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Cyclooctene, epoxide

Figure 22. Time-dependent yield of cyclooctene epoxide in the presence of 1 mol% 6(triangles), 7 (squares), 8 (circles), CpMo(CO)3Me (open squares), and CpMo(CO)3Cl (open circles) at 55°C [89]. Figure 22. Time-dependent yield of cyclooctene epoxide in the presence of 1 mol% 6(triangles), 7 (squares), 8 (circles), CpMo(CO)3Me (open squares), and CpMo(CO)3Cl (open circles) at 55°C [89].
Cyclooctene epoxidation catalyzed by supported sulfonated metalloporphyrins. [Pg.61]

Table 1 Cyclooctene epoxidation with TBHP/MCM-supported Mo02X2(THF)2... Table 1 Cyclooctene epoxidation with TBHP/MCM-supported Mo02X2(THF)2...
Table 2 Catalytic cyclooctene epoxidation with TBHP/zeolite-supported MoCp(CO)3Cl... Table 2 Catalytic cyclooctene epoxidation with TBHP/zeolite-supported MoCp(CO)3Cl...
Table4 Cyclooctene epoxidation with TBHP/MCM-spacer ligand-tethered Cp Mo(CO)3R complexes... [Pg.146]

The results for cyclooctene epoxidation with TBHP show that the method of heterogenisation plays a decisive role in the activity (Table 6). Indeed, the materials obtained from the complex grafted onto a fimctionahsed matrix (odd entries. Table 6) are less active (seen by comparing TOP values) than those synthesised via the tethering of fimctionahsed complexes on a mesoporous material (even entries. Table 6). [Pg.149]

The MCM samples show about 90-95% cyclooctene epoxidation with TBHP, with nearly 100% selectivity after a reaction time of 24 h (entries 2 and 3, Table 7). Conversion is lower with the SBA-15 catalysts (entry 4, Table 7). The TOPS are about one order of magnitude lower than the respective homo-... [Pg.149]

When Mo02Cl2(THF)2 is introduced into functionalised MCM (MCM-41 or MCM-48), cyclooctene epoxidation results are better than those observed... [Pg.152]

Materials synthesised by autocatalysis provide high activity (100% conversion in 3 h) and selectivity (100%) for cyclooctene epoxidation with TBHP, as well as excellent recycling ability (the catalytic properties are almost fully recovered after three rims). [Pg.155]

Table 9 Cyclooctene epoxidation with TBHP/complexes M0X2O2L2 (X = Cl, Me L = Lewis base) 1-3 and CpMo(CO)3Me, CpMo(CO)3Cl, Me5CpMo(CO)3Me in different RTlLs... Table 9 Cyclooctene epoxidation with TBHP/complexes M0X2O2L2 (X = Cl, Me L = Lewis base) 1-3 and CpMo(CO)3Me, CpMo(CO)3Cl, Me5CpMo(CO)3Me in different RTlLs...
Another method of MPFDCPP catalyst synthesis, applied in this work, was borrowed from Ref. [97], All these catalysts displayed extremely high stability. Nevertheless, a large number of catalytic cycles was observed only at cyclooctene epoxidation. Thus, these... [Pg.278]

The stereospecific conversion of c/s-cyclooctene epoxide to alcohol 51, first reported by Cope,87 has been examined in greater detail recently.88-90 Of importance is... [Pg.58]

R. Rinaldi, J. Sepulveda, U. Schuchardt, Cyclohexene and cyclooctene epoxidation with aqueous hydrogen peroxide using transition metal-free sol-gel alumina as catalyst, Adv. Synth. Catal. 346 (2004) 281. [Pg.81]

T. Luts, H. Papp, Novel ways of Mn-salen complex immobilization on modified silica support and their catalytic activity in cyclooctene epoxidation, Kinet. Catal. 48 (2007) 176. [Pg.84]

N. A. Stephenson, A. T. BeU, Influence of solvent composition on the kinetics of cyclooctene epoxidation by hydrogen peroxide catalyzed by iron(III) [tetrakis(pentafluorophenyl)] porphyrin chloride (I., TPP)I < 1. Inorg. Chem. 45 (2006) 2758. [Pg.98]


See other pages where Cyclooctene, epoxide is mentioned: [Pg.48]    [Pg.204]    [Pg.382]    [Pg.383]    [Pg.135]    [Pg.141]    [Pg.147]    [Pg.148]    [Pg.154]    [Pg.154]    [Pg.158]    [Pg.172]    [Pg.81]    [Pg.290]    [Pg.41]    [Pg.58]    [Pg.2920]    [Pg.30]    [Pg.98]    [Pg.395]    [Pg.399]    [Pg.415]   
See also in sourсe #XX -- [ Pg.387 ]




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