Startseite Crystal structure of (E)-2-((2-(pyrimidin-2-yl)hydrazono)methyl)quinolin-1-ium perchlorate – methanol (1/1), C15H16N5O5Cl
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Crystal structure of (E)-2-((2-(pyrimidin-2-yl)hydrazono)methyl)quinolin-1-ium perchlorate – methanol (1/1), C15H16N5O5Cl

  • Huanhuan Yang , Fanyu Shi , Qingqing Xu , Jinghai Wang und Ai-Ping Xing ORCID logo EMAIL logo
Veröffentlicht/Copyright: 25. März 2020

Abstract

C15H16N5O5Cl, monoclinic, P21/n (no. 14), a = 7.37210(10) Å, b = 13.30639(19) Å, c = 17.1682(2) Å, β = 97.2301(12)°, Z = 4, V = 1670.74(4) Å3, Rgt(F) = 0.0357, wRref(F2) = 0.1023, T = 173(1) K.

CCDC no.: 1977198

The asymmetric unit 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:Yellow cube
Size:0.20 × 0.10 × 0.10 mm
Wavelength:Cu Kα radiation (1.54184 Å)
μ:2.39 mm−1
Diffractometer, scan mode:SuperNova, ω
θmax, completeness:74.8°, >99%
N(hkl)measured, N(hkl)unique, Rint:6479, 3313, 0.018
Criterion for Iobs, N(hkl)gt:Iobs > 2 σ(Iobs), 3022
N(param)refined:241
Programs:CrysAlisPRO [1], Olex2 [2], SHELX [3], [4]
Table 2:

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

AtomxyzUiso*/Ueq
Cl10.57731(5)0.53745(3)0.84240(2)0.02563(13)
O10.6532(2)0.47832(11)0.90768(8)0.0467(4)
O20.52243(19)0.47407(10)0.77588(7)0.0424(3)
O30.42113(18)0.59200(10)0.86131(9)0.0456(3)
O40.71333(17)0.60872(10)0.82253(7)0.0364(3)
O50.59300(17)0.64623(9)0.43948(6)0.0330(3)
H5B0.57370.68350.47560.049*
C150.5755(3)0.70157(14)0.36811(9)0.0355(4)
H15A0.62510.66310.32850.053*
H15B0.64080.76390.37620.053*
H15C0.44860.71510.35150.053*
N10.51510(17)0.78806(10)0.55241(7)0.0258(3)
N20.51253(19)0.84204(11)0.68570(8)0.0297(3)
N30.63795(17)0.69064(10)0.65879(7)0.0257(3)
H30.66610.68230.70850.031*
N40.67750(16)0.61947(10)0.60863(7)0.0234(3)
N50.76895(16)0.47665(9)0.50539(7)0.0209(3)
C10.4247(2)0.87224(12)0.52842(9)0.0290(3)
H10.39540.88300.47480.035*
C20.3733(2)0.94339(13)0.57962(10)0.0317(4)
H20.30871.00080.56210.038*
C30.4233(2)0.92465(13)0.65863(10)0.0325(4)
H3A0.39320.97200.69470.039*
C40.5517(2)0.77768(12)0.63038(9)0.0242(3)
C50.7544(2)0.53839(12)0.63682(9)0.0252(3)
H5A0.77770.52870.69080.030*
C60.80431(19)0.46239(11)0.58312(9)0.0231(3)
C70.8932(2)0.37398(12)0.61188(9)0.0274(3)
H70.91690.36310.66570.033*
C80.9446(2)0.30409(12)0.56066(10)0.0286(3)
H81.00430.24590.57990.034*
C90.90804(19)0.31946(11)0.47871(9)0.0251(3)
C100.9560(2)0.24869(12)0.42337(10)0.0309(3)
H101.01820.19030.44030.037*
C110.9109(2)0.26629(13)0.34499(10)0.0336(4)
H110.94200.21950.30870.040*
C120.8175(2)0.35476(13)0.31860(9)0.0316(4)
H120.78740.36530.26500.038*
C130.7702(2)0.42562(12)0.37040(9)0.0267(3)
H130.70970.48410.35240.032*
C140.81479(19)0.40814(11)0.45139(9)0.0221(3)
H50.718(3)0.5315(16)0.4874(13)0.041(6)*

Source of material

All chemicals were of reagent grade and used without further purification. The title compound was synthesized according to the relevant literature [5].

