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101.
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Summary: Polypeptide‐shelled poly(propylene imine) dendrimers were realized by ring‐opening polymerization of α‐amino acid N‐carboxyanhydrides, initiated by dendrimers as core molecules. Polypeptides with 2nd generation core were used as model compounds to investigate interior complexes between metal ion and surface‐modified dendrimers. Micro‐calorimetric measurements outlined the formation of approximate 1:1 complexes between CuII and polypeptide‐shelled dendrimers and the influence of polypeptide chain compositions on differential molar heats of complexation.

Composition of one of the polypeptides synthesized.  相似文献   

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Single phase powders of (A19N7)[In4]2 (A = Ca, Sr) and (Ca4N)[In2] were prepared by reaction of melt beads of the metallic components with nitrogen. The crystal structure of (Ca19N7)[In4]2 was refined based on neutron and X‐ray powder diffraction data. The crystal structure of (Sr19N7)[In4]2 was solved from the X‐ray powder pattern. The structure refinements in combination with results from chemical analyses ascertain the compositions. The compounds (A19N7)[In4]2 (A = Ca, Sr) are isotypes of (Ca19N7)[Ag4]2; (Ca19N7)[In4]2 is probably identical to the earlier reported (Ca18.5N7)[In4]2. The crystal structure of the isotypes (A19N7)[In4]2 (A = Ca, Sr; cubic, , Ca: a = 1471.65(3) pm; Sr: a = 1561.0(1) pm) contains isolated [In4] tetrahedra embedded in a framework of edge‐ and vertex‐sharing (A6N) octahedra. Six of these octahedra are condensed by edge‐sharing around one central A2+ ion to form “superoctahedra” (A19N6) which are connected three‐dimensionally via further octahedra by corner‐sharing. The crystal structure of (Ca4N)[In2] (tetragonal, I41/amd, a = 491.14(4) pm, c = 2907.7(3) pm) consists of alternating layers of perovskite type slabs of vertex‐sharing octahedra (Ca2Ca4/2N) and parallel arranged infinite zigzag chains equation/tex2gif-stack-1.gif[In2]. In the sense of Zintl‐type counting the compounds (A2+)19(N3?)7[(In2.125?)4]2 present an electron excess, (Ca2+)4(N3?)[(In2.5?)2] is electron deficient. Metallic properties are supported by electrical resistivity and magnetic susceptibility measurements. The analysis of the electronic structures gives evidence for the existence of homoatomic interactions In–In and significant heteroatomic metal–metal interactions Ca–In which favor the deviations of the title compounds from the (8 – N) rule.  相似文献   
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By irradiating a natW target with 9 MeV/u 76Ge ions, neutron-rich isotopes in the chromiumgermanium region were produced. On-line mass-separated samples were investigated. The new isotopes 62Mn, 71Cu, 72Cu and 73Cu were identified and their half-lives measured to be 0.88(15), 19.5(16), 6.6(1) and 3.9(3) s, respectively. The half-life of 63Fe, a nucleus which has previously been detected using particle-identification techniques, was measured to be 4.9(5) s. Decay schemes were derived in most cases. Additional spectroscopic information was obtained on the decays of 73Zn and 74Zn. We give evidence that the earlier reported γ-ray activity attributed to 67Ni belongs to the decay of the 70Cu isomers. At A = 67 we observed a new β-ray activity of 21(1) s half-life which is here assigned to the decay of 67Ni.  相似文献   
109.
A biomimetic complex which mimics the arginine-phosphonate diester interaction of the arginine fork is investigated with respect to structure and energetics of stable configurations. Within this work, we provide knowledge on local minima of the isolated system obtained from first-principles calculations. Non-negligible solvation effects are studied in a microsolvation approach. The interactions which govern the structural patterns of molecular recognition in this tweezer-guest complex can be significantly modulated by the action of hydrogen bond accepting and donating solvent molecules, such as dimethyl sulfoxide or water, which were present in experimental investigations on this system. Different tweezer-guest structures are evaluated with respect to their temperature-dependent thermodynamical properties as products of the first association reaction step of the bisphosphonate tweezer template and the guanidinium moiety.  相似文献   
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Using on-line mass separation of evaporation residues from heavy-ion-induced fusion reactions, three new isotopes were identified by their alpha decay, Eα given in keV: 183Pb, 6715(20), 184Pb, 6632(10) and 188Bi, 6820(20). Half-lives were determined for 184Pb, 0.55(6)s, 185Pb, 4.1(3)s and 183Tl, 0.060(15) s. The alpha branching ratios were re-measured for 182–184Hg and 178, 179Pt, the results are discussed within the framework of alpha width systematics.  相似文献   
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