Synthesis and copolymerization of N-tert-butyldimethylsilylacrylamide: A new acrylamide precursor

European Polymer Journal

Volumn 32, Issue 4, 1996, Pages 475-479

  Dasgupta, A ^a,b  

^a TATA RESEARCH DEVELOPMENT AND DESIGN CENTRE   (India)

^b NATIONAL CHEMICAL LABORATORY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

MOLECULAR STRUCTURE;

ACRYLAMIDE DERIVATIVE COPOLYMER; EXPERIMENTAL STUDY; LATERAL GROUP; ORGANIC SILANE; PREPARATION; RADICAL COPOLYMERIZATION; RANDOM COPOLYMER; REACTIVITY RATIO; STYRENE COPOLYMER;

COPOLYMERS;

EID: 0029727044     PISSN: 00143057     EISSN: None     Source Type: Journal    
DOI: 10.1016/0014-3057(95)00156-5     Document Type: Article

References (11)

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6. Poor mechanical stability of acrylamide based supports have prevented it from becoming very popular for use in affinity separations, in spite of having some major advantages like resistance to microbial attack, relatively good pH stability (pH=2-10), excellent chemical stability, and low nonspecific binding characteristics (due to the lack of a biopolymer matrix based on sugar residues). G. T. Hermanson, A. Krishna Mallia and Paul K. Smith in Immobilized Affinity Ligand Techniques, p. 16. Academic Press, 1993.
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