Phenanthroline complexes of zinc and calcium carbamates.

Acta Crystallogr C

Bundesanstalt für Materialforschung und -prüfung, Richard-Willstätter-Strasse 11, D-12489 Berlin, Germany.

Published: March 2004

Bis(N,N-di-n-butyldithiocarbamato-kappa2S,S')(1,10-phenanthroline-kappa2N,N')zinc(II) ethanol hemisolvate, [Zn(C9H18NS2)2(C12H8N2)].0.5C2H6O, (I), and bis(N,N-di-n-hexyldithiocarbamato-kappa2S,S')bis(1,10-phenanthroline-kappa2N,N')calcium(II), [Ca(C13H26NS2)2(C12H8N2)2], (II), are mixed-ligand complexes. In the first compound, the Zn atom has a distorted octahedral coordination, while in the second compound, the Ca atom is eight-coordinate, with four S and four N atoms forming a highly distorted cube.

Download full-text PDF

Source
http://dx.doi.org/10.1107/S0108270104001441DOI Listing

Publication Analysis

Top Keywords

compound atom
8
phenanthroline complexes
4
complexes zinc
4
zinc calcium
4
calcium carbamates
4
carbamates bisnn-di-n-butyldithiocarbamato-kappa2ss'110-phenanthroline-kappa2nn'zincii
4
bisnn-di-n-butyldithiocarbamato-kappa2ss'110-phenanthroline-kappa2nn'zincii ethanol
4
ethanol hemisolvate
4
hemisolvate [znc9h18ns22c12h8n2]05c2h6o
4
[znc9h18ns22c12h8n2]05c2h6o bisnn-di-n-hexyldithiocarbamato-kappa2ss'bis110-phenanthroline-kappa2nn'calciumii
4

Similar Publications

Effect of Glycoconjugation on Cytotoxicity and Selectivity of 8-Aminoquinoline Derivatives Compared to 8-Hydroxyquinoline.

Molecules

January 2025

Department of Organic Chemistry, Bioorganic Chemistry and Biotechnology, Silesian University of Technology, B. Krzywoustego 4, 44-100 Gliwice, Poland.

Numerous emerging chemotherapeutic agents incorporate -heterocyclic fragments in their structures, with the quinoline skeleton being particularly significant. Our recent works have focused on glycoconjugates of 8-hydroxyquinoline (8-HQ), which demonstrated enhanced bioavailability and solubility compared to their parent compounds, although they fell short in selectivity. In this study, our objective was to improve the selectivity of glycoconjugates by replacing the oxygen atom with nitrogen by substituting the 8-HQ moiety with 8-aminoquinoline (8-AQ).

View Article and Find Full Text PDF

In recent years, a number of synthetic potentiators of antibiotics have been discovered. Their action can significantly enhance the antibacterial effect and limit the spread of antibiotic resistance through inhibition of bacterial cystathionine-γ-lyase. To expand the known set of potentiators, we developed methods for the synthesis of five new representatives of 6-bromoindole derivatives-potential inhibitors of bacterial cystathionine-γ-lyase-namely potassium 3-amino-5-((6-bromoindolyl)methyl)thiophene-2-carboxylate () and its 6-bromoindazole analogs ( and ), along with two 6-broindazole analogs of the parent compound .

View Article and Find Full Text PDF

Crystal Structure and Magnetic Properties of the Novel Compound ErMnGe.

Materials (Basel)

January 2025

MOE Key Laboratory of New Processing Technology for Nonferrous Metals and Materials, School of Resources, Environment and Materials, Guangxi University, Nanning 530004, China.

The RE-M-Ge systems (RE: rare earths, M: transition group elements) contain a large number of compounds with special magnetic properties. A novel compound ErMnGe was found during the investigation on the phase diagram of the Er-Mn-Ge ternary system, and its crystal structure and magnetic properties were investigated. Powder X-ray diffraction results show that ErMnGe crystallizes in an orthorhombic YNiSi-type structure with the space group Pnma (No.

View Article and Find Full Text PDF

Glutathione S-transferases (GSTs) are promising pharmacological targets for developing antiparasitic agents against helminths, as they play a key role in detoxifying cytotoxic xenobiotics and managing oxidative stress. Inhibiting GST activity can compromise parasite viability. This study reports the successful identification of two selective inhibitors for the mu-class glutathione S-transferase of 25 kDa (Ts25GST) from , named and , using a computationally guided approach.

View Article and Find Full Text PDF

The functional properties of tetraaryl compounds, M(aryl) (M = transition metal or group 14 element), are dictated not only by their common tetrahedral geometry but also by their central atom. The identity of this atom may serve to modulate the reactivity, electrochemical, magnetic, and optical behavior of the molecular species, or of extended materials built from appropriate tetraaryl building blocks, but this has not yet been systematically evaluated. Toward this goal, here we probe the influence of Os(IV), C, and Si central atoms on the spectroelectrochemical properties of a series of redox-active tetra(ferrocenylaryl) complexes.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!