research papers
Structure–mechanical property correlations in mechanochromic luminescent crystals of boron difluoride dibenzoylmethane derivatives
aDepartment of Chemical Sciences, Indian Institute of Science Education and Research (IISER) Kolkata, Mohanpur Campus, Mohanpur 741252, India, bDepartment of Materials Engineering, Indian Institute of Science, Bangalore 560012, India, cDepartment of Chemistry, University of Virginia, Charlottesville, Virginia 22904, USA, and dCenter of Excellence for Advanced Materials Research, King Abdulaziz University, Jeddah 21589, Saudi Arabia
*Correspondence e-mail: ramu@materials.iisc.ernet.in, cmreddy@iiserkol.ac.in
The structure and mechanical properties of crystalline materials of three boron difluoride dibenzoylmethane (BF2dbm) derivatives were investigated to examine the correlation, if any, among mechanochromic luminescence (ML) behaviour, solid-state structure, and the mechanical behaviour of single crystals. Qualitative mechanical deformation tests show that the crystals of BF2dbm(tBu)2 can be bent permanently, whereas those of BF2dbm(OMe)2 exhibit an inhomogeneous shearing mode of deformation, and finally BF2dbmOMe crystals are brittle. Quantitative mechanical analysis by nanoindentation on the major facets of the crystals shows that BF2dbm(tBu)2 is soft and compliant with low values of elastic modulus, E, and hardness, H, confirming its superior suceptibility for plastic deformation, which is attributed to the presence of a multitude of slip systems in the In contrast, both BF2dbm(OMe)2 and BF2dbmOMe are considerably stiffer and harder with comparable E and H, which are rationalized through analysis of the structural attributes such as the intermolecular interactions, slip systems and their relative orientation with respect to the indentation direction. As expected from the qualitative mechanical behaviour, prominent ML was observed in BF2dbm(tBu)2, whereas BF2dbm(OMe)2 exhibits only a moderate ML and BF2dbmOMe shows no detectable ML, all examined under identical conditions. These results confirm that the extent of ML in crystalline organic solid-state fluorophore materials can be correlated positively with the extent of plasticity (low recovery). In turn, they offer opportunities to design new and improved efficient ML materials using crystal engineering principles.
1. Introduction
Organic solid-state fluorophore materials exhibit considerable promise in applications such as light-emitting diodes (Strassert et al., 2011; Friend et al., 1999), lasers (Gao et al., 2010; Schmidtke et al., 2002), two-photon fluorescent materials (Denk et al., 1994) and in opto-electronic devices (Yoon et al., 2010). However, detailed understanding of the mechanism(s) behind their properties is essential before they can be successfully deployed. The mechanochromic luminescence (ML) in their solid state is mainly due to the chemical or physical structural changes, for example, the latter involves the reorganization of molecules by changes in conformation, relative position of the molecules, intermolecular interactions or all of the processes together, upon subjecting them to stress (Krishna et al., 2013; Zhang et al., 2010; Anthony et al., 2010). Usually, the solid-state reorganization of molecules is closely related to the mechanical properties of their crystals, because both the properties depend intricately upon the intermolecular interactions (Reddy, Padmanabhan et al., 2006; Reddy, Kirchner et al., 2006; Ghosh & Reddy, 2012; Reddy et al., 2010; Sun & Hou, 2008; Feng & Grant, 2006). The design of new molecular materials with target mechanical properties requires precise control over the weak intermolecular interactions in the structure because their strength and directionality play a crucial role in the deformation process (Ghosh et al., 2013, 2015). A number of studies show that the changes in solid-state luminescence can be brought about through either or by changes in (Perruchas et al., 2010; Yoon et al., 2010; Kozhevnikov et al., 2008; Zhang et al., 2010). However, almost nothing is known about how one can control ML behaviour through the engineering of solid-state packing in crystals, which is a considerable challenge as the precise control of weak intermolecular interactions is nontrivial (Desiraju & Steiner, 1999; Desiraju, 1997, 2005).
In recent work we have shown that the easy-to-deform polymorph of a BF2AVB derivative shows better ML behaviour, in terms of reversibility, compared with its brittle polymorph (near-instantaneous recovery) (Krishna et al., 2013). The presence of slip planes in the former, which facilitate plastic deformation through shear sliding, was suggested as the reason for the prominent reversible ML. This observation, in turn, indicates that the crystal engineering of ML materials should embody the key design principle of introducing slip planes in the crystal packing. It is important to note here that such principles are not only useful for ML materials, but also in other instances such as for improving the tabletability of pharmaceutical solids (Krishna et al., 2015; Bag et al., 2012; Karki et al., 2009; Jain, 1999; Chattoraj et al., 2010), for the design of flexible optoelectronic crystals (Briseno et al., 2006; Ruiz et al., 2012; Minemawari et al., 2011), flexible waveguides (Chandrasekhar & Chandrasekar, 2012; Chandrasekar, 2014; Balzer et al., 2003; Drain, 2002; Lehn, 2002) etc. In trying to further such knowledge, the present work examines the crystal structures, mechanical properties and ML in BF2dbm(tBu)2, BF2dbm(OMe)2 and BF2dbmOMe (Fig. 1) compounds, with a view to determining if any correlation exists amongst these three attributes. The mechanical behaviour of single crystals of the respective compounds was evaluated qualitatively as well as quantitatively. The former was accomplished by manually applying mechanical stress and deforming crystals using a pair of metal forceps and a metal needle while observing the crystal under a microscope, whereas the nanoindentation (NI) technique was utilized for quantitative property measurements. The measurements made and bulk ML properties are rationalized on the basis of the presence or absence of active slip planes in the respective crystal packing. In addition to both qualitative and quantitative analysis, we employ the Hirshfeld two-dimensional fingerprint plot analysis to quantify the dominant hydrogen bonding functionalities present in the three compounds (Fig. S5 ) (McKinnon et al., 2007).
Slip planes (weak interaction planes) are generally found in molecular crystals when the weakly interacting functional groups such as tBu, —OMe, —SMe, —Cl etc. are organized in such a way that the molecules interact only via dispersive and nonspecific van der Waals (vdW) interactions across a crystallographic plane. For this study, the molecular derivatives of boron difluoride dibenzoylmethane (BF2dbm) were selected for the following reasons: (i) they have the ability to absorb ultraviolet (UV) light over a wider range of wavelengths than many other organic sunscreen agents; (ii) they form stable crystalline complexes with boron trifluoride, which are highly fluorescent under UV irradiation; (iii) high sensitivity of the emission colour to the conformational changes. With this in mind, we introduced the hydrophobic groups such as tBu, —OMe as substituents to promote the formation of active slip planes in the crystal packing, which promote plastic deformation leading to the creation of low energy defects. In turn, we expect that the fluorophore crystals with higher levels of plasticity can exhibit reversible ML behaviour (Krishna et al., 2013; Anthony et al., 2010; Reddy, Kirchner et al., 2006; Reddy, Padmanabhan et al., 2006; Sun & Hou, 2008).
2. Results and disscussion
All three compounds were synthesized by following known procedures (Karasev & Korotkich, 1986; Yoshii et al., 2013; Sun et al., 2012; Zawadiak & Mrzyczek, 2012). Single crystals of the three compounds BF2dbm(tBu)2, BF2dbm(OMe)2 and BF2dbmOMe, prepared by the standard slow evaporation method, were utilized for X-ray as well as for the mechanical property studies. Among the three compounds, crystals of BF2dbm(tBu)2 are cyan in colour (450 nm), BF2dbm(OMe)2 green (498) and BF2dbmOMe yellow (554), as shown in Fig. 1. The initial qualitative mechanical deformation tests confirmed that molecular crystals of BF2dbm(tBu)2 and BF2dbm(OMe)2 undergo plastic bending and shearing deformation, respectively, whereas BF2dbmOMe was found to be brittle under the test conditions. Crystals of both BF2dbm(tBu)2 and BF2dbm(OMe)2 materials exhibited prominent ML properties when the powders of the respective crystals were scratched firmly using a mortar and pestle at room temperature, but no detectable ML behaviour was noticed in case of the brittle crystals of BF2dbmOMe under similar test conditions.
