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131.
Hartwig Möller Nikolaus Seiler Gottfried Werner 《Analytical and bioanalytical chemistry》1968,243(1):126-129
Some experiences are given with a measuring device for the determination of the specific radioactivity of 14C-labelled brain amino-acids. The apparatus consists of an automatic amino-acid analyzer combined with a flow cell filled with anthracene. The reproducibility of the method is ±5% to ±1% m.e. in the range of 1×10?3 μCi to 5×10?2 μCi. A quantitative determination of 3×10?4 μCi/ml eluant is still possible. 相似文献
132.
Gottfried Köthe 《Mathematische Annalen》1968,178(1):1-3
Ohne ZusammenfassungHeinrich Behnke zum 70. Geburtstag 相似文献
133.
Ohne ZusammenfassungHerrnHelmut Grunsky zum 60. Geburtstag am 11. Juli 1964 gewidmet 相似文献
134.
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136.
Gottfried Mrkl Andreas Pll Norbert G. Aschenbrenner Corinna Schmaus Theodor Troll Peter Kreitmeier Heinrich Nth Martin Schmidt 《Helvetica chimica acta》1996,79(5):1497-1517
Extremely Expanded Tetrathiafulvalenes with Polyene Spacers. Carotinoid Tetrathiafulvalenes. Polymethin-Tetracyanotetrathiafulvalene Radical Cations, a New Class of Violenes The synthesis of extended tetrathiafulvalenes 11 with di-, tetra-, hexa-, octa-, deca- and dodecamethine spacers is described by a PPh3-induced Wittig-reaction-like condensation of the corresponding polyenedials 10 with 2-thio-1,3-dithiole-4,5-dicarbonitrile ( 9 ). By the same procedure, the dimethyloctamethine- and the tetramethyl-hexadecamethine-tetrathiafulvalenes 14 and 15 , respectively, were obtained. The extended tetrathiafulvalenes represent multistep vinylogous redox systems of the ‘violene type’. They can be oxidized to give the cyanine-like radical cations, e.g. 11 sem, 14 sem, and 15 sem, and the dications, e.g. 11 ox, 14 ox, and 15 ox; their UV/VIS/NIR spectra are reported. The crystal and molecular structure of (all-E)-2,2′-(octa-2,4,6-trien-1,8-diylidene)bis[1,3-dithiole-4,5-dicarbonitrile] ( 11e ) was determined: it is a rod-like, planar molecule; in the crystal, it forms staples along the longest molecule axis. The CV measurements confirm that the redox potentials of 11, 14 , and 15 decrease asymptotically with the increasing length of the spacer. Because of the close relationship of the extended tetrathiafulvalenes (ETTF's) to the carotinoids, they are named ‘caroviologenes’; they formally belong to the class of molecular wires. 相似文献
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138.
Gottfried Spelsberg-Korspeter 《Journal of sound and vibration》2010,329(23):4829-4840
Self-excited vibrations are a severe problem in many technical applications. In many cases they are caused by friction as for example in disk and drum brakes, clutches, saws and paper calenders. The goal to suppress self-excited vibrations can be reached by active and passive techniques, the latter ones being preferable due to the lower costs. Among design engineers it is known that breaking the symmetries of structures is sometimes helpful to avoid self-excited vibrations. This has been verified from an analytical point of view in a recent paper. The goal of the present paper is to use this analytical insight for a systematic structural optimization of rotors in frictional contact. The first system investigated is a simple discrete model of a rotor in frictional contact. As a continuous example a rotating beam in frictional contact is considered and optimized with respect to its bending stiffness. Finally a brake disk is optimized giving some attention to the feasibility of the modifications for the production process. 相似文献
139.
Abstract Fluorescence correlation spectroscopy (FCS) is an important biophysical technique. FCS is currently being used in many areas of biology to solve several scientific problems. Its properties such as detection at the single molecular level, higher sensitivity, and use of lower sample volume make FCS a promising molecular diagnostic tool. The promising applications of FCS extend from DNA kinetics/dynamics studies to the comprehensive understanding of receptor–ligand interactions. In this article, we review various promising biological applications of FCS. 相似文献
140.
Two Histidines in an α‐Helix: A Rigid Co2+‐Binding Motif for PCS Measurements by NMR Spectroscopy
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Alireza Bahramzadeh Hailun Jiang Prof. Thomas Huber Prof. Gottfried Otting 《Angewandte Chemie (International ed. in English)》2018,57(21):6226-6229
Pseudocontact shifts (PCS) generated by paramagnetic metal ions present valuable long‐range information in the study of protein structural biology by nuclear magnetic resonance (NMR) spectroscopy. Faithful interpretation of PCSs, however, requires complete immobilization of the metal ion relative to the protein, which is difficult to achieve with synthetic metal tags. We show that two histidine residues in sequential turns of an α‐helix provide a binding site for a Co2+ ion, which positions the metal ion in a uniquely well‐defined and predictable location. Exchange between the bound and free cobalt is slow on the timescale defined by chemical shifts, but the NMR resonance assignments are nonetheless readily transferred from the diamagnetic to the paramagnetic NMR spectrum by an IzSz‐exchange experiment. The double‐histidine‐Co2+ motif offers a straightforward, inexpensive, and convenient way of generating precision PCSs in proteins. 相似文献