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N-(Siklohekzil(metil)karbamotiyoil)-4-nitrobenzamit Bileşiğinin Sentezi, Kristal Yapısı, DFT Çalışmaları ve Hirshfeld Yüzey Analizi

Year 2022, Volume: 5 Issue: 2, 681 - 706, 18.07.2022
https://doi.org/10.47495/okufbed.1090049

Abstract

Bu çalışmada, yeni N-(siklohekzil(metil)karbamotioil)-4-nitrobenzamit (1) bileşiği iyi verimle sentezlendi ve bileşik 1H NMR spektroskopik tekniğiyle karakterize edildi. Ayrıca, N-siklohekzil(metil)karbamotiyoil)-4-nitrobenzamit’in kristal yapısı, X-ışını tek kristal kırınım tekniği ile aydınlatıldı. Monoklinik sistemde kristallenen 1´in uzay grubu P21/c olarak tespit edildi. Kristal yapının birim hücre parametreleri a = 14,858(4) Å, b = 5,0386(14) Å, c = 22,336(7) Å ve β = 104,952(8)° olarak belirlendi. N-(Siklohekzil(metil)karbamotiyoil)-4-nitrobenzamit bileşiği için B3LYP/6-311G(d,p) teori seviyesinde gaz fazındaki yoğunluk fonksiyoneli teorisi ile optimize edilmiş yapı deneysel olarak tanımlanmış moleküler yapı ile karşılaştırıldı. 1 için HOMO ve LUMO enerjileri ve enerji boşluğu hesaplandı. Bileşiğin HOMO ve LUMO enerji seviyeleri arasında 0,7772 eV’luk bir enerji boşluğunun olduğu tespit edildi. Bu değer, molekülün kimyasal olarak reaksiyona girme eğiliminin yüksek olduğunu ve kararsız olduğunu gösterdi. Moleküller arası etkileşimlerin grafiksel yaklaşımı, Hirshfeld yüzey analizinden elde edildi ve çeşitli etkileşimleri ölçmek için 2D parmak izi çizimleri kullanıldı. Hirshfeld yüzey analizi, yüzey alanına en baskın katkının H···H (%42,10) etkileşimlerinden kaynaklandığı belirledi.