3. analysis
3.1. BF2dbm(tBu)2
BF2dbm(tBu)2 crystallizes in the centrosymmetric monoclinic C2/c, with half the molecule in an (Fig. S1(i) , for clarity the full molecule has been shown). Since there are no conventional hydrogen-bonding functional groups, the molecular packing is dominated mainly by weak C—H⋯F interactions. Plenty of examples are available in the literature on the utilization of C—H⋯O and C—H⋯F intermolecular interactions for crystal engineering (Hathwar et al., 2011; Thalladi et al., 1995; Schönleber et al., 2014; Thakur et al., 2010). Thalladi et al. suggested that C—H⋯F interactions can also be as important as C—H⋯O and C—H⋯N hydrogen bonds for stabilizing the specific crystal structures (Thalladi et al., 1998; Dunitz & Schweizer, 2006; Chopra & Row, 2011). In the present case, the bifurcated C—H⋯F (d/Å, θ/°; 2.56 Å, 167.36°) and C—H⋯B (3.058 Å, 160.76°) interactions between the phenyl and BF2O2 groups connect molecules along the b-axis in a head-to-tail fashion (Fig. 2d) (Alemany et al., 2014), which are further linked along the c-axis via an additional C—H⋯F (2.46 Å, 135.98°) interaction to form thick two-dimensional sheets as shown in Fig. 2(e). The two-dimensional sheets pack together via the close packing of hydrophobic tBu groups resulting in slip planes or weak interaction planes parallel to (100) in the crystal packing (Fig. 2c). The slip planes exist orthogonal to comparatively strong C—H⋯F interactions. Therefore, the overall crystal packing is anisotropic and hence promotes plasticity in the crystals (Reddy, Kirchner et al., 2006; Reddy, Padmanabhan et al., 2006; Ghosh & Reddy, 2012; Reddy et al., 2010; Sun & Hou, 2008; Feng & Grant, 2006; Reddy et al., 2005; Panda et al., 2015).
3.2. BF2dbm(OMe)2
BF2dbm(OMe)2 is known to crystallize in the centrosymmetric monoclinic C2/c, with half a molecule in the (Fig. S1(ii) , for clarity the full molecule is shown), which is redetermined here (Fig. 3) (Yoshii et al., 2013). The bifurcated C—H⋯F (2.67 Å, 157.56°) and C—H⋯B (3.019 Å, 162.24°) intermolecular interactions between the phenyl and BF2O2 groups form linear tapes, which are further linked by additional C—H⋯F interactions (2.57 Å, 118.26°) to form two-dimensional sheets. In the crystal packing slip planes are formed by —OCH3 functional groups. In this case the crystals undergo plastic shearing deformation (Ghosh & Reddy, 2012; Reddy et al., 2010; Krishna et al., 2015; Bag et al., 2012) and do not show plastic bending on any of the faces.
3.3. BF2dbmOMe
BF2dbmOMe crystallizes in triclinic with one molecule in the (Fig. S1(iii) ). Unlike the other two compounds, the molecule here does not possess mirror symmetry, because the hydrophobic —OCH3 is substituted only on one phenyl ring and not on both sides. Notably, the lone —OCH3 fails to form the slip planes in this structure. Instead, the H atom of the —OCH3 group forms a C—H⋯B (3.174 Å, 159.78°) interaction (shorter than the sum of van der Waals radii, 3.28 Å) with the BF2O2 group (Alemany et al., 2014). Molecules are further linked by multiple C—H⋯F interactions leading to the three-dimensional interlocking of the structure (Fig. 4b). As a result the crystals show brittle mechanical behaviour (Reddy, Krishner et al., 2006; Reddy, Padmanabhan et al., 2006; Ghosh & Reddy, 2012; Reddy et al., 2010; Sun & Hou, 2008; Feng & Grant, 2006).
4. Mechanical properties of molecular crystals
The qualitative mechanical deformation experiments performed on the crystals of three compounds revealed that their mechanical behaviour is distinct from each other. Even though the three compounds contain a common backbone, i.e. BF2dbm, the different substituent hydrophobic functional groups lead to unique crystal packing arrangements in them. The molecular crystals of BF2dbm(tBu)2 deformed plastically when bent on the (001) crystal face and the crystal packing is consistent with the established bending model, i.e. the existence of anisotropy in the crystal packing in such a way that the strong and weak interactions are arranged in nearly perpendicular directions (Reddy et al., 2005; Reddy, Padmanabhan et al., 2006). Furthermore, the molecules are connected via multiple weak C—H⋯F intermolecular interactions in two directions, but in the third direction the adjacent sheets pack via only the tBu functional groups (Fig. 2c). Thus, it is not surprising that the crystals plastically bend upon the application of a mechanical stress. In the case of BF2dbm(OMe)2, the molecular crystals undergo inhomogeneous shearing deformation, as shown in Fig. 1. Typically, the observation of such a deformation mode indicates that some specific crystallographic planes offer very low resistance to shearing upon the application of stress, whereas the other planes exhibit considerably more resistance. Therefore, plastic deformation is restricted only to those `easy sliding' molecular planes. This is consistent with the crystal packing features wherein the molecules are packed into flat two-dimensional layers with the support of C—H⋯F interactions. The —OCH3 functional groups close pack to form slip planes. Here the two-dimensional layers, comprising molecules between the slip planes (see Fig. 3e), are thick and hence are not ideal to slide one over the other to result in the easy shearing deformation. However, on application of a mechanical stress the layers slide to some extent and create striations on the crystal due to inhomogeneous shearing (Fig. 1). Further application of the mechanical stress leads to fracture of the crystal. As there are slip planes in the structure we also tried to bend them, but did not show any plastic bending nature. This is typically the case when the is comparable to or exceeds the fracture stress (Ghosh et al., 2013). In the molecular crystals of BF2dbmOMe, three-dimensional interlocked packing via the C—H⋯(BF2O2) and C—H⋯F intermolecular interactions do not allow for plastic deformation and hence fail in a brittle manner.
Quantification of mechanical properties by nanoindentation (NI) experiments: Recent work has successfully demonstrated that the NI technique can be utilized to quantify the mechanical properties of molecular crystals, and in turn not only establish the structure–property correlations, but also use such knowledge for designing organic solids with specific targeted properties. The major faces of the crystals of BF2dbm(tBu)2, BF2dbm(OMe)2 and BF2dbmOMe were all indented in load-control mode with a Berkovich tip, and (un)loading rates of 0.2 mN s−1, peak load, Pmax, of 1 mN, and Pmax hold time of 2 s. Representative load, P, versus depth, h, curves are displayed in Fig. 5, which reveal the following significant differences in the mechanical responses of the three compounds examined.
(a) The loading part of the P–h curve obtained on BF2dbmOMe is smooth, whereas the corresponding ones obtained on BF2dbm(OMe)2 and BF2dbm(tBu)2 are serrated with several discrete displacement bursts (or `pop-ins'). Prior work on nanoindentation of molecular crystals has shown that such displacement jumps, hpop-in, associated with the pop-ins are integer multiples of the relevant inter-planar spacing of the crystal, typically the slip plane. In the case of BF2dbm(tBu)2, the observed hpop-ins are multiple integers of ∼ 5 nm, which correspond to ∼ 10 times the d-spacing (0.0502 nm) of the slip planes. In the case of BF2dbm(OMe)2, the corresponding hpop-in is ∼ 5.4 nm, which again is an integer multiple of 0.3541 nm (about 15 times).
(b) The P–h responses obtained on BF2dbm(OMe)2 and BF2dbmOMe are nearly identical (in contrast to the distinct shearing and brittle behaviour in qualitative tests, respectively), except for the serrations in the former's loading curve. Indeed, the elastic modulus, E, and hardness, H, values extracted from these P–h curves using the standard Oliver–Pharr (O–P) method are also similar (see Table 1). Further, the indentation impressions are also similar (see Fig. 6), with no significant pile-up around the indents. The response obtained from BF2dbm(tBu)2, in contrast, is significantly different. First, for the same Pmax, the maximum hmax, is significantly larger. Yet, the residual depth upon complete unloading is nearly the same in all the three crystals. This suggests that BF2dbm(tBu)2 is significantly softer and compliant (as indicated by the high rate of elastic recovery during unloading), which is confirmed by the relatively smaller E and H values extracted from the P–h curves using the O–P method. Here it is important to note that significant pile-up around the indent (see Fig. 6a) is noted, which indicates the ease of However, the pile-up affects the accuracy of estimated E and H values, as the effective contact area altered significantly. In view of this, we will not utilize these quantitative metrics in further discussion, except to note that BF2dbm(tBu)2 is soft and compliant compared with the other two compounds examined in this work.
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Understanding the above observations, made on the NI results, requires the consideration of crystal packing with respect to the indentation direction. The qualitative tests indicate that BF2dbm(tBu)2, BF2dbm(OMe)2 and BF2dbmOMe crystals are bending, shearing and brittle types, respectively. The NI experiments indeed confirm that BF2dbm(tBu)2 is much softer (plastic) vis-à-vis the other two. As mentioned earlier, the presence of slip planes orthogonal to relatively stronger interactions in the crystal packing promotes plasticity (Reddy et al., 2005; Reddy, Padmanabhan et al., 2006; Panda et al., 2015). In BF2dbm(tBu)2 crystals, (100) formed by the hydrophobic tBu groups (Fig. 2c) is the slip plane. This allows for easy plastic deformation when the crystals are stressed through bending upon the (001) face that is orthogonal to the slip plane. The NI experiments, which were also performed on the (001) plane, i.e. the major face (Fig. S4a ). This means that the indentation direction [001] is parallel to the slip planes (bc-plane). Moreover, the indentation direction is oblique to the direction of the π-stacked molecules (Fig. 2c). These geometrical factors favour easier shearing of the molecular layers during deformation. Hence, the indenter penetrates easily into the crystal, giving rise to low H.
