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1.
1. | Ethylbenzene in acetonitrile is slowly oxidized by atmospheric oxygen to acetophenone in the presence of a catalytic amount of CrO3. |
2. | Ethylbenzene is oxidized to acetophenone by iodosobenzene in acetonitrile in the air in the presence of catalytic amounts of CrO3 and -picolinic acid. |
2.
>CrO3, (NBu4)2CrO4, (NBu4)2Cr2O7, and (NBu4)Cr4O13 catalyze the hydrogen peroxide oxidation of cyclohexane, ethylbenzene, and styrene in acetonitrile. The active species is apparently a Cr(VI) peroxo complex.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 1, pp. 210–211, January, 1990. 相似文献
3.
Irradiation by light with >520 nm of solutions of cyclohexane, n-hexane, and ethylbenzene in CH2Cl2 in air in the presence of the complexes (Bu4N)2. Cr2O7, (Bu4N)2Cr3O10, or (Bu4N)2Cr4O13 results in formation (after GLC) of the corresponding alcohols and ketones. Under these conditions, styrene epoxide, benzaldehyde, and acetophenone are produced from styrene; alcohols are oxidized to carbonyl compounds; and triphenylphosphine forms triphenylphosphine oxide.For previous communication, see [1]. Preliminary reports have been published [2, 3].Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 11, pp. 2463–2468, November, 1991. 相似文献
4.
Alkanes (cyclohexane, hexane, heptane isomers) are effectively oxidized in CH3CN at 20–70°C by hydrogen peroxide when catalyzed by a Bu4NVO3-pyrazine-2-carboxylic acid system. Alkyl hydroperoxide is the main product; an alcohol and a ketone or an aldehyde are also formed. Under these conditions benzene is oxidized to give phenol, while alkyl benzenes yield oxygenation products both of the ring and the side chain. It has been assumed that the interaction of H2O2 with VO3
– gives rise to generation of HO radicals and other radical-like vanadium containing species that abstract a hydrogen atom from an alkane, RH. The radical R. formed reacts with O2 to produce ROO. which is then transformed to alkyl hydroperoxide.Presented at the VIII International Symposium on Homogeneous Catalysis (Amsterdam, 1992).Translated fromIzvestiya Akademii Nauk, Seriya Khimicheskaya, No. 1, pp. 64–68, January, 1993. 相似文献
5.
D. Mandelli K. B. Voitiski U. Schuchardt G. B. Shul'pin 《Chemistry of Natural Compounds》2002,38(3):243-245
The complex of Mn(IV) with the macrocyclic N-containing ligand 1,4,7-trimethyl-1,4,7-triazacyclononane (L) [L2Mn2O3](PF6)2 catalyzes epoxidation of (+)-limonene in CH3CN solution at room temperature. Adding CH3COOH accelerates the reaction. The products are isomers of limonene epoxide with predominance of that with an epoxified ring double bond. Epoxidation of - and -pinene by this system is less effective, apparently due to extensive steric shielding of the double bonds in the pinenes. 相似文献
6.
7.
V. V. Zamashchikov E. S. Rudakov S. A. Mitchenko G. V. Nizova A. N. Kitaigorodskii G. B. Shul'pin 《Russian Chemical Bulletin》1984,33(7):1520-1522
Conclusions The reaction of K2PtCl4 with iodoacetone in aqueous solution at about 20C gives the -acetonyl Pt(IV) complex which is more stable to the action of nucleophilic reagents than the analogous methyl and ethyl complexes.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 7, pp. 1657–1660, July, 1984. 相似文献
8.
9.
[(-ArH)Fe(-C5H5)]+BF4
–, where ArH is benzene or toluene, catalyzes the photochemical oxidation of hydrocarbons by oxygen in acetonitrile. Cyclohexane and ethylbenzene are oxidized to the alcohol and ketone derivatives, which are formed in different amounts (after gas-liquid chromatography); benzaldehyde is obtained from styrene. The proposed mechanism involves the formation of a peroxide radical from the organometallic complex, which is capable of hydrogen atom abstraction from the alkane.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 7, pp. 1680–1683, July, 1991. 相似文献
10.
2-Propanol or 1-propanol in acetonitrile, when exposed to air and irradiated with a tungsten lamp in the presence of catalytic amounts of copper(ii) acetate and hydroquinone, are oxidized to give acetone or propanal, respectively.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 6, pp. 1147–1149, June, 1994.We express our gratitude to the administration of the University of Neuchfitel (Switzerland) for having provided the possibility and means to complete this work. We also thank Dr. S. Claude, Mr. A. Béguin, and Mr. G. Meister of the same University for their assistance in the experiments.The financial support of the Russian Foundation for Basic Research (Grant No. 93-03-5226) and the International Science Foundation (Grant MMS 000) is gratefully acknowledged. 相似文献