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Heavy Chalcogenide-Based Ionic Liquids in Syntheses of Metal Chalcogenide Materials near Room Temperature.


ABSTRACT: This minireview describes two strategically different and unexplored approaches to use ionic liquids (IL) containing weakly solvated and highly reactive chalcogenide anions [E-SiMe3 ]- and [E-H]- of the heavy chalcogens (E=S, Se, Te) in materials synthesis near room temperature. The first strategy involves the synthesis of unprecedented trimethylsilyl chalcogenido metalates Cat+ [M(E-SiMe3 )n ]- (Cat=organic IL cation) of main group and transition metals (M=Ga, In, Sn, Zn, Cu, Ag, Au). These fully characterized homoleptic metalates serve as thermally metastable precursors in low-temperature syntheses of binary, ternary and even quaternary chalcogenide materials such as CIGS and CZTS relevant for semiconductor and photovoltaics (PV) applications. Furthermore, thermally and protolytically metastable coinage metalates Cat+ [M(ESiMe3 )2 ]- (M=Cu, Ag, Au; E=S, Se) are accessible. Finally, the use of precursors BMPyr[E-SiMe3 ] (E=Se,Te; BMPyr=1-butyl-1-methylpyrrolidinium) as sources of activated selenium and tellurium in the synthesis of high-grade thermoelectric nanoparticles Bi2 Se3 and Bi2 Te3 is shortly highlighted. The second synthesis strategy involves the metalation of ionic liquids Cat[S-H] and Cat[Se-H] by protolytically highly active metal alkyls or amides Rn M. This rather general approach towards unknown chalcogenido metalates Catm [Rn-1 M(E)]m (E=S, Se) will be demonstrated in a research paper following this short review head-to-tail.

SUBMITTER: Guschlbauer J 

PROVIDER: S-EPMC7874248 | biostudies-literature | 2021 Feb

REPOSITORIES: biostudies-literature

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Heavy Chalcogenide-Based Ionic Liquids in Syntheses of Metal Chalcogenide Materials near Room Temperature.

Guschlbauer Jannick J   Sundermeyer Jörg J  

ChemistryOpen 20210201 2


This minireview describes two strategically different and unexplored approaches to use ionic liquids (IL) containing weakly solvated and highly reactive chalcogenide anions [E-SiMe<sub>3</sub> ]<sup>-</sup> and [E-H]<sup>-</sup> of the heavy chalcogens (E=S, Se, Te) in materials synthesis near room temperature. The first strategy involves the synthesis of unprecedented trimethylsilyl chalcogenido metalates Cat<sup>+</sup> [M(E-SiMe<sub>3</sub> )<sub>n</sub> ]<sup>-</sup> (Cat=organic IL cation)  ...[more]

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