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The title mol­ecular salt, C11H21N4+·C6H4NO3·C6H5NO3, (II), crystallizes with two independent three-component aggregates in the asymmetric unit. In the cations, the cyclo­hexane rings fused to the cage aza­adamantane systems both adopt a chair conformation. In the crystal structure, the aggregates are connected by C—H...O hydrogen bonds, forming a supra­molecular unit enclosing an R44(24) ring motif. These units are linked via C—H...O and C—H...N hydrogen bonds, forming a three-dimensional network. Even hydrogen-bond formation to one of the N atoms is enough to induce structural stereoelectronic effects in the normal donor→acceptor direction. The C—N bond distances provide structural evidence for a strong anomeric effect. The structure also displays O—H...O and N—H...O hydrogen bonding. Geometric optimization and natural bond orbital (NBO) analysis of (II) were undertaken by utilizing DFT/B3LYP with the 6-31+G(d,p) basis set. NBO second-order perturbation theory calculations indicate donor–acceptor inter­actions between nitro­gen lone pairs and the anti­bonding orbital of the C—C and C—N bonds for the protonated polyamine, in agreement with the occurrence of bond-length and bond-angle changes within the aminal cage structure.

Supporting information

cif

Crystallographic Information File (CIF) https://doi.org/10.1107/S2053229615004829/lg3159sup1.cif
Contains datablocks II, global

hkl

Structure factor file (CIF format) https://doi.org/10.1107/S2053229615004829/lg3159Isup2.hkl
Contains datablock I

pdf

Portable Document Format (PDF) file https://doi.org/10.1107/S2053229615004829/lg3159sup3.pdf
The <sup>1</sup>H NMR spectrum of (II)

CCDC reference: 1052946

Computing details top

Data collection: X-AREA (Stoe & Cie, 2001); cell refinement: X-AREA (Stoe & Cie, 2001); data reduction: X-AREA (Stoe & Cie, 2001); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL2014 (Sheldrick, 2015); molecular graphics: XP in SHELXTL-Plus (Sheldrick, 2008); software used to prepare material for publication: SHELXL2014 (Sheldrick, 2015).

8,10,12-Triaza-1-azoniatetracyclo[8.3.1.18,12.02,7]pentadecane 4-nitrophenolate 4-nitrophenol monosolvate top
Crystal data top
C11H21N4+·C6H4NO3·C6H5NO3F(000) = 1032
Mr = 486.53Dx = 1.343 Mg m3
Monoclinic, P21Mo Kα radiation, λ = 0.71073 Å
a = 6.2201 (6) ÅCell parameters from 10933 reflections
b = 22.964 (2) Åθ = 3.4–25.9°
c = 16.8626 (16) ŵ = 0.10 mm1
β = 92.879 (8)°T = 173 K
V = 2405.6 (4) Å3Plate, yellow
Z = 40.27 × 0.22 × 0.11 mm
Data collection top
Stoe IPDS II two-circle
diffractometer
6220 reflections with I > 2σ(I)
Radiation source: Genix 3D IµS microfocus X-ray sourceRint = 0.038
ω scansθmax = 25.6°, θmin = 3.4°
Absorption correction: multi-scan
(X-AREA; Stoe & Cie, 2001)
h = 77
Tmin = 0.944, Tmax = 0.970k = 2627
12586 measured reflectionsl = 1620
8218 independent reflections
Refinement top
Refinement on F2Hydrogen site location: mixed
Least-squares matrix: fullH atoms treated by a mixture of independent and constrained refinement
R[F2 > 2σ(F2)] = 0.044 w = 1/[σ2(Fo2) + (0.060P)2]
