Startseite The crystal structure of 4-(4-chlorophenyl)cyclohexane-1-carboxylic acid, C13H15ClO2
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The crystal structure of 4-(4-chlorophenyl)cyclohexane-1-carboxylic acid, C13H15ClO2

  • Chao-Jun Du ORCID logo EMAIL logo , Zong-Dong Wang , Xiao-Ke Wang und Yan Zeng
Veröffentlicht/Copyright: 25. März 2020

Abstract

C13H15ClO2, monoclinic, P21/n (no. 14), a = 14.4696(7) Å, b = 9.5385(4) Å, c = 18.7042(11) Å, β = 112.619(2)°, V = 2383.0(2) Å3, Z = 8, Rgt(F) = 0.0414, wRref(F2) = 0.1090, T = 150(2) K.

CCDC no.: 1985066

The asymmetric unit of the title structure is shown in the figure. 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:Colorless block
Size:0.25 × 0.15 × 0.10 mm
Wavelength:Mo Kα radiation (0.71073 Å)
μ:0.30 mm−1
Diffractometer, scan mode:Bruker APEX-II, φ and ω
θmax, completeness:26.4°, >99%
N(hkl)measured, N(hkl)unique, Rint:32366, 4858, 0.053
Criterion for Iobs, N(hkl)gt:Iobs > 2 σ(Iobs), 3550
N(param)refined:297
Programs:Bruker [1], SHELX [2], Olex2 [3], [4]
Table 2:

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

AtomxyzUiso*/Ueq
C10.46667(13)0.32592(19)0.60064(11)0.0271(4)
C20.36168(13)0.3092(2)0.54110(11)0.0270(4)
H20.3606990.2265190.5079610.032*
C30.33404(15)0.4400(2)0.48926(12)0.0369(5)
H3A0.3395030.5241520.5216120.044*
H3B0.3816850.4507080.4632630.044*
C40.22744(14)0.4291(2)0.42815(11)0.0356(5)
H4A0.2240370.3510550.3923080.043*
H4B0.2103110.5168260.3975810.043*
C50.15106(13)0.40370(19)0.46515(11)0.0269(4)
H50.1556910.4846920.5003130.032*
C60.17985(13)0.2720(2)0.51536(11)0.0290(4)
H6A0.1761140.1895720.4821850.035*
H6B0.1316340.2575270.5405300.035*
C70.28581(13)0.2837(2)0.57758(11)0.0313(4)
H7A0.2884060.3618290.6131190.038*
H7B0.3029240.1960380.6082780.038*
C80.04537(13)0.40065(19)0.40497(10)0.0251(4)
C9−0.01749(14)0.5152(2)0.39584(11)0.0321(5)
H90.0070620.5952820.4277580.038*
C10−0.11520(14)0.5160(2)0.34136(11)0.0339(5)
H10−0.1566930.5958270.3356600.041*
C11−0.15101(13)0.3993(2)0.29577(10)0.0274(4)
C12−0.09056(14)0.2846(2)0.30130(11)0.0294(4)
H12−0.1153400.2056880.2684650.035*
C130.00756(14)0.2865(2)0.35598(11)0.0290(4)
H130.0496410.2079790.3598900.035*
C140.76258(14)0.8498(2)0.74946(11)0.0285(4)
C150.65660(14)0.8546(2)0.69085(11)0.0298(4)
H150.6582940.8695610.6384500.036*
C160.60240(15)0.7184(2)0.68970(13)0.0417(6)
H16A0.6010220.7012090.7414800.050*
H16B0.6389190.6399400.6777190.050*
C170.49465(16)0.7233(2)0.62884(13)0.0430(6)
H17A0.4966150.7289240.5765920.052*
H17B0.4598520.6353560.6316210.052*
C180.43559(14)0.8471(2)0.64015(11)0.0313(4)
H180.4269490.8325540.6901640.038*
C190.49281(14)0.9834(2)0.64682(13)0.0400(5)
H19A0.4563831.0602090.6603170.048*
H19B0.4954561.0058740.5959650.048*
C200.59961(15)0.9761(2)0.70797(14)0.0414(6)
H20A0.6348311.0652230.7082720.050*
H20B0.5974580.9632590.7598270.050*
C210.33156(14)0.85609(19)0.57613(11)0.0277(4)
C220.24625(15)0.8430(2)0.59257(12)0.0370(5)
H220.2531020.8263090.6444420.044*
C230.15104(15)0.8537(2)0.53482(13)0.0405(5)
H230.0934730.8449320.5471780.049*
C240.14089(14)0.8771(2)0.45974(12)0.0311(4)
C250.22375(15)0.8890(2)0.44093(12)0.0351(5)
H250.2161500.9037590.3887390.042*
C260.31826(15)0.8790(2)0.49909(12)0.0347(5)
H260.3754240.8878800.4862250.042*
Cl1−0.27574(3)0.39643(6)0.23058(3)0.04083(16)
Cl20.02171(4)0.89427(6)0.38669(4)0.04856(18)
H10.599(2)0.314(3)0.6135(18)0.086(10)*
H30.892(2)0.875(3)0.7604(18)0.081(10)*
O10.53649(10)0.30102(18)0.57425(8)0.0404(4)
O20.48521(10)0.36194(14)0.66807(8)0.0339(3)
O30.83116(11)0.87893(16)0.72272(8)0.0383(4)
O40.78200(10)0.82055(18)0.81785(8)0.0427(4)

