2000
DOI: 10.1002/1521-3773(20001201)39:23<4376::aid-anie4376>3.0.co;2-2
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Tailored Alkene Oligomerization with H-ZSM-57 Zeolite

Abstract: The unique lobate‐pore structure of acidic ZSM‐57 zeolite favors the crosswise arrangement of light alkenes and thus their selective dimerization into C6–C12 oligomers (see picture). Allylic hydrogen abstraction and deactivation generally observed with other acidic zeolites is largely suppressed in ZSM‐57.

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Cited by 47 publications

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“…The products selectivities are markedly impacted by the microporous topology of the zeolite, as reported for example for ethylene, propene, or 2-butene oligomerization . The branching degree of the oligomerized products was found to decrease with the micropore diameter of the zeolite structure.…”
Section: Transformation Of Alkenes and Bifunctional Transformation Of...
mentioning
confidence: 69%
“…The products selectivities are markedly impacted by the microporous topology of the zeolite, as reported for example for ethylene, 411 propene, 412 or 2-butene oligomerization. 413 The branching degree of the oligomerized products was found to decrease with the micropore diameter of the zeolite structure. Contribution of external surface acid sites can, however, significantly lower the shape selectivity effect of the microporous structure.…”
Section: Oligomerization
mentioning
confidence: 99%
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