where P = (Fo2 + 2Fc2)/3
wR(F2) = 0.107(Δ/σ)max < 0.001
S = 0.94Δρmax = 0.17 e Å3
8218 reflectionsΔρmin = 0.21 e Å3
647 parametersAbsolute structure: Flack x parameter determined using 2249 quotients [(I+)-(I-)]/[(I+)+(I-)] (Parsons et al., 2013)
1 restraintAbsolute structure parameter: 0.9 (10)
Special details top

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.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top
xyzUiso*/Ueq
N10.7231 (5)0.76571 (16)0.9399 (2)0.0298 (8)
N21.1649 (4)0.72911 (16)0.9478 (2)0.0247 (8)
N30.8431 (5)0.66606 (17)0.9222 (2)0.0272 (8)
H30.811 (8)0.627 (3)0.927 (4)0.063 (18)*
N40.9398 (5)0.73696 (18)0.8260 (2)0.0322 (9)
C10.8648 (5)0.78687 (18)1.0059 (2)0.0287 (8)
H10.83470.76201.05270.034*
C21.1070 (6)0.78085 (17)0.9933 (3)0.0277 (9)
H21.14720.81520.96080.033*
C31.2284 (6)0.7873 (2)1.0724 (3)0.0395 (10)
H3B1.38440.78181.06590.047*
H3C1.17960.75751.10990.047*
C41.1867 (8)0.8484 (3)1.1050 (4)0.0545 (15)
H4A1.25590.85171.15900.065*
H4B1.25450.87751.07090.065*
C50.9496 (8)0.8624 (2)1.1087 (3)0.0536 (14)
H5A0.93340.90411.12210.064*
H5B0.88880.83931.15180.064*
C60.8215 (7)0.8497 (2)1.0307 (3)0.0419 (12)
H6A0.66580.85521.03790.050*
H6B0.86550.87690.98890.050*
C71.1560 (6)0.7400 (2)0.8630 (3)0.0294 (10)
H7A1.24810.71120.83730.035*
H7B1.21610.77920.85340.035*
C80.7856 (6)0.7783 (2)0.8596 (3)0.0343 (11)
H8A0.84990.81770.85920.041*
H8B0.65390.77920.82410.041*
C90.6672 (6)0.70603 (19)0.9480 (3)0.0299 (10)
H9A0.53340.69800.91560.036*
H9B0.63870.69801.00420.036*
C101.0617 (6)0.67514 (18)0.9663 (3)0.0275 (9)
H10A1.04160.67381.02410.033*
H10B1.15800.64260.95320.033*
C110.8652 (7)0.6779 (2)0.8351 (3)0.0347 (11)
H11A0.96930.65030.81310.042*
H11B0.72450.67270.80580.042*
N210.0853 (10)0.3926 (3)0.6506 (3)0.0650 (15)
O210.2755 (5)0.56016 (14)0.8783 (2)0.0340 (8)
H210.419 (9)0.560 (3)0.893 (3)0.054 (15)*
O220.2293 (9)0.3595 (3)0.6318 (4)0.099 (2)
O230.0995 (8)0.3900 (3)0.6218 (3)0.0927 (18)
C210.2347 (6)0.51935 (19)0.8242 (3)0.0289 (10)
C220.0252 (7)0.5146 (2)0.7908 (3)0.0348 (11)
H220.08410.54000.80760.042*
C230.0229 (7)0.4735 (2)0.7339 (3)0.0390 (12)
H230.16480.47060.71070.047*
C240.1355 (8)0.4364 (2)0.7107 (3)0.0405 (12)
C250.3430 (8)0.4395 (2)0.7430 (3)0.0398 (12)
H250.45020.41350.72600.048*
C260.3928 (7)0.4807 (2)0.7999 (3)0.0331 (11)
H260.53510.48300.82300.040*
N310.8656 (7)0.4095 (2)1.1831 (3)0.0433 (11)
O310.6592 (5)0.56054 (14)0.9352 (2)0.0331 (7)
O320.7276 (7)0.37614 (18)1.2066 (3)0.0559 (10)
O331.0507 (6)0.41117 (19)1.2132 (3)0.0597 (11)
C310.7077 (7)0.52352 (19)0.9923 (3)0.0302 (10)
C320.5536 (7)0.4843 (2)1.0218 (3)0.0344 (11)
H320.41110.48400.99870.041*
C330.6069 (7)0.4473 (2)1.0826 (3)0.0349 (11)
H330.50180.42141.10140.042*
C340.8126 (7)0.4472 (2)1.1170 (3)0.0347 (11)
C350.9691 (7)0.4840 (2)1.0886 (3)0.0342 (11)
H351.11120.48331.11190.041*
C360.9186 (6)0.5209 (2)1.0276 (3)0.0342 (11)
H361.02720.54541.00820.041*
N1A0.2438 (5)0.23971 (15)0.4399 (2)0.0258 (8)
N2A0.6609 (4)0.29117 (16)0.4552 (2)0.0261 (8)
N4A0.4377 (5)0.27791 (18)0.3291 (2)0.0321 (9)
N3A0.3343 (5)0.34582 (16)0.4274 (2)0.0264 (8)
C1A0.4121 (5)0.20952 (17)0.4880 (2)0.0269 (8)