Source of material

All of starting materials are used without further purification. Under stirring, 4-(4-chlorophenyl)cyclohexanecarboxylic acid (2.38 g, 10 mmol) was added to 25 mL THF in a warm water bath for 30 min. After cooling, the solution was filtered and evaporated in air at room temperature. Colorless crystals were harvested after one week, yield: 82.6%.

Experimental details

The structure was solved by direct methods with the SHELXS program. All of H-atoms from C atoms were positioned with idealized geometry with Uiso(H) = 1.2Ueq(C). The two hydrogen atoms from O atoms were positioned with Q peaks and refined freely.

Comment

It’s known that the methyl or ethyl esters of 4-arylcyclohexanecarboxylic acid and its derivatives are one of the most common kinds of the products of Diels-Alder reactions [5], [6], [7], [8]. These compounds mentioned above could although come from other organic reactions [9], [10]. Especially, these asymmetrically substituted products, are usually synthesized by the Michael addition [11], [12], [13], [14], [15]. However, the corresponding acids are rare [16].

As shown in the figure, X-ray diffraction indicates that the asymmetric unit contains two molecules of the title compound. All atoms of the chlorophenyl moiety are nearly co-planar, the cyclohexyl group adapts the chair conformation. A dimer is generated by the O—H⋯O hydrogen bond with a head to head model. All of the bond lengths and angles of the title compound are comparable with its analogues.

Acknowledgements

This study was supported by the project of tackling key problems in science and technology in Henan Province (No. 182102210460 and 182102311076).

References

1. Bruker. SAINT v8.37A. Bruker AXS Inc, Madison, WI, USA (2015).Suche in Google Scholar

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

3. Bourhis, L. J.; Dolomanov, O. V.; Gildea, R. J.; Howard, J. A. K.; Puschmann, H.: The anatomy of a comprehensive constrained, restrained refinement program for the modern computing environment-Olex2 dissected. Acta Crystallogr. A71 (2015) 59–75.10.1107/S2053273314022207Suche in Google Scholar

4. 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

5. Alza, E.; Sayalero, S.; Cambeiro, X. C.; Martin-Rapun, R.; Miranda, P. O.; Pericas, M. A.: Catalytic batch and continuous flow production of highly enantioenriched cyclohexane derivatives with polymer-supported diarylprolinol silyl ethers. Synlett 4 (2011) 464–468.10.1002/chin.201126054Suche in Google Scholar

6. Kirfel, A.; Kordy, M. E.; Troschutz, R.: Methyl 3-(4-chlorobenzoyl)-4-(4-chlorophenyl)-1-cyano-4-hydroxy-2,6-diphenylcyclohexanecarboxylate, C34H27Cl2NO4. Acta Crystallogr. C39 (1983) 1563–1565.10.1107/S0108270183009270Suche in Google Scholar