In the case of BF2dbm(OMe)2, while the qualitative experiments reveal its suceptibility to localized plastic shearing, the NI experiments yield high E and H values, implying high resistance to elastic and plastic deformations. These seemingly contradictory results can be rationalized as follows. We could perform the NI experiments only on the major face (010) of single crystals of BF2dbm(OMe)2 (Fig. S4b ). In this the (100) planes are the slip planes, and also parallel to the indentation direction of [010]. However, here along this direction molecules are linked by multiple and strong C—H⋯F interactions compared with the weak π-stacking interactions in BF2dbm(tBu)2 (see the orientation of molecules in Figs. 2c and 3e). The superior restorative nature of the C—H⋯F interactions produces higher E and H values in this case than for the other two samples. In this context it is worth noting that the crystal deformation is highly influenced by molecular arrangement and directional and/or non-directional interactions in the particular indentation direction (Varughese et al., 2013; Kiran et al., 2010; Varughese et al., 2012; Kiran, Varughese et al., 2013). Desiraju and coworkers state that `the short-range nondirectional interactions (such as van der Waals interactions) are likely to influence the plastic response as they will have a large bearing on how bonds break, whereas directional interactions (such as hydrogen bonds), being effective at long separations, influence elasticity because of their restorative character' (Varughese et al., 2013). Further, we recognize in this context that it would have been better if we had indented the crystal on other facets as well, so as to obtain a good idea on the anisotropy in plastic properties. Unfortunately, the small size of the crystals precluded us from pursuing this matter to its logical end.
The E and H values of the third compound, BF2dbmOMe, were found to be slightly lower than the respective values for BF2dbm(OMe)2. In this case, indentation experiments were performed on the major face (001) of the crystals. Notably, the orientation of molecules along the indentation direction is similar to that of BF2dbm(OMe)2. Indeed, the C—H⋯F interactions are slightly oblique to the indentation direction, which is probably the reason for the slightly lower E and H than that of BF2dbm(OMe)2. The —OCH3 functional groups in this structure do not form the slip planes, which would otherwise facilitate This makes stress relaxation in this crystal difficult and hence the crystals exhibit brittle behaviour, which is consistent with its three-dimensional interlocked structure with more contributions from directional interactions (Fig. S5 ) and the absence of slip planes in it.
5. Mechanochromic luminescence experiments
Experiments to examine the ML characteristics of the three compounds were performed by taking a few single crystals of the respective compounds (separately) in a mortar and gently crushing with a pestle to form a thin layer of powder particles. Firm mechanical stress was applied on the resulting thin powder layers and the prominence of mechanochromic luminescence was examined under UV light (365 nm). The bending type BF2dbm(tBu)2 crystals exhibited prominent colour changes from cyan (450 nm) to yellow (548 nm), while a reasonably good change in emission colour from green to yellow (only broadening of the peak) was observed for the shearing type BF2dbm(OMe)2 even at room temperature (Figs. 1 and S3 ). Moreover, both the materials healed back to their original colour, slow at room temperature but more quickly upon heating with a hot air gun. However, the third compound, BF2dbmOMe, did not exhibit any perceptible colour change at room temperature as well as at −98°C, which was obtained by immersing the mortar into frozen methanol using liquid N2 solution. This is in good agreement with the observed qualitative mechanical properties. The results support our earlier hypothesis that the plastic deformation behaviour effects the ML behaviour of solid-state fluorophores. The quantitative NI data does not allow ranking of plasticity in the three solids, which is mainly because of the absence of the data from the other observed faces.
The reversibility of ML behaviour depends on the plastic/elastic nature of the material. Longer recovery times are required for a material with high plastic behaviour. These observations are further supported by the elastic recovery rates of the P–h curves of the three compounds obtained from the NI experiments. BF2dbm(OMe)2 and BF2dbmOMe molecular crystals gave a higher elastic recovery rate than for BF2dbm(tBu)2 crystals. In addition to that, the perturbed yellow states on recovery emit the same colour as their parent forms, which suggests that the perturbed states must remain close enough to their original solid-state structure, but with defects that allow some changes in the molecular environment so that they return to the same form with time or on heating (Krishna et al., 2013). The powder X-ray also suggests that the recovery of the samples subjected to mechanical grinding is much slower in the case of BF2dbm(tBu)2 and BF2dbm(OMe)2 compared with the BF2dbmOMe samples. As expected, the recovery of the brittle BF2dbmOMe samples is so fast that it does not show any significant decrease in the intensities of the peaks upon ball milling for 30 min due to partial amorphization of the material, while the peaks in both bending type BF2dbm(tBu)2 and shearing type BF2dbm(OMe)2 show a significant decrease, confirming their superior plasticity than that of the former. On the other hand, the solid-state emission spectra of BF2dbm(tBu)2 showed a significant (from 450 to 548 nm) as well as broadening of the emission band upon mechanical grinding (FWHM from 41 to 115 nm), while BF2dbm(OMe)2 showed only a slight broadening of the emission band (FWHM from 56 to 77 nm), but no shift was observed in the maxima (Fig. S3 ). No change was observed in the case of BF2dbmOMe. These results are also in good agreement with the recovery dynamics of the three samples, expected from their plasticity order.
6. Conclusions
We have examined the mechanical properties of three compounds, namely BF2dbm(tBu)2, BF2dbm(OMe)2 and BF2dbmOMe crystals, using qualitative mechanical deformation tests and quantitative analysis using nanoindentation experiments. The preliminary qualitative tests revealed that BF2dbm(tBu)2, BF2dbm(OMe)2 and BF2dbmOMe crystals undergo bending, shearing and brittle deformation, respectively. Further, NI experiments confirmed that the BF2dbm(tBu)2 crystals are much softer with the lowest elastic modulus (0.369 ± 0.008 GPa) and hardness (92.45 ± 4.04 MPa) values compared with both shearing (BF2dbm(OMe)2) and brittle (BF2dbmOMe) type crystals. The observed mechanical properties in all the cases were consistent with their underlying crystal packing. In addition to that, BF2dbm(tBu)2 and BF2dbm(OMe)2 molecular crystals showed a prominent ML property from cyan to yellow and green to yellow, respectively, due to their higher plasticity, whereas BF2dbmOMe molecular crystals did not. After analyzing the results of these three examples, we conclude that the ML behaviour positively correlates with the plasticity. Hence introducing the slip planes into the crystal packing by keeping hydrophobic functional groups such as tBu and —OCH3 as substituents can help the design of efficient ML materials.
7. Experimental
BF2dbm(tBu)2, BF2dbm(OMe)2 and BF2dbmOMe compounds were synthesized according to previously reported procedures (Karasev & Korotkich, 1986; Yoshii et al., 2013; Sun et al., 2012; Zawadiak & Mrzyczek, 2012) and all the reagents and solvents were received from Aldrich chemicals which were used as such without any further purification. All the compounds were crystallized from commercially available solvents by the slow evaporation method at ambient conditions. BF2dbm(tBu)2 single crystals obtained from hexane:ethyl acetate (1:1 ratio), BF2dbm(OMe)2 and BF2dbmOMe were obtained from acetone solvent. After 2–3 days the crystals were suitable for single-crystal X-ray diffraction (SCXRD) experiments as well as for studying mechanical properties by: (i) qualitative experiments using metal forceps and a needle under the microscope and (ii) quantitative experiments using the NI technique. Initially, good quality crystals were selected under the microscope and face indexing experiments were carried out to identify the faces of all the three crystals and then used for NI experiments.
For indentation experiments, single crystals were firmly mounted on a stud using cyanoacrylate glue. Experiments were performed on each major facet of the three compounds using a nanoindenter (Triboindenter of Hysitron, Minneapolis, USA) with an in situ imaging capability. The machine continuously monitors and records the load, P, and displacement, h, of the indenter with force and displacement resolutions of 1 nN and 0.2 nm, respectively. A three-sided pyramidal Berkovich diamond indenter (tip radius ∼ 100 nm) was used to indent the crystals. Loading and unloading rates of 0.2 mN s−1 and a hold time of 2 s at peak load were employed. In order to identify flat regions for the experiment, the crystal surfaces were imaged prior to indentation using the same indenter tip. A minimum of 10 indentes were performed on each crystallographic face to ensure reproducibility. The indentation impressions were captured immediately after unloading so as to avoid any time-dependent elastic recovery of the residual impression. The P–h curves obtained were analyzed using the standard Oliver–Pharr method (Oliver & Pharr, 1992) to extract the elastic modulus, E, of the crystal in that orientation and the detailed methodology is given elsewhere (Bolshakov et al., 1996). However, this method was not used where the pile-up is found around the indenter.
