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Article Dans Une Revue ChemistrySelect Année : 2022

Solid‐State Structures of Primary Long‐Chain Alkylamine Borane Adducts – Synthesis, Properties and Computational Analysis

Kevin Turani-I-Belloto
  • Fonction : Auteur
María-José Valero-Pedraza
  • Fonction : Auteur
Eddy Petit
  • Fonction : Auteur
Rodica Chiriac
  • Fonction : Auteur
François Toche
  • Fonction : Auteur
Dominique Granier
  • Fonction : Auteur
Pascal G Yot
  • Fonction : Auteur
Johan G Alauzun
  • Fonction : Auteur

Résumé

Two new members of the amine boranes family are hexadecylamine borane C 16 H 33 NH 2 BH 3 (C16AB) and octadecylamine borane C 18 H 35 NH 2 BH 3 (C18AB). They are easily synthesized by reaction of the corresponding amines with borane dimethyl sulfide. Both are white solids; they are crystalline and isostructural (monoclinic, s.g. P2 1 /a (No. 14)). Their successful synthesis has been verified by molecular (FTIR, Raman, NMR) and structural analyses as well as computational calculations (e. g. Mulliken charges). These analyses have also pointed out the existence of dihydrogen bonds between H δ + of NH 2 of one molecule and H δÀ of BH 3 of another molecule. The thermal stability of C16AB and C18AB was studied. Both solids melts at 70-80 °C; between 100 and ca. 210 °C they dehydrogenate while releasing 1.1-1.4 wt% of pure H 2 ; and, above 210 °C, they decompose in high extent. All of these findings may open the way to future works on molecular self-assembly, synthesis of advanced materials and hydrogen storage. This is discussed hereafter.

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hal-03855968 , version 1 (16-11-2022)

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Kevin Turani-I-Belloto, María-José Valero-Pedraza, Eddy Petit, Rodica Chiriac, François Toche, et al.. Solid‐State Structures of Primary Long‐Chain Alkylamine Borane Adducts – Synthesis, Properties and Computational Analysis. ChemistrySelect, 2022, 7 (43), ⟨10.1002/slct.202203533⟩. ⟨hal-03855968⟩
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