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排序方式: 共有79条查询结果,搜索用时 31 毫秒
1.
Yoshiyuki Mizuhata Shiori Fujimori 《Phosphorus, sulfur, and silicon and the related elements》2020,195(11):936-939
AbstractThe reaction of 2-t-Bu-germabenzenylpotassium with Me2(t-Bu)SiCl (TBDMSCl) resulted in the coupling among two TBDMS-substituted germabenzenes and the germabenzenylpotassium. The structure of the product was determined by X-ray crystallographic analysis. Its formation mechanism was proposed with the help of theoretical calculations. 相似文献
2.
Huihui Xu Dr. Arseni Kostenko Dr. Catherine Weetman Dr. Shiori Fujimori Prof. Shigeyoshi Inoue 《Angewandte Chemie (International ed. in English)》2023,62(11):e202216021
Facile access to dimeric heavier aluminum chalcogenides [(NHC)Al(Tipp)-μ-Ch]2 (NHC=IiPr (1,3-diisopropyl-4,5-dimethylimidazol-2-ylidene, IMe4 (1,3,4,5-tetramethylimidazol-2-ylidene); Tipp=2,4,6-iPr3C6H2; Ch=Se, Te) by treatment of NHC-stabilized aluminum dihydrides with elemental Se and Te is reported. The higher affinity of IMe4 in comparison with IiPr toward the Al center in [(NHC)Al(Tipp)-μ-Ch]2 can be used for ligand exchange. Additionally, the presence of excess IMe4 allows for cleavage of the dimers to form a rare example of a neutral multiply bonded heavier aluminum chalcogenide in the form of a tetracoordinate aluminum complex, (IMe4)2(Tipp)Al=Te. This species reacts with three equivalents of CO2 across two Al−CNHC and the Al=Te bond affording a pentacoordinate aluminum complex containing a dianionic tellurocarbonate ligand [CO2Te]2−, which is the first example of tellurium analogue of a carbonate [CO3]2−. 相似文献
3.
Shiori Komai Mitsuhiro Hirano Naofumi Ohtsu 《Surface and interface analysis : SIA》2020,52(12):823-828
The Sr 3d X-ray photoelectron spectroscopy (XPS) spectrum of Sr-containing hydroxyapatite (SHAp) overlaps completely with the P 2p spectrum. Thus, the chemical state identification of Sr in SHAp is a challenging task. In this work, the Sr 3d spectrum was isolated from the overlapping spectra for analyzing the chemical state of Sr using a generic peak-fitting method. The SHAp layers containing various Sr concentrations were produced on a Ti substrate using a chemical treatment process with a calcium phosphate slurry that included Sr (NO3)2. The distribution of the constituent elements changed according to the Sr concentration, implying that the chemical state of Sr varied with concentration. The isolation of the Sr 3d XPS spectrum was conducted via spectral deconvolution using the P 2p spectrum corresponding to HAp. The isolated Sr 3d spectrum revealed that the chemical state of Sr was in SrO and Sr-substituted HAp states, and their ratio varied with the Sr concentration in the layer. The SrO to Sr-substituted HAp ratios affected the Sr ion releasing behavior from the SHAp layer, supporting the validity of the obtained analytical results. 相似文献
4.
Saiko Sugawara Toshihiko Ito Shiori Sato Yuki Sato Kano Kasuga Ikuo Kojima Masayuki Kobayashi 《Applied biochemistry and biotechnology》2014,172(1):206-215
Fibroblast growth factor 4 (FGF4) is considered as a crucial gene for tumorigenesis in humans and the development of mammalian embryos. The secreted, mature form of human FGF4 is thought to be comprised of 175 amino acid residues (proline32 to leucine206, Pro32-Leu206). Here, we found that bacterially expressed, 6× histidine (His)-tagged human FGF4 (Pro32-Leu206) protein, referred to as HishFGF4, was unstable such as in phosphate-buffered saline. In these conditions, site-specific cleavage, including between Ser54 and Leu55, in HishFGF4 was identified. In order to generate stable human FGF4 derivatives, a 6× His-tagged human FGF4 (Leu55-Leu206), termed HishFGF4L, was expressed in Escherichia coli. HishFGF4L could be purified from the supernatant of cell lysates by heparin column chromatography. In phosphate-buffered saline, HishFGF4L was considered as sufficiently stable. HishFGF4L exerted significant mitogenic activities in mouse embryonic fibroblast Balb/c 3T3 cells. In the presence of PD173074, an FGF receptor inhibitor, the growth-stimulating activity of HishFGF4L disappeared. Taken together, we suggest that HishFGF4L is capable of promoting cell growth via an authentic FGF signaling pathway. Our study provides a simple method for the production of a bioactive human FGF4 derivative in E. coli. 相似文献
5.
