Crystal structure of benz­yl(meth­yl)phen­yl[(piperidin-1-ium-1-yl)meth­yl]silane bromide

Barth, E.R.; Golz, C.; Koller, S.G.; Strohmann, C.

doi:10.1107/S2056989015016965

organic compounds

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Volume 71| Part 10| October 2015| Page o759

doi:10.1107/S2056989015016965

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Crystal structure of benzyl(methyl)phenyl[(piperidin-1-ium-1-yl)methyl]silane bromide

Eva Rebecca Barth,^a Christopher Golz,^a Stephan G. Koller ^a and Carsten Strohmann ^a ^*

^aFakultät für Chemie und Chemische Biologie, Technische Universität Dortmund, Otto-Hahn-Strasse 6, 44227 Dortmund, Germany
^*Correspondence e-mail: carsten.strohmann@tu-dortmund.de

Edited by J. Simpson, University of Otago, New Zealand (Received 29 August 2015; accepted 10 September 2015; online 17 September 2015)

The title compound, C₂₀H₂₉NSi⁺·Br⁻, contains a chiral silicon atom but crystallizes as a racemate. The C—Si—C bond angles in the range of 103.64 (8)–111.59 (9)° are usual for tetrahedral geometry. The piperidine ring shows a regular chair conformation with an equatorially positioned exocyclic N—C bond. In the crystal, there is a hydrogen bond between the ammonium cation and the bromide anion. The crystal packing shows the dominant intermolecular interaction to be the electrostatic attraction between the ammonium cation and the bromide anion.

Keywords: crystal structure; chiral organosilane; N—H⋯Br hydrogen bond.

CCDC reference: 1423495

1. Related literature

Benzylmethyl(piperidinomethyl)silane and its methyliodide salt are used as model systems to investigate the stereochemistry of substitution reactions with silyllithium compounds as nucleophiles, see: Strohmann et al. (2004 ).

2. Experimental

2.1. Crystal data

C₂₀H₂₈NSi⁺·Br⁻
M_r = 390.43
Monoclinic, P 2₁ /n
a = 13.9311 (12) Å
b = 7.4605 (6) Å
c = 19.3515 (17) Å
β = 100.926 (2)°
V = 1974.8 (3) Å³
Z = 4
Mo Kα radiation
μ = 2.14 mm⁻¹
T = 173 K
0.2 × 0.2 × 0.1 mm

2.2. Data collection

Bruker APEXII CCD diffractometer
Absorption correction: multi-scan (SADABS, Bruker, 2015 ) T_min = 0.421, T_max = 0.746
26749 measured reflections
4759 independent reflections
3948 reflections with I > 2σ(I)
R_int = 0.040

2.3. Refinement

R[F² > 2σ(F²)] = 0.031
wR(F²) = 0.080
S = 1.02
4759 reflections
213 parameters
H atoms treated by a mixture of independent and constrained refinement
Δρ_max = 0.66 e Å⁻³
Δρ_min = −0.25 e Å⁻³

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
N1—H1⋯Br1	0.82 (2)	2.41 (2)	3.2242 (15)	173.4 (17)

Data collection: APEX2 (Bruker, 2003 ); cell refinement: SAINT (Bruker, 2003); data reduction: SAINT; program(s) used to solve structure: SHELXT (Sheldrick, 2015a ); program(s) used to refine structure: SHELXL2014 (Sheldrick, 2015b ); molecular graphics: SHELXTL (Sheldrick, 2008 ); software used to prepare material for publication: OLEX2 (Dolomanov et al., 2009 ) and publCIF (Westrip, 2010 ).

Supporting information

CCDC reference: 1423495

Crystal structure: contains datablock I. DOI: 10.1107/S2056989015016965/sj5471sup1.cif

Structure factors: contains datablock I. DOI: 10.1107/S2056989015016965/sj5471Isup2.hkl

Supporting information file. DOI: 10.1107/S2056989015016965/sj5471Isup3.cml

checkCIF report

Synthesis and crystallization top

The title compound was synthesized to increase the enantiomeric ratio of the chiral benzylmethylphenyl(piperidinomethyl)silane. Therefore the silane was treated with 1 eq of HBr in Et₂O (1 M). Solvent was evaporated in vacuum, and the solid residue was recrystallized from isopropanol at 243 K for 24 h. The crystals were washed with cold isopropanol to prepare them for X-ray analysis.