7.1. Crystallography
Crystals of all three compounds were individually mounted on a glass pip. Intensity data were collected on a Bruker KAPPA APEX II CCD Duo system with graphite-monochromatic Mo Kα radiation (λ = 0.71073 Å). The data were collected at 100 K and the data reduction was performed using Bruker SAINT software (Bruker, 2003). Crystal structures were solved by using SHELXL97 and refined by full-matrix least-squares on F2 with anisotropic displacement parameters for non-H atoms using SHELXL97 (Bruker, 2000). H atoms associated with C atoms were fixed in geometrically constrained positions. H atoms associated with O and N atoms were included in the located positions. Structure graphics shown in the figures were created using the X-Seed software package Version 2.0.10.
7.2. (DSC)
DSC was conducted on a Mettler–Toledo DSI1 STARe instrument. Accurately weighed samples (3–4 mg) were placed in hermetically sealed aluminium crucibles (40 µL) and scanned from 30 to 300°C at a heating rate of 5°C min−1 under a dry nitrogen atmosphere (flow rate 80 ml min−1). The data were managed by STARe software (Fig. S2d ).
7.3. Powder X-ray diffraction (PXRD)
The PXRD patterns were collected on a Rigaku SmartLab with a Cu Kα radiation (1.540 Å). The tube voltage and amperage were set at 20 kV and 35 mA, respectively. Each sample was scanned between 5 and 50° 2θ with a step size of 0.02° (Fig. S2 ). The instrument was previously calibrated using a silicon standard.
7.4. Solid state UV–vis absorption and emission spectra
Spectra were collected using a JASCO V-670 spectrophotometer and a Horiba Jobin Yvon Fluorolog CP machine (USA), iHR 320 model spectrometer equipped with 450 W Xe lamp, respectively. Initially both absorption and emission spectra were recorded for a smoothly smeared powder sample (unground), after that the sample was gently ground for 5 min with a mortar and pestle, and both the spectra were immediately recorded (the same procedure was repeated for all three compounds; Fig. S3 ).
Supporting information
10.1107/S2052252515015134/ed5006sup1.cif
contains datablocks global, bf2dbmome2_a, bf2dbm_ome, bf2dbmtbu2_a. DOI:Structure factors: contains datablock bf2dbmome2_a. DOI: 10.1107/S2052252515015134/ed5006bf2dbmome2_asup2.hkl
Structure factors: contains datablock bf2dbm_ome. DOI: 10.1107/S2052252515015134/ed5006bf2dbm_omesup3.hkl
Structure factors: contains datablock bf2dbmtbu2_a. DOI: 10.1107/S2052252515015134/ed5006bf2dbmtbu2_asup4.hkl
Supporting tables and figures. DOI: 10.1107/S2052252515015134/ed5006sup5.pdf
Data collection: CrysAlis PRO, Agilent Technologies, Version 1.171.37.31 (release 14-01-2014 CrysAlis171 .NET) (compiled Jan 14 2014,18:38:05) for bf2dbm_ome. Cell
SAINT v7.68A (Bruker, 2009) for bf2dbmome2_a, bf2dbmtbu2_a; CrysAlis PRO, Agilent Technologies, Version 1.171.37.31 (release 14-01-2014 CrysAlis171 .NET) (compiled Jan 14 2014,18:38:05) for bf2dbm_ome. Data reduction: SAINT v7.68A (Bruker, 2009) for bf2dbmome2_a, bf2dbmtbu2_a; CrysAlis PRO, Agilent Technologies, Version 1.171.37.31 (release 14-01-2014 CrysAlis171 .NET) (compiled Jan 14 2014,18:38:05) for bf2dbm_ome. Program(s) used to solve structure: olex2.solve (Bourhis et al., 2015) for bf2dbmome2_a, bf2dbm_ome; SIR2004 (Burla et al., 2007) for bf2dbmtbu2_a. Program(s) used to refine structure: SHELXL (Sheldrick, 2008) for bf2dbmome2_a, bf2dbm_ome; olex2.refine (Bourhis et al., 2015) for bf2dbmtbu2_a. For all compounds, molecular graphics: Olex2 (Dolomanov et al., 2009); software used to prepare material for publication: Olex2 (Dolomanov et al., 2009).C17H15BF2O4 | F(000) = 688 |
Mr = 332.10 | Dx = 1.474 Mg m−3 |
Monoclinic, C2/c | Mo Kα radiation, λ = 0.71073 Å |
a = 21.1854 (15) Å | Cell parameters from 7514 reflections |
b = 7.0826 (5) Å | θ = 3.0–31.6° |
c = 10.0747 (7) Å | µ = 0.12 mm−1 |
β = 98.208 (2)° | T = 100 K |
V = 1496.20 (18) Å3 | Needle, green |
Z = 4 | 0.4 × 0.2 × 0.1 mm |
Bruker APEX-II CCD diffractometer | 1811 independent reflections |
Radiation source: fine-focus sealed tube | 1657 reflections with I > 2σ(I) |
Graphite monochromator | Rint = 0.026 |
φ and ω scans | θmax = 28.0°, θmin = 1.9° |
Absorption correction: multi-scan SADABS2008/1 (Bruker,2008) was used for absorption correction. wR2(int) was 0.1263 before and 0.0401 after correction. The Ratio of minimum to maximum transmission is 0.9314. The λ/2 correction factor is 0.0015. | h = −27→27 |
Tmin = 0.695, Tmax = 0.746 | k = −9→9 |
13225 measured reflections | l = −13→11 |
Refinement on F2 | Secondary atom site location: difference Fourier map |
Least-squares matrix: full | Hydrogen site location: inferred from neighbouring sites |
R[F2 > 2σ(F2)] = 0.033 | H-atom parameters constrained |
wR(F2) = 0.095 | w = 1/[σ2(Fo2) + (0.0514P)2 + 0.8028P] where P = (Fo2 + 2Fc2)/3 |
S = 1.08 | (Δ/σ)max = 0.001 |
1811 reflections | Δρmax = 0.36 e Å−3 |
112 parameters | Δρmin = −0.22 e Å−3 |
0 restraints | Extinction correction: SHELXL, Fc*=kFc[1+0.001xFc2λ3/sin(2θ)]-1/4 |
Primary atom site location: iterative | Extinction coefficient: 0.0139 (15) |
C17H15BF2O4 | V = 1496.20 (18) Å3 |
Mr = 332.10 | Z = 4 |
Monoclinic, C2/c | Mo Kα radiation |
a = 21.1854 (15) Å | µ = 0.12 mm−1 |
b = 7.0826 (5) Å | T = 100 K |
c = 10.0747 (7) Å | 0.4 × 0.2 × 0.1 mm |
β = 98.208 (2)° |
Bruker APEX-II CCD diffractometer | 1811 independent reflections |
Absorption correction: multi-scan SADABS2008/1 (Bruker,2008) was used for absorption correction. wR2(int) was 0.1263 before and 0.0401 after correction. The Ratio of minimum to maximum transmission is 0.9314. The λ/2 correction factor is 0.0015. | 1657 reflections with I > 2σ(I) |
