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From formulation to structure: 3D electron diffraction for the structure solution of a new indomethacin polymorph from an amorphous solid dispersion
aDepartment of Materials Science and Metallurgy, University of Cambridge, 27 Charles Babbage Road, Cambridge CB3 0FS, United Kingdom, bGSK R&D, Gunnels Wood Road, Stevenage SG1 2NY, United Kingdom, and cBeamline I11, Diamond Light Source, Didcot, Oxford OX11 0DE, United Kingdom
*Correspondence e-mail: hl585@cam.ac.uk, pam33@cam.ac.uk
3D electron diffraction (3DED) is increasingly employed to determine molecular and crystal structures from micro-crystals. Indomethacin is a well known, marketed, small-molecule non-steroidal anti-inflammatory drug with eight known polymorphic forms, of which four structures have been elucidated to date. Using 3DED, we determined the structure of a new ninth polymorph, σ, found within an amorphous solid dispersion, a product formulation sometimes used for active pharmaceutical ingredients with poor aqueous solubility. Subsequently, we found that σ indomethacin can be produced from direct solvent evaporation using dichloromethane. These results demonstrate the relevance of 3DED within drug development to directly probe product formulations.
Keywords: indomethacin; amorphous solid dispersions; drug development; 3D electron diffraction; polymorphism; structure determination; pharmaceutical formulation; active pharmaceutical ingredients.
CCDC reference: 2355453
1. Introduction
Interest in 3D electron diffraction (3DED) techniques for structure solution from micro-crystals has increased rapidly within drug discovery over the past 5 years (Gemmi et al., 2019; Jones et al., 2018
). 3DED (also known as MicroED) enables the determination of molecular structures from micro-crystals, eliminating the need for the larger crystals required for single-crystal X-ray diffraction (SCXRD) – the current gold standard for structure solution in the pharmaceutical industry – and unlocks possibilities for high-throughput The potential impact of 3DED within drug development has been less prominent (Lightowler et al., 2024
): the majority of compounds with previously unknown structures that have been solved were of a single phase, studied in isolation; although there has been success with determining structures from off-the-shelf products (Jones et al., 2018
; Karothu et al., 2023
; Gruene et al., 2018
). We present here a 3DED study on a type of sample that may be investigated at the product formulation stage of development, with the added complications of an unexpected form of the active pharmaceutical ingredient (API) and the presence of an excipient.
Indomethacin (Fig. 1) is a non-steroidal anti-inflammatory drug known to have eight polymorphic forms (Table 1
). Despite having been widely used for over 40 years, the structures of several polymorphs (δ and θ) have only recently been revealed using 3DED (Lightowler et al., 2022
; Andrusenko et al., 2021
). Indomethacin is classified using the Biopharmaceutics Classification System (BCS) as class II (Butler & Dressman, 2010
), indicating its poor aqueous solubility resulting in low oral bioavailability. Amorphous solid dispersions (ASDs) are a popular formulation strategy used to create superior dissolution performance – often referred to as the `spring effect' – of poorly soluble pharmaceutical molecules by creating a stable solid dispersion of the API within an amorphous water-soluble polymer, which acts as an (Vasconcelos et al., 2007
). Furthermore, ASDs aim to provide kinetic stability to prevent subsequent crystallization of the supersaturated drug within the gastrointestinal tract, often referred to as the `parachute effect' (Hu et al., 2019
; Guzmán et al., 2007
). However, ASDs may experience storage life complications caused by unwanted and crystallization of the API which may affect the performance of the drug product, subject to different storage conditions such as humidity and temperature (Ricarte et al., 2019
; Xie & Taylor, 2017
). Undesirable crystallinity found in ASDs may take the form of different polymorphs (S'ari et al., 2021
). These can be difficult to isolate from the formulation in the form of a single crystal of sufficient quality for SCXRD. This may be further exacerbated by the presence of multiple polymorphs, resulting in potential concern later on in the drug development process where the appearance of new forms can have serious consequences (Newman & Wenslow, 2016
).
![]() Van Duong et al. (2018 ![]() †Kistenmacher & Marsh (1972 ![]() ‡Chen et al. (2002 ![]() §Andrusenko et al. (2021 ![]() ¶Lightowler et al. (2022 ![]() |
![]() | Figure 1 Indomethacin molecule C19H16ClNO4. |
In this work, we formulate an ASD of indomethacin and polyvinylpyrrolidone (PVP), prepared via the solvent-evaporation method using dichloromethane (DCM) (Ricarte et al., 2019). We find crystallinity in the form of a new polymorph of indomethacin which grows in a whisker-like (∼30 nm wide) or lath-like (approximately several hundred nanometres wide) morphology [see Fig. 2
(a)]. We solved the structure of this new polymorph using 3DED.
