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901.
Hersa Milawati Dr. Yoshiyuki Manabe Takuya Matsumoto Dr. Masato Tsutsui Dr. Yoshihiro Ueda Ayane Miura Dr. Kazuya Kabayama Prof. Koichi Fukase 《Angewandte Chemie (International ed. in English)》2023,62(25):e202303750
We propose a de novo glycan display approach that combines metabolic labeling and a glycan-caging strategy as a facile editing method for cell-surface glycans. This method enables the introduction of antigen glycans onto cancer cells to induce immune responses through antibody recruiting. The caging strategy prevents the capture of α-rhamnose (an antigen glycan) by endogenous antibodies during the introduction of the glycan to the targeted cell surface, and subsequent uncaging successfully induces immune responses. Therefore, this study proposes a practical method for editing the cell-surface glycocalyx under promiscuous conditions, such as those in vivo, which paves the way for the development of glycan function analysis and regulation. 相似文献
902.
Dr. Hajime Kameo Yudai Tanaka Dr. Yoshihiro Shimoyama Daisuke Izumi Prof. Hiroyuki Matsuzaka Dr. Yumiko Nakajima Pierre Lavedan Arnaud Le Gac Dr. Didier Bourissou 《Angewandte Chemie (International ed. in English)》2023,62(20):e202382062
A T-shaped Pt0 complex with a diphosphine-borane (DPB) ligand was prepared. The Pt→B interaction enhances the electrophilicity of the metal and triggers the addition of Lewis bases to give the corresponding tetracoordinate complexes. For the first time, anionic Pt0 complexes are isolated and structurally authenticated. X-ray diffraction analyses show the anionic complexes [(DPB)PtX]− (X=CN, Cl, Br, I) to be square-planar. The d10 configuration and Pt0 oxidation state of the metal were unambiguously established by X-ray photoelectron spectroscopy and DFT calculations. The coordination of Lewis acids as Z-type ligands is a powerful mean to stabilize elusive electron-rich metal complexes and achieve uncommon geometry. 相似文献
903.
The preparation and characterization of n-alkane/water emulsions using beta-cyclodextrin (beta-CD) were studied. The prepared n-alkane/water emulsions were of the oil-in-water (O/W) type, and the stability of emulsions was in the order of n-hexadecane > n-dodecane > n-octane. From observations using polarized light microscopy and powder X-ray diffraction measurement, it was suggested that the formation of a dense film at the oil-water interface and the three-dimensional structural network created by precipitated complexes in the continuous phase are associated with the stability of emulsion. Furthermore, it was clarified that O/W-type emulsions were formed because the contact angle (theta ow) which the precipitate makes with the interface was theta ow < 90 degrees in all compounds (oils) used in this study. 相似文献
904.
Yoshihiro Nakashima Jia-Hua Xing Satoshi Inomata Takashi Imamura 《Chemical physics letters》2008,450(4-6):248-252
Rate coefficients for the reactions of cyclohexadienyl (c-C6H7) radicals with O2 and NO were measured at 296 ± 2 K. The c-C6H7 radicals were detected selectively by laser-induced fluorescence. The rate coefficient for the reaction of c-C6H7 with O2, (4.4 ± 0.5) × 10−14 cm3 molecule−1 s−1, was independent of the bath-gas (He) pressure (13–80 Torr). In the reaction of c-C6H7 with NO, thermal equilibrium among c-C6H7, NO, and C6H7NO was observed. The forward and reverse reactions were in the falloff region, and the equilibrium constant was (1.5 ± 0.6) × 10−15 cm3 molecule−1. 相似文献
905.
We have investigated the ground state and the two lowest excited states of the CeF molecule using four-component relativistic multiconfigurational quasidegenerate perturbation theory calculations, assuming the reduced frozen-core approximation. The ground state is found to be (4f(1))(5d(1))(6s(1)), with Omega = 3.5, where Omega is the total electronic angular momentum around the molecular axis. The lowest excited state with Omega = 4.5 is calculated to be 0.104 eV above the ground state and corresponds to the state experimentally found at 0.087 eV. The second lowest excited state is experimentally found at 0.186 eV above the ground state, with Omega = 3.5 based on ligand field theory calculations. The corresponding state having Omega = 3.5 is calculated to be 0.314 eV above the ground state. Around this state, we also have the state with Omega = 4.5. The spectroscopic constants R(e), omega(e), and nu(1-0) calculated for the ground and first excited states are in almost perfect agreement with the experimental values. The characteristics of the CeF ground state are discussed, making comparison with the LaF(+) and LaF molecules. We denote the d- and f-like polarization functions as d(*) and f(*). The chemical bond of CeF is constructed via {Ce(3.6+)(5p(6)d(*0.3)f(*0.1))F(0.6-)(2p(5.6))}(3+) formation, which causes the three valence electrons to be localized at Ce(3.6+). 相似文献
906.
