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121.
122.
Barron JA Glazier S Bernhard S Takada K Houston PL Abruña HD 《Inorganic chemistry》2003,42(5):1448-1455
The absorption and emission spectra, excited-state lifetimes, quantum yields, and electrochemical measurements have been obtained for a new series of chiral complexes based on three different chiral 2,2':6',2' '-terpyridine ligands, (-)-ctpy, (-)-[ctpy-x-ctpy], and (-)-[ctpy-b-ctpy], with one, two, or multiple Ru metal centers. The room-temperature absorption and emission maxima of [[((-)-ctpy)Ru]-(-)-[ctpy-b-ctpy]-[Ru((-)-ctpy)]](PF(6))(4) and ((-)-[ctpy-b-ctpy])-[[Ru((-)-[ctpy-b-ctpy])](PF(6))(2)](n) were shifted to lower energies and also exhibited significantly longer luminescence lifetimes when compared to [Ru((-)-ctpy)(2)](PF(6))(2), [[((-)-ctpy)Ru]-(-)-[ctpy-x-ctpy]-[Ru((-)-ctpy)]](PF(6))(4), and ((-)-[ctpy-x-ctpy])-[[Ru((-)-[ctpy-x-ctpy])](PF(6))(2)](n). In terms of their electrochemical behavior, all of the complexes studied exhibited one Ru-centered and two ligand-centered redox waves and the [[((-)-ctpy)Ru]-(-)-[ctpy-x-ctpy]-[Ru((-)-ctpy)]](PF(6))(4), ((-)-[ctpy-x-ctpy])-[[Ru((-)-[ctpy-x-ctpy])](PF(6))(2)](n), and ((-)-[ctpy-b-ctpy])-[[Ru((-)-[ctpy-b-ctpy])](PF(6))(2)](n)() complexes were found to electrodeposit upon ligand-based reduction. The difference between the formal potentials of the Ru-centered and the first ligand-centered (least negative) waves corresponded linearly with the changes in the observed emission energies. The shifts in energy are discussed using a particle-in-a-box model, and the luminescence lifetimes are discussed in terms of the structure of the excited-state manifold. 相似文献
123.
The thermal properties, i.e., heat capacity, enthalpy, entropy, and Gibbs function, and the transition behavior of the copolymer system of 4-hydroxybenzoic acid and 2,6-hydroxynaphthoic acid have been studied based on differential scanning calorimetry. The heat capacities of the glass, crystal, and anisotropic melt are shown to be largely additive on a molar basis. Additivity is lost in the two transition regions, glass transition and disordering transition. Isothermal crystallization experiments on the copolymers revealed the existence of two types of crystals which melt at high temperature (fast-grown crystals) and low temperature (slowly grown crystals). The ATHAS computation method is used to bring heat capacities of the solid state into agreement with approximate frequency spectra. The changes in heat capacity at the glass transitions occur at 434°K for the poly(oxy-1,4-benzoyl) [33.2 J/(K mol)] and at 420°K for poly(oxy-2,6-naphthoyl) [46.5 J/(K mol)]. The copolymers have a transition range of above 100°K. The anisotropic melt is linked to the well-known condis state of poly(oxy-1,4-benzoyl) by a continuous changes in disorder and mobility without an additional first-order transition. 相似文献
124.
125.
F. Bernhard 《Heat and Mass Transfer》1992,27(6):369-376
Zusammenfassung Die analytischen Lösungsfunktionen der Fourierschen Differentialgleichung für homogene, unendlich lange Zylinder bei Randbedingung 3. Art werden in verschiedenen Kennwertermittlungs-und -umrechnungsverfahren für das dynamische Verhalten industrieller Temperaturfühler in Flüssigkeiten und Gasen als Modellfunktionen benutzt. Werden dabei nur die ersten Glieder der unendlichen Reihe verwendet (Abbruchapproximation), treten für kleine Zeiten z. T. erhebliche Approximationsfehler auf. Ausgehend von der Zeitkonstantensumme eines homogenen Zylinders werden vereinfachte Approximationsmodelle niederer Ordnung angegeben, die auch für den Anfangsbereich der Übergangsfunktion nur geringe Abweichungen besitzen.
Herrn Prof. Dr.-Ing. U. Grigull zm 80. Geburtstag gewidmet 相似文献
Simplified model for the approximation of the temperature behaviour and the time response of homogeneous cylinders
The analytical solutions of Fourier differential equations for homogeneous cylinders of infinite length at convection boundary conditions of the 3th type are used to define the characteristic values and the transformation methods for the dynamic behaviour of industrial probes for temperature measurement in fluids. By using only the first terms of the series at smallt the errors of the approximation are becoming significant. Considering the sum of the time constant for homogeneous cylinders, simplified low order models for approximation are given. These models are exact even for the small time range.
Herrn Prof. Dr.-Ing. U. Grigull zm 80. Geburtstag gewidmet 相似文献
126.
Chryss Chryssomalakos Bernhard Drabant Michael Schlieker Wolfgang Weich Bruno Zumino 《Communications in Mathematical Physics》1992,147(3):635-646
Using previous results we construct theq-analogues of the left invariant vector fields of the quantum enveloping algebra corresponding to the complex Lie algebras of typeA
n–1
,B
n
,C
n
, andD
n
. These quantum vector fields are functionals over the complex quantum groupA. In the special caseA
1 it is shown that this Hopf algebra coincides withU
q
sl(2, ). 相似文献
127.
