Please use this identifier to cite or link to this item: http://dx.doi.org/10.14279/depositonce-6238
Main Title: Heavier congeners of CO and CO2 as ligands: from zero-valent germanium ('germylone') to isolable monomeric GeX and GeX2 complexes (X = S, Se, Te)
Author(s): Xiong, Yun
Yao, Shenglai
Karni, Miriam
Kostenko, Arseni
Burchert, Alexander
Apeloig, Yitzhak
Drieß, Matthias
Type: Article
Language Code: en
Abstract: In contrast to molecular CO and CO2, their heavier mono- and dichalcogenide homologues, EX and EX2 (E = Si, Ge, Sn, Pb; X = O, S, Se, Te), are important support materials (e.g., SiO2) and/or semiconductors (e.g., SiS2) and exist typically as insoluble crystalline or amorphous polymers under normal conditions. Herein, we report the first successful synthesis and characterisation of an extraordinary series of isolable monomeric GeX and GeX2 complexes (X = S, Se, Te), representing novel classes of compounds and heavier congeners of CO and CO2. This could be achieved by solvent-dependent oxidation reactions of the new zero-valent germanium ('germylone')-GaCl3 precursor adduct (bis-NHC)Ge-0 -> GaCl3 1 (bis-NHC = H2C[{NC(H)=C(H)N(Dipp)}C:](2), Dipp = 2,6-iPr(2)C(6)H(3)) with elemental chalcogens, affording the donor-acceptor stabilised monomeric germanium(IV) dichalcogenide (bis-NHC)Ge-IV(=X)=X -> GaCl3 (X = S, 2; X = Se, 3) and germanium(II) monochalcogenide complexes (bis-NHC)Ge-II= X -> GaCl3 (X = Se, 4; X = Te, 5), respectively. Moreover, the reactivity of 4 and 5 towards elemental sulphur, selenium, and tellurium has been investigated. In THF, the germanium(II) monoselenide complex 4 reacts with activated elemental selenium to afford the desired germanium(IV) diselenide complex 3. Unexpectedly, both reactions of 4 and 5 with elemental sulphur, however, lead to the formation of germanium(IV) disulfide complex 2 under liberation of elemental Se and Te as a result of further oxidation of the germanium centre and replacement of the Se and Te atoms by sulphur atoms. All novel compounds 1-5 have been fully characterised, including single-crystal X-ray diffraction analyses, and studied by DFT calculations.
URI: https://depositonce.tu-berlin.de//handle/11303/6899
http://dx.doi.org/10.14279/depositonce-6238
Issue Date: 2016
Date Available: 24-Oct-2017
DDC Class: 540 Chemie und zugeordnete Wissenschaften
Creative Commons License: https://creativecommons.org/licenses/by/3.0/
Journal Title: Chemical Science
Publisher: Royal Society of Chemistry
Publisher Place: Cambridge
Volume: 7
Issue: 8
Publisher DOI: 10.1039/c6sc01839d
Page Start: 5462
Page End: 5469
EISSN: 2041-6539
ISSN: 2041-6520
Appears in Collections:Fachgebiet Metallorganische Chemie und Anorganische Materialien » Publications

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