R?ntgenstruktur-Analyse von Trans-1-ethyl-2-(1-ethyl-2-adamantyliden)adamantan, Vergleich mit Kraftfeld-Rechnungen

Ohne Zusammenfassung

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X-ray structural analysis of trans-1-Ethyl-2-(1-ethyl-2-adamantylidene)-adamantane. Comparison with force field calculations

     

Fourth order approximation of harmonic maps from surfaces

Let be a compact Riemannian surface and let be a compact Riemannian manifold, both without boundary, and assume that N is isometrically embedded into some ℝ ^l . We consider a sequence of critical points of the functional with uniformly bounded energy. We show that this sequence converges weakly in and strongly away from finitely many points to a smooth harmonic map. One can perform a blow-up to show that there separate at most finitely many non-trivial harmonic two-spheres at these finitely many points. Finally we prove the so called energy identity for this approximation in the case that ↪ ℝ ^l . Mathematics Subject Classification (2000) 58E20, 35J60, 53C43     

A Rational Approach to Tetra-Functional Photo-Switches

α,ω-Bis(1,8-dichloroanthracen-10-yl)alkanes with (CH₂)_n-linker units (n=1–4) were synthesized starting from 1,8-dichloroanthracen-10(9H)-one. This was transformed into anthracenes with allyl, bromomethyl and propargyl substituents in position 10; these were converted in various C−C-bond formation reactions (plus hydrogenation), leading to two anthracene units flexibly linked by α,ω-alkandiyl groups. 1,2-Ethandiyl- and 1,3-propandiyl-linked derivatives were functionalized with ethynyl groups in positions 1, 8, 1’ and 8’, and these terminally functionalized by Me₃Sn groups using Me₂NSnMe₃. All linked bisanthracenes were subjected to UV light induced cyclomerization and a series of 9,10 : 9’,10’-photo-cyclomers were obtained. Their thermal cycloreversion and (repeated) switchability was demonstrated. 1,3-Bis{1,8-bis[(trimethylstannyl)ethynyl]anthracen-10-yl}propane served as model compound for photo-switchable acceptor molecules and its open and closed forms were characterized by NMR and DOSY experiments.     

Advantages of a two-detector system in automated substoichiometric radioisotope dilution analysis

Automation widens the scope of substoichiometric radioisotope dilution analysis. This is because the very strict requirement of the manual method-chemical separation of exactly equal quantities of the test substance-need no longer be fulfilled: reproducibility of the determination is reached by means of automated operation and activity measurement. The theory given in this paper shows how the choice of suitable chemical reactions is widened and why the reliability and the advantages of isotope dilution analysis are secured by the use of a two-detector system.     

1,2‐Azaborine: The Boron‐Nitrogen Derivative of ortho‐Benzyne

The BN analogue of ortho‐benzyne, 1,2‐azaborine, is generated by flash vacuum pyrolysis, trapped under cryogenic conditions, and studied by direct spectroscopic techniques. The parent BN aryne spontaneously binds N₂ and CO₂, thus demonstrating its highly reactive nature. The interaction with N₂ is photochemically reversible. The CO₂ adduct of 1,2‐azaborine is a cyclic carbamate which undergoes photocleavage, thus resulting in overall CO₂ splitting.     

Investigation of the 19Na nucleus via resonance elastic scattering

The structure of the unbound proton-rich isotope ¹⁹Na was studied in resonance elastic scattering of a radioactive ¹⁸Ne beam on a proton target using the thick-target inverse-kinematics method. The experiment covered the excitation energy range from 0.5 to 2.7 MeV in c.m.s. Only one state of ¹⁹Na (the second excited state) was observed. A combined R-matrix and potential model analysis was performed. The spin and parity assignment of this second excited state was confirmed to be 1/2⁺. We show that the position of the 1/2⁺ state significantly affects the reaction rate through that state, but the total reaction rate remains unchanged since the ¹⁸Ne(2p, γ) proceeds mostly via the ground and first excited states in ¹⁹Na at stellar temperatures. The text was submitted by the authors in English.     

Modeling styrene-styrene interactions

This study is the first step in the systematic investigation of substituted (carboxyl) polystyrene nanoparticles. Understanding the fundamental interactions between the p-carboxyl styrene monomers, where an ethyl group is used instead of a vinyl group (referenced, for convenience, as "p-carboxyl styrene"), provides the basic information needed to construct potentials for nanoparticles composed of these monomers. In this work, low-energy isomers of p-carboxyl styrene dimer were studied. The dimer structures and their relative and binding energies were determined using both M?ller-Plesset second-order perturbation theory (MP2) and the general effective fragment potential (EFP2) method. Sections of the intermolecular potential energy surface (PES) of the p-carboxylated styrene dimer in its global minimum orientation were also determined. As expected, double hydrogen bonding between the two carboxylic groups provides the strongest interaction in this system, followed by isomers with a single H-bond and strong benzene ring-benzene ring (pi-pi) type interactions. Generally, the EFP2 method reproduces the MP2 geometries and relative energies with good accuracy, so it appears to be an efficient alternative to the correlated ab initio methods, which are too computationally demanding to be routinely used in the study of the more-complex polymeric systems of interest.     

Determination of the strange quark content of the nucleon from a next-to-leading-order QCD analysis of neutrino charm production

We present the first next-to-leading-order QCD analysis of neutrino charm production, using a sample of 6090 ^– and -induced opposite-sign dimuon events observed in the CCFR detector at the Fermilab Tevatron. We find that the nucleon strange quark content is suppressed with respect to the non-strange sea quarks by a factor =0.477 _–0.053 ^+0.063 , where the error includes statistical, systematic and QCD scale uncertainties. In contrast to previous leading order analyses, we find that the strange seax-dependence is similar to that of the non-strange sea, and that the measured charm quark mass,m _c =1.70±0.19 GeV/c², is larger and consistent with that determined in other processes. Further analysis finds that the difference inx-distributions betweenxs(x) and is small. A measurement of the Cabibbo-Kobayashi-Maskawa matrix element |V _cd |=0.232 _–0.020 ^+0.018 is also presented.