Conformation behavior of azolium-linked cyclophane upon immobilization by hybrid supramolecule assembly: Synthesis and characterization

Article type: Research Article

Authors: Li, Yuan-Yuan | Xiao, Min | Zhang, Chong | Niu, Yun-Yin^{; *}

Affiliations: College of Chemistry and Molecular Engineering, Zhengzhou University, Henan, P.R. China

Correspondence: [*] Corresponding author: Yun-Yin Niu, College of Chemistry and Molecular Engineering, Zhengzhou University, Henan 450001, P.R. China. E-mail: [email protected].

Abstract: In this paper, one imidazole macrocyclic divalent cation with flexible configuration was chosen with the aim of the immobilization of its conformation. One novel organic-inorganic hybrid supramolecule {[syn/anti-did] (CuS3C3N3) (C2H3N)} (1), [did2+ = (12z, 52z)–11H, 51H–1, 5(1, 3)-diimidazol-3-iuma-3, 7(1, 2)-dibenzenacyclooctaphane-13, 53-diium] has been synthesized through the self-assembly reaction of did2+ with CuSCN under solvothermal reaction. This compound has been unambiguously confirmed by PXRD, IR, TG and X-ray single crystal diffraction. Crystallographic analysis shows that the anion of compound 1 is binuclear structure. The stability of compound 1 is relatively good.

DOI: 10.3233/MGC-190793

Journal: Main Group Chemistry, vol. 18, no. 4, pp. 437-443, 2019