tools for teaching crystallography
13H9Cl2F3N4OS): a case study of whole-molecule configurational disorder
of the insecticide ethiprole (CaDepartment of Studies in Chemistry, University of Mysore, Manasagangotri, Mysuru-570 006, India, bHoneychem Pharma Research Pvt. Ltd., Peenya Industrial Area, Bengaluru-560 058, India, and cDepartment of Chemistry, University of Kentucky, Lexington, KY, 40506-0055, USA
*Correspondence e-mail: ybb2706@gmail.com, yathirajan@hotmail.com, s.parkin@uky.edu
The H-imidazole-3-carbonitrile}, C13H9Cl2F3N4OS, a phenylpyrazole-based insecticide, is presented. The pyrazole ring carries four substituents: an N-bound 2,6-dichloro-4-trifluoromethylphenyl ring and C-bound amine, ethanesulfinyl, and cyano groups. The sulfur atom of the ethanesulfinyl group is trigonal–pyramidal and stereogenic. The structure exhibits whole-molecule due to superposition of enantiomers. The crystal packing is dominated by strong N—H⋯O and N—H⋯N hydrogen bonds, which form R44(18) and R22(12) ring motifs. Since the ethiprole molecule is quite small, and structure solution and were straightforward, the structure presents a convenient instructional example for modelling whole-body disorder of a non-rigid molecule. To this end, a step-by-step overview of the model-building and process is also given. The structure could form the basis of a useful classroom, practical, or workshop-style example.
of ethiprole {systematic name: 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-ethanesulfinyl-1Keywords: ethiprole; phenylpyrazole insecticide; whole-molecule disorder; configurational disorder; refinement strategy; instructional tool; crystal structure.
CCDC reference: 2235968
1. Chemical context
Ethiprole, H-pyrazole-3-carbonitrile (C13H9Cl2F3N4OS), is a phenylpyrazole-based insecticide. This class of compounds target an insect's central nervous system, making it toxic to the host by blocking the glutamate-gated chloride channel. They are effective against a broad spectrum of chewing and sucking insects, showing pronounced plant systemic activity (Wu, 1998), as well as offering protection against stored-grain insect pests (Arthur, 2002). Fipronil and fipronil sulfone are related insecticides. The design, synthesis, and mode of action of phenylpyrazoles containing the 2,2,2-trichloro-1-alkoxyethyl functionality has been published by Zhao et al. (2010). The synthesis and pharmacological activities of pyrazole derivatives were reviewed by Karrouchi et al. (2018), and advances in their synthesis were described by Fustero et al. (2011). Further developments in the synthesis and biological evaluations of pyrazole derivatives were reviewed recently by Ebenezer et al. (2022). In light of the general structure–function relationships of phenylpyrazole insecticides, it is surprising that the of ethiprole has not previously been published. One possible reason could be the presence of whole-molecule disorder (vide infra), which provided further impetus for our crystallographic study of ethiprole.
5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-(ethanesulfinyl)-1Ethiprole is a chiral molecule by virtue of the trigonal–pyramidal geometry at the sulfur atom of its ethanesulfinyl group. Commercial formulations are, however, racemic. The et al., 1962) and uric acid dihydrate (Parkin & Hope, 1998), amongst many others. Unlike ethiprole, both azulene and uric acid are rigid planar molecules. In azulene, disorder results from the molecule (which lacks symmetry) being situated on a crystallographic inversion centre (and is therefore disordered exactly 50:50), while in uric acid dihydrate the minor disorder component results from a non-crystallographic 180° flip of the molecule, which fortuitously happens to remain compatible with the hydrogen-bonding environment of its major-occupancy counterpart. In ethiprole, however, the molecule is not rigid; indeed it has several internal The disorder results from superposition of enantiomers, with concomitant torsional relaxation of the other functional groups to satisfy hydrogen-bonding requirements and best fill the available space. Since the ethiprole molecule is quite small, and structure solution and were relatively straightforward, we thought it might serve as a convenient instructional example to showcase the concept and treatment of whole-molecule disorder for a non-rigid molecule. To this end, we also present a step-by-step overview of one way to proceed from structure solution through model building and to a chemically and crystallographically sensible final model.
presented here is centrosymmetric, but was found to incorporate configurational whole-molecule disorder. The phenomenon of whole-molecule disorder is not new; well-known examples include azulene (Robertson2. Structural commentary
The ethiprole molecule (Fig. 1) consists of a phenylpyrazole backbone with Cl atoms at the 2- and 6-positions of the benzene ring and a CF3 group at the 4-position. The pyrazole ring connects to benzene by one of its ring nitrogen atoms, with dihedral angle 80.4 (2)° for the major component [minor is 79.7 (12)°] and carries an NH2 group on the carbon adjacent to the ring-linking nitrogen. The ethanesulfinyl substituent is attached to the middle carbon of the pyrazole ring, with a cyano group on the remaining carbon. All bond lengths and angles in ethiprole have normal values, but there is slight deviation of substituents away from the plane of the benzene ring, i.e., C13 by 0.174 (9) Å, N1 by 0.162 (8) Å on one side of the ring and Cl1 by 0.096 (7) Å and Cl2 by 0.078 (12) Å on the other side. The sulfur atom of the ethanesulfinyl group is trigonal–pyramidal and therefore stereogenic, but since the structure is centrosymmetric, the crystals are, of necessity, racemic. Despite the equal presence of both each contains disorder components [major and minor fractions are 86.70 (18)% and 13.30 (18)%, respectively] of the opposite hand (i.e., R or S at the sulfur superimposed on S or R, respectively), as shown in Fig. 2. In addition to the dihedral angle mentioned above, internal in the molecule correspond to torsions about the N1—C7, C10—C13, and C2—S1 bonds, which are summarized for both disorder components in Table 1. A detailed step-by-step breakdown of one way to build a satisfactory model for the whole-molecule is given in Section 6: Structure solution and step-by-step refinement overview.
3. Supramolecular features
Given the relatively small occupancy fraction of the minor disorder component (only ∼13%), detailed description of supramolecular interactions given here is limited to the major component. The proximity of superimposed disorder components (Fig. 2), however, suggests that the hydrogen-bonding motifs are compatible with both major–minor and minor–minor interactions. There are only two strong intermolecular hydrogen bonds for the major component (Table 2), and both involve the two hydrogens of the amine group at N3 as donor. These are N3—H3NA⋯O1i [DD⋯A = 2.820 (6) Å] to an inversion-related molecule and N3—H3NB⋯N4ii [DD⋯A = 3.150 (4) Å] involving a molecule adjacent along the a-axis direction (symmetry codes are as per Table 2). In combination with further inversion-related molecules, these hydrogen bonds generate R44(18) and R22(12) ring motifs (Fig. 3), which link together to form tapes parallel to the a-axis. There are weaker contacts involving C—H as donor included in Table 2, but of these, only C9—H9⋯O1iii at 3.17 (4) Å is likely to have any structural importance.
