Startseite Crystal structure of aqua-dichlorido-(4-(((3-ethoxy-2-oxidobenzylidene)hydrazono)(oxido)methyl)pyridin-1-ium-κ3N,O,O′)iron(III), C15H16Cl2N3O4Fe
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Crystal structure of aqua-dichlorido-(4-(((3-ethoxy-2-oxidobenzylidene)hydrazono)(oxido)methyl)pyridin-1-ium-κ3N,O,O′)iron(III), C15H16Cl2N3O4Fe

  • Yang Liguo ORCID logo EMAIL logo , Zhang Zhen , Niu Yongsheng , Wang Fang und Tian Dayong
Veröffentlicht/Copyright: 15. Februar 2020

Abstract

C15H16Cl2N3O4Fe, monoclinic, P21/n (no. 14), a = 8.7419(15) Å, b = 22.717(4) Å, c = 9.6256(16) Å, β = 112.546(2)°, V = 1765.4(5) Å3, Z = 4, Rgt(F) = 0.0255, wRref(F2) = 0.0622, T = 298 K [1–3].

CCDC no.: 1976174

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:0.08 × 0.06 × 0.04 mm
Wavelength:Mo Kα radiation (0.71073 Å)
μ:1.18 mm−1
Diffractometer, scan mode:Bruker APEX-II, φ and ω-scans
θmax, completeness:27.4°, >99%
N(hkl)measured, N(hkl)unique, Rint:18605, 3981, 0.017
Criterion for Iobs, N(hkl)gt:Iobs > 2 σ(Iobs), 3641
N(param)refined:258
Programs:Bruker programs [1], SHELX [2], [3]
Table 2:

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

AtomxyzUiso*/Ueq
Fe10.50777 (3)0.41040 (2)0.66793 (2)0.02454 (7)
Cl10.33527 (5)0.33308 (2)0.69679 (4)0.03778 (11)
Cl20.31552 (6)0.48323 (2)0.65479 (5)0.04196 (11)
O10.64449 (14)0.40756 (5)0.89001 (12)0.0290 (2)
O20.44854 (14)0.40170 (5)0.45607 (12)0.0300 (2)
O30.31207 (17)0.41924 (6)0.16413 (13)0.0402 (3)
O40.67867 (16)0.47691 (6)0.66340 (15)0.0343 (3)
H410.675 (3)0.4822 (11)0.585 (3)0.057 (8)*
H420.670 (3)0.5075 (12)0.697 (3)0.062 (8)*
N10.78490 (18)0.32936 (6)0.83829 (15)0.0333 (3)
N20.68413 (16)0.34384 (6)0.69017 (14)0.0283 (3)
N31.0670 (2)0.35455 (8)1.38555 (18)0.0452 (4)
H31.134 (3)0.3521 (10)1.475 (3)0.061 (7)*
C10.8464 (2)0.40060 (8)1.19415 (19)0.0368 (4)
H10.7636110.4302841.1623950.044*
C20.9533 (3)0.39705 (9)1.3421 (2)0.0461 (5)
H20.9461760.4247971.4132410.055*
C41.0822 (2)0.31410 (9)1.2913 (2)0.0444 (4)
H4A1.1636710.2840861.3274160.053*
C50.9797 (2)0.31600 (8)1.14178 (19)0.0384 (4)
H50.9897030.2874861.0735660.046*
C60.86106 (19)0.36020 (7)1.09158 (17)0.0287 (3)
C70.75342 (19)0.36606 (7)0.92894 (16)0.0273 (3)
C80.7033 (2)0.31207 (7)0.58725 (18)0.0319 (3)
H80.7828830.2812870.6180760.038*
C90.6119 (2)0.32021 (7)0.42840 (17)0.0288 (3)
C100.49312 (19)0.36543 (7)0.37048 (17)0.0261 (3)
C110.4196 (2)0.37282 (7)0.21209 (17)0.0289 (3)
C120.4578 (2)0.33485 (8)0.11767 (18)0.0341 (4)
H120.4067490.3399780.0117960.041*
C130.5707 (2)0.28913 (8)0.17654 (19)0.0369 (4)
H130.5941380.2627360.1107080.044*
C140.6477 (2)0.28220 (7)0.32882 (19)0.0357 (4)
H140.7262090.2514540.3680430.043*
C15a0.2826 (5)0.44513 (17)0.0158 (4)0.0350 (8)
H15Aa0.3747530.435170−0.0158640.042*
H15Ba0.2747410.4885180.0199830.042*
C16a0.1215 (5)0.41976 (19)−0.0942 (4)0.0535 (11)
H16Aa0.0977820.436068−0.1945780.080*
H16Ba0.1309450.376840−0.0974160.080*
H16Ca0.0313660.429956−0.0617240.080*
C15′b0.2208 (8)0.4208 (3)−0.0017 (6)0.0406 (14)
H15Cb0.2978870.428962−0.0524990.049*
H15Db0.1660620.382456−0.0381900.049*
C16′b0.0964 (6)0.4679 (2)−0.0337 (6)0.0473 (16)
H16Db0.0331770.470417−0.1424250.071*
H16Eb0.0209890.4592650.0171740.071*
H16Fb0.1522080.5055560.0029300.071*
  1. Occupancies: a = 0.605(5), b = 0.395(5).

