Supporting information
Crystallographic Information File (CIF) https://doi.org/10.1107/S160053680200452X/ci6109sup1.cif | |
Structure factor file (CIF format) https://doi.org/10.1107/S160053680200452X/ci6109Isup2.hkl |
CCDC reference: 183802
Key indicators
- Single-crystal X-ray study
- T = 200 K
- Mean (C-C) = 0.004 Å
- R factor = 0.060
- wR factor = 0.196
- Data-to-parameter ratio = 10.5
checkCIF results
No syntax errors found ADDSYM reports no extra symmetry
Data collection: COLLECT (Nonius, 2000); cell refinement: HKL SCALEPACK (Otwinowski & Minor, 1997); data reduction: HKL DENZO (Otwinowski & Minor, 1997) and SCALEPACK; program(s) used to solve structure: SHELXS86 (Sheldrick, 1985); program(s) used to refine structure: SHELXL97 (Sheldrick, 1997); molecular graphics: ORTEP-3 (Farrugia, 1997); software used to prepare material for publication: SHELXL97.
C13H12N+·BF4− | F(000) = 552 |
Mr = 269.05 | Dx = 1.385 Mg m−3 |
Monoclinic, P21/n | Cu Kα radiation, λ = 1.54178 Å |
Hall symbol: -P 2yn | Cell parameters from 2348 reflections |
a = 5.9727 (4) Å | θ = 2–70° |
b = 15.082 (1) Å | µ = 1.05 mm−1 |
c = 14.3364 (10) Å | T = 200 K |
β = 91.895 (4)° | Block, white |
V = 1290.72 (15) Å3 | 0.25 × 0.10 × 0.08 mm |
Z = 4 |
Nonius KappaCCD diffractometer | 1624 reflections with I > 2σ(I) |
Radiation source: fine-focus sealed tube | Rint = 0.065 |
Horizontally mounted graphite crystal monochromator | θmax = 68.4°, θmin = 4.3° |
Detector resolution: 9 pixels mm-1 | h = 0→7 |
CCD scans | k = 0→18 |
11038 measured reflections | l = −17→17 |
2306 independent reflections |
Refinement on F2 | Primary atom site location: structure-invariant direct methods |
Least-squares matrix: full | Secondary atom site location: difference Fourier map |
R[F2 > 2σ(F2)] = 0.060 | Hydrogen site location: inferred from neighbouring sites |
wR(F2) = 0.196 | All H-atom parameters refined |
S = 1.10 | w = 1/[σ2(Fo2) + (0.1069P)2 + 0.3137P] where P = (Fo2 + 2Fc2)/3 |
2306 reflections | (Δ/σ)max = 0.001 |
220 parameters | Δρmax = 0.32 e Å−3 |
0 restraints | Δρmin = −0.28 e Å−3 |
