Synthesis and Application of Robust Spiro [Fluorene 9] CAAC Ruthenium Alkylidene Complexes to the „One-Pot“ Conversion of Allyl Acetate to Butane-1,4-diol

23 May 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

A series of a novel CAAC ligands featuring a spiro-fluorene group have been synthesized and complexed with ruthenium alkylidenes, yielding the corresponding Hoveyda-type derivatives as a new family of olefin metathesis catalysts. The novel complexes have been characterized by XRD, HRMS and NMR measurements. The synthetized complexes were tested in catalysis and showed good activity in olefin metathesis, as demonstrated on diethyl diallylmalonate and allyl acetate substrates. The unique backbone in the ligand system with the large, yet inflexible condensed system renders interesting properties to the catalyst, exemplified by the good catalytic performance and improved Z selectivity. In addition, the catalyst can also serve as a hydrogenation catalyst in a consecutive (one-pot) reaction. The latter reaction can convert allyl acetate to butane 1,4 diol, a valuable chemical intermediate for biodegradable polybutylene succinate (PBS).

Keywords

fluorene
CAAC
olefin metathesis
allyl acetate

Supplementary materials

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Title
Synthesis and Application of Robust Spiro [Fluorene 9] CAAC Ruthenium Alkylidene Complexes to the „One-Pot“ Conversion of Allyl Acetate to Butane-1,4-diol
Description
Supplementary information containing synthesis and characterization of intermediates and key molecules, alongside description of catalytic tests.
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