Cation-controlled capture of polyoxovanadate-based organic-inorganic 1D architectures

Stefan Repp; Michael Steiner; Montaha Anjass; Dieter Sorsche; Carsten Streb

doi:10.1039/d2cc04379c

Cation-controlled capture of polyoxovanadate-based organic-inorganic 1D architectures

Chem Commun (Camb). 2022 Dec 1;58(96):13397-13400. doi: 10.1039/d2cc04379c.

Authors

Stefan Repp¹, Michael Steiner^{1

2}, Montaha Anjass^{1

2}, Dieter Sorsche¹, Carsten Streb^{1

2

3}

Affiliations

¹ Institute of Inorganic Chemistry I, Ulm University, Albert-Einstein-Allee 11, Ulm 89081, Germany. carsten.streb@uni-mainz.de.
² Helmholtz-Institute Ulm, Helmholtzstr. 11, Ulm 89081, Germany.
³ Department of Chemistry, Johannes Gutenberg University Mainz, Duesbergweg 10-14, Mainz 55128, Germany.

PMID: 36382678
DOI: 10.1039/d2cc04379c

Abstract

Metal cations are used to control the selective crystallization of organic-inorganic supramolecular polymers. Two complementary monomers, a dodecanuclear vanadate [V₁₂O₃₂(NO₃)]^5- and the organic macrocycle cyclen assemble into hybrid host-guest aggregates. In the presence of Ba²⁺ or La³⁺, supramolecular polymerization and crystallization is driven by a complex interplay of cyclene protonation, hydrogen-bonding and electrostatics.