Refinement top

Crystal data, data collection and structure refinement details are summarized in Table 1. Treatment of hydrogen atoms: U_iso(H) = 1.2 times U_iso(C) for CH and CH₂, U_iso(H) = 1.5 times U_iso(C) for CH₃; refinement: secondary CH₂ and aromatic H with riding coordinates, CH₃ as a rotating methyl group.

Related literature top

Preparation of the hydrobromide starting from benzylmethyl(piperidinomethyl)silane was used as a methyliodide-free alternative to determine the chirality of quarternary silicon centre. Benzylmethyl(piperidinomethyl)silane and its methyliodide salt is used as a model system to investigate the stereochemistry of substitution reactions with silyllithium compounds as nucleophiles (Strohmann et al., 2004).

Computing details top

Data collection: APEX2 (Bruker, 2003); cell refinement: SAINT (Bruker, 2003); data reduction: SAINT (Bruker, 2003); program(s) used to solve structure: SHELXT (Sheldrick, 2015a); program(s) used to refine structure: SHELXL2014 (Sheldrick, 2015b); molecular graphics: SHELXTL (Sheldrick, 2008); software used to prepare material for publication: OLEX2 (Dolomanov et al., 2009) and publCIF (Westrip, 2010).

Figures top

	Fig. 1. Molecular structure of the title compound with anisotropic displacement ellipsoids drawn at the 50% probability level. An intermolecular hydrogen bond is shown as a dashed line.
	Fig. 2. Crystal packing of the title compound viewed along b axis. H-atoms are omitted for clarity.

Benzyl(methyl)phenyl[(piperidin-1-ium-1-yl)methyl]silane bromide top

Crystal data top

C₂₀H₂₈NSi⁺·Br⁻	F(000) = 816
M_r = 390.43	D_x = 1.313 Mg m⁻³
Monoclinic, P2₁/n	Mo Kα radiation, λ = 0.71073 Å
a = 13.9311 (12) Å	Cell parameters from 7370 reflections
b = 7.4605 (6) Å	θ = 2.9–27.9°
c = 19.3515 (17) Å	µ = 2.14 mm⁻¹
β = 100.926 (2)°	T = 173 K
V = 1974.8 (3) Å³	Block, colourless
Z = 4	0.2 × 0.2 × 0.1 mm

Data collection top

Bruker APEXII CCD diffractometer	3948 reflections with I > 2σ(I)
φ and ω scans	R_int = 0.040
Absorption correction: multi-scan (SADABS, Bruker, 2015)	θ_max = 28.0°, θ_min = 2.1°
T_min = 0.421, T_max = 0.746	h = −18→18
26749 measured reflections	k = −9→9
4759 independent reflections	l = −25→25

Refinement top

Refinement on F²	Primary atom site location: structure-invariant direct methods
Least-squares matrix: full	Hydrogen site location: mixed
R[F² > 2σ(F²)] = 0.031	H atoms treated by a mixture of independent and constrained refinement
wR(F²) = 0.080	w = 1/[σ²(F_o²) + (0.0462P)² + 0.3152P] where P = (F_o² + 2F_c²)/3
S = 1.02	(Δ/σ)_max = 0.001
4759 reflections	Δρ_max = 0.66 e Å⁻³
213 parameters	Δρ_min = −0.25 e Å⁻³
0 restraints

Crystal data top

C₂₀H₂₈NSi⁺·Br⁻	V = 1974.8 (3) Å³
M_r = 390.43	Z = 4
Monoclinic, P2₁/n	Mo Kα radiation
a = 13.9311 (12) Å	µ = 2.14 mm⁻¹
b = 7.4605 (6) Å	T = 173 K
c = 19.3515 (17) Å	0.2 × 0.2 × 0.1 mm
β = 100.926 (2)°

Data collection top

Bruker APEXII CCD diffractometer	4759 independent reflections
Absorption correction: multi-scan (SADABS, Bruker, 2015)	3948 reflections with I > 2σ(I)
T_min = 0.421, T_max = 0.746	R_int = 0.040
26749 measured reflections

Refinement top

R[F² > 2σ(F²)] = 0.031	0 restraints
wR(F²) = 0.080	H atoms treated by a mixture of independent and constrained refinement
S = 1.02	Δρ_max = 0.66 e Å⁻³
4759 reflections	Δρ_min = −0.25 e Å⁻³
213 parameters

Special details top

Experimental. Absorption correction: SADABS-2014/5 (Bruker,2014/5) was used for absorption correction. wR2(int) was 0.1354 before and 0.0450 after correction. The Ratio of minimum to maximum transmission is 0.5649. The λ/2 correction factor is 0.00150.

