Abstract

A two-stage scheme was proposed for the synthesis of alkoxy derivatives of the closo-decaborate anion [B10H9(OR)]2–, where R = C2H5, iso-C3H7, C4H9. At the first stage, the oxonium derivatives with the general formula [B10H9(OR2)]– were synthesized by the reaction between the [B10H11]–anion and acyclic ethers. At the second stage, the synthesized oxonium derivatives reacted with hydrazine hydrate to form the alkoxy derivatives with the general formula [B10H9(OR)]2–, where R = C2H5, iso-C3H7, C4H9. This approach appreciably increased the yield of target products and simplified their separation. The alkoxy derivatives were separated and characterized by IR and 1H, 11B, and 13C NMR spectroscopy.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call