![]() | Figure 2 (a) Crystal from which structure solution was successful. It is positioned such that the [100]* direction is parallel to the direction of the electron beam at 0 ° tilt, based on the calculated orientation matrix. (b)–(d) Slices of planes from the reconstructed for indomethacin. suggest a monoclinic of C2/c or Cc. |
2. Methods
The presence of a new crystal form in the ASD was first identified using powder X-ray diffraction (PXRD). As expected, indomethacin (purchased from Sigma–Aldrich) was as polymorph γ, the most stable form. Given that a range of drug loadings are commonly found in commercial ASDs (He & Ho, 2015), ASDs across a range of drug loadings were produced using the solvent-evaporation method (see Section S1.1 of the supporting information). ASDs with loadings of 20:80 to 80:20 indomethacin:PVP appeared amorphous using PXRD. However, PXRD from 95:5 indomethacin:PVP ASDs feature a set of low-angle characteristic peaks which could not be matched to any of the polymorphs of indomethacin in the Cambridge Structural Database (CSD), but instead showed very strong similarities to the τ structure previously reported by Van Duong et al. (2018
) in an indomethacin:polyethylene glycol solid dispersion. Owing to the difficulty isolating single crystals of τ for SCXRD, the structure of this polymorph remains unsolved. For our structure, indexing the PXRD data was challenging, providing many possible monoclinic unit cells and options. Before turning to 3DED, several attempts to progress with from PXRD data via global optimization methods using some of the many candidate unit cells of our structure proved unsuccessful.
The ASD was deposited as a crushed powder onto Quantifoil R1.2/1.3 grids. 3DED data were collected from crystals several micrometres in size under cryogenic conditions using a Thermo Fisher Titan Krios G3i operated at 300 kV and a CETA-16M camera, revealing a monoclinic C2/c or Cc. Though the occurrence of Cc structures in the CSD is rarer than C2/c, structure solution using both space groups was attempted before further conclusions were drawn.
Based on observed the search was narrowed to two possible space groups:A dataset obtained from one crystal [shown in Fig. 2(a)] was of sufficient quality to proceed with the structure solution, giving a completeness of 77% up to 0.8 Å resolution. The monoclinic cell parameters were found to be a = 43.70 (12) Å, b = 5.19 (7) Å, c = 33.43 (7) Å, β = 100.73 (9)°, V = 7448 (104) Å3. From the orientation matrix, the short crystallographic b axis is parallel to the long axis of the crystals, as might be expected from Bravais–Friedel–Donnay–Harker (Donnay & Harker, 1937
) considerations. Crystals were found to lie with the (100) face flat on the grids [Fig. 2
(a)]. Due to this of the crystals, a problem documented in 3DED (Lightowler et al., 2022
; Woollam et al., 2020
), it was not possible to collect to a completeness of greater than 80% even with the merging of multiple crystals. Given the sufficient quality of an individual dataset, we decided not to merge data from multiple crystals.
3. Results and discussion
The structure was successfully solved via the ab initio dual space method implemented in SHELXD (Schneider & Sheldrick, 2002) using the C2/c with two indomethacin molecules per (Z′ = 2). All non-hydrogen atoms were found in the initial C2/c structure solution. Hydrogen atoms were generated in geometrically idealized positions. By comparison, structure solution using the Cc only yielded a partial solution. The positions of atoms found in the incomplete Cc solution matched the of those in the C2/c solution, but with an origin shift. However, of the partial solution was highly unstable even with restraints to control the Therefore, a final was carried out using the least-squares methods in SHELXL for the C2/c with electron scattering factors [International Tables Vol. C: Tables 4.2.6.8 and 6.1.1.4]. Restraints were limited to maintaining the same geometry in the two independent molecules: there was no need for any further geometric or atomic displacement restraints. Isotropic atomic displacement factors were preferred because anisotropic was not found to significantly improve the model. The final model gave an R factor of 28.22% refined using data to 0.8 Å resolution. Table S1 of the supporting information summarizes all relevant crystallographic information.
ED structures typically have higher R factors than those solved using SCXRD (Klar et al., 2023). In this case, this is likely due to several factors. Both the structure solution and the have been carried out using kinematical approximations assuming intensities are proportional to the square of the (Ihkl ∝ |Fhkl|2); dynamical effects (i.e. multiple scattering) which will affect the observed intensities are not considered here (Palatinus et al., 2015
). Another factor is the induced radiation damage to the sample. This is qualitatively described by the observation of higher-order spots reducing in intensity across the tilt series. Quantitative modelling of the effects of electron beam irradiation damage are not yet well established (Peet et al., 2019
). The CETA camera used is also less sensitive compared with a direct electron detector and required a higher dose (a cumulative dose of 20 e Å−2 per tilt series), thus exacerbating sample damage and accurate detection of intensities. Finally, no correction was made to account for the effects of inelastic scattering.
The (a), the torsion angles in the carboxyl groups of the different indomethacin molecules here are orthogonal but otherwise the molecules are highly similar. By considering the overlay for all non-hydrogen atoms except the carboxylic acid oxygens, the RMSD is reduced to 0.125 Å. The independent indomethacin molecules in this polymorph form a carboxylic dimer which is consistent with interactions found in the α, γ, θ and δ forms.
