1999
DOI: 10.1021/ma981941n
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High-Resolution13C NMR Configurational Analysis of Polypropylene Made with MgCl2-Supported Ziegler−Natta Catalysts. 1. The “Model” System MgCl2/TiCl4−2,6-Dimethylpyridine/Al(C2H5)3

Abstract: The stereosequence distribution of the “atactic” and “isotactic” fractions of a polypropylene sample made with a MgCl2-supported catalyst was determined by means of high-resolution 13C NMR and analyzed in terms of statistical models of increasing sophistication. Two-site models, including the one normally used for the interpretation of “routine” 13C NMR data at pentad level, were shown to be inconsistent with the much finer high-resolution data. A good agreement between experimental and calculated distribution… Show more

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Cited by 203 publications
(218 citation statements)
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References 36 publications
(123 reference statements)
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“…Below 0.1 wt-%, the mmmm value became constant at around 37 mol%, indicating that the interaction between TiCl 3 molecules disappears and each molecule becomes isolated. Above 0.1 wt-%, the mmmm value monotonously increased from 37 to 50 mol%, which corresponds to the formation of TiCl 3 multinuclear species [8,9]. The other properties, such as the polymerization activity and MWD, follow the same dependences on the Ti content.…”
Section: Introductionmentioning
confidence: 85%
“…Below 0.1 wt-%, the mmmm value became constant at around 37 mol%, indicating that the interaction between TiCl 3 molecules disappears and each molecule becomes isolated. Above 0.1 wt-%, the mmmm value monotonously increased from 37 to 50 mol%, which corresponds to the formation of TiCl 3 multinuclear species [8,9]. The other properties, such as the polymerization activity and MWD, follow the same dependences on the Ti content.…”
Section: Introductionmentioning
confidence: 85%
“…2 [33 -35]. As reported [13,33], Ti-species a, b could produce PPs with low isotacticity, while c, d with high isotacticity. The polymers synthesized by the equilibriums between a and c (or b and d) were of stereoblock structures.…”
Section: Possible Structures Of Catalytic Active Centersmentioning
confidence: 81%
“…It is clear that adding external donor lead to improvement in isotacticity of all the PP chains in the n-heptane-insoluble fraction. This kind of donor effect can be 6 explained by a mechanistic model proposed by Busico V. et al [14]. In this model, the silane coordinates at catalyst surface in vicinity to the active site and increase its isospecificity.…”
Section: Tabmentioning
confidence: 99%