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References

  • Abosadiya HM., Anouar EH., Yamin BM. Synthesis, X-Ray, Spectroscopic characterization (FT-IR, NMR, UV–Vis) and quantum chemical calculations of some substituted benzoylthiourea derivatives. Journal of Molecular Structure. 2019; 1194, 48-56. DOI: 10.1016/j.molstruc.2019.05.060
  • Abosadiya HM. Synthesis, crystal structure and antioxidant evaluation of N-(4-formylpiperazine-1-carbonothioyl)benzamide. European Journal of Chemistry. 2020; 11(2): 156-159. DOI: 10.5155/eurjchem.11.2.156-159.1981.
  • Angulo-Cornejo JR., Ayala-León K., Herbosa GG., Cuevas JV., Diez V., Richter R., Hennig L., Beyer L. Synthesis and structural characterization of N-[4-(2-hydroxyethyl)-1,2,4-oxathiazinan-3-ylidene]-benzamide and its mercury(II) chloride adduct. Zeitschrift Für Naturforschung B Journal of Chemical Sciences. 2005; 60(9): 945-950 DOI: 10.1515/znb-2005-0906.
  • Ashfaq M., Tahir MN., Muhammad S., Munawar KS., Ali A., Bogdanov G., Alarfaji SS. Single-crystal investigation, hirshfeld surface analysis, and DFT study of third-order NLO properties of unsymmetrical acyl thiourea derivatives. ACS Omega. 2021; 6(46): 31211-31225. DOI: 10.1021/acsomega.1c04884.
  • Asiri AM., Faidallah HM., Al-Youbi AO., Alamry KA., Ng SW. 1-Benzoyl-3-[3-cyano-8-methyl-4-(1-methyl-1H-pyrrol-2-Yl)-5,6,7,8-tetra-hydro-quinolin-2-Yl]thio-urea. Acta Crystallographica Section E Crystallographic Communications. 2011; 67(9): o2430- o2430. DOI: 10.1107/S1600536811033046.
  • Ayata S., Kaynak I., Merdivan M. Solid phase extractive preconcentration of silver from aqueous samples. Environmental Monitoring and Assessment. 2009; 153(1-4): 333-338. DOI: 10.1007/s10661-008-0359-6.
  • Aydın F., Aykaç D., Ünver H., İskeleli NO. Synthesis, spectral properties and structure of new novel 3,3′-dibenzoyl-1,1′-(propan-1,3-Diyl)-bisthiourea. Journal of Chemical Crystallography. 2012; 42(4): 381-387. DOI: 10.1007/s10870-011-0258-5.
  • Aydın F., Ünver H., Aykaç D., İskeleli NO. Spectroscopic studies and structure of 4-(3-benzoylthioureido) benzoic acid. Journal of Chemical Crystallography. 2010; 40(12): 1082-1086. DOI: 10.1007/s10870-010-9799-2.
  • Becke AD. Density‐functional thermochemistry. III. The role of exact exchange. The Journal of Chemical Physics .1993; 98(7): 5648-5652. DOI: 10.1063/1.464913.
  • Beyer L., Hoyer E., Hennig H., Kirmse R., Hartmann H., Liebscher J. Synthese und charakterisierung neuartiger übergangsmetallchelate von 1,1-dialkyl-3-benzoyl-thioharnstoffen. Journal Für Praktische Chemie. 1975; 317 (5): 829–839. DOI: 10.1002/prac.19753170518.
  • Bozkurt SS., Merdivan M. Solid phase extraction of gold (III) on silica gel modified with benzoylthiourea prior to its determination by flame atomic absorption spectrometry. Environmental Monitoring and Assessment. 2009; 158(1-4): 15-21. DOI: 10.1007/s10661-008-0561-6.
  • Bruce JC., Koch KR. N-benzoyl-N’,N’-dibutylselenourea and its palladium(II) complex. Acta Crystallographica Section C. 2008; 64 (Pt 1): m1-4. DOI: 10.1107/S0108270107053711.
  • Chermette HJ. Chemical reactivity indexes in density functional theory. Journal of computational chemistry. 1999; 20(1): 129-154.
  • Cornejo JA., Ayala K., Richter R., Böhlig H., Hennig L., Beyer L. Wasserstoffbrücken in 1,1-bis(2-hydroxyethyl)-3-benzoylthioharnstoff und seinen nickel (II)- und kupfer (II)-chelat-komplexen. Zeitschrift für anorganische und allgemeine Chemie. 2005; 631(15): 3040-3045. DOI: 10.1002/zaac.200500266.
  • Déchamps-Olivier I., Guillon E., Mohamadou A., Barbier JP. Coordination of nickel and cobalt with N-morpholine or N,N-diethyl, N’-monosubstituted benzoyl thioureas. Polyhedron. 1996; 15(20): 3617-3622. DOI: 10.1016/0277-5387(96)00081-2.
  • Dennington R., Keith TA., Millam JM. GaussView, Version 6, Semichem Inc., Shawnee Mission, KS, 2016.
  • Dolomanov OV., Bourhis LJ., Gildea RJ., Howard JA., Puschmann, H. OLEX2: a complete structure solution, refinement and analysis program. Journal of Applied Crystallography. 2009; 42(2): 339-341.
  • Douglass IB., Dains FB. Some derivatives of benzoyl and furoyl isothiocyanates and their use in synthesizing heterocyclic compounds1. Journal of the American Chemical Society. 1934a; 56(3): 719-721. DOI: 10.1021/ja01318a057.
  • Douglass IB., Dains FB. The preparation and hydrolysis of mono- and disubstituted benzoylthioureas1. Journal of the American Chemical Society. 1934b; 56(6): 1408-1409. DOI: 10.1021/ja01321a061.
  • Egan TJ., Koch KR., Swan PL., Clarkson C., Van Schalkwyk DA., Smith PJ. In vitro antimalarial activity of a series of cationic 2, 2 ‘-bipyridyl-and 1, 10-phenanthrolineplatinum (II) benzoylthiourea complexes. Journal of Medicinal Chemistry. 2004; 47(11): 2926-2934.
  • Fitzl G., Beyer L., Sieler J., Richter R., Kaiser J., Hoyer E. Kristall- und molekülstruktur von bis(1,1-diethyl-3-benzoyl-thioureato) palladium (II). Zeitschrift Für Anorganische und Allgemeine Chemie. 1977; 433 (1): 237-241. DOI: 10.1002/zaac.19774330127.
  • Frisch MJ., Trucks GW., Schlegel HB., Scuseria GE., Robb MA., Cheeseman JR., Scalmani G., Barone V., Petersson GA., Nakatsuji H., Li X., Caricato M. Marenich AV., Bloino J.,Janesko BG., Gompert R., Mennucci B., Hratchian HP., Ortiz JV., Izmaylov AF., Sonnenberg JL., Williams-Young D., Ding F., Lipparin F., Egidi F., Going J., Peng B., Petrone A., Henderson T., vd.. Gaussian 16, Revision C.01, Gaussian, Inc., Wallingford CT, 2016.
  • Gemili M., Sari H., Ulger M., Sahin E., Nural Y. Pt (II) and Ni (II) complexes of octahydropyrrolo[3,4-c] pyrrole N -benzoylthiourea derivatives: synthesis, characterization, physical parameters and biological activity. Inorganica Chimica Acta. 2017; 463, 88-96. DOI: 10.1016/j.ica.2017.04.026.
  • Gopiraman M., Selvakumaran N., Kesavan D., Kim IS., Karvembu R. Chemical and physical interactions of 1-benzoyl-3, 3-disubstituted thiourea derivatives on mild steel surface: corrosion inhibition in acidic media. Industrial & Engineering Chemistry Research. 2012; 51(23): 7910-7922.
  • Guillon E., Mohamadou A., Déchamps-Olivier I., Barbier JP. Synthesis and characterization of copper, cickel and cobalt complexes with N-disubstituted, N′-ethoxy carbonyl thioureas. Polyhedron. 1996; 15 (5-6): 947-952. DOI: 10.1016/0277-5387(95)00305-6.
  • Katritzky AR., Tala SR., Abo-Dya NE., Gyanda K., El-Gendy BED. M, Abdel-Samii ZK, Steel P J. Selective synthesis and structural elucidation of S-acyl- and N-acylcysteines. The Journal of Organic Chemistry. 2009; 74(18): 7165-7167.
  • Kavak G., Özbey S., Binzet G., Külcü N. Synthesis and single crystal structure analysis of three novel benzoylthiourea derivatives. Turkish Journal of Chemistry. 2009; 33(6): 857-868. DOI: 10.3906/kim-0901-1.
  • Ke SY., & Xue SJ. Synthesis and herbicidal activity of N-(o-fluorophenoxyacetyl) thioureas derivatives and related fused heterocyclic compounds. Arkivoc. 2006; 10, 63-68. DOI: 10.3998/ark.5550190.0007.a08.
  • Ketchemen KIY., Khan MD., Mlowe S., Akerman MP., Vitorica-Yrezabal I., Whitehead G., Nyamen LD., Ndifon PT., Revaprasadu N., O’Brien P. Crystal structures and physicochemical studies of some novel divalent and trivalent transition metal chelates of N-morpholine-N’-benzoylthiourea. Journal of Molecular Structure. 2021; 1229 (129791): 129791. DOI: 10.1016/j.molstruc.2020.129791.
  • Kirishnamaline G., Magdaline JD., Chithambarathanu T., Aruldhas D., Anuf AR. Theoretical investigation of structure, anticancer activity and molecular docking of thiourea derivatives. Journal of Molecular Structure. 2021; 1225(129118): 129118. DOI: 10.1016/j.molstruc.2020.129118.
  • Kirmse R., Beyer L., Hoyer E. A single-crystal and solution ESR study of bis(N,N-diethyl-N′-benzoylthioureato)-copper(II). Chemical Physics Letters. 1976; 44 (1): 173-176. DOI: 10.1016/0009-2614(76)80435-6.
  • Koch KR. New chemistry with old ligands: N-alkyl- and N, N-dialkyl-N′-acyl(aroyl)thioureas in co-ordination, analytical and process chemistry of the platinum group metals. Coordination Chemistry Reviews 2001; 216-217, 473-488 DOI: 10.1016/s0010-8545(01)00337-x.
  • Koch KR. New chemistry with old ligands: N-alkyl-and N, N-dialkyl-N′-acyl (aroyl) thioureas in co-ordination, analytical and process chemistry of the platinum group metals. Coordination Chemistry Reviews. 2001; 216: 473-488.
  • Koch KR., Sacht C., Grimmbacher T., Bourne S. New ligands for the platinum-group metals: deceptively simple coordination chemistry of N-acyl-N’-alkyl-and N-acyl-N’, N’-dialkyl-thioureas. South African Journal of Chemistry-Suid-Afrikaanse Tydskrif Vir Chemie. 1995; 48(1–2): 71-77.
  • Koch KR., Wang Y., Coetzee A. Platinum (II) and palladium (II) complexes of N-benzoyl-N′-propylthiourea (H2L): synthesis and geometric isomer distribution of [M(H2L-S )2X2] (M = Pt(II) or Pd(II); X = Cl−, Br− or I−); crystal structure of trans-[Pd(H2L-S )2Br2]. Journal of the Chemical Society Dalton Transactions. 1999; 6: 1013-1016. DOI: 10.1039/a809543d
  • Kotzé IA., Smith VJ., Kangara EF., Koch KR., Rare Hypodentate L-ΚS. Coordination mode of N, N-dialkyl-N′-aroylthioureas leads to unprecedented mixed-ligand [Pt(Phen)(L-ΚS)2] complexes. New Journal of Chemistry. 2017; 41(24): 14995-15002. DOI: 10.1039/c7nj03178e.
  • König KH., Schuster M., Schneeweis G., Steinbrech B. Zur chromatographie von metallchelaten: XIV. dünnschicht-chromatographie von N, N-Dialkyl-N′-benzoylthioharnstoff-chelaten. Fresenius’ Zeitschrift für Analytische Chemie. 1984; 319(1): 66-69. DOI: 10.1007/bf00476232.
  • Kurnakow NS. Über die beziehungen zwischen der farbe und der konstitution der haloïddoppelsalze. Zeitschrift Für Anorganische Chemie. 1898; 17(1): 207-235.
  • Kurt G., Mercimek B. Preparation of new benzoylthiourea-functionalized PVC resin and investigation of the complexation properties. Journal of Inorganic and Organometallic Polymers and Materials. 2009; 19(3): 367-373. DOI: 10.1007/s10904-009-9274-8.
  • Lee CT., Yang WT., Parr RG. Development of the colle-salvetti correlation-energy formula into a functional of the electron density. Physical review B. 1988; 37(2): 785-789. DOI: 10.1103/physrevb.37.785.
  • Li S., Cao X., Chen C., Ke S. Novel salicylic acid-oriented thiourea-type receptors as colorimetric chemosensor: Synthesis, characterizations and selective naked-eye recognition properties. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 2012; 96, 18-23.
