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Preparation and Reactivity of a Triphosphenium Bromide Salt: A Convenient and Stable Source of PhosphorusI
Published on: November 22, 2016
A bis(germylene) functionalized metal-coordinated polyphosphide and its isomerization
Ravi Yadav1, Bhupendra Goswami1, Thomas Simler1
1Institute of Inorganic Chemistry, Karlsruhe Institute of Technology (KIT), Engesserstraße 15, 76131 Karlsruhe, Germany. roesky@kit.edu.
Pentaphosphaferrocene served as a phosphorus source for novel germylene-polyphosphide complexes. Reactivity with a digermylene resulted in a unique iron-phosphorus-germanium complex exhibiting unprecedented isomerization.
Area of Science:
- Organometallic Chemistry
- Main Group Chemistry
- Coordination Chemistry
Background:
- Pentaphosphaferrocene, [Cp*Fe(η5-P5)], is a known source of polyphosphorus ligands.
- Germylene complexes are valuable building blocks in inorganic synthesis.
Purpose of the Study:
- To explore the reactivity of pentaphosphaferrocene with digermylenes.
- To synthesize and characterize novel germylene-polyphosphide complexes.
Main Methods:
- Reaction of [Cp*Fe(η5-P5)] with [LGe-GeL] (L = {PhC(NtBu)2}).
- Isolation and characterization of the resulting complex using spectroscopic and crystallographic techniques.
Main Results:
- A stepwise reaction involving reductive homolytic cleavage of the Ge-Ge bond was observed.
- Formation of the complex [(LGe)2{(μ,η4-P5)FeCp*}] with an unprecedented isomerization.
Conclusions:
- Pentaphosphaferrocene can serve as a versatile polyphosphorus source in reactions with low-valent main group element compounds.
- The observed isomerization highlights novel reactivity pathways in germylene-polyphosphide chemistry.
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