Experimental. Anal. and spectroscopic data: Calcd for C13H12BF4N (269.05): C, 58.03; H, 4.50; N, 5.21. Found: C, 58.10; H, 4.55; N, 5.17. 1H NMR (CD2Cl2): δ 9.90 (s, br, 2 H, NH2), 7.88–7.60 (m, 10 H, Ph2) p.p.m.. 13C NMR (CD2Cl2): 184.4 (1 C, CNH2), 136.59 (2 C, CH, Ph), 132.1 (4 C, CH, Ph), 130.3 (2 C, C, Ph), 129.7 (4 C, CH, Ph) p.p.m.. |
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 | ||
C1 | 0.8688 (4) | 0.27992 (16) | 0.51965 (18) | 0.0542 (7) | |
C2 | 0.7895 (4) | 0.20242 (17) | 0.46724 (18) | 0.0548 (7) | |
C3 | 0.9348 (5) | 0.13219 (18) | 0.45107 (19) | 0.0582 (7) | |
C4 | 0.8674 (5) | 0.0612 (2) | 0.3971 (2) | 0.0674 (8) | |
C5 | 0.6519 (6) | 0.0590 (2) | 0.3577 (2) | 0.0771 (9) | |
C6 | 0.5077 (6) | 0.1283 (3) | 0.3740 (3) | 0.0813 (10) | |
C7 | 0.5723 (5) | 0.1994 (2) | 0.4273 (2) | 0.0702 (8) | |
C8 | 1.0505 (4) | 0.27364 (16) | 0.59144 (17) | 0.0537 (7) | |
C9 | 1.0644 (6) | 0.20021 (19) | 0.6498 (2) | 0.0607 (7) | |
C10 | 1.2404 (6) | 0.1930 (2) | 0.7146 (2) | 0.0695 (8) | |
C11 | 1.4004 (6) | 0.2580 (2) | 0.7217 (2) | 0.0734 (9) | |
C12 | 1.3841 (5) | 0.3326 (2) | 0.6659 (2) | 0.0692 (8) | |
C13 | 1.2108 (5) | 0.34047 (19) | 0.6007 (2) | 0.0605 (7) | |
B1 | 0.2697 (5) | 0.4366 (2) | 0.3484 (2) | 0.0577 (8) | |
F1 | 0.4824 (3) | 0.45061 (15) | 0.38620 (18) | 0.1093 (8) | |
F2 | 0.2663 (3) | 0.45451 (15) | 0.25612 (13) | 0.0970 (7) | |
F3 | 0.1200 (3) | 0.48922 (14) | 0.39319 (16) | 0.1001 (7) | |
F4 | 0.2126 (3) | 0.35000 (12) | 0.36554 (14) | 0.0902 (7) | |
N1 | 0.7842 (5) | 0.35776 (17) | 0.5018 (2) | 0.0664 (7) | |
H1 | 0.668 (7) | 0.366 (3) | 0.458 (3) | 0.110 (14)* | |
H2 | 0.827 (7) | 0.410 (3) | 0.538 (3) | 0.116 (14)* | |
H3 | 1.079 (5) | 0.1321 (17) | 0.480 (2) | 0.060 (8)* | |
H4 | 0.966 (5) | 0.0156 (19) | 0.3835 (19) | 0.060 (8)* | |
H5 | 0.606 (5) | 0.009 (2) | 0.319 (2) | 0.072 (8)* | |
H6 | 0.362 (7) | 0.130 (3) | 0.346 (3) | 0.103 (12)* | |
H7 | 0.475 (5) | 0.247 (2) | 0.440 (2) | 0.076 (9)* | |
H9 | 0.959 (5) | 0.1592 (19) | 0.6452 (18) | 0.053 (7)* | |
H10 | 1.245 (5) | 0.143 (2) | 0.753 (2) | 0.065 (8)* | |
H11 | 1.535 (7) | 0.250 (3) | 0.766 (3) | 0.113 (13)* | |
H12 | 1.496 (6) | 0.378 (3) | 0.674 (2) | 0.094 (11)* | |
H13 | 1.199 (5) | 0.390 (2) | 0.563 (2) | 0.076 (9)* |
U11 | U22 | U33 | U12 | U13 | U23 | |
C1 | 0.0527 (14) | 0.0534 (14) | 0.0573 (15) | 0.0065 (12) | 0.0103 (11) | 0.0051 (11) |
