Display options
Share it on

Chemistry. 2015 Aug 17;21(34):12011-7. doi: 10.1002/chem.201501556. Epub 2015 Jun 30.

Facile Assembly of Chiral Metallosquares by Using Enantiopure Tribenzotriquinacene Corner Motifs.

Chemistry (Weinheim an der Bergstrasse, Germany)

Wen-Rong Xu, Guang-Jie Xia, Hak-Fun Chow, Xiao-Ping Cao, Dietmar Kuck

Affiliations

  1. Department of Chemistry, State Key Laboratory of Synthetic Chemistry and The Center of Novel Functional Molecules, The Chinese University of Hong Kong, Shatin (Hong Kong).
  2. Department of Chemistry, Center of Scientific Modelling and Computation, The Chinese University of Hong Kong, Shatin (Hong Kong).
  3. Department of Chemistry, State Key Laboratory of Synthetic Chemistry and The Center of Novel Functional Molecules, The Chinese University of Hong Kong, Shatin (Hong Kong). [email protected].
  4. State Key Laboratory of Applied Organic Chemistry and College of Chemistry and Chemical Engineering, Lanzhou University, 730000 Lanzhou (P. R. China). [email protected].
  5. Department of Chemistry and Center for Molecular Materials (CM2), Bielefeld University, 33615 Bielefeld (Germany). [email protected].

PMID: 26126897 DOI: 10.1002/chem.201501556

Abstract

A pair of enantiomerically pure metallosquares based on linear platinum-diacetylene edges and tribenzotriquinacene corner units was synthesized. Their structures were characterized by (1) H-, (13) C- and (31) P NMR spectroscopy as well as MALDI-TOF mass spectrometry and circular dichroism. Based on DFT calculation, the optimized geometry possesses a distorted square conformation in which the four edges are not sitting on the same plane. The molecular square further self-assembled in the solid state to afford microspheres with diameter of approximately 300 nm, as determined by scanning electron microscopy.

© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Keywords: metallosquares; molecular spheres; self-assembly; supramolecular chemistry; tribenzotriquinacenes

Publication Types