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Structural Defects in Polyallylcarbosilane Dendrimers and Their PolyolDerivatives Characterized by NMR and MALDI-TOF Mass Spectrometry

  1. 1.
    SYSNO ASEP0343150
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleStructural Defects in Polyallylcarbosilane Dendrimers and Their PolyolDerivatives Characterized by NMR and MALDI-TOF Mass Spectrometry
    Author(s) Krupková, Alena (UCHP-M) RID, ORCID, SAI
    Čermák, Jan (UCHP-M) RID, ORCID, SAI
    Walterová, Zuzana (UMCH-V)
    Horský, Jiří (UMCH-V) RID, ORCID
    Source TitleMacromolecules. - : American Chemical Society - ISSN 0024-9297
    Roč. 43, č. 10 (2010), s. 4511-4519
    Number of pages9 s.
    Languageeng - English
    CountryUS - United States
    Keywordscarbosilane dendrimers ; maldi-tof ms ; structural defects
    Subject RIVCC - Organic Chemistry
    R&D ProjectsLC06070 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    CEZAV0Z40720504 - UCHP-M (2005-2011)
    AV0Z40500505 - UMCH-V (2005-2011)
    UT WOS000277649500014
    DOI10.1021/ma100315w
    AnnotationA series of polyallylcarbosilane dendrimers and carbosilane-based dendritic polyols up to third generation was analyzed by means of MALDI-TOF MS and multinuclear NMR to determine the character, origin, and number of structural defects. Several side reactions accompanying hydrosilylation, from which isomerization of terminal double bonds was the most abundant, were detected during the synthesis of carbosilane skeleton. Despite increased steric hindrance, internal double bonds react in subsequent addition reactions. Depending on the synthetic sequence applied, the retained reactivity of the internal double bonds can lead either to suppression of the defect in the next generation or to creation of more significant defects such as dendrimer dimers. Hydroboration of allyl groups using dicyclohexylborane proceeded with near quantitative conversion; a small amount of hydrolysis accompanying the following oxidation step producing nonreactive alkyl groups at the periphery was detected.
    WorkplaceInstitute of Chemical Process Fundamentals
    ContactEva Jirsová, jirsova@icpf.cas.cz, Tel.: 220 390 227
    Year of Publishing2011
Number of the records: 1  

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