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81.
Tetsuo Kodama 《Archiv der Mathematik》1971,22(1):271-274
Ohne ZusammenfassungThe author acknowledges support received from the National Research Council of Canada, Grant A-7210.Herrn. Prof. E.Lamprecht und Herrn Dr. H.Mathieu dankt Verfasser für ihre Anmerkungen, die zu Verbesserungen der ursprünglichen Fassung führten. 相似文献
82.
Hanaoka K Kikuchi K Kojima H Urano Y Nagano T 《Journal of the American Chemical Society》2004,126(39):12470-12476
Detection of chelatable zinc (Zn(2+)) in biological studies has attracted much attention recently, because chelatable Zn(2+) plays important roles in many biological systems. Lanthanide complexes (Eu(3+), Tb(3+), etc.) have excellent spectroscopic properties for biological applications, such as long luminescence lifetimes of the order of milliseconds, a large Stoke's shift of >200 nm, and high water solubility. Herein, we present the design and synthesis of a novel lanthanide sensor molecule, [Eu-7], for detecting Zn(2+). This europium (Eu(3+)) complex employs a quinolyl ligand as both a chromophore and an acceptor for Zn(2+). Upon addition of Zn(2+) to a solution of [Eu-7], the luminescence of Eu(3+) is strongly enhanced, with high selectivity for Zn(2+) over other biologically relevant metal cations. One of the important advantages of [Eu-7] is that this complex can be excited with longer excitation wavelengths (around 340 nm) as compared with previously reported Zn(2+)-sensitive luminescent lamthanide sensors, whose excitation wavelength is at too high an energy level for biological applications. The usefulness of [Eu-7] for monitoring Zn(2+) changes in living HeLa cells was confirmed. This novel Zn(2+)-selective luminescent lanthanide chemosensor [Eu-7]should be an excellent lead compound for the development of a range of novel luminescent lanthanide chemosensors for biological applications. 相似文献
83.
We introduce a technique for computing approximate
solutions to optimization problems. If $X$ is the set
of feasible solutions, the standard goal
of approximation algorithms is to compute $x\in X$ that is an
$\varepsilon$-approximate solution in the following sense:
$$d(x) \leq (1+\varepsilon)\, d(x^*),$$
where $x^* \in X$ is an optimal solution,
$d\colon\ X\rightarrow {\Bbb R}_{\geq 0}$ is
the optimization function to be minimized, and
$\varepsilon>0$ is an input parameter.
Our approach is first to devise algorithms that
compute pseudo $\varepsilon$-approximate solutions
satisfying the bound
$$d(x) \leq d(x_R^*) + \varepsilon R,$$
where $R>0$ is a new input parameter.
Here $x^*_R$ denotes an optimal solution in the space $X_R$ of
$R$-constrained feasible solutions. The parameter $R$ provides
a stratification of $X$ in the sense that (1) $X_R \subseteq X_{R}$ for
$R < R$ and (2) $X_R = X$ for $R$ sufficiently large.
We first describe a highly efficient scheme
for converting a pseudo $\varepsilon$-approximation
algorithm into a true $\varepsilon$-approximation algorithm.
This scheme is useful because
pseudo approximation algorithms seem to be
easier to construct than $\varepsilon$-approximation algorithms.
Another benefit is that our algorithm is
automatically precision-sensitive.
We apply our technique to two problems in robotics:
(A) Euclidean Shortest Path (3ESP), namely
the shortest path for a point robot amidst polyhedral obstacles in
three dimensions, and
(B) $d_1$-optimal motion for a rod moving amidst
planar obstacles (1ORM).
Previously, no polynomial time $\varepsilon$-approximation algorithm
for (B) was known. For (A), our new solution
is simpler than previous solutions and has
an exponentially smaller complexity in terms
of the input precision. 相似文献
84.
The cationic ruthenium catalyst (Cp*RuCl2)2/AgOTf/Ligand promotes the addition reaction of carboxylic acids across olefins without beta-hydride elimination. 相似文献
85.
Kameda T Zhao C Ashida J Asakura T 《Journal of magnetic resonance (San Diego, Calif. : 1997)》2003,160(2):91-96
It is important to know the structure of silk I (Bombyx mori silk structure before spinning in the solid state) in order to understand the mechanism of fiber formation at the atomic level. In this study, 15N-dephased, 13C-observe REDOR has been carried out to determine the atomic distance of intra-molecular hydrogen bond between the 13C=O carbon of the 14th Gly residue and the 15N nitrogen of the 17th Ala residue of (AG)(6)A[1-13C]GAG[15N]AG(AG)(6) with silk I form after removal of the effect of MAS frequency on the re-coupling. The distance was determined to be 4.3A, which confirmed the intra-molecular hydrogen bonding formation between these two atomic sites. 相似文献
86.
87.
[reaction: see text] [60]Fullerenoacetyl chloride, one of the reactive derivatives of [60]fullerenoacetic acid, was isolated and identified for the first time. This acid chloride was easily synthesized in good yield from tert-butyl [60]fullerenoacetate through two steps. In the presence of 4-(dimethylamino)pyridine as a base, the acid chloride smoothly reacted with various alcohols under mild conditions to give the corresponding esters including [60]fullerene-biomolecule hybrids in moderate to high yields. 相似文献
88.
Recent theoretical advances have identified several computational algorithms that can be implemented utilizing quantum information
processing (QIP), which gives an exponential speedup over the corresponding (known) algorithms on conventional computers.
QIP makes use of the counter-intuitive properties of quantum mechanics, such as entanglement and the superposition principle.
Unfortunately it has so far been impossible to build a practical QIP system that outperforms conventional computers. Atomic
ions confined in an array of interconnected traps represent a potentially scalable approach to QIP. All basic requirements
have been experimentally demonstrated in one and two qubit experiments. The remaining task is to scale the system to many
qubits while minimizing and correcting errors in the system. While this requires extremely challenging technological improvements,
no fundamental roadblocks are currently foreseen. 相似文献
89.
Tetsuo Asaji Janez Seliger Veselko Žagar Hiroyuki Ishida 《Magnetic resonance in chemistry : MRC》2010,48(7):531-536
Proton transfer in hydrogen‐bonded organic co‐crystals of chloranilic acid with some organic bases was investigated by nuclear quadrupole resonance (NQR) spectroscopy. The 35Cl NQR frequencies of chloranilic acid molecule as well as 14N NQR frequencies of the organic base molecule were measured with the conventional pulse methods as well as double‐resonance methods, respectively. The extent of proton transfer in the O···H···N hydrogen bond was estimated from Townes–Dailey analysis of the 14N NQR parameters. The 35Cl NQR frequency and molecular geometry of chloranilic acid are correlated to the extent of proton transfer in the protonation process of the organic base molecule. It is shown that the hydrogen bond affects the π‐electron system of chloranilic acid. Geometry dependence of the O···H···N hydrogen bond, i.e. the H? N valence bond order versus the hydrogen‐bond geometry correlation is also discussed. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
90.
An acoustic field effectively affects chromatographic retention in some separation modes and, thus, can be a novel factor controlling retention. After being transmitted into the column, ultrasound energy is mostly converted into heat as a result of absorption by stationary and mobile phases. Thus, ultrasound brings about temperature increases. However, actual temperature increases measured by thermosensors are smaller than those calculated from chromatographic retention changes. In addition, larger ultrasound effects are observed in chromatographic modes involving ionic interactions. These results possibly imply that ultrasound directly influences ionic interactions involved in retention mechanisms. 相似文献