Source of material

The ligand 3-ethoxysalicylaldehyde-isonicotinohydrazide was synthesized by condensing 3-ethoxysalicylaldehyde with equimolar isonicotinohydrazide in ethanol. Iron trichloride hexahydrate (1 mmol) was added to a 30 mL methanol solution containing 3-ethoxysalicylaldehyde-isonicotinohydrazide (1 mmol). The resulting mixture was refluxed with stirring for 1.5 h, and then cooled slowly to room temperature and filtered. Black prism-shaped crystals were obtained from the solution after several days. Yield (0.13 g, 30%) m.p. 263–269 K. FTIR (KBr) ν (cm−1): 3201, 1694, 1564, 1467, 1255, 1040. Anal. Calc. for C19H17N9O2 (%): C, 41.96; H, 3.73; N, 9.79. Found (%): C, 41.92; H, 3.70; N, 9.70.

Experimental details

The C-bound H atoms were geometrically placed (C—H = 0.95–0.98 Å) and refined as riding with Uiso(H) = 1.2–1.5 Ueq(C). Other H atoms are refined freely (see Table 2).

Discussion

Schiff base play an important role in inorganic chemistry, because they can form stable complexes with most transition metal ions and Ln ions. The application of the complexes with the schiff base ligands is based on their biological activity [4]. Expecially, the mode of chelation with transition metal ions present in the living system have been of significant interest [5], [6], [7], [8]. Many complexes with aroylhydrazone ligands have been reported [9], [10].

The molecular structure of the complex and the labelling of the atoms as showing in the figure. The Fe(III) atom is meridionally coordinated by O, N, O of the ylidic hydrazonato ligand. Two chlorido and one aqua ligand complete the distorted pseudo-octahedral coordination sphere. The bond lengths of Fe1—O1, Fe1—O2, Fe1—O4, Fe1—N2, Fe1—Cl1 and Fe1—Cl2 are similar with those reported in the literature [11], [12], [13], [14], [15], [16], [17], [18], [19], [20]. The angles of Cl1—Fe1—Cl2, O1—Fe1—O4, O2—Fe1—O4, O1—Fe1—Cl1, O2—Fe1—Cl2, O1—Fe1—N2, O2—Fe1—N2 and N2—Fe1—Cl1 are 93.11°, 84.85°, 87.48°, 89.81°, 96.93°, 75.89°, 85.59° and 86.01°, respectively.

