High Complexation Ability of Thiacalixarene with Transition Metal Ions. The Effects of Replacing Methylene Bridges of Tetra(p-t-butyl)calix[4]arenetetrol by Epithio Groups

スポンサーリンク

概要

• 論文の詳細を見る
• 1998-07-15

著者

• 壹岐 伸彦

  東北大学大学院環境科学研究科環境科学専攻

• IKI Nobuhiko

  Department of Biomolecular Engineering, Graduate School of Engineering, Tohoku University

• MOROHASHI Naoya

  Department of Biomolecular Engineering, Graduate School of Engineering, Tohoku University

• MIYANO Sotaro

  Department of Biomolecular Engineering, Graduate School of Engineering, Tohoku University

• NARUMI Fumitaka

  Department of Biomolecular Engineering, Graduate School of Engineering, Tohoku University

• Iki Nobuhiko

  Department Of Biomolecular Engineering Graduate School Of Engineering Tohoku University

• Miyano S

  Department Of Biomolecular Engineering Graduate School Of Engineering Tohoku University

• Miyano Sotaro

  Department Of Biochemistry And Engineering Faculty Of Engineering Tohoku University

• 壹岐 伸彦

  Department Of Biomolecular Engineering Graduate School Of Engineering Tohoku University

• Morohashi Naoya

  Department Of Biomolecular Engineering Graduate School Of Engineering Tohoku University

• Narumi Fumitaka

  Department Of Biomolecular Engineering Graduate School Of Engineering Tohoku University

• Narumi Fumitaka

  Department Of Basic Sciences School Of Science And Engineering Ishinomaki Senshu University