  • Limban C., Chifiriuc MC., Caproiu MT., Dumitrascu F., Ferbinteanu M., Pintilie L., Stefaniu A., Vlad IM., Bleotu C., Marutescu LG., Nuta DC. New substituted benzoylthiourea derivatives: from design to antimicrobial applications. Molecules. 2020; 25(7): 1478. DOI: 10.3390/molecules25071478.
  • Mandal H., Ray D. Bis- and tris-chelates of NiII, CuII, CoII and FeIII bound to N, N-dialkyl/alkyl aryl-N′-benzoylthiourea ligands. Inorganica Chimica Acta. 2014; 414, 127-133. DOI: 10.1016/j.ica.2014.01.044.
  • McKinnon JJ., Jayatilaka D., Spackman MA. Towards quantitative analysis of intermolecular interactions with hirshfeld surfaces. Chemical Communications journal. 2007; 37, 3814-3816. DOI: 10.1039/b704980c.
  • Nencki M. Zur kenntniss des sulfoharnstoffs. Berichte der Deutschen Chemischen Gesellschaft. 1873; 6 (1): 598–600. DOI: 10.1002/cber.187300601186.
  • Nkabyo HA., Koch KR. Configurational E/Z and photo-induced cis-trans isomerism in the Pd(II) complex of asymmetrical N,N-methyl-ethyl-N′-benzoylthiourea. Journal of Molecular Structure. 2019; 1190: 47-53. DOI: 10.1016/j.molstruc.2019.04.038.
  • Nkabyo HA., Koch KR. New Trans-[Pd(L-κS,O)2] Complexes from N,N-dialkyl-N′-aroylthioureas prepared by photo-induced isomerization of their cis-[Pd(L-ΚS,O)2] counterparts and their thermal trans-cis isomerization. Inorganica Chimica Acta. 2018; 483: 440-447. DOI: 10.1016/j.ica.2018.08.028.
  • Nkabyo HA., Olaoye O. Synthesis, structural characterization, cis–trans isomerism, and dft studies on cis-bis(N, N-di-methyl-N′-benzoylthioureato) palladium(II). Journal of Structural Chemistry. 2020; 61(11): 1751-1759. DOI: 10.1134/s0022476620110098.
  • Nkabyo HA., Procacci B., Duckett SB., Koch KR. Reversible photo-isomerization of cis-[Pd(L-ΚS,O)2] (HL = N,N-diethyl-N’-1-naphthoylthiourea) to trans-[Pd(L-ΚS,O)2] and the unprecedented formation of trans-[Pd(L-ΚS,N)2] in solution. Dalton Transactions Journal. 2019; 48(46): 17241-17251. DOI: 10.1039/c9dt03672e.
  • Nordin NA., Chai TW., Tan BL., Choi CL., Abd Halim AN., Hussain H., Ngaini Z. Novel synthetic monothiourea aspirin derivatives bearing alkylated amines as potential antimicrobial agents. Journal of Chemistry. 2017; 1-7 DOI: 10.1155/2017/2378186.
  • Okuniewski A., Rosiak D., Chojnacki J., Becker B. Crystallographic study of self-organization in the solid state including quasi-aromatic pseudo-ring stacking interactions in 1-benzoyl-3-(3,4-dimethoxyphenyl)thiourea and 1-benzoyl-3-(2-hydroxypropyl)thiourea. Acta Crystallographica Section C: Structural Chemistry 2017; 73 (1): 52-56. DOI: 10.1107/S2053229616019495.
  • Ozer CK., Solmaz U., Arslan H. Crystal structure, hirshfeld surface analysis, and DFT studies of N-(2-chlorophenylcarbamothioyl) cyclohexanecarboxamide. European Journal of Chemistry. 2021; 12(4): 439-449.
  • Özgeriş B. Design, synthesis, characterization, and biological evaluation of nicotinoyl thioureas as antimicrobial and antioxidant agents. The Journal of Antibiotics. 2021b; 74(4): 233-243. DOI: 10.1038/s41429-020-00399-7.
  • Özgeriş B. Synthesis of substituted phenethylamine-based thioureas and their antimicrobial and antioxidant properties. Russian Journal of Organic Chemistry. 2021a; 57(3): 422-429. DOI: 10.1134/s1070428021030143.
  • Palatinus L., Chapuis GJ. SUPERFLIP–a computer program for the solution of crystal structures by charge flipping in arbitrary dimensions. Journal of Applied Crystallography. 2007; 40 (4): 786-790.
  • Palatinus L., Prathapa SJ., van Smaalen SJ. EDMA: a computer program for topological analysis of discrete electron densities. Journal of Applied Crystallography. 2012; 45(3): 575-580.
  • Palatinus L., van der Lee AJ. Symmetry determination following structure solution in P1. Journal of Applied Crystallography. 2008; 41(6): 975-984.
  • Pérez H., O’Reilly B., Plutín AM., Martínez R., Durán R., Collado IG., Mascarenhas YP. Synthesis, characterization, and crystal structure of Ni (II) and Cu (II) complexes with N-furoyl-N′,N′-diethylthiourea: antifungal activity. Journal of Coordination Chemistry. 2011; 64(16): 2890-2898. DOI: 10.1080/00958972.2011.608426.
  • Pinheiro LCS., Hoelz LVB., Ferreira MLG., Oliveira LG., Pereira RFA., do Valle AM., André LSP., Scaffo J., Pinheiro FR., Ribeiro TAN., Sachs D., Pascoal ACRF., Boechat N., Aguiar-Alves F. Synthesis of benzoylthiourea derivatives and analysis of their antibacterial performance against planktonic Staphylococcus aureus and its biofilms. Letters in Applied Microbiology. 2020; 71(6): 645-651. DOI: 10.1111/lam.13359.
  • Plutín AM., Alvarez A., Mocelo R., Ramos R., Castellano EE., da Silva MM., Colina-Vegas L., Pavan FR., Batista AA. Anti- mycobacterium tuberculosis activity of platinum (II)/ N, N -disubstituted- N ′-acyl thiourea complexes. Inorganic Chemistry Communications. 2016; 63, 74-80. DOI: 10.1016/j.inoche.2015.11.020.
  • Reinel M., Richter R., Kirmse R. Synthesen und strukturen von N-acylthioharnstoffkomplexen des zinks und des cadmiums. Zeitschrift für Anorganische und Allgemeine Chemie. 2002; 628(1): 41-44. DOI: 10.1002/1521-3749(200201)628:1<41::aid-zaac41>3.0.co;2-q.
  • Richter R., Dietze F., Schmidt S., Hoyer E., Poll W., Mootz D. Koordination von silber(I) durch N,N-diethyl-N’-benzoylthioharnstoff in Lösung und in festem Zustand. Zeitschrift für Anorganische und Allgemeine Chemie. 1997; 623 (1-6): 135-140. DOI: 10.1002/zaac.19976230122.
  • Saeed A., Flörke U., Erben MF. A review on the chemistry, coordination, structure and biological properties of 1-(Acyl/Aroyl)-3-(substituted) thioureas. Journal of Sulfur Chemistry 2014; 35(3): 318-355. DOI: 10.1080/17415993.2013.834904.
  • Saeed A., Qamar R., Fattah TA., Flörke U., Erben MF. Recent developments in chemistry, coordination, structure and biological aspects of 1-(acyl/aroyl)-3-(substituted) thioureas. Research on Chemical Intermediates. 2017; 43(5): 3053-3093. DOI: 10.1007/s11164-016-2811-5.
  • Schröder U., Beyer L., Richter R., Angulo-Cornejo J., Castillo-Montoya M., Lino-Pacheco M. Complex formation of N∩N-ethylene bridged bis(N′-benzoyl-O-ethyl-ısourea) and N-benzoylguanidines with late transition metals. Inorganica Chimica Acta. 2003; 353: 59-67. DOI: 10.1016/s0020-1693(03)00322-0.
  • Sheldrick GM. Crystal structure refinement with SHELXL Acta Crystallographica Section C Structural Chemistry. 2015; 71(1): 3-8.
  • Spackman MA., Jayatilaka D. Hirshfeld surface analysis. CrystEngComm 2009; 11(1): 19-32. DOI: 10.1039/B818330A.
  • Spackman MA., McKinnon JJ. Fingerprinting intermolecular interactions in molecular crystals. , CrystEngComm. 2002; 4 (66): 378-392 DOI: 10.1039/B203191B.
  • Spackman PR., Turner, MJ., McKinnon JJ., Wolff SK., Grimwood DJ., Jayatilaka D., Spackman MA. CrystalExplorer: A program for Hirshfeld surface analysis, visualization and quantitative analysis of molecular crystals. Journal of Applied Crystallography. 2021; 54(3): 1006-1011.
  • Suhud K., Hasbullah SA., Ahmad M., Heng LY., Kassim MB. Crystal structure of 4-meth-oxy-N-(piperidine-1-carbono-thio-Yl) benzamide. Acta Crystallographica Section E: Crystallographic Communications. 2017; 73(10): 1530-1533. DOI: 10.1107/S2056989017013317.
  • Suhud K., Heng LY., Hasbullah SA., Ahmad M., Kassim MB. Crystal structure of 4-meth-oxy-N-[(pyrrolidin-1-yl) carbothio-yl]benzamide. Acta Crystallographica Section E: Crystallographic Communications. 2015; 71(4): o225-o226. DOI: 10.1107/S2056989015003813.
  • Sun J., Cai S., Mei H., Li J., Yan N., Wang Q., Huo D. Molecular docking and QSAR studies on substituted Acyl (thio) urea and thiadiazolo [2, 3‐α] pyrimidine derivatives as potent inhibitors of influenza virus neuraminidase. Chemical Biology & Drug Design. 2010; 76(3): 245-254.
  • Tan SL., Azizan AHS., Jotani MM., Tiekink ERT. 3,3-bis(2-hy-droxy-eth-Yl)-1-(4-methyl-benzoyl)thio-urea: crystal structure, hirshfeld surface analysis and computational study. Acta Crystallographica Section E: Crystallographic Communications. 2019; 75(10): 1472-1478. DOI: 10.1107/S2056989019012581.
  • Telmore VM., Kumar P., Jaison PG. Study on complexation of palladium with thiourea-based ligands and its determination in simulated high-level liquid waste Using solid phase extraction-electrospray mass spectrometry. Journal of Radioanalytical and Nuclear Chemistry. 2018; 318(2): 1249-1259. DOI: 10.1007/s10967-018-6165-x.
  • Wei Q., Ning JY., Dai X., Gao YD., Su L., Zhao BX., Miao JY. Discovery of novel HSP90 inhibitors that induced apoptosis and impaired autophagic flux in A549 lung cancer cells. European Journal of Medicinal Chemistry. 2018; 145, 551-558.
  • Wilson D., de los Ángeles Arada M., Alegret S., del Valle M. Lead (II) ion selective electrodes with PVC membranes based on two bis-thioureas as ionophores: 1, 3-bis (N′-benzoylthioureido) benzene and 1, 3-bis (N′-furoylthioureido) benzene. Journal of Hazardous Materials. 2010; 181(1-3): 140-146.
  • Yamin BM., Osman UM. 1,2-Bis(N’-benzoyl-thio-ureido)-4-chloro-benzene. Acta Crystallographica Section E: Crystallographic Communications. 2011; 67(P6): o1286-o1286. DOI: 10.1107/S1600536811014954.
  • Yang W., Liu H., Li M., Wang F., Zhou W., Fan J. Synthesis, structures and antibacterial activities of benzoylthiourea derivatives and their complexes with cobalt. Journal of Inorganic Biochemistry. 2012; 116, 97-105. DOI: 10.1016/j.jinorgbio.2012.08.001.
  • Yaseen S., Rauf MK., Zaib S., Badshah A., Tahir MN., Ali MI., Imtiaz-ud-Din., Shahid M., Iqbal J. Synthesis, characterization and urease inhibition, in vitro anticancer and antileishmanial studies of Co (III) complexes with N, N, N′-trisubstituted acylthioureas. Inorganica Chimica Acta. 2016; 443, 69-77. DOI: 10.1016/j.ica.2015.12.027.
  • Yusof MSM., Jusoh RH., Khairul WM., Yamin BM. Synthesis and characterisation a series of N-(3,4-dichlorophenyl)-N′-(2,3 and 4-methylbenzoyl) thiourea derivatives. Journal of Molecular Structure. 2010; 975(1-3): 280-284. DOI: 10.1016/j.molstruc.2010.04.037.
  • Zade CM., Pete UD., Kadam MS., Bendre RS. Development of novel insect growth regulators: effect of 1-(substitutedbenzoyl)-3-[(2′-isopropyl-5′-methylphenoxy) acetamino] thiourea and urea derivatives on total haemocyte count of dysdercus koenigii. Chemistry for Sustainable Development. 2012; 69-79.
  • Zhang ZJ., Zeng Y., Jiang ZY., Shu BS., Sethuraman V., Zhong GH. Design, synthesis, fungicidal property and QSAR studies of novel β-carbolines containing urea, benzoylthiourea and benzoylurea for the control of rice sheath blight. Pest Management Science. 2018; 74(7); 1736-1746. DOI: 10.1002/ps.4873.

