Home Physical Sciences Crystal structure of {5,5′-((propane-1,3-diylbis(azanylylidene))bis(methanylylidene))bis(3-(ethoxycarbonyl)-2,4-dimethylpyrrol-1-ido)-κ4N,N′,N′′,N′′′}zinc(II), C23H30N4O4Cu
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Crystal structure of {5,5′-((propane-1,3-diylbis(azanylylidene))bis(methanylylidene))bis(3-(ethoxycarbonyl)-2,4-dimethylpyrrol-1-ido)-κ4N,N′,N′′,N′′′}zinc(II), C23H30N4O4Cu

  • Xue-Feng Han , Qing-Wen Yang , Miao Yang and Wei-Na Wu EMAIL logo
Published/Copyright: February 6, 2018

Abstract

C13H17N3OS, monoclinic, P1̅ (no. 2), a = 7.746(6) Å, b = 12.344(9) Å, c = 12.655(9) Å, α = 95.766(7)°, β = 98.007(7)°, γ = 101.595(13)°, V = 1163.4(15) Å3, Z = 2, Rgt(F) = 0.0550, wRref(F2) = 0.1616, T = 296(2) K.

CCDC no.: 1436155

The crystal structure is shown in the figure (Hydrogen atoms are omitted for clarity). Tables 1 and 2 contain details on crystal structure and measurement conditions and a list of the atoms including atomic coordinates and displacement parameters.

Table 1:

Data collection and handling.

Crystal:Brown block
Size:0.20 × 0.16 × 0.15 mm
Wavelength:Mo Kα radiation (0.71073 Å)
μ:0.98 mm−1
Diffractometer, scan mode:Bruker SMART, φ and ω-scans
θmax, completeness:27.5°, >99%
N(hkl)measured, N(hkl)unique, Rint:12740, 5310, 0.066
Criterion for Iobs, N(hkl)gt:Iobs > 2 σ(Iobs), 4099
N(param)refined:305
Programs:Bruker programs [1], SHELX [2]
Table 2:

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

AtomxyzUiso*/Ueq
Cu10.52283(5)0.51864(3)0.26879(3)0.03900(16)
O1−0.0819(4)0.1584(2)0.0234(2)0.0561(7)
O2−0.0996(5)0.2388(3)−0.1273(3)0.0801(10)
O30.7828(7)0.0999(3)0.3772(3)0.1045(14)
O40.7967(5)0.1575(3)0.5516(3)0.0808(10)
N10.3297(4)0.4329(2)0.1560(2)0.0398(6)
N20.5055(4)0.6401(2)0.1799(3)0.0480(7)
N30.6472(4)0.6234(2)0.3979(2)0.0437(7)
N40.6320(4)0.4110(2)0.3439(2)0.0398(6)
C1−0.2559(7)−0.0151(4)0.0457(4)0.0745(13)
H1B−0.346541−0.0783980.0109090.112*
H1C−0.2954980.0191430.1067080.112*
H1A−0.148002−0.0390180.0692560.112*
C2−0.2213(6)0.0666(4)−0.0311(4)0.0703(12)
H2A−0.1843340.032270−0.0940750.084*
H2B−0.3287700.092661−0.0542240.084*
C3−0.0289(5)0.2417(3)−0.0355(3)0.0476(8)
C40.1158(4)0.3298(3)0.0242(3)0.0390(7)
C50.1845(4)0.4302(3)−0.0156(3)0.0407(7)
C60.3126(4)0.4915(3)0.0675(3)0.0375(7)
C70.2081(4)0.3355(3)0.1305(3)0.0381(7)
C80.1285(5)0.4666(3)−0.1220(3)0.0493(8)
H8A0.1555980.417937−0.1785340.074*
H8B0.1917040.541634−0.1233050.074*
H8C0.0023580.463403−0.1325270.074*
C90.1787(6)0.2566(3)0.2115(3)0.0525(9)
H9A0.2694170.2811070.2739960.079*
H9B0.1845400.1832550.1809280.079*
H9C0.0633360.2545500.2318280.079*
C100.4089(5)0.6052(3)0.0865(3)0.0444(8)
H100.4022540.6520800.0337220.053*
C110.5866(7)0.7590(3)0.2090(3)0.0729(13)
H11Aa0.4917300.7987970.2151270.087*
H11Ba0.6454860.7847420.1504670.087*
H11Cb0.5225230.8016860.1635750.087*
H11Db0.7093870.7728950.1965460.087*
C12a0.7173(8)0.7896(4)0.3096(4)0.063(2)
H12Aa0.7464450.8703750.3248230.076*
H12Ba0.8255350.7667750.2955900.076*
C12Ab0.5823(18)0.7960(9)0.3232(5)0.055(5)
H12Cb0.6335260.8755240.3366050.066*
H12Db0.4576030.7865750.3312640.066*
C130.6702(6)0.7450(3)0.4103(3)0.0617(11)
H13Aa0.7642870.7782410.4704520.074*
H13Ba0.5605000.7648410.4257650.074*
H13Cb0.7973000.7772060.4207070.074*
H13Db0.6280020.7672910.4760850.074*
C140.7157(5)0.5735(3)0.4733(3)0.0437(8)
H140.7695800.6123100.5404550.052*
C150.7055(4)0.4567(3)0.4495(3)0.0396(7)
C160.7705(5)0.3801(3)0.5073(3)0.0433(8)
C170.7412(5)0.2822(3)0.4313(3)0.0455(8)
C180.6567(5)0.3058(3)0.3317(3)0.0418(7)
C190.8600(6)0.4010(4)0.6228(3)0.0566(10)
H19A0.9762690.3840260.6274970.085*
H19B0.7893330.3544580.6643640.085*
H19C0.8718170.4779520.6503750.085*
C200.6122(6)0.2342(3)0.2252(3)0.0580(10)
H20A0.5414230.2676800.1749820.087*
H20B0.5460810.1616970.2330510.087*
H20C0.7204880.2272010.1990030.087*
C210.7753(6)0.1715(4)0.4471(4)0.0628(11)
C220.8274(9)0.0514(4)0.5749(6)0.111(2)
H22A0.9522390.0586000.6043200.134*
H22B0.799019−0.0009510.5092400.134*
C230.7161(16)0.0102(6)0.6521(8)0.189(5)
H23A0.592478−0.0005660.6211790.283*
H23B0.7417200.0634990.7160220.283*
H23C0.740590−0.0594860.6701790.283*
  1. Occupancies: a = 0.721(11), b = 0.279(11).

