4.8 Article

Introducing Axial Chirality into Mesoionic 4,4′-Bis(1,2,3-triazole) Dicarbenes

Journal

ORGANIC LETTERS
Volume 14, Issue 7, Pages 1866-1868

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol3004657

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Funding

  1. Ministerio de Ciencia e Innovacion (MICINN, Spain) [CTQ2010-21625-C02-01]
  2. UPV/EHU
  3. Gobierno Vasco (ETORTEK-nanoIKER) [1E-11/304]
  4. Gobierno Vasco

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Mesoionic 4,4'-bis(1,2,3-triazole-5,5'-diylidene) Rh(I) complexes having a C2 chiral 4,4'-axis were accessed from 3-alkyltriazolium salts in virtually complete de. Their structure and configurational integrity were assessed by NMR spectroscopy, X-ray crystallography, and chiral HPLC. Computational analysis of the MICs involved in the reaction suggested the formation of a highly stable and unprecedented cation-carbene intermediate species, which could be evidenced experimentally by cyclic voltammetry analysis.

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