• Miyano Sotaro

  Department of Applied Chemistry, Faculty of Engineering, Tohoku University

関連論文

• キャピラリー電気泳動反応器を用いる亜鉛(II)-1, 5-ビス(2-ヒドロキシ-5-スルホフェニル)-3-シアノホルマザン錯体のオンキャピラリー解離反応特性の評価
• Sulfur-bridged Oligo(benzoic acid)s as a Novel Family of Metal Extractants
• Synthesis of a Sulfur-bridged Diphosphine Ligand and Its Unique Complexation Properties toward Palladium(II) Ion
• Tetra- and Di-Nuclear Copper(II) Complexes with Stereoisomers of Sulfinylcalix[4]arene Arising from the Disposition of Four S=O Groups
• Beneficial Effect of TMSCl in the Lewis Acid-mediated Carboxylation of Aromatic Compounds with Carbon Dioxide
• Synthesis and Characterization of Novel Chiral 1,2-Diamines Derived from α-Pinene
• Interaction between Quaternary Ammonium Ions and Dipeptides : Positive Anion Allosteric Effect
• Metal-Ion Extractability of Sulfur-Bridged Oligomers of Phenol ; Distinct Effect of the Number of Sulfur Bridges Rather Than the Cyclic/Acyclic Form^1
• 新規ホスト分子チアカリックスアレーン
• Complexing Ability of p-tert-Butylthiacalix[6]arene toward Metal Ions. Predominant Effect of Coordination by the Bridging Sulfur Rather than That of the Ring-Size
• Synthesis and Structural Characterization of a Pd^ Complex with p-tert-Butylsulfinylcalix[4]arene
• Sulfonylcalix[4]arene as a Bis-Tridentate Facial Ligand: Syntheses and Structures of Dinuclear Complexes, [M_2(L)(H_2O)_2(dmf)_4] (M = Co(II),Ni(II);H_4L = p-tert-Butylsulfonylcalix[4]arene
• Coordination of Epithio Groups of p - tert - Butylthiacalix [4]arene in a Zn^ Complex Studied by X-Ray Crystallography
• High Complexation Ability of Thiacalixarene with Transition Metal Ions. The Effects of Replacing Methylene Bridges of Tetra(p-t-butyl)calix[4]arenetetrol by Epithio Groups
• 水溶液中におけるテトラヒドロクルクミンの酸化安定性と酸解離特性の評価
• 「生命科学と分析化学」特集号の刊行にあたって(生命科学と分析化学)
• Topological Variation between Hexa- and Trithiacalix[6]arene-Copper(II) Complexes : From Sphere to Wheel by Reducing the Number of the Sulfur Bridges
• A p-tert-Butyldithiacalix[4]arene-Copper(II) Complex Having Double-cone Shape of Unique Heteroditopie Inclusion Behavior
• p-tert-Butylthiacalix[6]arene as a Clustering Ligand. Syntheses and Structures of Co^_5, Ni^_4, and Mixed-Metal M^Ni^_4 (M=Mn, Co, and Cu) Cluster Complexes, and a Novel Metal-Induced Cluster Core Rearrangement
• 超微量金属錯体の速度論的識別モードーキャピラリー電気泳動システムの設計
• 多彩な可能性を秘めた新規ホスト化合物 : チアカリックスアレーン
• チアカリックスアレーン - 分離・センシング機能試薬の新規プラットホームの創製 -
• チアカリックスアレーン
• A New Chiral Stationary Phase for Gas Chromatography by Use of a Chiral Thiacalix [4] arene Derivative
• 自己集合単分子層形成を用いる液体クロマトグラフィー固定相
• Almost Complete Removal of Trace Amount of Halogenated Organic Compounds in Water:An Approach by Use of a Combination of Water-Soluble Thiacalixarene and Ion-Exchange Resins
• A New Water-Soluble Host Molecule Derived from Thiacalixarene
• Lewis Acid-Mediated Carboxylation of Aryl- and Allylsilanes with Carbon Dioxide
• Lewis Acid-Mediated Carboxylation of Fused Aromatic Compounds with Carbon Dioxide
• Interconversion between syn and anti Conformations of 1, 3-Bis (O-cyanomethyl)-p-tert-butylthiacalix[4]arene
• Synthesis and Optical Resolution of an anti-O, O'-Dialkylated Calix[4]arene
• Ester-Mediated Nucleophilic Aromatic Substitution of 2, 3-Alkylidenedioxybenzoic Esters by Aryl Lithium Reagents
• New Entry to Chiral Base Catalyst. Asymmetric Michael Addition of α-Substituted β-Keto Esters to Methyl Vinyl Ketone Catalyzed by Podand-type Alkali Metal 2'-Substituted 1, 1'-Binaphthalen-2-oxides
• Highly Selective Luminescence Determination of Terbium at the Sub-ppb Level with Sulfonylcalix[4]arene-p-tetrasulfonate
• An Investigation of the Inherent Chiral Induction Ability of Axially Chiral 1,1'-Binaphthalene Framework in the Prelog's Atrolactic Acid Synthesis
• Acid-catalyzed Facile Racemization of Axially Dissymmetric 2'-Hydroxy-1,1'-binaphthyl-2-carboxylic Acid
• High-Performance Separation and Determination of Co(III) and Ni(II) Chelates of 4-(2-Pyridylazo)resorcinol at Femtomole Levels by Capillary Electrophoresis
• Chelating Adsorbent for Heavy Metal Ions Prepared by Loading Anion-Exchange Resin with Thiacalix[4]arenetetrasulfonate
• α-Methoxy-α-trifluoromethylpropionic Acid (MTPr). A New Chiral Derivatizing Reagent for GC Separation of Enantiomeric Amino Acids
• Design and Synthesis of Chiral Stationary Phase Derived from (S)-[10]Paracyclophane-13-carboxylic Acid for the HPLC Separation of Enantiomers
• Direct Carboxylation of Thiophenes and Benzothiophenes with the Aid of EtAlCl_2
• Selective Extraction of Heavy Rare-earth Metal Ions with a Novel Calix[4]arene-based Diphosphonic Acid
• Use of axially chiral 2'-methoxy-1,1'-binaphthyl-2-carboxylic acid as chiral derivatizing agent for discrimination of enantiomeric alcohols and amines by 1H NMR.
• The asymmetric Ullmann coupling reaction of chiral diol diesters of 1-bromo-2-naphthoic acid and 2-halo-3-nitrobenzoic acids: Highly diastereoselective synthesis of atropisomeric 6,6'-dinitrodiphenic acids.
• Carbon-carbon bond formation by use of chloroiodomethane as a C1 unit. I. Formation of chloromethyltriphenylphosphonium iodide, and its application for the Wittig chloromethylenation of aldehydes and ketones.
• Asymmetric synthesis of axially chiral, unsymmetrical diphenic acids via intramolecular Ullmann coupling reaction.
• The Ullmann coupling reaction of axially chiral (S)-2,2'-bis(1-iodo-2-naphthyloxycarbonyl)-1,1'-binaphthyl.
• Axially dissymmetric bis(aminophosphine)s derived from 2,2'-diamino-1,1'-binaphthyl. Synthesis and application to rhodium(I)-catalyzed asymmetric hydrogenations.
• The asymmetric Ullmann coupling reaction of (S)-2,2'-bis(1-bromo-2-naphthoyloxy)-1,1'-binaphthyl revisited. Formation of 24-membered optically pure cyclic dimer as well as 12-membered cyclic monomer.
• Absorption of Chlorinated Hydrocarbons Dissolved in Water with Pellets Made of p-tert-Butylcalix[4]arene and Silica Gel
• Carbon-carbon bond formation by the use of chloroiodomethane as a C1 unit. IV. The Mannich reaction of ketones by means of dihalomethane and secondary amine.
• Carbon-carbon bond formation by the use of chloroiodomethane as a C1 unit. III. A convenient synthesis of the Mannich base from enol silyl ether by a combination of chloroiodomethane and N,N,N',N'-tetramethylmethanediamine.
• Selective oxidation of 2-bromo-m-xylene to 2-bromo-3-methylbenzoic acid or 2-bromoisophthalic acid.
• Carbon-carbon bond formation by the use of chloroiodomethane as a C1 unit. II. The preparation and synthetic application of 1-chloro-3-iodoheptane.
• Oxygen-accelerated generation of the bromocarbenoid reagent of zinc from diethylzinc and bromoform. Bromocyclopropanes from olefins.
• Synthesis of Optically Active Polyamides Having Axially Dissymmetric 1,1'-Binaphthalene-2,2'-dicarboxylic Acid Component and Their Optical Resolution Ability as Chiral Adsorbent for HPLC.
• A practical method for optical resolution of 1,1'-binahthyl-2,2'-dicarboxylic acid via 1-phenylethylamides.

もっと見る 閉じる

スポンサーリンク