗肝门部胆管癌的首选方法,R0切除是提高肝门部胆管癌患者长期生存率的关键.目前多采用Bismuth分型方法对肿瘤进行临床分型,结合术前各种影像学检查结果了解血管、淋巴结和肝脏受侵情况,对肝门部胆管癌实施胆管切除联合包括尾叶在内的肝切除、淋巴结清扫以及必要时血管切除的治疗意见已趋一致. 展开更多
关键词 肝门部胆管癌 bismuth 肝切除 范围
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基于三氰基铁(Ⅲ)酸盐的Fe^(Ⅲ)_(4)Ni^(Ⅱ)_(2)六核配合物的合成、结构及磁性 被引量:2
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作者 李国玲 王蒙蒙 +2 位作者 唐新学 张然 倪中海 《无机化学学报》 SCIE CAS CSCD 北大核心 2023年第8期1564-1570,共7页
利用三氰基铁酸盐(Bu_(4)N)[FeⅢ(Tp)(CN)_(3)](Tp=氢化三(1-吡唑基)硼酸)与配体2,9-二吡唑基-1,10-菲咯啉(dpzpen)以及高氯酸镍反应合成了一例氰根桥联的Fe^(Ⅲ)_(4)Ni^(Ⅱ)_(2)六核配合物[Fe_(4)Ni_(2)(Tp)_(4)(CN)_(12)(dpzpen)_(2)]... 利用三氰基铁酸盐(Bu_(4)N)[FeⅢ(Tp)(CN)_(3)](Tp=氢化三(1-吡唑基)硼酸)与配体2,9-二吡唑基-1,10-菲咯啉(dpzpen)以及高氯酸镍反应合成了一例氰根桥联的Fe^(Ⅲ)_(4)Ni^(Ⅱ)_(2)六核配合物[Fe_(4)Ni_(2)(Tp)_(4)(CN)_(12)(dpzpen)_(2)]·12H_(2)O·3CH_(3)OH (1)。结构研究表明配合物1具有近似菱形的Fe^(Ⅲ)_(2)Ni^(Ⅱ)_(2)骨架结构,另外2个Fe则通过氰根延伸在菱形的外侧。磁性研究表明在配合物1中氰根桥联的Fe和Ni表现出铁磁相互作用。更为重要的是,基于配合物1的结构模型,对它的变温磁化率数据进行拟合得到了不同Fe-Ni之间的磁耦合常数,得到的最佳磁耦合常数J3d(15.73 cm^(-1))>J2d(3.53 cm^(-1))≈J1d(3.50 cm^(-1))与Ni-N键的键长以及Ni-N≡C键角的变化趋势有关(J3d:0.206 5 nm,169.8°;J2d:0.206 2 nm,163.1°;J1d:0.198 7 nm,161.6°)。以上结果表明Ni-N键长越短,Ni-N≡C键角越大,Fe与Ni之间的铁磁耦合越强。 展开更多
关键词 三氰基铁酸盐 FeNi配合物 晶体结构 磁性 磁性-结构相互关系
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三核铜(Ⅱ)-稀土(Ⅲ)席夫碱配合物的合成、分子结构和性质
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作者 刘一夫 马方伟 《黑龙江大学工程学报(中英俄文)》 2023年第4期18-25,共8页
通过四齿铜(Ⅱ)席夫碱配合物(CuSaltn)与硝酸镧(Ⅲ)反应,合成了一系列的3d-4f异金属席夫碱配合物(CuSaltn)_(2)Ln(H_(2)O)(NO_(3))_(3)(Ln=镧(1),铈(2),镨(3),钕(4),钐(5)),其中Saltn为1,3-丙二胺缩双水杨醛席夫碱配体。对配体和配合物... 通过四齿铜(Ⅱ)席夫碱配合物(CuSaltn)与硝酸镧(Ⅲ)反应,合成了一系列的3d-4f异金属席夫碱配合物(CuSaltn)_(2)Ln(H_(2)O)(NO_(3))_(3)(Ln=镧(1),铈(2),镨(3),钕(4),钐(5)),其中Saltn为1,3-丙二胺缩双水杨醛席夫碱配体。对配体和配合物进行了元素分析、热失重、红外光谱、紫外光谱等分析表征。在室温下测定了配合物5的晶体结构,钐(Ⅲ)离子与两个双齿铜配合物、两个双齿硝酸盐离子和一个水分子形成九配位构型。形成三核铜(Ⅱ)-稀土(Ⅲ)配合物后,配合物的荧光显著降低。该类化合物的结构研究为其他类似的席夫碱配合物的研究提供有价值的信息,并且会被应用于荧光性能的研究。 展开更多
关键词 铜(Ⅱ)-稀土()配合物 席夫碱 晶体结构
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Thermal Decomposition Kinetics and Mechanism of Tb(Ⅲ) m-Methylbenzoate Complex with 1,10-Phenanthroline in Static Air Atmosphere 被引量:5
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作者 ZHANG Jian-jun WANG Rui-fen +1 位作者 ZHANG Jian-ling WANG Shu-ping 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2002年第1期25-29,共5页
The thermal behavior of [Tb_2( m -MBA)_6(phen)_2](H_2O)_2( m -MBA=C_8H_7O_2, methoxybenzoate; phen=C_ 12 H_8N_2, 1,10-phenanthroline) in static air atmosphere was investigated by means of TG-DTG and DTA methods. The... The thermal behavior of [Tb_2( m -MBA)_6(phen)_2](H_2O)_2( m -MBA=C_8H_7O_2, methoxybenzoate; phen=C_ 12 H_8N_2, 1,10-phenanthroline) in static air atmosphere was investigated by means of TG-DTG and DTA methods. The thermal decomposition of the title compound takes place mainly in two steps. The intermediate and the residue for each decomposition were identified by the TG curve. By the kinetic method of processing thermal analysis data put forward by Malek et al ., it is defined that the kinetics model for the first-step thermal decomposition is SB( m,n ). 展开更多
关键词 Thermal decomposition Non-isothermal kinetics Tb() complex m-Methylbenzoate 1 10-PHENANTHROLINE
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Synthesis of Eu(Ⅲ) and Tb(Ⅲ) Complexes with New Aryl Amide Type Tetrapodal Ligand and Their Luminescence Properties 被引量:3
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作者 蔡正洪 谭民裕 《Journal of Rare Earths》 SCIE EI CAS CSCD 2002年第5期382-384,共3页
A new aryl amide type tetrapodal ligand L (1, 1, 1, 1 tetrakis-{[(2 benzylaminoformyl) phenoxyl]methyl}methane) and its europium and terbium nitrate complexes were synthesized. The luminescence properties of these c... A new aryl amide type tetrapodal ligand L (1, 1, 1, 1 tetrakis-{[(2 benzylaminoformyl) phenoxyl]methyl}methane) and its europium and terbium nitrate complexes were synthesized. The luminescence properties of these complexes were also studied. 展开更多
