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dc.contributor.author | Khodov I. | |
dc.contributor.author | Maltceva O. | |
dc.contributor.author | Klochkov V. | |
dc.contributor.author | Koifman O. | |
dc.contributor.author | Mamardashvili N. | |
dc.date.accessioned | 2018-04-05T07:09:42Z | |
dc.date.available | 2018-04-05T07:09:42Z | |
dc.date.issued | 2017 | |
dc.identifier.issn | 1144-0546 | |
dc.identifier.uri | http://dspace.kpfu.ru/xmlui/handle/net/129911 | |
dc.description.abstract | © 2017 The Royal Society of Chemistry and the Centre National de la Recherche Scientifique. The complexation of 2-aza-21-carba-tetraphenylporphyrin and 2-aza-2-methyl-5,10,15,20-tetraphenyl-21-carbaporphyrin with nickel and zinc acetates in organic solvents has been investigated by UV-Vis spectroscopy and 1 H NMR. It has been shown that the enhanced reactivity of these tetrapyrrolic macrocycles is mainly determined by their ability to exist in different tautomeric forms. | |
dc.relation.ispartofseries | New Journal of Chemistry | |
dc.title | N-Confused porphyrins: Complexation and<sup>1</sup>H NMR studies | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 16 | |
dc.relation.ispartofseries-volume | 41 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 7932 | |
dc.source.id | SCOPUS11440546-2017-41-16-SID85027164038 |