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dc.contributor.authorParthasarathi, D.en
dc.contributor.authorPadusha, M. S. A.en
dc.contributor.authorSuganya, S.en
dc.contributor.authorKumaradhas, P.en
dc.contributor.authorSajith, A. M.en
dc.contributor.authorJoy, M. N.en
dc.date.accessioned2022-05-12T08:22:46Z-
dc.date.available2022-05-12T08:22:46Z-
dc.date.issued2022-
dc.identifier.citationSynthesis, Characterization, Crystal Structure of 4-(4-Bromo-phenyl)-2,6-dimethyl-1,4-dihydro-pyridine-3,5-dicarboxylic Acid Diethyl Ester: Hirshfeld Surface Analysis and DFT Calculations / D. Parthasarathi, M. S. A. Padusha, S. Suganya et al. // Egyptian Journal of Chemistry. — 2022. — Vol. 65. — Iss. 2. — P. 439-448.en
dc.identifier.issn0449-2285-
dc.identifier.otherAll Open Access, Bronze3
dc.identifier.urihttp://elar.urfu.ru/handle/10995/111777-
dc.description.abstractThe title compound dihydro-pyridine was synthesized and structure is established by FT-IR, 1H NMR, and 13C NMR spectral analysis. The SC-XRD analysis has been carried out for the determination of molecular structure and its disclosed that crystal relates to monoclinic crystal phase, P21/n1 space group and cell parameters are a= 10.2314(2), b = 7.5215(1), c = 24.5475(4), α = 90, β = 97.921(1)° γ = 90 with 0.34 x 0.33 x 0.30 crystal size. The crystal lattice exhibits inter-molecular H-bonding between N1—H1A—O1. Further inter contacts of the crystal lattice were determined by 3-D Hirshfeld surface (HSA) as well as percentage of contributions have been computed through 2D finger plot depiction. Moreover, bond length, bond angle and torsion angles have been correlated to respective output results of B3LYP/6-311++G(d,p). The electrophilic and nucleophilic characters have been studied through molecular electrostatic potential (MEP) analysis. © 2020 NIODC. All rights reserved ©2022 National Information and Documentation Center (NIDOC).en
dc.description.sponsorshipWe record our sincere thanks to the (CIMF), Periyar University, Salem for providing the facilities for single crystal XRD analysis and SAIF-VIT for providing 1H, 13C NMR analysis. The authors also thanks to Jamal instrumentation facility (JIF), Post Graduate and Research Department of Chemistry, Jamal Mohamed College, Tiruchirappalli for providing necessary lab facilities.en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherNIDOC (Nat.Inform.Document.Centre)en1
dc.publisherEgypts Presidential Specialized Council for Education and Scientific Researchen
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.sourceEgypt. J. Chem.2
dc.sourceEgyptian Journal of Chemistryen
dc.subject1,4en
dc.subjectDFT ANALYSISen
dc.subjectDIHYDRO PYRIDINEen
dc.subjectHIRSHFELD SURFACESen
dc.subjectN-H-O INTERACTIONen
dc.subjectSC-XRDen
dc.titleSynthesis, Characterization, Crystal Structure of 4-(4-Bromo-phenyl)-2,6-dimethyl-1,4-dihydro-pyridine-3,5-dicarboxylic Acid Diethyl Ester: Hirshfeld Surface Analysis and DFT Calculationsen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.21608/EJCHEM.2021.88473.4256-
dc.identifier.scopus85121456982-
local.contributor.employeeParthasarathi, D., Post Graduate and Research Department of Chemistry, Jamal Mohamed College, Bharathidasan University, Tamilnadu, Tiruchirappalli, 620 020, India; Padusha, M.S.A., Post Graduate and Research Department of Chemistry, Jamal Mohamed College, Bharathidasan University, Tamilnadu, Tiruchirappalli, 620 020, India; Suganya, S., Laboratory of X-Ray Crystallography and Computational Molecular biology, Department of Physics, Periyar University, Salem, 636 01, India; Kumaradhas, P., Laboratory of X-Ray Crystallography and Computational Molecular biology, Department of Physics, Periyar University, Salem, 636 01, India; Sajith, A.M., Ortin laboratories Pvt.Ltd, Malkapur Village, Choutuppal Mandal, Telengana, Hyderabad, 508252, India; Joy, M.N., Innovation center for Chemical and Pharmaceutical Technologies, Institute of Chemical Technology, Ural Federal University, 19Mira Street, Yekaterinburg, 620002, Russian Federationen
local.description.firstpage439-
local.description.lastpage448-
local.issue2-
local.volume65-
dc.identifier.wos000739329900003-
local.contributor.departmentPost Graduate and Research Department of Chemistry, Jamal Mohamed College, Bharathidasan University, Tamilnadu, Tiruchirappalli, 620 020, India; Laboratory of X-Ray Crystallography and Computational Molecular biology, Department of Physics, Periyar University, Salem, 636 01, India; Ortin laboratories Pvt.Ltd, Malkapur Village, Choutuppal Mandal, Telengana, Hyderabad, 508252, India; Innovation center for Chemical and Pharmaceutical Technologies, Institute of Chemical Technology, Ural Federal University, 19Mira Street, Yekaterinburg, 620002, Russian Federationen
local.identifier.pure29140828-
local.identifier.eid2-s2.0-85121456982-
local.identifier.wosWOS:000739329900003-
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