关键词 rare earths aryl amide tetrapodal ligand Eu() and Tb() complexes luminescence property
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Synthesis,Fluorescence and Magnetic Properties of a New Europium(Ⅲ)Complex Eu(C14H9O3)2(C12H8N2)2(NO3) 被引量:5
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作者 杨颖群 李玉林 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2018年第11期1781-1785,共5页
A new europium(III)complex Eu(CHO)(CHN)(NO)has been synthesized with 2-benzoylbenzoic acid and 1,10-phenanthroline as ligands.Crystal data for the complex are as follows:monoclinic,space group P2/c,a=9.6733(6),b=22.95... A new europium(III)complex Eu(CHO)(CHN)(NO)has been synthesized with 2-benzoylbenzoic acid and 1,10-phenanthroline as ligands.Crystal data for the complex are as follows:monoclinic,space group P2/c,a=9.6733(6),b=22.9521(14),c=19.7701(12)?,β=94.9800(10)o,V=4372.8(5)?~3,D=1.557 g/cm~3,Z=4,μ(Mo Kα)=1.501 mm,F(000)=2064,the final R=0.0214 and w R=0.0510.The Eu(III)ion is coordinated by ten atoms to give a bicapped square antiprism coordination geometry.The complex shows two intense fluorescence emission bands arising from the transitions of Eu:~5D→~7F(594 nm)and ~5D→~7F(618 nm).In addition,its XT decreases from 1.29767 cm~3?mol?K at 300 K to 0.01531 cm~3?mol?K at 2 K. 展开更多
关键词 europium() complex crystal structure fluorescent and magnetic properties
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Intercalation Assembly, Characterization and Luminescent Properties of Novel Supramolecular Composite Materials, Tb(Ⅲ) Complex with Tetrapodal Ligand-Montmorillonite 被引量:3
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作者 Jiang Wei Tang Yu +2 位作者 Xu Li Liu Weisheng Tan Minyu 《Journal of Rare Earths》 SCIE EI CAS CSCD 2006年第5期537-537,共1页
Two kinds of Tb( Ⅲ ) complexes with tetrapodal ligand, [TbL(NO3)]^3+ and [TbL]^3+ (L: 1,1, 1', 1'-tera ( 2-pyridinecarboxylester )-di ( trimethylpropane)) were intercalated into the interlayer space of... Two kinds of Tb( Ⅲ ) complexes with tetrapodal ligand, [TbL(NO3)]^3+ and [TbL]^3+ (L: 1,1, 1', 1'-tera ( 2-pyridinecarboxylester )-di ( trimethylpropane)) were intercalated into the interlayer space of montmorillonite (MT) by ion exchange and coordination reaction of L with the Tb^3+ ion existing in the interlayer space of Tb-MT respectively. The obtained luminescent supramolecular composite materials, [ TbL (NO3) ]^2+-MT and [TbL]^3+-MT were characterized by elemental analysis, XRD, FT-IR, UV-vis and thermal analysis. At the same time, the luminescent properties of the materials were also studied. The results show that the intercalated materials with regular layered structure, good thermal stability and the interlayer spacing (d001) approximates to the size of the complex ions which are located in the interlayer space of MT in the form of a monolayer. 展开更多
关键词 Tb(ⅲ complexes with tetrapodal ligand MONTMORILLONITE supramolecular composite materials intercalation assembly luminescent properties rare earths
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Investigation on Molecular and Crystal Structures of Metal Complexes with Aminopolycarboxylic Acids——Synthesis and Structure of K[In~Ⅲ(EDTA)(H_2O)]·2H_2O 被引量:2
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作者 王君 陈冬松 +1 位作者 宋玉林 高敬群 《Rare Metals》 SCIE EI CAS CSCD 1998年第3期54-59,共6页