Acknowledgements

The authors gratefully acknowledge Scientific and technological project of Henan province (192102310232), the Anyang Key Laboratory for Chemical Biosensing (21302003), Key discipline of environmental engineer of Anyang Institute of Technology. The Natural Science Foundation of China (21471015, 21631003, 21561007, and 21701046), the Innovation Program for High-level Talents of Guizhou Province (No. 2016-5657), the Science and Technology Fund of Guizhou Province (No. 2016-1030), the Major Program for Creative Research Groups of Guizhou Provincial Education Department (2017-028), and the Fundamental Research Funds for the Central Universities (FRF-BD-17-016A).

References

1. SMART and SAINT for Windows NT Software Reference Manuals, Version 5.0, Bruker Analytical X-Ray Systems, Madison, WI (1997).Suche in Google Scholar

2. Sheldrick, G. M.: SADABS, A Software for Empirical Absorption Correction; University of Göttingen: Göttingen, Germany (1997).Suche in Google Scholar

3. SHELXL Reference Manual, version 5.1; Bruker analytical X-ray systems: Madison, WI (1997).Suche in Google Scholar

4. Chohan, Z. H.; Sherazi, S. K. A.: Synthesis and characterisation of some Co(II), Cu(II) and Ni(II) complexes with nicotinoylhydrazine derivatives and the biological role of metals and anions (SO42−, NO3, CzO42− and CH3CO2) on the antibacterial properties. Synth. React. Inorg. Met. Org. Chem. 29 (1999) 105–118.10.1080/00945719909349437Suche in Google Scholar

5. Savini, L.; Chiasserini, L.; Gaeta, A.; Pellerano, C.: Synthesis and anti-tubercular evaluation of 4-quinolylhydrazones. Biorg. Med. Chem. 10 (2002) 2193–2198.10.1016/S0968-0896(02)00071-8Suche in Google Scholar

6. Ochiai, E.: Bioinorganic chemistry: an introduction. Allyn and Bacon (1977).Suche in Google Scholar

7. Tossidis, I. A.; Bolos, C. A.; Aslanidis, P. N.; Katsoulos, G. A.: Monohalogenobenzoylhydrazones III. synthesis and structural studies of Pt (II), Pd (II) and Rh (III) complexes of di-(2-pyridyl) ketonechlorobenzoyl hydrazones. Inorg. Chim. Acta. 133 (1987) 275–280.10.1016/S0020-1693(00)87779-8Suche in Google Scholar

8. Dilworth, J. R.: The coordination chemistry of substituted hydrazines. Coord. Chem. Rev. 21 (1976) 29–62.10.1016/S0010-8545(00)82050-0Suche in Google Scholar

9. Yu, G. M.; Li, Y. H.; Zou, L. F.; Zhu, J. W.; Liu, X. Q.: Bis[μ-2-(2-benzoylhydrazinylidenemethyl)-6-methoxyphenolato][2-(2-benzoylhydrazinylidenemethyl)-6-methoxyphenolato]dimanganese(II) perchlorate methanol solvate. Acta. Crystallogr. E66 (2010) m693–m694.10.1107/S1600536810018040Suche in Google Scholar PubMed PubMed Central

10. Monfared, H. H.; Pounsaneh, E.; Sadighian, S.; Ng, S. W.; Tiekink, E. R. T.: Syntheses, structures, and catalytic activity of copper(II)- aroylhydrazone complexes. Z. Anorg. Allg. Chem. 639 (2013) 435–442.10.1002/zaac.201200395Suche in Google Scholar

11. Monfared, H. H.; Sadighian, S.; Kamyabi, M. A.; Mayer, P.: Iron(III) aroylhydrazone complexes: Structure, electrochemical studies and catalytic activity in oxidation of olefins. J. Mol. Catal. A-Chem. 304 (2009) 139–146.10.1016/j.molcata.2009.02.004Suche in Google Scholar

