Isolation of cyclic aluminium polysulfides by stepwise sulfurization

Huihui Xu, Catherine Weetman, Franziska Hanusch, Shigeyoshi Inoue

Research output: Contribution to journalArticlepeer-review

1 Downloads (Pure)

Abstract

Despite the notable progress in aluminium chalcogenides, their sulfur congeners have rarely been isolated under mild conditions owing to limited synthetic precursors and methods. Herein, facile isolation of diverse molecular aluminium sulfides is achievable, by the reaction of N -heterocyclic carbene-stabilized terphenyl dihydridoaluminium ( 1 ) with various thiation reagents. Different to the known dihydridoaluminium 1 Tipp , 1 features balanced stability and reactivity at the Al center. It is this balance that enables the first monomeric aluminium hydride hydrogensulfide 2 , the six-membered cyclic aluminium polysulfide 4 and the five-membered cyclic aluminium polysulfide 6 t o be isolated, by reaction with various equivalents of elemental sulfur. Moreover, a rare aluminium heterocyclic sulfide with Al-S-P five-membered ring ( 7 ) was obtained in a controlled manner. All new compounds were fully characterized by multinuclear NMR spectroscopy and elemental analysis. Their structures were confirmed by single-crystal X-ray diffraction studies.
Original languageEnglish
Article numbere202104042
Number of pages7
JournalChemistry - A European Journal
Volume28
Issue number8
Early online date21 Dec 2021
DOIs
Publication statusPublished - 7 Feb 2022

Keywords

  • aluminium hydride
  • chalogenide
  • controllable
  • desulfurization
  • polysulfide

Fingerprint

Dive into the research topics of 'Isolation of cyclic aluminium polysulfides by stepwise sulfurization'. Together they form a unique fingerprint.

Cite this