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1.
About the Fluorescence Thermochromism of Acetonitrile Copper Iodide with Dibenzo-18-Crown-6 Copper iodide reacts in actonitrile solution with dibenzo-18-crown-6 to form a compound,(CuJ)4(CH3CN)4(db-18-c-6), which fluoresces yellow at 298K, but pink at 77 K. It decomposes at 55.3°C. (5 Torr) by lost of acetonitrile and a heterogeneous mixture of copper iodide and polyether results. In absence of dibenzo-18-crown-6, copper iodide forms with acetonitrile a heterogeneous mixture of copper iodide and polyether results. In absence of dibenzo-18-crown-6, copper iodide forms with acetonitrile a solvate CuJ. CH3CN. It also shows fluorescence thermochromism (yellow at 298 K, but green at 77 k) but decomposes at 0°C and 760 Torr. The luminescences pectra of the macrocyclic polyether complex at 298 K is redshifted. This probably results from intersection between the crown and the acetonitrile copper iodide. 相似文献
2.
With
, we here construct, for each positive integer N, a smooth function
of degree zero so that there must be at least N singular points for any map that minimizes the energy
in the family
. The infimum of over U(g) is strictly smaller than the infimum of over the continuous functions in U(g). There are some generalizations to higher dimensions.Research partially supported by the National Science FoundationResearch supported by an Alfred P. Sloan Graduate Fellowship 相似文献
3.
On Fluorescent Compounds of Copper(I) Iodide with Aromatic Nitrogenous Bases The easily obtainable compounds of copper(I) iodide with esters of nicotinic acid, with nicotinic acid amide and nitrile, as well as with quinoline, isoquinoline and quinaldine are strongly fluorescent in ultraviolet light. They are remarkably stable against water and air, compared with analogous picoline and lutidine compounds. Only in one case (nicotinic acid hexyl ester-copper(I) iodide) the phenomenon of fluorescence thermochromism has been observed. 相似文献
4.
Highly pure chromium(II) acetate, was obtained from chromium powder and anhydrous acetic acid in the presence of a small amount of acetylhalide. CrII acetate reacts with acetyl halide in anhydrous acetic acid to sesquisolvates like CrCl2 · 3/2 CH3COOH. If one equivalent of alkali acetate or an organic nitrogen base is added to solutions of CrII acetate in acetyl halide/acetic acid mixtures, trihalochromates(II) are precipitated which are hexagonal in structure, except the ammonium and the potassium salt. With two equivalents of alkali or ammonium acetate tetrachlorochromates(II) of cesium, rubidium and ammonium are precipitated. They are tetragonal in structure (K2NiF4 type). Using pyridinium acetate with various mixtures of acetyl bromide and acetic acid, only the solvates (PyH)3(CrBr5) · 2CH3COOH is formed. 相似文献
5.
6.
Suppose Ω is a smooth domain in Rm,N is a compact smooth Riemannian manifold, andZ is a fixed compact subset of Ω having finite (m − 3)-dimensional Minkowski content (e.g.,Z ism − 3 rectifiable). We consider various spaces of harmonic mapsu: Ω →N that have a singular setZ and controlled behavior nearZ. We study the structure of such spacesH and questions of existence, uniqueness, stability, and minimality under perturbation. In caseZ = 0,H is a Banach manifold locally diffeomorphic to a submanifold of the product of the boundary data space with a finite-dimensional
space of Jacobi fields with controlled singular behavior. In this smooth case, the projection ofu εH tou |ϖΩ is Fredholm of index 0.
R. H.’s research partially supported by the National Science Foundation. 相似文献
7.
K. Hardt R. Kroth G. Mikus C. Günther M. Guttormsen H. Hübel J. Recht R. Tischler 《Zeitschrift für Physik A Hadrons and Nuclei》1982,305(1):1-7
The magnetic moment of the 11 ns, 15? isomer in204Po and the internal magnetic field of Po in Ni were determined in an in-beam recoil implantation experiment. Time-differential perturbed angular distributions of conversion electrons were measured in an iron-free orange spectrometer. The magnetic hyperfine field of ¦H(PoNi)¦=555(22) kOe is in agreement with the systematic trend for the 6p elements. Theg-factorg(15?) =0.41(2) is discussed, together with theB (E2, 15?→13?). within the shell model. 相似文献
8.
Thierry?De?PauwEmail author Robert?Hardt 《Calculus of Variations and Partial Differential Equations》2003,17(4):405-442
We consider Plateau type variational problems related to the size minimization of rectifiable currents. We realize the limit of a size minimizing sequence as a stationary varifold and a minimal set. Other examples of functionals to be minimized include the integral over the underlying carrying set of a power q of the multiplicity function, with
.Because minimizing sequences may have unbounded mass we make use of a more general object called a rectifiable scan for describing the limit. This concept is motivated by the possibility of recovering a flat chain from a sufficiently large collection of its slices. In case the given boundary is smooth and compact, the limiting scan has finite mass and corresponds to a rectifiable current.Received: 11 February 2002, Accepted: 16 June 2002, Published online: 17 December 2002Mathematics Subject Classification (2000):
49Q15, 28A75Thierry De Pauw: The research of the first author was supported by a Marie Curie fellowship of the European Community program Human Potential under contract HMPF-CT-2001-01235Robert Hardt: The research of the second author was partially supported by NSF grant DMS-0072486 相似文献
9.
T Wang M Barber I Hardt D B Kassel 《Rapid communications in mass spectrometry : RCM》2001,15(22):2067-2075
An automated packed-column semi-preparative supercritical fluid chromatography/mass spectrometry (SFC/MS) system incorporating mass-directed fraction collection has been designed and implemented as an alternative to preparative HPLC and preparative HPLC/MS (PrepLC/MS) for the purification of pharmaceutical compounds. The system incorporates a single quadrupole mass spectrometer and a supercritical fluid chromatograph. Separations were achieved using a binary solvent system consisting of carbon dioxide and methanol. Purification of SFC-separated compounds was achieved incorporating mass-directed fraction collection, enabling selective isolation of the target molecular weight compound and eliminating the collection of undesired compounds (e.g., by-products, excess starting materials, etc.). Cross contamination between fractions and recoveries of the system were investigated. Mass spectrometer ionization with basic mobile additives is discussed, and examples of preparative SFC/MS chiral separations are presented. Early experiences suggest SFC will be a powerful and complementary technique to HPLC for the purification of pharmaceutical compounds. 相似文献
10.