Synthesis, Crystal Structure, DFT Studies and Hirshfeld Surface Analysis of N-(cyclohexyl(methyl)carbamothioyl)-4-nitrobenzamide

Year 2022, Volume: 5 Issue: 2, 681 - 706, 18.07.2022
https://doi.org/10.47495/okufbed.1090049

Abstract

In this study, new N-(cyclohexyl(methyl)carbamothioyl)-4-nitrobenzamide was synthesized in good yield and the compound was characterized by 1H NMR spectroscopic technique. In addition, the crystal structure of N-(cyclohexyl (methyl)carbamothioyl)-4-nitrobenzamide clarified by the X-ray single crystal diffraction technique. The compound crystallizes into monoclinic system with space group P21/c symmetry. The unit cell parameters of the crystal structure were determined as a = 14.858(4) Å, b = 5.0386(14) Å, c = 22.336(7) Å and β = 104.952(8)°. Density functional theory optimized structure in the gaseous phase at B3LYP/6-311G(d,p) level of theory has been compared with the experimentally defined molecular structure for N-(cyclohexyl(methyl)carbamothioyl)-4-nitrobenzamide compound. The HOMO and LUMO energies and energy gap were calculated for title compound. It was determined that there is an energy gap of 0.7772 eV between the HOMO and LUMO energy levels of the compound. This value indicated that the molecule had a high tendency to react chemically and was unstable. The graphical approach of the intermolecular interactions was obtained from the Hirshfeld surface analysis and 2D fingerprint plots was employed to quantifies various interaction. Hirshfeld surface analysis determined that the most dominant contribution to the surface area was due to H···H (42.10%) interactions.

