Branched oligophenylenes containing octylphenotiazine and dioctylfluorene groups and phen-1,3,5-triyl branching center


Дәйексөз келтіру

Толық мәтін

Ашық рұқсат Ашық рұқсат
Рұқсат жабық Рұқсат берілді
Рұқсат жабық Тек жазылушылар үшін

Аннотация

A series of branched oligophenylenes containing the dioctylfluorene and octylphenothiazine moieties was synthesized using the Suzuki reaction applied within the framework of the A2 + B2 + B3 approach. 1,3,5-tris(7-Bromo-9,9-di-n-octylfluoren-2-yl)benzene and 1,3,5-tris- (4-bromophenyl)benzene were used as the branching co-monomers. It was shown that the fluorescence spectra of co-oligomers containing phenothiazine moieties are shifted to the longwavelength region as compared to the spectra of that without such moieties.

Авторлар туралы

A. Kovalev

A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences

Email: khotina@ineos.ac.ru
Ресей, 28 ul. Vavilova, Moscow, 119991

E. Martyanova

A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences

Email: khotina@ineos.ac.ru
Ресей, 28 ul. Vavilova, Moscow, 119991

M. Sycheva

A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences

Email: khotina@ineos.ac.ru
Ресей, 28 ul. Vavilova, Moscow, 119991

I. Suntsova

A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences

Email: khotina@ineos.ac.ru
Ресей, 28 ul. Vavilova, Moscow, 119991

N. Kushakova

A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences

Email: khotina@ineos.ac.ru
Ресей, 28 ul. Vavilova, Moscow, 119991

I. Abramov

A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences

Email: khotina@ineos.ac.ru
Ресей, 28 ul. Vavilova, Moscow, 119991

I. Khotina

A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences

Хат алмасуға жауапты Автор.
Email: khotina@ineos.ac.ru
Ресей, 28 ul. Vavilova, Moscow, 119991

Қосымша файлдар

Қосымша файлдар
Әрекет
1. JATS XML

© Springer Science+Business Media, LLC, part of Springer Nature, 2018