Source of material

Ethyl 5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylate (2 mmol) and propane-1,3-diamine (1 mmol) were dissolved in an ethanol/THF (1:1) solution (10 mL). The mixture was stirred for 4 h at room temperture, and then copper actetate monohydrate (1 mmol) was added. The resulting solution was left in air for a few days, yielding brown block-shaped crystals.

Experimental details

The C12 atom splitted over two positions, with the occupancy value of C12/C12A being 0.72/0.28. The hydrogen atoms were placed at calculated positions and refined as riding atoms with isotropic displacement parameters.

Discussion

Schiff base ligands bearing pyrrole units have attracted much attention due to their excellent coordination abilities [3, 4] . The crystal structures of copper(II) and zinc(II) complexes with bis(pyrrol-2-ylmethyleneamine) ligands have been widely investigated [3], [4], [5], [6]. As part of our ongoing studies of pyrrol complexes [5], [6], [7], the title complex was synthesized and characterized.

In the title complex, the Cu(II) ion is surrounded by the ligand via its four N atoms, thus giving a distorted square planar geometry (r.m.s. deviation 0.2679 Å). The dihedral angle, defined by the intersection of two pyrrol-2-ylmethyleneamine planes (N1/C4—C7, r.m.s. deviation 0.0067 Å; N4/C15—C18, r.m.s. deviation 0.0091 Å) at the copper center, is 43.3°. The N—Cu—N angles range from 82.94(13) to 160.35(12)°, and the bond distances of Cu—N span from 1.965(3) to 1.977(3) Å. The molecular structure of the title complex is similar to that of [N,N-bis((pyrrol-2-yl)methylidene)butane-1,4-diamine-κ4N,N′,N′′,N′′′]copper(II) [1].

References

Bruker. SMART and SAINT. Bruker AXS Inc., Madison, WI, USA (2007).Search in Google Scholar

Sheldrick, G. M.: Crystal refinement with SHELX. Acta Crystallogr. C71 (2015) 3–8.10.1107/S2053273314026370Search in Google Scholar PubMed PubMed Central

Wu, Z.; Chen, Q.; Xiong, S.; Xin, B.; Zhao, Z.; Jiang, L.; Ma, J. S.: Double-stranded helicates, triangles, and squares formed by the self-assembly of pyrrol-2-ylmethyleneamines and ZnII Ions. Angew. Chem. Int. Ed. 42 (2003) 3271–3274.10.1002/anie.200350908Search in Google Scholar PubMed

Yang, L.; Chen, Q.; Li, Y.; Xiong, S.; Li, G.; Ma, J. S.: Self-assembly of bis(pyrrol-2-ylmethyleneamine) ligands with Cu(II) controlled by bridging [-(CH2)n-] spacers and weak intermolecular C—H⋯Cu hydrogen bonding. Eur. J. Inorg. Chem. 2004 (2004) 1478–1487.10.1002/ejic.200300639Search in Google Scholar

Wang, Y.; Yang, Z.-Y.; Chen, Z.-N.: Synthesis, characterization and DNA binding properties of four Zn(II) complexes with Bis(pyrrol-2-yl-methyleneamine) ligands. Bioorg. Med. Chem. Lett. 18 (2008) 298–303.10.1016/j.bmcl.2007.10.085Search in Google Scholar PubMed

Wang, Y.; Wu, W.-N.; Wang, Q.; Yang, Z.-Y.: Synthesis, characterization, and antioxidant activities of three Cu(II) complexes with Schiff-base ligands. J. Coord. Chem. 63 (2010) 147–155.10.1080/00958970903295836Search in Google Scholar

Mao, P. D.; Yan, L.-L.; Wu, W.-N.; Song, Y.-H.; Yao, B.-X.: Ni(II)/Cu(II)/Zn(II) complexes baded on a bis(pyrrol-2-yl-methyleneamine) ligand: syntheses, characterization, fluorescence properties and crystal structures of Ni(II)/Cu(II) complexes. Chin. J. Inorg. Chem. 32 (2016) 879–883.Search in Google Scholar

Received: 2017-10-16
Accepted: 2018-1-23
Published Online: 2018-2-6
Published in Print: 2018-3-28

©2018 Xue-Feng Han 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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