Yayın: Crystal Structure and Hirshfeld Surface Analysis of 1-(4-Chlorophenyl)-5-{4-[(2-methylphenyl)methoxy]phenyl}-1H-Pyrazole
| dc.contributor.author | Aydin, Abdullah | |
| dc.contributor.author | Akkurt, Mehmet | |
| dc.contributor.author | Turanli, Sumeyye | |
| dc.contributor.author | Banoglu, Erden | |
| dc.contributor.author | Ozcelik, Nefise | |
| dc.date.accessioned | 2026-01-04T14:57:30Z | |
| dc.date.issued | 2021-01-01 | |
| dc.description.abstract | The aim of the study is to explore the crystal structure and performe Hirshfeld surface analysis of 1-(4-chlorophenyl)-5-{4-[(2-methylphenyl)methoxy]phenyl}-1H-pyrazole. In the title compound, C23H19ClN2O, the 4-chlorophenyl, 2-methylphenyl and benzene rings are oriented with dihedral angles of 71.22(10), 31.82(9) and 59.76(9)degrees, respectively, with respect to the pyrazole ring. Pairs of molecules are linked by intermolecular C-H center dot center dot center dot O hydrogen contacts with R-2(2)(8) ring motifs forming sheets lying parallel to (100). Furthermore C-H center dot center dot center dot pi interactions also contribute to stabilizing the molecular packing. A Hirshfeld surface analysis has been used to confirm and quantify the supramolecular interactions which indicate that the most important contributions for the crystal packing are from H center dot center dot center dot H (42.5%) and H center dot center dot center dot C/C center dot center dot center dot H (35%) and H center dot center dot center dot Cl/Cl center dot center dot center dot H (12%) interactions. | |
| dc.description.uri | https://avesis.gazi.edu.tr/publication/details/462a235d-cc94-4c7e-a2d8-b77e0c01c6f0/oai | |
| dc.description.uri | https://avesis.erciyes.edu.tr/publication/details/462a235d-cc94-4c7e-a2d8-b77e0c01c6f0/oai | |
| dc.description.uri | http://dx.doi.org/10.48623/aperta.230312 | |
| dc.identifier.openaire | dedup_wf_002::26e1d3dcde1b9fde8dad41cb603a4d91 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12597/38499 | |
| dc.language.iso | eng | |
| dc.publisher | Aperta | |
| dc.rights | OPEN | |
| dc.title | Crystal Structure and Hirshfeld Surface Analysis of 1-(4-Chlorophenyl)-5-{4-[(2-methylphenyl)methoxy]phenyl}-1H-Pyrazole | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| local.api.response | {"authors":[{"fullName":"Aydin, Abdullah","name":"Abdullah","surname":"Aydin","rank":1,"pid":null},{"fullName":"Akkurt, Mehmet","name":"Mehmet","surname":"Akkurt","rank":2,"pid":null},{"fullName":"Turanli, Sumeyye","name":"Sumeyye","surname":"Turanli","rank":3,"pid":null},{"fullName":"Banoglu, Erden","name":"Erden","surname":"Banoglu","rank":4,"pid":null},{"fullName":"Ozcelik, Nefise","name":"Nefise","surname":"Ozcelik","rank":5,"pid":null}],"openAccessColor":null,"publiclyFunded":null,"type":"publication","language":{"code":"eng","label":"English"},"countries":null,"subjects":null,"mainTitle":"Crystal Structure and Hirshfeld Surface Analysis of 1-(4-Chlorophenyl)-5-{4-[(2-methylphenyl)methoxy]phenyl}-1H-Pyrazole","subTitle":null,"descriptions":["The aim of the study is to explore the crystal structure and performe Hirshfeld surface analysis of 1-(4-chlorophenyl)-5-{4-[(2-methylphenyl)methoxy]phenyl}-1H-pyrazole. In the title compound, C23H19ClN2O, the 4-chlorophenyl, 2-methylphenyl and benzene rings are oriented with dihedral angles of 71.22(10), 31.82(9) and 59.76(9)degrees, respectively, with respect to the pyrazole ring. Pairs of molecules are linked by intermolecular C-H center dot center dot center dot O hydrogen contacts with R-2(2)(8) ring motifs forming sheets lying parallel to (100). Furthermore C-H center dot center dot center dot pi interactions also contribute to stabilizing the molecular packing. A Hirshfeld surface analysis has been used to confirm and quantify the supramolecular interactions which indicate that the most important contributions for the crystal packing are from H center dot center dot center dot H (42.5%) and H center dot center dot center dot C/C center dot center dot center dot H (35%) and H center dot center dot center dot Cl/Cl center dot center dot center dot H (12%) interactions."],"publicationDate":"2021-01-01","publisher":"Aperta","embargoEndDate":null,"sources":null,"formats":null,"contributors":null,"coverages":null,"bestAccessRight":{"code":"c_abf2","label":"OPEN","scheme":"http://vocabularies.coar-repositories.org/documentation/access_rights/"},"container":null,"documentationUrls":null,"codeRepositoryUrl":null,"programmingLanguage":null,"contactPeople":null,"contactGroups":null,"tools":null,"size":null,"version":null,"geoLocations":null,"id":"dedup_wf_002::26e1d3dcde1b9fde8dad41cb603a4d91","originalIds":["50|od_____10046::84abbb825cb34f8eb823e66e6ac5172a","462a235d-cc94-4c7e-a2d8-b77e0c01c6f0","50|od______9447::84abbb825cb34f8eb823e66e6ac5172a","oai:aperta.ulakbim.gov.tr:230312","50|r39c86a4b39b::736f8d88a9ea2d2d15702ba7da9f6563"],"pids":null,"dateOfCollection":null,"lastUpdateTimeStamp":null,"indicators":{"citationImpact":{"citationCount":0,"influence":2.5349236e-9,"popularity":1.6119823e-9,"impulse":0,"citationClass":"C5","influenceClass":"C5","impulseClass":"C5","popularityClass":"C5"}},"instances":[{"type":"Article","urls":["https://avesis.gazi.edu.tr/publication/details/462a235d-cc94-4c7e-a2d8-b77e0c01c6f0/oai"],"publicationDate":"2021-11-01","refereed":"nonPeerReviewed"},{"type":"Article","urls":["https://avesis.erciyes.edu.tr/publication/details/462a235d-cc94-4c7e-a2d8-b77e0c01c6f0/oai"],"publicationDate":"2021-11-01","refereed":"nonPeerReviewed"},{"alternateIdentifiers":[{"scheme":"doi","value":"10.48623/aperta.230312"}],"license":"CC BY","type":"Other literature type","urls":["http://dx.doi.org/10.48623/aperta.230312"],"publicationDate":"2021-01-01","refereed":"nonPeerReviewed"}],"isGreen":null,"isInDiamondJournal":null} | |
| local.import.source | OpenAire |
