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排序方式: 共有2796条查询结果,搜索用时 31 毫秒
1.
Mitsuki Yamashita Yuna Kawasumi Yuki Tachibana Dr. Shinnosuke Horiuchi Dr. Koji Yamamoto Prof. Tetsuro Murahashi 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(5):1212-1216
Although small cyclic- and open-chain unsaturated hydrocarbon anions such as cyclopentadienide and open-chain pentadienide are used as the strongly electron-donating auxiliary ligands for metal complexes, more extended π-conjugated unsaturated hydrocarbon anions have rarely been used in coordination chemistry, despite their potential ability to serve as the multiply bridging π-ligands for metal clusters. This work reports isolation of metal chain clusters bearing the multi-dentate, open-chain extended unsaturated hydrocarbon anion ligands. The extended open-chain π-conjugated polyenyl ligands could effectively stabilize oxidized palladium chains, including an unprecedented [Pd4]4+ chain. 相似文献
2.
Hideaki Murasugi Dr. Shohei Kumagai Dr. Hiroaki Iguchi Prof. Dr. Masahiro Yamashita Dr. Shinya Takaishi 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(42):9885-9891
Crystal structures of a series of organic–inorganic hybrid gold iodide perovskites, formulated as A2[AuII2][AuIIII4] [A=methylammonium (MA) ( 1 ) and formamidinium (FA) ( 2 )], A′2[I3]1−x[AuII2]x[AuIIII4] [A′=imidazolium (IMD) ( 3 ), guanidinium (GUA) ( 4 ), dimethylammonium (DMA) ( 5 ), pyridinium (PY) ( 6 ), and piperizinium (PIP) ( 7 )], systematically changed depending on the cation size. In addition, triiodide (I3−) ions were partly incorporated into the AuI2− sites of 3 – 7 , whereas they were not incorporated into those of 1 and 2 . Such a difference comes from the size of the organic cation. Optical absorption spectra showed characteristic intervalence charge-transfer bands from AuI to AuIII species, and the optical band gap increased as the size of the cation became larger. 相似文献
3.
Tsutomu KumagaiMasaaki Tomura Jun-ichi NishidaYoshiro Yamashita 《Tetrahedron letters》2003,44(36):6845-6848
1,3-Dithiol-2-ylidene derivatives containing bis(ethynylpyridine) units were synthesized using a Pd-catalyzed reaction of the corresponding dibromide. X-Ray crystal analysis revealed unique crystal structures depending on the aromatic groups. The absorption spectra and redox properties indicated intramolecular charge-transfer interactions between the 1,3-dithiole unit and the pyridyl parts. 相似文献
4.
5.
Yamashita Hiromi Ariyuki Masao Yoshizawa Katsuhiro Kida Keiko Ohshiro Satoshi Anpo Masakazu 《Research on Chemical Intermediates》2004,30(2):235-245
The photocatalytic reactivities of chromium-containing mesoporous silica molecular sieves (Cr-HMS) under visible light irradiation have been investigated. Cr-HMS involves tetrahedral chromium oxide (Cr-oxide) moieties which are highly dispersed and incorporated in the framework of molecular sieve with two terminal Cr=O groups. In the presence of propane with molecular oxygen, a partial oxidation proceeded under visible light irradiation to produce acetone and acrolein, with high selectivity, while a complete oxidation proceeded under UV light irradiation mainly to produce CO2. The charge-transfer excited state of the tetrahedral Cr-oxide moieties plays a significant role in the photocatalytic reactions. 相似文献
6.
In this paper we focus on the problem of identifying the index sets P(x):=i|xi>0, N(x):={i|Fi(x)>0 and C(x):=i|xi=Fi(x)=0} for a solution x of the monotone nonlinear complementarity problem NCP(F). The correct identification of these sets is important from both theoretical and practical points of view. Such an identification enables us to remove complementarity conditions from the NCP and locally reduce the NCP to a system which can be dealt with more easily. We present a new technique that utilizes a sequence generated by the proximal point algorithm (PPA). Using the superlinear convergence property of PPA, we show that the proposed technique can identify the correct index sets without assuming the nondegeneracy and the local uniqueness of the solution.This work was supported in part by a Grant-in-Aid for Scientific Research from the Ministry of Education, Science, Sports and Culture of Japan.Mathematics Subject Classification (2000): 90C33, 65K10 相似文献
7.
Toshiyuki Sugawa 《Monatshefte für Mathematik》2003,139(1):61-68
The inner radius of univalence of a domain D with Poincaré density ρ
D
is the possible largest number σ such that the condition ∥ S
f
∥
D
= sup
w∈ D
ρ
D
(w)
−2∥ S
f
(z) ∥ ≤ σ implies univalence of f for a nonconstant meromorphic function f on D, where S
f
is the Schwarzian derivative of f. In this note, we give a lower bound of the inner radius of univalence for strongly starlike domains of order α in terms
of the order α.
The author was partially supported by the Ministry of Education, Grant-in-Aid for Encouragement of Young Scientists, 11740088.
A part of this work was carried out during his visit to the University of Helsinki under the exchange programme of scientists
between the Academy of Finland and the JSPS.
Received November 26, 2001; in revised form September 24, 2002
Published online May 9, 2003 相似文献
8.
We have investigated the photoluminescence (PL) properties of trace amounts of Pr and Tb in single-crystal samples of yttria-stabilized zironia (YSZ), and found that Pr of the order of 10−6 mass% and Tb of the order of 10−5 mass% in YSZ can be detected by the PL spectroscopy. The PL spectra of the YSZ samples for the 280 nm excitation were comprised of several peaks and a broad emission. The peaks were attributed to transitions of Pr3+ and Tb3+ in the YSZ samples, whereas the broad emission seemed to be attributed to the yttria-associated oxygen vacancies. The peak intensities corresponded to the amounts of Pr and Tb in the YSZ samples, the amounts of which were analyzed by glow discharge mass spectrometry. In the PL excitation spectra, but not in the photoabsorption spectra, small peaks at 376 and 381 nm were observed, and were attributed to the transitions of Tb3+ in the YSZ samples. The results of the PL excitation spectra corresponding to the Pr3+ line emissions suggest that the charge transfer occurs between the YSZ and Pr ion in it. The trace amounts of these lanthanoids in YSZ would disturb the decay process of the photoinduced electrons to the yttria-associated oxygen vacancies. 相似文献
9.
Toshiyuki Kuruma 《Zeitschrift fur Physik C Particles and Fields》1993,57(4):551-558
The top quark, once produced, should be an important window to the electroweak symmetry breaking sector. We compute electroweak radiative corrections to the decay processt→b+W + in order to extract information on the Higgs sector and to fix the background in searches for a possible new physics contribution. The large Yukawa coupling of the top quark induces a new form factor through vertex corrections and causes discrepancy from the tree-level longitudinalW-boson production fraction, but the effect is of order 1% or less form H<1 TeV. 相似文献
10.
A spinel-type structure was found in cadmium stannate CdSnO3 prepared by thermal decomposition of the hydroxostannate CdSn(OH)6 at 550–800°C. Its occurrence depends strongly on the precipitation conditions of CdSn(OH)6 from CdCl2 and Na2Sn(OH)6 aqueous solutions. In the (Cd1–xCax)SnO3 system, the spinel phase appears in the composition range of 0.0 ≤ x ≤ 0.35. The experimental results suggest the presence of cation vacancies in the spinel octahedral sites. 相似文献