4. Database and literature survey
There are a large number of structurally and chemically related compounds present in the CSD (CSD version 5.43 with all updates through September 2022; Groom et al., 2016). A recent paper by Priyanka et al. (2022) on N-{3-cyano-1-[2,6-dichloro-4-(trifluoro-methyl)phenyl]-4-(ethylsulfanyl)-1H-pyrazol-5-yl}-2,2,2-trifluoroacetamide (CSD entry FERPOL) recorded 82 matches for a 1-phenyl-cyanopyrazole search fragment. Fine tuning of this search fragment by specifying any N-bound group at C1 reduced the number of matches to 76, while inclusion of 2,6-dichloro-4-(trifluoromethyl)phenyl at N1 gave 60 hits. The requirement of a sulfur-bound group at C2 reduced this to eight unique structures, two of which were dimers. A table of the six best structural matches, plus three closely related compounds was given (see Priyanka et al., 2022 and references therein). The structure of ethiprole would fit well in that table.
The phenomenon of whole-molecule disorder is not uncommon. A search of the CSD for `whole-molecule disorder', however, gave only 39 hits, but we suspect the true number is higher as not all relevant entries would have been flagged as such in the CSD. A search for `configurational disorder' affecting only whole molecules returned three structures (CUHDOY, CUHDUE, CUHFAM; Bouwstra et al., 1985), but these involve mixed crystals of trans-stilbene and trans-azobenzene. In those three structures the configurations are exclusively trans, so the disorder is better described as orientational because each disorder component has the same (i.e., trans) configuration. One other case is a structure purported to be a monoclinic polymorph of meso-(E,E)-1,10-[1,2-bis(4-chlorophenyl)ethane-1,2-diyl]-bis(phenyldiazene), CSD entry PAGCEI01 (Mohamed et al., 2016), but the model as presented is severely distorted, including C—C distances as long as 1.695 (7) Å and bond angles in the range 85.9 (4)–139.9 (6)° for ostensibly sp3-hybridized carbon atoms. The improbable distortions result from inversion symmetry in the assigned of type C2/c (see in particular Fig. 2 of Mohamed et al., 2016). A superposition of S,S and R,R isomers, with a smaller amount of the meso form, is more likely.
5. Synthesis and crystallization
Trifluoroacetic acid (0.5 mL) was added to a stirred solution of 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-ethylthio-1H-pyrazole-3-carbonitrile (0.19 g, 0.5 mmol) in CH2Cl2 (2.5 mL) at 283–285 K. Hydrogen peroxide (0.1 mL of 30%, w/w) was added over 20 min. while maintaining the temperature at 283–285 K and the mixture was kept at the same temperature for a further 3 h. Then, CH2Cl2 (5 mL) was added followed by sodium hydrogen sulfite to quench any remaining hydrogen peroxide, and the mixture was maintained below 288 K for 20 min. Water (10 mL) was then added, and the mixture was subjected to a careful extraction with a portion of CH2Cl2 (50 mL). The organic phase was separated off and dried over anhydrous MgSO4 and the volatile substances were removed under reduced pressure. The residue was subjected to on a column of silica gel, eluting with petroleum ether and ethyl acetate (7:3). The solvent was removed under reduced pressure, leaving the white solid sulfoxide (Yield: 80%). A general reaction scheme is given in Fig. 4. X-ray-quality crystals were obtained from methanol solution by slow evaporation (m.p.: 421–423 K).
6. Structure solution and step-by-step overview
In this section, the process of model building and , with corresponding summarized in Table 3. SHELXL RES files for each step are included in the supporting information.
from an initial solution through to a final model incorporating whole-molecule is described as a series of logical steps. A few snapshots of the model at each stage are given in Fig. 5Step 1: The structure solved quite easily using SHELXT, to give a starting model with all atom types assigned correctly apart from the amine nitrogen, which had been tagged as a carbon. This starting model, depicted in Fig. 5a, was readily corrected while assigning a sensible atom-numbering scheme to the model.
Step 2: Upon of anisotropic displacement parameters (ADPs), the model looked quite reasonable. One fluorine ellipsoid is elongated (Fig. 5b), but disorder of CF3 groups is common and easy to model. The difference map, however, revealed a few substantial electron-density peaks. In Fig. 5b, the largest peak (labelled Q1) corresponded to 4.85 e Å−3, which is far too big to be ignored. The next three largest, labelled Q2, Q3, and Q4 ranged from 1.64–1.05 e Å−3. By inspection, a disorder model with a minor component for the ethanesulfinyl substituent comprising Q1 (as S1′), O1 (copied as O1′) and Q4/Q3 (as C5′/C6′) looks plausible, but inverts the stereochemistry at the sulfur atom, thereby dictating In the subsequent model, the major and minor components were assigned separate PARTs in SHELXL, occupancies were constrained to sum to unity via an FVAR (`free variable') parameter, and similarity restraints on geometry (SAME) and ADPs (SIMU) were added.
Step 3: of partial ethanesulfinyl disorder gave the model depicted in Fig. 5c. Here, the largest difference map peak (Q1) is now 1.44 e Å−3 and only about 0.8 Å from Cl1. A further problem with this partial disorder model is that the geometry of the bonding of the minor ethanesulfinyl group to the pyrazole ring is severely distorted. In order to fix this, a second component for the pyrazole ring and consequently, much of the rest of the molecule would be required. Thus, a model for whole-molecule disorder was constructed by simply copying the previously non-disordered (`PART 0') atoms into the major and minor PARTs and tying the occupancies using the same FVAR parameter. The similarity (SAME and SIMU) restraints were strengthened (assigned a smaller effective uncertainty) so as to ensure that the minor-component bond distances and angles conform to those of the major.
Step 4: The resulting initial of whole-molecule disorder gave the model shown in Fig. 5d. The previous largest difference map peak is now accounted for by the minor component Cl1′, such that the largest peaks now all correspond to hydrogen atoms.
Step 5: For the final stage, hydrogen atoms were added and the constraints/restraints were optimized. For this structure, many of the disordered atom pairs are in very close proximity, so most were constrained using the SHELXL command EADP. For the minor ethanesulfinyl group, the ADPs were restrained using RIGU (Thorn et al., 2012). The trifluoromethyl group adds an additional complication because the available electron density is not quite compatible with the occupancy factors refined for the main disorder model. For this reason, a separate occupancy for the fluorine atoms (but not the carbon) was set, which refined to 0.61 (4) for the major component. This is an approximate treatment, but wholly satisfactory in this case. Construction of a more sophisticated four-component disorder model is possible, but ultimately of limited scientific value. RIGU restraints were also sufficient to keep the minor CF3 group ADPs in check. The particular combination of constraints and restraints is largely dependent upon the nature of the disorder, and so should be decided on a case-by-case basis. Experimentation with different approaches provides a valuable learning opportunity. Overlap of disorder components in the final model is shown in Fig. 2. The main take-away message here is that construction of sensible disorder models can be straightforward and logical, but the essential criterion is that the model must make good chemical and crystallographic sense. Crystal-structure requires more than an uncritical quest for low R-values.
