Home Crystal structure of 3,3′-(1,2-phenylenebis(methylene))bis(1-methyl-1H-imidazol-3-ium) bis(hexafluoridophosphate), C16H20F12N4P2
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Crystal structure of 3,3′-(1,2-phenylenebis(methylene))bis(1-methyl-1H-imidazol-3-ium) bis(hexafluoridophosphate), C16H20F12N4P2

  • Zhou Yao-Hong , Huang Ting , Nie Xu-Liang ORCID logo , Chen Jing and Xiong Wan-Ming EMAIL logo
Published/Copyright: July 2, 2020

Abstract

C16H20F12N4P2, monoclinic, P21/c (no. 14), a = 7.3086(15) Å, b = 12.174(3) Å, c = 26.355(6) Å, β = 94.500(2)°, V = 2337.6(8) Å3, Z = 4, Rgt(F) = 0.0742, wRref(F2) = 0.2262, T = 296(2) K.

CCDC no.: 2010830

The molecular structure is shown in the figure. Table 1 contains crystallographic data and Table 2 contains the list of the atoms including atomic coordinates and displacement parameters.

Table 1:

Data collection and handling.

Crystal:Colorless block
Size:0.20 × 0.17 × 0.15 mm
Wavelength:Mo Kα radiation (0.71073 Å)
μ:0.29 mm−1
Diffractometer, scan mode:Bruker APEX-II, φ and ω
θmax, completeness:25.5°, >99%
N(hkl)measured, N(hkl)unique, Rint:17696, 4351, 0.027
Criterion for Iobs, N(hkl)gt:Iobs > 2 σ(Iobs), 3316
N(param)refined:309
Programs:Bruker [1], SHELX [2], [3], Diamond [4]
Table 2:

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

AtomxyzUiso*/Ueq
C10.1649(5)0.3971(3)0.66220(14)0.0431(8)
C20.1323(5)0.3453(3)0.70776(15)0.0512(10)
H20.20910.28890.72020.061*
C3−0.0137(6)0.3775(4)0.73465(15)0.0541(10)
H3−0.03650.34200.76470.065*
C4−0.1249(6)0.4623(4)0.71665(16)0.0550(10)
H4−0.22150.48520.73510.066*
C5−0.0940(5)0.5136(3)0.67144(15)0.0506(9)
H5−0.17040.57060.65950.061*
C60.0497(5)0.4811(3)0.64378(14)0.0413(8)
C70.3283(6)0.3650(4)0.63315(18)0.0583(11)
H7A0.29250.36790.59690.070*
H7B0.42580.41810.64040.070*
C80.0856(5)0.5355(3)0.59381(15)0.0502(9)
H8A0.20120.57490.59820.060*
H8B0.09820.47890.56840.060*
C90.5603(5)0.2327(3)0.66977(15)0.0496(9)
H90.64710.28400.68210.060*
C100.4231(7)0.0776(4)0.6510(2)0.0699(13)
H100.39980.00260.64850.084*
C110.3106(7)0.1585(4)0.6337(2)0.0695(13)
H110.19510.15040.61660.083*
C120.7366(7)0.0673(5)0.6973(2)0.0797(16)
H12A0.78750.01990.67300.120*
H12B0.69890.02420.72520.120*
H12C0.82750.11960.70980.120*
C13−0.0521(6)0.7197(4)0.57865(16)0.0545(10)
H130.04420.76020.59440.065*
C14−0.2220(6)0.5833(4)0.54924(17)0.0602(11)
H14−0.26230.51250.54120.072*
C15−0.3128(6)0.6771(4)0.53787(19)0.0672(13)
H15−0.42830.68320.52060.081*
C16−0.2498(9)0.8783(4)0.5513(2)0.0917(19)
H16A−0.14240.92100.56120.138*
H16B−0.34520.89620.57300.138*
H16C−0.29080.89450.51660.138*
N10.3987(4)0.2555(3)0.64592(13)0.0506(8)
N20.5776(5)0.1254(3)0.67302(13)0.0554(9)
N3−0.0582(4)0.6119(3)0.57502(12)0.0477(8)
N4−0.2057(5)0.7611(3)0.55623(14)0.0600(10)
P10.53757(15)0.23823(9)0.82279(4)0.0523(3)
P20.19576(15)0.77518(10)0.45696(4)0.0531(3)
F10.6281(5)0.3101(3)0.86834(13)0.1000(11)
F20.4456(5)0.1675(3)0.77745(12)0.0878(9)
F30.5182(4)0.1379(3)0.86050(12)0.0839(9)
F40.5557(4)0.3382(2)0.78450(11)0.0794(8)
F50.7355(4)0.1961(3)0.81161(14)0.0931(10)
F60.3417(4)0.2803(3)0.83457(12)0.0913(10)
F70.2538(5)0.7065(6)0.50536(17)0.169(3)
F80.1368(6)0.8391(6)0.40864(18)0.180(3)
F90.1263(10)0.8624(4)0.4912(3)0.205(3)
F100.2708(10)0.6852(3)0.4248(2)0.198(3)
F110.3860(5)0.8305(5)0.45589(17)0.1450(19)
F120.0058(5)0.7173(4)0.45793(15)0.1268(16)

Source of material

1-Methylimidazole (2.62 g, 0.032 mol) and 1,2-bis(bromomethyl)benzene (4.22 g, 0.016 mol) was added into a flask containing toluene (25 mL). Then the mixture was stirred vigorously at 105 °C for 16 h. After the reaction has been completed (monitored by TLC), the toluene top phase was decanted and the product was washed with ethyl acetate and anhydrous diethyl ether 3 times respectively. The intermediate product was dried in vacuo at 60 °C for 1 h to give a white powder in 98.9% yield. During the anion exchange reaction, the intermediate (1.07 g, 0.0025 mol) and KPF6 (0.92 g, 0.005 mol) were dissolved in water (25 mL), and the reaction proceeded at 95 °C for 10 h before the reaction mixture was allowed to cool slowly to room temperature. After deionized water washing and air drying, the final product was obtained in 90.5% yield.