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. 1. Fixed U_iso At 1.2 times of: All C(H) groups, All C(H,H) groups At 1.5 times of: All C(H,H,H) groups 2.a Secondary CH2 refined with riding coordinates: C2(H2A,H2B), C15(H15A,H15B), C16(H16A,H16B), C17(H17A,H17B), C18(H18A,H18B), C19(H19A,H19B), C20(H20A,H20B) 2.b Aromatic/amide H refined with riding coordinates: C4(H4), C5(H5), C6(H6), C7(H7), C8(H8), C10(H10), C11(H11), C12(H12), C13(H13), C14(H14) 2.c Idealized Me refined as rotating group: C1(H1A,H1B,H1C)

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å²) top

	x	y	z	U_iso*/U_eq
Si1	0.27017 (3)	0.16579 (6)	0.40241 (2)	0.02506 (11)
N1	0.47332 (10)	0.2487 (2)	0.38731 (7)	0.0226 (3)
H1	0.4648 (13)	0.358 (3)	0.3882 (9)	0.026 (5)*
C1	0.22693 (15)	−0.0080 (3)	0.33465 (11)	0.0397 (5)
H1A	0.2388	0.0327	0.2889	0.060*
H1B	0.1568	−0.0282	0.3317	0.060*
H1C	0.2624	−0.1202	0.3477	0.060*
C2	0.22659 (14)	0.3967 (3)	0.37105 (10)	0.0332 (4)
H2A	0.2580	0.4872	0.4055	0.040*
H2B	0.2463	0.4217	0.3255	0.040*
C3	0.11714 (13)	0.4124 (2)	0.36237 (9)	0.0287 (4)
C4	0.05486 (15)	0.3325 (2)	0.30609 (11)	0.0365 (4)
H4	0.0816	0.2690	0.2716	0.044*
C5	−0.04527 (17)	0.3443 (3)	0.29963 (13)	0.0494 (6)
H5	−0.0867	0.2876	0.2612	0.059*
C6	−0.08555 (16)	0.4373 (3)	0.34831 (14)	0.0533 (6)
H6	−0.1546	0.4453	0.3435	0.064*
C7	−0.02525 (17)	0.5190 (3)	0.40435 (12)	0.0499 (6)
H7	−0.0528	0.5845	0.4379	0.060*
C8	0.07535 (15)	0.5058 (3)	0.41163 (10)	0.0376 (4)
H8	0.1163	0.5609	0.4507	0.045*
C9	0.22505 (12)	0.1129 (2)	0.48553 (9)	0.0274 (4)
C10	0.15034 (14)	−0.0107 (3)	0.48712 (11)	0.0375 (4)
H10	0.1224	−0.0726	0.4452	0.045*
C11	0.11604 (16)	−0.0451 (3)	0.54855 (12)	0.0463 (5)
H11	0.0652	−0.1301	0.5482	0.056*
C12	0.15485 (16)	0.0426 (3)	0.60973 (11)	0.0466 (5)
H12	0.1311	0.0186	0.6517	0.056*
C13	0.22922 (17)	0.1669 (3)	0.60999 (11)	0.0423 (5)
H13	0.2564	0.2284	0.6521	0.051*
C14	0.26369 (15)	0.2009 (3)	0.54857 (10)	0.0339 (4)
H14	0.3147	0.2859	0.5493	0.041*
C15	0.40836 (12)	0.1599 (2)	0.43050 (9)	0.0250 (3)
H15A	0.4242	0.2126	0.4783	0.030*
H15B	0.4278	0.0322	0.4352	0.030*
C16	0.57838 (13)	0.2155 (3)	0.41985 (9)	0.0296 (4)
H16A	0.5913	0.0849	0.4209	0.036*
H16B	0.5911	0.2596	0.4690	0.036*
C17	0.64701 (14)	0.3085 (3)	0.37913 (10)	0.0351 (4)
H17A	0.7155	0.2796	0.4007	0.042*
H17B	0.6385	0.4399	0.3818	0.042*
C18	0.62716 (14)	0.2504 (3)	0.30259 (10)	0.0369 (4)
H18A	0.6428	0.1216	0.2994	0.044*
H18B	0.6695	0.3190	0.2764	0.044*
C19	0.52035 (14)	0.2826 (3)	0.26998 (9)	0.0319 (4)
H19A	0.5070	0.4130	0.2682	0.038*
H19B	0.5071	0.2364	0.2211	0.038*
C20	0.45269 (13)	0.1907 (2)	0.31190 (9)	0.0276 (4)
H20A	0.3840	0.2195	0.2908	0.033*
H20B	0.4611	0.0592	0.3094	0.033*
Br1	0.45737 (2)	0.67990 (2)	0.38635 (2)	0.03319 (7)

