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21.
Deutsch JM 《Physical review letters》1992,69(10):1536-1539
22.
Lothar Helm Karen Deutsch Edward A. Deutsch Andr E. Merbach 《Helvetica chimica acta》1992,75(1):210-217
The kinetics of pyridine exchange on trans-[MO2(py)4]+ have been followed by 1H-NMR in CD3NO2 for M = Re, Tc: k298S?1 = (5.5 ± 0.1) × 10?6, 0.04 ± 0.02; ΔH≠/kJmol?1 = 111 ± 3, 101 ± 9; ΔS≠/JK?1mol?1 = +28 ± 10, +68 ± 35. For the Rev complex, pyridine and oxygen exchanges have been measured simultaneously by 1H- and 17O-NMR in deuterated water: k298/s?1 = (8.6 ± 0.2) × 10?6 (py), (14.5 ± 0.3) × 10?6 (oxygen); ΔH≠/kJmol?1 = 111 ± 1, 91 ± 1; ΔS /JK?1mol?1 = +32 ± 3, ?32 ± 4. For both complexes, the rate law for pyridine exchange is first-order in complex and zero-order in pyridine; together with the activation parameter values, and the fact that the rate does not depend significantly on the nature of the solvent, this strongly implies the operation of a dissociative mechanism. The ratio of pyridine exchange rates for the Tc and Re complexes at room temperature is ca. 8000. The consequences of these observations for radiopharmaceutical synthesis are discussed. 相似文献
23.
Michael Deutsch 《Bulletin of the Brazilian Mathematical Society》2013,44(1):1-23
We investigate a Goursat-type transformation for Bryant surfaces and a few of its geometric features. The basic result is that, when regarded as a non-isometric group action on the moduli space of CMC1 immersions of a fixed surface, the Lawson correspondence is equivariant with respect to the more familiar Goursat transform on minimal immersions. This generalizes certain well-known deformations of critical surfaces and enlarges the number of explicitly computable cousin pairs, visualized here in a quaternionic upper-half space. 相似文献
24.
Jan Maier Marian Deutsch Dr. Julia Merz Prof. Dr. Qing Ye Oliver Diamond Maja-Tessa Schilling Dr. Alexandra Friedrich Prof. Dr. Bernd Engels Prof. Dr. Todd B. Marder 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(68):15989-16000
We have investigated the cannibalistic self-trapping reaction of an ortho-benzyne derivative generated from 1,11-bis(p-tolyl)undeca-1,3,8,10-tetrayne in an HDDA reaction. Without adding any specific trapping agent, the highly reactive benzyne is trapped by another bisdiyne molecule in at least three different modes. We have isolated and characterized the resulting products and performed high-level calculations concerning the reaction mechanism. During the cannibalistic self-trapping process, either a C≡C triple bond or an sp–sp3 C−C single bond is cleaved. Up to seven rings and nine C−C bonds are formed starting from two 1,11-bis(p-tolyl)undeca-1,3,8,10-tetrayne molecules. Our experiments and calculations provide considerable insight into the variety of reaction pathways which the ortho-benzyne derivative, generated from a bisdiyne, can take when reacting with another bisdiyne molecule. 相似文献
25.
THE REACTIONS OF N3P3CL6 AND RELATED COMPOUNDS WITH DIFUNCTIONAL REAGENTS. COMPARISONS AND CONTRASTS
Abdulla H. Alkubaisi W. Francis Deutsch Michael B. Hursthouse Harold G. Parkes Leylacaron S. Shaw Robert A. Shaw 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1-2):229-237
Abstract The reactions of N3P3Cl6 with a variety of difunctional reagents are discussed. NMR spectroscopic and X-ray crystallographic investigations are presented. 相似文献
26.
In many magnetic materials, spin dynamics at short times are dominated by precessional motion as damping is relatively small. We describe how avalanches evolve under these conditions. The growth front is spread out over a large region and consists of rapidly fluctuating spins often above the ferromagnetic transition temperature. In the limit of no damping the system will transition to an ergodic state if the initial instability is large enough, but otherwise can die out. This dynamic nucleation phenomenon is analyzed theoretically and the implications for real materials are discussed. 相似文献
27.
Andreev VA Banks TI Case TA Chitwood DB Clayton SM Crowe KM Deutsch J Egger J Freedman SJ Ganzha VA Gorringe T Gray FE Hertzog DW Hildebrandt M Kammel P Kiburg B Knaack S Kravtsov PA Krivshich AG Lauss B Lynch KL Maev EM Maev OE Mulhauser F Ozben CS Petitjean C Petrov GE Prieels R Schapkin GN Semenchuk GG Soroka MA Tishchenko V Vasilyev AA Vorobyov AA Vznuzdaev ME Winter P;MuCap Collaboration 《Physical review letters》2007,99(3):032002
The rate of nuclear muon capture by the proton has been measured using a new technique based on a time projection chamber operating in ultraclean, deuterium-depleted hydrogen gas, which is key to avoiding uncertainties from muonic molecule formation. The capture rate from the hyperfine singlet ground state of the microp atom was obtained from the difference between the micro(-) disappearance rate in hydrogen and the world average for the micro(+) decay rate, yielding Lambda(S)=725.0+/-17.4 s(-1), from which the induced pseudoscalar coupling of the nucleon, g(P)(q(2)=-0.88m(2)(micro))=7.3+/-1.1, is extracted. 相似文献
28.
We propose a method for laser cooling group-II-like atoms without changing the quantum state of their nuclear spins, thus preserving coherences that are usually destroyed by optical pumping in the cooling process. As group-II-like atoms have a (1)S(0) closed-shell ground state, nuclear spin and electronic angular momentum are decoupled, allowing for their independent manipulation. The hyperfine interaction that couples these degrees of freedom in excited states can be suppressed through the application of external magnetic fields. Our protocol employs resolved-sideband cooling on the forbidden clock transition, (1)S(0) --> (3)P(0), with quenching via coupling to the rapidly decaying (1)P(1) state, deep in the Paschen-Back regime. This makes it possible to laser cool neutral atomic qubits without destroying the quantum information stored in their nuclear spins, as shown in two examples, (171)Yb and (87)Sr. 相似文献
29.
Leon N. Schneider Dr. Eva-Maria Tanzer Krauel Dr. Carl Deutsch Dr. Klaus Urbahns Tobias Bischof Kristina A. M. Maibom Dr. Johannes Landmann Dr. Fabian Keppner Dr. Christoph Kerpen Dr. Michael Hailmann Ludwig Zapf Tanja Knuplez Dr. Rüdiger Bertermann Dr. Nikolai V. Ignat'ev Prof. Dr. Maik Finze 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(42):10973-10978
Fluorinated groups are essential for drug design, agrochemicals, and materials science. The bis(trifluoromethyl)amino group is an example of a stable group that has a high potential. While the number of molecules containing perfluoroalkyl, perfluoroalkoxy, and other fluorinated groups is steadily increasing, examples with the N(CF3)2 group are rare. One reason is that transfer reagents are scarce and metal-based storable reagents are unknown. Herein, a set of CuI and AgI bis(trifluoromethyl)amido complexes stabilized by N- and P-donor ligands with unprecedented stability are presented. The complexes are stable solids that can even be manipulated in air for a short time. They are bis(trifluoromethyl)amination reagents as shown by nucleophilic substitution and Sandmeyer reactions. In addition to a series of benzylbis(trifluoromethyl)amines, 2-bis(trifluoromethyl)amino acetate was obtained, which, upon hydrolysis, gives the fluorinated amino acid N,N-bis(trifluoromethyl)glycine. 相似文献
30.