C2 | 0.0508 (15) | 0.0606 (15) | 0.0532 (15) | 0.0041 (11) | 0.0042 (11) | 0.0023 (11) |
C3 | 0.0546 (16) | 0.0596 (16) | 0.0602 (16) | 0.0054 (12) | −0.0011 (13) | 0.0022 (12) |
C4 | 0.0710 (19) | 0.0606 (17) | 0.0706 (18) | 0.0061 (15) | 0.0010 (15) | −0.0093 (14) |
C5 | 0.073 (2) | 0.082 (2) | 0.075 (2) | −0.0102 (17) | −0.0034 (16) | −0.0134 (17) |
C6 | 0.0579 (19) | 0.106 (3) | 0.080 (2) | −0.0065 (18) | −0.0018 (16) | −0.0106 (19) |
C7 | 0.0545 (17) | 0.086 (2) | 0.0696 (19) | 0.0094 (15) | 0.0016 (14) | −0.0063 (16) |
C8 | 0.0575 (15) | 0.0508 (14) | 0.0533 (14) | 0.0074 (11) | 0.0072 (12) | −0.0013 (11) |
C9 | 0.0731 (19) | 0.0532 (15) | 0.0559 (16) | −0.0011 (14) | 0.0034 (14) | 0.0007 (12) |
C10 | 0.092 (2) | 0.0623 (17) | 0.0539 (16) | 0.0110 (16) | −0.0038 (15) | 0.0045 (13) |
C11 | 0.078 (2) | 0.080 (2) | 0.0617 (18) | 0.0083 (17) | −0.0065 (15) | −0.0093 (15) |
C12 | 0.0672 (19) | 0.076 (2) | 0.0644 (18) | −0.0044 (16) | 0.0013 (15) | −0.0081 (15) |
C13 | 0.0677 (18) | 0.0544 (16) | 0.0599 (16) | 0.0017 (13) | 0.0111 (13) | −0.0017 (13) |
B1 | 0.0534 (17) | 0.0536 (17) | 0.0656 (19) | 0.0085 (13) | −0.0033 (14) | −0.0024 (14) |
F1 | 0.0732 (13) | 0.1164 (17) | 0.1357 (19) | −0.0103 (11) | −0.0365 (12) | 0.0279 (14) |
F2 | 0.1037 (15) | 0.1168 (17) | 0.0706 (12) | 0.0269 (12) | 0.0039 (10) | 0.0219 (11) |
F3 | 0.1015 (14) | 0.0831 (13) | 0.1166 (16) | 0.0259 (11) | 0.0147 (12) | −0.0212 (11) |
F4 | 0.1120 (16) | 0.0637 (11) | 0.0945 (14) | −0.0016 (9) | −0.0034 (12) | −0.0002 (9) |
N1 | 0.0642 (15) | 0.0639 (16) | 0.0714 (16) | 0.0152 (12) | 0.0067 (13) | 0.0058 (12) |
C1—N1 | 1.300 (3) | C9—C10 | 1.384 (4) |
C1—C2 | 1.460 (4) | C9—H9 | 0.88 (3) |
C1—C8 | 1.474 (4) | C10—C11 | 1.371 (5) |
C2—C3 | 1.393 (4) | C10—H10 | 0.93 (3) |
C2—C7 | 1.402 (4) | C11—C12 | 1.382 (5) |
C3—C4 | 1.373 (4) | C11—H11 | 1.02 (4) |
C3—H3 | 0.94 (3) | C12—C13 | 1.377 (4) |
C4—C5 | 1.389 (4) | C12—H12 | 0.96 (4) |
C4—H4 | 0.93 (3) | C13—H13 | 0.93 (3) |
C5—C6 | 1.379 (5) | B1—F2 | 1.350 (4) |
C5—H5 | 0.97 (3) | B1—F3 | 1.370 (4) |
C6—C7 | 1.366 (5) | B1—F4 | 1.375 (4) |
C6—H6 | 0.95 (4) | B1—F1 | 1.380 (4) |
C7—H7 | 0.95 (3) | N1—H1 | 0.93 (5) |