12. Huo, L. H.; Gao, S.; Liu, J. W.; Li, J.; Zhao, H.; Zhao, J. G.: Dichloro(methanol-κO)[3-methoxysalicyl-aldehyde (4-methoxybenzoyl) hydrazonato-κ3N,O′,N]iron(III) methanol solvate. Acta. Cryst. E60 (2004) m673–m675.10.1107/S160053680400950XSuche in Google Scholar

13. Kia, R.; Kargar, H.: Synthesis, spectral characterization and crystal structure studies of a new hydrazone-Schiff base and its dioxomolybdenum(VI) complex. J. Coord. Chem. 68 (2015) 1441–1451.10.1080/00958972.2015.1011146Suche in Google Scholar

14. Vrdoljak, V.; Cindrić, M.; Milić, D.; Matković-Čalogović, D.; Novak, P.; Kamenar, B.: Synthesis of five new molybdenum (VI) thiosemicarbazonato complexes. Crystal structures of salicylaldehyde and 3-methoxy-salicylaldehyde 4-methylthiosemi carbazones and their molybdenum(VI) complexes. Polyhedron 24 (2005) 1717–1726.10.1016/j.poly.2005.05.002Suche in Google Scholar

15. Ding, S. B.; Li, W. H.: Dioxomolybdenum(VI) complexes of hydrazones of two substituted salicylaldehydes: synthesis, structures, and catalytic properties. J. Coord. Chem. 66 (2013) 2023–2031.10.1080/00958972.2013.797079Suche in Google Scholar

16. Li, A.-M.: Vanadium(V) complexes with hydrazone and benzohydroxamate ligands: synthesis, structures and catalytic epoxidation. J. Coord. Chem. 67 (2014) 2076–2085.10.1080/00958972.2014.931577Suche in Google Scholar

17. He, X.-Q.: Syntheses, X-ray structures, and catalytic oxidations of dioxomolybdenum(VI) complexes with tridentate benzohydrazones. J. Coord. Chem. 66 (2013) 966–976.10.1080/00958972.2013.773587Suche in Google Scholar

18. Jin, N. Y.: Syntheses, crystal structures, and catalytic properties of dioxomolybdenum(VI) complexes with hydrazone ligands. J. Coord. Chem. 65 (2012) 4013–4022.10.1080/00958972.2012.731049Suche in Google Scholar

19. Rana, A.; Dinda, R.; Sengupta, P.; Ghosh, S.; Falvello, L. R.: Synthesis, characterisation and crystal structure of cis-dioxomolybdenum(VI) complexes of some potentially pentadentate but functionally tridentate (ONS) donor ligands. Polyhedron 21 (2002) 1023–1030.10.1016/S0277-5387(02)00913-0Suche in Google Scholar

20. Li, Z.-P.; Li, Y.-J.; Li, Z.-X.; Li, H.; Xiao, Z.-P.: Synthesis and crystal structures of N′-3,5-dibromo-2-hydroxybenzylidene)-2-hydroxy-3-methylbenzohydrazide and its oxovanadium(V) complex [N′-(3,5-dibromo-2-oxidobenzylidene-κO)-2-hydroxy-3- methylbenzohydrazidato-κ2N′,O](methanol-κO)(methanolato-κO)oxidovanadium(V). J. Chem. Crystallogr. 41 (2011) 1568.10.1007/s10870-011-0141-4Suche in Google Scholar

Received: 2019-10-13
Accepted: 2020-01-08
Published Online: 2020-02-15
Published in Print: 2020-04-28

