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Synthesis and Characterization of Pyridine-Ligated Bicyclic (Alkyl)(Amino)Carbene (BICAAC) Ruthenium Alkylidene Complexes
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DOI：10.1002/cctc.70703.png)
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Abstract
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Grubbs-type ruthenium–alkylidene catalysts are pivotal in olefin metathesis, with improved activity and initiation achieved through ligand design. While NHC- and CAAC-based systems are well established, robust and strongly σ-donating BICAACs remain underexplored, particularly in pyridine-activated third-generation catalysts important for Ring-Opening Metathesis Polymerization (ROMP). Here we report the first synthesis and full characterization of pyridine-ligated BICAAC–Ru alkylidene complexes. Using a modified Grubbs protocol that avoids bis-carbene formation, pyridine complexes (1a–3a, 3b) were prepared from in situ generated BICAACs and bis-pyridine phosphine intermediates. Spectroscopic, crystallographic, and DFT studies show that steric congestion at Ru disfavors bis-pyridine coordination, with a second pyridine. These results establish pyridine-coordinated BICAAC–Ru complexes as a well-defined platform for next-generation metathesis catalysts.
Keywords:
BICAAC complex
pyridine ligand
ruthenium alkylidene complex
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