Ferric ethoxide

Ferric citrate, molecular formula, 6 638t Ferric ethoxide, 14 533 Ferric ethylenediaminetetraacetic acid (ferric EDTA), 19 261 Ferric ferrocyanide, 8 186 22 810 pigment used in makeups, 7 836t Ferrichromes, 14 557 Ferric ion, acrylamide stabilizer, 1 289 Ferric nitrate bright pickle, 15 375 Ferric oxide... 

Ferric ethoxide has also been used for carboxylation of ketones, but yields 3... 

P Keto esters (t.g., ethyl ocetoacetate) are soluble in solutions of caustic alkalis but not in sodium carbonate solution. They give colours with freshly prepared ferric chloride solution a little alcohol should be added to bring the ester into solution. Sodium ethoxide solution reacts to yield sodio compounds, which usually crystallise out in the cold. Phenylhydrazine yields pyrazolones. They are hydrolysed by boiling sulphuric acid to the Corresponding ketones, which can be identified as usual (Section 111,74). 

N-Methyl-2-pyrrolidone Ferric chloride hexahydrate Glycol monomethyl ether Lithium aluminum hydride Ruthenium on charcoal Magnesium ethoxide 4-Toluenesulfonic acid Sodium bicarbonate 1,2,3,4-Tetrafluoro benzene Palladium on charcoal Cyclopropylamine N-benzylimide... 

A common feature of the complexes [Nac Fe6(L13)6 ]Cl (36) and [Csc- Fe8(L13)g ]Cl (37, Sect. 6) is that one p -OT ethoxide donor of the triethano-lateamine ligands [N(CH2CH20)iCH2CH20 ] of (L13) 3 does not participate in the formation of the ferric wheels. They function solely as ligands for the coordi-native saturation of the iron centers. Therefore, any monoanionic donor, such as a chloride ion, could also be a candidate for this function. As expected, reaction of /V-alkyldiethanolamines H2L14 17 (38) with calcium hydride and iron(III) chloride yielded the neutral iron coronands [Fe6Cl6(L14 17)6] (39) with unoccupied centers (Scheme 14) [114-116],... 

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