Open Access Article
This Open Access Article is licensed under a
Creative Commons Attribution 3.0 Unported Licence

Pressure-induced preference for solvation of 5,6-dimethylbenzimidazole

Witold Zielinski and Andrzej Katrusiak *
Faculty of Chemistry, Adam Mickiewicz University, Umultowska 89b, 61-614 Poznań, Poland. E-mail: katran@amu.edu.pl

Received 22nd February 2016 , Accepted 1st April 2016

First published on 4th April 2016


Abstract

5,6-Dimethylbenzimidazole (C9H9N2) crystallizes exclusively in the unsolvated form from an aqueous solution up to 0.25 GPa and from methanol, ethanol or their mixed solutions up to 0.6 GPa. At still higher pressures, solvated crystals with water, methanol and ethanol are formed depending on the solvent used for recrystallization. The NH⋯N bonds of the neat crystals are replaced by NH⋯OH⋯N bonds in the solvates. This preference for high-pressure solvation has been rationalized in terms of changed hydrogen bonds as well as volume balance between neat and solvated compounds. The methanol solvate C9H9N2·MeOH undergoes a pressure-induced phase transition at 1.40 GPa, lowering its symmetry from monoclinic space group P21/c (phase α) to triclinic space group P[1 with combining macron] (high-pressure phase β) and ordering the H-atoms in hydrogen bonds NH⋯OH⋯N, disordered in phase α.


Introduction

Most organic compounds preferentially form either unsolvated or solvated crystals under normal conditions. There are also substances forming solvates1–6 depending on concentration and temperature.7 The formation of solvates is often desired in the agriculture and pharmaceutical industry,8 because the solvation efficiently modifies such properties as solubility, melting and stability, most important for practical applications.9–11 There are also examples of the effect of pressure on the solvation preferences.12 Presently we have investigated the effect of pressure for the crystallization of 5,6-dimethylbenzimidazole (dMBzIm). The obtained solvates are most intriguing when compared to the crystallization preferences of analogous benzimidazole (BzIm),13 and 2-methylbenzimidazole (MBzIm),14 none of which formed any solvates neither at ambient or high pressure. The compression of neat crystals as well as high-pressure recrystallization of BzIm and of MBzIm resulted in the same phases. Recently, we reported the pressure-induced hydration of dMBzIm.15 The formation of hemihydrate dMBzIm·1/2H2O above 0.25 GPa is counterintuitive because the molecular volume (V/Z) of the hemihydrate is significantly smaller than that of neat dMBzIm. Moreover, the hemihydrate crystals recovered to ambient pressure have not changed in open vials for years. Presently we have extended the study on dMBzIm to its high-pressure crystallization of methanol and ethanol solutions. We found that the crystallization of dMBzIm can be controlled by the pressure, favoring the methanol (dMBzIm·MeOH) and ethanol (dMBzIm·EtOH) solvates. Fig. 1 shows the series of benzimidazole derivatives recrystallized at high pressure, and the obtained dMBzIm solvates. It was our intention to explain this different preferential high-pressure crystallization of BzIm, MBzIm and dMBzIm as well as the solvation of this latter compound.
image file: c6ce00419a-f1.tif
Fig. 1 H-Bonded aggregates of benzimidazole, BzIm (a) and its derivatives, 2-methylbenzimidazole, MBzIm (b), and 5,6-dimethylbenzimidazole, dMBzIm (c), as well as the solvates of dMBzIm: hemihydrate dMBzIM·1/2H2O (d), methanol solvate dMBzIm·MeOH (e) and ethanol solvate dMBzIm·EtOH (f). This drawing also lists the high-pressure phases (labeled β and γ) of the neat compounds (a–c) and the methanol solvate (e).