![]() | Figure 3 (a) Comparison between the two independent molecules of σ showing their conformational similarity (RMSD = 0.5003 Å). The biggest difference comes from the torsion angle of the carboxyl groups. Overlaying all atoms except the carboxylic acid oxygens leads to RMSD = 0.125 Å. (b) Conformational comparison between one of the indomethacin molecules in σ with one of the independent molecules in the δ structure (RMSD = 0.392 Å). Similarly to (a), the difference comes from the torsion angle of the carboxyl groups. Overlaying all atoms except the carboxylic acid oxygens leads to RMSD = 0.153 Å. (c) Yellow graphics highlight the channels in the σ structure which suggest that solvent templating was the mechanism for formation. |
To confirm our 3DED model and show consistency with the bulk sample, a Rietveld rigid-body supporting information). This converged with a satisfactory fit (Rwp = 1.40%, χ2 = 2.09) without significant modification of the structure. Although characteristic peak positions from the new structure are very similar to that of the τ polymorph identified by Van Duong et al. (2018), the relative intensities of the peaks do not match, and this cannot be accounted for by the effects of texture. Most notably, the very weak intensity of the (400) peak in the new PXRD data contrasts with the strong peak at the corresponding location in τ. This cannot be explained by because the lower-order peak (200) is the strongest peak detected in the new structure: this is more than 8000 times stronger than (400), as shown in Fig. S4. The difference in observed intensities in PXRD data must instead come from differences within the unit cells. It is not possible to see these peaks in the ED data because these low-order reflections are covered by the shadow of the beam stop, which acts to protect the electron detector from the direct beam. However, given the similar characteristic peak positions, the τ polymorph and our structure are likely to be closely related and share strong structural similarities. We propose to name the new structure σ, the ninth polymorph of indomethacin.
On further inspection of σ, we note that 12% of the unit-cell volume is composed of predominantly hydrophobic open channels parallel to the b axis [Fig. 3(c)]. Large void spaces in crystal structures can be associated with metastable phases (Kitaigorodskii, 1965
; Barbas et al., 2018
; Sundareswaran & Karuppannan, 2020
). The metastable nature of polymorph σ relative to the most thermodynamically stable γ phase is supported by the emergence of new peaks corresponding to the latter phase in the PXRD data collected around 10 months after the production of σ. Based on the spatial distribution of the channels, we considered the possibility that a smaller molecule (such as solvent) is responsible for the empty space in the structure and is relevant to the crystallization mechanism of σ. We propose that DCM molecules (the solvent used) may have acted as a backbone solvent template, running in channels through the structure during solvent evaporation as crystals formed. The total channel volume in the is 903 Å3, with 8 channels in each The molar volume of DCM is ∼68 Å3, suggesting that each channel could fit two solvent molecules given that we would expect channels in the structure to decrease in volume upon The volatility of DCM makes it highly unlikely to remain within the indomethacin structure on drying. This is further reinforced by the lack of residual electron density observed in the channels. To confirm this hypothesis, evaporation of a DCM solution of pure indomethacin was carried out (on a crystallization dish left at room temperature, with no additional heating or pressure necessary), also yielding the σ structure observed using PXRD. This is consistent with the theory of crystallization via solvent templating (Gnutzmann et al., 2014
; Klimakow et al., 2010
).
Consequently, based on our observations from the solved structure, we have developed a simpler route to forming this polymorph. Although DCM is not a solvent generally used in manufacturing processes within the pharmaceutical industry owing to its environmental impact, the more open structure of this metastable form of indomethacin may be of potential interest as it will likely have different dissolution properties compared with the most thermodynamically stable γ phase. A similar theory was proposed for the crystallization of the δ polymorph, whereby the indomethacin methanol solvate first crystallizes before (Andrusenko et al., 2021). However, the methanol directly disrupts the hydrogen bonding between indomethacin molecules, whereas in σ the positions of the channels suggest that the DCM molecules do not interact strongly with indomethacin, as would be expected based on its lack of hydrogen bond donors and acceptors. Interestingly, although σ and δ have different packing arrangements, the conformations of the individual indomethacin molecules are broadly comparable [an example of this conformational fit is shown in Fig. 3
(b)].
To conclude, we have isolated a metastable phase of indomethacin from an amorphous solid dispersion and reported the structure of a new polymorph (which we call σ) using 3DED. The solution obtained suggested a crystallization mechanism of solvent templating and provided an easier experimental route to the new form via evaporation of pure indomethacin from DCM. This demonstrates the applicability of 3DED to drug development in addition to drug discovery.
4. Related literature
The following references are cited in the supporting information: Coelho (2018); Macrae et al. (2020
); Pham et al. (2010
); Rigaku (2020
).
