Autoxidation of mercaptans promoted by a bifunctional catalyst

Zwart, J.; Weide, H.; Bröker, N.; Rummens, Cpj Kees; Schuit, G.C.A.; German, Anton L.

doi:10.1016/0304-5102(77)80040-0

Cited by 78 publications

(11 citation statements)

References 17 publications

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“…The experiments have revealed that the peroxodimer D, as well as Со II TPP complex, [13] did not oxidize 1-propanethiol, what was confirmed by conclusions made earlier [11,12] ). Only Co III TPP is able to oxidize 1-propanethiol rapidly in the oxygen-free solution.…”

Section: Resultssupporting

confidence: 78%

Oxidation of Cobalt(II) Tetraphenylporphyrinate with Molecular Oxygen

Tatyana¹,

Vladimir²,

Alexandr³

et al. 2015

MHC

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Section: Resultssupporting

confidence: 78%

Oxidation of Cobalt(II) Tetraphenylporphyrinate with Molecular Oxygen

Tatyana¹,

Vladimir²,

Alexandr³

et al. 2015

MHC

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“…The thermogravimetric analytical curves for the polymeric phthalocyanines prepared from 3,Y,4,4'-benzophenonetetracarboxylic dianhydride are given in Figures 4 and 5, the analytical data are presented in Tables IV and V. These polymers showed good thermal stability, similar to the properties of many phthalocyanine polymers recently reported by other authors [19].…”

Section: Thermal Propertiessupporting

confidence: 65%

Synthesis and characterization of metal polymeric phthalocyanine from 3,3?,4,4?benzophenonetetracarboxylic dianhydride

Tian

Wang

1994

J Polym Res

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Metal polymeric phthalocyanines were prepared by reaction of 3,3',4,4'-benzophenonetetracarboxylic dianhydride with urea, metal salts and ammonium molybdate. The structure of these polymers was characterized by infrared spectra, visible spectra and X-ray powder diffraction. The electrical conductivity of the polymers after iodine doping was in the range of 10 -4~ l0 7 S/cm. Thermogravimetric analyses showed that these polymers have good thermal stability, and have different break mechanism under nitrogen and air condition.

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“…Thus, cobalt(II) 4,4',4",4"'-tetrasulfophthalocyanine with a bis(3-aminopropyl)amine base bound to poly(acrylamide) was found to be more active by a factor of 32 than the corresponding homogeneous complex [109].…”

Section: Cooperative Catalysismentioning

confidence: 97%