Abstract
Abstract A facile aerobic oxidation of 1,2-bis(meso-octaethylporphyrinyl)ethane and other similar dimers to the corresponding trans-1,2-bis(meso-porphyrinyl)ethenes in several organic acids has been studied by UV-vis and 1H NMR spectroscopy and the general mechanism of the oxidation has been proposed. The key step of the oxidation is monoprotonation of the two porphyrin rings in dimer followed by two electron oxidation.
References
14
Referenced
13
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{'key': '2024011821590708100_r11'}
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Dates
Type | When |
---|---|
Created | 19 years, 4 months ago (April 28, 2006, 2:20 a.m.) |
Deposited | 1 year, 7 months ago (Jan. 18, 2024, 4:59 p.m.) |
Indexed | 1 year, 7 months ago (Jan. 18, 2024, 7:02 p.m.) |
Issued | 32 years, 1 month ago (Aug. 1, 1993) |
Published | 32 years, 1 month ago (Aug. 1, 1993) |
Published Online | 19 years, 4 months ago (April 27, 2006) |
Published Print | 32 years, 1 month ago (Aug. 1, 1993) |
@article{Borovkov_1993, title={Mechanistic Studies on Oxidation Reaction of Ethane-Bridged Porphyrin Dimers to trans-Ethylene-Bridged Species}, volume={22}, ISSN={1348-0715}, url={http://dx.doi.org/10.1246/cl.1993.1409}, DOI={10.1246/cl.1993.1409}, number={8}, journal={Chemistry Letters}, publisher={Oxford University Press (OUP)}, author={Borovkov, Victor V and Ponomarev, Gelii V and Ishida, Akito and Kaneda, Takahiro and Sakata, Yoshiteru}, year={1993}, month=aug, pages={1409–1412} }