7. Lv, H.; Mo, J.; Fang, X.; Chi, Y. R.: Formal Diels-Alder reactions of chalcones and formylcyclopropanes catalyzed by chiral N-heterocyclic carbenes. Org. Lett. 13 (2011) 5366–5369.10.1021/ol202250sSuche in Google Scholar PubMed

8. Huang, X.; Liu, M.; Jasinski, J. P.; Peng, B.; Zhang, W.: Recyclable organocatalysts for a one-pot asymmetric synthesis of 2-fluorocyclohexanols bearing six contiguous stereocenters. Adv. Synth. Catal. 359 (2017) 1919–1926.10.1002/adsc.201700129Suche in Google Scholar

9. Chu, X.-J.; Bartkovitz, D.; Danho, W.; Swistok, J.; Cheung, A. W.-H.; Kurylko, G.; Rowan, K.; Yeon, M.; Franco, L.; Qi, L.; Chen, L.; Yagaloff, K.: Discovery of 1-amino-4-phenylcyclohexane-1-carboxylic acid and its influence on agonist selectivity between human melanocortin-4 and -1 receptors in linear pentapeptides. Bioorg. Med. Chem. Lett. 15 (2005) 4910–4914.10.1016/j.bmcl.2005.08.012Suche in Google Scholar PubMed

10. Caron, S.; Vazquez, E.: The synthesis of a selective PDE4/TNF α inhibitor. Org. Process Res. Dev. 5 (2001) 587–592.10.1021/op010223pSuche in Google Scholar

11. Sun, P.; Meng, C.-Y.; Zhou, F.; Li, X.-S.; Xie, J.-W.: Organocatalytic asymmetric one-pot sequential reaction: synthesis of highly substituted spirocyclohexanepyrazolones with six contiguous stereogenic carbons. Tetrahedron 70 (2014) 9330–9336.10.1016/j.tet.2014.10.038Suche in Google Scholar

12. Cai, L.; Zhang, B.; Wu, G.; Song, H.; He, Z.: Chemoselective phosphine-catalyzed cascade annulations between two different activated alkenes: highly diastereoselective syntheses of polysubstituted cyclohexanes and cyclopentenes. Chem. Commun. 47 (2011) 1045–1047.10.1039/C0CC02817GSuche in Google Scholar PubMed

13. Chauhan, P.; Urbanietz, G.; Raabe, G.; Enders, D.: Asymmetric synthesis of functionalized cyclohexanes bearing five stereocenters via a one-pot organocatalytic Michael-Michael-1,2-addition sequence. Chem. Commun. 50 (2014) 6853–6855.10.1039/C4CC01885KSuche in Google Scholar

14. Chauhan, P.; Urbanietz, G.; Raabe, G.; Enders, D.: Organocatalytic one-pot 1,4-/1,6-/1,2-addition sequence for the stereocontrolled formation of six consecutive stereocenters. Chem. Commun. 51 (2015) 2270–2272.10.1039/C4CC09730KSuche in Google Scholar

15. Blumel, M.; Chauhan, P.; Vermeeren, C.; Dreier, A.; Lehmann, C. W.; Enders, D.: Asymmetric organocatalytic synthesis of highly functionalized spirocyclohexane indandiones via a one-pot Michael/Michael/Aldol sequence. Synthesis 47 (2015) 3618–3628.10.1002/chin.201614070Suche in Google Scholar

16. Shi, D.; Xie, Y.; Zhou, H.; Xia, C.; Huang, H.: A highly diastereo-and enantioselective reaction for constructing functionalized cyclohexanes: six contiguous stereocenters in one step. Angew. Chem. Int. Ed. 51 (2012) 1248–1251.10.1002/anie.201107495Suche in Google Scholar PubMed

Received: 2020-01-06
Accepted: 2020-02-19
Published Online: 2020-03-25
Published in Print: 2020-06-25