Results and discussion

The dMeBzIm crystallization performed above 0.6 GPa from methanol and ethanol solutions resulted in solvates. The crystallization of methanol and of methanol[thin space (1/6-em)]:[thin space (1/6-em)]ethanol[thin space (1/6-em)]:[thin space (1/6-em)]water mixture (16[thin space (1/6-em)]:[thin space (1/6-em)]3[thin space (1/6-em)]:[thin space (1/6-em)]1 vol) solutions yields methanol solvate crystals in a monoclinic system, space group P21/c. The pressure preference for the solvate formation could be determined visually by recognizing the characteristic elongated plate morphology of neat dMBzIm and rhomboid plates of its solvates (Fig. 6). Likewise, a pressure of 0.6 GPa was required to obtain solvate dMBzIm·EtOH from an ethanol solution. The X-ray diffraction measurements revealed the apparent differences in the lattice dimensions (Table 1 and Fig. 2), the symmetry and the molecular association between neat dMBzIm and its solvates.
Table 1 Selected crystal data for the high-pressure structures of dMBzIm and the methanol and ethanol solvates, all at 296 K. Low- and high-pressure polymorphs of solvate dMBzIm·MeOH are labeled with Greek letters α and β, respectively
dMBzIm α-dMBzIm MeOH β-dMBzIm MeOH dMBzIm EtOH
P (GPa) 0.33(2) 0.92(2) 1.53(2) 1.50(2)
Space group P21/c P21/c P[1 with combining macron] P[1 with combining macron]
a (Å) 6.538(3) 9.977(7) 10.111(5) 7.0048(7)
b (Å) 26.99(14) 7.1746(3) 7.1012(7) 8.453(3)
c (Å) 13.930(5) 12.7576(6) 6.6980(9) 9.3834(12)
α (°) 90 90 114.719(11) 66.49(2)
β (°) 102.68(4) 93.545(13) 94.60(2) 81.840(9)
γ (°) 90 90 90.206(18) 71.705(18)
Volume (Å3) 2398(13) 911.4(6) 435.1(2) 483.6(2)
Z/Z 12/3 4/1 2/1 2/1
D x (g cm−3) 1.212 1.299 1.36 1.32
R 1/wR2 0.086/0.198 0.050/0.129 0.083/0.181 0.057/0.141



image file: c6ce00419a-f2.tif
Fig. 2 Unit-cell parameters as a function of pressure in (a) dMBzIm·MeOH (the dashed line marks the transition between monoclinic and triclinic phases); and (b) dMBzIm·EtOH.

The anomalous compression of dMBzIm·MeOH indicates its phase transition at 1.40 GPa: the monoclinic phase below 1.40 GPa has been denoted with the Greek letter α and the high-pressure triclinic phase with the letter β. The phase transition at 1.40 GPa occurred upon increasing pressure, but the crystal cracked and crystallization had to be repeated above 1.40 GPa in order to obtain good quality single crystals for X-ray diffraction studies. The unit-cell dimensions of phases α and β are similar, apart from the triclinic strain in phase β and the unit-cell volume and contents of phase β being half those of phase α; parameter c of the triclinic unit cell is halved in the triclinic β phase (see Fig. 2 and 3).


image file: c6ce00419a-f3.tif
Fig. 3 Chains of NH⋯OH⋯N hydrogen bonded molecules in (a) dMBzIm·MeOH phase α; (b) dMBzIm·MeOH phase β; and (c) dMBzIm·EtOH. Also, the structures projected down the NH⋯OH⋯N bonded chains are shown in the bottom (the voids in these structures are shown in Fig. S1 in ESI).

In the solvated crystals, the dMBzIm and solvent molecules are NH⋯OH⋯N bonded (Fig. 3). In dMBzIm·MeOH the chains run along axis [y] and this direction of the crystal is the least compressed. A similar interval of H-bonded chains parallel to axis [x] in dMBzIm·EtOH is reflected in the similar unit-cell parameter a and its small compressibility. The unit-cell of phase β has been chosen as the halved unit-cell of phase α (stable between 0.1 MPa and 0.6 GPa) along [z]. This choice of unit-cell in phase β is not the conventional unit cell, but it allows a convenient comparison of these related structures.

