Measurements of theg-factor ratio of the first 3− and 5− states in40Ca and the lifetime of the 5− state

[Theg-factor ratio of the first excited 3^? and 5^? states in⁴⁰Ca was measured to beg ₃/g ₅=1.01(10) employing the implantation perturbed angular correlation technique. The static hyperfine fields (SF) in Fe and Gd hosts were used. In addition the lifetime of the 5^? state was measured to be τ=426(7)ps. The values of the SF in Gd and Fe hosts were deduced and compared with systematics in this element region.     

Crystallization of Arthrobacter sp. strain 1C N-(1-D-carboxyethyl)-L-norvaline dehydrogenase and its complex with NAD+

The novel NAD+-linked opine dehydrogenase from a soil isolate Arthrobacter sp. strain 1C belongs to an enzyme superfamily whose members exhibit quite diverse substrate specificites. Crystals of this opine dehydrogenase, obtained in the presence or absence of co-factor and substrates, have been shown to diffract to beyond 1.8 ? resolution. X-ray precession photographs have established that the crystals belong to space group P21212, with cell parameters a = 104.9, b = 80.0, c = 45.5 ? and a single subunit in the asymmetric unit. The elucidation of the three-dimensional structure of this enzyme will provide a structural framework for this novel class of dehydrogenases to enable a comparison to be made with other enzyme families and also as the basis for mutagenesis experiments directed towards the production of natural and synthetic opine-type compounds containing two chiral centres.     

Plunger measurements on highly stripped O-ions as tool for detecting electron polarization on emergence from thin ferromagnetic layers

From hyperfine interaction studles on free single electron¹⁶O(3⁻) ions. in a time differential mode using the recoil distance technique. It is shown that these ions are polarized when emerging from magnetized thin layers of Fe. The observed degree of polarization , however, is smaller than expected from transient field measurements.     

New aspect in transient magnetic fields using heavy ion beams

Transient field precessions have been measured with the first excited 2 ₁ ⁺ -state as probe for ions of²⁸Si traversing Fe at v_ion?1v₀ and 13v₀(v₀=c/137) and⁶²Ni being stopped in Fe. The degree of polarization deduced for the Si ions, p_1s=0.19(6), is consistent with low-velocity data. There is clear evidence that the field strength is attenuated by heavy ion beams. For the⁶²Ni(2 ₁ ⁺ ) state at 1.173 MeV a g-factor value of g=0.34(7) was obtained in good agreement with a previous result.     

Measurements of lifetime andg-factor of the 32S(4 1 + ) state at 4.459 MeV

Precessions of the very short-lived 2 ₁ ⁺ - and 4 ₁ ⁺ -states in³²S have been measured using the transient field technique. The deducedg-factor of the 4 ₁ ⁺ -state g=+0.40(15) agrees with the known value of the 2 ₁ ⁺ -state and with theoretical predictions. In addition, the lifetimes of both states were redetermined and are consistent with previous results.     

Aromatic-aromatic interactions in crystal structures of helical peptide scaffolds containing projecting phenylalanine residues

Aromatic-aromatic interactions between phenylalanine side chains in peptides have been probed by the structure determination in crystals of three peptides: Boc-Val-Ala-Phe-Aib-Val-Ala-Phe-Aib-OMe, I; Boc-Val-Ala-Phe-Aib-Val-Ala-Phe-Aib-Val-Ala-Phe-Aib-OMe, II; Boc-Aib-Ala-Phe-Aib-Phe-Ala-Val-Aib-OMe, III. X-ray diffraction studies reveal that all three peptides adopt helical conformations in the solid state with the Phe side chains projecting outward. Interhelix association in the crystals is promoted by Phe-Phe interactions. A total of 15 unique aromatic pairs have been characterized in the three independent crystal structures. In peptides I and II, the aromatic side chains lie on the same face of the helix at i/i + 4 positions resulting in both intrahelix and interhelix aromatic interactions. In peptide III, the Phe side chains are placed on the opposite faces of the helix, resulting in exclusive intermolecular aromatic interactions. The distances between the centroids of aromatic pair ranges from 5.11 to 6.86 A, while the distance of closest approach of ring carbon atoms ranges from 3.27 to 4.59 A. Examples of T-shaped and parallel-displaced arrangements of aromatic pairs are observed, in addition to several examples of inclined arrangements. The results support the view that the interaction potential for a pair of aromatic rings is relatively broad and rugged with several minima of similar energies, separated by small activation barriers.     

TransientK-shell hyperfine fields and deduced polarizations for single-electron C and O ions in different ferromagnets

Effective transient magnetic fields have been measured for single-electron carbon and oxygen ions traversing ferromagnetic Ni and Gd hosts, respectively. The deduced values ofK-shell polarization are well explained considering spin exchange scattering as a dominant mode of polarization.     

Aza-analogues of cage compounds: Potential precursors to azacubanes and 1-azahomocubanes

Exploration of the reactions of the 9-azahomocubane system led to derivatives of two small-ring systems containing aza-bridging atoms, 5-azatetracyclo[4.2.0.0^3,8.0^4,7]octane and 9-azatetracyclo[4.3.0.0^2,5.0^4,7]nonane. The structures were characterized by X-ray diffraction analyses. There are no prior X-ray structural reports on these systems.