Co‐Crystallization of Half‐Sandwich ( R M , R C )/( S M , R C ) Diastereomers in Single Crystals

Autor: Henri Brunner, Takashi Tsuno, Michael Bodensteiner, Stefanie Gärtner, Chiemi Miyahara, Seera Ito, Takaki Kurosawa, Kazuhiro Koyama
Rok vydání: 2016
Předmět:
Zdroj: European Journal of Inorganic Chemistry. 2016:5405-5410
ISSN: 1099-0682
1434-1948
DOI: 10.1002/ejic.201600962
Popis: Diastereomer separation by fractional crystallization is the most important method for the resolution of enantiomers in research as well as in industry. Herein we describe two different types of diastereomer co-crystallization, which impede diastereomer separation. - The two diastereomers (RFe,RC)- and (SFe,RC)-[CpFe(Prophos)PPh(OMe)2]PF6, differing only in the metal configuration, form 1:1 co-crystals with a racemate-like lattice. Between the (RFe,RC)- and (SFe,RC)-diastereomers there is an almost-inversion center and the (RFe,RC)/(SFe,RC)-pair repeats as a kind of 'dimer' in the lattice. - Crystallization of a 50:50 diastereomer mixture of (RRu,RC)- and (SRu,RC)-[MeCpRu(Prophos)Cl] gave (RRu,RC)/(SRu,RC) 7:93 co-crystals and another crystallization diastereomerically pure (SRu,RC)-[MeCpRu(Prophos)Cl]. In the co-crystal the 93% component (SRu,RC)-[MeCpRu(Prophos)Cl] dictates the build-up of a conglomerate-like lattice and the 7% component (RRu,RC)-[MeCpRu(Prophos)Cl] has to adopt its M-Prophos chelate ring conformation, although diastereomerically pure (RRu,RC)-[MeCpRu(Prophos)Cl] has a completely different chelate ring conformation.
Databáze: OpenAIRE
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