Another structural transformation in dMBzIm·MeOH at Pc is that in phase α, the azole and hydroxyl H-atoms are disordered in the hydrogen bonds, while in phase β they are ordered. This ordering of H-atom results in the changed orientation of the dMBzIm and methanol molecules, in connection to the directional character of the hydrogen bonds, different at their H-donor and H-acceptor sites.16,17 The effect of the molecular orientation for the H-sites in hydrogen bonds NH⋯OH⋯N can be correlated to angles C–N⋯O and C–O⋯N, also known as Donohue angles.18 Their pressure dependence is shown in Fig. 4. It can be observed that the phase transition in dMBzIm·MeOH makes the angles on both sites of the methanol molecule significantly different, and one of these angles becomes much closer to the ideal angle of 109°, consistent with the hydroxyl H-atom position.


image file: c6ce00419a-f4.tif
Fig. 4 Angles C–N⋯O and C–O⋯N in the NH⋯OH⋯N bonds in the crystal structures of the solvates: (a) dMBzIm·MeOH phases; (b) dMBzIm·EtOH as a function of pressure; and (c) the NH⋯OH⋯N bonds with indicated Donohue angles.

The origin of the preference between unsolvated and solvated crystallization of dMBzIm at different pressures can be connected with the interplay of transformed intermolecular interactions (H-bonds) as well as with the volume difference between the neat and solvated components. These volume changes are illustrated in Fig. 5. The volume difference between the solvate formula unit and the volume of one solvate-molecule assumed in the pure solvent under the same conditions for both the methanol solvate phases α and β as well as for the ethanol solvate is smaller than that of the neat dMBzIm crystal. It means that the work-energy contribution PΔV performed via pressure for the formation of the solvate is negative, equal to −0.6 kJ mol−1, i.e. favorable for the solvate formation.


image file: c6ce00419a-f5.tif
Fig. 5 Pressure dependence of the molecular volume (V/Z) of dMBzIm as well as its methanol (MeOH) and ethanol (EtOH) solvates. At 1.40 GPa dMBzIm·MeOH transforms from monoclinic space group P21/c to triclinic phase β space group P[1 with combining macron]. Dashed lines mark the molecular volume of MeOH and EtOH in their neat liquid form19 subtracted from the volume of the solvates.

On the other hand, the volume increase ΔV of the solvates compared to that of neat dMBzIm is about 45 Å3 for dMBzIm·MeOH and 70 Å for dMBzIm·EtOH, which is consistent with such a volume increase in the solvates deposited in the Cambridge Structural Database.20 It is an indication that dMBzIm·MeOH and dMBzIm·EtOH do not differ significantly from other solvates obtained under normal conditions, although a high pressure is indispensable for their generation. However, according to our observations both of these solvates decompose below 0.60 GPa.

Conclusions

High pressure has been successfully used for inducing the solvation of dMBzIm with methanol and ethanol. In several respects it proceeds differently than it was previously observed for dMBzIm·1/2H2O hemihydrate. The analogy of the methanol and ethanol solvates with the hemihydrate includes also the substitution of NH⋯N bonds in neat dMBzIm with bonds NH⋯OH⋯N in the solvates. However the apparent difference between the hemihydrate and the solvates investigated is the magnitude of ΔVs, much smaller for dMBzIm·1/2H2O, which agrees well with the stability of this hemihydrate under normal conditions. In this respect the pressure-induced solvation of dMBzIm considerably differs depending on the solvate, although the intermolecular interactions involved in the solvation are similar. Most importantly, it has been shown that apart from the dMBzIm·1/2H2O hemihydrate, the pressure provides an efficient method, and is the only one known so far for obtaining other solvates of 5,6-dimethylbenzimidazole.

Experimental section

Crystal growth at high pressure

5,6-Dimethylbenzimidazole (m.p. 475 K), analytical grade, from Acros Organics, was used as delivered. High pressure studies were performed in a Merrill–Bassett diamond-anvil cell (DAC)21 modified by mounting the diamond anvils directly on steel supports with conical windows;22 tungsten gaskets of a 0.2 mm thickness with a spark-eroded hole of 0.40 mm in diameter were used. Single crystals of dMBzIm·MeOH and dMBzIm·EtOH solvates were obtained above 0.6 GPa from saturated solutions in methanol and ethanol, respectively. The pressure was calibrated via the ruby-fluorescence method23 with a Photon Control Inc. spectrometer, affording an accuracy of 0.02 GPa, before and after the diffraction measurements. Single crystals were grown in isothermal and isochoric conditions in the DAC. A hot-air gun with a digital control of temperature, and an independent measurement of temperature using a thermocouple at one of the anvils inside the DAC were applied. The polycrystalline mass, obtained via isothermal compression, was heated until a single grain was left and then the sample was slowly cooled to room temperature. Single crystals of the dMBzIm solvates obtained in situ in the DAC are shown in Fig. 6.
image file: c6ce00419a-f6.tif
Fig. 6 Single crystals grown in situ inside the DAC chamber: (a–b) a neat dMBzIm crystal grown from the methanol solution at 0.22 GPa; (c–d) from the same solution, a dMBzIm·MeOH crystal at 0.92 GPa; and (e–f) from the ethanol solution, a dMBzIm·EtOH crystal grown at 1.42 GPa. Small irregular ruby chips in the chamber are for pressure calibration. The sample crystal and the ruby chips were loose in the chamber (c) before the crystal was jammed between the gasket edges (d).