Tmin = 0.695, Tmax = 0.746 | Rint = 0.026 |
13225 measured reflections |
R[F2 > 2σ(F2)] = 0.033 | 0 restraints |
wR(F2) = 0.095 | H-atom parameters constrained |
S = 1.08 | Δρmax = 0.36 e Å−3 |
1811 reflections | Δρmin = −0.22 e Å−3 |
112 parameters |
Geometry. All e.s.d.'s (except the e.s.d. in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell e.s.d.'s are taken into account individually in the estimation of e.s.d.'s in distances, angles and torsion angles; correlations between e.s.d.'s in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell e.s.d.'s is used for estimating e.s.d.'s involving l.s. planes. |
Refinement. Refinement of F2 against ALL reflections. The weighted R-factor wR and goodness of fit S are based on F2, conventional R-factors R are based on F, with F set to zero for negative F2. The threshold expression of F2 > σ(F2) is used only for calculating R-factors(gt) etc. and is not relevant to the choice of reflections for refinement. R-factors based on F2 are statistically about twice as large as those based on F, and R- factors based on ALL data will be even larger. |
x | y | z | Uiso*/Ueq | ||
B1 | 0.5000 | 0.06398 (19) | 0.2500 | 0.0147 (3) | |
C1 | 0.41783 (4) | 0.45810 (12) | 0.40667 (9) | 0.0133 (2) | |
C2 | 0.38118 (4) | 0.34871 (13) | 0.48329 (10) | 0.0162 (2) | |
H2 | 0.3836 | 0.2177 | 0.4801 | 0.019* | |
C3 | 0.34166 (5) | 0.43343 (14) | 0.56332 (10) | 0.0184 (2) | |
H3 | 0.3176 | 0.3595 | 0.6137 | 0.022* | |
C4 | 0.33771 (4) | 0.63041 (14) | 0.56867 (9) | 0.0157 (2) | |
C5 | 0.37337 (4) | 0.74130 (14) | 0.49256 (10) | 0.0173 (2) | |
H5 | 0.3706 | 0.8722 | 0.4953 | 0.021* | |
C6 | 0.41314 (4) | 0.65471 (13) | 0.41262 (10) | 0.0168 (2) | |
H6 | 0.4371 | 0.7288 | 0.3621 | 0.020* | |
C7 | 0.29790 (5) | 0.90162 (15) | 0.67053 (11) | 0.0239 (2) | |
H7A | 0.3402 | 0.9429 | 0.7057 | 0.036* | |
H7B | 0.2691 | 0.9333 | 0.7326 | 0.036* | |
H7C | 0.2844 | 0.9630 | 0.5863 | 0.036* | |
C8 | 0.46058 (4) | 0.36583 (13) | 0.32466 (9) | 0.0128 (2) | |
C9 | 0.5000 | 0.46405 (18) | 0.2500 | 0.0150 (3) | |
H9 | 0.5000 | 0.5954 | 0.2500 | 0.018* | |
F1 | 0.53917 (3) | −0.04842 (8) | 0.33814 (6) | 0.02054 (18) | |
O1 | 0.45954 (3) | 0.18135 (9) | 0.32582 (7) | 0.01788 (19) | |
O2 | 0.29794 (3) | 0.70101 (10) | 0.65105 (8) | 0.0219 (2) |
U11 | U22 | U33 | U12 | U13 | U23 | |
B1 | 0.0173 (6) | 0.0096 (6) | 0.0178 (7) | 0.000 | 0.0043 (5) | 0.000 |
C1 | 0.0136 (4) | 0.0129 (4) | 0.0131 (4) | 0.0002 (3) | 0.0013 (3) | 0.0002 (3) |
C2 | 0.0172 (4) | 0.0123 (4) | 0.0194 (5) | 0.0001 (3) | 0.0037 (3) | 0.0020 (3) |
C3 | 0.0183 (4) | 0.0174 (5) | 0.0209 (5) | −0.0007 (3) | 0.0073 (4) | 0.0038 (3) |
C4 | 0.0135 (4) | 0.0183 (5) | 0.0156 (5) | 0.0018 (3) | 0.0030 (3) | −0.0010 (3) |
C5 | 0.0197 (5) | 0.0123 (4) | 0.0208 (5) | 0.0006 (3) | 0.0054 (4) | −0.0015 (3) |
C6 | 0.0194 (4) | 0.0134 (4) | 0.0189 (5) | −0.0014 (3) | 0.0074 (3) | 0.0003 (3) |
C7 | 0.0217 (5) | 0.0222 (5) | 0.0296 (6) | 0.0038 (4) | 0.0094 (4) | −0.0068 (4) |
C8 | 0.0139 (4) | 0.0113 (4) | 0.0125 (4) | 0.0004 (3) | −0.0004 (3) | −0.0001 (3) |
C9 | 0.0173 (6) | 0.0108 (5) | 0.0174 (6) | 0.000 | 0.0039 (5) | 0.000 |
F1 | 0.0204 (3) | 0.0192 (3) | 0.0218 (3) | 0.0032 (2) | 0.0021 (2) | 0.0047 (2) |
O1 | 0.0229 (4) | 0.0099 (3) | 0.0230 (4) | −0.0004 (2) | 0.0104 (3) | 0.0001 (2) |
O2 | 0.0216 (4) | 0.0212 (4) | 0.0257 (4) | 0.0030 (3) | 0.0126 (3) | −0.0016 (3) |
B1—F1i | 1.3786 (10) | C3—C4 | 1.3991 (13) |
B1—F1 | 1.3786 (10) | C4—C5 | 1.3931 (13) |
B1—O1i | 1.4819 (10) | C4—O2 | 1.3596 (11) |
B1—O1 | 1.4819 (10) | C5—C6 | 1.3887 (13) |
C1—C2 | 1.4038 (12) | C7—O2 | 1.4343 (12) |
C1—C6 | 1.3979 (12) | C8—C9 | 1.3880 (11) |
C1—C8 | 1.4641 (12) | C8—O1 | 1.3068 (11) |
C2—C3 | 1.3797 (13) | C9—C8i | 1.3880 (11) |
F1i—B1—F1 | 109.45 (11) | C5—C4—C3 | 120.06 (8) |
F1—B1—O1i | 108.47 (4) | O2—C4—C3 | 115.85 (8) |
F1i—B1—O1 | 108.46 (4) | O2—C4—C5 | 124.10 (9) |
F1i—B1—O1i | 109.34 (4) | C6—C5—C4 | 119.46 (9) |
F1—B1—O1 | 109.34 (4) | C5—C6—C1 | 121.17 (8) |
O1i—B1—O1 | 111.76 (10) | C9—C8—C1 | 123.41 (9) |
C2—C1—C8 | 119.95 (8) | O1—C8—C1 | 115.38 (8) |
C6—C1—C2 | 118.55 (8) | O1—C8—C9 | 121.21 (8) |
C6—C1—C8 | 121.49 (8) | C8—C9—C8i | 119.84 (11) |
C3—C2—C1 | 120.72 (9) | C8—O1—B1 | 122.99 (7) |
C2—C3—C4 | 120.05 (8) | C4—O2—C7 | 117.41 (8) |
Symmetry code: (i) −x+1, y, −z+1/2. |
C16H13BF2O3 | Z = 2 |
Mr = 302.07 | F(000) = 312 |
Triclinic, P1 | Dx = 1.407 Mg m−3 |
a = 8.0234 (7) Å | Mo Kα radiation, λ = 0.71073 Å |
b = 9.0901 (8) Å | Cell parameters from 1505 reflections |
c = 10.7916 (8) Å | θ = 2.7–26.6° |
α = 75.514 (7)° | µ = 0.11 mm−1 |
β = 80.766 (7)° | T = 100 K |
γ = 69.797 (8)° | Needle, yellow |
V = 712.79 (11) Å3 | 0.5 × 0.35 × 0.1 mm |
SuperNova, Dual, Cu at zero, Eos diffractometer | 2991 independent reflections |
Radiation source: SuperNova (Mo) X-ray Source | 2092 reflections with I > 2σ(I) |
Mirror monochromator | Rint = 0.021 |
Detector resolution: 7.9580 pixels mm-1 | θmax = 28.1°, θmin = 2.0° |
ω scans | h = −10→10 |
Absorption correction: multi-scan CrysAlis PRO, Agilent Technologies, Version 1.171.37.31 (release 14-01-2014 CrysAlis171 .NET) (compiled Jan 14 2014,18:38:05) Empirical absorption correction using spherical harmonics, implemented in SCALE3 ABSPACK scaling algorithm. | k = −9→11 |
Tmin = 0.866, Tmax = 1.000 | l = −14→12 |
4141 measured reflections |
Refinement on F2 | Primary atom site location: iterative |
Least-squares matrix: full | Secondary atom site location: difference Fourier map |
R[F2 > 2σ(F2)] = 0.057 | Hydrogen site location: inferred from neighbouring sites |
wR(F2) = 0.136 | H-atom parameters constrained |