H1A0.47380.17970.45230.032*
C2A0.5992 (5)0.24895 (18)0.5150 (3)0.0280 (10)
H2A0.54940.27200.56090.034*
C3A0.7870 (6)0.2114 (2)0.5473 (3)0.0387 (10)
H3A10.83710.18590.50470.046*
H3A20.90840.23670.56570.046*
C4A0.7147 (7)0.1745 (3)0.6160 (3)0.0453 (13)
H4A10.83330.14800.63370.054*
H4A20.68420.20030.66110.054*
C5A0.5169 (7)0.1389 (2)0.5943 (3)0.0428 (11)
H5A10.46820.11910.64230.051*
H5A20.55380.10850.55550.051*
C6A0.3343 (6)0.1762 (2)0.5586 (3)0.0347 (10)
H6A10.21110.15110.54150.042*
H6A20.28520.20380.59900.042*
C7A0.1905 (5)0.29833 (18)0.4614 (3)0.0264 (9)
H7A10.19910.30140.52000.032*
H7A20.03940.30610.44310.032*
C8A0.6512 (6)0.2730 (2)0.3711 (3)0.0328 (11)
H8A10.69920.23200.36830.039*
H8A20.75470.29700.34250.039*
C9A0.2786 (6)0.2360 (2)0.3552 (3)0.0315 (10)
H9A10.14020.24290.32520.038*
H9A20.32720.19620.34270.038*
C10A0.5600 (6)0.34641 (19)0.4639 (3)0.0278 (10)
H10C0.64490.37680.43790.033*
H10D0.55630.35610.52100.033*
C11A0.3545 (7)0.3354 (2)0.3401 (3)0.0342 (11)
H11C0.21190.33930.31180.041*
H11D0.45270.36450.31830.041*
N21A0.4123 (8)0.6241 (2)0.1464 (3)0.0542 (13)
O21A0.2318 (5)0.45706 (14)0.3764 (2)0.0339 (7)
O22A0.2682 (8)0.6576 (2)0.1291 (3)0.0799 (15)
O23A0.5939 (7)0.6252 (2)0.1142 (3)0.0763 (14)
C21A0.2713 (6)0.49818 (19)0.3222 (3)0.0272 (9)
C22A0.1133 (6)0.5371 (2)0.2992 (3)0.0311 (10)
H22A0.02790.53480.32320.037*
C23A0.1595 (7)0.5783 (2)0.2424 (3)0.0363 (11)
H23A0.05200.60500.22740.044*
C24A0.3652 (8)0.5808 (2)0.2071 (3)0.0360 (11)
C25A0.5245 (7)0.5435 (2)0.2289 (3)0.0373 (11)
H25A0.66510.54620.20450.045*
C26A0.4783 (6)0.5020 (2)0.2866 (3)0.0335 (11)
H26A0.58760.47610.30210.040*
N31A0.3632 (8)0.6054 (2)0.6795 (3)0.0476 (12)
O31A0.1472 (5)0.45273 (14)0.4355 (2)0.0334 (7)
O32A0.5466 (7)0.60263 (19)0.7114 (3)0.0608 (11)
O33A0.2261 (7)0.63961 (18)0.7021 (3)0.0593 (11)
C31A0.1982 (6)0.48961 (19)0.4917 (3)0.0282 (10)
C32A0.4079 (7)0.4921 (2)0.5263 (3)0.0361 (11)
H32A0.51530.46720.50690.043*
C33A0.4622 (7)0.5296 (2)0.5877 (3)0.0391 (12)
H33A0.60440.52990.61100.047*
C34A0.3072 (7)0.5670 (2)0.6151 (3)0.0335 (11)
C35A0.0989 (7)0.5677 (2)0.5811 (3)0.0356 (11)
H35A0.00580.59390.59940.043*
C36A0.0477 (7)0.5293 (2)0.5201 (3)0.0339 (11)
H36A0.09410.52970.49640.041*
H3A0.269 (6)0.384 (2)0.434 (3)0.028 (11)*
H21A0.058 (13)0.461 (5)0.408 (5)0.14 (3)*
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
N10.0226 (15)0.0328 (19)0.034 (2)0.0021 (13)0.0017 (13)0.0079 (17)
N20.0226 (14)0.0250 (17)0.027 (2)0.0019 (13)0.0004 (13)0.0028 (16)
N30.0268 (16)0.027 (2)0.027 (2)0.0017 (14)0.0025 (14)0.0013 (17)
N40.0328 (17)0.039 (2)0.025 (2)0.0029 (16)0.0015 (15)0.0045 (19)
C10.0269 (16)0.029 (2)0.031 (2)0.0040 (15)0.0046 (14)0.0023 (18)
C20.0292 (18)0.0223 (19)0.032 (2)0.0027 (14)0.0054 (15)0.0044 (18)
C30.037 (2)0.043 (2)0.038 (2)0.0050 (18)0.0030 (17)0.014 (2)
C40.062 (3)0.052 (3)0.049 (3)0.015 (2)0.003 (2)0.025 (3)
C50.065 (3)0.040 (3)0.058 (3)0.001 (2)0.021 (3)0.019 (3)
C60.045 (2)0.032 (2)0.050 (3)0.0049 (18)0.014 (2)0.002 (2)
C70.0278 (19)0.034 (2)0.026 (2)0.0025 (17)0.0027 (16)0.001 (2)
C80.031 (2)0.039 (3)0.033 (3)0.0028 (18)0.0013 (17)0.016 (2)
