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Crystal Structure and Hirshfeld Surface Analysis of 3-(Hydroxymethyl)

dc.authorscopusid57213972060
dc.authorscopusid57194716371
dc.authorscopusid6508118425
dc.authorscopusid57201620841
dc.authorscopusid57218830659
dc.authorwosidGumus, Mustafa/Hdm-9549-2022
dc.authorwosidN, Dege/B-2545-2016
dc.authorwosidDege, Necmi/B-2545-2016
dc.authorwosidKansız, Sevgi/Aaq-1908-2020
dc.authorwosidSaif, Eiad/Aak-4944-2021
dc.contributor.authorGumus, Mustafa Kemal
dc.contributor.authorKansiz, Sevgi
dc.contributor.authorTulemisova, Gulzhamal Bagitovna
dc.contributor.authorDege, Necmi
dc.contributor.authorSaif, Eiad
dc.contributor.authorIDN, Dege/0000-0003-0660-4721
dc.date.accessioned2025-12-11T01:05:54Z
dc.date.issued2022
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Gumus, Mustafa Kemal] Artvin Coruh Univ, Sci Technol Res & Applicat Ctr, Artvin, Turkey; [Gumus, Mustafa Kemal; Tulemisova, Gulzhamal Bagitovna] Atyrau State Univ, Fac Nat & Agr Sci, Dept Chem & Chem Technol, Atyrau 060011, Kazakhstan; [Kansiz, Sevgi] Samsun Univ, Dept Fundamental Sci, Fac Engn, TR-55420 Samsun, Turkey; [Dege, Necmi] Ondokuz Mayis Univ, Fac Arts & Sci, Dept Phys, TR-55139 Samsun, Turkey; [Saif, Eiad] Sanaa Community Coll, Dept Comp & Elect Engn Technol, Sanaa, Yemen; [Saif, Eiad] Ondokuz May S Univ, Fac Engn, Dept Elect & Elect Engn, TR-55139 Samsun, Turkeyen_US
dc.descriptionN, Dege/0000-0003-0660-4721;en_US
dc.description.abstractA new synthesis of the title compound, C19H21NO2, was developed with good yield and purity using the reaction of 4-hydroxy-3-methyl-2-butanone, benzaldehyde and ammonium acetate in glacial acetic acid as a solvent. The central piperidine ring adopts a chair conformation, and its least-squares basal plane forms dihedral angles of 85.71 (11) and 77.27 (11)degrees with the terminal aromatic rings. In the crystal, the molecules are linked by O-H center dot center dot center dot O and C-H center dot center dot center dot O hydrogen bonds into double ribbons. The Hirshfeld surface analysis shows that the most important contributions are from H center dot center dot center dot H (68%), C center dot center dot center dot H/H center dot center dot center dot C (19%) and O center dot center dot center dot H/H center dot center dot center dot O (12%) interactions.en_US
dc.description.woscitationindexEmerging Sources Citation Index
dc.identifier.doi10.1107/S2056989021012640
dc.identifier.endpage+en_US
dc.identifier.issn2056-9890
dc.identifier.pmid35079418
dc.identifier.scopus2-s2.0-85123077787
dc.identifier.scopusqualityQ3
dc.identifier.startpage29en_US
dc.identifier.urihttps://doi.org/10.1107/S2056989021012640
dc.identifier.urihttps://hdl.handle.net/20.500.12712/41345
dc.identifier.volume78en_US
dc.identifier.wosWOS:000760208800006
dc.language.isoenen_US
dc.publisherInt Union Crystallographyen_US
dc.relation.ispartofActa Crystallographica Section E-Crystallographic Communicationsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCrystal Structureen_US
dc.subjectPiperidoneen_US
dc.subjectBenzaldehydeen_US
dc.subject4-Hydroxy-3-Methyl-2-Butanoneen_US
dc.subjectAmmonium Acetateen_US
dc.subjectHirshfeld Surfaceen_US
dc.subjectHydrogen Bondingen_US
dc.titleCrystal Structure and Hirshfeld Surface Analysis of 3-(Hydroxymethyl)en_US
dc.typeArticleen_US
dspace.entity.typePublication

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