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
Si1	0.0243 (2)	0.0241 (2)	0.0264 (2)	0.00079 (18)	0.00388 (18)	−0.00076 (18)
N1	0.0252 (8)	0.0172 (6)	0.0254 (7)	0.0034 (5)	0.0050 (6)	−0.0016 (5)
C1	0.0374 (11)	0.0395 (11)	0.0399 (10)	−0.0018 (9)	0.0013 (8)	−0.0105 (9)
C2	0.0316 (10)	0.0306 (9)	0.0383 (10)	0.0021 (8)	0.0090 (8)	0.0082 (8)
C3	0.0312 (10)	0.0260 (8)	0.0294 (9)	0.0031 (7)	0.0072 (7)	0.0102 (7)
C4	0.0406 (11)	0.0298 (10)	0.0364 (10)	0.0061 (8)	−0.0001 (8)	0.0057 (8)
C5	0.0436 (13)	0.0386 (12)	0.0582 (14)	−0.0035 (9)	−0.0100 (11)	0.0160 (10)
C6	0.0292 (11)	0.0587 (14)	0.0730 (16)	0.0058 (10)	0.0125 (11)	0.0356 (13)
C7	0.0494 (13)	0.0592 (14)	0.0475 (12)	0.0228 (11)	0.0256 (11)	0.0215 (11)
C8	0.0427 (11)	0.0385 (10)	0.0316 (9)	0.0089 (9)	0.0068 (8)	0.0074 (8)
C9	0.0250 (9)	0.0249 (8)	0.0323 (9)	0.0042 (7)	0.0058 (7)	0.0044 (7)
C10	0.0333 (10)	0.0359 (10)	0.0420 (10)	−0.0051 (8)	0.0037 (8)	0.0071 (8)
C11	0.0355 (11)	0.0475 (12)	0.0578 (14)	−0.0038 (9)	0.0137 (10)	0.0193 (10)
C12	0.0447 (12)	0.0572 (13)	0.0427 (12)	0.0113 (10)	0.0200 (10)	0.0164 (10)
C13	0.0456 (12)	0.0479 (13)	0.0355 (10)	0.0088 (9)	0.0130 (9)	−0.0018 (9)
C14	0.0339 (10)	0.0333 (10)	0.0361 (10)	0.0014 (8)	0.0110 (8)	−0.0032 (8)
C15	0.0254 (9)	0.0248 (8)	0.0251 (8)	0.0012 (6)	0.0052 (6)	0.0018 (6)
C16	0.0243 (9)	0.0356 (9)	0.0280 (9)	0.0052 (7)	0.0028 (7)	−0.0006 (7)
C17	0.0246 (9)	0.0437 (11)	0.0375 (10)	0.0002 (8)	0.0075 (8)	−0.0023 (8)
C18	0.0331 (11)	0.0444 (11)	0.0362 (10)	0.0042 (9)	0.0144 (8)	−0.0007 (9)
C19	0.0365 (10)	0.0340 (9)	0.0264 (8)	0.0038 (8)	0.0091 (7)	0.0000 (7)
C20	0.0302 (9)	0.0286 (9)	0.0234 (8)	0.0022 (7)	0.0035 (7)	−0.0030 (7)
Br1	0.04173 (13)	0.02011 (10)	0.03668 (11)	0.00323 (7)	0.00476 (8)	−0.00210 (7)