Project Number

-

References

  • Abosadiya HM., Anouar EH., Yamin BM. Synthesis, X-Ray, Spectroscopic characterization (FT-IR, NMR, UV–Vis) and quantum chemical calculations of some substituted benzoylthiourea derivatives. Journal of Molecular Structure. 2019; 1194, 48-56. DOI: 10.1016/j.molstruc.2019.05.060
  • Abosadiya HM. Synthesis, crystal structure and antioxidant evaluation of N-(4-formylpiperazine-1-carbonothioyl)benzamide. European Journal of Chemistry. 2020; 11(2): 156-159. DOI: 10.5155/eurjchem.11.2.156-159.1981.
  • Angulo-Cornejo JR., Ayala-León K., Herbosa GG., Cuevas JV., Diez V., Richter R., Hennig L., Beyer L. Synthesis and structural characterization of N-[4-(2-hydroxyethyl)-1,2,4-oxathiazinan-3-ylidene]-benzamide and its mercury(II) chloride adduct. Zeitschrift Für Naturforschung B Journal of Chemical Sciences. 2005; 60(9): 945-950 DOI: 10.1515/znb-2005-0906.
  • Ashfaq M., Tahir MN., Muhammad S., Munawar KS., Ali A., Bogdanov G., Alarfaji SS. Single-crystal investigation, hirshfeld surface analysis, and DFT study of third-order NLO properties of unsymmetrical acyl thiourea derivatives. ACS Omega. 2021; 6(46): 31211-31225. DOI: 10.1021/acsomega.1c04884.
  • Asiri AM., Faidallah HM., Al-Youbi AO., Alamry KA., Ng SW. 1-Benzoyl-3-[3-cyano-8-methyl-4-(1-methyl-1H-pyrrol-2-Yl)-5,6,7,8-tetra-hydro-quinolin-2-Yl]thio-urea. Acta Crystallographica Section E Crystallographic Communications. 2011; 67(9): o2430- o2430. DOI: 10.1107/S1600536811033046.
  • Ayata S., Kaynak I., Merdivan M. Solid phase extractive preconcentration of silver from aqueous samples. Environmental Monitoring and Assessment. 2009; 153(1-4): 333-338. DOI: 10.1007/s10661-008-0359-6.
  • Aydın F., Aykaç D., Ünver H., İskeleli NO. Synthesis, spectral properties and structure of new novel 3,3′-dibenzoyl-1,1′-(propan-1,3-Diyl)-bisthiourea. Journal of Chemical Crystallography. 2012; 42(4): 381-387. DOI: 10.1007/s10870-011-0258-5.
  • Aydın F., Ünver H., Aykaç D., İskeleli NO. Spectroscopic studies and structure of 4-(3-benzoylthioureido) benzoic acid. Journal of Chemical Crystallography. 2010; 40(12): 1082-1086. DOI: 10.1007/s10870-010-9799-2.
  • Becke AD. Density‐functional thermochemistry. III. The role of exact exchange. The Journal of Chemical Physics .1993; 98(7): 5648-5652. DOI: 10.1063/1.464913.
  • Beyer L., Hoyer E., Hennig H., Kirmse R., Hartmann H., Liebscher J. Synthese und charakterisierung neuartiger übergangsmetallchelate von 1,1-dialkyl-3-benzoyl-thioharnstoffen. Journal Für Praktische Chemie. 1975; 317 (5): 829–839. DOI: 10.1002/prac.19753170518.
  • Bozkurt SS., Merdivan M. Solid phase extraction of gold (III) on silica gel modified with benzoylthiourea prior to its determination by flame atomic absorption spectrometry. Environmental Monitoring and Assessment. 2009; 158(1-4): 15-21. DOI: 10.1007/s10661-008-0561-6.
  • Bruce JC., Koch KR. N-benzoyl-N’,N’-dibutylselenourea and its palladium(II) complex. Acta Crystallographica Section C. 2008; 64 (Pt 1): m1-4. DOI: 10.1107/S0108270107053711.
  • Chermette HJ. Chemical reactivity indexes in density functional theory. Journal of computational chemistry. 1999; 20(1): 129-154.
  • Cornejo JA., Ayala K., Richter R., Böhlig H., Hennig L., Beyer L. Wasserstoffbrücken in 1,1-bis(2-hydroxyethyl)-3-benzoylthioharnstoff und seinen nickel (II)- und kupfer (II)-chelat-komplexen. Zeitschrift für anorganische und allgemeine Chemie. 2005; 631(15): 3040-3045. DOI: 10.1002/zaac.200500266.
  • Déchamps-Olivier I., Guillon E., Mohamadou A., Barbier JP. Coordination of nickel and cobalt with N-morpholine or N,N-diethyl, N’-monosubstituted benzoyl thioureas. Polyhedron. 1996; 15(20): 3617-3622. DOI: 10.1016/0277-5387(96)00081-2.
  • Dennington R., Keith TA., Millam JM. GaussView, Version 6, Semichem Inc., Shawnee Mission, KS, 2016.
  • Dolomanov OV., Bourhis LJ., Gildea RJ., Howard JA., Puschmann, H. OLEX2: a complete structure solution, refinement and analysis program. Journal of Applied Crystallography. 2009; 42(2): 339-341.
  • Douglass IB., Dains FB. Some derivatives of benzoyl and furoyl isothiocyanates and their use in synthesizing heterocyclic compounds1. Journal of the American Chemical Society. 1934a; 56(3): 719-721. DOI: 10.1021/ja01318a057.
  • Douglass IB., Dains FB. The preparation and hydrolysis of mono- and disubstituted benzoylthioureas1. Journal of the American Chemical Society. 1934b; 56(6): 1408-1409. DOI: 10.1021/ja01321a061.
  • Egan TJ., Koch KR., Swan PL., Clarkson C., Van Schalkwyk DA., Smith PJ. In vitro antimalarial activity of a series of cationic 2, 2 ‘-bipyridyl-and 1, 10-phenanthrolineplatinum (II) benzoylthiourea complexes. Journal of Medicinal Chemistry. 2004; 47(11): 2926-2934.
  • Fitzl G., Beyer L., Sieler J., Richter R., Kaiser J., Hoyer E. Kristall- und molekülstruktur von bis(1,1-diethyl-3-benzoyl-thioureato) palladium (II). Zeitschrift Für Anorganische und Allgemeine Chemie. 1977; 433 (1): 237-241. DOI: 10.1002/zaac.19774330127.
  • Frisch MJ., Trucks GW., Schlegel HB., Scuseria GE., Robb MA., Cheeseman JR., Scalmani G., Barone V., Petersson GA., Nakatsuji H., Li X., Caricato M. Marenich AV., Bloino J.,Janesko BG., Gompert R., Mennucci B., Hratchian HP., Ortiz JV., Izmaylov AF., Sonnenberg JL., Williams-Young D., Ding F., Lipparin F., Egidi F., Going J., Peng B., Petrone A., Henderson T., vd.. Gaussian 16, Revision C.01, Gaussian, Inc., Wallingford CT, 2016.
  • Gemili M., Sari H., Ulger M., Sahin E., Nural Y. Pt (II) and Ni (II) complexes of octahydropyrrolo[3,4-c] pyrrole N -benzoylthiourea derivatives: synthesis, characterization, physical parameters and biological activity. Inorganica Chimica Acta. 2017; 463, 88-96. DOI: 10.1016/j.ica.2017.04.026.
  • Gopiraman M., Selvakumaran N., Kesavan D., Kim IS., Karvembu R. Chemical and physical interactions of 1-benzoyl-3, 3-disubstituted thiourea derivatives on mild steel surface: corrosion inhibition in acidic media. Industrial & Engineering Chemistry Research. 2012; 51(23): 7910-7922.
  • Guillon E., Mohamadou A., Déchamps-Olivier I., Barbier JP. Synthesis and characterization of copper, cickel and cobalt complexes with N-disubstituted, N′-ethoxy carbonyl thioureas. Polyhedron. 1996; 15 (5-6): 947-952. DOI: 10.1016/0277-5387(95)00305-6.
  • Katritzky AR., Tala SR., Abo-Dya NE., Gyanda K., El-Gendy BED. M, Abdel-Samii ZK, Steel P J. Selective synthesis and structural elucidation of S-acyl- and N-acylcysteines. The Journal of Organic Chemistry. 2009; 74(18): 7165-7167.
  • Kavak G., Özbey S., Binzet G., Külcü N. Synthesis and single crystal structure analysis of three novel benzoylthiourea derivatives. Turkish Journal of Chemistry. 2009; 33(6): 857-868. DOI: 10.3906/kim-0901-1.
  • Ke SY., & Xue SJ. Synthesis and herbicidal activity of N-(o-fluorophenoxyacetyl) thioureas derivatives and related fused heterocyclic compounds. Arkivoc. 2006; 10, 63-68. DOI: 10.3998/ark.5550190.0007.a08.
