1,1?,3,3?-tetraalkyl-2,2?-biperimidinylidenes

dc.authoridHokelek, Tuncer/0000-0002-8602-4382
dc.authoridCetinkaya, Bekir/0000-0002-4551-8650
dc.authorwosidHokelek, Tuncer/G-6068-2013
dc.authorwosidHokelek, Tuncer/JCE-0691-2023
dc.contributor.authorAlici, B
dc.contributor.authorHökelek, T
dc.contributor.authorÇetinkaya, E
dc.contributor.authorÇetinkaya, B
dc.date.accessioned2024-08-04T20:13:14Z
dc.date.available2024-08-04T20:13:14Z
dc.date.issued2003
dc.departmentİnönü Üniversitesien_US
dc.description.abstractC-2 deprotonation of 1,3-dibutylperimidinium bromide (1a) with sodium hydride and a catalytic amount of potassium tert-butoxide in dry THF led to the formation of the exceptionally inert tetraaminoalkene 2a. In contrast, isostructural tetrakis(2-methoxyethyl)-tetraaminoalkene (2b) instantaneously reacted with O-2 to yield urea 3b, and silver nitrate was readily reduced with 2b to form a silver mirror. Compound 2a has been characterized by X-ray diffraction studies; the naphtho-pyrimidine skeleton imposes structural constraints and some rigidity to the C=C bonding. (C) 2003 Wiley Periodicals, Inc.en_US
dc.identifier.doi10.1002/hc.10088
dc.identifier.endpage87en_US
dc.identifier.issn1042-7163
dc.identifier.issue1en_US
dc.identifier.scopus2-s2.0-0037277589en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage82en_US
dc.identifier.urihttps://doi.org/10.1002/hc.10088
dc.identifier.urihttps://hdl.handle.net/11616/93486
dc.identifier.volume14en_US
dc.identifier.wosWOS:000180824700013en_US
dc.identifier.wosqualityQ2en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherJohn Wiley & Sons Incen_US
dc.relation.ispartofHeteroatom Chemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectEnetetraminesen_US
dc.subjectCatalystsen_US
dc.subjectComplexesen_US
dc.subjectChemistryen_US
dc.subjectCarbenesen_US
dc.title1,1?,3,3?-tetraalkyl-2,2?-biperimidinylidenesen_US
dc.typeArticleen_US

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