Issue 40, 2021

Selective crystallization of four bis(phthalocyaninato)lanthanoid(iii) polymorphs

Abstract

Bis(phthalocyaninato)lanthanoid(III) (LnPc2) complexes have attracted significant attention for their exceptional optical, electronic and magnetic properties. Crystallization of these compounds usually requires cumbersome methods such as sublimation and electrocrystallization, which is a significant limitation to both structural determinations and the preparation of high purity materials at scale. We report here the selective crystallization of four polymorphs of LnPc2 obtained exclusively by the slow evaporation of saturated solutions. The obtained phase depends on the initial oxidation state of the LnPc2 molecule and the choice of solvent. Single-crystal X-ray diffraction studies were used to determine 14 new structures including Ln = La, Pr, Nd, Sm, Gd, Tb, Dy, Er and Yb, as well as correct previous mis-identifications from the literature. We provide a detailed comparison of molecular structure and crystal packing in all LnPc2 polymorphs. The primary feature in all phases is columnar stacking based on parallel π–π interactions, with a variety of slip angles within those stacks as well as secondary interactions between them. Chemical redox and acid–base titrations, performed on re-dissolved crystals demonstrate that LnPc2+ and LnPc2 are easily obtained through weak oxidizing and reducing agents, respectively. Additionally, we show that the protonated form of the NdPc2 complex has a nearly identical UV-vis spectrum to that of neutral NdPc2, explaining some of the confusion over chemical composition in previously published literature.

Graphical abstract: Selective crystallization of four bis(phthalocyaninato)lanthanoid(iii) polymorphs

Supplementary files

Article information

Article type
Paper
Submitted
18 jul 2021
Accepted
20 sep 2021
First published
21 sep 2021

CrystEngComm, 2021,23, 7151-7161

Author version available

Selective crystallization of four bis(phthalocyaninato)lanthanoid(III) polymorphs

M. Dailey and C. Besson, CrystEngComm, 2021, 23, 7151 DOI: 10.1039/D1CE00936B

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