Synthesis and Electrochemical Studies of Porphyrin Dimers Linked by Metallocarbenes
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文摘
The functionalization of porphyrins at the meso positions by azoles led, after subsequent alkylation, to several precursors of N-heterocyclic carbenes. Porphyrin dimers linked by palladium (or rhodium) bis-carbene spacers were prepared and characterized. Spectroscopic data and X-ray structures showed that the coordination geometry for the two carbenes around the palladium linker was trans-anti. Electrochemical studies revealed significant electronic communication between the two porphyrins, despite the absence of conjugation pathways.

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