Synthesis, structural characterization, and cytotoxic activity of new spirocyclic octachlorocyclotetraphosphazenes
dc.authorid | Hokelek, Tuncer -- 0000-0002-8602-4382 | |
dc.contributor.author | Işıklan, Muhammed | |
dc.contributor.author | Sayın, Levent | |
dc.contributor.author | Sonkaya, Ömer | |
dc.contributor.author | Hökelek, Tuncer | |
dc.contributor.author | Türk, Mustafa | |
dc.contributor.author | Oğuztüzün, Serpil | |
dc.date.accessioned | 13.07.201910:50:10 | |
dc.date.accessioned | 2019-07-29T19:30:19Z | |
dc.date.available | 13.07.201910:50:10 | |
dc.date.available | 2019-07-29T19:30:19Z | |
dc.date.issued | 2016 | |
dc.department | Aksaray Teknik Bilimler Meslek Yüksekokulu | |
dc.description.abstract | Octachlorocyclotetraphosphazene, N4P4Cl8, (1) was reacted with N, N-dibenzylethylenediamine to synthesize partially substituted monospiro- (2), dispiro- (5) and tetraspirocyclotetraphosphazene (8) derivatives. The reactions of 2 and 5 with excess pyrrolidine and morpholine produced fully substituted pyrrolidino (3 and 6) and morpholino (4 and 7) spirocyclotetraphosphazenes. The structures of the compounds were determined with 1D (H-1, C-13, P-31, and DEPT) NMR, 2D (HSQC) NMR, ESI-MS, FTIR, and elemental analysis. The solid-state structures of 6 and 7 were examined by X-ray crystallography. In 7, intramolecular C-H...O hydrogen bonds link the molecules into centrosymmetric dimmers. The cytotoxic activity of all the compounds against human cervix carcinoma cell lines (HeLa) was investigated. The study showed that these compounds exert limited cytotoxic, apoptotic and necrotic effects on HeLa cancer cell lines. | |
dc.description.sponsorship | Kirikkale University, Scientific Research Projects Coordination Unit [2005/19]; Hacettepe University, Scientific Research Unit [0202602002] | |
dc.description.sponsorship | The authors gratefully acknowledge the "Kirikkale University, Scientific Research Projects Coordination Unit" Grant No. 2005/19 and "Hacettepe University, Scientific Research Unit" Grant No. 0202602002 for financial support. | |
dc.identifier.doi | 10.1080/10426507.2016.1160240 | |
dc.identifier.endpage | 1222 | en_US |
dc.identifier.issn | 1042-6507 | |
dc.identifier.issn | 1563-5325 | |
dc.identifier.issue | 9 | en_US |
dc.identifier.scopusquality | Q3 | |
dc.identifier.startpage | 1216 | en_US |
dc.identifier.uri | https://doi.org/10.1080/10426507.2016.1160240 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12451/6263 | |
dc.identifier.volume | 191 | en_US |
dc.identifier.wos | WOS:000382941000006 | |
dc.identifier.wosquality | N/A | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.language.iso | en | |
dc.publisher | Taylor & Francis Ltd | |
dc.relation.ispartof | Phosphorus Sulfur and Silicon and the Related Elements | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
dc.rights | info:eu-repo/semantics/embargoedAccess | |
dc.subject | Cyclotetraphosphazenes | |
dc.subject | Spirophosphazenes | |
dc.subject | Crystal Structure | |
dc.subject | Spectroscopy | |
dc.subject | HeLa Cancer Cell Line | |
dc.subject | Cytotoxicity | |
dc.title | Synthesis, structural characterization, and cytotoxic activity of new spirocyclic octachlorocyclotetraphosphazenes | |
dc.type | Article |
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