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Published on: September 5, 2014
Syntheses and Solid-State Structure Analyses of Pentafluoroethylated Arsanes
Lukas Hartmann1, Nagat Dündar1, Hans-Georg Stammler1
1Centrum für Molekulare Materialien, Fakultät für Chemie, Universität Bielefeld, Universitätsstraße 25, Bielefeld 33615, Germany.
This study presents an improved synthesis for pentafluoroethylated arsanes, creating new organoarsenic compounds. These novel compounds, including tris(pentafluoroethyl)arsane, offer versatile applications in chemistry.
Area of Science:
- Organometallic Chemistry
- Fluorine Chemistry
- Arsenic Chemistry
Background:
- Pentafluoroethylated arsanes are valuable compounds with diverse applications.
- Existing synthesis methods may have limitations in yield or control.
Purpose of the Study:
- To develop an improved and controlled synthesis of pentafluoroethylated arsanes.
- To characterize the synthesized compounds using advanced analytical techniques.
Main Methods:
- Deprotonation of pentafluoroethane using n-butyllithium to form pentafluoroethyllithium.
- Reaction of pentafluoroethyllithium with arsenic trichloride and subsequent functionalization using diethylamino protecting groups.
- Characterization of products via multinuclear NMR spectroscopy and X-ray diffraction analysis.
Main Results:
- Successful synthesis of tris(pentafluoroethyl)arsane in good yields.
- Controlled synthesis of partially substituted arsanes, As(C2F5)2(NEt2) and As(C2F5)(NEt2)2, using protecting groups.
- Isolation and characterization of novel halogenoarsanes, As(C2F5)nCl3-n and As(C2F5)nBr3-n (n=1,2).
Conclusions:
- The developed method provides an efficient route to various pentafluoroethylated arsanes.
- The use of protecting groups allows for precise control over the degree of substitution at the arsenic center.
- The synthesized compounds are characterized as colorless, volatile liquids with determined solid-state structures.
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