  • Ketchemen KIY., Khan MD., Mlowe S., Akerman MP., Vitorica-Yrezabal I., Whitehead G., Nyamen LD., Ndifon PT., Revaprasadu N., O’Brien P. Crystal structures and physicochemical studies of some novel divalent and trivalent transition metal chelates of N-morpholine-N’-benzoylthiourea. Journal of Molecular Structure. 2021; 1229 (129791): 129791. DOI: 10.1016/j.molstruc.2020.129791.
  • Kirishnamaline G., Magdaline JD., Chithambarathanu T., Aruldhas D., Anuf AR. Theoretical investigation of structure, anticancer activity and molecular docking of thiourea derivatives. Journal of Molecular Structure. 2021; 1225(129118): 129118. DOI: 10.1016/j.molstruc.2020.129118.
  • Kirmse R., Beyer L., Hoyer E. A single-crystal and solution ESR study of bis(N,N-diethyl-N′-benzoylthioureato)-copper(II). Chemical Physics Letters. 1976; 44 (1): 173-176. DOI: 10.1016/0009-2614(76)80435-6.
  • Koch KR. New chemistry with old ligands: N-alkyl- and N, N-dialkyl-N′-acyl(aroyl)thioureas in co-ordination, analytical and process chemistry of the platinum group metals. Coordination Chemistry Reviews 2001; 216-217, 473-488 DOI: 10.1016/s0010-8545(01)00337-x.
  • Koch KR. New chemistry with old ligands: N-alkyl-and N, N-dialkyl-N′-acyl (aroyl) thioureas in co-ordination, analytical and process chemistry of the platinum group metals. Coordination Chemistry Reviews. 2001; 216: 473-488.
  • Koch KR., Sacht C., Grimmbacher T., Bourne S. New ligands for the platinum-group metals: deceptively simple coordination chemistry of N-acyl-N’-alkyl-and N-acyl-N’, N’-dialkyl-thioureas. South African Journal of Chemistry-Suid-Afrikaanse Tydskrif Vir Chemie. 1995; 48(1–2): 71-77.
  • Koch KR., Wang Y., Coetzee A. Platinum (II) and palladium (II) complexes of N-benzoyl-N′-propylthiourea (H2L): synthesis and geometric isomer distribution of [M(H2L-S )2X2] (M = Pt(II) or Pd(II); X = Cl−, Br− or I−); crystal structure of trans-[Pd(H2L-S )2Br2]. Journal of the Chemical Society Dalton Transactions. 1999; 6: 1013-1016. DOI: 10.1039/a809543d
  • Kotzé IA., Smith VJ., Kangara EF., Koch KR., Rare Hypodentate L-ΚS. Coordination mode of N, N-dialkyl-N′-aroylthioureas leads to unprecedented mixed-ligand [Pt(Phen)(L-ΚS)2] complexes. New Journal of Chemistry. 2017; 41(24): 14995-15002. DOI: 10.1039/c7nj03178e.
  • König KH., Schuster M., Schneeweis G., Steinbrech B. Zur chromatographie von metallchelaten: XIV. dünnschicht-chromatographie von N, N-Dialkyl-N′-benzoylthioharnstoff-chelaten. Fresenius’ Zeitschrift für Analytische Chemie. 1984; 319(1): 66-69. DOI: 10.1007/bf00476232.
  • Kurnakow NS. Über die beziehungen zwischen der farbe und der konstitution der haloïddoppelsalze. Zeitschrift Für Anorganische Chemie. 1898; 17(1): 207-235.
  • Kurt G., Mercimek B. Preparation of new benzoylthiourea-functionalized PVC resin and investigation of the complexation properties. Journal of Inorganic and Organometallic Polymers and Materials. 2009; 19(3): 367-373. DOI: 10.1007/s10904-009-9274-8.
  • Lee CT., Yang WT., Parr RG. Development of the colle-salvetti correlation-energy formula into a functional of the electron density. Physical review B. 1988; 37(2): 785-789. DOI: 10.1103/physrevb.37.785.
  • Li S., Cao X., Chen C., Ke S. Novel salicylic acid-oriented thiourea-type receptors as colorimetric chemosensor: Synthesis, characterizations and selective naked-eye recognition properties. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 2012; 96, 18-23.
  • Limban C., Chifiriuc MC., Caproiu MT., Dumitrascu F., Ferbinteanu M., Pintilie L., Stefaniu A., Vlad IM., Bleotu C., Marutescu LG., Nuta DC. New substituted benzoylthiourea derivatives: from design to antimicrobial applications. Molecules. 2020; 25(7): 1478. DOI: 10.3390/molecules25071478.
  • Mandal H., Ray D. Bis- and tris-chelates of NiII, CuII, CoII and FeIII bound to N, N-dialkyl/alkyl aryl-N′-benzoylthiourea ligands. Inorganica Chimica Acta. 2014; 414, 127-133. DOI: 10.1016/j.ica.2014.01.044.
  • McKinnon JJ., Jayatilaka D., Spackman MA. Towards quantitative analysis of intermolecular interactions with hirshfeld surfaces. Chemical Communications journal. 2007; 37, 3814-3816. DOI: 10.1039/b704980c.
  • Nencki M. Zur kenntniss des sulfoharnstoffs. Berichte der Deutschen Chemischen Gesellschaft. 1873; 6 (1): 598–600. DOI: 10.1002/cber.187300601186.
  • Nkabyo HA., Koch KR. Configurational E/Z and photo-induced cis-trans isomerism in the Pd(II) complex of asymmetrical N,N-methyl-ethyl-N′-benzoylthiourea. Journal of Molecular Structure. 2019; 1190: 47-53. DOI: 10.1016/j.molstruc.2019.04.038.
  • Nkabyo HA., Koch KR. New Trans-[Pd(L-κS,O)2] Complexes from N,N-dialkyl-N′-aroylthioureas prepared by photo-induced isomerization of their cis-[Pd(L-ΚS,O)2] counterparts and their thermal trans-cis isomerization. Inorganica Chimica Acta. 2018; 483: 440-447. DOI: 10.1016/j.ica.2018.08.028.
  • Nkabyo HA., Olaoye O. Synthesis, structural characterization, cis–trans isomerism, and dft studies on cis-bis(N, N-di-methyl-N′-benzoylthioureato) palladium(II). Journal of Structural Chemistry. 2020; 61(11): 1751-1759. DOI: 10.1134/s0022476620110098.
  • Nkabyo HA., Procacci B., Duckett SB., Koch KR. Reversible photo-isomerization of cis-[Pd(L-ΚS,O)2] (HL = N,N-diethyl-N’-1-naphthoylthiourea) to trans-[Pd(L-ΚS,O)2] and the unprecedented formation of trans-[Pd(L-ΚS,N)2] in solution. Dalton Transactions Journal. 2019; 48(46): 17241-17251. DOI: 10.1039/c9dt03672e.
  • Nordin NA., Chai TW., Tan BL., Choi CL., Abd Halim AN., Hussain H., Ngaini Z. Novel synthetic monothiourea aspirin derivatives bearing alkylated amines as potential antimicrobial agents. Journal of Chemistry. 2017; 1-7 DOI: 10.1155/2017/2378186.
  • Okuniewski A., Rosiak D., Chojnacki J., Becker B. Crystallographic study of self-organization in the solid state including quasi-aromatic pseudo-ring stacking interactions in 1-benzoyl-3-(3,4-dimethoxyphenyl)thiourea and 1-benzoyl-3-(2-hydroxypropyl)thiourea. Acta Crystallographica Section C: Structural Chemistry 2017; 73 (1): 52-56. DOI: 10.1107/S2053229616019495.
  • Ozer CK., Solmaz U., Arslan H. Crystal structure, hirshfeld surface analysis, and DFT studies of N-(2-chlorophenylcarbamothioyl) cyclohexanecarboxamide. European Journal of Chemistry. 2021; 12(4): 439-449.
  • Özgeriş B. Design, synthesis, characterization, and biological evaluation of nicotinoyl thioureas as antimicrobial and antioxidant agents. The Journal of Antibiotics. 2021b; 74(4): 233-243. DOI: 10.1038/s41429-020-00399-7.
  • Özgeriş B. Synthesis of substituted phenethylamine-based thioureas and their antimicrobial and antioxidant properties. Russian Journal of Organic Chemistry. 2021a; 57(3): 422-429. DOI: 10.1134/s1070428021030143.
  • Palatinus L., Chapuis GJ. SUPERFLIP–a computer program for the solution of crystal structures by charge flipping in arbitrary dimensions. Journal of Applied Crystallography. 2007; 40 (4): 786-790.
  • Palatinus L., Prathapa SJ., van Smaalen SJ. EDMA: a computer program for topological analysis of discrete electron densities. Journal of Applied Crystallography. 2012; 45(3): 575-580.