A summary of crystal data, data collection, and . All major-component hydrogen atoms were found in difference maps and all carbon-bound hydrogens were refined using riding models with constrained distances set to 0.95 Å (Csp2—H), 0.98 Å (RCH3), 0.99 Å (R2CH2). The major-component NH2 hydrogen coordinates refined in a stable manner, but those of the minor component used a riding model with N—H distances set to 0.88 Å. Uiso(H) parameters were assigned values of either 1.2Ueq or 1.5Ueq (RCH3 only) of the attached atom.
details is given in Table 4
|
|
|
Supporting information
CCDC reference: 2235968
https://doi.org/10.1107/S205698902300035X/dj2062sup1.cif
contains datablocks I, global. DOI:Structure factors: contains datablock I. DOI: https://doi.org/10.1107/S205698902300035X/dj2062Isup2.hkl
Intermediate models (RES files disguised as TXT) for the five steps given in the main manuscript, also the last checkCIF report for the revised https://doi.org/10.1107/S205698902300035X/dj2062sup3.txt
DOI:Supporting information file. DOI: https://doi.org/10.1107/S205698902300035X/dj2062sup4.txt
Supporting information file. DOI: https://doi.org/10.1107/S205698902300035X/dj2062sup5.txt
Supporting information file. DOI: https://doi.org/10.1107/S205698902300035X/dj2062sup6.txt
Supporting information file. DOI: https://doi.org/10.1107/S205698902300035X/dj2062sup7.txt
Supporting information file. DOI: https://doi.org/10.1107/S205698902300035X/dj2062sup8.pdf
Supporting information file. DOI: https://doi.org/10.1107/S205698902300035X/dj2062Isup9.cml
Data collection: APEX3 (Bruker, 2016); cell
APEX3 (Bruker, 2016); data reduction: APEX3 (Bruker, 2016); program(s) used to solve structure: SHELXT (Sheldrick, 2015a); program(s) used to refine structure: SHELXL2019/2 (Sheldrick, 2015b); molecular graphics: XP in SHELXTL (Sheldrick, 2008); software used to prepare material for publication: SHELX (Sheldrick, 2008) and publCIF (Westrip, 2010).C13H9Cl2F3N4OS | F(000) = 800 |
Mr = 397.20 | Dx = 1.604 Mg m−3 |
Monoclinic, P21/n | Mo Kα radiation, λ = 0.71073 Å |
a = 8.6199 (3) Å | Cell parameters from 9978 reflections |
b = 12.7967 (5) Å | θ = 2.7–27.5° |
c = 14.9178 (5) Å | µ = 0.56 mm−1 |
β = 91.280 (1)° | T = 90 K |
V = 1645.12 (10) Å3 | Tablet, colourless |
Z = 4 | 0.27 × 0.13 × 0.07 mm |
Bruker D8 Venture dual source diffractometer | 3792 independent reflections |
Radiation source: microsource | 3437 reflections with I > 2σ(I) |
Detector resolution: 7.41 pixels mm-1 | Rint = 0.031 |
φ and ω scans | θmax = 27.6°, θmin = 2.1° |
Absorption correction: multi-scan (SADABS; Krause et al., 2015) | h = −11→11 |
Tmin = 0.856, Tmax = 0.971 | k = −15→16 |
23236 measured reflections | l = −19→19 |
Refinement on F2 | Secondary atom site location: difference Fourier map |
Least-squares matrix: full | Hydrogen site location: mixed |
R[F2 > 2σ(F2)] = 0.037 | H atoms treated by a mixture of independent and constrained refinement |
wR(F2) = 0.077 | w = 1/[σ2(Fo2) + (0.0083P)2 + 1.5062P] where P = (Fo2 + 2Fc2)/3 |
S = 1.26 | (Δ/σ)max = 0.001 |
3792 reflections | Δρmax = 0.37 e Å−3 |
341 parameters | Δρmin = −0.25 e Å−3 |
108 restraints | Extinction correction: SHELXL-2019/2 (Sheldrick 2015b), Fc*=kFc[1+0.001xFc2λ3/sin(2θ)]-1/4 |
Primary atom site location: structure-invariant direct methods | Extinction coefficient: 0.0013 (3) |
Experimental. The crystal was mounted using polyisobutene oil on the tip of a fine glass fibre, which was fastened in a copper mounting pin with electrical solder. It was placed directly into the cold gas stream of a liquid-nitrogen based cryostat (Hope, 1994; Parkin & Hope, 1998). Diffraction data were collected with the crystal at 90K, which is standard practice in this laboratory for the majority of flash-cooled crystals. |
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. Refinement progress was checked using Platon (Spek, 2020) and by an R-tensor (Parkin, 2000). The final model was further checked with the IUCr utility checkCIF. |
