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71.
The diluted-field Ising model, a random nonnegative field ferromagnetic model, is shown to have a unique Gibbs measure with probability I when the field mean is positive. Our methods involve comparisons with ordinary uniform field Ising models. They yield as a corollary a way of obtaining spontaneous magnetization through the application of a vanishing random magnetic field. The correlation lengths of this model defined as (lim
n-(1/n) log 0;
n)-1, wheren is the site on the first coordinate axis at distancen from the origin and 0;
n
is the origin ton two-point truncated correlation function, is non-random. We derive an upper bound for it in terms of the correlation length of an ordinary nonrandom model with uniform field related to the field distribution of the diluted model. 相似文献
72.
Bogumil Zelent Józef Kuśba Ignacy Gryczynski Michael L. Johnson Joseph R. Lakowicz 《Journal of fluorescence》1993,3(3):199-207
We examined the time-dependent intensity decays ofN-acetyl-l-tryptophanamide (NATA) when collisionally quenched by acrylamide in propylene glycol over a range of temperatures. The intensity decays of NATA became increasingly heterogeneous in the presence of acrylamide. The NATA intensity decays were not consistent with the Collins-Kimball radiation boundary condition (RBC) model for quenching. The steady-state Stern-Volmer plots show significant upward curvature, and quenching of NATA by acrylamide was observed even in vitrified propylene glycol, where translational diffusion cannot occur during the lifetime of the excited state. These frequencydomain and steady-state data indicate a through-space quenching interaction between NATA and acrylamide, and the results are consistent with a rate constant for quenching that depends exponentially on the fluorophore-quencher separation distance. The exponential distance-dependent rate of quenching also explains the upward curvature of the Stern-Volmer plot, and the steady-state data aid in determining the interaction distance between NATA and acrylamide. These results suggest that the distance-dependent quenching rates need to be considered in the interpretation of acrylamide quenching of proteins. 相似文献
73.
Uulke A. van der Heide Marc A. M. J. Zandvoort Ernst van Faassen Gijs van Ginkel Yehudi K. Levine 《Journal of fluorescence》1993,3(4):271-279
Measurements of fluorescence depolarization decays are widely used to obtain information about the molecular order and rotational dynamics of fluorescent probe molecules in membrane systems. This information is obtained by least-squares fits of the experimental data to the predictions of physical models for motion. Here we present a critical review of the ways and means of the data analysis and address the question how and why totally different models such as Brownian rotational diffusion and wobble-in-cone provide such convincing fits to the fluorescence anistropy decay curves. We show that while these models are useful for investigating the general trends in the behavior of the probe molecules, they fail to describe the underlying motional processes. We propose to remedy this situation with a model in which the probe molecules undergo fast, though restricted local motions within a slowly rotating cage in the lipid bilayer structure. The cage may be envisaged as a free volume cavity between the lipid molecules, so that its position and orientation change with the internal conformational motions of the lipid chains. This approach may be considered to be a synthesis of the wobble-in-cone and Brownian rotational diffusion models. Importantly, this compound motion model appears to provide a consistent picture of fluorescent probe behavior in both oriented lipid bilayers and lipid vesicle systems. 相似文献
74.
A new calix[4]crown chemosensor based on dual sensing probes reveals Pb2+ ion selectivity over other metal ions, which arises from a hypsochromic shift of azo units in UV spectrum as well as a fluorescence enhancement of pyrenyl parts in fluorescence spectrum via a suppressed FRET. 相似文献
75.
We investigate a piecewise linear (area-preserving) mapT describing two coupled baker transformations on two squares, with coupling parameter 0c1. The resulting dynamical system is Kolmogorov for anyc0. For rational values ofc, we construct a generating partition on whichT induces a Markov chain. This Markov structure is used to discuss the decay of correlation functions: exponential decay is found for a class of functions related to the partition. Explicit results are given forc=2–n. The macroscopic analog of our model is a leaking process between two (badly) stirred containers: according to the Markov analysis, the corresponding progress variable decays exponentially, but the rate coefficients characterizing this decay are not those determined from the one-way flux across the cell boundary. The validity of the macroscopic rate law is discussed. 相似文献
76.
