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201.
Several human lung samples were dissected into lobes and uranium and silicon contents in each lobe were determined by the fission track method and the inductively coupled plasma-atomic emission spectrometry (ICP-AES), respectively. It was found that both uranium and silicon concentrations were high in the upper lobe compared with those in the lower one. Though the tendency may be mainly interpreted by the deposition way of airborne dust in the lung, the higher U/Si concentration ratio in the upper part than that in the lower part of lungs may suggest the partial removal of uranium deposited in the lower part of the tissue. 相似文献
202.
Yoshimasa Makita Tomofumi Danno Keisuke Ikeda Hsien-Han Lee Taro Abe Kento Sogawa Akihiro Nomoto Shin-ichi Fujiwara Akiya Ogawa 《Tetrahedron letters》2017,58(48):4507-4509
Hemicryptophanes are covalent molecular cages, constructed from a cyclotriveratrylene-based host unit and a functional unit linked by covalent spacers, which have been designed to accommodate endohedral functionalities in the cavity. In this study, the synthesis and characterization of the rigid, biphenyl-linked hemicryptophane 1 were investigated by NMR, ESI-MS, and X-ray crystallography. The structure of the inclusion complex, in which a dichloromethane molecule was constructed encapsulated within 1, was characterized by X-ray crystallography. An endohedral, cobalt(II) hemicryptophane complex 2 was also synthesized and characterized ESI-MS and X-ray crystallography. The X-ray crystal structure of 2 showed that the biphenyl-linked hemicryptophane had three components—a molecule each of chloroform and acetonitrile, and a cobalt(II) ion—within its cavity. 相似文献
203.
Harada T Ikeda S Hashimoto F Sakata T Ikeue K Torimoto T Matsumura M 《Langmuir : the ACS journal of surfaces and colloids》2010,26(22):17720-17725
A core-shell composite consisting of a palladium (Pd) nanoparticle and a hollow carbon shell (Pd@hmC) was employed as a catalyst for aerobic oxidation of various alcohols. The core-shell structure was synthesized by consecutive coatings of Pd nanoparticles with siliceous and carbon layers followed by removal of the intermediate siliceous layer. Structural characterizations using TEM and N(2) adsorption-desorption measurements revealed that Pd@hmC thus-obtained was composed of a Pd nanoparticle core of 3-6 nm in diameter and a hollow carbon shell with well-developed mesopore (ca. 2.5 nm in diameter) and micropore (ca. 0.4-0.8 nm in diameter) systems. When compared to some Pd-supported carbons, Pd@hmC showed a high level of catalytic activity for oxidation of benzyl alcohol into benzaldehyde using atmospheric pressure of O(2) as an oxidant. The Pd@hmC composite also exhibited a high level of catalytic activity for aerobic oxidations of other primary benzylic and allylic alcohols into corresponding aldehydes. The presence of a well-developed pore system in the lateral carbon shell enabled efficient diffusion of both substrates and products to reach the central Pd nanoparticles, leading to such high catalytic activities. This core-shell structure also provided high thermal stability of Pd nanoparticles toward coalescence and/or aggregation due to the physical isolation of each Pd nanoparticle from neighboring particles by the carbon shell: this specific property of Pd@hmC resulted in possible regeneration of catalytic activity for these aerobic oxidations by a high-temperature heat treatment of the sample recovered after catalytic reactions. 相似文献
204.
205.
Metal-ion complexation of 7-benzylimidazo[1,2-a]pyrazin-3(7H)-one derivative (2) with Li+, Mg2+, Ca2+, Ba2+, Sc3+, and La3+ in acetonitrile resulted in successive modulations of its UV/vis absorption and fluorescence spectroscopic properties. This result indicates that 2 can be used as a colorimetric and fluorometric sensor of the Lewis acidity of a metal ion in aprotic solutions. The hypothesis that the metal-ion complex has a O10(imidazopyrazinone)-metal ion bond was supported by X-ray crystallographic analysis and quantum chemical calculations for a Li+ complex of 7-methylimidazo[1,2-a]pyrazin-3(7H)-one derivative (1). 相似文献
206.
