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Inorganics 2018, 6(3), 68; https://doi.org/10.3390/inorganics6030068

Synthesis of Ferrocenyl-Substituted Organochalcogenyldichlorogermanes

1
Graduate School of Natural Sciences, Nagoya City University, Yamanohata 1, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8501, Japan
2
Institute for Chemical Research, Gokasho, Uji, Kyoto 611-0011, Japan
3
Department of Chemistry, College of Science, Rikkyo University, 3-34-1 Nishi-Ikebukuro, Toshima-ku, Tokyo 171-8501, Japan
*
Author to whom correspondence should be addressed.
Received: 13 June 2018 / Revised: 6 July 2018 / Accepted: 9 July 2018 / Published: 11 July 2018
(This article belongs to the Special Issue Metallocene Complexes)
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Abstract

Reaction of the isolable ferrocenyldichlorogermyl anion, Fc*GeCl2 (Fc* = 2,5-bis(3,5-di-t-butylphenyl)-1-ferrocenyl), with the isolable chalcogenenyl halides resulted in the formation of the corresponding organochalcogenyldichlorogermanes that were structurally characterized. Thus, it was demonstrated the use of sterically demanding ferrocenyl groups allowed isolating stable crystalline organochalcogenyldichlorogermanes. View Full-Text
Keywords: ferrocene; steric protection; germanium; selenide; telluride; selenenylchloride; tellurenylchloride ferrocene; steric protection; germanium; selenide; telluride; selenenylchloride; tellurenylchloride
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This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. (CC BY 4.0).

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Sasamori, T.; Suzuki, Y.; Sugamata, K.; Sugahara, T.; Tokitoh, N. Synthesis of Ferrocenyl-Substituted Organochalcogenyldichlorogermanes. Inorganics 2018, 6, 68.

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