©2020 Yang Liguo et al., published by De Gruyter, Berlin/Boston

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

Artikel in diesem Heft

  1. Frontmatter
  2. Crystal structure of catena-poly[(μ2-3-(benzo[d]thiazol-2-yl)-5-carboxybenzoato-κ2N:O)silver(I)], C15H8AgNO4S
  3. Crystal structure of bis(4-phenylpiperazin-1-ium) bis(2-(4-phenylpiperazin-1-yl)succinato-κ2O,O′)copper(II) tetrahydrate, C48H70CuN8O12, [C10H14N2]2[Cu(C14H17N2O4)2] ⋅ 4 H2O
  4. Crystal structure of triaqua-bis(2-(6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylenedecahydronaphthalen-1-yl)-1-(2-oxo-2,5-dihydrofuran-3-yl)ethane-1-sulfonato-κ2O,O′)calcium(II) – ethanol (1/2), C44H76CaO19S2
  5. The crystal structure of ethyl 5-(4-(diphenylamino)phenyl)thiophene-2-carboxylate, C25H21NO2S
  6. The crystal structure of 5-bromo-2-(2-methyl-2H-tetrazol-5-yl)pyridine, C7H6BrN5
  7. The crystal structure of (E)-5-chloro-2-hydroxy-N′-(2-hydroxy-4-methoxybenzylidene)benzohydrazide, C15H13ClN2O4
  8. The crystal structure of (2Z,2′Z)-N′,N′′′′-(pyridine-2,6-dicarbonyl)dipicolinohydrazonamide, C19H17N9O2
  9. Photochromic properties and crystal structure of 3,3′-(perfluorocyclopent-1-ene-1,2-diyl)bis(5-(4-(azidomethyl)phenyl)-2-methylthiophene), C29H20F6N6S2
  10. Crystal structure of aqua-dichlorido-(4-(((3-ethoxy-2-oxidobenzylidene)hydrazono)(oxido)methyl)pyridin-1-ium-κ3N,O,O′)iron(III), C15H16Cl2N3O4Fe
  11. Crystal structure of catena-poly[diaqua-(μ2-4,4′-bipyridine-κ2N:N′)-bis(2,3,4,5-tetrabromo-6-carboxybenzoato-κ1O)-nickel(II)], C26H14Br8NiN2O10
  12. Crystal structure of diethanol-κ1O-bis(μ2-N-((2-oxidonaphthalen-1-yl)methylene)pyrazine-2-carbohydrazonato-κ5N,O,O′:O′:N′)-bis(nitrato-κ2O,O′)dieuropium(III), C36H32N10O12Eu2
  13. The crystal structure of 2-aminoisophthalic acid, C8H7NO4
  14. Crystal structure of (E)-2-(4-((3,4-difluorobenzyl)oxy)styryl)-4,6-dimethoxybenzaldehyde, C24H20F2O4
  15. Crystal structure of 2-benzoylpyrene, C23H14O
  16. Crystal structure of chlorido-(η6-p-cymene)-(N-(2-fluorophenyl)-1-(pyridin-2-yl)methanimine-κ2N,N′)ruthenium(II) – acetone (1/1), C22H23ClN2F7OPRu
  17. The crystal structure of 2-bromoisonicotinic acid, C6H4BrNO2
  18. Crystal structure of 1,3,5,7-tetraphenyl-8-(N-phenylformamido)-2-oxa-5-azabicyclo[4.2.0]oct -3-en-7-yl benzoate, C44H34N2O4
  19. Synthesis and crystal structure of 4-(3-acetyl-5-(thiophen-2-yl)-2,3-dihydro-1,3,4-oxadiazol-2-yl)-7-(diethylamino)-2H-chromen-2-one, C21H21N3O4S
  20. Crystal structure of poly[diaqua-(μ2-4,4′-bipyridine-κ2N:N′)-(μ2-3,4,5,6-tetrafluorophthalato-κ2O:O′)nickel(II)], C18H12F4NiN2O6