Emi Evangelio Dr. Marie‐Laure Bonnet Dr. Miquel Cabañas Dr. Motohiro Nakano Dr. Jean‐Pascal Sutter Dr. Andrea Dei Prof. Vincent Robert Dr. Daniel Ruiz‐Molina Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(22):6666-6677
The different thermally induced intermolecular electron transfer (IET) processes that can take place in the series of complexes [M(Cat‐N‐BQ)(Cat‐N‐SQ)]/[M(Cat‐N‐BQ)2], for which M=Co ( 2 ), Fe ( 3 ) and Ni( 4 ), and Cat‐N‐BQ and Cat‐N‐SQ denote the mononegative (Cat‐N‐BQ?) or dinegative (Cat‐N‐SQ2?) radical forms of the tridentate Schiff‐base ligand 3,5‐di‐tert‐butyl‐1,2‐quinone‐1‐(2‐hydroxy‐3,5‐di‐tert‐butylphenyl)imine, have been studied by variable‐temperature UV/Vis and NMR spectroscopies. Depending on the metal ion, rather different behaviors are observed. Complex 2 has been found to be one of the few examples so far reported to exhibit the coexistence of two thermally induced electron transfer processes, ligand‐to‐metal (IETLM) and ligand‐to‐ligand (IETLL). IETLL was only found to take place in complex 3 , and no IET was observed for complex 4 . Such experimental studies have been combined with ab initio wavefunction‐based CASSCF/CASPT2 calculations. Such a strategy allows one to solicit selectively the speculated orbitals and to access the ground states and excited‐spin states, as well as charge‐transfer states giving additional information on the different IET processes. 相似文献
207.
Yoshida T Nishi I Ideta S Fujimori A Kubota M Ono K Kasahara S Shibauchi T Terashima T Matsuda Y Ikeda H Arita R 《Physical review letters》2011,106(11):117001
We have studied the three-dimensional shapes of the Fermi surfaces (FSs) of BaFe(2)(As(1-x)P(x))(2) (x=0.38), where superconductivity is induced by isovalent P substitution and by angle-resolved photoemission spectroscopy. Moderately strong electron mass enhancement has been identified for both the electron and hole FSs. Among two observed hole FSs, the nearly two-dimensional one shows good nesting with the outer two-dimensional electron FS, but its orbital character is different from the outer electron FS. The three-dimensional hole FS shows poor nesting with the electron FSs. The present results suggest that the three dimensionality and the difference in the orbital character weaken FS nesting while partial nesting among the outer electron FSs of d(xy) character and/or that within the three-dimensional hole FS becomes dominant, which may lead to the nodal superconductivity. 相似文献
208.
T. Ino Y. ArimotoT. Yoshioka K. MishimaK. Taketani S. MutoH.M. Shimizu H. KiraY. Sakaguchi T. OkuK. Sakai T. ShinoharaJ. Suzuki H. OtonoH. Oide S. YamashitaS. Imajo H. FunahashiM. Yamada Y. IwashitaM. Kitaguchi M. HinoZ. Suzuki T. SanukiT. Seki K. HirotaK. Ikeda H. SatoY. Otake H. OhmoriT. Morishima T. Shima 《Physica B: Condensed Matter》2011,406(12):2424-2428
We measured the neutron beam polarization of the BL05/NOP (Neutron Optics and Physics) beamline at J-PARC with an accuracy of less than 10−3 using polarized 3He gas as a neutron spin analyzer. Precise polarimetry of the neutron beam is necessary to understand the beamline optics as well as for the asymmetry measurements of the neutron beta decay, which are planned in this beamline. 相似文献
209.
Naofumi Naga Takeshi Shiono Tomiki Ikeda 《Journal of molecular catalysis. A, Chemical》1999,150(1-2):155-162
Ethylene polymerization was conducted with bis(cyclopentadienyl)zirconium dichloride (1) and rac-dimethylsilylenebis(indenyl)zirconium dichloride (2) combined with trialkylaluminum (AlR3; R=methyl (Me), ethyl (Et), isobutyl (iBu))/triphenylcarbenium tetrakis(pentafluorophenyl)borate (Ph3CB(C6F5)4) or tris(pentafluorophenyl)borane (B(C6F5)3) to study the effect of cocatalysts on polymerization rate (Rp). When AlMe3 was used, no activity or very low activity was observed with both zirconocenes regardless of the borane compounds used. The replacement of AlMe3 to AlEt3 or AliBu3 with 1–AlR3/Ph3CB(C6F5)4 caused polymerization and induction time was observed to reach the maximum Rp. Especially in the case of using AlEt3, it took about 30 min to show the activity. When B(C6F5)3 was used, AlEt3 was not effective but AliBu3 gave the highest activity among all the combinations of AlR3 and the borane compounds. In the case of polymerization with 2 using Ph3CB(C6F5)4, high activity was observed with both AlEt3 and AliBu3 without any induction period. When B(C6F5)3 was used instead of Ph3CB(C6F5)4, very low activity was observed with AlEt3. On the other hand, high activity was observed with AliBu3, and the maximum Rp was found at the beginning of the polymerization. The effect of AlR3 on the formation of active species was discussed based on these results. 相似文献