Home The crystal structure of N′1,N′2-bis((E)-3-(tert-butyl)-2-hydroxybenzylidene)oxalohydrazide, C24H30N4O4
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The crystal structure of N′1,N′2-bis((E)-3-(tert-butyl)-2-hydroxybenzylidene)oxalohydrazide, C24H30N4O4

  • Zhenxiu Xiao , Tiantian Wang , Xin Deng , Wujiu Jiang ORCID logo EMAIL logo and Yuxing Tan ORCID logo EMAIL logo
Published/Copyright: February 14, 2023

Abstract

C24H30N4O4, monoclinic, C2/c (no. 15), a = 21.170(3) Å, b = 13.2938(17) Å, c = 9.7133(12) Å, β = 114.423(2)°, V = 2489.0(5) Å3, Z = 4, Rgt(F) = 0.0473, wRref(F2) = 0.1424, T = 296(2) K.

CCDC no.: 2235010

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: Yellow block
Size: 0.22 × 0.16 × 0.14 mm
Wavelength: Mo Kα radiation (0.71073 Å)
μ: 0.08 mm−1
Diffractometer, scan mode: Bruker APEX-II, φ and ω
θmax, completeness: 26.0°, >99%
N(hkl)measured, N(hkl)unique, Rint: 6844, 2444, 0.023
Criterion for Iobs, N(hkl)gt: Iobs > 2σ(Iobs), 1719
N(param)refined: 149
Programs: Bruker [1], SHELX [2, 3], WinGX/ORTEP [4]
Table 2:

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

Atom x y z Uiso*/Ueq
O2 0.55557 (5) 0.52894 (9) 0.18663 (12) 0.0549 (4)
N2 0.57546 (6) 0.53478 (9) −0.02416 (13) 0.0393 (3)
H2 0.559044 0.525743 −0.120343 0.047*
N1 0.64290 (6) 0.56723 (10) 0.05581 (14) 0.0422 (3)
O1 0.74778 (6) 0.63101 (11) 0.29471 (14) 0.0700 (4)
H1 0.708476 0.610180 0.244137 0.105*
C8 0.53672 (7) 0.51794 (11) 0.05156 (16) 0.0358 (4)
C7 0.68021 (8) 0.57718 (12) −0.01866 (18) 0.0448 (4)
H7 0.661441 0.560874 −0.120907 0.054*
C1 0.75101 (8) 0.61328 (12) 0.0527 (2) 0.0490 (4)
C2 0.78283 (8) 0.63888 (13) 0.2063 (2) 0.0530 (5)
C6 0.78744 (9) 0.62431 (15) −0.0369 (2) 0.0649 (5)
H6 0.766461 0.607652 −0.138911 0.078*
C3 0.85189 (9) 0.67449 (14) 0.2725 (2) 0.0645 (5)
C4 0.88480 (10) 0.68317 (16) 0.1760 (3) 0.0792 (7)
H4 0.930336 0.706275 0.215892 0.095*
C5 0.85418 (11) 0.65966 (17) 0.0246 (3) 0.0810 (7)
H5 0.878531 0.667682 −0.035338 0.097*
C9 0.88717 (11) 0.70263 (17) 0.4402 (3) 0.0841 (7)
C12 0.84792 (14) 0.7907 (2) 0.4716 (3) 0.1059 (9)
H12A 0.801281 0.770306 0.450114 0.159*
H12B 0.847009 0.846698 0.408360 0.159*
H12C 0.870955 0.810132 0.575835 0.159*
C10 0.96207 (12) 0.7377 (2) 0.4845 (4) 0.1205 (11)
H10A 0.962559 0.791370 0.418922 0.181*
H10B 0.989301 0.682504 0.475150 0.181*
H10C 0.981226 0.761010 0.587234 0.181*
C11 0.88997 (17) 0.6127 (2) 0.5402 (3) 0.1410 (14)
H11A 0.915630 0.630573 0.644445 0.211*
H11B 0.912377 0.557290 0.515232 0.211*
H11C 0.843670 0.593639 0.523910 0.211*

Source of material

All chemicals were purchased from commercial sources and used as received without further purification. The 3-(tert-butyl)-2-hydroxybenzaldehyde (20 mmol, 3.564 g) and oxalohydrazide (10 mmol, 1.18 g) were dissolved in MeOH (100 mL). The mixture was refluxed for 6 h. Finally, the title crystal was precipitated by controlling slowly cooling.

Experimental details

All H-atoms bonded to C atoms were placed geometrically and refined using a riding model with common isotropic displacement factors Uiso(H) = 1.2 or 1.5 Ueq(parent C-atom).

Comment

Acylhydrazones have found widespread use in many disciplines. In the field of coordination chemistry, acylhydrazones are important organic ligands [5, 6]. Bis(salicylaldehyde)oxaldihydrazone is a special class of acylhydrazone with fluorescent properties which have important applications in the field of analytical chemistry [7, 8], in general, the fluorescence intensity can be significantly enhanced by connecting large steric hindrance electron donor substituents to salicylaldehyde azine. So, the synthesis and crystal structure of the title compound are of great significance to study the application.

The title molecule in the crystal structure is a symmetric molecule. The ORTEP diagram is presented in the Figure. Bond lengths and angles are all in the expected ranges. The title molecule exhibits an E configuration. The bond length of C7=N1 is 1.2795(18) Å, which is similar to those reported in the literature [9, 10]. The bond length of C1–C7 is 1.449(2) Å, shorter than normal C–C single bonds, which is similar to those reported in the literature [11, 12].

Intramolecular and intermolecular hydrogen bonding exist in the crystal structure of the title compound. The oxygen atom O1 provides one intramolecular hydrogen bond to N1 (N1⋯O1 = 2.6026(16) Å). The carbon atom C7 provides one intermolecular hydrogen bond to O2″ of another molecule, the nitrogen atom N2 provides one intermolecular hydrogen bond to O2″ of another molecule (C7⋯O2″ = 3.302(2) Å, N2⋯O2″ = 2.7943(16) Å; ″ = −x + 3/2, y − 1/2, −z + 3/2).


Corresponding authors: Wujiu Jiang and Yuxing Tan, School of Chemistry and Materials Science, Key Laboratory of Functional Metal-Organic Compounds of Hunan Province, Key Laboratory of Metal Organic New Materials of College of Hunan Province Hengyang, Normal University, Hengyang, Hunan 421008, China, E-mail: ,

  1. Author contribution: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: This work was supported by the 2022 Innovation and Entrepreneurship Training Program for Hunan College students (Nos. NYD202211, cxcy2022038), the 22nd College students Extracurricular Academic Science and Technology Works Competition Project of Hengyang Normal University (Nos. 13, 14), Hunan Provincial Natural Science Foundation of China (No. 2022JJ30096) and Foundation of Key Laboratory of Functional Metal–Organic Compounds of Hunan Province (No. 2022HSKFJJ028).

  3. Conflict of interest statement: The authors declare no conflicts of interest regarding this article.

References

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Received: 2023-01-08
Accepted: 2023-02-01
Published Online: 2023-02-14
Published in Print: 2023-04-25

© 2023 the author(s), published by De Gruyter, Berlin/Boston

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

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