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Isolable Geminal Bisgermenolates: A New Synthon in Organometallic Chemistry

We have synthesized the first isolable geminal bisenolates L(2)K(2)Ge[(CO)R](2) (R=2,4,6‐trimethylphenyl (2 a,b), L=THF for (2 a) or [18]‐crown‐6 for (2 b)), a new synthon for the synthesis of organometallic reagents. The formation of these derivatives was confirmed by NMR spectroscopy and X‐ray cry...

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Detalles Bibliográficos
Autores principales: Drusgala, Manfred, Frühwirt, Philipp, Glotz, Gabriel, Hogrefe, Katharina, Torvisco, Ana, Fischer, Roland C., Wilkening, H. Martin R., Kelterer, Anne‐Marie, Gescheidt, Georg, Haas, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596710/
https://www.ncbi.nlm.nih.gov/pubmed/34464492
http://dx.doi.org/10.1002/anie.202111636
Descripción
Sumario:We have synthesized the first isolable geminal bisenolates L(2)K(2)Ge[(CO)R](2) (R=2,4,6‐trimethylphenyl (2 a,b), L=THF for (2 a) or [18]‐crown‐6 for (2 b)), a new synthon for the synthesis of organometallic reagents. The formation of these derivatives was confirmed by NMR spectroscopy and X‐ray crystallographic analysis. The UV/Vis spectra of these anions show three distinct bands, which were assigned by DFT calculations. The efficiency of 2 a,b to serve as new building block in macromolecular chemistry is demonstrated by the reactions with two different types of electrophiles (acid chlorides and alkyl halides). In all cases the salt metathesis reaction gave rise to novel Ge‐based photoinitiators in good yields.