x | y | z | Uiso*/Ueq | Occ. (<1) | |
N1 | 0.5445 (4) | 0.5998 (6) | 0.7093 (3) | 0.0182 (5) | 0.8670 (18) |
N2 | 0.6936 (3) | 0.6209 (5) | 0.6832 (2) | 0.0196 (5) | 0.8670 (18) |
N3 | 0.4028 (2) | 0.5309 (3) | 0.82962 (18) | 0.0230 (5) | 0.8670 (18) |
H3NA | 0.396 (3) | 0.512 (2) | 0.8842 (14) | 0.028* | 0.8670 (18) |
H3NB | 0.320 (3) | 0.552 (2) | 0.8046 (18) | 0.028* | 0.8670 (18) |
N4 | 1.0770 (3) | 0.6082 (3) | 0.75630 (19) | 0.0389 (7) | 0.8670 (18) |
C1 | 0.5370 (3) | 0.5576 (3) | 0.7931 (2) | 0.0171 (5) | 0.8670 (18) |
C2 | 0.6907 (3) | 0.5514 (2) | 0.82449 (16) | 0.0173 (5) | 0.8670 (18) |
C3 | 0.7781 (3) | 0.5921 (2) | 0.75424 (16) | 0.0174 (5) | 0.8670 (18) |
C4 | 0.9451 (3) | 0.6026 (3) | 0.75381 (18) | 0.0254 (6) | 0.8670 (18) |
S1 | 0.76917 (6) | 0.50533 (5) | 0.92572 (3) | 0.01963 (17) | 0.8670 (18) |
O1 | 0.6751 (7) | 0.5486 (3) | 1.0009 (3) | 0.0260 (8) | 0.8670 (18) |
C5 | 0.7180 (3) | 0.36919 (18) | 0.91758 (16) | 0.0272 (5) | 0.8670 (18) |
H5A | 0.604079 | 0.361134 | 0.921067 | 0.033* | 0.8670 (18) |
H5B | 0.751054 | 0.340844 | 0.859280 | 0.033* | 0.8670 (18) |
C6 | 0.7973 (4) | 0.3095 (3) | 0.9937 (2) | 0.0364 (7) | 0.8670 (18) |
H6A | 0.909024 | 0.323806 | 0.993807 | 0.055* | 0.8670 (18) |
H6B | 0.779664 | 0.234421 | 0.985451 | 0.055* | 0.8670 (18) |
H6C | 0.754503 | 0.331730 | 1.050923 | 0.055* | 0.8670 (18) |
C7 | 0.4240 (4) | 0.6102 (3) | 0.6436 (2) | 0.0168 (6) | 0.8670 (18) |
C8 | 0.3596 (4) | 0.7075 (2) | 0.6246 (2) | 0.0186 (6) | 0.8670 (18) |
Cl1 | 0.41063 (10) | 0.81431 (6) | 0.68914 (5) | 0.02727 (17) | 0.8670 (18) |
C9 | 0.2533 (5) | 0.7197 (4) | 0.5541 (3) | 0.0234 (6) | 0.8670 (18) |
H9 | 0.210998 | 0.786461 | 0.540059 | 0.028* | 0.8670 (18) |
C10 | 0.2102 (8) | 0.6321 (4) | 0.5045 (3) | 0.0228 (5) | 0.8670 (18) |
C11 | 0.2662 (8) | 0.5337 (4) | 0.5248 (4) | 0.0226 (9) | 0.8670 (18) |
H11 | 0.233081 | 0.474522 | 0.491027 | 0.027* | 0.8670 (18) |
C12 | 0.372 (1) | 0.5234 (4) | 0.5956 (5) | 0.0203 (6) | 0.8670 (18) |
Cl2 | 0.4408 (3) | 0.4005 (3) | 0.6233 (3) | 0.0286 (4) | 0.8670 (18) |
C13 | 0.1079 (4) | 0.6471 (3) | 0.4223 (3) | 0.0295 (5) | 0.8670 (18) |
F1 | 0.1853 (13) | 0.6876 (12) | 0.3572 (8) | 0.056 (2) | 0.61 (4) |
F2 | −0.0122 (15) | 0.7092 (14) | 0.4396 (10) | 0.066 (3) | 0.61 (4) |
F3 | 0.0463 (14) | 0.5561 (8) | 0.3945 (8) | 0.0377 (15) | 0.61 (4) |
N1' | 0.527 (3) | 0.594 (4) | 0.7149 (19) | 0.0182 (5) | 0.1330 (18) |
N2' | 0.680 (2) | 0.610 (4) | 0.6972 (18) | 0.0196 (5) | 0.1330 (18) |
N3' | 0.359 (2) | 0.522 (2) | 0.8202 (16) | 0.0230 (5) | 0.1330 (18) |
H3NC | 0.279354 | 0.534504 | 0.784121 | 0.028* | 0.1330 (18) |
H3ND | 0.345134 | 0.491878 | 0.872482 | 0.028* | 0.1330 (18) |
N4' | 1.049 (2) | 0.589 (3) | 0.7759 (16) | 0.0389 (7) | 0.1330 (18) |
C1' | 0.501 (2) | 0.548 (3) | 0.7958 (17) | 0.0171 (5) | 0.1330 (18) |
C2' | 0.6496 (17) | 0.5301 (16) | 0.8317 (11) | 0.0173 (5) | 0.1330 (18) |
C3' | 0.7518 (17) | 0.5701 (17) | 0.7724 (13) | 0.0174 (5) | 0.1330 (18) |
C4' | 0.9195 (18) | 0.582 (2) | 0.7715 (16) | 0.0254 (6) | 0.1330 (18) |
S1' | 0.6671 (4) | 0.4649 (3) | 0.9351 (2) | 0.0217 (11) | 0.1330 (18) |
O1' | 0.712 (5) | 0.545 (3) | 1.006 (2) | 0.034 (7) | 0.1330 (18) |
C5' | 0.844 (2) | 0.3953 (15) | 0.9178 (10) | 0.041 (4) | 0.1330 (18) |
H5'1 | 0.833948 | 0.350034 | 0.864145 | 0.049* | 0.1330 (18) |
H5'2 | 0.930407 | 0.445072 | 0.908355 | 0.049* | 0.1330 (18) |
C6' | 0.878 (3) | 0.329 (2) | 1.0011 (15) | 0.046 (6) | 0.1330 (18) |
H6'1 | 0.974518 | 0.289973 | 0.993367 | 0.069* | 0.1330 (18) |
H6'2 | 0.888340 | 0.374509 | 1.053665 | 0.069* | 0.1330 (18) |
H6'3 | 0.792253 | 0.279836 | 1.009625 | 0.069* | 0.1330 (18) |
C7' | 0.404 (3) | 0.6039 (18) | 0.6499 (16) | 0.0168 (6) | 0.1330 (18) |
C8' | 0.334 (3) | 0.6994 (16) | 0.6320 (15) | 0.0186 (6) | 0.1330 (18) |
Cl1' | 0.3635 (7) | 0.7996 (5) | 0.7076 (4) | 0.02727 (17) | 0.1330 (18) |
C9' | 0.240 (3) | 0.715 (2) | 0.5570 (17) | 0.0234 (6) | 0.1330 (18) |