Supporting information
CCDC reference: 2355453
https://doi.org/10.1107/S2052252524008121/of5005sup1.cif
contains datablock I. DOI:Structure factors: contains datablock indomethacin_sigma. DOI: https://doi.org/10.1107/S2052252524008121/of5005sup2.hkl
Input file from the https://doi.org/10.1107/S2052252524008121/of5005sup3.txt
carried out on the PXRD data. DOI:Supporting figures and table. DOI: https://doi.org/10.1107/S2052252524008121/of5005sup4.pdf
C19H16ClNO4 | F(000) = 1114 |
Mr = 357.79 | Dx = 1.276 Mg m−3 |
Monoclinic, C2/c | Electron radiation, λ = 0.0197 Å |
a = 43.70 (12) Å | Cell parameters from 6711 reflections |
b = 5.19 (7) Å | θ = 0.1–0.7° |
c = 33.43 (7) Å | µ = 0.000 mm−1 |
β = 100.73 (9)° | T = 87 K |
V = 7448 (104) Å3 | Lath, off-white |
Z = 16 | 0.01 × 0.001 × 0.0001 mm |
Thermo Scientific Krios G3i diffractometer | 4062 reflections with I > 2σ(I) |
Radiation source: transmission electron microscope | Rint = 0.137 |
3D–ED scans | θmax = 0.7°, θmin = 0.1° |
Absorption correction: multi-scan CrysAlisPro 1.171.41.93a (Rigaku Oxford Diffraction, 2020) Empirical absorption correction using spherical harmonics, implemented in SCALE3 ABSPACK scaling algorithm. | h = −48→47 |
Tmin = 0.015, Tmax = 1.000 | k = −6→6 |
15410 measured reflections | l = −41→41 |
5885 independent reflections |
Refinement on F2 | Hydrogen site location: inferred from neighbouring sites |
Least-squares matrix: full | H-atom parameters constrained |
R[F2 > 2σ(F2)] = 0.282 | w = 1/[σ2(Fo2) + (0.2913P)2 + 28.140P] where P = (Fo2 + 2Fc2)/3 |
wR(F2) = 0.635 | (Δ/σ)max < 0.001 |
S = 1.17 | Δρmax = 0.45 e Å−3 |
5885 reflections | Δρmin = −0.42 e Å−3 |
208 parameters | Extinction correction: SHELXL-2017/1 (Sheldrick 2017), Fc*=kFc[1+0.001xFc2λ3/sin(2θ)]-1/4 |
66 restraints | Extinction coefficient: 534 (71) |
Primary atom site location: dual |
Experimental. On the TEM is is impossible to determine the crystal colour. However, the colour of the bulk powder is off-white as described above. |
Geometry. All esds (except the esd in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell esds are taken into account individually in the estimation of esds in distances, angles and torsion angles; correlations between esds in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell esds is used for estimating esds involving l.s. planes. |
Refinement. The co-ordinates for the non-hydrogen atoms were refined with 'SAME 0.005' restraints that held the two independent molecules to have the same geometry. There was no need for any further geometric restraints e.g. FLAT. Isotropic ADPs were refined for all the non-hydrogen atoms. No restraints were necessary on these. Hydrogen atoms were geometrically placed and refined using a riding model with isotropic ADPs as an appropriate multiple of the bonded atom. |
x | y | z | Uiso*/Ueq | ||
N1 | 0.6296 (3) | 0.541 (2) | 0.4378 (3) | 0.024 (3)* | |
C2 | 0.6399 (3) | 0.667 (2) | 0.4750 (3) | 0.019 (3)* | |
C3 | 0.6675 (3) | 0.563 (2) | 0.4933 (3) | 0.026 (3)* | |
C4 | 0.7019 (3) | 0.185 (2) | 0.4719 (3) | 0.024 (3)* | |
H4 | 0.717877 | 0.189689 | 0.495482 | 0.029* | |
C5 | 0.7032 (4) | 0.007 (3) | 0.4416 (3) | 0.036 (4)* | |
C6 | 0.6795 (3) | 0.003 (2) | 0.4063 (3) | 0.024 (3)* | |
H6 | 0.680803 | −0.119154 | 0.385499 | 0.029* | |
