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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 51 (1998), S. 121-127 
    ISSN: 1572-879X
    Keywords: esterification ; 2-(1-cyclohexenyl)cyclohexanone ; acetic acid ; cation exchange resin ; acid-treated clay ; 2-(2-cyclohexyl acetate)cyclohexanone
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Self-aldol condensation of cyclohexanone yields a mixture of 2-(1-cyclohexenyl)cyclohexanone (I), 2-cyclohexylidenecyclohexanone (II) and subsequent condensation products. An acid-treated clay catalyst was employed to selectively obtain the β γ-unsaturated ketone (I). (I) was separated from the reaction mixture by fractional vacuum distillation and subsequently esterified with acetic acid to synthesise the corresponding ester, 2-(2-cyclohexyl acetate)cyclohexanone, a precursor of [1,1-biphenyl]-2,2'-diol, which has applications in plasticizers, pesticides, as a diluent in epoxy resins, etc. The applicability of cation exchange resins and an acid-treated clay for the esterification of 2-(1-cyclohexenyl)cyclohexanone with acetic acid was explored.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 29 (1997), S. 225-230 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the oxidation of formate, oxalate, and malonate by |NiIII(L1)|2+ (where HL1 = 15-amino-3-methyl-4,7,10,13-tetraazapentadec-3-en-2-one oxime) were carried out over the regions pH 3.0-5.75, 2.80-5.50, and 2.50-7.58, respectively, at constant ionic strength and temperature 40°C. All the reactions are overall second-order with first-order on both the oxidant and reductant. A general rate law is given as - d/dt|NiIII(L1)2+| = kobs|NiIII(L1)2+| = (kd + nks |R|)|NiIII(L1)2+|, where kd is the auto-decomposition rate constant of the complex, ks is the electron transfer rate constant, n is the stoichiometric factor, and R is either formate, oxalate, or malonate. The reactivity of all the reacting species of the reductants in solution were evaluated choosing suitable pH regions. The reactivity orders are: kHCOOH 〉 kHCOO-; kH2ox 〉 kHox- 〉 kox2-, and kH2mal 〉 kHmal- 〈 kmal2- for the oxidation of formate, oxalate, and malonate, respectively, and these trends were explained considering the effect of hydrogen bonded adduct formation and thermodynamic potential. © 1997 John Wiley & Sons, Inc. Int J Chem Kinet 29: 225-230, 1997.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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