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1.
Thomas Pautzsch Elisabeth Klemm 《Journal of polymer science. Part A, Polymer chemistry》2004,42(12):2911-2919
Poly{bis(4,4′‐tert‐butyl‐2,2′‐bipyridine)–(2,2′‐bipyridine‐5,5′‐diyl‐[1,4‐phenylene])–ruthenium(II)bishexafluorophosphate} ( 3a ), poly{bis(4,4′‐tert‐butyl‐2,2′‐bipyridine)–(2,2′‐bipyridine‐4,4′‐diyl‐[1,4‐phenylene])–ruthenium(II)bishexafluorophosphate} ( 3b ), and poly{bis(2,2′‐bipyridine)–(2,2′‐bipyridine‐5,5′‐diyl‐[1,4‐phenylene])–ruthenium(II)bishexafluorophosphate} ( 3c ) were synthesized by the Suzuki coupling reaction. The alternating structure of the copolymers was confirmed by 1H and 13C NMR and elemental analysis. The polymers showed, by ultraviolet–visible, the π–π* absorption of the polymer backbone (320–380 nm) and at a lower energy attributed to the d–π* metal‐to‐ligand charge‐transfer absorption (450 nm for linear 3a and 480 nm for angular 3b ). The polymers were characterized by a monomodal molecular weight distribution. The degree of polymerization was approximately 8 for polymer 3b and 28 for polymer 3d . © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 2911–2919, 2004 相似文献
2.
Thomas Pautzsch Lars Blankenburg Elisabeth Klemm 《Journal of polymer science. Part A, Polymer chemistry》2004,42(3):722-732
A series of novel π-conjugated polymers containing ruthenium bipyridine complexes was synthesized by a cross-coupling reaction and characterized. These polymers exhibit absorption maxima around 330–350 nm (π-π*) and 460–500 nm metal-to-ligand charge transfer (MLCT), respectively. They are soluble in common organic solvents, and all polymers can be converted into transparent films. We investigated the influence of different donating and acceptor diethynylarenes of the ultraviolet-visible spectra. The oxidation potential, which was measured by cyclic- and square-wave voltametry, showed a typical Ru2+/3+ exhibited at 1.25 V versus the saturated calomel electrode. The polymers were further characterized with photoluminescence measurements. When excited at 442 nm ( 11a ), the polymer exhibited an emission peak at 690 nm. This peak was attributed to the MLCT states. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 722–732, 2004 相似文献
3.
4.
In order to replace silicones in some of their biomedical applications, e.g. syringe lubrication, implants ets., a series of digermoxanes (R1R2R3Ge)2O (R = n–alkyl, aryl) were synthesized. These compounds are thermally stable oils; their viscosities, depending on the nature of substituents, lie in the range 1–72 cPo (mPa s) at 20°C. 相似文献
5.
Frédéric Coquel Thierry Gallouët Jean-Marc Hérard Nicolas Seguin 《Comptes Rendus Mathematique》2002,334(10):927-932
Closure laws for interfacial pressure and interfacial velocity are proposed within the frame work of two-pressure two-phase flow models. These enable us to ensure positivity of void fractions, mass fractions and internal energies when investigating field by field waves in the Riemann problem. To cite this article: F. Coquel et al., C. R. Acad. Sci. Paris, Ser. I 334 (2002) 927–932. 相似文献
6.
The surface body is a generalization of the floating body. Its relation to p-affine surface area is studied. 相似文献
7.
Aziridines react with trifluoromethyl hypofluorite at ? 40°C to produce mixtures of 1-(aziridine)carbonyl fluoride and 1-fluoroaziridine , the proportions of which depend on steric effects. Several compounds react with starting materials to give 1, 1′-(carbonyl)bisaziridines . Most compounds and all compounds are isolated. Chemical properties and ir and nmr data of , , are described; the formation of an isocyanate and a substituted urea from a compound is observed. A mechanism for this reaction is suggested. 相似文献
8.
Steric and electronic influences of various substituted pyridines support the hypothesis of the coordination of pyridine in the manganese porphyrin-catalysed epoxidation of olefins with sodium hypochlorite solution. 相似文献
9.
C. Auguet J. L. Seguin F. Martorell F. Moll V. Torra J. Lerchner 《Journal of Thermal Analysis and Calorimetry》2006,86(2):521-529
Micro-calorimetric
devices using Si-based sensors are very useful for the study of gas–solid
reactions, in which very low mass of reactants are necessary. But in fact
the consequence of using flat detectors is an increase of the uncertainty
in the measured energy. In this work a calorimetric gas sensor based on Xensor
chip is analysed studying the local x–y
contributions of dissipation to the sensitivity related to the value in the
centre. We study also the effects of the gas-flow on the sensitivity, comparing
the results obtained with two Xensor type chips. Finally we carry out a deeper
analysis of the x–y effects on the
calorimetric detector for dissipations in the reactant shell extremely close
to the detector surface to visualize the link between the power density distribution
and the output signal. 相似文献
10.
Joachim Heidberg Elisabeth Kampshoff Helmut Stein Helmut Weiss Michael Warskulat 《Mikrochimica acta》1988,94(1-6):105-108
Sample/spectrum relationships are investigated using both a low resolution rapid-scanning NIR monochromator and a Fourier transform instrument capable of high resolution and are evaluated in terms of whether or not the resolution of the instrument is sufficient for measuring the natural bandwidths corresponding to the sample. Based on the sample/spectrum relationship a criterion is developed which must be followed in order to apply either derivative spectroscopy or deconvolution to enhance the resolution of overlapped bands without generating spectral artifacts. 相似文献