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71.
Shoichi Katsuta Tokutaro Kimura Yoshihiro Kudo Ryozo Nakagawa Yasuyuki Takeda Mikio Ouchi 《Journal of inclusion phenomena and macrocyclic chemistry》1998,31(2):89-98
The overall extraction constants (Kex) of uni- andbivalent metal picrates with 15-(2,5-dioxahexyl)-15-methyl-16-crown-5(L16C5) were determined between benzene and water at 25°C. TheKex values were analyzed into the constituent equilibriumconstants, i.e., the extraction constant of picric acid, the distributionconstant of the crown ether, the stability constant of the metalion–crown ether complex in water, and the ion-pair extraction constantof the complex cation with the picrate anion. The Kex valuedecreases in the orders Ag+ > Na+ >Tl+ > K+ > Li+ andPb2+ > Ba2+ > Sr2+ for theuni- and bivalent metals, respectively, which are the same as those observedfor 16C5. The extraction selectivity was found to be governed by theselectivity of the ion-pair extraction of the L16C5–metal picratecomplex rather than by that of the complex formation in water. Theextraction ability of L16C5 is smaller for all the metals than that of 16C5,which is mostly attributed to the higher lipophilicity of L16C5. Differencesin the extraction selectivity between L16C5 and 16C5 were observed for thebivalent metals but little for the univalent metals. The side-arm effect onthe extraction selectivity was interpreted on the basis of the negativecorrelation between the effect on the complex stability constant in waterand that on the ion-pair extraction constant. 相似文献
72.
Junko Iida Takehiro Takeda Takumi Takasuga John Moncur Phil Ireland Barry Wright 《Journal of separation science》1991,14(2):103-109
A hybrid mass spectrometer with an EBQQ configuration was used to investigate two approaches to trace dioxin analysis: high resolution gas chromatography – high resolution mass spectrometry (HRGC-HRMS) and high resolution gas chromatography – mass spectrometry – mass spectrometry (HRGC-MS-MS). It is shown that selected ion monitoring (SIM) HRGC-HRMS exhibits better selectivity for dioxins separated on a cyanopropyl column than is otherwise obtained under medium resolution mass spectrometry (3,000 resolution), while optimization of conditions for HRGC-MS-MS allowed the observation of 350 femtograms of the highly toxic 2,3,7,8-TCDF at a S/N ratio of 5:1. Both methods were applied to environmental samples with good results. 相似文献
73.
Identification and formation mechanism of individual degradation products in lithium‐ion batteries studied by liquid chromatography/electrospray ionization mass spectrometry and atmospheric solid analysis probe mass spectrometry 下载免费PDF全文
74.
Yoshiyuki Mizuhata Nobuhiro Takeda Norihiro Tokitoh 《Phosphorus, sulfur, and silicon and the related elements》2013,188(4-5):947-948
The reductive debromination of an very crowded bis(bromodiaryl- silyl)butadiyne 2 was performed with potassium graphite to give the corresponding 2-allenyl-1-benzosilole 3 was isolated as a main product. 相似文献
75.
76.
Mechanism of Macroscopic Motion of Oleate Helical Assemblies: Cooperative Deprotonation of Carboxyl Groups Triggered by Photoisomerization of Azobenzene Derivatives 下载免费PDF全文
Dr. Yoshiyuki Kageyama Tomonori Ikegami Yuta Kurokome Prof. Dr. Sadamu Takeda 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(25):8669-8675
Macroscopic and spatially ordered motions of self‐assemblies composed of oleic acid and a small amount of an azobenzene derivative, induced by azobenzene photoisomerization, was previously reported. However, the mechanism of the generation of submillimeter‐scale motions by the nanosized structural transition of azobenzene was not clarified. Herein, an underlying mechanism of the motions is proposed in which deprotonation of carboxyl groups in cooperation with azobenzene photoisomerization causes a morphological transition of the self‐assembly, which in turn results in macroscopic forceful dynamics. The photoinduced deprotonation was investigated by potentiometric pH titration and FTIR spectroscopy. The concept of hierarchical molecular interaction generating macroscale function is expected to promote the next stage of supramolecular chemistry. 相似文献
77.
Takeshi Takeda Shuichi Kuroi Makoto Ozaki Akira Tsubouchi 《Phosphorus, sulfur, and silicon and the related elements》2013,188(5-6):1291-1296
Abstract Trialkylsilyl group-directed regioselective transformations of alkynyl thioacetals to alkynylcyclopropanes and enynes are described. 相似文献
78.
79.
Nobuhiro Takeda Norihiro Tokitoh Renji Okazaki 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1):633-636
The first rotational isomers of stable selenoaldehydes are synthesized by deselenation of cyclic polyselenides having an efficient steric protection group, 2, 4, 6-tris[bis(trimetylsilyl)methyl]phenyl (Tbt). Reactions of these selenoaldehydes with W(CO)5.THF gives the corresponding η1-selenoaldehyde tungsten complexes, the structures of which are established by X-ray crystallography. 相似文献
80.
Tsuneyuki Sato Toshio Kadowaki Hiroshi Takeda Takayuki Otsu 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(8):1225-1239
(S)-4-Methyl-2-N,N-dimethylaminopentyl methacrylate (DMAPM) was synthesized from the reaction of N,N-dimethyl-L-leucinol with methacryl chloride, and its radical polymerization was investigated. It was found that DMAPM readily polymerized by α,α1-azobisisobutyronitrile (AIBN) as an initiator to give poly-DMAPM. The copolymerization of DMAPM(M1) with styrene(Mz) was also studied in various solvents with AIBN as an initiator at 60°C. From the result obtained in benzene, Q and e values of DMAPM were determined to be 0.64 and -0.04, respectively. Specific rotations of the copolymers of DMAPM with styrene were not proportional to the weight percent of the DMAPM unit incorporated, but the observed relation gave a downward curve. The copolymerizations DMAPM with α, β-disubstituted monomers such as maleic acid, maleimide, and N-phenylmaleimide were carried out in order to induce asymmetric center in the polymer chain. After hydrolysis of the copolymers obtained, the hydrolyzed polymers were found to be optically active, suggesting an induction of asymmetric center into the polymer chain. 相似文献