Related Experiment Video
Updated: Dec 24, 2025
![The Synthesis of [Sn10SiSiMe334]2- Using a Metastable SnI Halide Solution Synthesized via a Co-condensation Technique](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F54498.jpg&w=3840&q=50)
The Synthesis of [Sn10SiSiMe334]2- Using a Metastable SnI Halide Solution Synthesized via a Co-condensation Technique
Published on: November 28, 2016
Trapping of ZnCl2 by bipyridyl-functionalized organotin sulfide clusters, and its effect on optical properties
Eugenie Geringer1, Eliza Leusmann, Frank Tambornino
1Fachbereich Chemie and Wissenschaftliches Zentrum für Materialwissenschaften (WZMW), Philipps-Universität Marburg, Hans-Meerwein-Strasse 4, D-35043 Marburg, Germany. dehnen@chemie.uni-marburg.de.
Abstract:
We report the syntheses of two new organotin sulfide clusters with heteroaromatic substituents. A phenanthroline-functionalized tin sulfide cluster [(RPhenSn)4S6] (1; RPhen = CMe2CH2C(Me)N-NC(H)C12H7N2) and a bipyridyl-terminated cluster [(R4-bipySn)4S6] (2; R4-bipy = CMe2CH2C(Me)N-NC(H)-4-C10H7N2) were obtained from reactions of the hydrazone-functionalized organotin sulfide cluster [(RNSn)4S6] (RN = CMe2CH2C(Me)N-NH2) with 1,10-phenanthroline-5-carboxaldehyde or 2,2'-bipyridine-4-carbaldehyde. 1 and 2 were tested towards their capability of trapping metal ions by means of the terminal chelating ligands. The reaction of 2 with ZnCl2 afforded the cluster compound [(R4-bipyZnCl2Sn)4S6] (5), in which four ZnCl2 units are coordinated by the heteroaromatic organic groups. We discuss the structures and demonstrate the effect of ZnCl2 trapping on optical absorption and luminescence properties.
Related Concept Videos
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation reactions,...
Preparation and Reactions of Sulfides