Hidenobu Tsuji Takayuki Nakano Yoshihiro Matsumoto Shumpei Kameyama 《Optical Review》2016,23(2):155-160
We have developed an illumination optical system for 3D imaging ladar (laser detection and ranging) which forms flattop beam shape by transformation of the Gaussian beam in the wide distance range. The illumination is achieved by beam division and recombination using a prism and a negative powered lens. The optimum condition of the transformation by the optical system is derived. It is confirmed that the flattop distribution can be formed in the wide range of the propagation distance from 1 to 1000 m. The experimental result with the prototype is in good agreement with the calculation result. 相似文献
907.
Stereoretentive Addition of N‐tert‐Butylsulfonyl‐α‐Amido Silanes to Aldehydes,Ketones, α,β‐Unsaturated Esters,and Imines
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Dr. Tsuyoshi Mita Keisuke Saito Masumi Sugawara Prof. Dr. Yoshihiro Sato 《化学:亚洲杂志》2016,11(10):1528-1531
Enantioenriched N‐tert‐butylsulfonyl‐α‐amido silanes were successfully reacted with aldehydes, ketones, imines, and α,β‐unsaturated esters in the presence of a sub‐stoichiometric amount of CsF (0.5 equiv) in 1,2‐dimethoxyethane (DME) at ?20 °C to afford the corresponding coupling products with up to 89 % enantiospecificity in a retentive manner. 相似文献
908.
Equilibrium constants () for the ion-pair formation of a complex ion NaL+ with ReO4− in water were determined potentiometrically at 25 °C and the ionic strength (I) of 0 mol dm−3 using a Na+-selective electrode. Here, crown ethers, L, were 15-crown-5 ether (15C5), benzo-15C5, 18-crown-6 ether (18C6) and benzo-18C6. Also, NaReO4 was extracted by the L into 1,2-dichloroethane and then extraction constants (Kex/mol−2 dm6) for the species, NaLReO4, were determined at 25 °C by AAS. These Kex values were resolved into four component equilibrium constants containing KMLA calculated at given I values. Based on these data, extraction-abilities of the L against the perrhenate were discussed in comparison with those of sodium picrate-L systems reported previously. 相似文献
909.
Grid pattern of nanothick microgel network 总被引:1,自引:0,他引:1
Chen G Kawazoe N Fan Y Ito Y Tateishi T 《Langmuir : the ACS journal of surfaces and colloids》2007,23(11):5864-5867
A novel grid pattern of two kinds of nanothick microgels was developed by alternate patterning using photolithography. At first, 100-microm-wide nanothick PAAm microgel stripes were grafted on a polystyrene surface by UV irradiation of the photoreactive azidobenzoyl-derivatized polyallylamine-coated surface through a photomask with 100-microm-wide stripes. Then, a second set of 100-microm-wide nanothick PAAc microgel stripes were grafted across the PAAm-grated polystyrene surface by UV irradiation of the photoreactive azidophenyl-derivatized poly(acrylic acid)-coated surface through a photomask placed perpendicularly to the first set of PAAm microgel stripes. The PAAc microgel stripe pattern was formed over the PAAm microgel stripe pattern. The cross angle of the two microgel stripes could be controlled by adjusting the position of the photomask when the second microgel pattern was prepared. Swelling and shrinking of the microgels were investigated by scanning probe microscopy (SPM) in an aqueous solution. SPM observation indicated that the thickness of the gel network was 100 to 500 nm. The regions containing PAAm, PAAc, and the PAAc-PAAm overlapping microgels showed different swelling and shrinking properties when the pH was changed. The PAAm microgel swelled at low pH and shrank at high pH whereas the PAAc microgel swelled at high pH and shrank at low pH. However, the PAAc-PAAm overlapping microgel did not change as significantly as did the two microgels, indicating that the swelling and shrinking of the two gels was partially offset. The pH-induced structural change was repeatedly reversible. The novel grid pattern of nanothick microgels will find applications in various fields such as smart actuators, artificial muscles, sensors, and drug delivery systems as well as in tissue engineering and so forth. 相似文献
910.
Ito Y Heydari M Hashimoto A Konno T Hirasawa A Hori S Kurita K Nakajima A 《Langmuir : the ACS journal of surfaces and colloids》2007,23(4):1845-1850
A hydrophobic to hydrophilic gradient surface was prepared using the tuned photodegradation of an alkylsilane self-assembled monolayer (SAM) using irradiation of vacuum ultraviolet light (wavelength=172 nm). The water contact angle on the photodegraded SAM surface was adjusted using the intensity and time photoirradiation parameters. The formation of a gradient was confirmed by fluorescent labeling. The water drop moved from the hydrophobic to hydrophilic surface with a velocity that depended on the gradient. The higher the gradient, the faster the water moved. For the first time, we have prepared a gradient surface using photodegradation where the movement of a water drop was regulated by the degree of gradation. Considering that the photodegradation technique can be applied to various surfaces and to lithography, this technique will be useful for various material surfaces. 相似文献