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|Title:||Reactivity of digermylenes toward potassium graphite : synthesis and characterization of germylidenide anions||Authors:||Chia, Siew-Peng
|Issue Date:||2011||Source:||Chia, S.-P., Yeong, H.-X., & So, C.-W. (2012). Reactivity of Digermylenes toward Potassium Graphite: Synthesis and Characterization of Germylidenide Anions. Inorganic Chemistry, 51(2), 1002-1010.||Series/Report no.:||Inorganic chemistry||Abstract:||The synthesis and characterization of the digermylenes [LGe–GeL] [L = L1 (3A), L2 (3B)] supported by the 2,6-diiminophenyl (L1) and 2-imino-5,6-methylenedioxylphenyl (L2) ligands are described. Their reactivities toward potassium graphite are also reported. The reaction of [LGeCl] [L = L1 (2A), L2 (2B)] with KC8 in tetrahydrofuran (THF) at room temperature afforded the digermylenes [LGe–GeL] [L = L1 (3A), L2 (3B)], which are the first examples of diaryldigermylenes stabilized by o-imino donor(s). The treatment of 3A with 2 equiv of KC8 in Et2O, followed by the addition of excess tetramethylethylenediamine (TMEDA), results in cleavage of the GeI–GeI bond to afford the germylidenide anion [L1GeK·TMEDA] (4A). Similarly, the reaction of 3B with excess KC8 in THF afforded the germylidenide anion [L2GeK] (4B). The molecular structures of compounds 4A and 4B as determined by single-crystal X-ray diffraction analysis show that the K atoms are η1-coordinated with the low-valent Ge atoms. Moreover, the negative charges at the Ge atoms in compounds 4A and 4B are stabilized by electron delocalization in the germanium heterocycles.||URI:||https://hdl.handle.net/10356/96788
|ISSN:||0020-1669||DOI:||http://dx.doi.org/10.1021/ic202138t||Rights:||© 2011 American Chemical Society.||Fulltext Permission:||none||Fulltext Availability:||No Fulltext|
|Appears in Collections:||SPMS Journal Articles|
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