©2020 Chao-Jun Du 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 bis [1-(phenylsulfonyl)-2-(1-(pyrazin-2-yl)ethylidene)hydrazin-1-ido-κ3N,N′,O]cobalt(II), C24H22N8O4S2Co
  3. The crystal structure of 1,3-bis(4-(methoxycarbonyl)benzyl)-2-methyl-1H-benzo[d]imidazol-3-ium bromide, C26H25BrN2O4
  4. Crystal structure of {tris((1H-benzo[d]imidazol-2-yl)methyl)amine-κ4N,N′,N′′,N′′′}-(nitrito-κ2O,O′)nickel(II) perchlorate – ethanol (1/1), C26H27ClN8NiO7
  5. Crystal structure of catena-poly[aqua[(μ2-4,5-dicarboxylato-2-(2-carboxylatophenyl)imidazol-1-ido-κ4N,O,O′:N′)](μ2-4,4′-bipyridine-κ2N:N′)dicopper(II)], C22H14Cu2N4O7
  6. Crystal structure of chlorido-tris(4-methylbenzyl-κC)-(triphenylarsine oxide-κO)tin(IV), C42H42AsClOSn
  7. The crystal structure of 4,4′-bipyridinium bis(3-carboxy-2-nitrobenzoate) tetrahydrate, C13H13N2O8
  8. Crystal structure of 1-(3-chlorophenyl)-4-(4-(((2,3-dihydro-1H-inden-5-yl)oxy)methyl)phenethyl)piperazine, C28H31ClN2O
  9. Crystal structure of catena-poly[diaqua-bis(μ2-5,5′-(1H-imidazole-4,5-diyl)bis(tetrazol-2-ido)-κ4N,N′:N′′,N′′′)magnesium], C10H8N20O2Mg
  10. The crystal structure of (E)-2-((2-hydroxy-4-ethoxybenzylidene)amino)-2-methylpropane-1,3-diol monohydrate, C13H21NO5
  11. Crystal structure of catena-poly[diaqua-(μ2-bipyridine-κ2N:N′)-bis(3,5-dichloroisonicotinato-κO)cadmium(II)] dihydrate, C22H20CdCl4N4O8
  12. The crystal structure of 4-(4-chlorophenyl)cyclohexane-1-carboxylic acid, C13H15ClO2
  13. Redetermination of the crystal structure of yttrium(III) trinitrate(V) pentahydrate, Y(NO3)3 ⋅ 5 H2O, H10N3O14Y
  14. Crystal structure of catena-poly[di-μ2-chlorido-1,10-phenanthroline-κ2N,N′-cadmium(II)], C12H8Cl2CdN2
  15. Crystal structure of 4-((2-methyl-6-(trifluoromethyl)pyrimidin-4-yl)oxy)benzoic acid, C13H9F3N2O3
  16. Crystal structure of 3-acetyl-4-hydroxybenzoic acid, C18H16O8
  17. Crystal structure of bis(N,2-bis(4-ethoxybenzylidene)hydrazine-1-carbohydrazonothioato-κ2N,S)nickel(II) — N,N-dimethylformamide (1/2), C44H56N10S2O6Ni
  18. The crystal structure of 5-chloro-4,6-dimethoxypyrimidin-2-amine, C6H8ClN3O2
  19. Crystal structure of poly[aqua-(μ4-benzene-1,2,4,5-tetracarboxylato-κ4O,O′,O′′,O′′′)bis(μ2-1-(4-(1H-imidazol-1-yl)benzyl)-1H-1,2,4-triazole-κ2N:N)dinickel(II)], NiC17H14N5O5
  20. Crystal structure of poly[aqua(5-dimethylamino)naphthalene-1-sulfonato-κ2N:O)(μ2-4,4′-bipyridyl -κ2N:N′)silver(I)], C44H44Ag2N6O8S2
  21. Crystal structure of 1-[3-(trifluoromethyl)cinnamoyl]-3-(pyridin-2-yl-κN)pyrazole-κ2N-bis(2-phenylpyridinato-k2C,N)iridium(III) hexafluorophosphate complex, [C40H28F3IrN5O]PF6
