Varying the Interplay of Calix[5]arenes through Chloromethane Inclusion

Thomas Clark, Mohamed Makha, Colin Raston, Alexandre Sobolev

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

Three inclusion complexes of calix[5] arenes as dichloromethane (DCM) or chloroform solvates have been structurally authenticated, namely, the complexes of p-Bu-t-calix[5] arene, 1, or p-H-calix[5] arene, with DCM, 2, and a new polymorph of the complex of p-phenyl-calix[5] arene with chloroform, 3. Complex 1 has two adjacent tbutyl groups of one calixarene embracing the analogous groups from another calixarene. Complex 2 has a slipped head-to-head arrangement of calixarenes with a DCM molecule in the cavity of each calixarene. In complex 3, the calixarenes form dimers through interdigitation, and these dimers are assembled with back-to-back arrangement of calixarenes from adjacent dimers. All solvate complexes were crystallized in the presence of p-carborane, which has complementarity of size of the cavity of the calixarenes yet is not incorporated in the structures.
Original languageEnglish
Pages (from-to)2783-2787
JournalCrystal Growth & Design
Volume6
Issue number12
DOIs
Publication statusPublished - 2006

Fingerprint Dive into the research topics of 'Varying the Interplay of Calix[5]arenes through Chloromethane Inclusion'. Together they form a unique fingerprint.

  • Cite this