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Cyclohexene

About: Cyclohexene is a research topic. Over the lifetime, 7295 publications have been published within this topic receiving 126499 citations. The topic is also known as: Benzene tetrahydride & Tetrahydrobenzene.


Papers
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Journal ArticleDOI
R. A. Sheldon1
TL;DR: In this paper, it was shown that an active epoxidation catalyst should be both a weak oxidant and a fairly strong Lewis acid, and that these requirements are best met by compounds of certain metals in high oxidation states.

246 citations

Journal ArticleDOI
TL;DR: In this paper, the rhodium-catalyzed hydroformylation of oct-1-ene, cyclohexene, and styrene has been studied using Rh(C0)Acac as the catalyst precursor and tris(2-tert-butyl-4-methylphenyl) phosphite as the ligand.

241 citations

Journal ArticleDOI
TL;DR: In this paper, the performance of oxygen and hydrogen peroxide as preferred oxidants for the selective oxidation of cyclohexene and n-hexane to adipic acid is summarized.

238 citations

Journal ArticleDOI
TL;DR: The synthesis and characterization of three highly active dimagnesium catalysts for the copolymerization of cyclohexene oxide and carbon dioxide, active under just 1 atm of carbon dioxide pressure, are reported.
Abstract: The synthesis and characterization of three highly active dimagnesium catalysts for the copolymerization of cyclohexene oxide and carbon dioxide, active under just 1 atm of carbon dioxide pressure, are reported. The catalysts have turnover numbers up to 6000 and turnover frequencies of up to 750 h–1. These values are, respectively, 75 and 20 times higher than those of the other three known magnesium catalysts. Furthermore, the catalysts operate at 1/500th the loading of the best reported magnesium catalyst. The catalyst selectivities are excellent, yielding polymers with 99% carbonate repeat units and >99% selectivity for copolymer. Using a dimagnesium bis(trifluoroacetate) catalyst, and water as a renewable chain transfer reagent, poly(cyclohexene carbonate) polyols are synthesized with high selectivity.

237 citations

Journal ArticleDOI
TL;DR: In this paper, the performance of cobalt phthalocyanine and iron porphyrin network polymers of intrinsic microporosity (network-PIMs) was compared with that of low molar mass analogues.
Abstract: Cobalt phthalocyanine and iron porphyrin network polymers of intrinsic microporosity (network-PIMs) were prepared and their performance as heterogeneous catalysts compared with that of low molar mass analogues. Spiro-linked Co phthalocyanine network-PIMs prepared from preformed chlorinated phthalocyanines showed lower surface areas and lower catalytic activity than those prepared by a phthalocyanine-forming reaction from a rigid precursor incorporating a spiro-centre. However, all the phthalocyanine network-PIMs were much more effective catalysts than low molar mass Co phthalocyanine for the decomposition of hydrogen peroxide, the oxidation of cyclohexene and the oxidation of hydroquinone. An Fe porphyrin network-PIM showed a higher surface area than any of the phthalocyanine polymers and showed higher activity for the oxidation of hydroquinone, also outperforming a low molar mass FeCl porphyrin.

236 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
202364
2022152
2021128
2020141
2019142
2018181