  21. Crystal structure of 4-hydroxynaphtho[2,3-b]benzofuran-6,11-dione, C16H8O4
  22. The crystal structure of 3,10-bis(4-methoxyphenyl)-6,12-dibenzyl-2,9-acetyl-6,12-diazapentacyclo[6.3.1.02,7.04,11.05,9]dodecane – acetone (1/1), C45H48N2O5
  23. The crystal structure of (E)-2-(((2-(1H-indol-3-yl)ethyl)iminio)methyl)-6-bromophenolate, C17H15N2BrO
  24. Crystal structure of catena-poly[diaqua-(μ2-oxalyl dihydrazide-κ4N,O:N′,O′)-bis(μ2-pyridine-2,3-dicarboxylato-κ3N,O,O′)dicadmium(II)] hexahydrate, C16H28O18N6Cd2
  25. Crystal structure of poly[tetra-(μ4-naphthalene-1,8-dicarboxylato-κ4O:O,O′: O′′:O′′,O′′′)-(μ4-oxo-κ4O:O:O:O) penta-lead(II)], C48H24O17Pb5
  26. Crystal structure of 5H-dibenzo[c,f][1,5]oxabismocin-12 (7H)-yl acetate, C16H15O3Bi
  27. The crystal structure of 2-(4-chloro-6-nitrophenyl)-1-(4-chloro-3-nitrophenyl)diazene 1-oxide, C12H6Cl2N4O5
  28. Crystal structure of bis(3-methyl-N-(1-(pyrazin-2-yl)ethylidene)benzohydrazonato-κ3O,N,N′)nickel(II), C28H26N8O2Ni
  29. Crystal structure of 3,10-bis(4-chlorophenyl)-6,12-dibenzyl-2,9-acetyl-6,12-diazapentacyclo[6.3.1.02,7.04,11.05,9]-dodecane, C40H36Cl2N2O2
  30. Crystal structure of bis[(μ2-4⋯O,O′:O′)-(4-hydroxybenzoato-κ2O,O′)-(1,10-phenanthroline-κ2N,N′)]-di-lead(II)μ-4-hydroxybenzoato-κ3O,O′:O′3O,O′:O′-bis-[(4-hydroxybenzoato-κ2O,O′)bis(1,10-phenanthroline-κ2N,N′)di-lead(II)] monohydrate, C52H36N4O12Pb2 ⋅ H2O
  31. Crystal structure of poly[diaqua-(μ3-3,4,5,6-tetrafluoro-phthalato-κ3O:O′:O′′)-(μ2-1,2-bis(4-pyridyl)ethene-κ2N:N′)cobalt(II)], C14H9CoF4NO6
  32. Crystal structure of 7-hydroxy-4-phenyl-2H-chromen-2-one, C15H10O3
  33. Crystal structure of 3,7-dimethyl-1-(5-oxohexyl)-3,7-dihydro-1H-purine-2,6-dione 4-hydroxybenzoic acid, C20H24N4O6
  34. Crystal structure of catena-poly[(μ2-1,5-dimethyl-2-phenyl-4-((pyridin-4-ylmethylene)amino)-1,2-dihydro-3H-pyrazol-3-one-κ2N:O)-bis(nitrato-κ1O)zinc(II)], C17H16N6O7Zn
  35. The crystal structure of diaqua-bis(6-aminopicolinato-κ2N,O)magnesium(II), C12H14O6N4Mg
  36. Crystal structure of (pyridine-2-carboxamide-κ2N,O)-[tris((1H-benzo[d]imidazol-2-yl)methyl)amine-κ4N,N′,N′′,N′′′]nickel(II) diperchlorate — methanol (1/3), C33H39Cl2N9NiO12
  37. Crystal structure of catena-poly[diaqua-bis(3-(4-trifluoromethyl-phenyl)-acrylato-κO1)-(μ2-1,4-bis(1-imidazolyl)benzene-κ2N3:N3)cobalt(II)], C32H26CoF6N4O6
  38. Crystal structure of (E)-3-(2-(2-hydroxy-4-methoxystyryl)-3,3-dimethyl-3H-indol-1-ium-1-yl)propane-1-sulfonate monohydrate, C22H25NO5S⋅H2O
  39. The crystal structure of bis(N-oxy-2-(1H-tetrazol-1-yl) acetamide κ2O,O′)-diaqua-zinc(II), C6H12ZnN10O6
