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81.
L. Adiels G. Backenstoss I. Bergström S. Carius S. Charalambous M. D. Cooper Ch. Findeisen D. Hatzifotiadou M. Hugi A. Kerek H. O. Meyer P. Pavlopoulos J. Repond L. Tauscher D. Tröster M. C. S. Williams K. Zioutas 《Zeitschrift fur Physik C Particles and Fields》1987,35(1):15-19
The branching ratios of \(p\bar p\) annihilations into the neutral final states 2π0, π0γ, and 2γ are measured by stopping antiprotons in liquid hydrogen. They are \(B_{2\pi ^0 } = \left( {2.06 \pm 0.14} \right) \times 10^{ - 4} \) , \(B_{\pi ^0 \gamma } = \left( {1.74 \pm 0.22} \right) \times 10^{ - 5} \) , andB γγ<1.7×10?6 (95% c.l.). 相似文献
82.
Grosnick D Wright SC Bolton RD Cooper MD Frank JS Hallin AL Heusi PA Hoffman CM Hogan GE Mariam FG Matis HS Mischke RE Piilonen LE Sandberg VD Sanders GH Sennhauser U Werbeck R Williams RA Wilson SL Hofstadter R Hughes EB Ritter MW Highland VL McDonough J 《Physical review letters》1986,57(26):3241-3244
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The new isocyanato carborane anion, [7-OCN-7-CB10H12]− was prepared by the reaction of 7-H3N-7-CB10H12 with triphosgene in the presence of triethylamine. The structure of this compound was established by 1H, 11B and 13C NMR as well as IR spectroscopy. The reactivigty of this compound with a series of organic amines was investigated. The resulting ureas were obtained in good to excellent yields. This approach is suitable for development of compounds for use in tumor selective Boron Neutron Capture Therapy (BNCT). 相似文献
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Fluorogenic probes dual-labeled with reporter and quencher dyes use a change in fluorescence to monitor biochemical events (e.g., substrate binding or enzyme digestion). Such events change the reporter-quencher distance, which affects fluorescence. Recently, it is has been shown that static quenching through intramolecular dimers is an important mechanism that can sometimes be more efficient than F?rster resonance energy transfer (FRET). 相似文献
90.
Margaret C. Gerthoffer Sikai Wu Bo Chen Tao Wang Steven Huss Shalisa M. Oburn Vincent H. Crespi John V. Badding Elizabeth Elacqua 《Chemical science》2020,11(42):11419
Limited supramolecular strategies have been utilized to synthesize sequence-defined polymers, despite the prominence of noncovalent interactions in materials design. Herein, we illustrate the utility of ‘sacrificial’ aryl-perfluoroaryl supramolecular synthons to synthesize sp3-hybridized nanothreads from sp2-enriched reactants. Our strategy features A–B reactant pairs in the form of a phenol:pentafluorophenol co-crystal that is preorganized for an electronically-biased and sequence-defined polymerization. The polymerization, initiated at 12 GPa, affords an alternating copolymer featuring exogenous –OH functionalities. The external substitution is confirmed through IR spectroscopy. Importantly, the inclusion of the functional unit provides the first experimental glimpse at reaction mechanism: keto–enol tautomerization that can only occur during cycloaddition is observed through IR spectroscopy. Our approach realizes the first example of a functionalized nanothread and attains sequence definition through sacrificial supramolecular preorganization and presents a further approach for de novo design of complex nanothreads.Supramolecular synthons are exploited to synthesize –OH functionalized sp3-rich sequence-defined nanothreads using pressure-induced polymerization of a phenol:pentafluorophenol co-crystal. 相似文献