Specific reactivity of 2,4,6-tri-tert-butylanilide anions and its application to benzylation reagent
The reaction of methyl iodide with an anilide anion prepared from 2,4,6-tri-tert-butylanilide and NaH in CH3CN gave N-methyl anilide (N-alkylation product) as a major product, while in the reaction of benzyl bromide with the anilide anion in DMF, O-benzyl imidate (O-alkylation product) was obtained with almost complete selectivity. The treatment of O-benzyl imidate with alcohols and carboxylic acids in the presence of trifluoromethane sulfonic acid gave benzyl ethers and benzyl esters, respectively. 相似文献
6.
7.
Chiral separations of 1-aminoindan (AI) by cyclodextrin electrokinetic chromatography (CDEKC) were investigated on microfluidic quartz chips. By using a microchip electrophoresis (MCE) instrument equipped with a linear-imaging UV detector, the separation process of the enantiomeric compounds was observed. When sulfated beta-cyclodextrin was employed as a chiral selector, the baseline separation of AI could be achieved within 1 min with a high repeatability. The relative standard deviation of the migration time was less than 6%. The fastest separation was achieved in 14 s, utilizing a separation length of only 6.1 mm. These results show that the MCE analysis employing a linear imaging UV detector has a significant potential for fast chiral analysis. 相似文献
8.
Susumu Yonezawa Shiori Nishibu Masayuki Takashima 《Journal of fluorine chemistry》2007,128(4):438-447
The preparation of the rare earth containing oxide fluoride glasses LnF3 (Ln; Y through Lu)-BaF2-AlF3-GeO2 in which the nominal content of LnF3 reached 60 mol% in maximum and their basic properties such as density, refractive index and glass transition temperature were investigated and summarized in detail. Especially, in order to discuss the local structure around the rare earth ion in the glass, the Judd-Ofelt analysis (discussion with Ω parameters) of the HoF3-BaF2-AlF3-GeO2 glasses was carried out. The unique fluorescent behavior and the magnetic properties of LnF3-BaF2-AlF3-GeO2 glasses (Ln = Tb and/or Sm) were also studied. 相似文献
9.
10.
A triruthenium cluster, (mu3,eta2,eta3,eta5-acenaphthylene)Ru3(CO)7 (1) catalyzes the reaction of secondary amides with hydrosilanes, yielding a mixture of secondary amines, tertiary amines, and silyl enamines. Production of secondary amines with complete selectivity is achieved by the use of higher concentration of the catalyst (3 mol %) and the use of bifunctional hydrosilanes such as 1,1,3,3-tetramethyldisiloxane. Acidic workup of the reaction mixture affords the corresponding ammonium salts, which can be treated with a base, providing a facile method for isolation of secondary amines with high purity. In contrast, tertiary amines are formed with high selectivity by using lower concentration of the catalyst (1 mol %) and polymeric hydrosiloxanes (PMHS) as reducing agent. Reduction with PMHS encapsulates the ruthenium catalyst and organic byproducts to the insoluble silicone resin. The two reaction manifolds are applicable to various secondary amides and are practical in that the procedures provide the desired secondary or tertiary amine as a single product. The product contaminated with only minimal amounts of ruthenium and silicon residues. On the basis of the products and observed side products as well as NMR studies a mechanistic scenario for the reaction is also described. 相似文献