1978
DOI: 10.1002/macp.1978.021790715
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Über die copolymerisation von (3‐vinylphenylazo)‐methylmalonodinitril mit styrol 7. Mitteilung über azo‐initiatoren

Abstract: 3-Vinylphenylazo)-methylmalonodinitrile (2) was copolymerized with styrene up to high conversion giving no remarkable change in the monomer composition. The reactions were carried out in emulsion at 5"C, in bulk at 50°C, and in solution at 60°C. The azo compound displays not only the properties of an initiator (thermolysis) and monomer (vinyl group), but also the behaviour of a retardation reagent (azo-function) explaining the decrease of polymerization rates and of molecular weights with increasing amounts of… Show more

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Cited by 22 publications
(7 citation statements)
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“…In contrast, linear azo polymers have been obtained via copolymerization of asymmetric azo monomers (25)(26)(27)(28)(29)(30)(31)(32)(33).…”
Section: N2o3mentioning
confidence: 99%
See 3 more Smart Citations
“…In contrast, linear azo polymers have been obtained via copolymerization of asymmetric azo monomers (25)(26)(27)(28)(29)(30)(31)(32)(33).…”
Section: N2o3mentioning
confidence: 99%
“…Molecular weight is determined by osmometry, viscometry, or HPLC (25)(26)(27)(28)(29)(31)(32)(33). Elemental analyses (25)(26)(27)(28)(29), UV spectroscopy (25)(26)(27)29,31,32), derivative UV spectroscopy (35), DSC (36), and 1 H NMR spectroscopy (28,30) are used for determining azo content. The thermal properties of polymers containing side-chain azo groups are similar to those of the low molecular-weight monomers.…”
Section: N2o3mentioning
confidence: 99%
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“…[1 -5] It was as early as 1976 that the synthesis and application of (3-vinylphenyl)azomethylmalonodinitrile (1) was described for the first time. [6][7][8] Compound 1 is a typical inimer (initiating monomer). Due to its vinyl group 1 can function both as a monomer and comonomer in radical polymerization.…”
Section: Introductionmentioning
confidence: 99%