Tunable π-interactions in monomeric organozinc complexes: Solution and solid-state studies

Ella Bukhaltsev, Israel Goldberg, Revital Cohen, Arkadi Vigalok

Research output: Contribution to journalArticlepeer-review

Abstract

A series of the calix[4]arene ligands, partially oxygen-depleted at the 1 and 3 positions via the Sonogashira cross-coupling reaction with several arylacetylenes, were prepared. Upon reaction with R2-Zn (R = Me, Et, C6F5), the corresponding organozinc complexes were obtained. X-ray analysis showed weak π-interactions between the organozinc fragment and the triple bonds. In addition, the solution 13C NMR studies showed good correlation between the strength of these interactions and electron density at the acetylene group, with more electron-rich alkynes binding stronger to the Zn center. The latter was also supported by DFT calculations on a model compound. These results show that, albeit weak, π-interactions of organozinc compounds can be observed and fine-tuned in both solution and the solid state.

Original languageEnglish
Pages (from-to)4015-4020
Number of pages6
JournalOrganometallics
Volume26
Issue number16
DOIs
StatePublished - 30 Jul 2007

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