Home Physical Sciences The crystal structure of diaqua-2,2′-((cyclohexane-1,2-diylbis(azanylylidene))bis(methanylylidene))diphenolato-κ4N,N′,O,O′)manganese(III) perchlorate, C20H24MnClN2O4
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The crystal structure of diaqua-2,2′-((cyclohexane-1,2-diylbis(azanylylidene))bis(methanylylidene))diphenolato-κ4N,N′,O,O′)manganese(III) perchlorate, C20H24MnClN2O4

  • Hongping Ju , Zihao Chen , Jing Qin , Yu Lang , Yunhui Ren , Ping Li , Nan Li and Kaihua Zhou EMAIL logo
Published/Copyright: February 13, 2018

Abstract

C20H24MnClN2O4, triclinic, P1̅ (no. 2), a = 7.9912(8) Å, b = 11.8174(9) Å, c = 12.7781(15) Å, α = 112.855(9)°, β = 97.649(9)°, γ = 91.215(7)°, V = 1098.6(2) Å3, Z = 2; Rgt(F) = 0.0491, wRref(F2) = 0.1319, T = 250(2) K.

CCDC no.:: 1817607

A part of the title crystal structure is shown in the figure. Tables 1 and 2 contain details of the measurement method and a list of the atoms including atomic coordinates and displacement parameters.

Table 1:

Data collection and handling.

Crystal:Block, brown
Wavelength:Mo Kα radiation (0.71073 Å)
μ:0.77 mm−1
Diffractometer, scan mode:Xcalibur, ω-scans
2θmax, completeness:25°, >99%
N(hkl)measured, N(hkl)unique, Rint:7226, 3855, 0.033
Criterion for Iobs, N(hkl)gt:Iobs > 2 σ(Iobs), 3038
N(param)refined:305
Programs:CrysAlisPRO[1], SHELX [2, 3] , DIAMOND [4]
Table 2:

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

AtomxyzUiso*/Ueq
Cl10.78794(13)0.29436(9)0.27489(9)0.0503(3)
Mn10.24919(7)0.38384(4)0.04312(4)0.03245(18)
O10.2438(3)0.3987(2)−0.09764(19)0.0395(6)
H1WA−0.096(7)0.373(5)−0.034(5)0.10(2)*
H1WB−0.005(5)0.411(4)0.077(4)0.044(11)*
O1W−0.0367(4)0.3427(3)0.0041(3)0.0498(7)
O20.2364(4)0.5532(2)0.1210(2)0.0501(7)
H2WA0.523(4)0.344(3)0.006(3)0.021(8)*
H2WB0.592(6)0.482(4)0.091(4)0.078(15)*
O2W0.5332(4)0.4092(3)0.0828(3)0.0612(8)
O40.8001(5)0.2809(3)0.1598(3)0.0884(12)
O50.7699(7)0.1771(3)0.2743(3)0.1138(16)
O60.9284(5)0.3615(4)0.3502(4)0.1182(16)
O70.6434(4)0.3576(4)0.3044(3)0.0854(11)
N10.2647(4)0.2043(2)−0.0261(2)0.0348(7)
N20.2509(4)0.3535(3)0.1848(2)0.0383(7)
C10.2879(5)0.6196(3)0.2330(3)0.0412(9)
C20.3174(6)0.7447(3)0.2704(3)0.0589(12)
H2A0.30590.78110.21650.071*
C30.3631(8)0.8176(4)0.3844(4)0.0806(17)
H3A0.38330.90320.40770.097*
C40.3798(8)0.7672(4)0.4657(4)0.0827(17)
H4A0.41160.81740.54400.099*
C50.3495(6)0.6436(4)0.4303(3)0.0619(12)
H5A0.35880.60900.48560.074*
C60.3052(5)0.5661(3)0.3147(3)0.0406(9)
C70.2784(5)0.4374(3)0.2861(3)0.0414(9)
H7A0.28130.41200.34740.050*
C80.2161(5)0.2212(3)0.1592(3)0.0457(9)
H8A0.09330.19980.13140.055*
C90.2615(6)0.1833(3)0.2603(3)0.0510(10)
H9A0.38180.20610.29200.061*
H9B0.19460.22610.32100.061*
C100.2248(7)0.0450(4)0.2189(4)0.0722(14)
H10A0.26160.01990.28240.087*
H10B0.10230.02470.19660.087*
C110.3102(7)−0.0252(4)0.1205(4)0.0718(14)
H11A0.2754−0.11310.09430.086*
H11B0.4330−0.01390.14570.086*
C120.2695(6)0.0144(3)0.0206(3)0.0499(10)
H12A0.3366−0.0292−0.03970.060*
H12B0.1493−0.0071−0.01190.060*
C130.3088(5)0.1517(3)0.0614(3)0.0459(10)
H13A0.43190.17020.08970.055*
C140.2410(5)0.1389(3)−0.1346(3)0.0395(8)
H14A0.24540.0533−0.15770.047*
C150.2084(5)0.1840(3)−0.2239(3)0.0382(8)
C160.1768(6)0.0987(4)−0.3372(3)0.0588(12)
H16A0.17900.0144−0.35220.071*
C170.1429(7)0.1337(4)−0.4267(4)0.0768(16)
H17A0.12120.0744−0.50260.092*
C180.1408(7)0.2581(4)−0.4045(4)0.0725(15)
H18A0.11700.2830−0.46600.087*
C190.1726(6)0.3445(4)−0.2952(3)0.0557(11)
H19A0.17030.4284−0.28200.067*
C200.2086(5)0.3101(3)−0.2022(3)0.0375(8)