  • Palatinus L., van der Lee AJ. Symmetry determination following structure solution in P1. Journal of Applied Crystallography. 2008; 41(6): 975-984.
  • Pérez H., O’Reilly B., Plutín AM., Martínez R., Durán R., Collado IG., Mascarenhas YP. Synthesis, characterization, and crystal structure of Ni (II) and Cu (II) complexes with N-furoyl-N′,N′-diethylthiourea: antifungal activity. Journal of Coordination Chemistry. 2011; 64(16): 2890-2898. DOI: 10.1080/00958972.2011.608426.
  • Pinheiro LCS., Hoelz LVB., Ferreira MLG., Oliveira LG., Pereira RFA., do Valle AM., André LSP., Scaffo J., Pinheiro FR., Ribeiro TAN., Sachs D., Pascoal ACRF., Boechat N., Aguiar-Alves F. Synthesis of benzoylthiourea derivatives and analysis of their antibacterial performance against planktonic Staphylococcus aureus and its biofilms. Letters in Applied Microbiology. 2020; 71(6): 645-651. DOI: 10.1111/lam.13359.
  • Plutín AM., Alvarez A., Mocelo R., Ramos R., Castellano EE., da Silva MM., Colina-Vegas L., Pavan FR., Batista AA. Anti- mycobacterium tuberculosis activity of platinum (II)/ N, N -disubstituted- N ′-acyl thiourea complexes. Inorganic Chemistry Communications. 2016; 63, 74-80. DOI: 10.1016/j.inoche.2015.11.020.
  • Reinel M., Richter R., Kirmse R. Synthesen und strukturen von N-acylthioharnstoffkomplexen des zinks und des cadmiums. Zeitschrift für Anorganische und Allgemeine Chemie. 2002; 628(1): 41-44. DOI: 10.1002/1521-3749(200201)628:1<41::aid-zaac41>3.0.co;2-q.
  • Richter R., Dietze F., Schmidt S., Hoyer E., Poll W., Mootz D. Koordination von silber(I) durch N,N-diethyl-N’-benzoylthioharnstoff in Lösung und in festem Zustand. Zeitschrift für Anorganische und Allgemeine Chemie. 1997; 623 (1-6): 135-140. DOI: 10.1002/zaac.19976230122.
  • Saeed A., Flörke U., Erben MF. A review on the chemistry, coordination, structure and biological properties of 1-(Acyl/Aroyl)-3-(substituted) thioureas. Journal of Sulfur Chemistry 2014; 35(3): 318-355. DOI: 10.1080/17415993.2013.834904.
  • Saeed A., Qamar R., Fattah TA., Flörke U., Erben MF. Recent developments in chemistry, coordination, structure and biological aspects of 1-(acyl/aroyl)-3-(substituted) thioureas. Research on Chemical Intermediates. 2017; 43(5): 3053-3093. DOI: 10.1007/s11164-016-2811-5.
  • Schröder U., Beyer L., Richter R., Angulo-Cornejo J., Castillo-Montoya M., Lino-Pacheco M. Complex formation of N∩N-ethylene bridged bis(N′-benzoyl-O-ethyl-ısourea) and N-benzoylguanidines with late transition metals. Inorganica Chimica Acta. 2003; 353: 59-67. DOI: 10.1016/s0020-1693(03)00322-0.
  • Sheldrick GM. Crystal structure refinement with SHELXL Acta Crystallographica Section C Structural Chemistry. 2015; 71(1): 3-8.
  • Spackman MA., Jayatilaka D. Hirshfeld surface analysis. CrystEngComm 2009; 11(1): 19-32. DOI: 10.1039/B818330A.
  • Spackman MA., McKinnon JJ. Fingerprinting intermolecular interactions in molecular crystals. , CrystEngComm. 2002; 4 (66): 378-392 DOI: 10.1039/B203191B.
  • Spackman PR., Turner, MJ., McKinnon JJ., Wolff SK., Grimwood DJ., Jayatilaka D., Spackman MA. CrystalExplorer: A program for Hirshfeld surface analysis, visualization and quantitative analysis of molecular crystals. Journal of Applied Crystallography. 2021; 54(3): 1006-1011.
  • Suhud K., Hasbullah SA., Ahmad M., Heng LY., Kassim MB. Crystal structure of 4-meth-oxy-N-(piperidine-1-carbono-thio-Yl) benzamide. Acta Crystallographica Section E: Crystallographic Communications. 2017; 73(10): 1530-1533. DOI: 10.1107/S2056989017013317.
  • Suhud K., Heng LY., Hasbullah SA., Ahmad M., Kassim MB. Crystal structure of 4-meth-oxy-N-[(pyrrolidin-1-yl) carbothio-yl]benzamide. Acta Crystallographica Section E: Crystallographic Communications. 2015; 71(4): o225-o226. DOI: 10.1107/S2056989015003813.
  • Sun J., Cai S., Mei H., Li J., Yan N., Wang Q., Huo D. Molecular docking and QSAR studies on substituted Acyl (thio) urea and thiadiazolo [2, 3‐α] pyrimidine derivatives as potent inhibitors of influenza virus neuraminidase. Chemical Biology & Drug Design. 2010; 76(3): 245-254.
  • Tan SL., Azizan AHS., Jotani MM., Tiekink ERT. 3,3-bis(2-hy-droxy-eth-Yl)-1-(4-methyl-benzoyl)thio-urea: crystal structure, hirshfeld surface analysis and computational study. Acta Crystallographica Section E: Crystallographic Communications. 2019; 75(10): 1472-1478. DOI: 10.1107/S2056989019012581.
  • Telmore VM., Kumar P., Jaison PG. Study on complexation of palladium with thiourea-based ligands and its determination in simulated high-level liquid waste Using solid phase extraction-electrospray mass spectrometry. Journal of Radioanalytical and Nuclear Chemistry. 2018; 318(2): 1249-1259. DOI: 10.1007/s10967-018-6165-x.
  • Wei Q., Ning JY., Dai X., Gao YD., Su L., Zhao BX., Miao JY. Discovery of novel HSP90 inhibitors that induced apoptosis and impaired autophagic flux in A549 lung cancer cells. European Journal of Medicinal Chemistry. 2018; 145, 551-558.
  • Wilson D., de los Ángeles Arada M., Alegret S., del Valle M. Lead (II) ion selective electrodes with PVC membranes based on two bis-thioureas as ionophores: 1, 3-bis (N′-benzoylthioureido) benzene and 1, 3-bis (N′-furoylthioureido) benzene. Journal of Hazardous Materials. 2010; 181(1-3): 140-146.
  • Yamin BM., Osman UM. 1,2-Bis(N’-benzoyl-thio-ureido)-4-chloro-benzene. Acta Crystallographica Section E: Crystallographic Communications. 2011; 67(P6): o1286-o1286. DOI: 10.1107/S1600536811014954.
  • Yang W., Liu H., Li M., Wang F., Zhou W., Fan J. Synthesis, structures and antibacterial activities of benzoylthiourea derivatives and their complexes with cobalt. Journal of Inorganic Biochemistry. 2012; 116, 97-105. DOI: 10.1016/j.jinorgbio.2012.08.001.
  • Yaseen S., Rauf MK., Zaib S., Badshah A., Tahir MN., Ali MI., Imtiaz-ud-Din., Shahid M., Iqbal J. Synthesis, characterization and urease inhibition, in vitro anticancer and antileishmanial studies of Co (III) complexes with N, N, N′-trisubstituted acylthioureas. Inorganica Chimica Acta. 2016; 443, 69-77. DOI: 10.1016/j.ica.2015.12.027.
  • Yusof MSM., Jusoh RH., Khairul WM., Yamin BM. Synthesis and characterisation a series of N-(3,4-dichlorophenyl)-N′-(2,3 and 4-methylbenzoyl) thiourea derivatives. Journal of Molecular Structure. 2010; 975(1-3): 280-284. DOI: 10.1016/j.molstruc.2010.04.037.
  • Zade CM., Pete UD., Kadam MS., Bendre RS. Development of novel insect growth regulators: effect of 1-(substitutedbenzoyl)-3-[(2′-isopropyl-5′-methylphenoxy) acetamino] thiourea and urea derivatives on total haemocyte count of dysdercus koenigii. Chemistry for Sustainable Development. 2012; 69-79.
  • Zhang ZJ., Zeng Y., Jiang ZY., Shu BS., Sethuraman V., Zhong GH. Design, synthesis, fungicidal property and QSAR studies of novel β-carbolines containing urea, benzoylthiourea and benzoylurea for the control of rice sheath blight. Pest Management Science. 2018; 74(7); 1736-1746. DOI: 10.1002/ps.4873.
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Details

