Publication:
Crystallographic and Spectroscopic Characterization of 2-[(7

dc.authorscopusid6507332027
dc.authorscopusid57221969135
dc.authorscopusid7004018699
dc.authorscopusid57210290492
dc.authorscopusid7003532104
dc.authorscopusid36951865300
dc.authorscopusid36951865300
dc.authorwosidRamli, Youssef/W-8033-2019
dc.authorwosidDemirtaş, Güneş/C-1943-2012
dc.contributor.authorAl-Taifi, Elham A.
dc.contributor.authorMaraei, Islam S.
dc.contributor.authorBakhite, Etify A.
dc.contributor.authorDemirtas, Gunes
dc.contributor.authorMague, Joel T.
dc.contributor.authorMohamed, Shaaban K.
dc.contributor.authorRamli, Youssef
dc.contributor.authorIDMohamed, Shaaban Kamel/0000-0003-4265-5315
dc.contributor.authorIDDemirtaş, Güneş/0000-0001-9953-4026
dc.contributor.authorIDAl-Taifi, Elham/0000-0002-9758-1969
dc.contributor.authorIDRamli, Youssef/0000-0002-6885-5692
dc.contributor.authorIDMarae, Islam/0000-0002-9290-0174
dc.date.accessioned2025-12-11T01:36:21Z
dc.date.issued2021
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Al-Taifi, Elham A.] Sanaa Univ, Fac Sci, Dept Chem, Sanaa, Yemen; [Maraei, Islam S.; Bakhite, Etify A.] Assiut Univ, Fac Sci, Dept Chem, Assiut, Egypt; [Demirtas, Gunes] Ondokuz Mayis Univ, Fac Arts & Sci, Dept Phys, TR-55139 Samsun, Turkey; [Mague, Joel T.] Tulane Univ, Dept Chem, New Orleans, LA 70118 USA; [Mohamed, Shaaban K.] Manchester Metropolitan Univ, Chem & Environm Div, Manchester M1 5GD, Lancs, England; [Mohamed, Shaaban K.] Minia Univ, Fac Sci, Chem Dept, El Minia 61519, Egypt; [Ramli, Youssef] Mohammed V Univ Rabat, Fac Med & Pharm, Drug Sci Res Ctr, Lab Med Chem, Rabat, Moroccoen_US
dc.descriptionMohamed, Shaaban Kamel/0000-0003-4265-5315; Demirtaş, Güneş/0000-0001-9953-4026; Al-Taifi, Elham/0000-0002-9758-1969; Ramli, Youssef/0000-0002-6885-5692; Marae, Islam/0000-0002-9290-0174en_US
dc.description.abstractIn the title molecule, C28H27N3O3S, the heterocyclic portion of the tetrahydroisoquinoline unit is planar and an intramolecular N-H center dot center dot center dot N hydrogen bond and a C-H center dot center dot center dot pi(ring) interaction help to determine the overall conformation. In the crystal, a layer structure with the layers parallel to (101) is generated by O-H center dot center dot center dot O and C-H center dot center dot center dot O hydrogen bonds.en_US
dc.description.sponsorshipNSF-MRI grant [1228232]; Tulane Universityen_US
dc.description.sponsorshipThe support of NSF-MRI grant No. 1228232 for the purchase of the diffractometer and Tulane University for support of the Tulane Crystallography Laboratory are gratefully acknowledged.en_US
dc.description.woscitationindexEmerging Sources Citation Index
dc.identifier.doi10.1107/S2056989021000372
dc.identifier.endpage+en_US
dc.identifier.issn2056-9890
dc.identifier.pmid33614138
dc.identifier.scopus2-s2.0-85100759192
dc.identifier.scopusqualityQ3
dc.identifier.startpage121en_US
dc.identifier.urihttps://doi.org/10.1107/S2056989021000372
dc.identifier.urihttps://hdl.handle.net/20.500.12712/44824
dc.identifier.volume77en_US
dc.identifier.wosWOS:000618622000010
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.subjectTetrahydroisoquinolineen_US
dc.subjectPhenylacetamideen_US
dc.subjectHydrogen Bonden_US
dc.subjectC-H Center Dot Center Dot Center Dot Pi(Ring) Interactionen_US
dc.titleCrystallographic and Spectroscopic Characterization of 2-[(7en_US
dc.typeArticleen_US
dspace.entity.typePublication

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