S = 1.04 | w = 1/[σ2(Fo2) + (0.042P)2 + 0.1821P] where P = (Fo2 + 2Fc2)/3 |
2991 reflections | (Δ/σ)max < 0.001 |
200 parameters | Δρmax = 0.14 e Å−3 |
0 restraints | Δρmin = −0.18 e Å−3 |
C16H13BF2O3 | γ = 69.797 (8)° |
Mr = 302.07 | V = 712.79 (11) Å3 |
Triclinic, P1 | Z = 2 |
a = 8.0234 (7) Å | Mo Kα radiation |
b = 9.0901 (8) Å | µ = 0.11 mm−1 |
c = 10.7916 (8) Å | T = 100 K |
α = 75.514 (7)° | 0.5 × 0.35 × 0.1 mm |
β = 80.766 (7)° |
SuperNova, Dual, Cu at zero, Eos diffractometer | 2991 independent reflections |
Absorption correction: multi-scan CrysAlis PRO, Agilent Technologies, Version 1.171.37.31 (release 14-01-2014 CrysAlis171 .NET) (compiled Jan 14 2014,18:38:05) Empirical absorption correction using spherical harmonics, implemented in SCALE3 ABSPACK scaling algorithm. | 2092 reflections with I > 2σ(I) |
Tmin = 0.866, Tmax = 1.000 | Rint = 0.021 |
4141 measured reflections |
R[F2 > 2σ(F2)] = 0.057 | 0 restraints |
wR(F2) = 0.136 | H-atom parameters constrained |
S = 1.04 | Δρmax = 0.14 e Å−3 |
2991 reflections | Δρmin = −0.18 e Å−3 |
200 parameters |
Geometry. All e.s.d.'s (except the e.s.d. in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell e.s.d.'s are taken into account individually in the estimation of e.s.d.'s in distances, angles and torsion angles; correlations between e.s.d.'s in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell e.s.d.'s is used for estimating e.s.d.'s involving l.s. planes. |
Refinement. Refinement of F2 against ALL reflections. The weighted R-factor wR and goodness of fit S are based on F2, conventional R-factors R are based on F, with F set to zero for negative F2. The threshold expression of F2 > σ(F2) is used only for calculating R-factors(gt) etc. and is not relevant to the choice of reflections for refinement. R-factors based on F2 are statistically about twice as large as those based on F, and R- factors based on ALL data will be even larger. |
x | y | z | Uiso*/Ueq | ||
C5 | 0.2844 (2) | 0.9028 (2) | 0.02628 (18) | 0.0446 (4) | |
C6 | 0.1661 (3) | 1.0443 (2) | 0.05682 (18) | 0.0481 (5) | |
H6 | 0.1572 | 1.1407 | −0.0016 | 0.058* | |
C13 | 0.4028 (2) | 0.8911 (2) | −0.09117 (16) | 0.0426 (4) | |
O19 | 0.7263 (2) | 0.85683 (19) | −0.43237 (14) | 0.0690 (5) | |
O4 | 0.2958 (2) | 0.76623 (17) | 0.10723 (14) | 0.0683 (5) | |
F22 | 0.26920 (19) | 0.66067 (17) | 0.32537 (12) | 0.0809 (5) | |
O2 | 0.0695 (2) | 0.91116 (17) | 0.25399 (14) | 0.0710 (5) | |
C16 | 0.6255 (3) | 0.8596 (3) | −0.31833 (18) | 0.0503 (5) | |
C1 | 0.0618 (3) | 1.0454 (2) | 0.17142 (18) | 0.0458 (5) | |
F21 | 0.05436 (19) | 0.68278 (16) | 0.20442 (13) | 0.0789 (4) | |
C17 | 0.5168 (3) | 1.0108 (2) | −0.29896 (19) | 0.0569 (5) | |
H17 | 0.5186 | 1.1016 | −0.3617 | 0.068* | |
C14 | 0.5146 (3) | 0.7408 (2) | −0.11221 (18) | 0.0496 (5) | |
H14 | 0.5142 | 0.6498 | −0.0493 | 0.060* | |
C7 | −0.0624 (3) | 1.1914 (2) | 0.21219 (18) | 0.0479 (5) | |
C18 | 0.4074 (3) | 1.0264 (2) | −0.18794 (19) | 0.0519 (5) | |
H18 | 0.3353 | 1.1278 | −0.1766 | 0.062* | |
C15 | 0.6250 (3) | 0.7236 (2) | −0.22341 (19) | 0.0527 (5) | |
H15 | 0.6983 | 0.6225 | −0.2349 | 0.063* | |
C8 | −0.1536 (3) | 1.1787 (3) | 0.3343 (2) | 0.0611 (6) | |
H8 | −0.1355 | 1.0789 | 0.3895 | 0.073* | |
C12 | −0.0944 (3) | 1.3422 (3) | 0.1305 (2) | 0.0592 (6) | |
H12 | −0.0359 | 1.3521 | 0.0486 | 0.071* | |
C10 | −0.3006 (3) | 1.4640 (3) | 0.2916 (3) | 0.0713 (7) | |
H10 | −0.3791 | 1.5548 | 0.3184 | 0.086* | |
B3 | 0.1727 (4) | 0.7518 (3) | 0.2246 (2) | 0.0567 (6) | |
C9 | −0.2714 (3) | 1.3153 (3) | 0.3731 (2) | 0.0739 (7) | |
H9 | −0.3309 | 1.3065 | 0.4546 | 0.089* | |
C20 | 0.8293 (4) | 0.7036 (3) | −0.4626 (2) | 0.0795 (8) | |
H20A | 0.8902 | 0.7197 | −0.5465 | 0.119* | |
H20B | 0.7514 | 0.6432 | −0.4611 | 0.119* | |
H20C | 0.9149 | 0.6459 | −0.4003 | 0.119* | |
C11 | −0.2131 (3) | 1.4775 (3) | 0.1704 (3) | 0.0695 (6) | |
H11 | −0.2337 | 1.5775 | 0.1152 | 0.083* |
U11 | U22 | U33 | U12 | U13 | U23 | |
C5 | 0.0469 (11) | 0.0451 (10) | 0.0452 (10) | −0.0198 (9) | −0.0061 (8) | −0.0066 (8) |
C6 | 0.0512 (12) | 0.0427 (10) | 0.0480 (11) | −0.0155 (9) | −0.0025 (9) | −0.0058 (8) |
C13 | 0.0446 (11) | 0.0456 (10) | 0.0410 (10) | −0.0187 (9) | −0.0032 (8) | −0.0090 (8) |
O19 | 0.0734 (11) | 0.0710 (10) | 0.0533 (9) | −0.0211 (8) | 0.0154 (7) | −0.0123 (7) |
O4 | 0.0856 (12) | 0.0434 (8) | 0.0588 (9) | −0.0148 (8) | 0.0210 (8) | −0.0059 (7) |
F22 | 0.0828 (10) | 0.0834 (10) | 0.0554 (8) | −0.0061 (8) | −0.0026 (7) | −0.0078 (7) |
O2 | 0.0899 (12) | 0.0476 (9) | 0.0605 (9) | −0.0185 (8) | 0.0231 (8) | −0.0079 (7) |
C16 | 0.0486 (11) | 0.0617 (13) | 0.0423 (11) | −0.0215 (10) | −0.0006 (8) | −0.0104 (9) |
C1 | 0.0473 (11) | 0.0473 (11) | 0.0466 (11) | −0.0198 (9) | −0.0039 (8) | −0.0101 (8) |
F21 | 0.0813 (10) | 0.0769 (10) | 0.0850 (10) | −0.0344 (8) | 0.0087 (7) | −0.0256 (7) |
C17 | 0.0650 (14) | 0.0482 (12) | 0.0500 (12) | −0.0185 (10) | 0.0019 (10) | −0.0010 (9) |
C14 | 0.0594 (13) | 0.0417 (11) | 0.0465 (11) | −0.0188 (9) | −0.0009 (9) | −0.0054 (8) |
C7 | 0.0448 (11) | 0.0520 (12) | 0.0519 (11) | −0.0185 (9) | −0.0035 (8) | −0.0158 (9) |
C18 | 0.0547 (12) | 0.0432 (11) | 0.0534 (12) | −0.0131 (9) | −0.0004 (9) | −0.0087 (9) |
C15 | 0.0559 (13) | 0.0482 (11) | 0.0520 (12) | −0.0145 (10) | 0.0009 (9) | −0.0134 (9) |
C8 | 0.0615 (14) | 0.0644 (14) | 0.0557 (13) | −0.0174 (11) | 0.0003 (10) | −0.0166 (10) |
C12 | 0.0591 (14) | 0.0524 (12) | 0.0659 (13) | −0.0192 (11) | 0.0045 (10) | −0.0162 (10) |
C10 | 0.0569 (14) | 0.0643 (16) | 0.0961 (19) | −0.0109 (12) | −0.0005 (13) | −0.0384 (14) |
B3 | 0.0666 (16) | 0.0456 (13) | 0.0512 (14) | −0.0173 (12) | 0.0066 (11) | −0.0062 (10) |