C90.0233 (17)0.032 (2)0.034 (2)0.0018 (15)0.0020 (15)0.006 (2)
C100.0231 (18)0.026 (2)0.033 (3)0.0021 (15)0.0023 (16)0.001 (2)
C110.037 (2)0.043 (3)0.024 (2)0.0095 (19)0.0049 (18)0.004 (2)
N210.088 (4)0.067 (4)0.040 (3)0.026 (3)0.002 (3)0.018 (3)
O210.0355 (17)0.0281 (17)0.038 (2)0.0000 (13)0.0005 (14)0.0077 (16)
O220.114 (4)0.103 (4)0.080 (4)0.012 (3)0.018 (3)0.065 (4)
O230.100 (3)0.103 (4)0.072 (4)0.034 (3)0.029 (3)0.034 (3)
C210.031 (2)0.023 (2)0.032 (3)0.0025 (16)0.0011 (18)0.005 (2)
C220.033 (2)0.027 (2)0.044 (3)0.0019 (18)0.002 (2)0.004 (2)
C230.037 (2)0.039 (3)0.040 (3)0.011 (2)0.007 (2)0.008 (3)
C240.058 (3)0.037 (3)0.027 (3)0.016 (2)0.003 (2)0.009 (2)
C250.042 (3)0.042 (3)0.036 (3)0.007 (2)0.012 (2)0.011 (3)
C260.034 (2)0.030 (2)0.036 (3)0.0029 (18)0.0064 (19)0.003 (2)
N310.066 (3)0.034 (3)0.030 (3)0.020 (2)0.000 (2)0.005 (2)
O310.0344 (15)0.0339 (17)0.0304 (19)0.0086 (12)0.0049 (13)0.0020 (16)
O320.088 (3)0.039 (2)0.041 (2)0.005 (2)0.011 (2)0.009 (2)
O330.071 (2)0.061 (3)0.046 (3)0.028 (2)0.0137 (19)0.004 (2)
C310.038 (2)0.022 (2)0.031 (3)0.0023 (16)0.0002 (19)0.004 (2)
C320.031 (2)0.038 (3)0.035 (3)0.0057 (19)0.0052 (19)0.002 (2)
C330.044 (2)0.026 (2)0.035 (3)0.0038 (19)0.008 (2)0.001 (2)
C340.044 (2)0.028 (2)0.031 (3)0.0071 (19)0.000 (2)0.003 (2)
C350.033 (2)0.037 (3)0.032 (3)0.0070 (18)0.0057 (18)0.003 (2)
C360.029 (2)0.034 (3)0.040 (3)0.0061 (17)0.0022 (19)0.004 (2)
N1A0.0247 (15)0.0237 (17)0.029 (2)0.0009 (12)0.0024 (13)0.0021 (16)
N2A0.0218 (14)0.0281 (19)0.028 (2)0.0005 (13)0.0001 (13)0.0061 (17)
N4A0.0318 (17)0.038 (2)0.027 (2)0.0066 (15)0.0003 (15)0.0014 (19)
N3A0.0257 (15)0.0242 (19)0.029 (2)0.0063 (13)0.0032 (14)0.0011 (17)
C1A0.0252 (16)0.0271 (19)0.028 (2)0.0016 (14)0.0012 (14)0.0033 (18)
C2A0.0229 (17)0.031 (2)0.031 (2)0.0022 (13)0.0010 (15)0.0044 (18)
C3A0.0267 (18)0.045 (2)0.044 (3)0.0069 (17)0.0033 (16)0.015 (2)
C4A0.036 (2)0.055 (3)0.044 (3)0.008 (2)0.0031 (19)0.021 (3)
C5A0.046 (2)0.044 (3)0.038 (3)0.008 (2)0.0036 (19)0.019 (2)
C6A0.0327 (19)0.034 (2)0.037 (3)0.0043 (16)0.0001 (17)0.010 (2)
C7A0.0200 (15)0.027 (2)0.032 (2)0.0007 (14)0.0002 (14)0.0001 (18)
C8A0.0275 (19)0.039 (3)0.032 (3)0.0062 (17)0.0069 (17)0.006 (2)
C9A0.033 (2)0.033 (2)0.027 (3)0.0037 (18)0.0054 (17)0.003 (2)
C10A0.0222 (18)0.024 (2)0.036 (3)0.0031 (15)0.0040 (16)0.001 (2)
C11A0.031 (2)0.038 (3)0.033 (3)0.0060 (18)0.0002 (19)0.007 (2)
N21A0.071 (3)0.055 (3)0.036 (3)0.017 (2)0.003 (2)0.014 (3)
O21A0.0352 (15)0.0298 (17)0.036 (2)0.0016 (13)0.0022 (14)0.0073 (16)
O22A0.095 (3)0.081 (4)0.064 (3)0.003 (3)0.004 (2)0.046 (3)
O23A0.081 (3)0.086 (4)0.059 (3)0.023 (3)0.023 (2)0.021 (3)
C21A0.033 (2)0.022 (2)0.027 (3)0.0034 (16)0.0019 (17)0.000 (2)
C22A0.028 (2)0.032 (2)0.033 (3)0.0015 (18)0.0001 (18)0.002 (2)
C23A0.039 (2)0.034 (3)0.037 (3)0.0008 (19)0.006 (2)0.001 (2)
C24A0.045 (2)0.035 (3)0.027 (3)0.011 (2)0.002 (2)0.000 (2)
C25A0.040 (2)0.037 (3)0.034 (3)0.010 (2)0.011 (2)0.006 (2)
C26A0.028 (2)0.032 (3)0.040 (3)0.0020 (18)0.0001 (18)0.008 (2)
N31A0.078 (3)0.033 (3)0.033 (3)0.020 (2)0.010 (2)0.001 (2)
O31A0.0372 (15)0.0299 (17)0.0325 (19)0.0071 (13)0.0051 (13)0.0039 (16)
