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A new synthetic route to 5,6,11,12-tetraarylethynyltetracenes
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| dc.date.accessioned | 2019-01-22T20:46:11Z | |
| dc.date.available | 2019-01-22T20:46:11Z | |
| dc.date.issued | 2018 | |
| dc.identifier.issn | 1477-0520 | |
| dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/148675 | |
| dc.description.abstract | © 2018 The Royal Society of Chemistry. A new synthetic route to 5,6,11,12-tetrakis(arylethynyl)tetracenes, π-extended rubrenes, was developed via [4 + 2] cycloadditions of dialkynylisobenzofuran and 1,4-naphthoquinone. Introduction of arylethynyl groups by double nucleophilic additions to tetracenequinone gave sterically congested (arylethynyl)tetracenes after reductive aromatization. The photophysical properties of the newly prepared π-conjugated molecules are also evaluated. | |
| dc.relation.ispartofseries | Organic and Biomolecular Chemistry | |
| dc.title | A new synthetic route to 5,6,11,12-tetraarylethynyltetracenes | |
| dc.type | Article | |
| dc.relation.ispartofseries-issue | 47 | |
| dc.relation.ispartofseries-volume | 16 | |
| dc.collection | Публикации сотрудников КФУ | |
| dc.relation.startpage | 9143 | |
| dc.source.id | SCOPUS14770520-2018-16-47-SID85058172478 |
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Публикации сотрудников КФУ Scopus [24551]
Коллекция содержит публикации сотрудников Казанского федерального (до 2010 года Казанского государственного) университета, проиндексированные в БД Scopus, начиная с 1970г.