X-ray diffraction analyses

The single-crystal diffraction data for dMBzIm at high pressures were measured at 296 K on a KUMA KM-4 CCD diffractometer with the graphite-monochromated MoKα radiation. The DAC was centered via the gasket-shadow method.24 The reflections were collected in the ω-scan mode, 0.75° frames and 30 s exposures. The CrysAlisCCD and CrysAlisRED programs25 were used for data collection, determination of the UB-matrix, and for initial data reduction and Lp corrections; reflections intensities have been accounted for the effects of absorption of X-rays through the DAC, shadowing of the beams by the gasket edges, and absorption of the sample crystal itself using the program REDSHABS.26 The structures of the solvates were solved using direct methods.27 The OLEX2 program28 with implemented SHELXL27 was used for all high-pressure data refinements. The positions of carbon H-atoms were calculated from the molecular geometry assuming a C–H bond length of 0.93 Å.

The azole and hydroxyl hydrogen atoms were located from difference Fourier maps and then restrained to the molecular geometry by instructions AFIX 43 and AFIX 134 with the N–H distance of 0.86 Å and 0.82 Å, respectively. Their location was also checked in this way, that the H-atoms were constrained at the idealized positions at both N-atoms, and then their site occupation factors (SOF) were refined with boundary condition assuming one H-atom in each H-bond, SOF(H1) + SOF(H3) = 1 for N1–H1⋯N3′ bond (H3 atom is the disordered H-site at N3 atom); SOF(H1) + SOF(H1a) = 1 and SOF(H1b) + SOF(H3) = 1 for N1–H1⋯O1–H1b⋯N3′ (H1a and H1b are the sites of disordered hydroxyl H-atoms in methanol and ethanol molecules). All these tests corroborated the ordered H-atom position in the NH⋯OH⋯N bonds found in the difference Fourier maps: disordered azole and hydroxyl H-locations in the low-pressure phase α of dMBzIm·MeOH are ordered in the β-phase and in dMBzIm·EtOH. In all plots and discussion of hydrogen bonding NH⋯N geometry the H-positions were normalized to the N–H bond length of 1.013 Å, C–H of 1.099 Å and O–H of 0.98 Å determined in neutron-diffraction studies.29 The crystallographic information of selected experiments is summarized in Table 1 (cf. Table S1 in ESI). The crystallographic data of the dMBzIm·EtOH structures at 0.84, 1.20, 1.50, 2.17 GPa and dMBzIm·MeOH structures at 0.92, 2.24, 1.53, 1.90, 2.19, 2.31 GPa have been deposited to the Cambridge Crystallographic Database Center as supplementary publications CCDC 1451562–1451571, respectively. The molecular and intermolecular dimensions were calculated with programs OLEX2 (ref. 27) and Mercury.30