H9' | 0.192939 | 0.780913 | 0.545476 | 0.028* | 0.1330 (18) |
C10' | 0.214 (5) | 0.631 (2) | 0.499 (2) | 0.0228 (5) | 0.1330 (18) |
C11' | 0.277 (6) | 0.534 (3) | 0.517 (3) | 0.0226 (9) | 0.1330 (18) |
H11' | 0.253091 | 0.476032 | 0.479105 | 0.027* | 0.1330 (18) |
C12' | 0.376 (7) | 0.522 (2) | 0.591 (3) | 0.0203 (6) | 0.1330 (18) |
Cl2' | 0.461 (3) | 0.4036 (19) | 0.619 (2) | 0.0286 (4) | 0.1330 (18) |
C13' | 0.114 (2) | 0.6495 (17) | 0.4167 (14) | 0.0295 (5) | 0.1330 (18) |
F1' | 0.1932 (13) | 0.6559 (17) | 0.3441 (8) | 0.044 (3) | 0.39 (4) |
F2' | 0.028 (2) | 0.7355 (9) | 0.4227 (9) | 0.044 (2) | 0.39 (4) |
F3' | 0.012 (2) | 0.5720 (13) | 0.4029 (13) | 0.038 (3) | 0.39 (4) |
U11 | U22 | U33 | U12 | U13 | U23 | |
N1 | 0.0171 (11) | 0.0231 (12) | 0.0145 (9) | −0.0004 (12) | 0.0000 (9) | 0.0037 (8) |
N2 | 0.0165 (9) | 0.0266 (18) | 0.0159 (15) | −0.0032 (9) | 0.0013 (9) | 0.0046 (11) |
N3 | 0.0154 (13) | 0.0370 (13) | 0.0167 (10) | −0.0001 (12) | −0.0010 (11) | 0.0069 (9) |
N4 | 0.0218 (12) | 0.067 (2) | 0.0278 (16) | −0.0038 (12) | −0.0001 (10) | 0.0073 (13) |
C1 | 0.0185 (14) | 0.0194 (14) | 0.0133 (9) | 0.0001 (14) | 0.0009 (11) | 0.0016 (8) |
C2 | 0.0158 (12) | 0.0227 (14) | 0.0134 (9) | 0.0001 (9) | 0.0001 (10) | 0.0019 (9) |
C3 | 0.0159 (11) | 0.0210 (15) | 0.0153 (13) | −0.0015 (9) | 0.0000 (9) | 0.0028 (9) |
C4 | 0.0219 (13) | 0.0375 (19) | 0.0169 (15) | −0.0041 (11) | −0.0009 (9) | 0.0056 (11) |
S1 | 0.0170 (3) | 0.0269 (3) | 0.0149 (2) | −0.0014 (2) | −0.00284 (18) | 0.0052 (2) |
O1 | 0.038 (3) | 0.0251 (13) | 0.0155 (11) | −0.0019 (12) | 0.0043 (11) | 0.0007 (9) |
C5 | 0.0363 (14) | 0.0218 (12) | 0.0234 (11) | 0.0061 (10) | −0.0017 (10) | 0.0010 (9) |
C6 | 0.054 (2) | 0.0304 (15) | 0.0248 (14) | 0.0151 (16) | 0.0026 (14) | 0.0066 (11) |
C7 | 0.0147 (13) | 0.0246 (11) | 0.0112 (10) | −0.0020 (9) | 0.0023 (9) | 0.0034 (8) |
C8 | 0.0182 (15) | 0.0207 (11) | 0.0170 (11) | −0.0018 (9) | 0.0002 (9) | −0.0008 (9) |
Cl1 | 0.0333 (4) | 0.0225 (3) | 0.0256 (4) | 0.0016 (3) | −0.0092 (3) | −0.0049 (3) |
C9 | 0.0221 (13) | 0.0256 (12) | 0.0221 (10) | 0.0039 (10) | −0.0042 (9) | 0.0016 (9) |
C10 | 0.0186 (10) | 0.0303 (11) | 0.0194 (11) | −0.0013 (8) | −0.0032 (9) | 0.0002 (9) |
C11 | 0.0230 (16) | 0.0252 (10) | 0.0195 (15) | −0.0047 (9) | −0.0010 (14) | −0.0030 (9) |
C12 | 0.0211 (10) | 0.0209 (10) | 0.0189 (12) | 0.0001 (8) | 0.0036 (10) | 0.0033 (8) |
Cl2 | 0.0366 (10) | 0.0199 (3) | 0.0290 (6) | 0.0021 (6) | −0.0037 (7) | 0.0017 (3) |
C13 | 0.0243 (11) | 0.0371 (13) | 0.0269 (12) | 0.0011 (9) | −0.0082 (9) | −0.0025 (10) |
F1 | 0.061 (3) | 0.075 (5) | 0.031 (3) | −0.027 (3) | −0.025 (2) | 0.028 (3) |
F2 | 0.047 (4) | 0.084 (6) | 0.066 (4) | 0.037 (4) | −0.036 (3) | −0.033 (4) |
F3 | 0.032 (3) | 0.046 (3) | 0.034 (2) | −0.002 (2) | −0.017 (2) | −0.0078 (18) |
N1' | 0.0171 (11) | 0.0231 (12) | 0.0145 (9) | −0.0004 (12) | 0.0000 (9) | 0.0037 (8) |
N2' | 0.0165 (9) | 0.0266 (18) | 0.0159 (15) | −0.0032 (9) | 0.0013 (9) | 0.0046 (11) |
N3' | 0.0154 (13) | 0.0370 (13) | 0.0167 (10) | −0.0001 (12) | −0.0010 (11) | 0.0069 (9) |
N4' | 0.0218 (12) | 0.067 (2) | 0.0278 (16) | −0.0038 (12) | −0.0001 (10) | 0.0073 (13) |
C1' | 0.0185 (14) | 0.0194 (14) | 0.0133 (9) | 0.0001 (14) | 0.0009 (11) | 0.0016 (8) |
C2' | 0.0158 (12) | 0.0227 (14) | 0.0134 (9) | 0.0001 (9) | 0.0001 (10) | 0.0019 (9) |
C3' | 0.0159 (11) | 0.0210 (15) | 0.0153 (13) | −0.0015 (9) | 0.0000 (9) | 0.0028 (9) |
C4' | 0.0219 (13) | 0.0375 (19) | 0.0169 (15) | −0.0041 (11) | −0.0009 (9) | 0.0056 (11) |
S1' | 0.020 (2) | 0.026 (2) | 0.0183 (17) | −0.0026 (15) | −0.0009 (13) | 0.0052 (14) |
O1' | 0.033 (15) | 0.038 (9) | 0.030 (7) | 0.005 (7) | −0.006 (6) | −0.004 (6) |
C5' | 0.048 (9) | 0.048 (9) | 0.026 (7) | 0.018 (8) | 0.005 (6) | 0.013 (6) |
C6' | 0.046 (11) | 0.061 (14) | 0.032 (9) | 0.019 (11) | 0.008 (9) | 0.027 (10) |
C7' | 0.0147 (13) | 0.0246 (11) | 0.0112 (10) | −0.0020 (9) | 0.0023 (9) | 0.0034 (8) |