  40. Crystal structure of (E)-4-((4-chlorophenylimino)methyl)pyridinium 3,5-dinitrobenzoate, C19H13ClN4O6
  41. Crystal structure of dichlorido-bis((E)-2-((pyridin-4-ylmethylene)amino)phenol)zinc(II), C24H20Cl2N4O2Zn
  42. Crystal structure of cyclo-[tetrachlorido-bis(μ2-p-xylylenediamine-κ2N:N′)dipalladium(II)] dimethyl sulfoxide solvate, C20H36Cl4N4O2Pd2S2
  43. Crystal structure of 4-(3-fluorophenyl)-7-hydroxy-2H-chromen-2-one, C15H9FO3
  44. Crystal structure of (E)-2-((2-(pyrimidin-2-yl)hydrazono)methyl)quinolin-1-ium perchlorate – methanol (1/1), C15H16N5O5Cl
  45. The crystal structure of bis(N-(amino(pyridin-2-yl)methylene)-5-chloro-2-hydroxybenzohydrazonato-κ3N,N′,O)zinc(II) – methanol (2/5), C57H60Cl2N16O13Zn2
  46. Synthesis and crystal structure of 4,4′-di(4-pyridyl)-6,6′-di(tert-butyl)-2,2′-[propylenedioxybis(nitrilomethylidyne)]diphenol, C35H40N4O4
  47. Crystal structure of (3E,3′E)-3,3′-((1,3,4-thiadiazole-2,5-diyl)bis(sulfanediyl))bis(4-hydroxy-4-phenylbut-3-en-2-one), C22H18N2O4S3
  48. Crystal structure of (N-benzyl-N-methyl-dithiocarbamato-κ2S,S′)di(4-chlorobenzyl)chloridotin(IV), C23H22Cl3NS2Sn
  49. Crystal structure of (1,4,7,10,13,16-hexaoxacyclooctadecane-κ6O6) sodium bromide hydrate, [Na(18-crown-6)]Br ⋅ H2O, C12H26BrNaO7
  50. Crystal structure of 7-ethoxyl-6,8-difluoro-4-oxo-1-phenyl-1,4-dihydro-quinoline-3-carboxylic acid, C18H13F2N1O4
  51. Crystal structure of chlorido (2-(4-ethylphenyl)pyrimidine-k2C,N)(triphenylphosphane-kP) palladium(II), C30H26ClN2PPd
  52. Crystal structure of 18-crown-6 – 1,4-diiodotetrafluorobenzene – acetonitrile (1/1/2), C22H30F4I2N2O6
  53. Crystal structure of diisobutyl 2,5-dihydroxycyclohexa-1,4-diene-1,4-dicarboxylate, C16H24O6
  54. Crystal structure of poly[[tris(μ2-cis-1,2-cyclohexanedicarboxylato)-κ2O, O′]-bis[μ3-1,3,5-tris[(1H-imidazol-1-yl)methyl]benzene-κ3N, N′,N′′]-trizinc(II)] – water (1/20), C60H106N12O32Zn3
  55. The synthesis and crystal structure of 5-amino-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-4-((trifluoromethyl)sulfinyl)-1H-pyrazole-3-carboxamide–tetrahydrofuran (1/1), C16H14N4Cl2F6O3S
  56. Crystal structure of dimethylbis(diisopropyldithiocarbamato-κ2S,S′)tin(IV), C16H34N2S4Sn
  57. Crystal structure of diisopropyl 2,5-dihydroxycyclohexa-1,4-diene-1,4-dicarboxylate, C14H20O6
  58. The synthesis and crystal structure of ethyl (E)-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-5-((2-methoxybenzylidene)amino)-4-((trifluoromethyl)sulfinyl)-1H-pyrazole-3-carboxylate, C22H15N3Cl2F6O4S
  59. The crystal structure of a matrine derivative, 13-(methylamine-1-yl) carbodithioate matrine, C17H27N3OS2
