Synthesis, crystal structures, spectral FT-IR, NMR and UV-Vis investigations and Hirshfeld surface analysis of two new 2-hydroxyethyl-substituted N-heterocyclic carbene precursors
| dc.authorid | Aktaş, Aydın/0000-0001-8496-6782 | |
| dc.authorwosid | Gök, Yetkin/AAA-5669-2021 | |
| dc.authorwosid | Barut Celepci, Duygu/M-6189-2017 | |
| dc.authorwosid | Aktaş, Aydın/J-6194-2019 | |
| dc.contributor.author | Aktas, Aydin | |
| dc.contributor.author | Celepci, Duygu Barut | |
| dc.contributor.author | Gok, Yetkin | |
| dc.date.accessioned | 2024-08-04T20:45:56Z | |
| dc.date.available | 2024-08-04T20:45:56Z | |
| dc.date.issued | 2019 | |
| dc.department | İnönü Üniversitesi | en_US |
| dc.description.abstract | This study discusses the synthesis of two new 2-hydroxyethyl substituted N-heterocyclic carbene (NHC) precursors. The NHC precursors were prepared from 1-(alkyl/aryl)benzimidazole and alkyl halides. They were characterized using H-1 NMR, C-13 NMR, FT-IR, UV-Vis spectroscopy, and elemental analysis techniques. Molecular and crystal structures of 1 and 2 were determined using the single-crystal X-ray diffraction method. Crystal structure of the compounds features NHC precursors and chloride anions. Additionally in 2, the asymmetric unit has a water molecule, which forms a tetrameric chloride-hydrate assembly with the chloride anion. The chloride anions play an important role in the stabilization of crystal structures to form a two-dimensional supramolecular architecture. The 3D Hirshfeld surface and the associated 2D fingerprint plots were also drawn to gain insights into the behavior of the interactions in the compounds. | en_US |
| dc.description.sponsorship | Dokuz Eylul University [KB.FEN.13] | en_US |
| dc.description.sponsorship | Dokuz Eylul University, Grant/Award Number: 2010.KB.FEN.13 | en_US |
| dc.identifier.doi | 10.1002/jccs.201900020 | |
| dc.identifier.endpage | 1396 | en_US |
| dc.identifier.issn | 0009-4536 | |
| dc.identifier.issn | 2192-6549 | |
| dc.identifier.issue | 10 | en_US |
| dc.identifier.scopus | 2-s2.0-85065639208 | en_US |
| dc.identifier.scopusquality | Q3 | en_US |
| dc.identifier.startpage | 1389 | en_US |
| dc.identifier.uri | https://doi.org/10.1002/jccs.201900020 | |
| dc.identifier.uri | https://hdl.handle.net/11616/98795 | |
| dc.identifier.volume | 66 | en_US |
| dc.identifier.wos | WOS:000491034300020 | en_US |
| dc.identifier.wosquality | Q3 | en_US |
| dc.indekslendigikaynak | Web of Science | en_US |
| dc.indekslendigikaynak | Scopus | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Wiley-V C H Verlag Gmbh | en_US |
| dc.relation.ispartof | Journal of The Chinese Chemical Society | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | chloride hydrate | en_US |
| dc.subject | crystal structure | en_US |
| dc.subject | FT-IR and NMR | en_US |
| dc.subject | Hirshfeld surface analysis | en_US |
| dc.subject | N-heterocyclic carbene | en_US |
| dc.subject | UV-Vis | en_US |
| dc.title | Synthesis, crystal structures, spectral FT-IR, NMR and UV-Vis investigations and Hirshfeld surface analysis of two new 2-hydroxyethyl-substituted N-heterocyclic carbene precursors | en_US |
| dc.type | Article | en_US |











