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21.
22.
L. Sommer 《Fresenius' Journal of Analytical Chemistry》1966,220(3):222-223
Ohne Zusammenfassung 相似文献
23.
Gavrilova AL Qin CJ Sommer RD Rheingold AL Bosnich B 《Journal of the American Chemical Society》2002,124(8):1714-1722
The di-Co(2+) complex, [Co(2+)(mu-OH)(oxapyme)Co(2+)(H(2)O)](+), contains an unsymmetrical binucleating ligand (oxapyme) which provides five- and six-coordinate metal sites when a hydroxide bridge is introduced. This complex absorbs 1 equiv of O(2) irreversibly in solution, producing an unstable di-Co(3+) oxygenated product. The oxygenated product has been studied at low temperatures, where its electronic absorption and (1)H NMR spectra were recorded. It is probable that the oxygenation reaction involves a one-site addition two-metal oxidation reaction to produce an end-on-bonded peroxide ligand at the available coordination site, giving the complex [Co(3+)(mu-OH)(oxapyme)Co(3+)(mu(1)-O(2))](+). Addition of 1 equiv of HClO(4) to this oxygenation product gives a stable peroxide complex, [Co(3+)(mu,eta(1):eta(2)-O(2))(oxapyme)Co(3+)](2+), where one of the oxygen atoms bridges the two metals and is sideways bonded to one of the metals. The formation of this stable complex involves expulsion of the OH(-) bridge. Addition of NO(2)(-) to the sideways-bonded peroxide complex leads to the formation of another stable complex, [Co(3+)(mu,eta(1):eta(1)-O(2))(oxapyme)Co(3+)(NO(2))](+), where the peroxide forms a classic di-end-on bridge to the two metals. Both of these complexes have been fully characterized. Addition of acid to this second stable dioxygen complex leads to the release of HNO(2) and the formation of the mu,eta(1):eta(2) sideways-bonded peroxide complex. 相似文献
24.
D. Grunenberg D. Sommer K. H. Koch 《Fresenius' Journal of Analytical Chemistry》1995,353(5-8):514-520
For the analysis of surfaces with poor conductivity the use of the direct current sputter process, usual in SNMS, produces unreproducible depth profiles with often widened transition widths. An efficient method for eliminating static charging in the case of non-coducting samples is the use of a high-frequency discharge. By comparison of the direct current mode with high frequency mode it is shown, that the use of SNMS with HF sputtering is the universal analysis method for most matrices, technical surfaces as well as oxidic materials. For non-conducting or poorly conducting samples, however, matrix-adjusted factors are to be used. 相似文献
25.
For the analysis of surfaces with poor conductivity the use of the “direct current sputter process”, usual in SNMS, produces unreproducible depth profiles with often widened transition widths. An efficient method for eliminating static charging in the case of non-coducting samples is the use of a high-frequency discharge. By comparison of the direct current mode with high frequency mode it is shown, that the use of SNMS with HF sputtering is the universal analysis method for most matrices, technical surfaces as well as oxidic materials. For non-conducting or poorly conducting samples, however, matrix-adjusted factors are to be used. 相似文献
26.
Beurer E Venkataraman NV Sommer M Spencer ND 《Langmuir : the ACS journal of surfaces and colloids》2012,28(6):3159-3166
An orthogonal, charge-density-versus-net-charge, surface-chemical gradient, composed of ternary mixed self-assembled monolayers, has been prepared from three hydrophilic components: positively chargeable amine-terminated, negatively chargeable carboxylic-acid-terminated, and hydroxyl-terminated alkanethiols, with the latter bearing a slight negative charge in electrolytes. The chemical composition and its distribution have been monitored by X-ray photoelectron spectroscopy. The adsorption behavior of negatively charged SiO(2) nanoparticles and positively charged amine-modified SiO(2) nanoparticles has been studied. Additionally, negatively charged proteins (bovine serum albumin and fibrinogen) and positively charged proteins (lysozyme) were adsorbed on the gradients. Negatively charged nanoparticles and proteins adsorb mainly in the positively charged region and vice versa, illustrating that the adsorption behavior is mainly influenced by electrostatic interactions, and showing the potential of the gradient for sorting applications. Despite literature reports to the contrary, no area was found that was completely resistant to protein adsorption. 相似文献
27.
Steffen Blaurock Thomas Koch Olaf Kühl Peter Lönnecke Felicite Majoumo René Sommer 《Phosphorus, sulfur, and silicon and the related elements》2013,188(6-7):1451-1456
Substituted bifunctional phosphorus-based ligands HX(CRR') n PR"H (or -PR" 2 ) [where X = O, S, NR', (substituted) cyclopentadienyl; n = 1, 2, 3; R, R', R" = alkyl, aryl, H] were employed as bridging ligands in the synthesis of early/late bridged transition metal complexes. Synthetic routes to the bifunctional ligands were also developed. First, mononuclear complexes, such as [TpZr(OCH 2 PPh 2 ) 3 ] (Tp = trispyrazolylborato), [Cp 2 Zr(1-O-2-PHR-C 6 H 10 )(Me)] (R = 2,4,6-Pr i 3 C 6 H 2 (Tipp)), [Cp 2 Zr(SCH 2 CH 2 PHR) 2 ] (R = Ph, Mes, Tipp), and phosphinoferrocene derivatives, were prepared. These complexes are suitable precursors for the introduction of a second metal (as in, for example, [TpZr( w -OCH 2 PPh 2 ) 3 Mo(CO) 3 ]). 相似文献
28.
Using the continous Edwards–chain model the simultaneous influence of harmonic–like constraints and of a stochastic order parameter field on the segment orientation in polymer networks is investigated. The harmonic potential reduces the orientation order parameter in comparison to the value for an unconstrained freely jointed chain. This reference value is approached from below in the case of strong topological constraints. The introduction of a stochastic order parameter field enlarges the orientation but the reference value remains the upper boundary. 相似文献
29.
30.
We studied the conformations of polymer chains embedded in regular lamellar matrices such as microphase-separated block copolymer melts or lipid/water systems. In such quasi-one-dimensional systems, the host plays the role of a nearly-periodic external potential. A probe chain can get trapped with the localization length L at isolated defects, when its degree of polymerization N exceeds a cross-over value NL. Interestingly, the radius of gyration, Rg, of the chain displays a minimum as a function of the defect density, ρ, the minimum being estimated by ρcL ≃ NL/N. Using Monte Carlo simulation, we underline the non-monotonic behavior of Rg and calculate Green's function for various defect densities. On the same vein, the mean square displacement of the monomer units at large times shows a pronounced minimum as a function of the defect density, ρ. 相似文献