O32A0.074 (3)0.059 (3)0.048 (3)0.033 (2)0.013 (2)0.005 (2)
O33A0.099 (3)0.036 (2)0.043 (3)0.011 (2)0.014 (2)0.012 (2)
C31A0.032 (2)0.027 (2)0.026 (2)0.0006 (16)0.0001 (17)0.005 (2)
C32A0.034 (2)0.034 (3)0.039 (3)0.0018 (18)0.0012 (19)0.000 (2)
C33A0.038 (2)0.038 (3)0.040 (3)0.006 (2)0.003 (2)0.005 (3)
C34A0.051 (3)0.030 (2)0.020 (3)0.012 (2)0.003 (2)0.000 (2)
C35A0.041 (2)0.033 (3)0.034 (3)0.0012 (19)0.006 (2)0.002 (2)
C36A0.034 (2)0.030 (2)0.037 (3)0.0016 (18)0.0044 (19)0.002 (2)
Geometric parameters (Å, º) top
N1—C91.422 (6)N1A—C9A1.457 (6)
N1—C81.456 (6)N1A—C1A1.466 (5)
N1—C11.467 (5)N2A—C10A1.426 (5)
N2—C101.437 (5)N2A—C2A1.464 (5)
N2—C71.450 (6)N2A—C8A1.476 (6)
N2—C21.469 (5)N4A—C11A1.433 (6)
N3—C111.508 (6)N4A—C9A1.463 (6)
N3—C91.509 (5)N4A—C8A1.477 (5)
N3—C101.530 (5)N3A—C11A1.503 (6)
N3—H30.93 (7)N3A—C10A1.504 (5)
N4—C111.444 (6)N3A—C7A1.539 (5)
N4—C71.455 (5)N3A—H3A0.98 (5)
N4—C81.482 (6)C1A—C6A1.514 (6)
C1—C61.530 (6)C1A—C2A1.526 (5)
C1—C21.538 (5)C1A—H1A1.0000
C1—H11.0000C2A—C3A1.530 (5)
C2—C31.506 (6)C2A—H2A1.0000
C2—H21.0000C3A—C4A1.522 (7)
C3—C41.534 (7)C3A—H3A10.9900
C3—H3B0.9900C3A—H3A20.9900
C3—H3C0.9900C4A—C5A1.508 (7)
C4—C51.514 (7)C4A—H4A10.9900
C4—H4A0.9900C4A—H4A20.9900
C4—H4B0.9900C5A—C6A1.523 (6)
C5—C61.531 (8)C5A—H5A10.9900
C5—H5A0.9900C5A—H5A20.9900
C5—H5B0.9900C6A—H6A10.9900
C6—H6A0.9900C6A—H6A20.9900
C6—H6B0.9900C7A—H7A10.9900
C7—H7A0.9900C7A—H7A20.9900
C7—H7B0.9900C8A—H8A10.9900
C8—H8A0.9900C8A—H8A20.9900
C8—H8B0.9900C9A—H9A10.9900
C9—H9A0.9900C9A—H9A20.9900
C9—H9B0.9900C10A—H10C0.9900
C10—H10A0.9900C10A—H10D0.9900
C10—H10B0.9900C11A—H11C0.9900
C11—H11A0.9900C11A—H11D0.9900
C11—H11B0.9900N21A—O22A1.227 (7)
N21—O231.226 (6)N21A—O23A1.229 (6)
N21—O221.227 (8)N21A—C24A1.448 (7)
N21—C241.452 (7)O21A—C21A1.329 (6)
O21—C211.324 (6)O21A—H21A1.18 (9)
O21—H210.91 (6)C21A—C26A1.396 (6)
C21—C221.398 (6)C21A—C22A1.397 (6)
C21—C261.401 (6)C22A—C23A1.367 (7)
C22—C231.367 (7)C22A—H22A0.9500
C22—H220.9500C23A—C24A1.385 (7)
C23—C241.374 (7)C23A—H23A0.9500
C23—H230.9500C24A—C25A1.373 (7)
C24—C251.377 (7)C25A—C26A1.381 (7)
C25—C261.372 (7)C25A—H25A0.9500
C25—H250.9500C26A—H26A0.9500
C26—H260.9500N31A—O33A1.234 (6)
N31—O321.230 (6)N31A—O32A1.239 (6)
N31—O331.235 (6)N31A—C34A1.428 (7)
N31—C341.437 (7)O31A—C31A1.298 (6)
O31—C311.308 (6)O31A—H21A1.35 (9)
C31—C361.415 (6)C31A—C32A1.404 (6)
C31—C321.423 (6)C31A—C36A1.408 (6)
C32—C331.359 (7)C32A—C33A1.375 (7)
C32—H320.9500C32A—H32A0.9500
C33—C341.378 (7)C33A—C34A1.388 (7)
C33—H330.9500C33A—H33A0.9500
C34—C351.392 (7)C34A—C35A1.391 (6)
C35—C361.356 (7)C35A—C36A1.379 (7)
C35—H350.9500C35A—H35A0.9500
C36—H360.9500C36A—H36A0.9500
N1A—C7A1.437 (5)
C9—N1—C8111.0 (4)C7A—N1A—C1A118.1 (3)
C9—N1—C1112.7 (3)C9A—N1A—C1A112.2 (3)
C8—N1—C1117.5 (3)C10A—N2A—C2A112.7 (3)
C10—N2—C7111.6 (3)C10A—N2A—C8A110.7 (4)
C10—N2—C2117.4 (3)C2A—N2A—C8A118.4 (4)
C7—N2—C2112.1 (3)C11A—N4A—C9A108.2 (3)
C11—N3—C9105.9 (3)C11A—N4A—C8A109.2 (4)
C11—N3—C10109.0 (3)C9A—N4A—C8A114.3 (3)
C9—N3—C10114.6 (3)C11A—N3A—C10A106.2 (3)
C11—N3—H3107 (4)C11A—N3A—C7A109.3 (3)
C9—N3—H3114 (3)C10A—N3A—C7A113.7 (3)
C10—N3—H3106 (3)C11A—N3A—H3A108 (3)
