Butane-1,4-diammonium bis(perchlorate)

Abstract

The butane-1,4-diammonium cation of the title compound, C₄H₁₄N₂ ²⁺·2ClO₄ ⁻, lies on a special position of site symmetry 2/m, whereas the perchlorate anion is located on a crystallographic mirror plane. An intricate three-dimensional hydrogen-bonding network exists in the crystal structure with each H atom of the ammonium group exhibiting bifurcated inter­actions to the perchlorate anion. Complex hydrogen-bonded ring and chain motifs are also evident, in particular a 50-membered ring with graph-set notation R ¹⁰ ₁₀(50) is identified.

Related literature

For related structural studies of butane-1,4-diammonium salts, see: van Blerk & Kruger (2007 ▶); Lemmerer & Billing (2006 ▶); Gabro et al. (2009 ▶). For hydrogen-bond motifs, see: Bernstein et al. (1995 ▶).

Experimental

Crystal data

• C₄H₁₄N₂ ²⁺·2ClO₄ ⁻

• M _r = 289.07

• Monoclinic,

• a = 19.4755 (10) Å

• b = 5.6210 (3) Å

• c = 5.3470 (2) Å

• β = 97.222 (3)°

• V = 580.70 (5) ų

• Z = 2

• Mo Kα radiation

• μ = 0.59 mm⁻¹

• T = 296 K

• 0.50 × 0.34 × 0.16 mm

Data collection

• Bruker APEXII CCD diffractometer

• Absorption correction: multi-scan (AX-Scale; Bruker, 2008 ▶) T _min = 0.757, T _max = 0.912

• 3067 measured reflections

• 793 independent reflections

• 694 reflections with I > 2s(I)

• R _int = 0.028

Refinement

• R[F ² > 2σ(F ²)] = 0.056

• wR(F ²) = 0.155

• S = 1.17

• 793 reflections

• 46 parameters

• H-atom parameters constrained

• Δρ_max = 0.47 e Å⁻³

• Δρ_min = −0.44 e Å⁻³

Data collection: APEX2 (Bruker, 2008 ▶); cell refinement: SAINT (Bruker, 2008 ▶; data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 ▶); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 ▶); molecular graphics: X-SEED (Barbour, 2001 ▶) and Mercury (Macrae et al., 2006 ▶); software used to prepare material for publication: publCIF (Westrip, 2010 ▶) and PLATON (Spek, 2009 ▶).

Supplementary Material

Additional supplementary materials: crystallographic information; 3D view; checkCIF report

Table 1. Hydrogen-bond geometry (Å, °).

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
N1—H1N⋯O1i	0.89	2.35	3.035 (3)	134
N1—H1N⋯O1ii	0.89	2.35	3.035 (3)	134
N1—H2N⋯O1	0.89	2.68	3.435 (4)	143
N1—H2N⋯O3	0.89	2.21	3.0308 (14)	153

Symmetry codes: (i) ; (ii) .

supplementary crystallographic information

Comment

The crystal structure of the title compound (I) adds to our current ongoing studies of long-chained diammonium mineral acid salts. Colourless rectangular crystals of butane-1,4-diammonium diperchlorate were synthesized and formed part of our structural chemistry study of the inorganic mineral acid salts of butane-1,4-diamine.

The butane-1,4-diammonium cation lies over an inversion centre and a twofold rotation axis. It also straddles a crystallographic mirror plane. The asymmetric unit contains one-half of a perchlorate anion and one-half of the butane-1,4-diammonium cation. The hydrocarbon chain is also fully extended and is of necessity completely planar as it lies in the crystallographic mirror plane. The molecular structure of (I) is shown in Figure 1.

Figure 2 illustrates the packing arrangement of the title compound (I). Single stacked layers of cations pack together with perchlorate anions inserted between the cation chains in line with the ammonium groups showing a distinct inorganic - organic layering effect that is a common feature of these long-chained diammonium salts. An extensive three-dimensional hydrogen-bonding network is formed.

A close-up view of the hydrogen bonding interactions can be viewed in Figure 3 where very clear evidence of bifurcated interactions can be seen on each hydrogen atom of both ammonium groups. The hydrogen bond distances and angles for (I) can be found in Table 2.

Since the hydrogen bonding network is extremely intricate and complex, we focus on one particularly interesting hydrogen-bonding ring motif in the structure. Figure 4 shows a view of five diammonium cations and five perchlorate anions (viewed down the a axis) that are hydrogen bonded together to form a large, level 2, 50-membered ring motif with graph set notation R¹⁰₁₀(50). Numerous other ring and chain motifs were identified with Mercury (Macrae et al.), but since the one in Figure 4 is the highest level motif obtainable in the structure, the other motifs of lower level are not depicted here.

Experimental

The title compound was prepared by adding butane-1,4-diamine (0.50 g, 5.67 mmol) to 30% perchloric acid (HClO₄, 2 ml, 9.138 mmol, Merck) in a sample vial. The mixture was then refluxed at 363 K for 2 h. The solution was cooled at 2 K h^-1 to room temperature. Colourless crystals of butane-1,4-diammonium diperchlorate were collected and a suitable single-crystal was selected for the X-ray diffraction study.

Refinement

Hydrogen atoms could be identified from the difference Fourier map but once these atoms were refined, their distances from the parent atoms were found to be significantly shorter than the ideal distances for C—H and N—H respectively. The H-atoms were therefore geometrically positioned and refined in the riding-model approximation, with C—H = 0.97 Å, N—H = 0.89 Å, and U_iso(H) = 1.2Ueq(C) or 1.5Ueq(N). The highest peak in the final difference map is 0.69Å from O2 and the deepest hole is 0.69Å from Cl1.

