Please use this identifier to cite or link to this item: 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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