C8' | 0.0182 (15) | 0.0207 (11) | 0.0170 (11) | −0.0018 (9) | 0.0002 (9) | −0.0008 (9) |
Cl1' | 0.0333 (4) | 0.0225 (3) | 0.0256 (4) | 0.0016 (3) | −0.0092 (3) | −0.0049 (3) |
C9' | 0.0221 (13) | 0.0256 (12) | 0.0221 (10) | 0.0039 (10) | −0.0042 (9) | 0.0016 (9) |
C10' | 0.0186 (10) | 0.0303 (11) | 0.0194 (11) | −0.0013 (8) | −0.0032 (9) | 0.0002 (9) |
C11' | 0.0230 (16) | 0.0252 (10) | 0.0195 (15) | −0.0047 (9) | −0.0010 (14) | −0.0030 (9) |
C12' | 0.0211 (10) | 0.0209 (10) | 0.0189 (12) | 0.0001 (8) | 0.0036 (10) | 0.0033 (8) |
Cl2' | 0.0366 (10) | 0.0199 (3) | 0.0290 (6) | 0.0021 (6) | −0.0037 (7) | 0.0017 (3) |
C13' | 0.0243 (11) | 0.0371 (13) | 0.0269 (12) | 0.0011 (9) | −0.0082 (9) | −0.0025 (10) |
F1' | 0.025 (3) | 0.090 (8) | 0.017 (2) | −0.002 (3) | −0.005 (2) | 0.008 (3) |
F2' | 0.048 (5) | 0.043 (4) | 0.041 (4) | 0.018 (3) | −0.030 (3) | −0.008 (3) |
F3' | 0.029 (5) | 0.044 (4) | 0.041 (5) | −0.012 (4) | −0.019 (3) | 0.007 (3) |
N1—C1 | 1.364 (3) | N1'—C1' | 1.369 (16) |
N1—N2 | 1.378 (3) | N1'—N2' | 1.369 (16) |
N1—C7 | 1.419 (3) | N1'—C7' | 1.428 (15) |
N2—C3 | 1.325 (3) | N2'—C3' | 1.368 (16) |
N3—C1 | 1.335 (3) | N3'—C1' | 1.323 (16) |
N3—H3NA | 0.85 (2) | N3'—H3NC | 0.8800 |
N3—H3NB | 0.85 (2) | N3'—H3ND | 0.8800 |
N4—C4 | 1.139 (3) | N4'—C4' | 1.123 (16) |
C1—C2 | 1.398 (3) | C1'—C2' | 1.397 (15) |
C2—C3 | 1.404 (3) | C2'—C3' | 1.362 (14) |
C2—S1 | 1.743 (2) | C2'—S1' | 1.757 (13) |
C3—C4 | 1.446 (3) | C3'—C4' | 1.455 (15) |
S1—O1 | 1.504 (4) | S1'—O1' | 1.519 (18) |
S1—C5 | 1.801 (3) | S1'—C5' | 1.793 (13) |
C5—C6 | 1.518 (3) | C5'—C6' | 1.527 (16) |
C5—H5A | 0.9900 | C5'—H5'1 | 0.9900 |
C5—H5B | 0.9900 | C5'—H5'2 | 0.9900 |
C6—H6A | 0.9800 | C6'—H6'1 | 0.9800 |
C6—H6B | 0.9800 | C6'—H6'2 | 0.9800 |
C6—H6C | 0.9800 | C6'—H6'3 | 0.9800 |
C7—C8 | 1.389 (3) | C7'—C8' | 1.383 (16) |
C7—C12 | 1.391 (4) | C7'—C12' | 1.392 (16) |
C8—C9 | 1.388 (3) | C8'—C9' | 1.385 (16) |
C8—Cl1 | 1.724 (3) | C8'—Cl1' | 1.723 (16) |
C9—C10 | 1.389 (4) | C9'—C10' | 1.391 (16) |
C9—H9 | 0.9500 | C9'—H9' | 0.9500 |
C10—C11 | 1.379 (4) | C10'—C11' | 1.382 (16) |
C10—C13 | 1.507 (3) | C10'—C13' | 1.503 (15) |
C11—C12 | 1.386 (4) | C11'—C12' | 1.384 (16) |
C11—H11 | 0.9500 | C11'—H11' | 0.9500 |
C12—Cl2 | 1.728 (3) | C12'—Cl2' | 1.727 (16) |
C13—F1 | 1.299 (8) | C13'—F1' | 1.294 (18) |
C13—F2 | 1.334 (6) | C13'—F2' | 1.333 (17) |
C13—F3 | 1.342 (7) | C13'—F3' | 1.338 (17) |
C1—N1—N2 | 113.6 (2) | C1'—N1'—N2' | 114.4 (15) |
C1—N1—C7 | 128.4 (3) | C1'—N1'—C7' | 120.2 (18) |
N2—N1—C7 | 117.4 (3) | N2'—N1'—C7' | 124.2 (19) |
C3—N2—N1 | 102.6 (2) | C3'—N2'—N1' | 101.8 (14) |
C1—N3—H3NA | 122.6 (18) | C1'—N3'—H3NC | 120.0 |
C1—N3—H3NB | 118 (2) | C1'—N3'—H3ND | 120.0 |
H3NA—N3—H3NB | 116 (3) | H3NC—N3'—H3ND | 120.0 |
N3—C1—N1 | 122.3 (2) | N3'—C1'—N1' | 121.5 (17) |
N3—C1—C2 | 132.3 (2) | N3'—C1'—C2' | 134.3 (17) |
N1—C1—C2 | 105.4 (2) | N1'—C1'—C2' | 104.0 (13) |
C1—C2—C3 | 104.42 (19) | C3'—C2'—C1' | 106.9 (12) |
C1—C2—S1 | 130.98 (19) | C3'—C2'—S1' | 134.8 (12) |
C3—C2—S1 | 124.60 (17) | C1'—C2'—S1' | 118.2 (12) |
N2—C3—C2 | 113.9 (2) | C2'—C3'—N2' | 112.8 (13) |
N2—C3—C4 | 120.0 (2) | C2'—C3'—C4' | 134.7 (15) |
C2—C3—C4 | 126.1 (2) | N2'—C3'—C4' | 112.4 (15) |
N4—C4—C3 | 177.2 (3) | N4'—C4'—C3' | 176 (2) |
O1—S1—C2 | 108.4 (2) | O1'—S1'—C2' | 107.9 (17) |
O1—S1—C5 | 105.8 (2) | O1'—S1'—C5' | 103.5 (15) |
C2—S1—C5 | 100.32 (12) | C2'—S1'—C5' | 99.6 (8) |
C6—C5—S1 | 109.32 (19) | C6'—C5'—S1' | 107.8 (12) |
C6—C5—H5A | 109.8 | C6'—C5'—H5'1 | 110.2 |
S1—C5—H5A | 109.8 | S1'—C5'—H5'1 | 110.2 |
C6—C5—H5B | 109.8 | C6'—C5'—H5'2 | 110.2 |
S1—C5—H5B | 109.8 | S1'—C5'—H5'2 | 110.2 |
H5A—C5—H5B | 108.3 | H5'1—C5'—H5'2 | 108.5 |
C5—C6—H6A | 109.5 | C5'—C6'—H6'1 | 109.5 |
C5—C6—H6B | 109.5 | C5'—C6'—H6'2 | 109.5 |
H6A—C6—H6B | 109.5 | H6'1—C6'—H6'2 | 109.5 |
C5—C6—H6C | 109.5 | C5'—C6'—H6'3 | 109.5 |
H6A—C6—H6C | 109.5 | H6'1—C6'—H6'3 | 109.5 |
H6B—C6—H6C | 109.5 | H6'2—C6'—H6'3 | 109.5 |
C8—C7—C12 | 119.2 (3) | C8'—C7'—C12' | 118.6 (15) |