Notes and references

  1. F. P. A. Fabbiani, D. R. Allan, W. I. David, S. A. Moggach, S. Parsons and C. R. Pulham, CrystEngComm, 2004, 6, 504 RSC.
  2. P. Vishweshwar, J. A. McMahon, J. A. Bis and M. J. Zaworotko, J. Pharm. Sci., 2006, 95, 499 CrossRef CAS PubMed.
  3. E. Boldyreva, Z. Kristallogr., 2014, 229, 236 CAS.
  4. F. P. A. Fabbiani, D. R. Allan, S. Parsons and C. R. Pulham, CrystEngComm, 2005, 7, 179 RSC.
  5. H. Hirai, T. Kondo, M. Hasegawa, T. Yagi, Y. Yamamoto, T. Komai, K. Nagashima, M. Sakashita, H. Fujihisa and K. Aoki, J. Phys. Chem. B, 2000, 104, 1429 CrossRef CAS.
  6. B. P. van Eijck and J. Kroon, Acta Crystallogr., Sect. B: Struct. Sci., 2000, 56, 535 CrossRef.
  7. H. H. Tung, E. L. Paul, M. Midler and J. A. McCauley, Crystallization of Organic Compounds: An Industrial Perspective, John Wiley & Sons, Inc., Hoboken, New Jersey, 2009 Search PubMed.
  8. E. H. Lee, Asian J. Pharm. Sci., 2014, 9, 163 CrossRef.
  9. N. Shan and M. J. Zaworotko, Drug Discovery Today, 2008, 13, 440 CrossRef CAS PubMed.
  10. S. Dharmendra and C. William, Adv. Drug Delivery Rev., 2004, 56, 335 CrossRef PubMed.
  11. G. R. Desiraju, J. Am. Chem. Soc., 2013, 135, 9952 CrossRef CAS PubMed.
  12. M. Anioła, A. Olejniczak and A. Katrusiak, Cryst. Growth Des., 2014, 14, 2187 Search PubMed.
  13. W. Zielinski and A. Katrusiak, Cryst. Growth Des., 2013, 13, 696 CAS.
  14. W. Zielinski and A. Katrusiak, Cryst. Growth Des., 2014, 14(9), 4247 CAS.
  15. W. Zielinski and A. Katrusiak, CrystEngComm, 2015, 17, 5468 RSC.
  16. A. Katrusiak, M. Ratajczak-Sitarz and E. Grech, J. Mol. Struct., 1999, 474, 135 CrossRef CAS.
  17. M. Ratajczak-Sitarz, M. D. Rozwadowska and A. Katrusiak, Pol. J. Chem., 1998, 72, 2493 CAS.
  18. J. Donohue, Selected topics in hydrogen bonding, in Structural Chemistry and Molecular Biology, ed. A. Rich and N. Davison, Freeman, San Francisco, 1968, pp. 443–465 Search PubMed.
  19. P. W. Bridgman, Proc. Am. Acad. Arts Sci., 1942, 74, 399 CrossRef CAS.
  20. M. Zaworotko, Am. Pharm. Outsorc., 2004, 5, 16 Search PubMed.
  21. L. Merrill and W. A. Bassett, Rev. Sci. Instrum., 1974, 45, 290 CrossRef.
  22. A. Katrusiak, Acta Crystallogr., Sect. A: Found. Crystallogr., 2008, 64, 135 CrossRef CAS PubMed.
  23. H. K. Mao, J. Xu and P. M. Bell, J. Geophys. Res., B, 1986, 91, 4673 CrossRef CAS.
  24. A. Budzianowski and A. Katrusiak, High-Pressure Crystallographic Experiments with a CCD Detector, High-Pressure Crystallography, ed. Katrusiak, A. and McMillan, P., Kluwer, Dordrecht, 2004 Search PubMed.
  25. CrysAlisCCD, CrysAlisRed, Oxford Diffraction, Oxford Diffraction Ltd, Abingdon, England, 2006 Search PubMed.
  26. A. Katrusiak, Z. Kristallogr., 2004, 219, 461 CAS.
  27. G. M. Sheldrick, Acta Crystallogr., Sect. A: Found. Crystallogr., 2008, 64, 112 CrossRef CAS PubMed.
  28. O. V. Dolomanov, L. J. Bourhis, R. J. Gildea, J. A. K. Howard and H. Puschmann, J. Appl. Crystallogr., 2009, 42, 339 CrossRef CAS.
  29. F. H. Allen and I. J. Bruno, Acta Crystallogr., Sect. B: Struct. Sci., 2010, 66, 380 CrossRef CAS PubMed.
  30. C. F. Macrae, P. R. Edgington, P. McCabe, E. Pidcock, G. P. Shields, R. Taylor, M. Towler and J. van de Streek, J. Appl. Crystallogr., 2006, 39, 453 CrossRef CAS.

Footnote

Electronic supplementary information (ESI) available. CCDC 1451562–1451571. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c6ce00419a

This journal is © The Royal Society of Chemistry 2016
Click here to see how this site uses Cookies. View our privacy policy here.