Source of material

A mixture of salicylaldehyde (0.045 g, 0.2 mmol), (+ −)1.2-cyclohexanediamine (0.011 g, 0.1 mmol) and triethylamine (0.005 g, 0.01 mmol) were dissolved in ethanol (2 mL), forming a yellow solution. A second solution made by dissolving 0.361 g (1.0 mmol) of Mn(ClO4)2⋅6H2O (0.072 g, 0.2 mmol) in 20 mL of water was added dropwise to the aforementioned solution. After left to stir overnight in a conical flask at 40 °C, a brown solution was obtained. After filtration, the filtrate was sealed with parafilm containing tiny pores for slow evaporation. Dark-brown crystals of the title compound were isolated after 2 weeks. In 69.7% yield by filtration, washed with metanol, and dried in air.

Experimental details

H atoms were generated geometrically and refined as riding atoms with C—H = 0.93 Å and Uiso(H) = 1.2 times Ueq(C) for benzene H atoms, with C—H = 0.98 Åand Uiso(H) = 1.2 times, Ueq(C) for cyclohexane H atoms.

Discussion

The design and synthesis of manganese tetradentate Schiff-base ligands (salen) complexes have provoked wide interest for their specific magnetic and catalytic behaviors [5, 6] . So far, although, dozens of Mn-salen type complexes have been isolated [7], [8], [9], [10], the isolation of new salen based Mn complexes remains a highly rewarding research area, since the Mn-salen family is a well researched field, systematically explore the relationship between reaction conditions and the structures may provide more clues for further understanding the formation mechanisms of complexes or crystalline materials [11], [12], [13].

The title compound crystallizes in the triclinic space group P1̅, which is constructed by one mononuclear Mn-salcy cation as well as one perchlorate. The central manganese atom is chelated with one salcy ligand via N2O2 in the equatorial plane. The bond lengths of Mn(1)—N(1), Mn(1)—N(2), Mn(1)—O(1) and Mn(1)—O(1) are 1.9759(32), 1.9702(22), 1.8689(27) and 1.8695(22) Å, respectively. In the apical position, MnIII is coordinated by two oxygen atoms from water ligands. The bond lengths of Mn1—O1W and Mn1—O2W are 2.273(3) Å and 2.246(3) Å, respectively. ClO4 act as counter-anion. It is noteworthy that the unit cell of the title compound contains two racemic units [Mn((+)-salcy)(H2O)2]+ and [Mn((+)-salcy)(H2O)2]+and overall exhibiting centrosymmetry.

Acknowledgements

This work was supported by Fund for Less Developed Regions of the National Natural Science Foundation of China (No. 31760257); Science and Technology Bureau of Kunming projects (No. 2017-1-S-16405), (No. 2017-1-S-16406). Joint Research Projects of Yunnan province of Local of institutions (partial) of higher education (2017FH001-002), (2017FH001-083)

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Received: 2017-9-28
Accepted: 2018-1-17
Published Online: 2018-2-13
Published in Print: 2018-3-28

©2018 Hongping Ju et al., published by De Gruyter, Berlin/Boston

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

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