Figures

Fig. 1.

: Molecular structure of the title compound, with atomic numbering scheme and displacement ellipsoids drawn at the 50% probability level.

Fig. 2.

: Packing arrangement of the title compound viewed down the b axis. Hydrogen bonds are indicated by red dashed lines.

Fig. 3.

: Close-up view of the title compound clearly showing the bifurcated hydrogen-bonding interactions. Hydrogen bonds are indicated by red dashed lines.

Fig. 4.

: Close up view of the title compound viewed down the a axis showing the 50-membered level 2 ring motif.

Crystal data

C4H14N22+·2ClO4−	F(000) = 300
Mr = 289.07	Dx = 1.653 Mg m−3
Monoclinic, C2/m	Mo Kα radiation, λ = 0.71073 Å
Hall symbol: -C 2y	Cell parameters from 1622 reflections
a = 19.4755 (10) Å	θ = 3.8–28.2°
b = 5.6210 (3) Å	µ = 0.59 mm−1
c = 5.3470 (2) Å	T = 296 K
β = 97.222 (3)°	Block, colourless
V = 580.70 (5) Å3	0.50 × 0.34 × 0.16 mm
Z = 2

Data collection

Bruker APEXII CCD diffractometer	793 independent reflections
Radiation source: fine-focus sealed tube	694 reflections with I > 2s(I)
graphite	Rint = 0.028
φ and ω scans	θmax = 28.3°, θmin = 3.8°
Absorption correction: multi-scan (AX-Scale; Bruker, 2008)	h = −23→25
Tmin = 0.757, Tmax = 0.912	k = −7→7
3067 measured reflections	l = −6→7

Refinement

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)] = 0.056	Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.155	H-atom parameters constrained
S = 1.17	w = 1/[σ2(Fo2) + (0.0955P)2 + 0.3477P] where P = (Fo2 + 2Fc2)/3
793 reflections	(Δ/σ)max < 0.001
46 parameters	Δρmax = 0.47 e Å−3
0 restraints	Δρmin = −0.44 e Å−3

Special details

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.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Ų)

	x	y	z	Uiso*/Ueq
C1	0.57860 (17)	0.0000	0.7538 (6)	0.0466 (8)
H1	0.5661	0.1394	0.8450	0.056*
C2	0.53822 (16)	0.0000	0.4976 (6)	0.0467 (8)
H2	0.5508	−0.1394	0.4065	0.056*
Cl1	0.65841 (4)	0.5000	0.27016 (13)	0.0403 (3)
N1	0.65459 (14)	0.0000	0.7476 (5)	0.0450 (7)
H1N	0.6762	0.0000	0.9045	0.068*
H2N	0.6666	0.1293	0.6673	0.068*
O1	0.69616 (13)	0.2898 (5)	0.2214 (5)	0.0755 (7)
O2	0.59205 (16)	0.5000	0.1238 (6)	0.0698 (9)
O3	0.65031 (17)	0.5000	0.5341 (5)	0.0633 (8)

Atomic displacement parameters (Ų)

	U11	U22	U33	U12	U13	U23
C1	0.0461 (18)	0.061 (2)	0.0321 (15)	0.000	0.0021 (12)	0.000
C2	0.0403 (18)	0.068 (2)	0.0315 (15)	0.000	0.0028 (12)	0.000
Cl1	0.0480 (5)	0.0380 (5)	0.0344 (5)	0.000	0.0031 (3)	0.000
N1	0.0425 (15)	0.0501 (17)	0.0398 (14)	0.000	−0.0049 (11)	0.000
O1	0.0818 (14)	0.0697 (16)	0.0730 (14)	0.0253 (12)	0.0014 (11)	−0.0236 (11)
O2	0.0619 (18)	0.069 (2)	0.071 (2)	0.000	−0.0187 (14)	0.000
O3	0.095 (2)	0.0596 (17)	0.0377 (14)	0.000	0.0171 (13)	0.000

Geometric parameters (Å, °)

C1—N1	1.484 (4)	Cl1—O1	1.433 (2)
C1—C2	1.492 (4)	Cl1—O1ii	1.433 (2)
C1—H1	0.9700	Cl1—O3	1.440 (3)
C2—C2i	1.492 (6)	N1—H1N	0.8900
C2—H2	0.9700	N1—H2N	0.8900
Cl1—O2	1.424 (3)
N1—C1—C2	113.0 (3)	O2—Cl1—O1ii	110.54 (12)
N1—C1—H1	109.0	O1—Cl1—O1ii	111.1 (2)
C2—C1—H1	109.0	O2—Cl1—O3	109.6 (2)
H1—C1—H1iii	107.8	O1—Cl1—O3	107.48 (13)
C1—C2—C2i	113.3 (3)	O1ii—Cl1—O3	107.48 (13)
C1—C2—H2	108.9	C1—N1—H1N	109.5
C2i—C2—H2	108.9	C1—N1—H2N	109.5
H2—C2—H2iii	107.7	H1N—N1—H2N	109.5
O2—Cl1—O1	110.54 (12)
N1—C1—C2—C2i	180.0

Symmetry codes: (i) −x+1, −y, −z+1; (ii) x, −y+1, z; (iii) x, −y, z.

Hydrogen-bond geometry (Å, °)

D—H···A	D—H	H···A	D···A	D—H···A
N1—H1N···O1iv	0.89	2.35	3.035 (3)	134
N1—H1N···O1v	0.89	2.35	3.035 (3)	134
N1—H2N···O1	0.89	2.68	3.435 (4)	143
N1—H2N···O3	0.89	2.21	3.0308 (14)	153

Symmetry codes: (iv) x, y, z+1; (v) x, −y, z+1.