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 |
|