  22. Crystal structure of catena-poly[aqua(μ6-piperazine-1,4-bisethanesulfonato-κ6N:N′:O:O′:O′′:O′′′)(μ2-pyrazinyl-κ2N:N′)disilver(I)sesquihydrate], C12H30Ag2N4O11S2
  23. Crystal structure of (E)-1-(2-nitrophenyl)-N-(o-tolyl)methanimine, C14H12N2O2
  24. Crystal structure of 4′-amino-3′,5′-diisopropyl-(1,1′-biphenyl)-4-carbonitrile, C19H22N2
  25. The crystal structure of poly[bis(N,N-dimethylformamide-κ1O)-tetrakis(μ2-cyanido-κ2C:N)dinickel(II)], C10H14N6O2Ni2
  26. Crystal structure of rac-trans-N,N′-bis(3-bromo-5-chlorosalicylidene)-1,2-cyclohexanediamine, C20H18Br2Cl2N2O2
  27. Crystal structure of rac-trans-N,N′-bis(3,5-dibromosalicylidene)-1,2-cyclohexanediamine, C20H18Br4N2O2
  28. The crystal structure of (dichromato-κ2O,O′)bis(1,10-phenanthroline-κ2N,N′)nickel(II), C12H16N4O7Cr2Ni
  29. The crystal structure of 3-((1R,2S)-1-methylpyrrolidin-1-ium-2-yl)pyridin-1-ium tetrachloridozincate(II) monohydrate, C10H18Cl4ZnN2O
  30. Crystal structure of bis(μ2-azido-k2N,N)-bis(2-amino-1-(N-(3-bromosalicylaldiminato))ethane)-dicopper(II), C20H18Br4N2O2
  31. Crystal structure of (η6-1-methyl-4-isopropylbenzene)-[5-bromo-2-(2-pyridyl)phenyl-κ2C,N]-chloro-ruthenium(II), C21H21BrClNRu
  32. Crystal structure of N-(methyl(oxo)(1-(6-(trifluoromethyl)pyridin-3-yl)ethyl)-λ6-sulfanylidene)cyanamide, C10H10F3N3OS
  33. Crystal structure of 6,6′-((cyclohexane-1,2-diylbis(azanylylidene))bis(methanylylidene))bis(2-bromo-4-chlorophenolato-κ4N,N′,O,O′)nickel(II), C20H16Br2Cl2NiN2O2
  34. Redetermination of the crystal structure of catena-poly[aqua-(1,10-phenanthroline-κ2N,N′)-(μ2-tetraoxidomolybdato(VI)-κ2O:O′)manganese(II) monohydrate, C12H12N2O6MoMn
  35. The crystal structure tetrakis(μ2-o-chlorobenzoato-κ2O:O′)-bis(methanol-κ1O)dirhodium(II), C30H24Cl4O10Rh2
  36. Crystal structure of bis(2,3-diphenyltetrazolidine-5-thione-κ1S)-(nitrato-κ1O)-(nitrato-κ2O,O′)lead(II), C26H20N10O6S2Pb
  37. Crystal structure of bis(3-bromo-N-(1-(3-methylpyrazin-2-yl)ethylidene)benzohydrazonato-κ3O,N,N′)cadmium(II) hemihydrate, C28H25N8O2.5Br2Cd
  38. Crystal structure of catena-poly[tetrakis(μ2-trifluoroacetato-κ2O:O′)(μ2-2,5-dimethylpyrazine-κ2N,N′)dicopper(II)], C7H4CuF6NO4
  39. The crystal structure of catena-poly[bis[3-azoniapentane-1,5-diammonium][bis(μ4-oxo)-tetrakis(μ3-oxo)-heptakis(μ2-oxo)-tetradecaoxo-octa-molybdenum] dihydrate], (C8H36N6O29Mo8)n
  40. Crystal structure of tetraaqua-bis(2-((3,5,6-trichloropyridin-2-yl)oxy)acetato-κO)-nickel(II)—diaqua-bis(2-((3,5,6-trichloropyridin-2-yl)oxy)acetato-nickel(II), C28H24Cl12N4Ni2O18
  41. The crystal structure of bis(2-hydroxypyrimidinium) pentachloridobismuthate(III), (C4N2H5O)2BiCl5
