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.
Inorganics 2018, 6(3), 68; https://doi.org/10.3390/inorganics6030068
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)
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.
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Keywords:
ferrocene; steric protection; germanium; selenide; telluride; selenenylchloride; tellurenylchloride
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MDPI and ACS Style
Sasamori, T.; Suzuki, Y.; Sugamata, K.; Sugahara, T.; Tokitoh, N. Synthesis of Ferrocenyl-Substituted Organochalcogenyldichlorogermanes. Inorganics 2018, 6, 68. https://doi.org/10.3390/inorganics6030068
AMA Style
Sasamori T, Suzuki Y, Sugamata K, Sugahara T, Tokitoh N. Synthesis of Ferrocenyl-Substituted Organochalcogenyldichlorogermanes. Inorganics. 2018; 6(3):68. https://doi.org/10.3390/inorganics6030068
Chicago/Turabian StyleSasamori, Takahiro; Suzuki, Yuko; Sugamata, Koh; Sugahara, Tomohiro; Tokitoh, Norihiro. 2018. "Synthesis of Ferrocenyl-Substituted Organochalcogenyldichlorogermanes" Inorganics 6, no. 3: 68. https://doi.org/10.3390/inorganics6030068
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