The synthesis of the intermediate 2-hydrazinopyrimidine: 2-chloropyrimidine (20 mmol, 2.29 g) was dissolved in absolute ethanol (30 mL). Then, excess hydrazine hydrate (8 mL, 80%) was added to the solution under stirring; a pale yellow solution formed immediately, accompanied with the release of heat. About 2 h later, colorless needle crystals appeared. The crystals were filtered and purified by recrystallization in ethanol. Yield: ca. 80%.

The synthesis of the target compound: 2-hydrazinopyrimidine (10 mmol, 1.10 g) was dissolved in absolute ethanol, furthermore 2-quinolinecarboxaldehyde (10 mmol, 1.57 g) and 2-hydrazinopyrimidine (10 mmol, 1.10 g) were dissolved in ethanol, respectively. And then, both solutions were mixed and reacted by reflux for 6 h to form a bright yellow solution. The pale yellow powder appeared by vacuum distillation and filtration. Yield: ca. 65%. The yellow powder (0.1 mmol, 24.9 mg) was dissolved in methanol to form a solution, and then a drop of perchloric acid was added. This solution was filtered and evaporated slowly at room temperature. A few days later, pale yellow crystals appeared. Yield: ca. 70%.

Experimental details

The H atoms were added geometrically using riding models and refined isotropically. Their Uiso values were set to 1.2Ueq of the parent C and N atoms, and 1.5Ueq of the parent O atoms.

Comment

As far as we know, pyrimidine derivatives have biological activities, such as anti-tumor, bactericidal, insecticidal and plant growth promotion. They are important pharmaceutical intermediates [6], [7], [8], [9]. Quinoline derivatives have also attracted great interest for the variety of biological activities such as antibacterial and anticancer activities [10], [11]. Moreover, the nitrogen atoms of the quinoline and pyrimidine derivatives have strong coordination ability to transition metals and rare-earth metals [12], [13].

The asymmetric unit of the title compound contains one organic cation, one perchlorate anion and one methanol molecule (see the figure). The C=N bond length of the title compound is 1.285(2) Å, which proved that the synthesis of title compound was successful. All geometric parameters are in the expected ranges [14], [15]. The nitrogen atom of quinoline section got a proton from perchloric acid in solution and formed a cationic structure. The dihedral angle between the quinoline plane and the pyrimidine plane is 1.33°. Abundant hydrogen bonds are formed between adjacent molecules through perchlorate anions and solvent methanol molecules as well.

References

1. Rigaku Oxford Diffraction. CrysAlis Pro Software system, version 1. 171. 38. 43f. Rigaku Oxford Diffraction (2015).Suche in Google Scholar

2. Dolomanov, O. V.; Bourhis, L. J.; Gildea, R. J.; Howard, J. A. K.; Puschmann, H.: OLEX2: a complete structure solution, refinement and analysis program. J. Appl. Crystallogr. 42 (2009) 339–341.10.1107/S0021889808042726Suche in Google Scholar

3. Sheldrick, G. M.: Crystal structure refinement with SHELXL. Acta Crystallogr. C71 (2015) 3–8.10.1107/S2053229614024218Suche in Google Scholar PubMed PubMed Central

4. Sheldrick, G. M.: SHELXT-integrated space-group and crystal-structure determination. Acta Crystallogr. A71 (2015) 3–8.10.1107/S2053273314026370Suche in Google Scholar PubMed PubMed Central

5. Yuan, J.; Chu, Y.-X.; Kou, H.-Z.: Synthesis, crystal structures, and magnetic properties of methoxido-bridged dinuclear MnIII complexes derived from tri-dentate chelating ligands. J. Coord. Chem. 69 (2016) 1218–1225.10.1080/00958972.2016.1166217Suche in Google Scholar

6. Dehnhardt, C. M.; Venkatesan, A. M.; Santos, E. D.; Chen, Z.; Santos, O.; Ayral-Kaloustian, S.; Brooijmans, N.; Mallon, R.; Hollander, I.; Feldberg, L.; Lucas, J.; Chaudhary, I.; Yu, K.; Gibbons, J.; Abraham, R.; Mansour, T. S.: Lead optimization of N-3-substituted 7-morpholinotriazolopyrimidines as dual phosphoinositide 3-kinase/mammalian target of rapamycin inhibitors: discovery of PKI-402. J. Med. Chem. 53 (2010) 798–810.10.1021/jm9014982Suche in Google Scholar PubMed