Geometric parameters (Å, º) top

Si1—C1	1.8614 (19)	C9—C14	1.400 (3)
Si1—C2	1.8883 (19)	C10—H10	0.9500
Si1—C9	1.8766 (18)	C10—C11	1.387 (3)
Si1—C15	1.8991 (18)	C11—H11	0.9500
N1—H1	0.82 (2)	C11—C12	1.371 (3)
N1—C15	1.498 (2)	C12—H12	0.9500
N1—C16	1.500 (2)	C12—C13	1.389 (3)
N1—C20	1.497 (2)	C13—H13	0.9500
C1—H1A	0.9800	C13—C14	1.387 (3)
C1—H1B	0.9800	C14—H14	0.9500
C1—H1C	0.9800	C15—H15A	0.9900
C2—H2A	0.9900	C15—H15B	0.9900
C2—H2B	0.9900	C16—H16A	0.9900
C2—C3	1.506 (3)	C16—H16B	0.9900
C3—C4	1.391 (3)	C16—C17	1.518 (3)
C3—C8	1.394 (3)	C17—H17A	0.9900
C4—H4	0.9500	C17—H17B	0.9900
C4—C5	1.379 (3)	C17—C18	1.518 (3)
C5—H5	0.9500	C18—H18A	0.9900
C5—C6	1.373 (4)	C18—H18B	0.9900
C6—H6	0.9500	C18—C19	1.521 (3)
C6—C7	1.382 (4)	C19—H19A	0.9900
C7—H7	0.9500	C19—H19B	0.9900
C7—C8	1.385 (3)	C19—C20	1.519 (3)
C8—H8	0.9500	C20—H20A	0.9900
C9—C10	1.395 (3)	C20—H20B	0.9900

C1—Si1—C2	111.59 (9)	C10—C11—H11	119.7
C1—Si1—C9	109.93 (9)	C12—C11—C10	120.6 (2)
C1—Si1—C15	111.14 (8)	C12—C11—H11	119.7
C2—Si1—C15	111.09 (8)	C11—C12—H12	120.2
C9—Si1—C2	109.14 (8)	C11—C12—C13	119.55 (19)
C9—Si1—C15	103.64 (8)	C13—C12—H12	120.2
C15—N1—H1	108.7 (13)	C12—C13—H13	120.1
C15—N1—C16	109.70 (13)	C14—C13—C12	119.9 (2)
C16—N1—H1	106.7 (13)	C14—C13—H13	120.1
C20—N1—H1	107.8 (12)	C9—C14—H14	119.3
C20—N1—C15	113.03 (13)	C13—C14—C9	121.48 (19)
C20—N1—C16	110.67 (13)	C13—C14—H14	119.3
Si1—C1—H1A	109.5	Si1—C15—H15A	107.0
Si1—C1—H1B	109.5	Si1—C15—H15B	107.0
Si1—C1—H1C	109.5	N1—C15—Si1	121.12 (11)
H1A—C1—H1B	109.5	N1—C15—H15A	107.0
H1A—C1—H1C	109.5	N1—C15—H15B	107.0
H1B—C1—H1C	109.5	H15A—C15—H15B	106.8
Si1—C2—H2A	109.4	N1—C16—H16A	109.3
Si1—C2—H2B	109.4	N1—C16—H16B	109.3
H2A—C2—H2B	108.0	N1—C16—C17	111.52 (14)
C3—C2—Si1	111.32 (12)	H16A—C16—H16B	108.0
C3—C2—H2A	109.4	C17—C16—H16A	109.3
C3—C2—H2B	109.4	C17—C16—H16B	109.3
C4—C3—C2	121.46 (17)	C16—C17—H17A	109.4
C4—C3—C8	118.03 (18)	C16—C17—H17B	109.4
C8—C3—C2	120.50 (17)	C16—C17—C18	111.09 (16)
C3—C4—H4	119.5	H17A—C17—H17B	108.0
C5—C4—C3	120.9 (2)	C18—C17—H17A	109.4
C5—C4—H4	119.5	C18—C17—H17B	109.4
C4—C5—H5	119.7	C17—C18—H18A	109.7
C6—C5—C4	120.5 (2)	C17—C18—H18B	109.7
C6—C5—H5	119.7	C17—C18—C19	110.05 (15)
C5—C6—H6	120.2	H18A—C18—H18B	108.2
C5—C6—C7	119.7 (2)	C19—C18—H18A	109.7
C7—C6—H6	120.2	C19—C18—H18B	109.7
C6—C7—H7	120.0	C18—C19—H19A	109.4
C6—C7—C8	120.1 (2)	C18—C19—H19B	109.4
C8—C7—H7	120.0	H19A—C19—H19B	108.0
C3—C8—H8	119.6	C20—C19—C18	111.38 (15)
C7—C8—C3	120.8 (2)	C20—C19—H19A	109.4
C7—C8—H8	119.6	C20—C19—H19B	109.4
C10—C9—Si1	122.04 (14)	N1—C20—C19	111.48 (14)
C10—C9—C14	117.13 (17)	N1—C20—H20A	109.3
C14—C9—Si1	120.80 (14)	N1—C20—H20B	109.3
C9—C10—H10	119.3	C19—C20—H20A	109.3
C11—C10—C9	121.40 (19)	C19—C20—H20B	109.3
C11—C10—H10	119.3	H20A—C20—H20B	108.0