C7 | 0.6538 (3) | 0.177 (2) | 0.4012 (3) | 0.020 (3)* | |
H7 | 0.638012 | 0.171727 | 0.377400 | 0.024* | |
C8 | 0.6524 (3) | 0.357 (2) | 0.4320 (3) | 0.031 (4)* | |
C9 | 0.6770 (3) | 0.361 (2) | 0.4679 (3) | 0.029 (3)* | |
C10 | 0.6046 (3) | 0.602 (2) | 0.4058 (3) | 0.017 (3)* | |
O11 | 0.6052 (3) | 0.543 (2) | 0.3708 (3) | 0.034 (3)* | |
C12 | 0.5760 (3) | 0.744 (2) | 0.4149 (3) | 0.026 (3)* | |
C13 | 0.5658 (4) | 0.957 (2) | 0.3912 (4) | 0.028 (3)* | |
H13 | 0.576682 | 1.014649 | 0.370862 | 0.033* | |
C14 | 0.5380 (4) | 1.089 (3) | 0.3982 (4) | 0.037 (4)* | |
H14 | 0.531084 | 1.237820 | 0.382500 | 0.044* | |
C15 | 0.5214 (4) | 1.005 (3) | 0.4268 (4) | 0.035 (4)* | |
C16 | 0.5336 (4) | 0.796 (3) | 0.4517 (4) | 0.045 (5)* | |
H16 | 0.523301 | 0.740220 | 0.472837 | 0.054* | |
C17 | 0.5615 (4) | 0.667 (3) | 0.4453 (4) | 0.033 (4)* | |
H17 | 0.569667 | 0.527492 | 0.462412 | 0.040* | |
Cl18 | 0.4879 (3) | 1.1646 (18) | 0.4353 (3) | 0.061 (3)* | |
C19 | 0.6240 (4) | 0.889 (3) | 0.4913 (4) | 0.041 (4)* | |
H19A | 0.615059 | 1.003764 | 0.468858 | 0.062* | |
H19B | 0.639110 | 0.984147 | 0.511158 | 0.062* | |
H19C | 0.607298 | 0.823626 | 0.504528 | 0.062* | |
C20 | 0.6883 (3) | 0.641 (2) | 0.5329 (3) | 0.040 (4)* | |
H20A | 0.709865 | 0.661959 | 0.528114 | 0.048* | |
H20B | 0.681289 | 0.809433 | 0.541577 | 0.048* | |
C21 | 0.6884 (4) | 0.456 (3) | 0.5652 (4) | 0.038 (4)* | |
O22 | 0.7071 (5) | 0.279 (3) | 0.5741 (5) | 0.059 (4)* | |
O23 | 0.6636 (5) | 0.483 (4) | 0.5841 (6) | 0.077 (6)* | |
H23 | 0.666226 | 0.390582 | 0.605172 | 0.115* | |
O24 | 0.7285 (3) | −0.159 (2) | 0.4480 (3) | 0.043 (3)* | |
C25 | 0.7305 (5) | −0.337 (3) | 0.4165 (4) | 0.036 (4)* | |
H25A | 0.733326 | −0.243157 | 0.391963 | 0.054* | |
H25B | 0.711245 | −0.438281 | 0.410463 | 0.054* | |
H25C | 0.748214 | −0.452250 | 0.425131 | 0.054* | |
N51 | 0.6343 (3) | −0.0402 (19) | 0.7580 (3) | 0.018 (3)* | |
C52 | 0.6454 (3) | −0.168 (2) | 0.7266 (3) | 0.021 (3)* | |
C53 | 0.6736 (3) | −0.068 (2) | 0.7232 (3) | 0.025 (3)* | |
C54 | 0.7070 (3) | 0.314 (2) | 0.7618 (3) | 0.018 (3)* | |
H54 | 0.723889 | 0.305447 | 0.747555 | 0.021* | |
C55 | 0.7071 (3) | 0.498 (2) | 0.7919 (3) | 0.017 (3)* | |
C56 | 0.6829 (3) | 0.501 (2) | 0.8147 (3) | 0.014 (3)* | |
H56 | 0.684017 | 0.619080 | 0.836664 | 0.017* | |
C57 | 0.6568 (3) | 0.331 (2) | 0.8058 (3) | 0.016 (3)* | |
H57 | 0.640052 | 0.341766 | 0.820235 | 0.019* | |
C58 | 0.6566 (3) | 0.147 (2) | 0.7751 (3) | 0.021 (3)* | |
C59 | 0.6820 (3) | 0.141 (2) | 0.7524 (3) | 0.018 (3)* | |
C60 | 0.6080 (3) | −0.096 (2) | 0.7755 (3) | 0.016 (3)* | |
O61 | 0.6068 (3) | −0.033 (2) | 0.8102 (3) | 0.025 (3)* | |
C62 | 0.5798 (3) | −0.228 (2) | 0.7497 (3) | 0.025 (3)* | |
C63 | 0.5671 (4) | −0.435 (2) | 0.7666 (4) | 0.031 (4)* | |
H63 | 0.575114 | −0.488539 | 0.793690 | 0.038* | |
C64 | 0.5412 (4) | −0.571 (2) | 0.7419 (3) | 0.029 (3)* | |
H64 | 0.532560 | −0.716461 | 0.752875 | 0.035* | |
C65 | 0.5289 (4) | −0.492 (2) | 0.7029 (3) | 0.031 (4)* | |
C66 | 0.5419 (4) | −0.274 (3) | 0.6875 (4) | 0.038 (4)* | |
H66 | 0.533081 | −0.210789 | 0.661150 | 0.046* | |
C67 | 0.5684 (4) | −0.146 (3) | 0.7113 (3) | 0.032 (4)* | |
H67 | 0.577815 | −0.004628 | 0.700170 | 0.039* | |
Cl68 | 0.4979 (2) | −0.6560 (15) | 0.6727 (2) | 0.044 (2)* | |
C69 | 0.6302 (4) | −0.395 (2) | 0.7030 (4) | 0.023 (3)* | |
