4.1 Article

Catalytic epoxidation of stilbenes with non-peripherally alkyl substituted carbonyl ruthenium phthalocyanine complexes

Journal

JOURNAL OF PORPHYRINS AND PHTHALOCYANINES
Volume 16, Issue 4, Pages 403-412

Publisher

WORLD SCI PUBL CO INC
DOI: 10.1142/S1088424612500459

Keywords

non-peripherally alkyl substituted phthalocyanine; carbonyl; ruthenium; epoxidation; stilbene; 2,6-dichloropyridine N-oxide

Funding

  1. SASOL

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A number of novel carbonyl(1,4,8,11,15,18,22,25-octaalkylphthalocyaninato)ruthenium(II) complexes were prepared by metal insertion with Ru-3(CO)(12). The new compounds have been characterized by H-1 NMR, C-13 NMR, IR, UV-vis and mass spectroscopy. This study demonstrated that this type of complexes and specifically carbonyl(1,4,8,11,15,18,22,25-octahexylphthalocyaninato)ruthenium(II) and carbonyl[1,4,8,11,15,18,22,25-octa(2-cyclohexylethyl)phthalocyaninato]ruthenium(II), exhibit high catalytic activity and stability in the epoxidation of stilbenes with 2,6-dichloropyridine N-oxide as oxidant.

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