Incommensurate Phase in Λ-cobalt (III) Sepulchrate Trinitrate Governed by Highly Competitive N−H⋅⋅⋅O and C−H⋅⋅⋅O Hydrogen Bond Networks

Titelangaben

Dey, Somnath ; Schönleber, Andreas ; van Smaalen, Sander ; Morgenroth, Wolfgang ; Krebs Larsen, Finn:
Incommensurate Phase in Λ-cobalt (III) Sepulchrate Trinitrate Governed by Highly Competitive N−H⋅⋅⋅O and C−H⋅⋅⋅O Hydrogen Bond Networks.
In: Chemistry : a European Journal. Bd. 28 (1 März 2022) Heft 13 . - Nr. e202104151.
ISSN 1521-3765
DOI der Verlagsversion: https://doi.org/10.1002/chem.202104151

Volltext

	Format: PDF Name: Chemistry A European J - 2022 - Dey - Incommensurate Phase in ‐cobalt III Sepulchrate Trinitrate Governed by Highly.pdf Version: Veröffentlichte Version Verfügbar mit der Lizenz Creative Commons BY 4.0: Namensnennung
	Download (1MB)

Abstract

Phase transitions in molecular crystals are often determined by intermolecular interactions. The cage complex of [Co(C₁₂H₃₀N₈)]³⁺ ⋅ 3 NO₃⁻ is reported to undergo a disorder-order phase transition at T꜀₁≈133 K upon cooling. Temperature-dependent neutron and synchrotron diffraction experiments revealed satellite reflections in addition to main reflections in the diffraction patterns below T꜀₁. The modulation wave vector varies as function of temperature and locks in at T꜀₃≈98 K. Here, we demonstrate that the crystal symmetry lowers from hexagonal to monoclinic in the incommensurately modulated phases in T꜀₁<T<T꜀₃. Distinctive levels of competitions: trade-off between longer N−H⋅⋅⋅O and shorter C−H⋅⋅⋅O hydrogen bonds; steric constraints to dense C−H⋅⋅⋅O bonds give rise to pronounced modulation of the basic structure. Severely frustrated crystal packing in the incommensurate phase is precursor to optimal balance of intermolecular interactions in the lock-in phase.