  60. Crystal structure of bis(2-hydroxy-6-((phenylimino)methyl)phenolato-κ2N,O)copper(II), C26H20CuN2O4
  61. The crystal structure of 2-p-fluorophenyl-5-dihydroxymethyl-1,3,4-oxadiazole, C9H7FN2O3
  62. Crystal structure of dichloridobis(4-chlorophenyl-κC1)(1,10-phenanthroline-κ2N,N′)tin(IV), C24H16Cl4N2Sn
  63. Crystal structure of bis{bromido-triphenyltin(IV)}(μ2-[4,4′-bipyridine]1,1′-dioxide-κ2O:O′), C46H38Br2N2O2Sn2
  64. Crystal structure of 2-(5-chloro-quinolin-8-yloxy)-N-quinolin-8-yl-acetamide, C20H14N3O2Cl
  65. Crystal structure of bis(N-(1-(3-ethylpyrazin-2-yl)ethylidene)-3-hydroxy-2-naphthohydrazonato-κ3N,N′,O)cobalt(II) — dimethylformamide (1/1), C41H41N9O5Co
  66. Crystal structure of bis[2-(1-(3-ethylpyrazin-2-yl)ethylidene)-1-tosylhydrazin-1-ido-κ3-N,N′,O]copper(II), C30H34N8O4S2Cu
  67. Crystal structure of (2-p-tolylpyrimidine-κ2C,N)(triphenylphosphane-κP) palladium(II), C29H24ClN2PPd
  68. Halogen bonding in crystal structure of bis(1,4,7,10-tetraoxacyclododecane-κ4O,O′,O′′,O′′′)cesium triiodide, C16H32CsI3O8
  69. The synthesis and crystal structure of N-(3-cyano-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-4-(trifluoromethylsulfinyl)-1H-pyrazol-5-yl)-2-phenylacetamide, C20H10N4Cl2F6O2S
  70. The crystal structure of 4-(trifluoromethyl)nicotinic acid, C7H4F3NO2
  71. Crystal structure of 3-(2-methylbenzyl)thiazolidin-2-one, C11H13ONS
  72. The crystal structure of 2,2,2-trifluoro-1-(isoquinolin-1-yl)ethane-1,1-diol, C11H8F3NO2
  73. The crystal structure of 3-bromoisonicotinic acid, C6H4BrNO2
  74. The crystal structure of 5-nitropicolinic acid monohydrate, C6H6N2O5
  75. The crystal structure of 3-(4-hydroxybenzyl)-1,5-dioxaspiro[5.5]undecane-2,4-dione, C16H18O5
  76. Crystal structure of [[Mo3Se7(S2CNEt2)3]2(μ-Se)] ⋅ 2(C6H4Cl2), C42H68Cl4Mo6N6S12Se15
  77. Crystal structure of (E)-4-hydroxy-3-((5-phenyl-1,3,4-oxadiazol-2-yl)thio)pent-3-en-2-one, C13H12N2O3S
  78. The crystal structure of (2,3-dioxo-5,6:13,14-dibenzo-9,10-benzo-1,4,8,11-7, 11-diene-κ4N,N′,N′′,N′′′)-nickel(II), Ni(C22H14N4O2)
  79. Crystal structure of 3-(1-benzyl-2-ethyl-4-nitro-1H-imidazol-5-ylthio)-propanoic acid, C15H17N3O4S
  80. The crystal structure of dichlorobis(2-(dicyclohexylphosphino)-2′,4′,6′-tri-i-propyl-1,1′-biphenyl) palladium(II)-dichloroform, C68H100Cl8P2Pd
  81. Crystal structure and antimicrobial properties of (1,4,7,10-tetraoxacyclododecane-κ4O,O′,O′′,O′′′)cesium(I) pentaiodide, C16H32CsI5O8
Heruntergeladen am 3.10.2025 von https://www.degruyterbrill.com/document/doi/10.1515/ncrs-2019-0760/html
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