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Zeolites acenaphthylene

In agreement with this, the analysis of the products forming during the alkylation over MCM-22 samples at different reaction time showed that about 80-90 wt. % of the recovered material is adsorbed on the external surface (phenol, o-TBP and p-TBP), whereas only about 10-20 wt.% is formed inside the zeolite ( coke constituted by p-TBP, naphthalenes, 9,10-dihydro-phenanthrene and acenaphthylene). Coke molecules could be formed in both supercages and sinusoidal channels. However, in the large supercages they would be converted into bulkier compounds, which is not the case. Therefore they are most likely located in the sinusoidal channels. [Pg.360]

The hydrogenation of aromatics (benzene, toluene, a-methylstyrene) can be carried out under very low (1 12,000) catalyst substrate ratio, and mild conditions on Rh and Ni organometallic complexes anchored to USY zeolites.474 A Rh complex anchored to functionalized MCM-41 exhibits excellent performance in the hydrogenation of arenes (benzene, toluene, p-xylene, mesitylene) under mild conditions (45°C and 1 atm) 475 A uniquely selective hydrogenation of acenaphthene and acenaphthylene was performed by using a triruthenium carbonyl cluster 476... [Pg.675]

The dimerisation of acenaphthylene has been used as a probe reaction to investigate the properties of the cavities of a zeolite.In solution acenaphthylene photodimerises to the syn and anti dimers (304) and (305) the singlet excited state yields the syn isomer exclusively, while the triplet excited state produces both the... [Pg.242]

Ramamurthy, V., Corbin, D.R., Kumar, C.V., and Turro, N.J., Modification of photochemical reactivity by zeolites cation controlled photodimerization of acenaphthylene within faujasites. Tetrahedron Lett., 31, 47,1990. [Pg.453]


See other pages where Zeolites acenaphthylene is mentioned: [Pg.244]    [Pg.244]    [Pg.264]    [Pg.1501]   


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