The title complex was synthesised and its molecular and crystal structures were determined by single crystal X ray reflection structure analysis. The crystal data are as follows: K[In Ⅲ(EDTA)(H 2O)]·2H 2O (... The title complex was synthesised and its molecular and crystal structures were determined by single crystal X ray reflection structure analysis. The crystal data are as follows: K[In Ⅲ(EDTA)(H 2O)]·2H 2O (EDTA=ethylene diamine N, N, N′, N′ tetraacetate), Monoclinic, C c space group, a=0.9096(2) nm,b=1.1996(2) nm, c =1.5144(3) nm, β =99.40(3)°, V =1.6302(6) 3, Z =3, D c=1.498 g·cm -3 , μ =1.325 mm -1 , F (000)=726, R =0.0320 and R W=0.0903 for 2315 observed independent reflections. The complex anion [In Ⅲ(EDTA)(H 2O)] - has a seven coordinate pseudo pentagonal bipyramidal (PB D 5h ) structure, in which the EDTA serves as a hexadentate ligand with two N atoms and four O atoms and one water molecule (H 2O) directly coordinated to the central metal ion In Ⅲ as a seventh ligand. 〓〓 展开更多
关键词 In Ethylenediaminetetraacetate (EDTA) complex Seven coordinate structures
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Synthesis and Characterization of Some Lanthanide(Ⅲ) Complexes with 4-[N-(2-methoxybenzylimine)formyl]-2, 3-dimethyl-1-phenyl-3-pyazolin-5-one 被引量:2
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作者 G. Rijulal P. Indrasenan 《Journal of Rare Earths》 SCIE EI CAS CSCD 2007年第6期670-673,共4页
A series of seven novel lanthanide(Ⅲ ) nitrato complexes with 4-[ N-(2-methoxybenzylimine)formyl] 1-2, 3- dimethyl-1-phenyl-3-pyazolin-5-one (2mbfa), were synthesized. These complexes were characterized by elem... A series of seven novel lanthanide(Ⅲ ) nitrato complexes with 4-[ N-(2-methoxybenzylimine)formyl] 1-2, 3- dimethyl-1-phenyl-3-pyazolin-5-one (2mbfa), were synthesized. These complexes were characterized by elemental analysis, molecular mass determination, conductance and magnetic moment measurements, IR, UV-visible, and ^13CNMR spectral studies, In these complexes, the Schiff base, 2mbfa, acts as neutral bidentate ligand by utilizing the carbonyl oxygen and azomethine nitrogen as donor sites. All the three nitrate ions are also coordinated unidentately with 7 coordination for the lanthanide(Ⅲ) ions with a tentative monocapped octahedral geometry for the complexes. All the seven lanthanide(Ⅲ) complexes have a general formula, [ Ln(2mbfa):(NO3)3 ]. 展开更多
关键词 synthesis characterization lanthanide(ⅲ complexes Schiff bases rare earths
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Crystal Structure and Fluorescent Study of a Binuclear Europium(Ⅲ) Complex 被引量:3
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作者 黄玲 刘荫秋 曾锡瑞 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2009年第9期1126-1130,共5页
A novel binuclear Eu(Ⅲ) complex [Eu2(dpa dioxide)2(NO3)4(bpdioxide)-(EtOH)] (dpa dioxide = di-2-pyridylamine N,N'-dioxide, bpdioxide = 2,2'-bipyridine N,N'-dioxide) has been synthesized and it exhibits... A novel binuclear Eu(Ⅲ) complex [Eu2(dpa dioxide)2(NO3)4(bpdioxide)-(EtOH)] (dpa dioxide = di-2-pyridylamine N,N'-dioxide, bpdioxide = 2,2'-bipyridine N,N'-dioxide) has been synthesized and it exhibits strong and sharp fluorescent emission at 614 nm under UV radiation of 245 nm at room temperature. X-ray structural determination indicates two independent Eu(Ⅲ) ions in the structure with different EuO8N and EuOgN environments. The compound crystallizes in the triclinic system, space group P1, with a = 10.8089(7), b = 11.4670(8), c = 17.1440(12) A, α = 92.834(2), β = 93.854(3), γ = 95.433(2)°, Z = 2, Dc = 1.876 g/cm3, V= 2107.3(2) A3, F(000) = 1168.0, the final R = 0.032 and wR = 0.086 for 6331 observed reflections with I 〉 2σ(I). 展开更多
关键词 rare earth complex europium(ⅲ LUMINESCENCE
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