Experimental details

All H atoms were included in calculated positions and refined as riding atoms, with C—H = 0.90–0.97 Å with Uiso(H) = 1.5 Ueq(C) for methyl H atoms and 1.2 Ueq(C) for all other H atoms.

Comment

Ionic liquid (ILs) refers to a salt composed solely of ions which generally has a melting point of 100 °C or below [5]. Because of the advantages of low volatility, non-flammability, high polarity, wide window of electrochemical performance, and large structural adjustability, it has been widely studied and applied [6], [7], [8], [9]. When the anion is hexafluorophosphate, this imidazole-based ionic liquids may show good hydrophobicity, and even temperature sensitivity of solubility. They can realize the function of “low temperature heterogeneous, high temperature homogeneous” in water or some organic solvents, which has application prospect in synthesis and natural product extraction [10], [11]. On the basis of our earlier work on aliphatic chain hydrocarbons [12], [13], [14], we now used halogenated arenes as starting material to react with methylimidazole, and the corresponding compound was obtained.

In the molecule of the title compound bond lengths and angles are very similar to those given in the literature [14]. The atoms of imidazole ring are coplanar, and the dihedral angle of the two imidazole rings and the phenyl group are 3.8(2)°, 82.8(2)° and 79.5(2)°, respectively. The torsion angles of C1—C7—N1—C9, and C6—C8—N3—C13 are 101.0(5)° and −112.9(4)°, respectively.

Acknowledgements

X-ray data were collected at Instrumental Analysis Center Nanchang Hangkong University, Nanchang, China. This work was supported by the National Natural Science Foundation of China (No. 31760193) and the Key Research Foundation of Educational Department of Jiangxi Province of China [GJJ190181].

References

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Received: 2020-06-02
Accepted: 2020-06-19
Published Online: 2020-07-02
Published in Print: 2020-08-26

©2020 Zhou Yao-Hong et al., published by De Gruyter, Berlin/Boston

This work is licensed under the Creative Commons Attribution 4.0 International License.

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  66. The crystal structure of 4a-formyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydro-1-2-6a,6b,9,9,12a-heptamethylpicen-10-yl acetate, C32H50O3
  67. Crystal structure of 3,3′-(1,2-phenylenebis(methylene))bis(1-methyl-1H-imidazol-3-ium) bis(hexafluoridophosphate), C16H20F12N4P2
  68. Crystal structure of catena-poly[diaqua-(μ2-tartrato-κ4O,O′:O′′,O′′′)zinc(II)], C4H8O8Zn
  69. The crystal structure of (6aR,6bS,8aS,8bR,9S,11aS,12aS,12bS)-10-(4-acetoxy-3-methylbutyl)-6a,8a,9-trimethyl-3,4,5,6,6a,6b,7,8,8a,8b,9,10,11a,12,12a,12b-hexadecahydro-1H-naphtho[2′,1′:4,5]indeno[2,1-b]furan-4-yl acetate, C31H48O5
  70. Crystal structure of 4,4′-(oxybis(methylene))bis(bromobenzene), C14H12Br2O
  71. Crystal structure of (N,N-dimethylsulphoxide)-[N-(3-ethoxy-2-(oxide)benzylidene)-3-methoxybenzenecarbohydrazonato-κ3N,O,O′]-dioxo-molybdenum(VI), C19H22MoN2O7S
  72. Crystal structure of dichlorido-bis(dimethyl sulphoxide-κO)-bis(4-methylbenzyl-κC1)tin(IV), C20H30Cl2O2S2Sn
  73. Crystal structure of (E)-2-amino-N′-(2-hydroxy-4-(2-(piperidin-1-yl)ethoxy)benzylidene)benzohydrazide monohydrate, C21H26N4O3 ⋅ H2O
  74. Crystal structure of chloridotris(4-chlorophenyl)(dimethyl sulfoxide-κO)tin(IV), C20H18Cl4OSSn
  75. Crystal structure of catena{di-aqua-sodium-[N-(hydroxyethyl), N-isopropyl-dithiocarbamato]}n, [C6H16NNaO2S2]n
  76. Crystal structure of 2,2,4,4,6,6-hexakis(4-chlorophenyl)-1,3,5,2,4,6-trithiatristanninane, C36H24Cl6S3Sn3
  77. Crystal structure of 6-methoxy-3-(5-(3-methoxyphenyl)-1,3,4-oxadiazol-2-yl)-4H-chromen-4-one-methanol (1/1), C20H18N2O6
  78. Crystal structure of hexanedihydrazide, C6H14N4O2
  79. Crystal structure of tert-butyl 2-(hydroxymethyl)-5-{4-[(methoxycarbonyl)amino]phenyl}-2,5-dihydro-1H-pyrrole-1-carboxylate, C18H24N2O5
  80. Crystal structure of [(Z)-O-isopropyl N-(4-nitrophenyl)thiocarbamato-κS]-(triphenylphosphine-κP)-gold(I), C28H26AuN2O3PS
  81. Crystal structure of [O-ethyl N-(4-nitrophenyl)thiocarbamato-κS](tri-4-tolylphosphine-κP)gold(I) tetrahydrofuran solvate, C30H30AuN2O3PS, C4H8O
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