7. Li, Z. H.; Liu, X. Q.; Geng, P. F.; Suo, F. Z.; Ma, J. L.: Discovery of [1,2,3]triazolo[4,5-d]pyrimidine derivatives as novel LSD1 inhibitors. ACS Med. Chem. Lett. 8 (2017) 384–389.10.1021/acsmedchemlett.6b00423Suche in Google Scholar PubMed PubMed Central

8. Yu, W.; Goddard, C.; Clearfield, E.; Mills, C.; Xiao, T.; Guo, H.; Morrey, J. D.; Motter, N. E.; Zhao, K.; Block, T. M.; Cuconati, A.; Xu, X.: Design, synthesis, and biological evaluation of triazolo-pyrimidine derivatives as novel inhibitors of hepatitis B virus surface antigen (HBsAg) secretion. J. Med. Chem. 54 (2011) 5660–5670.10.1021/jm200696vSuche in Google Scholar PubMed PubMed Central

9. Baraldi, P. G.; Cacciari, B.; Moro, S.; Spalluto, G.; Pastorin, G.; Ros, T. D.; Klotz, K.-N.; Varani, K.; Gessi, S.; Borea, P. A.: Synthesis, biological activity, and molecular modeling investigation of new pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine derivatives as human A3 adenosine receptor antagonists. J. Med. Chem. 45 (2002) 770–780.10.1021/jm0109614Suche in Google Scholar PubMed

10. Ding, W. Q.; Liu, B.; Vaught, J. L.; Yamauchi, H.; Lind, S. E.: Anticancer activity of the antibiotic clioquinol. Cancer Res. 65 (2005) 3389–3395.10.1158/0008-5472.CAN-04-3577Suche in Google Scholar PubMed

11. Jiang, H.; Taggart, J. E.; Zhang, X.; Benbrook, D. M.; Lind, S. E.; Ding, W.-Q.: Nitroxoline (8-hydroxy-5-nitroquinoline) is more a potent anti-cancer agent than clioquinol(5-chloro-7-iodo-8-quinoline). Cancer Lett. 312 (2011) 11–17.10.1016/j.canlet.2011.06.032Suche in Google Scholar PubMed PubMed Central

12. Tardito, S.; Barilli, A.; Bassanetti, I.; Tegoni, M.; Bussolati, O.; Franchi-Gazzola, R.; Mucchino, C.; Marchio, L.: Copper-dependent cytotoxicity of 8-hydroxyquinoline derivatives correlates with their hydrophobicity and does not require caspase activation. J. Med. Chem. 55 (2012) 10448–10459.10.1021/jm301053aSuche in Google Scholar PubMed

13. Qin, Q.-P.; Chen, Z.-F.; Qin, J.-L.; He, X.-J.; Li, Y.-L.; Liu, Y.-C.; Huang, K.-B.; Liang, H.: Studies on antitumor mechanism of two planar platinum(II) complexes with 8-hydroxyquinoline: synthesis, characterization, cytotoxicity, cell cycle and apoptosis. Eur. J. Med. Chem. 92 (2015) 302–313.10.1016/j.ejmech.2014.12.052Suche in Google Scholar PubMed

14. Buvaylo, E. A.; Kokozay, V. N.; Yu. Vassilyeva, O.; Skelton, B. W.; Nesterova, O. V.; Pombeiro, A. J. L.: Copper(II) complex of the 2-pyridinecarbaldehyde aminoguanidine Schiff base: crystal structure and catalytic behaviour in mild oxidation of alkanes. Inorg. Chem. Commun. 78 (2017) 85–90.10.1016/j.inoche.2017.03.008Suche in Google Scholar

15. Valdes-Martinez, J.; Alstrum-Acevedo, J. H.; Toscano, R. A.; Espinosa-Perez, G.; Helfrich, B. A.; West, D. X.: Bis(2-pyridiniomethyleneaminoguanidinium) trans-tetraaquadichloronickel(II) dichloride tetrahydrate. Acta Crystallogr. E57 (2001) m137–m139.10.1107/S1600536801003725Suche in Google Scholar

Received: 2019-11-29
Accepted: 2020-01-13
Published Online: 2020-03-25
Published in Print: 2020-04-28

©2020 Huanhuan Yang 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 17.11.2025 von https://www.degruyterbrill.com/document/doi/10.1515/ncrs-2019-0873/html
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