H69A | 0.612868 | −0.334872 | 0.682176 | 0.035* | |
H69B | 0.622331 | −0.513204 | 0.721601 | 0.035* | |
H69C | 0.645474 | −0.484251 | 0.689980 | 0.035* | |
C70 | 0.6946 (3) | −0.149 (2) | 0.6942 (3) | 0.027 (3)* | |
H70A | 0.716556 | −0.137458 | 0.708582 | 0.033* | |
H70B | 0.690292 | −0.331112 | 0.686541 | 0.033* | |
C71 | 0.6910 (5) | 0.005 (3) | 0.6577 (4) | 0.044 (4)* | |
O72 | 0.6739 (4) | 0.193 (3) | 0.6500 (4) | 0.044 (4)* | |
O73 | 0.7093 (4) | −0.075 (2) | 0.6314 (4) | 0.038 (3)* | |
H73 | 0.705679 | 0.014798 | 0.610131 | 0.057* | |
O74 | 0.7322 (3) | 0.666 (2) | 0.7985 (3) | 0.027 (3)* | |
C75 | 0.7336 (5) | 0.842 (3) | 0.8312 (4) | 0.033 (4)* | |
H75A | 0.732756 | 0.746967 | 0.856351 | 0.050* | |
H75B | 0.715865 | 0.960833 | 0.825421 | 0.050* | |
H75C | 0.753050 | 0.940049 | 0.834568 | 0.050* |
N1—C2 | 1.403 (13) | N51—C52 | 1.401 (13) |
N1—C10 | 1.414 (15) | N51—C60 | 1.413 (15) |
N1—C8 | 1.419 (18) | N51—C58 | 1.417 (18) |
C2—C3 | 1.360 (17) | C52—C53 | 1.360 (17) |
C2—C19 | 1.500 (19) | C52—C69 | 1.500 (19) |
C3—C9 | 1.456 (17) | C53—C59 | 1.458 (17) |
C3—C20 | 1.515 (15) | C53—C70 | 1.515 (15) |
C4—C5 | 1.384 (15) | C54—C55 | 1.386 (15) |
C4—C9 | 1.405 (18) | C54—C59 | 1.406 (18) |
C4—H4 | 0.9500 | C54—H54 | 0.9500 |
C5—O24 | 1.384 (18) | C55—O74 | 1.385 (18) |
C5—C6 | 1.416 (17) | C55—C56 | 1.416 (16) |
C6—C7 | 1.430 (17) | C56—C57 | 1.430 (17) |
C6—H6 | 0.9500 | C56—H56 | 0.9500 |
C7—C8 | 1.398 (15) | C57—C58 | 1.399 (15) |
C7—H7 | 0.9500 | C57—H57 | 0.9500 |
C8—C9 | 1.457 (17) | C58—C59 | 1.458 (17) |
C10—O11 | 1.216 (11) | C60—O61 | 1.214 (11) |
C10—C12 | 1.528 (17) | C60—C62 | 1.530 (17) |
C12—C17 | 1.356 (15) | C62—C67 | 1.356 (15) |
C12—C13 | 1.381 (19) | C62—C63 | 1.379 (19) |
C13—C14 | 1.450 (19) | C63—C64 | 1.452 (19) |
C13—H13 | 0.9500 | C63—H63 | 0.9500 |
C14—C15 | 1.375 (16) | C64—C65 | 1.375 (16) |
C14—H14 | 0.9500 | C64—H64 | 0.9500 |
C15—C16 | 1.41 (2) | C65—C66 | 1.41 (2) |
C15—Cl18 | 1.753 (17) | C65—Cl68 | 1.753 (17) |
C16—C17 | 1.44 (2) | C66—C67 | 1.44 (2) |
C16—H16 | 0.9500 | C66—H66 | 0.9500 |
C17—H17 | 0.9500 | C67—H67 | 0.9500 |
C19—H19A | 0.9800 | C69—H69A | 0.9800 |
C19—H19B | 0.9800 | C69—H69B | 0.9800 |
C19—H19C | 0.9800 | C69—H69C | 0.9800 |
C20—C21 | 1.443 (17) | C70—C71 | 1.443 (16) |
C20—H20A | 0.9900 | C70—H70A | 0.9900 |
C20—H20B | 0.9900 | C70—H70B | 0.9900 |
C21—O22 | 1.23 (2) | C71—O72 | 1.23 (2) |
C21—O23 | 1.362 (18) | C71—O73 | 1.361 (17) |
O23—H23 | 0.8400 | O73—H73 | 0.8400 |
O24—C25 | 1.416 (16) | O74—C75 | 1.418 (16) |
C25—H25A | 0.9800 | C75—H75A | 0.9800 |
C25—H25B | 0.9800 | C75—H75B | 0.9800 |
C25—H25C | 0.9800 | C75—H75C | 0.9800 |
C2—N1—C10 | 129.7 (10) | C52—N51—C60 | 129.5 (10) |
C2—N1—C8 | 108.5 (10) | C52—N51—C58 | 108.6 (10) |
C10—N1—C8 | 120.8 (8) | C60—N51—C58 | 121.4 (8) |
C3—C2—N1 | 109.0 (10) | C53—C52—N51 | 109.0 (10) |
C3—C2—C19 | 125.1 (10) | C53—C52—C69 | 125.2 (10) |
N1—C2—C19 | 125.9 (11) | N51—C52—C69 | 125.6 (11) |
C2—C3—C9 | 110.5 (10) | C52—C53—C59 | 110.4 (10) |
C2—C3—C20 | 128.8 (10) | C52—C53—C70 | 127.8 (10) |
C9—C3—C20 | 120.6 (11) | C59—C53—C70 | 121.8 (12) |
C5—C4—C9 | 120.1 (11) | C55—C54—C59 | 119.9 (11) |
C5—C4—H4 | 120.0 | C55—C54—H54 | 120.0 |
C9—C4—H4 | 120.0 | C59—C54—H54 | 120.0 |
C4—C5—O24 | 116.3 (11) | O74—C55—C54 | 116.3 (11) |
C4—C5—C6 | 119.8 (11) | O74—C55—C56 | 123.8 (9) |
