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排序方式: 共有96条查询结果,搜索用时 15 毫秒
21.
Köhler T Hodgson MC Seidel D Veauthier JM Meyer S Lynch V Boyd PD Brothers PJ Sessler JL 《Chemical communications (Cambridge, England)》2004,(9):1060-1061
In contrast to octaethylporphyrin, which forms a very labile bis-BF(2) complex, treatment of the hexa- and octapyrrolic expanded porphyrins amethyrin and [32]octaphyrin with BF(3).Et(2) under standard reaction and work-up conditions gives rise to stable, non-labile mono- and bis-BF(2) complexes; these were readily characterised by, inter alia, X-ray diffraction analyses. 相似文献
22.
23.
Michael Quinones Yazhou Zhang Penelope Riascos Huey‐Min Hwang Winfred G. Aker Xiaojia He Ruomei Gao 《Photochemistry and photobiology》2014,90(2):374-379
Many biomolecules contain photoactive reducing agents, such as reduced nicotinamide adenine dinucleotide (NADH) and 6‐thioguanine (6‐TG) incorporated into DNA through drug metabolism. These reducing agents may produce reactive oxygen species under UVA irradiation or act as electron donors in various media. The interactions of C60 fullerenes with biological reductants and light energy, especially via the Type‐I electron‐transfer mechanism, are not fully understood although these factors are often involved in toxicity assessments. The two reductants employed in this work were NADH for aqueous solutions and 6‐TG for organic solvents. Using steady‐state photolysis and electrochemical techniques, we showed that under visible light irradiation, the presence of reducing agents enhanced C60‐mediated Type‐I reactions that generate superoxide anion (O2.?) at the expense of singlet oxygen (1O2) production. The quantum yield of O2.? production upon visible light irradiation of C60 is estimated below 0.2 in dipolar aprotic media, indicating that the majority of triplet C60 deactivate via Type‐II pathway. Upon UVA irradiation, however, both C60 and NADH undergo photochemical reactions to produce O2.?, which could lead to a possible synergistic toxicity effects. C60 photosensitization via Type‐I pathway is not observed in the absence of reducing agents. 相似文献
24.
Brothers PJ 《Chemical communications (Cambridge, England)》2008,(18):2090-2102
The coordination of boron to a range of polypyrrole-containing ligands is explored in this feature article. The boron dipyrromethenes are well-known as laser dyes and fluorescent labels in biology. Subphthalocyanine and subporphyrin macrocycles containing only three pyrrole rings can exist only when templated by a central boron atom. Boron complexes of expanded porphyrins (six or eight pyrroles) can complex boron in dipyrromethene (but not bipyrrole) sites. The primary focus of the article is on boron porphyrin and corrole complexes, where the tight fit of two boron atoms within the very constrained coordination site gives rise to unexpected chemistry at both boron and the porphyrin ligand. These unusual features are described and reasons for their occurrence postulated. 相似文献
25.
Convergence of Rothe's method for the fully nonlinear parabolic equation ut+F(D2u, Du, u, x, t)=0 is considered under some continuity assumptions on F. We show that the Rothe solutions are Lipschitz in time, Hölder in space, and they solve the equation in the viscosity sense. As an immediate corollary we get Lipschitz behavior in time of the viscosity solutions of our equation. 相似文献
26.
Penelope Schobinger-Papamantellos A. Niggli 《Journal of Physics and Chemistry of Solids》1981,42(7):583-586
The chemical and magnetic structures of the intermetallic compound Nd5Ge4 were determined from neutron diffraction powder data. In contrast to the isomorphous heavy rare-earth compounds, Nd5Ge4 orders with a canted ferrimagnetic arrangement below Tc = 52 K. The ordered Nd moments are 2.6, 3.1 and 2.4 μB for the three sites respectively. The magnetic space group is Pnm'a' and the plane of easy magnetization (010). 相似文献
27.
V.Nambi Aiyar Penelope W. Codding K.Ann Kerr M.H. Benn Alan J. Jones 《Tetrahedron letters》1981,22(6):483-484
The structure of delphinifoline, a minor alkaloid of DC, was established by spectroscopic methods, and X-ray crystallography. 相似文献
28.
Ohne ZusammenfassungMit 1 Abbildung 相似文献
29.
Lewis PA Inman CE Yao Y Tour JM Hutchison JE Weiss PS 《Journal of the American Chemical Society》2004,126(39):12214-12215
We have studied oligo(phenylene-ethynylene)s inserted into amide-containing alkanethiol self-assembled monolayers using scanning tunneling microscopy to demonstrate switching based on chemical functionality of the environment of the inserted molecules. The molecules show stability in two conductance states: an ON and an OFF state. We demonstrate bias-dependent switching due to hydrogen bonding between the inserted oligo(phenylene-ethynylene) and the matrix molecules. In addition, the inserted molecules exhibit fewer switching events than previously reported for alkanethiol matrixes, which we attribute to the rigidity of the hydrogen-bonded matrix. 相似文献
30.
Zusammenfassung Nach Dehydratation des Germanat-Zeoliths Tl3HGe7O16· · 4 H2O bildet sich bei 650°C das zu Me2Ge4O9 (Me=Na, K, Rb) isotype Thalliumtetragermanat. Durch Entwässerung bei 700°C entsteht aus dem Zeolith ein stabiles Hexagermanat Tl2Ge6O13, welches auch aus Schmelzen der Zusammensetzung Tl2O:GeO2=1:6 gewonnen wird. Mit Hilfe von DK- undWeissenberg-Aufnahmen werden für die rhombische Elementarzelle die Gitterparameter:a=37,247,b=13,743 undc=4,733 kX·E. ermittelt. Wahrscheinliche Raumgruppe ist D
2h
17
. 相似文献