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https://hdl.handle.net/11499/8055
Title: | Synthesis and characterization of metal-free phthalocyanine containing 16-membered N2S2-donor macrocycles linked to a 2-pyridinyl methyl moiety | Authors: | Kabay, Nilgün Gök, Yaşar |
Keywords: | Detosylation Macrocyclization Metal-free phthalocyanine Mixed donor macrocycle Pendant arms macrocyclic compound methyl group nitrile phthalocyanine derivative pyridine derivative article carbon nuclear magnetic resonance chemical modification cyclotetramerization infrared spectroscopy mass spectrometry proton nuclear magnetic resonance synthesis ultraviolet spectroscopy |
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. | URI: | https://hdl.handle.net/11499/8055 https://doi.org/10.1016/j.tetlet.2013.05.125 |
ISSN: | 0040-4039 |
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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