Phosphorus-nitrogen compounds
dc.authorid | Begeç, Saliha/0000-0001-5331-6736 | |
dc.authorid | Hokelek, Tuncer/0000-0002-8602-4382; | |
dc.authorwosid | Begeç, Saliha/AAA-9708-2021 | |
dc.authorwosid | Hokelek, Tuncer/G-6068-2013 | |
dc.authorwosid | Hokelek, Tuncer/JCE-0691-2023 | |
dc.contributor.author | Kiliç, A | |
dc.contributor.author | Begeç, S | |
dc.contributor.author | Kiliç, Z | |
dc.contributor.author | Hökelek, T | |
dc.date.accessioned | 2024-08-04T20:12:11Z | |
dc.date.available | 2024-08-04T20:12:11Z | |
dc.date.issued | 2000 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | The reactions of Cl3P=N-P(O)Cl-2 (1) with Sodium 2,4,6-tert-butylphenoxide and sodium 2,6-di-tert-butyl-4-methylphenoxide give geminal bis products (2) and (3), respectively. Compounds (2) and (3) have been characterised by elemental analysis, IR, H-1-, C-13 and P-31-NMR and the structure of compound (2) has been examined crystallographically. It crystallizes in the monoclinic space group P2(1)/n with a = 10.056(1), b = 25.986(1), c = 15.533(1)Angstrom, beta = 95.9(1)degrees, V = 4037.6(1)Angstrom(3), Z = 4 and D-x = 1.19 g cm(-3). The bulky substituents are instrumental in determining the molecular geometry. The P-N bonds have neither single-nor double-bond character and are substantially shorter than the ideal P-N single bond. The P=O double bond is abnormally long and it has a single bond character. The P-N-P angle [158.0(3)degrees] is the largest one for the reported acyclic phosphazene derivatives in the literature. (C) 2000 Elsevier Science B.V. All rights reserved. | en_US |
dc.identifier.doi | 10.1016/S0022-2860(99)00232-X | |
dc.identifier.endpage | 262 | en_US |
dc.identifier.issn | 0022-2860 | |
dc.identifier.issue | 2-3 | en_US |
dc.identifier.scopus | 2-s2.0-0034711781 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.startpage | 255 | en_US |
dc.identifier.uri | https://doi.org/10.1016/S0022-2860(99)00232-X | |
dc.identifier.uri | https://hdl.handle.net/11616/93278 | |
dc.identifier.volume | 516 | en_US |
dc.identifier.wos | WOS:000084761200016 | 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 | Elsevier Science Bv | en_US |
dc.relation.ispartof | Journal of Molecular Structure | 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 | phosphorus-nitrogen compounds | en_US |
dc.subject | crystal structures of phosphazene compounds | en_US |
dc.subject | spectroscopic studies of phosphazene derivatives | en_US |
dc.subject | phenolysis of acyclic monophosphazene | en_US |
dc.title | Phosphorus-nitrogen compounds | en_US |
dc.type | Article | en_US |