Logo BSU

Пожалуйста, используйте этот идентификатор, чтобы цитировать или ссылаться на этот документ: https://elib.bsu.by/handle/123456789/337590
Полная запись метаданных
Поле DCЗначениеЯзык
dc.contributor.authorCaki, Y.B.-
dc.contributor.authorMakarevich, M.-
dc.contributor.authorBohdan, M.-
dc.contributor.authorCelike, T.-
dc.contributor.authorHulnik, M.-
dc.contributor.authorVasilenko, I.V.-
dc.contributor.authorKiskan, B.-
dc.contributor.authorKostjuk, S.V.-
dc.date.accessioned2025-11-25T11:26:22Z-
dc.date.available2025-11-25T11:26:22Z-
dc.date.issued2025-
dc.identifier.citationMacromol. Chem. Phys.2025; 226: 2400261ru
dc.identifier.urihttps://elib.bsu.by/handle/123456789/337590-
dc.description.abstractThe strategy for the preparation of polyisobutylene‐based block copolymers via mechanistic transformation from cationic to radical polymerization is reported. This strategy involves the synthesis of 2‐bromo‐2‐methylpropanoyl‐terminated difunctional polyisobutylene macroinitiator (BiBB‐PIB‐BiBB) via consecutive cationic polymerization, in situ preparation of hydroxyl‐terminated polyisobutylene and its acylation by 2‐bromo‐2‐methylpropanoyl bromide. The Mn 2 (CO) 10 −triggered photo‐induced radical polymerization of styrene in bulk using this macroinitiator leads to the formation of multiblock copolymer, while predominantly triblock copolymer is generated during the polymerization of methyl methacrylate. The possibility to functionalize the polyisobutylene by pyrene via photo‐induced radical addition of 1‐bromomethyl pyrene in the presence of Mn 2 (CO) 10 is also demonstrated in this work.ru
dc.description.sponsorshipThis work was carried out with financial support from the Ministry of Science and Higher Education of the Russian Federation under grant agreement № 075-15-2024-633 (Sechenov University). In part, this work was also supported by State Program for Scientific Research of Belarus “Chemical processes, reagents and technologies, bioregulators and bioorganic chemistry” (project 2.1.01.03). The authors YBC, TC, and BK also thank the Scientific and Technological Research Council of Turkey (TUBITAK) (Project Number: 220N159), and the Council of Higher Education (YÖK) – Istanbul Technical University Research Fund (Project Number: TGA-2023-44004). SK thanks Dr. Dmitriy Shiman for the DSC measurements.ru
dc.language.isoenru
dc.publisherWiley-VCH GmbHru
dc.rightsinfo:eu-repo/semantics/openAccessru
dc.subjectЭБ БГУ::ЕСТЕСТВЕННЫЕ И ТОЧНЫЕ НАУКИ::Химияru
dc.titleFunctionalized Polyisobutylene and Polyisobutylene-BasedBlock Copolymers by Mechanistic Transformation fromCationic to Radical Processru
dc.typearticleru
dc.rights.licenseCC BY 4.0ru
dc.identifier.DOI10.1002/macp.202400261-
dc.identifier.scopus105001835218-
Располагается в коллекциях:Статьи химического факультета

Полный текст документа:
Файл Описание РазмерФормат 
Macro Chemistry Physics - 2024 - Cakir - Functionalized Polyisobutylene and Polyisobutylene‐Based Block Copolymers by.pdf1,28 MBAdobe PDFОткрыть
Показать базовое описание документа Статистика Google Scholar



Все документы в Электронной библиотеке защищены авторским правом, все права сохранены.