O24—C5—C6 | 124.0 (10) | C54—C55—C56 | 119.8 (11) |
C5—C6—C7 | 121.9 (9) | C55—C56—C57 | 121.9 (9) |
C5—C6—H6 | 119.1 | C55—C56—H56 | 119.1 |
C7—C6—H6 | 119.1 | C57—C56—H56 | 119.1 |
C8—C7—C6 | 118.3 (11) | C58—C57—C56 | 118.0 (11) |
C8—C7—H7 | 120.8 | C58—C57—H57 | 121.0 |
C6—C7—H7 | 120.8 | C56—C57—H57 | 121.0 |
C7—C8—N1 | 132.6 (12) | C57—C58—N51 | 132.3 (11) |
C7—C8—C9 | 119.3 (11) | C57—C58—C59 | 119.6 (11) |
N1—C8—C9 | 108.0 (9) | N51—C58—C59 | 107.9 (8) |
C4—C9—C3 | 135.3 (11) | C54—C59—C53 | 135.5 (11) |
C4—C9—C8 | 120.6 (9) | C54—C59—C58 | 120.5 (9) |
C3—C9—C8 | 104.0 (10) | C53—C59—C58 | 104.0 (10) |
O11—C10—N1 | 121.1 (11) | O61—C60—N51 | 121.6 (11) |
O11—C10—C12 | 118.6 (10) | O61—C60—C62 | 119.0 (10) |
N1—C10—C12 | 120.3 (8) | N51—C60—C62 | 119.3 (8) |
C17—C12—C13 | 121.3 (12) | C67—C62—C63 | 121.8 (12) |
C17—C12—C10 | 121.3 (10) | C67—C62—C60 | 120.6 (10) |
C13—C12—C10 | 117.4 (10) | C63—C62—C60 | 117.6 (10) |
C12—C13—C14 | 118.5 (11) | C62—C63—C64 | 118.4 (11) |
C12—C13—H13 | 120.7 | C62—C63—H63 | 120.8 |
C14—C13—H13 | 120.7 | C64—C63—H63 | 120.8 |
C15—C14—C13 | 121.7 (12) | C65—C64—C63 | 121.5 (12) |
C15—C14—H14 | 119.1 | C65—C64—H64 | 119.3 |
C13—C14—H14 | 119.1 | C63—C64—H64 | 119.3 |
C14—C15—C16 | 117.8 (13) | C64—C65—C66 | 118.2 (13) |
C14—C15—Cl18 | 121.8 (10) | C64—C65—Cl68 | 121.8 (10) |
C16—C15—Cl18 | 120.2 (10) | C66—C65—Cl68 | 120.0 (10) |
C15—C16—C17 | 120.4 (12) | C65—C66—C67 | 120.4 (12) |
C15—C16—H16 | 119.8 | C65—C66—H66 | 119.8 |
C17—C16—H16 | 119.8 | C67—C66—H66 | 119.8 |
C12—C17—C16 | 120.0 (12) | C62—C67—C66 | 119.7 (12) |
C12—C17—H17 | 120.0 | C62—C67—H67 | 120.2 |
C16—C17—H17 | 120.0 | C66—C67—H67 | 120.2 |
C2—C19—H19A | 109.5 | C52—C69—H69A | 109.5 |
C2—C19—H19B | 109.5 | C52—C69—H69B | 109.5 |
H19A—C19—H19B | 109.5 | H69A—C69—H69B | 109.5 |
C2—C19—H19C | 109.5 | C52—C69—H69C | 109.5 |
H19A—C19—H19C | 109.5 | H69A—C69—H69C | 109.5 |
H19B—C19—H19C | 109.5 | H69B—C69—H69C | 109.5 |
C21—C20—C3 | 113.4 (11) | C71—C70—C53 | 113.9 (10) |
C21—C20—H20A | 108.9 | C71—C70—H70A | 108.8 |
C3—C20—H20A | 108.9 | C53—C70—H70A | 108.8 |
C21—C20—H20B | 108.9 | C71—C70—H70B | 108.8 |
C3—C20—H20B | 108.9 | C53—C70—H70B | 108.8 |
H20A—C20—H20B | 107.7 | H70A—C70—H70B | 107.7 |
O22—C21—O23 | 121.0 (13) | O72—C71—O73 | 121.2 (12) |
O22—C21—C20 | 125.8 (12) | O72—C71—C70 | 125.6 (11) |
O23—C21—C20 | 112.9 (12) | O73—C71—C70 | 113.1 (12) |
C21—O23—H23 | 109.5 | C71—O73—H73 | 109.5 |
C5—O24—C25 | 116.6 (12) | C55—O74—C75 | 116.6 (11) |
O24—C25—H25A | 109.5 | O74—C75—H75A | 109.5 |
O24—C25—H25B | 109.5 | O74—C75—H75B | 109.5 |
H25A—C25—H25B | 109.5 | H75A—C75—H75B | 109.5 |
O24—C25—H25C | 109.5 | O74—C75—H75C | 109.5 |
H25A—C25—H25C | 109.5 | H75A—C75—H75C | 109.5 |
H25B—C25—H25C | 109.5 | H75B—C75—H75C | 109.5 |
C10—N1—C2—C3 | −170.7 (13) | C60—N51—C52—C53 | −172.2 (13) |
C8—N1—C2—C3 | −2.3 (15) | C58—N51—C52—C53 | −0.3 (15) |
C10—N1—C2—C19 | 7 (2) | C60—N51—C52—C69 | 3 (2) |
C8—N1—C2—C19 | 175.2 (14) | C58—N51—C52—C69 | 174.5 (13) |
N1—C2—C3—C9 | 0.9 (16) | N51—C52—C53—C59 | −1.6 (16) |
C19—C2—C3—C9 | −176.6 (13) | C69—C52—C53—C59 | −176.5 (12) |
N1—C2—C3—C20 | 177.3 (12) | N51—C52—C53—C70 | 178.6 (12) |
C19—C2—C3—C20 | 0 (2) | C69—C52—C53—C70 | 4 (2) |
C9—C4—C5—O24 | −180.0 (14) | C59—C54—C55—O74 | −178.4 (12) |