  42. The crystal structure of catena-poly[(μ2-4,4′-dipyridine-κ2N,N′)-bis(3,5,6-trichloropyridine-2-oxyacetato-κO)-bis(ethanol-κO)nickel(II)], C28H26Cl6N4NiO8
  43. Crystal structure and anti-inflammatory activity of (3E,5E)-1-((4-chlorophenyl)sulfonyl)-3,5-bis(4-fluorobenzylidene)piperidin-4-one-dichloromethane (1/1), C26H20Cl3F2NO3S
  44. The crystal structure of 5-bromopicolinic acid monohydrate, C6H6BrNO3
  45. The crystal structure of 2-(3-(4-bromophenyl)-5-(4-fluorophenyl)-4,5-dihydro-1H-pyrazol-1-yl)-8H-indeno[1,2-d]thiazole, C25H17BrFN3S
  46. The crystal structure of catena-poly[(μ2-2-((3-bromo-2-oxidobenzylidene)amino)acetato-κ4O,N,O′:O′′)-(dimethylformamide-κ1O)]zinc(II), C12H13N2O4BrZn
  47. Crystal structure of aqua-azido-κ1N-(6,6′-((propane-1,3-diylbis(azanylylidene))bis(methanylylidene))bis(3-bromophenolato)-κ4N,N′,O,O′iron(III), C17H16Br2FeN5O3
  48. The crystal structure of tris(1-ethylimidazole-κ1N)-(sulfato-κ2O,O′)vanadium(IV), C15H24N6O5SV
  49. Crystal structure of (E)-3-methoxy-N′-(1-(pyridin-2-yl)ethylidene)benzohydrazide, C15H15N3O2
  50. Crystal structure of dichloro-bis-(1-butyl-1H-benzo[d]imidazole)-nickel(II), C22H28Cl2N4Ni
  51. The crystal structure of 2-(2,3-dimethoxyphenyl)-3-hydroxy-4H-chromen-4-one, C17H14O5
  52. The crystal structure of 5-(2-(4-fluorophenyl)hydrazono)-4-methyl-2-((3-(5-methyl-1-(4-methylphenyl)-1H-1,2,3-triazol-4-yl)-1-phenyl-1H-pyrazol-4-yl)methylene) hydrazono)-2,5-dihydrothiazole dimethylformamide monosolvate, C30H25FN10S⋅C3H7NO
  53. The crystal structure of 1,8-bis(pyridin-4-ylethynyl)anthracene-1,2,4,5-tetrafluoro-3,6-diiodobenzene (2/1), C62H32F4I2N4
  54. The crystal structure of 3,6-di-tert-butyl-1,8-diiodo-9-methyl-9H-carbazole, C21H25I2N
  55. The crystal structure of 8-((4-chlorophenylamino)methylene)-6,10-dioxaspiro[4.5]decane-7,9-dione, C15H14ClNO4
  56. The crystal structure of catena-poly[oktaaqua-bis(μ2-4,4′-ethene-1,2-diyldipyridine-κ2N:N′)-(μ2-3,3′-(1-oxidodiazene-1,2-diyl)diphthalato-κ2O:O′)dicobalt(II)] dihydrate, C28H36N4O19Co2
  57. Crystal structure of (E)-1-(2-cyano-3-oxo-1-phenylprop-1-en-1-yl)-3,7-diphenylindolizine-6-carbonitrile, C31H19N3O
  58. Crystal structure of 1,1′-bis(diphenylphosphino)ferrocene-(1,1′-bis(diphenylphosphino)ferrocene-κ2P,P′)-(O-isobutyl sulfurodithioito-κ2S,S′)copper(I), C39H37CuFeOP2S2
  59. Crystal structure of poly[(5-bimethylamino-1-naphthalenesulfonato-κO)-(μ3-hexamethylenetetramino-κ3N:N′:N′′)silver(I)] dihydrate, C36H52Ag2N10O8S2
  60. Crystal structure of poly[μ2-diaqua-(μ2-2-amino-4,5-dicyano-κ2N:N′-imidazol-1-ide)sodium(I)], C5H6N5O2Na
  61. Crystal structure of (1,3-propanediamine-κ2N,N′)(N-(3-aminopropyl)-α-methyl aspartato-κ4N,N′,O,O′)cobalt(III) chloride, C11H24ClCoN4O4
