Chimeric supramolecular synthons in Ph2Te2(I2)Se

Research output: Contribution to journalArticlepeer-review

Abstract

Iodination of Ph2Te2Se by molecular iodine is directed towards the Te atom and yields {diiodo[(phenyltellanyl)selanyl]-λ4-tellanyl}benzene, PhTeSeTeI2Ph or C12H10I2SeTe2. The molecule can be considered as a chimera of PhTeSeR, PhTeSeTePh and R′TeI2Ph fragments. The crystal structure features a complex interplay of the supramolecular synthons Te⋯π(Ph), Se⋯Te and I⋯Te, combining molecules into a three-dimensional framework. Their combination affords long-range supramolecular synthons which are fused in a way resembling the mythological chimera and could be defined as chimeric supramolecular synthons. The energies of the intermolecular interactions have also been calculated and analyzed.

Original languageAmerican English
Pages (from-to)579-584
Number of pages6
JournalActa crystallographica. Section C, Structural chemistry
Volume76
DOIs
StatePublished - 1 Jun 2020
Externally publishedYes

Keywords

  • chalcogenide
  • crystal structure
  • energy framework
  • halogen bonding
  • secondary bonding
  • supramolecular synthon
  • σ-hole

All Science Journal Classification (ASJC) codes

  • Condensed Matter Physics
  • Physical and Theoretical Chemistry
  • Inorganic Chemistry
  • Materials Chemistry

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