Si1—C2—C3—C4	−74.37 (19)	C9—Si1—C2—C3	−55.09 (15)
Si1—C2—C3—C8	104.58 (17)	C9—Si1—C15—N1	−160.77 (12)
Si1—C9—C10—C11	−178.33 (15)	C9—C10—C11—C12	0.2 (3)
Si1—C9—C14—C13	178.18 (15)	C10—C9—C14—C13	0.0 (3)
N1—C16—C17—C18	−56.7 (2)	C10—C11—C12—C13	0.0 (3)
C1—Si1—C2—C3	66.61 (15)	C11—C12—C13—C14	−0.1 (3)
C1—Si1—C9—C10	−15.24 (18)	C12—C13—C14—C9	0.2 (3)
C1—Si1—C9—C14	166.66 (15)	C14—C9—C10—C11	−0.2 (3)
C1—Si1—C15—N1	81.20 (15)	C15—Si1—C2—C3	−168.75 (12)
C2—Si1—C9—C10	107.45 (16)	C15—Si1—C9—C10	−134.11 (15)
C2—Si1—C9—C14	−70.65 (16)	C15—Si1—C9—C14	47.79 (16)
C2—Si1—C15—N1	−43.69 (15)	C15—N1—C16—C17	−178.06 (14)
C2—C3—C4—C5	178.46 (17)	C15—N1—C20—C19	−179.63 (14)
C2—C3—C8—C7	−179.31 (17)	C16—N1—C15—Si1	−177.28 (11)
C3—C4—C5—C6	0.8 (3)	C16—N1—C20—C19	−56.13 (18)
C4—C3—C8—C7	−0.3 (3)	C16—C17—C18—C19	55.3 (2)
C4—C5—C6—C7	−0.3 (3)	C17—C18—C19—C20	−55.1 (2)
C5—C6—C7—C8	−0.6 (3)	C18—C19—C20—N1	56.0 (2)
C6—C7—C8—C3	0.9 (3)	C20—N1—C15—Si1	−53.24 (17)
C8—C3—C4—C5	−0.5 (3)	C20—N1—C16—C17	56.54 (19)

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
N1—H1···Br1	0.82 (2)	2.41 (2)	3.2242 (15)	173.4 (17)

Hydrogen-bond geometry (Å, º) top

D—H···A	D—H	H···A	D···A	D—H···A
N1—H1···Br1	0.82 (2)	2.41 (2)	3.2242 (15)	173.4 (17)

Acknowledgements

We are grateful to the Deutsche Forschungsgemeinschaft (DFG) for financial support.

References

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Bruker (2015). SADABS. Bruker AXS Inc., Madison, Wisconsin, USA. Google Scholar
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Volume 71| Part 10| October 2015| Page o759

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organic compounds\(\def\hfill{\hskip 5em}\def\hfil{\hskip 3em}\def\eqno#1{\hfil {#1}}\)

Crystal structure of benz­yl(meth­yl)phen­yl[(piperidin-1-ium-1-yl)meth­yl]silane bromide

1. Related literature

2. Experimental

2.1. Crystal data

2.2. Data collection

2.3. Refinement

Supporting information

Acknowledgements

References

organic compounds

Crystal structure of benzyl(methyl)phenyl[(piperidin-1-ium-1-yl)methyl]silane bromide