C8—C9 | 1.388 (4) | N1—H2 | 0.97 (4) |
C8—C13 | 1.394 (4) | ||
N1—C1—C2 | 120.3 (3) | C10—C9—C8 | 119.8 (3) |
N1—C1—C8 | 117.9 (3) | C10—C9—H9 | 121.1 (18) |
C2—C1—C8 | 121.8 (2) | C8—C9—H9 | 119.1 (18) |
C3—C2—C7 | 118.7 (3) | C11—C10—C9 | 120.4 (3) |
C3—C2—C1 | 120.1 (2) | C11—C10—H10 | 121.9 (18) |
C7—C2—C1 | 121.1 (2) | C9—C10—H10 | 117.8 (18) |
C4—C3—C2 | 120.9 (3) | C10—C11—C12 | 120.3 (3) |
C4—C3—H3 | 119.4 (16) | C10—C11—H11 | 120 (2) |
C2—C3—H3 | 119.6 (16) | C12—C11—H11 | 120 (2) |
C3—C4—C5 | 119.9 (3) | C13—C12—C11 | 120.0 (3) |
C3—C4—H4 | 121.1 (17) | C13—C12—H12 | 122 (2) |
C5—C4—H4 | 118.9 (17) | C11—C12—H12 | 118 (2) |
C6—C5—C4 | 119.2 (3) | C12—C13—C8 | 120.1 (3) |
C6—C5—H5 | 121.3 (18) | C12—C13—H13 | 120.6 (19) |
C4—C5—H5 | 119.4 (18) | C8—C13—H13 | 119.3 (19) |
C7—C6—C5 | 121.6 (3) | F2—B1—F3 | 110.8 (2) |
C7—C6—H6 | 117 (2) | F2—B1—F4 | 111.6 (3) |
C5—C6—H6 | 122 (2) | F3—B1—F4 | 107.3 (3) |
C6—C7—C2 | 119.7 (3) | F2—B1—F1 | 109.8 (3) |
C6—C7—H7 | 122.7 (19) | F3—B1—F1 | 109.5 (3) |
C2—C7—H7 | 117.7 (19) | F4—B1—F1 | 107.8 (2) |
C9—C8—C13 | 119.5 (3) | C1—N1—H1 | 122 (2) |
C9—C8—C1 | 120.0 (2) | C1—N1—H2 | 122 (3) |
C13—C8—C1 | 120.5 (2) | H1—N1—H2 | 115 (4) |
N1—C1—C2—C3 | 149.0 (3) | N1—C1—C8—C9 | 144.1 (3) |
C8—C1—C2—C3 | −28.8 (4) | C2—C1—C8—C9 | −38.0 (4) |
N1—C1—C2—C7 | −26.8 (4) | N1—C1—C8—C13 | −36.7 (4) |
C8—C1—C2—C7 | 155.4 (3) | C2—C1—C8—C13 | 141.2 (3) |
C7—C2—C3—C4 | 0.0 (4) | C13—C8—C9—C10 | −1.7 (4) |
C1—C2—C3—C4 | −175.9 (3) | C1—C8—C9—C10 | 177.4 (3) |
C2—C3—C4—C5 | 0.1 (5) | C8—C9—C10—C11 | 0.2 (5) |
C3—C4—C5—C6 | −0.4 (5) | C9—C10—C11—C12 | 1.8 (5) |
C4—C5—C6—C7 | 0.6 (5) | C10—C11—C12—C13 | −2.2 (5) |
C5—C6—C7—C2 | −0.5 (5) | C11—C12—C13—C8 | 0.6 (4) |
C3—C2—C7—C6 | 0.2 (4) | C9—C8—C13—C12 | 1.3 (4) |
C1—C2—C7—C6 | 176.1 (3) | C1—C8—C13—C12 | −177.9 (3) |
D—H···A | D—H | H···A | D···A | D—H···A |
N1—H1···F1 | 0.93 (4) | 1.96 (4) | 2.786 (4) | 147 (4) |
N1—H2···F3i | 0.97 (5) | 1.83 (4) | 2.804 (3) | 175 (4) |
C7—H7···F4 | 0.95 (3) | 2.43 (3) | 3.230 (4) | 142 (2) |
C11—H11···F4ii | 1.02 (4) | 2.31 (4) | 3.183 (4) | 143 (3) |
Symmetry codes: (i) −x+1, −y+1, −z+1; (ii) x+3/2, −y+1/2, z+1/2. |
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