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21.
Development of a New Benzylating Reagent Spontaneously Releasing Benzyl Cation Equivalents at Room Temperature
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Dr. Kohei Yamada Yuichi Tsukada Yukiko Karuo Dr. Masanori Kitamura Prof. Dr. Munetaka Kunishima 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(38):12274-12278
A new O‐benzylating reagent, that is, 4‐(4,6‐diphenoxy‐1,3,5‐triazin‐2‐yl)‐4‐benzylmorpholinium trifluoromethanesulfonate (DPT‐BM), has been developed. Benzyl cation equivalents are generated from DPT‐BM by dissolving the compound in a solvent at room temperature under non‐acidic conditions. The benzylation of various alcohols by using a combination of DPT‐BM and magnesium oxide provided the benzyl ethers in good yields. 相似文献
22.
Munetaka Iwamura Airi Fukui Koichi Nozaki Hikaru Kuramochi Satoshi Takeuchi Tahei Tahara 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(51):23354-23361
Femtosecond time-resolved absorption and picosecond time-resolved emission measurements were carried out for highly concentrated aqueous solutions of K2[Pt(CN)4] to investigate excited-state dynamics of the [Pt(CN)42−] oligomers formed with metallophilic interactions. Time-resolved absorption spectra exhibit complicated dynamics that are represented with five time constants. Among them, the 90-ps and 400-ps dynamics were assigned to the S1 → T1 intersystem crossing of the trimer and tetramer coexisting in the solution by comparison with the fluorescence decays. Clear oscillations of transient absorption were observed in the first few picoseconds, and the frequency-detected-wavelength 2D analysis revealed that the 135-cm−1 and 65-cm−1 oscillations arise from the Pt–Pt stretch motions of the S1 trimer and S1 tetramer, respectively. The obtained time-resolved spectroscopic data provide a clear view of the excited-state dynamics of the [Pt(CN)42−] oligomers in the femto-/picosecond time region. 相似文献
23.
采用一步化学原位还原法将球形纳米铂颗粒直接修饰在玻碳电极上,用SEM、EDS和电化学方法对该电极进行表征并与铂片电极、裸玻碳电极进行了对比。结果表明,纳米铂修饰电极的峰电流与扫描速度呈线性关系,纳米铂在电极表面覆盖率为1.28×10-7mol/cm2。循环伏安法研究结果表明纳米铂修饰电极对半胱氨酸的催化氧化作用和铂片电极相比提高了数倍,且峰电位负移了0.3V。在纳米铂修饰的玻碳电极上,半胱氨酸的浓度在1.0×10-7mol/L到1.0×10-5mol/L范围内和催化电流呈线性关系。 相似文献
24.
在不使用交联剂的情况下,借助种子媒介纳米金属生长法将纳米金直接修饰到玻碳电极表面.试验发现纳米金粒子在电极表面覆盖率为5.4×10-10 mol·cm-2,[Fe(CN)6]3-/[Fe(CN)6]4-氧化还原电子探针的试验证明,纳米金修饰玻碳电极表面的电子传递速率是使用交联剂制备电极的四倍.与裸玻碳电极相比,抗坏血酸在该电极表面的氧化峰电位负移150 mV,峰电流提高2.2μA,同时与尿酸的氧化峰电位差达到186 mV,可用于抗坏血酸和尿酸的同时检测. 相似文献
25.
Selective Host–Guest Interactions of a Transformable Coordination Capsule/Tube with Fullerenes
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Norifumi Kishi Prof. Dr. Munetaka Akita Dr. Michito Yoshizawa 《Angewandte Chemie (International ed. in English)》2014,53(14):3604-3607
An M2L4 coordination capsule or an M2L2 coordination tube was selectively formed by the combination of HgII hinges and bent bispyridine ligands. The two structures reversibly interconvert at room temperature in response to modulation of the metal‐to‐ligand ratio and exhibit different host–guest interaction behavior. The capsule alone encapsulates large spherical molecules, fullerenes C60 and C70, and the bound guests are released upon capsule‐to‐tube transformation by the simple addition of metal ions. 相似文献
26.
