Design of Highly Selective Recognition and Separation System for Metal Ions
金属离子高选择性识别与分离系统的设计
基本信息
- 批准号:13640603
- 负责人:
- 金额:$ 2.11万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for Scientific Research (C)
- 财政年份:2001
- 资助国家:日本
- 起止时间:2001 至 2002
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
(1) Several bi- and tridentate ligands had been prepared, and in addition to the monodentate ligand, tri-n-octylphosphine oxide (TOPO), they were applied to the synergistic extraction of alkaline earth metals and lanthanide metals. Bis (diphenylphosphinyl) methane (BDPPM) was found to be the most powerful adduct forming ligand. The compositions of the extracted species were confirmed by a graphical method. The extraction constants were calculated on the basis of the composition of the extracted species and elucidated in terms of the molecular structure.(2) Novel 4-acyl-5-pyrazolones having the crown ether moiety as the intramolecular synergist have been synthesized and the solvent extraction of various metal ions are examined. It is expected that the crown ether moiety could behave as the intramolecular synergist and that the selectivity could be governed by the acylpyrazolone and the crown ether parts. These ligands are powerful and selective extracting reagents for alkali, alkaline earth and divalent transition metal ions, and the selectivity is quite unique depending on the intramolecular synergist.
(1)已经制备了几种双齿配体,除了单次配体三辛基膦氧化物(TOPO)外,还将它们应用于碱接地金属和灯笼金属的协同提取。发现BIS(二苯基磷酸)甲烷(BDPPM)是形成最强大的加合物。通过图形方法证实了提取物种的组成。根据提取物种的组成来计算提取常数,并根据分子结构阐明。(2)已合成具有冠状醚部分的新型4-酰基-5-吡唑酮,作为分子内的协同作用,并检查了各种金属离子的溶液提取。可以预期,冠状部分可以表现为分子内协同作用,并且选择性可以由酰基吡唑酮和牙冠醚部分控制。这些配体具有强大的选择性提取试剂,用于碱,碱土和二价过渡金属离子,根据分子内协同作用,选择性非常独特。
项目成果
期刊论文数量(22)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Y. Komatsu: "Separation of potassium and calcium by centrifugal partition chromatograph system"RIKEN Accel. Prog. Rep.. 36. 207 (2003)
Y.小松:“通过离心分配色谱系统分离钾和钙”RIKEN Accel。
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- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
S.Umetani, K.Ogura, S.Yamazaki: "Novel Acylpyrazolones Having Crown Ether Moiety as Intramolecular Synergist"Anal.Sci.. 17. 241-244 (2001)
S.Umetani、K.Ogura、S.Yamazaki:“具有冠醚部分作为分子内增效剂的新型酰基吡唑啉酮”Anal.Sci.. 17. 241-244 (2001)
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- 影响因子:0
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- 通讯作者:
S.Umetani, Y.Komatsu, H.Yamada, S.Enomoto: "Acylpyrazolones with crown ether moiety as intramolecular synergist"RIKEN Accel. Prog. Rep.. 36. 129 (2003)
S.Umetani,Y.Komatsu,H.Yamada,S.Enomoto:“具有冠醚部分作为分子内增效剂的酰基吡唑啉酮”RIKEN Accel。
- DOI:
- 发表时间:
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- 影响因子:0
- 作者:
- 通讯作者:
S. Umetani: "Solvent Extraction of Metal Ions with Novel 4-Acyl-5-pyrazolones Having Crown Ether Moiety as Intramolecular Synergist"Proceedings of the International Solvent Extraction Conference (ISEC2002). 420-424 (2002)
S. Umetani:“用具有冠醚部分作为分子内增效剂的新型 4-酰基-5-吡唑酮进行金属离子的溶剂萃取”国际溶剂萃取会议 (ISEC2002) 会议记录。
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- 影响因子:0
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Y.Komatsu, S.Umetani, S.Tsurubou: "Separation of Cesium and Strontium from S-Block Metal Ions by Double and Triple Phase Systems"Solvent Extraction for the 21st Century (Proceedings of ISEC'99). 1249-1253
Y.Komatsu、S.Umetani、S.Tsurubou:“通过双相和三相系统从 S 区金属离子中分离铯和锶”21 世纪的溶剂萃取(ISEC99 会议记录)。
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UMETANI Shigeo其他文献
UMETANI Shigeo的其他文献
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{{ truncateString('UMETANI Shigeo', 18)}}的其他基金
Molecular Design of Organic Ligands with Highly Selective Recognition and Separation Function for Metal Ions
具有金属离子高选择性识别和分离功能的有机配体的分子设计
- 批准号:
11640607 - 财政年份:1999
- 资助金额:
$ 2.11万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Molecular Design of Highly Selective Ligand Controlling the Geometry of the Donating Atoms
控制供体原子几何形状的高选择性配体的分子设计
- 批准号:
07640803 - 财政年份:1995
- 资助金额:
$ 2.11万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Molecular Recognition Study Based on a Multi-point Interaction Utilizing Metal Complexes
基于金属配合物多点相互作用的分子识别研究
- 批准号:
04640550 - 财政年份:1992
- 资助金额:
$ 2.11万 - 项目类别:
Grant-in-Aid for General Scientific Research (C)
Studies on Polydentate Organic Phosphorus Compounds as Extraction Reagents.
多齿有机磷化合物作为萃取剂的研究。
- 批准号:
01540475 - 财政年份:1989
- 资助金额:
$ 2.11万 - 项目类别:
Grant-in-Aid for General Scientific Research (C)
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12640518 - 财政年份:2000
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Molecular Design of Organic Ligands with Highly Selective Recognition and Separation Function for Metal Ions
具有金属离子高选择性识别和分离功能的有机配体的分子设计
- 批准号:
11640607 - 财政年份:1999
- 资助金额:
$ 2.11万 - 项目类别:
Grant-in-Aid for Scientific Research (C)