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Search for "fluoride sensing" in Full Text gives 2 result(s) in Beilstein Journal of Organic Chemistry.

Synthesis of dibenzosuberenone-based novel polycyclic π-conjugated dihydropyridazines, pyridazines and pyrroles

  • Ramazan Koçak and
  • Arif Daştan

Beilstein J. Org. Chem. 2021, 17, 719–729, doi:10.3762/bjoc.17.61

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  • tautomerization A with a [1,7]-H shift 13 would be formed. Alternatively, in the second mechanism, 13 is thought to occur by tautomerization B and a [1,5]-H shift (Scheme 9). Photophysical properties In our previous work, we examined the photophysical and fluoride sensing properties of dihydropyridazine
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Published 15 Mar 2021

Tetrathiafulvalene-based azine ligands for anion and metal cation coordination

  • Awatef Ayadi,
  • Aziz El Alamy,
  • Olivier Alévêque,
  • Magali Allain,
  • Nabil Zouari,
  • Mohammed Bouachrine and
  • Abdelkrim El-Ghayoury

Beilstein J. Org. Chem. 2015, 11, 1379–1391, doi:10.3762/bjoc.11.149

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  • prepared electroactive rhenium complex the TTF is neutral and the rhenium cation is hexacoordinated. The electrochemical behavior of the three compounds indicates that they are promising for the construction of crystalline radical cation salts. Keywords: azine ligand; fluoride sensing; rhenium
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Published 07 Aug 2015
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