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31.
Dietmar Stuewer 《Fresenius' Journal of Analytical Chemistry》1990,337(7):737-742
Summary Among recent MS techniques for elemental analysis, Glow Discharge Mass Spectrometry (GDMS) covers the field of direct analysis of conducting and semiconducting solids. In GDMS, a glow discharge in a working gas — usually Ar — at reduced pressure serves to atomize a solid sample by cathodic sputtering and to ionize the vapourized atoms. Ions are separated according to mass by a quadrupole filter (with low mass resolution) or a double focusing device (with high mass resolution). Use of a working gas implies the appearance of spectral interferences by molecular ions. Analysis may be impeded by these interferences, even in the case of high mass resolution. GDMS shows convincing analytical performance. Detection limits in the low ng/g region and even below can easily be realized. Precision is normally in the low percentage region, and a dynamic region of about nine orders of magnitude may be covered. Matrix effects are of no significant influence, and elemental sensitivities are within one order of magnitude. Semiquantitative analysis without standards is possible with limited accuracy, which is of considerable practical interest in the sub-microtrace region. Application experiences have mainly been gathered in analysis of very pure materials and semiconductors. GDMS has also been applied successfully for analytical characterization of technical surface layers. 相似文献
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Sabine Rentsch Gudrun Hermann Mark Bischoff Dietmar Strehlow Manfred Rentsch 《Photochemistry and photobiology》1997,66(5):585-590
Abstract— The excited state behavior of the red light-absorbing form of phytochrome (Pr) was studied on the femtosecond time scale. After excitation of Pr with 75 fs laser pulses at 616 nm the kinetics of the transient absorption changes was recorded at selected wavelengths probing mainly the bleaching of the Pr ground-state absorption and the stimulated emission. The kinetic data obtained indicate the population of an excited state with a 3 ps lifetime immediately after excitation. This state precedes the formation of another excited state with a 32 ps lifetime. The decay of the latter state is followed by the appearance of a first product state that is assumed to represent lunii-R. In addition, 2,3-dihydrobiliverdin, which is considered to be an adequate model of the Pr chro-mophore, was included in the femtosecond studies. The absorption difference spectra recorded at various delay times show an immediate bleaching of the ground-state absorption. Simultaneously with bleaching a broad transient absorption appears between 410 and 525 nm. The data analysis yields similar kinetic components as they were observed in the decay of Pr. It is suggested from this finding that within the first tens of picoseconds after excitation the excited-state properties of Pr are mainly determined by the properties of the chromophore itself. 相似文献
39.
Dr. Mohd Nazish Dr. Mujahuddin M. Siddiqui Dr. Samir Kumar Sarkar Dr. Annika Münch Christina M. Legendre Dr. Regine Herbst-Irmer Prof. Dietmar Stalke Prof. Dr. Herbert W. Roesky 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(5):1744-1752
This work describes the synthesis and coordination behavior of a new mixed-donor ligand PhC(NtBu)2SiC6H4PPh2 ( 1 ) containing both silylene and phosphine donor sites. Ligand 1 was synthesized from a reaction of ortho-lithiated diphenylphosphinobenzene (LiC6H4PPh2) with chlorosilylene (PhC(NtBu)2SiCl). Treatment of 1 with Se and GeCl2 resulted in SiIV compounds 2 and 3 by selective oxidation of the silylene donor. This strong σ-donor ligand induces dissociation of CuCl and PhBCl2 leading to formation of ionic complexes 4 and 5 respectively. The reaction of 1 with ZnCl2 and AlCl3 resulted in the formation of chelate complexes 5 and 7 , respectively, while treatment with EtAlCl2 and GaCl3 forms monodentate complexes 8 and 9 . X-ray analysis of 4 showed that the copper is in the spiro center of the two five-membered rings. Moreover, the copper(I)chloride has not been oxidized but dissociates to Cu+ and [CuCl2]−. All the compounds are well characterized by mass spectrometry, elemental analysis, NMR spectroscopy, and single-crystal X-ray diffraction studies. 相似文献
40.
Johannes Kretsch Anne-Kathrin Kreyenschmidt Timo Schillmöller Dr. Märt Lõkov Dr. Regine Herbst-Irmer Prof. Dr. Ivo Leito Prof. Dr. Dietmar Stalke 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(38):9858-9865
A novel sterically demanding bis(4-benzhydryl-benzoxazol-2-yl)methane ligand 6 (4−BzhH2BoxCH2) was gained in a straightforward six-step synthesis. Starting from this ligand monomeric [M(4-BzhH2BoxCH)] (M=Na ( 7 ), K ( 81 )) and dimeric [{M(4-BzhH2BoxCH)}2] (M=K ( 82 ), Rb ( 9 ), Cs ( 10 )) alkali metal complexes were synthesised by deprotonation. Abstraction of the potassium ion of 8 by reaction with 18-crown-6 resulted in the solvent separated ion pair [{(THF)2K@(18-crown-6)}{bis(4-benzhydryl-benzoxazol-2-yl)methanide}] ( 11 ), including the energetically favoured monoanionic (E,E)-(4-BzhH2BoxCH) ligand. Further reaction of 4−BzhH2BoxCH2 with three equivalents KH and two equivalents 18-crown-6 yielded polymeric [{(THF)2K@(18-crown-6)}{K@(18-crown-6)K(4-BzhBoxCH)}]n (n→∞) ( 12 ) containing a trianionic ligand. The neutral ligand and herein reported alkali complexes were characterised by single X-ray analyses identifying the latter as a promising precursor for low-valent main group complexes. 相似文献