Uebergangsmetall-methylen-komplexe. XII. Zur reversiblen protonierung einer elektronenreichen metall-metall-bindung

Wolfgang A. Herrmann, Johann Plank, Doris Riedel

Research output: Contribution to journalArticlepeer-review

21 Scopus citations

Abstract

The dinuclear cationic μ-hydridorhodium complex [(μ-CO)(μ-H) (η5-C5H5)-Rh(CO)2]BF4 has been synthesized in quantitative yield by metal-metal bond protonation of the parent carbonyl compound (μ-CO)[(η5-C5H5)Rh(CO)]2 with HBF4/diethyl ether, the complex is characterized by conductivity measurements and IR, 1H NMR and {1H}-13 C NMR spectroscopy, rapid deprotonation is effected by sodium methoxide. The C3υ-isomer of (η5-C5H5)3Rh3(CO)3 is isolated in 92% yield from reaction of the parent compound with HBF4/H2O in tetrahydrofuran.

Original languageEnglish
Pages (from-to)C47-C50
JournalJournal of Organometallic Chemistry
Volume190
Issue number2
DOIs
StatePublished - 6 May 1980
Externally publishedYes

Fingerprint

Dive into the research topics of 'Uebergangsmetall-methylen-komplexe. XII. Zur reversiblen protonierung einer elektronenreichen metall-metall-bindung'. Together they form a unique fingerprint.

Cite this