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A previously unknown cocrystal of olanzapine and phenol was identified from a volatile deep eutectic solvent as the intermediate species in the crystallization of olanzapine. This new nanocrystalline phase was investigated by electron diffraction, powder X-ray diffraction and differential scanning calorimetry. The structure was determined by simulated annealing using 3D electron diffraction data and confirmed using DFT-D optimizations. Olanzapine and phenol cocrystallize in the triclinic space group P1, supporting the hypothesis of a dimeric growth unit, where a centrosymmetric dimer is stabilized by multiple weak C—H...π interactions and forms double N—H...N hydrogen bonding with adjacent dimers.

Supporting information

cif

Crystallographic Information File (CIF) https://doi.org/10.1107/S2052520620012779/je5035sup1.cif
3D ED data, CCDC 2027602 (I). Powder XRD data, CCDC 2030951 (II)

hkl

Structure factor file (CIF format) https://doi.org/10.1107/S2052520620012779/je5035Isup2.hkl
Contains datablock I

CCDC references: 2027602; 2030951


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