C11—N4—C7107.2 (4)C10A—N3A—H3A109 (2)
C11—N4—C8110.1 (3)C7A—N3A—H3A110 (2)
C7—N4—C8114.0 (4)N1A—C1A—C6A115.2 (3)
N1—C1—C6114.4 (3)N1A—C1A—C2A113.4 (3)
N1—C1—C2114.9 (3)C6A—C1A—C2A109.6 (3)
C6—C1—C2108.0 (3)N1A—C1A—H1A106.0
N1—C1—H1106.3C6A—C1A—H1A106.0
C6—C1—H1106.3C2A—C1A—H1A106.0
C2—C1—H1106.3N2A—C2A—C1A114.2 (3)
N2—C2—C3114.6 (3)N2A—C2A—C3A113.4 (3)
N2—C2—C1114.4 (3)C1A—C2A—C3A109.2 (3)
C3—C2—C1108.7 (3)N2A—C2A—H2A106.5
N2—C2—H2106.2C1A—C2A—H2A106.5
C3—C2—H2106.2C3A—C2A—H2A106.5
C1—C2—H2106.2C4A—C3A—C2A109.6 (3)
C2—C3—C4108.7 (4)C4A—C3A—H3A1109.8
C2—C3—H3B109.9C2A—C3A—H3A1109.8
C4—C3—H3B109.9C4A—C3A—H3A2109.8
C2—C3—H3C109.9C2A—C3A—H3A2109.8
C4—C3—H3C109.9H3A1—C3A—H3A2108.2
H3B—C3—H3C108.3C5A—C4A—C3A112.7 (4)
C5—C4—C3113.1 (4)C5A—C4A—H4A1109.1
C5—C4—H4A109.0C3A—C4A—H4A1109.1
C3—C4—H4A109.0C5A—C4A—H4A2109.1
C5—C4—H4B109.0C3A—C4A—H4A2109.1
C3—C4—H4B109.0H4A1—C4A—H4A2107.8
H4A—C4—H4B107.8C4A—C5A—C6A112.0 (4)
C4—C5—C6112.9 (4)C4A—C5A—H5A1109.2
C4—C5—H5A109.0C6A—C5A—H5A1109.2
C6—C5—H5A109.0C4A—C5A—H5A2109.2
C4—C5—H5B109.0C6A—C5A—H5A2109.2
C6—C5—H5B109.0H5A1—C5A—H5A2107.9
H5A—C5—H5B107.8C1A—C6A—C5A109.5 (3)
C1—C6—C5108.9 (4)C1A—C6A—H6A1109.8
C1—C6—H6A109.9C5A—C6A—H6A1109.8
C5—C6—H6A109.9C1A—C6A—H6A2109.8
C1—C6—H6B109.9C5A—C6A—H6A2109.8
C5—C6—H6B109.9H6A1—C6A—H6A2108.2
H6A—C6—H6B108.3N1A—C7A—N3A115.1 (3)
N2—C7—N4113.8 (3)N1A—C7A—H7A1108.5
N2—C7—H7A108.8N3A—C7A—H7A1108.5
N4—C7—H7A108.8N1A—C7A—H7A2108.5
N2—C7—H7B108.8N3A—C7A—H7A2108.5
N4—C7—H7B108.8H7A1—C7A—H7A2107.5
H7A—C7—H7B107.7N2A—C8A—N4A115.5 (3)
N1—C8—N4115.9 (4)N2A—C8A—H8A1108.4
N1—C8—H8A108.3N4A—C8A—H8A1108.4
N4—C8—H8A108.3N2A—C8A—H8A2108.4
N1—C8—H8B108.3N4A—C8A—H8A2108.4
N4—C8—H8B108.3H8A1—C8A—H8A2107.5
H8A—C8—H8B107.4N1A—C9A—N4A113.1 (4)
N1—C9—N3112.0 (3)N1A—C9A—H9A1109.0
N1—C9—H9A109.2N4A—C9A—H9A1109.0
N3—C9—H9A109.2N1A—C9A—H9A2109.0
N1—C9—H9B109.2N4A—C9A—H9A2109.0
N3—C9—H9B109.2H9A1—C9A—H9A2107.8
H9A—C9—H9B107.9N2A—C10A—N3A110.9 (3)
N2—C10—N3114.1 (3)N2A—C10A—H10C109.5
N2—C10—H10A108.7N3A—C10A—H10C109.5
N3—C10—H10A108.7N2A—C10A—H10D109.5
N2—C10—H10B108.7N3A—C10A—H10D109.5
N3—C10—H10B108.7H10C—C10A—H10D108.0
H10A—C10—H10B107.6N4A—C11A—N3A108.8 (4)
N4—C11—N3108.5 (4)N4A—C11A—H11C109.9
N4—C11—H11A110.0N3A—C11A—H11C109.9
N3—C11—H11A110.0N4A—C11A—H11D109.9
N4—C11—H11B110.0N3A—C11A—H11D109.9
N3—C11—H11B110.0H11C—C11A—H11D108.3
H11A—C11—H11B108.4O22A—N21A—O23A123.3 (5)
O23—N21—O22123.3 (6)O22A—N21A—C24A118.4 (5)
O23—N21—C24118.3 (6)O23A—N21A—C24A118.4 (5)
O22—N21—C24118.3 (5)C21A—O21A—H21A113 (5)
C21—O21—H21109 (4)O21A—C21A—C26A118.4 (4)
O21—C21—C22118.4 (4)O21A—C21A—C22A122.5 (4)
O21—C21—C26122.4 (4)C26A—C21A—C22A119.1 (4)
C22—C21—C26119.1 (4)C23A—C22A—C21A120.7 (4)
C23—C22—C21120.2 (4)C23A—C22A—H22A119.6
C23—C22—H22119.9C21A—C22A—H22A119.6
C21—C22—H22119.9C22A—C23A—C24A119.1 (5)
C22—C23—C24119.5 (4)C22A—C23A—H23A120.5
C22—C23—H23120.3C24A—C23A—H23A120.5
C24—C23—H23120.3C25A—C24A—C23A121.5 (5)
C23—C24—C25121.8 (5)C25A—C24A—N21A119.7 (5)
C23—C24—N21119.8 (5)C23A—C24A—N21A118.8 (5)
C25—C24—N21118.4 (5)C24A—C25A—C26A119.4 (4)
C26—C25—C24119.1 (5)C24A—C25A—H25A120.3
C26—C25—H25120.4C26A—C25A—H25A120.3