4,5-二溴苯基荧光酮-溴化十六烷基三甲铵荧光熄灭法测定微量铁 总被引:2,自引:0,他引:2
本文利用DBPF为荧光试剂,在大量CTMAB存在下,用荧光熄灭法测定微量铁,λ_(ex)为362nm,λ_(em)560nm。线性范围为0.002~0.12μg/mL。三元络合物中,Fe:DBPF=1:3。 相似文献
77.
Hiroshi Ikeda Takumi Sugiyama Akihiko Ueno 《Journal of inclusion phenomena and macrocyclic chemistry》2007,57(1-4):83-87
A new chemosensor for larger guests was prepared. The new chemosensor bears hydrophobic units at the primary hydroxy side
and a dansyl unit at the secondary hydroxy side of β-cyclodextrin. Due to the hydrophobic units, the new chemosensor is sensitive
to large or slender guests such as SDS and insensitive to 1-adamantanol, which is a good guest for the natural β-CD. 相似文献
78.
规整链球型含C_(60)聚(丙烯酸β-羟乙酯)的合成及其在水中的自组装 总被引:2,自引:0,他引:2
C60 由于其独特的物理化学性质 ,在生命科学中引起了人们的广泛兴趣 .例如 :水溶性C60 的羧酸衍生物 ,羟基取代C60 ,C60 的氨基酸水溶性衍生的合成已有报道[1~ 3] ,并被用来研究C60 的生物化学及医学活性 .Tokuyama[4 ] 等合成了酶功能化C60及与核酸连接的C60 ,研究并证明了它的细胞毒性及G 选择DNA切割能力等生化活性 .Friedman[5]等合成了水溶性C60 的羧酸衍生物 ,研究了它对HIV 1艾滋病毒的抑制作用 ,此外 ,关于不同C60含量的C60 蛋白质衍生物的合成及性质的研究也有报道[6] .C60 是一个直径为 0 71… 相似文献
79.
Summary The highly complex matrix of diesel particulate extracts was analyzed for nitrated polycyclic aromatic hydrocarbons (nitro-PAH)
using fused-silica capillary-column gas chromatography along with a thermionic nitrogen-phosphorus detector (TID) and high-performance
liquid chromatography followed by on-line catalytic reduction of the nitro-PAH to amino-PAH and subsequent fluorescence detection.
Positive isomer identification and quantitation of nitro-PAH are from retention times of authentic standards and their mass
spectra. The ease of nitro-PAH formation by nitration of PAH raises the question regarding the origin of these species, whether
they are produced as “native” products during the engine combustion process and/or in the exhaust, or instead, formed as the
result of chemical conversion to produce artifacts during the sampling procedure. This problem is assessed examing 1-nitropyrene-concentration
in particulates of three light-duty diesel engines for different sampling times. 1-Nitropyrene concentrations show only a
moderate increase with sampling time under average sampling conditions.
Presented at the 15th International Symposium on Chromatography, Nürnberg, October 1984 相似文献
80.
Fluorescence decay and quenching of pyrene labels on copolymers of 2-acrylamido-2-methylpropanesulphonic acid (AMPS) and N,N-dimethylacrylamide were observed in dilute salt-free aqueous solutions as a function of the mole fraction FAMPS of AMPS from 0 to 0.896. Monoexponential decay was found for the samples of FAMPS<0.35 and biexponential decay for the samples of FAMPS>0.35. The fast decay component is 80%, and the averaged lifetime 〈τ〉 and lifetime τ1 of the fast decay is decreased with increasing FAMPS. Quenching efficiency of Cu2+, I−, CH3NO2, and dinitrobenzene to the pyrene label was investigated in the framework of Stern-Volmer plot. With increasing FAMPS the quenching efficiency of Cu2+ is increased while that of I− decreased. For the neutral quenchers, the quenching rate constant kq increases when FAMPS<0.449 then decreases, showing a decline of accessibility to the pyrene label. These results were interpreted consistently with the counterion condensation concept, where condensed counterions caused the polyelectrolyte chains to aggregate. The existence of less-polar “temporal aggregated domain” in highly charged polyelectrolytes appears to lead to the slower decay and lower accessibility of the pyrene labels. 相似文献