Yasushi Koyama Ichiro Takatsuka Munetaka Nakata Mitsuo Tasumi 《Journal of Raman spectroscopy : JRS》1988,19(1):37-49
Raman and infrared spectra in the region of 1800-150 cm−1 were recorded for a set of cis-trans isomers of d̃-carotene, i.e. the all-trans, 7-cis, 9-cis, 13-cis and 15-cis isomers. Spectral comparison revealed Raman and infrared key bands which (1) distinguish stretched or terminal-bent configurations (all-trans, 7-cis and 9-cis) from central-bent configurations (13-cis and 15-cis), and (2) distinguish unmethylated 7-cis and 15-cis configuratios. Keybands (1) include Raman bands at 1160 and 1140 cm−1 and infrared bands at 825 and 775 cm−1 (the intensity varies with the position of the cis-bend) Key bands (2) include Raman bands at 1274 and 962 cm−1 and an infrared band at 741 cm−1 (characteristic of the 7-cis configuration), and also a Raman band at 1247 cm−1 and an infrared band at 775 cm−1 (characteristic of the 15-cis configuration). The normal modes for the key bands were determined by a set of normal coordinate calculations for the isomeric configurations of a simplified model of d̃-carotene. The key bands were mainly related to the C H in-plane bendings, coupled with the CC or C C stretching, or to the C H out-of-plane wagging vibrations, some of which coupled with the CC torsion. 相似文献
27.
Polycationic‐Shelled Capsular and Tubular Nanostructures and Their Anionic–Guest Binding Properties
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Dr. Kohei Yazaki Dr. Yoshihisa Sei Prof. Dr. Munetaka Akita Dr. Michito Yoshizawa 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(49):17557-17561
For the development of novel nanospace with unique electrostatic character, we prepared new capsular and tubular nanostructures by the quantitative assembly of metal ions and bent bisacridinium ligands. The capsule and tube have closed spherical and open cylindrical cavities, respectively, with diameters of around 1 nm surrounded by cationic polyaromatic panels. Thanks to the facile synthetic protocol (three steps), another polycationic capsule with an elliptical nanocavity was also prepared by using an elongated ligand. In spite of the absence of pendant hydrophilic groups, the spherical polyaromatic capsule shows sufficient water solubility due to the polycationic shell. Moreover, the highly cationic cavity (12+) can selectively encapsulate anionic organic compounds in water. 相似文献
28.
Solubility Switching of Metallophthalocyanines and Their Larger Derivatives upon Encapsulation
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Dr. Kei Kondo Prof. Dr. Munetaka Akita Dr. Michito Yoshizawa 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(6):1937-1940
Metallophthalocyanines (MPcs) are very useful pigments but scarcely soluble without appropriate functional groups in common solvents. Herein, we report that bent polyaromatic amphiphiles act as excellent solubilizing reagents for nonfunctionalized MPcs and larger MPc derivatives (e.g., CuPc, perhalogenated CuPcs, Cu‐naphthalocyanine, CuPc polymers, and double‐decker MPcs) in neutral water upon encapsulation. The resultant MPc nanocomposites display high stability towards heat and pH change. More importantly, the encapsulated MPcs can be released by simple protocols under mild conditions both into a bulk solvent and onto glass or polymer plates. 相似文献
29.
Munetaka Nakata Masaaki Sugie Harutoshi Takeo Chi Matsumura Tsutomu Fukuyama Kozo Kuchitsu 《Journal of Molecular Spectroscopy》1981,86(1):241-249
The microwave spectra of four isotopic species of dichlorine monoxide (OCl2) have been observed, and the rotational constants have been obtained. The rm structure for each isotopic species has been determined by Watson's method. The equilibrium structure has been estimated by taking proper averages of rm structures to be and ∠eClOCl = 110.886(6)°. The general applicability and the merit of the present method for estimating the equilibrium structure are pointed out. 相似文献
30.
Munetaka Nakata Tsutomu Fukuyama Kozo Kuchitsu Harutoshi Takeo Chi Matsumura 《Journal of Molecular Spectroscopy》1980,83(1):118-129
The microwave spectra of eight isotopic species of COCl2 have been observed, and the following rotational constants have been obtained: An analysis of the rotational constants has resulted in the rs and rm structures. The equilibrium structure, re, has been estimated by combining the rm parameters derived according to Watson's method and the re bond distances estimated in our recent electron-diffraction and spectroscopic studies to be , , ∠eClCCl = 111.79 ± 0.24°. 相似文献