C24—C25—H25120.4C25A—C26A—C21A120.1 (4)
C25—C26—C21120.3 (4)C25A—C26A—H26A120.0
C25—C26—H26119.9C21A—C26A—H26A120.0
C21—C26—H26119.9O33A—N31A—O32A122.3 (5)
O32—N31—O33122.6 (5)O33A—N31A—C34A118.8 (5)
O32—N31—C34119.2 (4)O32A—N31A—C34A118.8 (5)
O33—N31—C34118.2 (5)C31A—O31A—H21A111 (4)
O31—C31—C36120.8 (4)O31A—C31A—C32A121.2 (4)
O31—C31—C32122.3 (4)O31A—C31A—C36A121.9 (4)
C36—C31—C32116.9 (4)C32A—C31A—C36A116.9 (4)
C33—C32—C31121.1 (4)C33A—C32A—C31A121.7 (4)
C33—C32—H32119.5C33A—C32A—H32A119.1
C31—C32—H32119.5C31A—C32A—H32A119.1
C32—C33—C34120.3 (4)C32A—C33A—C34A119.4 (5)
C32—C33—H33119.8C32A—C33A—H33A120.3
C34—C33—H33119.8C34A—C33A—H33A120.3
C33—C34—C35120.3 (5)C33A—C34A—C35A121.1 (5)
C33—C34—N31120.0 (4)C33A—C34A—N31A119.3 (5)
C35—C34—N31119.7 (4)C35A—C34A—N31A119.6 (5)
C36—C35—C34120.1 (4)C36A—C35A—C34A118.5 (4)
C36—C35—H35120.0C36A—C35A—H35A120.8
C34—C35—H35120.0C34A—C35A—H35A120.8
C35—C36—C31121.3 (4)C35A—C36A—C31A122.3 (4)
C35—C36—H36119.3C35A—C36A—H36A118.8
C31—C36—H36119.3C31A—C36A—H36A118.8
C7A—N1A—C9A110.4 (4)
C9—N1—C1—C6143.5 (4)C7A—N1A—C1A—C6A89.1 (4)
C8—N1—C1—C685.5 (4)C9A—N1A—C1A—C6A140.8 (4)
C9—N1—C1—C290.7 (4)C7A—N1A—C1A—C2A38.3 (5)
C8—N1—C1—C240.4 (5)C9A—N1A—C1A—C2A91.9 (4)
C10—N2—C2—C383.7 (4)C10A—N2A—C2A—C1A94.6 (4)
C7—N2—C2—C3145.2 (3)C8A—N2A—C2A—C1A36.8 (4)
C10—N2—C2—C142.8 (5)C10A—N2A—C2A—C3A139.5 (4)
C7—N2—C2—C188.3 (4)C8A—N2A—C2A—C3A89.2 (4)
N1—C1—C2—N234.2 (5)N1A—C1A—C2A—N2A38.8 (4)
C6—C1—C2—N2163.2 (4)C6A—C1A—C2A—N2A169.0 (3)
N1—C1—C2—C3163.6 (4)N1A—C1A—C2A—C3A166.9 (3)
C6—C1—C2—C367.3 (4)C6A—C1A—C2A—C3A62.9 (4)
N2—C2—C3—C4168.5 (4)N2A—C2A—C3A—C4A172.9 (4)
C1—C2—C3—C462.2 (5)C1A—C2A—C3A—C4A58.5 (5)
C2—C3—C4—C553.8 (6)C2A—C3A—C4A—C5A54.1 (6)
C3—C4—C5—C649.9 (7)C3A—C4A—C5A—C6A53.0 (6)
N1—C1—C6—C5169.7 (3)N1A—C1A—C6A—C5A170.2 (4)
C2—C1—C6—C561.0 (4)C2A—C1A—C6A—C5A60.5 (5)
C4—C5—C6—C153.1 (6)C4A—C5A—C6A—C1A55.4 (5)
C10—N2—C7—N453.2 (5)C9A—N1A—C7A—N3A46.1 (4)
C2—N2—C7—N480.9 (4)C1A—N1A—C7A—N3A84.9 (4)
C11—N4—C7—N263.6 (5)C11A—N3A—C7A—N1A48.4 (4)
C8—N4—C7—N258.5 (5)C10A—N3A—C7A—N1A70.1 (5)
C9—N1—C8—N447.2 (5)C10A—N2A—C8A—N4A48.4 (5)
C1—N1—C8—N484.6 (5)C2A—N2A—C8A—N4A83.8 (4)
C11—N4—C8—N150.6 (5)C11A—N4A—C8A—N2A51.7 (5)
C7—N4—C8—N169.9 (5)C9A—N4A—C8A—N2A69.7 (5)
C8—N1—C9—N353.7 (5)C7A—N1A—C9A—N4A53.9 (4)
C1—N1—C9—N380.5 (4)C1A—N1A—C9A—N4A80.1 (4)
C11—N3—C9—N163.0 (4)C11A—N4A—C9A—N1A64.6 (5)
C10—N3—C9—N157.3 (5)C8A—N4A—C9A—N1A57.3 (5)
C7—N2—C10—N345.6 (4)C2A—N2A—C10A—N3A81.1 (4)
C2—N2—C10—N385.8 (5)C8A—N2A—C10A—N3A54.0 (4)
C11—N3—C10—N249.2 (5)C11A—N3A—C10A—N2A63.4 (4)
C9—N3—C10—N269.3 (5)C7A—N3A—C10A—N2A56.8 (5)
C7—N4—C11—N365.5 (4)C9A—N4A—C11A—N3A64.9 (4)
C8—N4—C11—N359.0 (4)C8A—N4A—C11A—N3A60.1 (4)
C9—N3—C11—N464.9 (4)C10A—N3A—C11A—N4A66.4 (4)
C10—N3—C11—N458.9 (4)C7A—N3A—C11A—N4A56.7 (4)
O21—C21—C22—C23179.2 (4)O21A—C21A—C22A—C23A179.2 (4)
C26—C21—C22—C231.4 (7)C26A—C21A—C22A—C23A0.2 (7)
C21—C22—C23—C240.9 (7)C21A—C22A—C23A—C24A0.7 (7)
C22—C23—C24—C250.2 (8)C22A—C23A—C24A—C25A1.3 (7)
C22—C23—C24—N21179.8 (5)C22A—C23A—C24A—N21A179.3 (5)
O23—N21—C24—C230.2 (8)O22A—N21A—C24A—C25A178.7 (5)
O22—N21—C24—C23179.0 (6)O23A—N21A—C24A—C25A2.1 (8)
