Crystal structure and Hirshfeld surface analysis of 2,2,2-trifluoro-1-(7-methylimidazo[1,2-a]pyridin-3- yl)ethan-1-one

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dc.authorid0000-0002-1141-5151
dc.contributor.authorGuseinov, Firudin I.
dc.contributor.authorKobrakov, Konstantin I.
dc.contributor.authorUgrak, Bogdan I.
dc.contributor.authorAtioğlu, Zeliha
dc.contributor.authorAkkurt, Mehmet
dc.contributor.authorBhattarai, Ajaya
dc.date.accessioned2022-02-15T06:39:54Z
dc.date.available2022-02-15T06:39:54Z
dc.date.issued2022en_US
dc.departmentKapadokya Üniversitesi, Uygulamalı Bilimler Yüksekokulu, Havacılık Elektrik ve Elektroniği Bölümü
dc.descriptionTARAMAWOS
dc.descriptionTARAMAPUBMED
dc.descriptionTARAMASCOPUS
dc.description.abstractThe bicyclic imidazo[1,2-a]pyridine core in the molecule of the title compound, C10H7F3N2O, is planar within 0.004 (1) A ° . In the crystal, the molecules are linked by pairs of C—H N and C—H O hydrogen bonds, forming strips. These strips are connected by the F F contacts into layers, which are further joined by – stacking interactions. The Hirshfeld surface analysis and fingerprint plots reveal that molecular packing is governed by F H/H F (31.6%), H H (16.8%), C H/H C (13.8%) and O H/H O (8.5%) contacts. 1. Chemical context The imidazo[1,2-a]pyridine synthon is one of the important fused bicyclic 5–6 heterocycles and it is recognized as a ‘drug prejudice’ scaffold because of its wide range of applications in medicinal chemistry (Bagdi et al., 2015). This synthon is also useful in coordination chemistry and catalysis because of its coordination ability and non-covalent donor–acceptor bonding (Guseinov et al., 2022; Ma et al., 2020, 2021; Mahmudov et al., 2020, 2021). Synthesis of this synthon from easily available chemicals is desirable due to its importance in the various branches of chemistry (Bagdi et al., 2015). Along with this, intermolecular interactions organize molecular architectures, which play a crucial role in synthesis, catalysis, micellization, etc. (Gurbanov et al., 2020a,b; Kopylovich et al., 2011; Ma et al., 2017a,b). The non-covalent bond–acceptor ability of both nitrogen atoms in the imidazo[1,2-a]pyridine synthon can be used in crystal engineering and in the design of dyes and other materials (Maharramov et al., 2018; Mizar et al., 2012; Shixaliyev et al., 2014; Shikhaliyev et al., 2018, 2019). Herein, we report a one-pot synthesis of 2,2,2-trifluoro-1-(7- methylimidazo[1,2-a]pyridin-3-yl)ethan-1-one (I) from (E/Z)- 3-bromo-1,1,1-trifluoro-4-isopropoxybut-3-en-2-one and 4-methylpyridin-2-amine, which provides multiple intermolecular non-covalent
dc.identifier.endpage17en_US
dc.identifier.issueE78en_US
dc.identifier.scopusqualityN/A
dc.identifier.startpage12en_US
dc.identifier.urihttps://doi.org/10.1107/S2056989021012676
dc.identifier.urihttps://hdl.handle.net/20.500.12695/1474
dc.identifier.wosWOS:000760208800003
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Sceince
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.institutionauthorAtioğlu, Zeliha
dc.language.isoen
dc.relation.ispartofActa Cryst
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectcrystal structure
dc.subjectimidazo[1,2- a]pyridine
dc.subjecthydrogen bonds
dc.subjectFF contacts
dc.subjectHirshfeld surface analysis
dc.titleCrystal structure and Hirshfeld surface analysis of 2,2,2-trifluoro-1-(7-methylimidazo[1,2-a]pyridin-3- yl)ethan-1-one
dc.typeArticle

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