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Volumn 49, Issue 3, 2011, Pages 781-795

Grafting of functional nitroxyl free radicals to polyolefins as a tool to postreactor modification of polyethylene-based materials with control of macromolecular architecture

Author keywords

FTIR; functionalization of polymers; nitroxyl free radicals; polyethylene; stoichiometric reaction

Indexed keywords

1-OCTENE; CALIBRATION CURVES; CHAIN EXTENSION; COUPLING REACTION; FTIR; FTIR SPECTROSCOPY; FUNCTIONALIZATION OF POLYMERS; FUNCTIONALIZATIONS; FUNCTIONALIZED POLYOLEFINS; GRAFTING LEVELS; GRAFTING SITES; H-ABSTRACTION; HIGH TEMPERATURE; MACROMOLECULAR ARCHITECTURE; MACROMOLECULAR STRUCTURES; MACRORADICALS; NITROXYL FREE RADICALS; NITROXYL RADICAL; PRISTINE POLYMERS; PROPER MODELS; QUANTITATIVE DETERMINATIONS; SEC ANALYSIS; SIDE REACTIONS; STOICHIOMETRIC REACTION;

EID: 78650831921     PISSN: 0887624X     EISSN: 10990518     Source Type: Journal    
DOI: 10.1002/pola.24493     Document Type: Article
Times cited : (34)

References (59)
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    • Parameters provided in commercial product literature (initiators for Polymer Production; Akzo Chemicals). The half-life of peroxide was determined by differential scanning calorimetry (DSC) and thermal activity monitoring (TAM) of a dilute solution of the initiator in monochlorobenzene.
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    • The synthesis of this compound was carried out adopting a procedure already described for a different alkoxyamine
    • The synthesis of this compound was carried out adopting a procedure already described for a different alkoxyamine:, Molawi, K.,;, Schulte, T.,;, Siegenthaler, K. O.,;, Wetter, C.,;, Studer, A., Chem Eur J 2005, 11, 2335-2350.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.