C8—C7—N1 | 120.6 (3) | C8'—C7'—N1' | 121 (2) |
C12—C7—N1 | 120.2 (3) | C12'—C7'—N1' | 119 (2) |
C9—C8—C7 | 120.7 (3) | C7'—C8'—C9' | 121.8 (18) |
C9—C8—Cl1 | 119.3 (3) | C7'—C8'—Cl1' | 118.4 (16) |
C7—C8—Cl1 | 120.0 (2) | C9'—C8'—Cl1' | 119.8 (16) |
C8—C9—C10 | 118.4 (3) | C8'—C9'—C10' | 118.2 (19) |
C8—C9—H9 | 120.8 | C8'—C9'—H9' | 120.9 |
C10—C9—H9 | 120.8 | C10'—C9'—H9' | 120.9 |
C11—C10—C9 | 122.2 (3) | C11'—C10'—C9' | 121.3 (17) |
C11—C10—C13 | 119.4 (3) | C11'—C10'—C13' | 121.0 (18) |
C9—C10—C13 | 118.3 (3) | C9'—C10'—C13' | 117.7 (17) |
C10—C11—C12 | 118.4 (4) | C10'—C11'—C12' | 119 (2) |
C10—C11—H11 | 120.8 | C10'—C11'—H11' | 120.5 |
C12—C11—H11 | 120.8 | C12'—C11'—H11' | 120.5 |
C11—C12—C7 | 121.0 (3) | C11'—C12'—C7' | 120.9 (18) |
C11—C12—Cl2 | 119.0 (3) | C11'—C12'—Cl2' | 122.9 (18) |
C7—C12—Cl2 | 119.9 (3) | C7'—C12'—Cl2' | 116.1 (17) |
F1—C13—F2 | 108.7 (6) | F1'—C13'—F2' | 108.0 (16) |
F1—C13—F3 | 108.8 (7) | F1'—C13'—F3' | 105.8 (16) |
F2—C13—F3 | 105.9 (5) | F2'—C13'—F3' | 104.8 (15) |
F1—C13—C10 | 111.0 (5) | F1'—C13'—C10' | 113 (2) |
F2—C13—C10 | 111.2 (5) | F2'—C13'—C10' | 112.7 (17) |
F3—C13—C10 | 111.1 (6) | F3'—C13'—C10' | 111.8 (19) |
C1—N1—N2—C3 | −1.1 (8) | C1'—N1'—N2'—C3' | 0 (6) |
C7—N1—N2—C3 | −172.6 (5) | C7'—N1'—N2'—C3' | −167 (4) |
N2—N1—C1—N3 | −179.3 (5) | N2'—N1'—C1'—N3' | −176 (4) |
C7—N1—C1—N3 | −8.9 (10) | C7'—N1'—C1'—N3' | −8 (7) |
N2—N1—C1—C2 | 0.6 (8) | N2'—N1'—C1'—C2' | −1 (6) |
C7—N1—C1—C2 | 171.0 (6) | C7'—N1'—C1'—C2' | 167 (3) |
N3—C1—C2—C3 | 180.0 (5) | N3'—C1'—C2'—C3' | 176 (4) |
N1—C1—C2—C3 | 0.1 (5) | N1'—C1'—C2'—C3' | 2 (4) |
N3—C1—C2—S1 | 0.1 (7) | N3'—C1'—C2'—S1' | −3 (6) |
N1—C1—C2—S1 | −179.8 (4) | N1'—C1'—C2'—S1' | −177 (3) |
N1—N2—C3—C2 | 1.1 (6) | C1'—C2'—C3'—N2' | −2 (4) |
N1—N2—C3—C4 | −179.7 (5) | S1'—C2'—C3'—N2' | 177 (3) |
C1—C2—C3—N2 | −0.8 (5) | C1'—C2'—C3'—C4' | 176 (3) |
S1—C2—C3—N2 | 179.0 (4) | S1'—C2'—C3'—C4' | −5 (5) |
C1—C2—C3—C4 | −180.0 (3) | N1'—N2'—C3'—C2' | 1 (5) |
S1—C2—C3—C4 | −0.1 (5) | N1'—N2'—C3'—C4' | −177 (3) |
C1—C2—S1—O1 | −45.6 (4) | C3'—C2'—S1'—O1' | 75 (3) |
C3—C2—S1—O1 | 134.5 (3) | C1'—C2'—S1'—O1' | −106 (3) |
C1—C2—S1—C5 | 64.9 (4) | C3'—C2'—S1'—C5' | −33 (3) |
C3—C2—S1—C5 | −114.9 (3) | C1'—C2'—S1'—C5' | 146 (2) |
O1—S1—C5—C6 | −75.9 (3) | O1'—S1'—C5'—C6' | 71 (2) |
C2—S1—C5—C6 | 171.4 (2) | C2'—S1'—C5'—C6' | −178.0 (17) |
C1—N1—C7—C8 | 107.1 (7) | C1'—N1'—C7'—C8' | 107 (4) |
N2—N1—C7—C8 | −82.8 (7) | N2'—N1'—C7'—C8' | −86 (5) |
C1—N1—C7—C12 | −74.7 (8) | C1'—N1'—C7'—C12' | −87 (5) |
N2—N1—C7—C12 | 95.4 (8) | N2'—N1'—C7'—C12' | 80 (6) |
C12—C7—C8—C9 | −4.9 (5) | C12'—C7'—C8'—C9' | 0 (3) |
N1—C7—C8—C9 | 173.2 (3) | N1'—C7'—C8'—C9' | 166 (2) |
C12—C7—C8—Cl1 | 174.8 (5) | C12'—C7'—C8'—Cl1' | 177 (3) |
N1—C7—C8—Cl1 | −7.1 (4) | N1'—C7'—C8'—Cl1' | −16 (2) |
C7—C8—C9—C10 | 1.6 (5) | C7'—C8'—C9'—C10' | 0 (2) |
Cl1—C8—C9—C10 | −178.1 (4) | Cl1'—C8'—C9'—C10' | −178 (3) |
C8—C9—C10—C11 | 1.8 (8) | C8'—C9'—C10'—C11' | 2 (5) |
C8—C9—C10—C13 | −173.8 (4) | C8'—C9'—C10'—C13' | −179 (3) |
C9—C10—C11—C12 | −1.7 (11) | C9'—C10'—C11'—C12' | −4 (8) |
C13—C10—C11—C12 | 173.8 (7) | C13'—C10'—C11'—C12' | 176 (5) |
C10—C11—C12—C7 | −1.8 (12) | C10'—C11'—C12'—C7' | 4 (8) |
C10—C11—C12—Cl2 | 178.8 (7) | C10'—C11'—C12'—Cl2' | −180 (5) |
C8—C7—C12—C11 | 5.1 (10) | C8'—C7'—C12'—C11' | −2 (7) |
N1—C7—C12—C11 | −173.1 (7) | N1'—C7'—C12'—C11' | −168 (5) |
C8—C7—C12—Cl2 | −175.6 (5) | C8'—C7'—C12'—Cl2' | −178 (3) |
N1—C7—C12—Cl2 | 6.3 (9) | N1'—C7'—C12'—Cl2' | 15 (5) |
C11—C10—C13—F1 | −102.0 (11) | C11'—C10'—C13'—F1' | −76 (5) |
C9—C10—C13—F1 | 73.7 (10) | C9'—C10'—C13'—F1' | 105 (3) |
C11—C10—C13—F2 | 136.9 (12) | C11'—C10'—C13'—F2' | 161 (4) |
C9—C10—C13—F2 | −47.4 (12) | C9'—C10'—C13'—F2' | −18 (4) |
C11—C10—C13—F3 | 19.2 (9) | C11'—C10'—C13'—F3' | 44 (5) |
C9—C10—C13—F3 | −165.1 (7) | C9'—C10'—C13'—F3' | −136 (3) |
D—H···A | D—H | H···A | D···A | D—H···A |
N3—H3NA···O1i | 0.85 (2) | 1.99 (2) | 2.820 (6) | 164 (3) |
