A complementary experimental and computational study of loxapine succinate and its monohydrate

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Bhardwaj, Rajni M. and Johnston, Blair F. and Oswald, Iain D. H. and Florence, Alastair J. (2013) A complementary experimental and computational study of loxapine succinate and its monohydrate. Acta Crystallographica Section C: Crystal Structure Communications, 69 (11). pp. 1273-1378. ISSN 0108-2701 (https://doi.org/10.1107/S0108270113029363)

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Abstract

The crystal structures of loxapine succinate [systematic name: 4-(2-chlorodibenzo[b,f][1,4]oxazepin-11-yl)-1-methylpiperazin-1-ium 3-carboxypropanoate], C18H19ClN3O+center dot C4H5O4-, and loxapine succinate monohydrate systematic name: bis[4-(2-chlorodibenzo[b,f][1,4]oxazepin-11-yl)-1-methylpiperazin- 1-ium] succinate succinic acid dihydrate, 2C(18)H(19)ClN(3)O(+)center dot C4H4O42-center dot C4H6O4 center dot 2H(2)O, have been determined using X-ray powder diffraction and single-crystal X-ray diffraction, respectively. Fixed cell geometry optimization calculations using density functional theory confirmed that the global optimum powder diffraction derived structure also matches an energy minimum structure. The energy calculations proved to be an effective tool in locating the positions of the H atoms reliably and verifying the salt configuration of the structure determined from powder data. Crystal packing analysis of these structures revealed that the loxapine succinate structure is based on chains of protonated loxapine molecules while the monohydrate contains dispersion stabilized centrosymmetric dimers. Incorporation of water molecules within the crystal lattice significantly alters the molecular packing and protonation state of the succinic acid.

ORCID iDs

Bhardwaj, Rajni M., Johnston, Blair F. ORCID logoORCID: https://orcid.org/0000-0001-9785-6822, Oswald, Iain D. H. ORCID logoORCID: https://orcid.org/0000-0003-4339-9392 and Florence, Alastair J. ORCID logoORCID: https://orcid.org/0000-0002-9706-8364;
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