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Biomedical subjects

C Grüning

Publications and source records attributed to C Grüning.

3 recordsLinked to original sources

First observation of atomic levels for the element fermium (Z=100).

The atomic level structure of the element fermium was investigated for the first time using a sample of 2.7x10(10) atoms of the isotope 255Fm with a half-life of 20.1 h. The atoms were evaporated from a filament and stored in the argon buffer gas of an optical cell. Atomic levels were sought by the method of resonance ionization spectroscopy using an excimer-dye-laser combination. Two atomic levels were found at wave numbers (25 099.8+/-0.2) and (25 111.8+/-0.2) cm(-1). Partial transition rates to the 5f(12)7s(2) (3)H(e)(6) ground state have been determined from their saturation characteristics. Multiconfiguration Dirac-Fock calculations suggest that the leading orders of these levels could be the 5f(12)7s7p (5)I(o)(6) and 5f(12)7s7p (5)G(o)(5) terms.

Journal Article↗

Thiofunctional vanadium complexes.

The neutral tetradentate ligand 1,6-bis(2'-pyridyl)-2,5-dithiahexane (N(2)S(2)), containing two thioether functions, reacts with [VX(2)L(4)] (X = Br, L(4) = 2 tmeda (tmeda = Me(2)NCH(2)CH(2)NMe(2)); X = I, L = tetrahydrofuran (THF)) and [VX(3)(THF)(3)] (X = Br, I) to form the complexes [VX(2)(N(2)S(2))] (1) and [VX(2)(N(2)S(2))]X (2), respectively. [V(2)(mu-Cl)(3)(THF)(6)]I and N(2)S(2) yield the V(IV) complex [VOCl(N(2)S(2)]I (3). The pentadentate, dianionic ligand 2,6-bis(2'-mercaptophenylthio)dimethylpyridine, NS(2)S'(2)(2-), which contains two thioether (S) and two thiophenolate (S') functions, reacts with [VBr(3)(THF)(3)] to afford [VBr(NS(2)S'(2))] (4). The complex [VO(Cl)S'NS'] (5; H(2)S'NS' is the Schiff base formed between o-mercaptoaniline and o-mercaptobenzaldehyde) is obtained by redox interaction between [VCl(3)(THF)(3)] and 2,2'-dithiodibenzaldehyde in the presence of o-mercaptoaniline. The crystal and molecular structures have been obtained for 3. THF, 4. THF, and 5. n-C(5)H(12). The relevance of these compounds and their formation for the interaction between vanadium and thiofunctional biomolecules is addressed.

Journal Article↗