C9—C4—C5—C6 | 1 (2) | C59—C54—C55—C56 | 4 (2) |
C4—C5—C6—C7 | −1 (2) | O74—C55—C56—C57 | 177.5 (12) |
O24—C5—C6—C7 | 179.8 (13) | C54—C55—C56—C57 | −5 (2) |
C5—C6—C7—C8 | 0 (2) | C55—C56—C57—C58 | 4.1 (19) |
C6—C7—C8—N1 | −175.0 (14) | C56—C57—C58—N51 | −177.3 (13) |
C6—C7—C8—C9 | 0 (2) | C56—C57—C58—C59 | −2.3 (19) |
C2—N1—C8—C7 | 178.5 (14) | C52—N51—C58—C57 | 177.5 (14) |
C10—N1—C8—C7 | −12 (2) | C60—N51—C58—C57 | −10 (2) |
C2—N1—C8—C9 | 2.8 (15) | C52—N51—C58—C59 | 2.1 (15) |
C10—N1—C8—C9 | 172.5 (12) | C60—N51—C58—C59 | 174.8 (12) |
C5—C4—C9—C3 | 177.3 (15) | C55—C54—C59—C53 | 178.4 (14) |
C5—C4—C9—C8 | 0 (2) | C55—C54—C59—C58 | −2.3 (19) |
C2—C3—C9—C4 | −176.8 (16) | C52—C53—C59—C54 | −177.9 (15) |
C20—C3—C9—C4 | 6 (2) | C70—C53—C59—C54 | 2 (2) |
C2—C3—C9—C8 | 0.8 (16) | C52—C53—C59—C58 | 2.8 (15) |
C20—C3—C9—C8 | −176.0 (12) | C70—C53—C59—C58 | −177.4 (12) |
C7—C8—C9—C4 | 0 (2) | C57—C58—C59—C54 | 1 (2) |
N1—C8—C9—C4 | 175.9 (12) | N51—C58—C59—C54 | 177.6 (11) |
C7—C8—C9—C3 | −178.6 (12) | C57—C58—C59—C53 | −179.0 (12) |
N1—C8—C9—C3 | −2.2 (16) | N51—C58—C59—C53 | −2.9 (15) |
C2—N1—C10—O11 | 151.5 (14) | C52—N51—C60—O61 | 153.9 (13) |
C8—N1—C10—O11 | −16 (2) | C58—N51—C60—O61 | −17.1 (19) |
C2—N1—C10—C12 | −29 (2) | C52—N51—C60—C62 | −29 (2) |
C8—N1—C10—C12 | 164.2 (11) | C58—N51—C60—C62 | 160.2 (11) |
O11—C10—C12—C17 | 131.6 (15) | O61—C60—C62—C67 | 131.5 (15) |
N1—C10—C12—C17 | −48 (2) | N51—C60—C62—C67 | −45.8 (19) |
O11—C10—C12—C13 | −49.2 (18) | O61—C60—C62—C63 | −50.2 (18) |
N1—C10—C12—C13 | 130.9 (14) | N51—C60—C62—C63 | 132.4 (13) |
C17—C12—C13—C14 | −3 (2) | C67—C62—C63—C64 | 1 (2) |
C10—C12—C13—C14 | 177.6 (13) | C60—C62—C63—C64 | −177.1 (13) |
C12—C13—C14—C15 | −2 (2) | C62—C63—C64—C65 | −1 (2) |
C13—C14—C15—C16 | 5 (3) | C63—C64—C65—C66 | −1 (2) |
C13—C14—C15—Cl18 | 179.9 (13) | C63—C64—C65—Cl68 | 179.4 (13) |
C14—C15—C16—C17 | −4 (3) | C64—C65—C66—C67 | 3 (2) |
Cl18—C15—C16—C17 | −178.9 (14) | Cl68—C65—C66—C67 | −176.9 (13) |
C13—C12—C17—C16 | 4 (2) | C63—C62—C67—C66 | 1 (2) |
C10—C12—C17—C16 | −176.6 (14) | C60—C62—C67—C66 | 179.6 (13) |
C15—C16—C17—C12 | −1 (3) | C65—C66—C67—C62 | −4 (2) |
C2—C3—C20—C21 | 108.9 (17) | C52—C53—C70—C71 | 95.9 (19) |
C9—C3—C20—C21 | −75.0 (17) | C59—C53—C70—C71 | −83.9 (19) |
C3—C20—C21—O22 | 93.3 (19) | C53—C70—C71—O72 | 3 (3) |
C3—C20—C21—O23 | −81.6 (18) | C53—C70—C71—O73 | −178.1 (15) |
C4—C5—O24—C25 | −178.0 (14) | C54—C55—O74—C75 | −175.4 (13) |
C6—C5—O24—C25 | 1 (2) | C56—C55—O74—C75 | 2 (2) |
D—H···A | D—H | H···A | D···A | D—H···A |
O23—H23···O72 | 0.84 | 1.79 | 2.63 (3) | 177 |
O73—H73···O22 | 0.84 | 1.83 | 2.64 (3) | 161 |
Acknowledgements
We thank Rigaku for access to the CrysAlisPro software suite.
Conflict of interest
The authors declare no competing interests.
Data availability
The authors confirm that the data supporting the findings of this study are available within the article and its supplementary materials.
Funding information
HL and PAM acknowledge funding from the Engineering and Physical Sciences Research Council (Nos. EP/W522120/1 and EP/R008779/1) and a GSK ICASE studentship (grant No. 210193). We also thank Diamond Light Source for access and support in using the I11 beam (award No. CY34800) which contributed to the results presented here.
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