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排序方式: 共有62条查询结果,搜索用时 15 毫秒
1.
M. Fischer W. Knoche P. D. I. Fletcher B. H. Robinson N. C. White 《Colloid and polymer science》1980,258(6):733-742
Summary Complex formation between divalent metal ions and the hydrophilic murexide anion in the presence of anionic micelles has been employed to study aspects of micelle formation, the binding of divalent metal ions to micelles, and the kinetics of metal-complex formation in the presence of micelles.
With 8 figures and 1 table
Dedicated to Prof.G. Rehage on the occasion of his 60th birthday. 相似文献
Zusammenfassung Die Komplexbildung zweiwertiger Metallionen mit dem hydrophilen Indikator Murexid wurde in Gegenwart anionischer Mizellen untersucht. Die Indikatorreaktion wurde benutzt, um Aussagen über Mizellbildung, Bindung zweiwertiger Metallionen an Mizellen und die Kinetik der Metallkomplexbildung bei Anwesenheit von Mizellen zu erhalten.
With 8 figures and 1 table
Dedicated to Prof.G. Rehage on the occasion of his 60th birthday. 相似文献
2.
Jannik Brückmann Dr. Carolin Müller Tamar Maisuradze Dr. Alexander K. Mengele Dr. Djawed Nauroozi Sven Fauth Andreas Gruber Prof. Dr. Stefanie Gräfe Prof. Dr. Kerstin Leopold Dr. Stephan Kupfer Prof. Dr. Benjamin Dietzek-Ivanšić Prof. Dr. Sven Rau 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(51):e202200766
The synthesis and detailed characterization of a new Ru polypyridine complex containing a heteroditopic bridging ligand with previously unexplored metal-metal distances is presented. Due to the twisted geometry of the novel ligand, the resultant division of the ligand in two distinct subunits leads to steady state as well as excited state properties of the corresponding mononuclear Ru(II) polypyridine complex resembling those of prototype [Ru(bpy)3]2+ (bpy=2,2'-bipyridine). The localization of the initially optically excited and the nature of the long-lived excited states on the Ru-facing ligand spheres is evaluated by resonance Raman and fs-TA spectroscopy, respectively, and supported by DFT and TDDFT calculations. Coordination of a second metal (Zn or Rh) to the available bis-pyrimidyl-like coordination sphere strongly influences the frontier orbitals, apparent by, for example, luminescence quenching. Thus, the new bridging ligand motif offers electronic properties, which can be adjusted by the nature of the second metal center. Using the heterodinuclear Ru−Rh complex, visible light-driven reduction of NAD+ to NADH was achieved, highlighting the potential of this system for photocatalytic applications. 相似文献
3.
Jannik Brückmann Dr. Carolin Müller Ilse Friedländer Dr. Alexander K. Mengele Prof. Kalina Peneva Prof. Benjamin Dietzek-Ivanšić Prof. Sven Rau 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(61):e202201931
The ambitious goal of artificial photosynthesis is to develop active systems that mimic nature and use light to split water into hydrogen and oxygen. Intramolecular design concepts are particularly promising. Herein, we firstly present an intramolecular photocatalyst integrating a perylene-based light-harvesting moiety and a catalytic rhodium center ( RhIIIphenPer ). The excited-state dynamics were investigated by means of steady-state and time-resolved absorption and emission spectroscopy. The studies reveal that photoexcitation of RhIIIphenPer yields the formation of a charge-separated intermediate, namely RhIIphenPer ⋅ + , that results in a catalytically active species in the presence of protons. 相似文献
4.
D. Brüggemann J. Hertzberg B. Wies Y. Waschke R. Noll K.-F. Knoche G. Herziger 《Applied physics. B, Lasers and optics》1992,55(4):378-380
An optical parametric oscillator (OPO), as a novel kind of broadband Stokes source, is employed for coherent anti-Stokes Raman spectroscopy (CARS). Compared to the conventional dye laser configuration OPO-CARS offers practical advantages. The tunable OPO allows a fast and comfortable frequency tuning. The excitation bandwidth of about 35 cm–1 (FWHM) limits the spectral range of effective and stable single pulse CARS generation but can be used to enhance selected spectral structures. 相似文献
5.
We present a new exact algorithm for the Steiner tree problem in edge-weighted graphs. Our algorithm improves the classical dynamic programming approach by Dreyfus and Wagner. We achieve a significantly better practical performance via pruning and future costs, a generalization of a well-known concept to speed up shortest path computations. Our algorithm matches the best known worst-case run time and has a fast, often superior, practical performance: on some large instances originating from VLSI design, previous best run times are improved upon by orders of magnitudes. We are also able to solve larger instances of the d-dimensional rectilinear Steiner tree problem for \(d \in \{3, 4, 5\}\), whose Hanan grids contain up to several millions of edges. 相似文献
6.
Jannik Matuschke S. Thomas McCormick Gianpaolo Oriolo Britta Peis Martin Skutella 《Operations Research Letters》2017,45(1):53-59
We present a new robust optimization model for the problem of maximizing the amount of flow surviving the attack of an interdictor. Given some path flow, our model allows the interdictor to specify the amount of flow removed from each path individually. In contrast to previous models, for which no efficient algorithms are known, the most important basic variants of our model can be solved in poly-time. We also consider extensions where there is a budget to set the interdiction costs. 相似文献
7.
For diffusion controlled reactions in solution a theory is proposed which includes the diffusion process, the lifetime of an encounter complex, and the rotation of the reacting species in the encounter complex. For some types of reaction the analytical equations of this scheme are solved and discussed. 相似文献
8.
9.
Comparison of monomethoxy‐, dimethoxy‐, and trimethoxysilane anchor groups for surface‐initiated RAFT polymerization from silica surfaces
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Dennis Huebner Vanessa Koch Bastian Ebeling Jannik Mechau Judith Elisabeth Steinhoff Philipp Vana 《Journal of polymer science. Part A, Polymer chemistry》2015,53(1):103-113
The immobilization of reversible addition–fragmentation chain transfer (RAFT) agents on silica for surface‐initiated RAFT polymerizations (SI‐RAFT) via the Z‐group approach was studied systematically in dependence of the functionality of the RAFT‐agent anchor group. Monoalkoxy‐, dialkoxy‐, and trialkoxy silyl ether groups were incorporated into trithiocarbonate‐type RAFT agents and bound to planar silica surfaces as well as to silica nanoparticles. The immobilization efficiency and the structure of the bound RAFT‐agent film varied strongly in dependence of the used solvent (toluene vs. 1,2‐dimethoxyethane) and the anchor group functionality, as evidenced by atomic force microscopy, transmission electron microscopy, dynamic light scattering, and UV/Vis spectroscopy. Surface‐initiated RAFT polymerizations using functionalized silica nanoparticles revealed that grafted oligomers, which often occur in SI‐RAFT, are not formed within the crosslinked structures that originate from the immobilization, and that RAFT‐agent films that show less aggregation during the immobilization are more efficient during SI‐RAFT in terms of polymer grafting density. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015 , 53, 103–113 相似文献
10.
Kavitha Telikepalli Király Tamás Matuschke Jannik Schlotter Ildikó Schmidt-Kraepelin Ulrike 《Mathematical Programming》2022,192(1-2):567-595
Mathematical Programming - Let G be a digraph where every node has preferences over its incoming edges. The preferences of a node extend naturally to preferences over branchings, i.e., directed... 相似文献