C9 | 0.0687 (16) | 0.0873 (19) | 0.0668 (15) | −0.0212 (14) | 0.0119 (12) | −0.0344 (14) |
C20 | 0.0819 (18) | 0.0842 (18) | 0.0659 (15) | −0.0226 (15) | 0.0232 (13) | −0.0282 (13) |
C11 | 0.0668 (15) | 0.0498 (13) | 0.0892 (18) | −0.0150 (11) | −0.0006 (13) | −0.0187 (12) |
C5—C6 | 1.390 (3) | C16—C17 | 1.397 (3) |
C5—C13 | 1.460 (3) | C16—C15 | 1.395 (3) |
C5—O4 | 1.310 (2) | C1—C7 | 1.479 (3) |
C6—C1 | 1.378 (3) | F21—B3 | 1.374 (3) |
C13—C14 | 1.402 (3) | C17—C18 | 1.374 (3) |
C13—C18 | 1.408 (3) | C14—C15 | 1.381 (3) |
O19—C16 | 1.361 (2) | C7—C8 | 1.400 (3) |
O19—C20 | 1.440 (3) | C7—C12 | 1.395 (3) |
O4—B3 | 1.484 (3) | C8—C9 | 1.390 (3) |
F22—B3 | 1.358 (3) | C12—C11 | 1.389 (3) |
O2—C1 | 1.307 (2) | C10—C9 | 1.381 (3) |
O2—B3 | 1.484 (3) | C10—C11 | 1.380 (3) |
C6—C5—C13 | 125.28 (17) | C15—C14—C13 | 122.08 (18) |
O4—C5—C6 | 119.51 (17) | C8—C7—C1 | 119.61 (18) |
O4—C5—C13 | 115.20 (17) | C12—C7—C1 | 121.53 (18) |
C1—C6—C5 | 121.67 (18) | C12—C7—C8 | 118.85 (19) |
C14—C13—C5 | 120.07 (16) | C17—C18—C13 | 120.94 (19) |
C14—C13—C18 | 117.52 (17) | C14—C15—C16 | 119.20 (19) |
C18—C13—C5 | 122.39 (17) | C9—C8—C7 | 120.0 (2) |
C16—O19—C20 | 118.45 (17) | C11—C12—C7 | 120.5 (2) |
C5—O4—B3 | 122.93 (16) | C11—C10—C9 | 119.9 (2) |
C1—O2—B3 | 122.63 (16) | F22—B3—O4 | 109.0 (2) |
O19—C16—C17 | 115.89 (17) | F22—B3—O2 | 108.81 (19) |
O19—C16—C15 | 124.32 (19) | F22—B3—F21 | 110.94 (19) |
C15—C16—C17 | 119.79 (18) | O2—B3—O4 | 111.38 (17) |
C6—C1—C7 | 124.67 (18) | F21—B3—O4 | 108.59 (19) |
O2—C1—C6 | 120.30 (18) | F21—B3—O2 | 108.1 (2) |
O2—C1—C7 | 115.03 (17) | C10—C9—C8 | 120.5 (2) |
C18—C17—C16 | 120.47 (18) | C10—C11—C12 | 120.2 (2) |
C23H27BF2O2 | F(000) = 816.4661 |
Mr = 384.29 | Dx = 1.261 Mg m−3 |
Monoclinic, C2/c | Mo Kα radiation, λ = 0.71073 Å |
a = 28.575 (4) Å | Cell parameters from 6711 reflections |
b = 7.0402 (9) Å | θ = 2.9–31.2° |
c = 10.3208 (13) Å | µ = 0.09 mm−1 |
β = 102.920 (3)° | T = 100 K |
V = 2023.7 (5) Å3 | Needle, green |
Z = 4 | 0.52 × 0.25 × 0.1 mm |
Bruker APEX-II CCD diffractometer | 2124 reflections with I ≥ 2u(I) |
Graphite monochromator | Rint = 0.038 |
φ and ω scans | θmax = 28.0°, θmin = 1.5° |
Absorption correction: multi-scan SADABS2008/1 (Bruker,2008) was used for absorption correction. wR2(int) was 0.1101 before and 0.0482 after correction. The Ratio of minimum to maximum transmission is 0.9414. The λ/2 correction factor is 0.0015. | h = −41→41 |
Tmin = 0.703, Tmax = 0.746 | k = −10→10 |
21860 measured reflections | l = −7→15 |
2442 independent reflections |
Refinement on F2 | 22 constraints |
Least-squares matrix: full | Primary atom site location: structure-invariant direct methods |
R[F2 > 2σ(F2)] = 0.035 | H-atom parameters constrained |
wR(F2) = 0.100 | w = 1/[σ2(Fo2) + (0.0516P)2 + 1.2985P] where P = (Fo2 + 2Fc2)/3 |
S = 1.06 | (Δ/σ)max = 0.0002 |
2442 reflections | Δρmax = 0.39 e Å−3 |
131 parameters | Δρmin = −0.19 e Å−3 |
0 restraints |
C23H27BF2O2 | V = 2023.7 (5) Å3 |
Mr = 384.29 | Z = 4 |
Monoclinic, C2/c | Mo Kα radiation |
a = 28.575 (4) Å | µ = 0.09 mm−1 |
b = 7.0402 (9) Å | T = 100 K |
c = 10.3208 (13) Å | 0.52 × 0.25 × 0.1 mm |
β = 102.920 (3)° |
Bruker APEX-II CCD diffractometer | 2442 independent reflections |
Absorption correction: multi-scan SADABS2008/1 (Bruker,2008) was used for absorption correction. wR2(int) was 0.1101 before and 0.0482 after correction. The Ratio of minimum to maximum transmission is 0.9414. The λ/2 correction factor is 0.0015. | 2124 reflections with I ≥ 2u(I) |
Tmin = 0.703, Tmax = 0.746 | Rint = 0.038 |
21860 measured reflections |
R[F2 > 2σ(F2)] = 0.035 | 0 restraints |
wR(F2) = 0.100 | H-atom parameters constrained |
S = 1.06 | Δρmax = 0.39 e Å−3 |
2442 reflections | Δρmin = −0.19 e Å−3 |
131 parameters |
x | y | z | Uiso*/Ueq | ||
B1 | 0.5 | 0.0782 (2) | 1.25 | 0.0154 (3) | |
C1 | 0.43854 (3) | 0.47264 (13) | 1.03271 (9) | 0.0127 (2) | |
C2 | 0.41542 (3) | 0.36165 (14) | 0.92499 (10) | 0.0139 (2) | |
H2 | 0.42268 (3) | 0.23311 (14) | 0.92257 (10) | 0.0166 (2)* | |
C3 | 0.38167 (3) | 0.44212 (14) | 0.82151 (10) | 0.0144 (2) | |
H3 | 0.36680 (3) | 0.36640 (14) | 0.75033 (10) | 0.0173 (2)* | |
C4 | 0.36961 (3) | 0.63428 (14) | 0.82217 (9) | 0.0134 (2) | |
C5 | 0.39418 (4) | 0.74521 (14) | 0.92869 (10) | 0.0168 (2) | |
H5 | 0.38753 (4) | 0.87443 (14) | 0.92988 (10) | 0.0202 (3)* | |
C6 | 0.42806 (4) | 0.66732 (14) | 1.03210 (10) | 0.0158 (2) | |
H6 | 0.44393 (4) | 0.74425 (14) | 1.10136 (10) | 0.0189 (3)* | |
C7 | 0.32948 (4) | 0.72312 (14) | 0.71573 (10) | 0.0158 (2) | |
C8 | 0.28815 (4) | 0.77798 (17) | 0.78196 (11) | 0.0234 (3) | |
H8a | 0.2778 (2) | 0.6678 (3) | 0.8228 (8) | 0.0352 (4)* | |
H8b | 0.29907 (10) | 0.8732 (9) | 0.8484 (6) | 0.0352 (4)* | |
H8c | 0.26180 (13) | 0.8271 (12) | 0.71596 (19) | 0.0352 (4)* | |
C9 | 0.31020 (4) | 0.58491 (16) | 0.60151 (10) | 0.0194 (2) | |
H9a | 0.33600 (7) | 0.5450 (9) | 0.5622 (6) | 0.0291 (3)* | |
H9b | 0.2965 (3) | 0.4761 (6) | 0.63521 (18) | 0.0291 (3)* | |
H9c | 0.2860 (2) | 0.6471 (4) | 0.5356 (4) | 0.0291 (3)* | |
C10 | 0.34791 (4) | 0.90250 (16) | 0.65792 (11) | 0.0236 (3) | |
H10a | 0.3590 (3) | 0.9924 (5) | 0.72797 (18) | 0.0354 (4)* | |
H10b | 0.3739 (2) | 0.8691 (3) | 0.6173 (8) | 0.0354 (4)* | |
H10c | 0.32233 (9) | 0.9579 (7) | 0.5925 (6) | 0.0354 (4)* | |
C11 | 0.47139 (3) | 0.38164 (14) | 1.14558 (9) | 0.0122 (2) | |
C12 | 0.5 | 0.4811 (2) | 1.25 | 0.0148 (3) | |
H12 | 0.5 | 0.6132 (2) | 1.25 | 0.0178 (3)* | |
F1 | 0.53097 (2) | −0.03347 (9) | 1.19864 (6) | 0.02402 (19) | |
O1 | 0.47140 (3) | 0.19649 (10) | 1.14224 (7) | 0.01850 (19) |
U11 | U22 | U33 | U12 | U13 | U23 | |
B1 | 0.0180 (7) | 0.0102 (7) | 0.0158 (7) | −0.000000 | −0.0008 (6) | 0.000000 |