A series of alkaline uranyl carbonates, M[UO2(CO3)3]·nH2O (M=Mg2, Ca2, Sr2, Ba2, Na2Ca, and CaMg) was synthesized and characterized by inductively coupled plasma mass spectrometry (ICP-MS) and atomic absorption spectrometry (AAS) after nitric acid digestion, X-ray powder diffraction (XRD), and thermal analysis (TGA/DTA). The molecular structure of these compounds was characterized by extended X-ray absorption fine-structure (EXAFS) spectroscopy and X-ray photoelectron spectroscopy (XPS). Crystalline Ba2[UO2(CO3)3]·6H2O was obtained for the first time. The EXAFS analysis showed that this compound consists of (UO2)(CO3)3 clusters similar to the other alkaline earth uranyl carbonates. The average U-Ba distance is 3.90±0.02 Å.Fluorescence wavelengths and life times were measured using time-resolved laser-induced fluorescence spectroscopy (TRLFS). The U-O bond distances determined by EXAFS, TRLFS, XPS, and Raman spectroscopy agree within the experimental uncertainties. The spectroscopic signatures observed could be useful for identifying uranyl carbonate species adsorbed on mineral surfaces. 相似文献
128.
Oliver Mechnich Gerhard Messier Horst Kessler Michael Bernd Bernhard Kutscher 《Helvetica chimica acta》1997,80(5):1338-1354
The conformational analysis of naturally occurring cytostatic cyclic heptapeptides axinastatin 2, 3, and 4 was carried out by two-dimensional NMR spectroscopy in combination with distance-geometry (DG) and molecular-dynamics (MD) calculations in explicit solvents. The synthesized secondary metabolites were examined in (D6)DMSO. Axinastatin 2 was also investigated in CD3OH. In all structures, Pro2 is in the i + 1 position of a βI turn and Pro6 occupies the i + 2 position of a βVIa turn about the cis amide bond between residue 5 and Pro6. In all peptides, a bifurcated H-bond occurs between residue 4 CO and the amide protons of residue 1 and 7. For axinastatin 2 and 3, an Asn Ig turn was found about Asn1 and Pro2. We compared these structures with conformations of cyclic heptapeptides obtained by X-ray and NMR studies. A β-bulge motif with two β turns and one bifurcated H-bond is found as the dominating backbone conformation of cyclic all-L-heptapeptides. Axinastatin 2, 3, and 4 can be characterized by six trans and one cis amide bond resulting in a β/βVI(a)-turn motif, a conformation found for many cyclic heptapeptides. Detailed biological tests of the synthetic compounds in different human cancer cell lines indicates these axinastatins to be inactive or of low activity. 相似文献
129.
Synthesis and Crystal Structure of [Se3N2Cl]+GaCl4? [Se3N2Cl]+GaCl4? has been prepared by the reduction of [Se2NCl2]+GaC14? with SbPh3 in CH2Cl2 solution, forming red crystals, which were characterized by an X-ray structure determination. Space group P21/n, Z = 4, 1640 observed unique reflections, R = 0.050. Lattice dimensions at ? 80 °C: a = 929.4(1), b= 1078.8(1), c = 1135.7(1) pm, β = 92.026(9)°. The cations from nearly planar Se3N2 five membered rings with Se? N bond lengths from 170 to 176pm and a Se? Se bond of 242.2 pm. One of the selenium atoms is bonded to the chlorine atom. 相似文献
130.
Zhijia Wang Antonio Toffoletti Yuqi Hou Jianzhang Zhao Antonio Barbon Bernhard Dick 《Chemical science》2021,12(8):2829
The triplet state lifetimes of organic chromophores are crucial for fundamental photochemistry studies as well as applications as photosensitizers in photocatalysis, photovoltaics, photodynamic therapy and photon upconversion. It is noteworthy that the triplet state lifetime of a chromophore can vary significantly for its analogues, while the exact reason was rarely studied. Herein with a few exemplars of typical BODIPY derivatives, which show triplet lifetimes varying up to 110-fold (1.4–160 μs), we found that for these derivatives with short triplet state lifetimes (ca. 1–3 μs), the electron spin polarization (ESP) pattern of the time-resolved electron paramagnetic resonance (TREPR) spectra of the triplet state is inverted at a longer delay time after laser pulse excitation, as a consequence of a strong anisotropy in the decay rates of the zero-field state sublevel of the triplet state. For the derivatives showing longer triplet state lifetimes (>50 μs), no such ESP inversion was observed. The observed fast decay of one sublevel is responsible for the short triplet state lifetime; theoretical computations indicate that it is due to a strong coupling between the Tz sublevel and the ground state mediated by the spin–orbit interaction. Another finding is that the heavy atom effect on the shortening of the triplet state lifetime is more significant for the T1 states with lower energy. To the best of our knowledge, this is the first systematic study to rationalize the short triplet state lifetime of visible-light-harvesting organic chromophores. Our results are useful for fundamental photochemistry and the design of photosensitizers showing long-lived triplet states.The electron spin polarization inversion and anisotropic decay of triplet substates explain the short triplet state lifetime of BODIPY derivatives. 相似文献