N3—H3NB···N4ii | 0.85 (2) | 2.31 (2) | 3.150 (4) | 172 (3) |
C9—H9···O1iii | 0.95 | 2.21 | 3.138 (6) | 165 |
N3′—H3ND···O1′i | 0.88 | 1.94 | 2.81 (5) | 167 |
N3′—H3NC···N4′ii | 0.88 | 2.10 | 2.87 (3) | 145 |
C9′—H9′···O1′iii | 0.95 | 2.31 | 3.17 (4) | 151 |
Symmetry codes: (i) −x+1, −y+1, −z+2; (ii) x−1, y, z; (iii) x−1/2, −y+3/2, z−1/2. |
Standard uncertainties for the minor component are much larger than for the major component as a result of its much lower occupancy factor. |
Major | Torsion | Minor | Torsion |
C1—N1—C7—C8 | 107.1 (7) | C1'—N1'—C7'—C8' | 107 (4) |
C9—C10—C13—F1 | 73.7 (10) | C9'—C10'—C13'—F1' | 105 (3) |
C1—C2—S1—O1 | -45.6 (4) | C1'—C2'—S1'—O1' | -106 (3) |
Steps 1–4 in the table correspond to the sequential snapshots shown in Fig. 5. The result of step 5 is shown in Fig. 2. |
Step | R1 (%) | wR2 (%) | Δρmax (e Å-3) | Δρmin (e Å-3) |
1 | 16.49 | 49.05 | 4.73 | -2.23 |
2 | 9.22 | 32.70 | 4.87 | -1.16 |
3 | 6.73 | 25.49 | 1.40 | -1.07 |
4 | 5.51 | 21.73 | 0.81 | -0.65 |
5 | 3.65 | 7.65 | 0.37 | -0.25 |
Acknowledgements
One of the authors (V) is grateful to the DST–PURSE Project, Vijnana Bhavana, UOM for providing research facilities. HSY thanks UGC for a BSR Faculty fellowship for three years.
Funding information
Funding for this research was provided by: NSF (MRI CHE1625732) and the University of Kentucky (Bruker D8 Venture diffractometer) to SP.
References
Arthur, F. H. (2002). J. Econ. Entomol. 95, 1314–1318. Web of Science CrossRef PubMed CAS Google Scholar
Bouwstra, J. A., Schouten, A., Kroon, J. & Helmholdt, R. B. (1985). Acta Cryst. C41, 420–426. CSD CrossRef CAS Web of Science IUCr Journals Google Scholar
Bruker (2016). APEX3. Bruker AXS Inc., Madison, Wisconsin, USA. Google Scholar
Ebenezer, O., Shapi, M. & Tuszynski, J. A. (2022). Biomedicines 10, 1124. CrossRef PubMed Google Scholar
Fustero, S., Sánchez-Roselló, M., Barrio, P. & Simón-Fuentes, A. (2011). Chem. Rev. 111, 6984–7034. Web of Science CrossRef CAS PubMed Google Scholar
Groom, C. R., Bruno, I. J., Lightfoot, M. P. & Ward, S. C. (2016). Acta Cryst. B72, 171–179. Web of Science CrossRef IUCr Journals Google Scholar
Karrouchi, K., Radi, S., Ramli, Y., Taoufik, J., Mabkhot, Y. N., Al-Aizari, F. A. & Ansar, M. (2018). Molecules, 23. https://doi.org/10.3390/molecules23010134 Google Scholar
Krause, L., Herbst-Irmer, R., Sheldrick, G. M. & Stalke, D. (2015). J. Appl. Cryst. 48, 3–10. Web of Science CSD CrossRef ICSD CAS IUCr Journals Google Scholar
Mohamed, S. K., Younes, S. H. H., Abdel-Raheem, E. M. M., Horton, P. N., Akkurt, M. & Glidewell, C. (2016). Acta Cryst. C72, 57–62. Web of Science CSD CrossRef IUCr Journals Google Scholar
Parkin, S. & Hope, H. (1998). Acta Cryst. B54, 339–344. Web of Science CSD CrossRef CAS IUCr Journals Google Scholar
Priyanka, P., Jayanna, B. K., Sunil Kumar, Y. C., Shreenivas, M. T., Srinivasa, G. R., Divakara, T. R., Yathirajan, H. S. & Parkin, S. (2022). Acta Cryst. E78, 1084–1088. CSD CrossRef IUCr Journals Google Scholar
Robertson, J. M., Shearer, H. M. M., Sim, G. A. & Watson, D. G. (1962). Acta Cryst. 15, 1–8. CSD CrossRef IUCr Journals Web of Science Google Scholar
Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122. Web of Science CrossRef CAS IUCr Journals Google Scholar
Sheldrick, G. M. (2015a). Acta Cryst. A71, 3–8. Web of Science CrossRef IUCr Journals Google Scholar
Sheldrick, G. M. (2015b). Acta Cryst. C71, 3–8. Web of Science CrossRef IUCr Journals Google Scholar
Thorn, A., Dittrich, B. & Sheldrick, G. M. (2012). Acta Cryst. A68, 448–451. Web of Science CrossRef CAS IUCr Journals Google Scholar
Westrip, S. P. (2010). J. Appl. Cryst. 43, 920–925. Web of Science CrossRef CAS IUCr Journals Google Scholar
Wu, T.-T. (1998). US Patent 5,814,652. Google Scholar
Zhao, Q., Li, Y., Xiong, L. & Wang, Q. (2010). J. Agric. Food Chem. 58, 4992–4998. Web of Science CrossRef CAS PubMed Google Scholar
This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.