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. 2019 Mar 1;25(13):3267-3271.
doi: 10.1002/chem.201806346. Epub 2019 Feb 4.

Pseudo-One-Coordinate Tetrylenium Salts Bearing a Bulky Carbazolyl Substituent

Affiliations

Pseudo-One-Coordinate Tetrylenium Salts Bearing a Bulky Carbazolyl Substituent

Alexander Hinz. Chemistry. .

Abstract

Syntheses of a bulky carbazole-based substituent, the parent 1,8-bis(3,5-di-tert-butylphenyl)-3,6-di-tert-butyl-carbazole (R-H) and a series of chlorotetrylenes, RECl (E=Ge, Sn, Pb), are described. Detailed analysis of the properties of the carbazole-based substituent revealed that it features flexible high bulkiness and electronic non-innocence, which may make it suitable for many applications in both main-group and transition-metal chemistry. To further showcase the employability of the novel substituent, the chlorotetrylenes were subjected to halide abstraction reactions, affording the corresponding tetrylenium salts [RE][Al(OC4 F9 )4 ] (E=Ge, Sn, Pb) as strongly coloured compounds.

Keywords: cations; germanium; lead; steric hindrance; tin.

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