Primary Language Turkish
Subjects Chemical Engineering
Journal Section RESEARCH ARTICLES
Authors

Gün Binzet

Project Number -
Publication Date July 18, 2022
Submission Date March 18, 2022
Acceptance Date May 5, 2022
Published in Issue Year 2022 Volume: 5 Issue: 2

Cite

APA Binzet, G. (2022). N-(Siklohekzil(metil)karbamotiyoil)-4-nitrobenzamit Bileşiğinin Sentezi, Kristal Yapısı, DFT Çalışmaları ve Hirshfeld Yüzey Analizi. Osmaniye Korkut Ata Üniversitesi Fen Bilimleri Enstitüsü Dergisi, 5(2), 681-706. https://doi.org/10.47495/okufbed.1090049
AMA Binzet G. N-(Siklohekzil(metil)karbamotiyoil)-4-nitrobenzamit Bileşiğinin Sentezi, Kristal Yapısı, DFT Çalışmaları ve Hirshfeld Yüzey Analizi. Osmaniye Korkut Ata University Journal of Natural and Applied Sciences. July 2022;5(2):681-706. doi:10.47495/okufbed.1090049
Chicago Binzet, Gün. “N-(Siklohekzil(metil)karbamotiyoil)-4-Nitrobenzamit Bileşiğinin Sentezi, Kristal Yapısı, DFT Çalışmaları Ve Hirshfeld Yüzey Analizi”. Osmaniye Korkut Ata Üniversitesi Fen Bilimleri Enstitüsü Dergisi 5, no. 2 (July 2022): 681-706. https://doi.org/10.47495/okufbed.1090049.
EndNote Binzet G (July 1, 2022) N-(Siklohekzil(metil)karbamotiyoil)-4-nitrobenzamit Bileşiğinin Sentezi, Kristal Yapısı, DFT Çalışmaları ve Hirshfeld Yüzey Analizi. Osmaniye Korkut Ata Üniversitesi Fen Bilimleri Enstitüsü Dergisi 5 2 681–706.
IEEE G. Binzet, “N-(Siklohekzil(metil)karbamotiyoil)-4-nitrobenzamit Bileşiğinin Sentezi, Kristal Yapısı, DFT Çalışmaları ve Hirshfeld Yüzey Analizi”, Osmaniye Korkut Ata University Journal of Natural and Applied Sciences, vol. 5, no. 2, pp. 681–706, 2022, doi: 10.47495/okufbed.1090049.
ISNAD Binzet, Gün. “N-(Siklohekzil(metil)karbamotiyoil)-4-Nitrobenzamit Bileşiğinin Sentezi, Kristal Yapısı, DFT Çalışmaları Ve Hirshfeld Yüzey Analizi”. Osmaniye Korkut Ata Üniversitesi Fen Bilimleri Enstitüsü Dergisi 5/2 (July 2022), 681-706. https://doi.org/10.47495/okufbed.1090049.
JAMA Binzet G. N-(Siklohekzil(metil)karbamotiyoil)-4-nitrobenzamit Bileşiğinin Sentezi, Kristal Yapısı, DFT Çalışmaları ve Hirshfeld Yüzey Analizi. Osmaniye Korkut Ata University Journal of Natural and Applied Sciences. 2022;5:681–706.
MLA Binzet, Gün. “N-(Siklohekzil(metil)karbamotiyoil)-4-Nitrobenzamit Bileşiğinin Sentezi, Kristal Yapısı, DFT Çalışmaları Ve Hirshfeld Yüzey Analizi”. Osmaniye Korkut Ata Üniversitesi Fen Bilimleri Enstitüsü Dergisi, vol. 5, no. 2, 2022, pp. 681-06, doi:10.47495/okufbed.1090049.
Vancouver Binzet G. N-(Siklohekzil(metil)karbamotiyoil)-4-nitrobenzamit Bileşiğinin Sentezi, Kristal Yapısı, DFT Çalışmaları ve Hirshfeld Yüzey Analizi. Osmaniye Korkut Ata University Journal of Natural and Applied Sciences. 2022;5(2):681-706.

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