  62. Crystal structure and anti-inflammatory activity of (3E,5E)-3,5-bis(4-fluorobenzylidene)-1-((4-fluorophenyl)sulfonyl)piperidin-4-one-dichloromethane (1/1), C26H20Cl2F3NO3S
  63. Crystal structure of (S)-(+)-1-cyclohexylethylaminium chloride, C8H18NCl
  64. The crystal structure of tris(nitrato-κ2O,O′)-bis(4,4,5,5-tetramethyl-2-(o-pyridyl)imidazoline-1-oxyl 3-oxide-κ2N,O)yttrium(III), C24H32N9O13Y
  65. Hydrogen bonding versus packing effects in the crystal structure of 3-((1R,2S)-1-methylpyrrolidin-1-ium-2-yl)pyridin-1-ium tetraiodidozincate(II), C10H16I4ZnN2
  66. Dimerization of 2-[(2-((2-aminophenyl)thio)phenyl)amino]-cyclohepta-2,4,6-trien-1-one through hydrogen bonding, C19H16N2OS
  67. Crystal structure of 1-(4-chloro-phenyl)-7-ethoxyl-6,8-difluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid, C18H12ClF2NO4
  68. Crystal structure of 7-ethoxy-6,8-difluoro-4-oxo-1-pyridin-2-ylmethyl-1,4-dihydro-quinoline-3-carboxylic acid, C18H14F2N2O4
  69. Crystal structure of octahydro-7aR,8′R-dimethylspiro[isobenzofuran-4(1H), 4′ (3′H)-[1H-7,9a]methanocyclohepta[c]pyran]-1′,3, 9′ (3aH,4′aH)-trione, C20H26O5
  70. Crystal structure of bis(5-ethoxy-2-(((1-hydroxy-2-methyl-3-oxidopropan-2-yl)imino)methyl)phenolato-κ3N,O,O’)manganese(IV) – methanol (1/1), C27H38MnN2O9
  71. Crystal structure of 8a,8a′′-oxybis(8aH-8,9-dioxa-3a1λ4-aza-8aλ4-borabenzo[fg]tetracene), C34H22B2N2O5
  72. Crystal structure of bromido-triphenyl-(triphenylarsine oxide-κO)tin(IV), C36H30AsBrOSn
  73. Crystal structure of catena-poly[chlorido-(μ2-formato-κ2O:O′)-(1,10-phenathroline-κ2N,N′)copper(II)], C26H18Cl2Cu2N4O4
  74. The crystal structure of poly[(μ10-5-carboxyisophthalato-κ10O)disodium], C9H4Na2O6
  75. The crystal structure of 3,5-difluoroisonicotinic acid, C6H3F2NO2
  76. The crystal structure of ethyl-1-(N-(adamantan-1-yl)-carbamothioyl)piperidine-4-carboxylate, C19H30N2O2S
  77. Crystal structure of 5-methyl-3-phenyl-1-tosyl-1,2,3,4-tetrahydropyridine, C19H21NO2S
  78. Crystal structure of bis((3-chlorosalicylidene)-ethylenediaminato-κ4N,N′,O,O′)nickel (II), C16H12Cl2NiN2O2
  79. Crystal structure of (E)-N′-(2-chloro-6-hydroxybenzylidene)-4-hydroxybenzohydrazide — dihydrofuran-2(3H)-one (1/1), C18H17ClN2O5
  80. Crystal structure of bis((3-bromosalicylidene)-ethylenediaminato-κ4N,N′,O,O′) nickel (II), C16H12Br2NiN2O2
  81. Crystal structure of trimethylsulfoxonium tetrachloridocobaltate(II) [(CH3)3SO]2CoCl4
Heruntergeladen am 29.11.2025 von https://www.degruyterbrill.com/document/doi/10.1515/ncrs-2020-0013/html
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