O23—N21—C24—C25179.7 (6)O22A—N21A—C24A—C23A0.8 (8)
O22—N21—C24—C251.0 (8)O23A—N21A—C24A—C23A178.5 (5)
C23—C24—C25—C260.1 (8)C23A—C24A—C25A—C26A0.9 (7)
N21—C24—C25—C26180.0 (5)N21A—C24A—C25A—C26A179.7 (5)
C24—C25—C26—C210.6 (7)C24A—C25A—C26A—C21A0.1 (7)
O21—C21—C26—C25179.3 (4)O21A—C21A—C26A—C25A178.8 (4)
C22—C21—C26—C251.3 (7)C22A—C21A—C26A—C25A0.6 (7)
O31—C31—C32—C33178.3 (4)O31A—C31A—C32A—C33A177.8 (5)
C36—C31—C32—C331.7 (7)C36A—C31A—C32A—C33A2.9 (7)
C31—C32—C33—C340.1 (7)C31A—C32A—C33A—C34A1.4 (7)
C32—C33—C34—C351.5 (7)C32A—C33A—C34A—C35A0.7 (7)
C32—C33—C34—N31177.7 (5)C32A—C33A—C34A—N31A179.2 (5)
O32—N31—C34—C332.5 (7)O33A—N31A—C34A—C33A178.1 (4)
O33—N31—C34—C33178.9 (4)O32A—N31A—C34A—C33A3.0 (7)
O32—N31—C34—C35178.3 (4)O33A—N31A—C34A—C35A2.0 (7)
O33—N31—C34—C350.2 (7)O32A—N31A—C34A—C35A176.9 (5)
C33—C34—C35—C361.0 (7)C33A—C34A—C35A—C36A1.2 (7)
N31—C34—C35—C36178.2 (4)N31A—C34A—C35A—C36A178.7 (4)
C34—C35—C36—C310.9 (7)C34A—C35A—C36A—C31A0.4 (7)
O31—C31—C36—C35177.8 (4)O31A—C31A—C36A—C35A178.3 (4)
C32—C31—C36—C352.2 (7)C32A—C31A—C36A—C35A2.5 (7)
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
O21—H21···O310.91 (6)1.62 (6)2.527 (5)169 (5)
O21A—H21A···O31A1.18 (9)1.35 (9)2.515 (4)166 (9)
N3—H3···O310.93 (7)1.80 (6)2.693 (5)161 (5)
N3A—H3A···O31A0.98 (5)1.74 (5)2.723 (5)174 (4)
C11—H11B···O32A0.992.483.294 (7)139
C7A—H7A1···O220.992.313.197 (8)149
C9—H9A···N2i0.992.493.169 (5)126
C10A—H10C···O21Aii0.992.273.241 (5)167
C11—H11A···O33Aii0.992.533.369 (7)142
C8A—H8A1···O33Aiii0.992.493.404 (6)154
C9A—H9A2···O32Aiii0.992.483.456 (6)170
C8—H8A···O33iv0.992.563.461 (6)151
C9—H9B···O22Av0.992.353.256 (7)152
C10—H10B···O21ii0.992.413.338 (5)156
Symmetry codes: (i) x1, y, z; (ii) x+1, y, z; (iii) x+1, y1/2, z+1; (iv) x+2, y+1/2, z+2; (v) x+1, y, z+1.
C—N bond lengths around the protonated N atom for free and protonated azaadamantane structures (Å) top
CompoundαC—NβC—NReference
(I)1.458–1.4741.461, 1.472Rivera et al. (2012)
(III)1.4621.462Grochowski et al. (1994)
(II)1.503–1.5391.422–1.444Present work
(III)+OS1.472–1.5101.441–1.472Chandrasekhar & Mukherjee (2015)
(III)+FM1.509–1.5151.439–1.447Bowes et al. (2003)
Notes: OS = organic salts (succinate, malate, phthalate and 4-hydroxybenzoate) and FM = fumarate.
The most important donor–acceptor natural bond orbital interactionsa and their second-order perturbation stabilization energies, ΔE2 (kcal mol-1) calculated for (Ia). top
Donor NBO (i)Acceptor NBO (j)InteractionΔE2
LPN2σ*N3—C10nσ*21.21
LPN1σ*N3—C9nσ*18.75
LPN4σ*N3—C11nσ*14.97
LPN1σ*N4—C8nσ*10.61
LPN2σ*N4—C7nσ*10.14
LPN4σ*N1—C8nσ*10.01
LPN4σ*N2—C7nσ*9.79
Partial sum of above most important interactions95.50
Sum of all E2 interactions128.6
Notes: (a) selected interactions are those with the largest E2 contribution and, as expected, they are delocalizations of neighbouring C—N bonds. The remainder (ca 25% of E2 energy) are delocalizations of the C—C antibonding orbitals of the cyclohexane ring (mostly the C1—C2 bond, which is thus the longest in the ring) and of the C—H antibonding orbitals of the CH2 groups of the cage.
 

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