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https://hdl.handle.net/11499/8055
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kabay, Nilgün | - |
dc.contributor.author | Gök, Yaşar | - |
dc.date.accessioned | 2019-08-16T12:34:54Z | |
dc.date.available | 2019-08-16T12:34:54Z | |
dc.date.issued | 2013 | - |
dc.identifier.issn | 0040-4039 | - |
dc.identifier.uri | https://hdl.handle.net/11499/8055 | - |
dc.identifier.uri | https://doi.org/10.1016/j.tetlet.2013.05.125 | - |
dc.description.abstract | A metal-free phthalocyanine (H2Pc) containing four diazadithiamacrocycles a with 2-pyridinyl methyl groups attached was synthesized via cyclotetramerization of 4,5-bis{2-[13(2-pyridinylmethyl)-1,9-dithia-5,13- diazacyclohexadecanyl-5]ethyl} thiophthalonitrile in the presence of DBU as a strong organic base. New compounds were characterized by a combination of elemental analysis, 1H NMR, 13C NMR, IR, UV/vis, and MS spectral data. © 2013 Elsevier Ltd. All rights reserved. | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | Tetrahedron Letters | en_US |
dc.relation.ispartof | Uluslararası Hakemli Dergi | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Detosylation | en_US |
dc.subject | Macrocyclization | en_US |
dc.subject | Metal-free phthalocyanine | en_US |
dc.subject | Mixed donor macrocycle | en_US |
dc.subject | Pendant arms | en_US |
dc.subject | macrocyclic compound | en_US |
dc.subject | methyl group | en_US |
dc.subject | nitrile | en_US |
dc.subject | phthalocyanine derivative | en_US |
dc.subject | pyridine derivative | en_US |
dc.subject | article | en_US |
dc.subject | carbon nuclear magnetic resonance | en_US |
dc.subject | chemical modification | en_US |
dc.subject | cyclotetramerization | en_US |
dc.subject | infrared spectroscopy | en_US |
dc.subject | mass spectrometry | en_US |
dc.subject | proton nuclear magnetic resonance | en_US |
dc.subject | synthesis | en_US |
dc.subject | ultraviolet spectroscopy | en_US |
dc.title | Synthesis and characterization of metal-free phthalocyanine containing 16-membered N2S2-donor macrocycles linked to a 2-pyridinyl methyl moiety | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 54 | en_US |
dc.identifier.issue | 31 | en_US |
dc.identifier.startpage | 4086 | |
dc.identifier.startpage | 4086 | en_US |
dc.identifier.endpage | 4090 | en_US |
dc.identifier.doi | 10.1016/j.tetlet.2013.05.125 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.scopus | 2-s2.0-84879686006 | en_US |
dc.identifier.wos | WOS:000321603200020 | en_US |
dc.identifier.scopusquality | Q2 | - |
dc.owner | Pamukkale University | - |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
item.languageiso639-1 | en | - |
item.openairetype | Article | - |
item.cerifentitytype | Publications | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
crisitem.author.dept | 20.03. Biomedical Engineering | - |
crisitem.author.dept | 17.01. Chemistry | - |
Appears in Collections: | Mühendislik Fakültesi Koleksiyonu Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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