C1 | 0.0129 (4) | 0.0133 (5) | 0.0115 (5) | 0.0001 (3) | 0.0022 (3) | 0.0007 (3) |
C2 | 0.0165 (4) | 0.0120 (4) | 0.0130 (5) | 0.0007 (3) | 0.0034 (4) | −0.0008 (4) |
C3 | 0.0161 (4) | 0.0156 (5) | 0.0109 (4) | −0.0009 (3) | 0.0018 (4) | −0.0020 (3) |
C4 | 0.0133 (4) | 0.0156 (4) | 0.0113 (4) | 0.0012 (3) | 0.0026 (3) | 0.0021 (3) |
C5 | 0.0202 (5) | 0.0118 (4) | 0.0170 (5) | 0.0015 (4) | 0.0012 (4) | 0.0001 (4) |
C6 | 0.0179 (5) | 0.0133 (5) | 0.0142 (5) | −0.0013 (4) | −0.0006 (4) | −0.0013 (4) |
C7 | 0.0153 (4) | 0.0183 (5) | 0.0124 (5) | 0.0032 (4) | 0.0002 (4) | 0.0012 (4) |
C8 | 0.0197 (5) | 0.0311 (6) | 0.0188 (5) | 0.0082 (4) | 0.0028 (4) | −0.0016 (4) |
C9 | 0.0181 (5) | 0.0245 (5) | 0.0133 (5) | 0.0034 (4) | −0.0016 (4) | −0.0010 (4) |
C10 | 0.0262 (5) | 0.0210 (5) | 0.0214 (6) | 0.0028 (4) | 0.0004 (4) | 0.0075 (4) |
C11 | 0.0131 (4) | 0.0120 (4) | 0.0123 (5) | 0.0006 (3) | 0.0041 (3) | 0.0002 (3) |
C12 | 0.0170 (6) | 0.0116 (6) | 0.0141 (7) | −0.000000 | −0.0001 (5) | 0.000000 |
F1 | 0.0261 (3) | 0.0247 (4) | 0.0199 (3) | 0.0089 (3) | 0.0020 (3) | −0.0027 (3) |
O1 | 0.0237 (4) | 0.0108 (4) | 0.0166 (4) | 0.0005 (3) | −0.0049 (3) | −0.0005 (3) |
B1—F1 | 1.3755 (11) | C4—C5 | 1.4023 (13) |
B1—F1i | 1.3755 (11) | C4—C7 | 1.5328 (13) |
B1—O1 | 1.4804 (11) | C5—C6 | 1.3839 (13) |
B1—O1i | 1.4804 (11) | C7—C8 | 1.5400 (15) |
C1—C2 | 1.3980 (13) | C7—C9 | 1.5328 (14) |
C1—C6 | 1.4026 (13) | C7—C10 | 1.5391 (15) |
C1—C11 | 1.4696 (13) | C11—C12 | 1.3878 (11) |
C2—C3 | 1.3897 (13) | C11—O1 | 1.3040 (12) |
C3—C4 | 1.3965 (14) | ||
F1i—B1—F1 | 110.27 (12) | C6—C5—C4 | 121.69 (9) |
O1i—B1—F1 | 108.45 (4) | C5—C6—C1 | 120.16 (9) |
O1i—B1—F1i | 109.06 (4) | C8—C7—C4 | 108.01 (8) |
O1—B1—F1 | 109.06 (4) | C9—C7—C4 | 112.01 (8) |
O1—B1—F1i | 108.45 (4) | C9—C7—C8 | 108.73 (8) |
O1i—B1—O1 | 111.55 (11) | C10—C7—C4 | 110.28 (8) |
C6—C1—C2 | 118.70 (9) | C10—C7—C8 | 109.21 (9) |
C11—C1—C2 | 119.42 (9) | C10—C7—C9 | 108.54 (9) |
C11—C1—C6 | 121.83 (9) | C12—C11—C1 | 123.83 (9) |
C3—C2—C1 | 120.44 (9) | O1—C11—C1 | 114.75 (8) |
C4—C3—C2 | 121.39 (9) | O1—C11—C12 | 121.41 (9) |
C5—C4—C3 | 117.55 (9) | C11i—C12—C11 | 119.41 (13) |
C7—C4—C3 | 122.53 (9) | C11—O1—B1 | 123.07 (8) |
C7—C4—C5 | 119.86 (9) |
Symmetry code: (i) −x+1, y, −z+5/2. |
Experimental details
(bf2dbmome2_a) | (bf2dbm_ome) | (bf2dbmtbu2_a) | |
Crystal data | |||
Chemical formula | C17H15BF2O4 | C16H13BF2O3 | C23H27BF2O2 |
Mr | 332.10 | 302.07 | 384.29 |
Crystal system, space group | Monoclinic, C2/c | Triclinic, P1 | Monoclinic, C2/c |
Temperature (K) | 100 | 100 | 100 |
a, b, c (Å) | 21.1854 (15), 7.0826 (5), 10.0747 (7) | 8.0234 (7), 9.0901 (8), 10.7916 (8) | 28.575 (4), 7.0402 (9), 10.3208 (13) |
α, β, γ (°) | 90, 98.208 (2), 90 | 75.514 (7), 80.766 (7), 69.797 (8) | 90, 102.920 (3), 90 |
V (Å3) | 1496.20 (18) | 712.79 (11) | 2023.7 (5) |
Z | 4 | 2 | 4 |
Radiation type | Mo Kα | Mo Kα | Mo Kα |
µ (mm−1) | 0.12 | 0.11 | 0.09 |
Crystal size (mm) | 0.4 × 0.2 × 0.1 | 0.5 × 0.35 × 0.1 | 0.52 × 0.25 × 0.1 |
Data collection | |||
Diffractometer | Bruker APEX-II CCD diffractometer | SuperNova, Dual, Cu at zero, Eos diffractometer | Bruker APEX-II CCD diffractometer |
Absorption correction | Multi-scan SADABS2008/1 (Bruker,2008) was used for absorption correction. wR2(int) was 0.1263 before and 0.0401 after correction. The Ratio of minimum to maximum transmission is 0.9314. The λ/2 correction factor is 0.0015. | Multi-scan CrysAlis PRO, Agilent Technologies, Version 1.171.37.31 (release 14-01-2014 CrysAlis171 .NET) (compiled Jan 14 2014,18:38:05) Empirical absorption correction using spherical harmonics, implemented in SCALE3 ABSPACK scaling algorithm. | Multi-scan SADABS2008/1 (Bruker,2008) was used for absorption correction. wR2(int) was 0.1101 before and 0.0482 after correction. The Ratio of minimum to maximum transmission is 0.9414. The λ/2 correction factor is 0.0015. |
Tmin, Tmax | 0.695, 0.746 | 0.866, 1.000 | 0.703, 0.746 |
No. of measured, independent and observed reflections | 13225, 1811, 1657 [I > 2σ(I)] | 4141, 2991, 2092 [I > 2σ(I)] | 21860, 2442, 2124 [I ≥ 2u(I)] |
Rint | 0.026 | 0.021 | 0.038 |
(sin θ/λ)max (Å−1) | 0.661 | 0.663 | 0.660 |
Refinement | |||
R[F2 > 2σ(F2)], wR(F2), S | 0.033, 0.095, 1.08 | 0.057, 0.136, 1.04 | 0.035, 0.100, 1.06 |
No. of reflections | 1811 | 2991 | 2442 |
No. of parameters | 112 | 200 | 131 |
H-atom treatment | H-atom parameters constrained | H-atom parameters constrained | H-atom parameters constrained |
Δρmax, Δρmin (e Å−3) | 0.36, −0.22 | 0.14, −0.18 | 0.39, −0.19 |
Computer programs: CrysAlis PRO, Agilent Technologies, Version 1.171.37.31 (release 14-01-2014 CrysAlis171 .NET) (compiled Jan 14 2014, 18:38:05), SAINT v7.68A (Bruker, 2009), olex2.solve (Bourhis et al., 2015), SIR2004 (Burla et al., 2007), SHELXL (Sheldrick, 2008), olex2.refine (Bourhis et al., 2015), Olex2 (Dolomanov et al., 2009).
Footnotes
‡Present address: Department of Metallurgical and Materials Engineering, National Institute of Technology, Rourkela 769008, India
Acknowledgements
RD thanks IISER Kolkata for a fellowship. CMR thanks CSIR (02(0156)/13/EMR-II) for financial support. UR thank the funding by the Deanship of Scientific Research (DSR), King Abdulaziz University, under grant No. (16-130-35-HiCi) and therefore acknowledge the financial and technical support from KAU. CLF thank the US National Science Foundation (CHE 1213915) for support for this research. We thank Rahul Maji, AVN Kishor Babu (IISER-K) for helping to record the solid-state UV–vis absorption and emission spectra.
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