2017
DOI: 10.1002/celc.201700199
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Protonation and Electrochemical Properties of Pyridyl‐ and Sulfonatophenyl‐Substituted Porphyrins in Nonaqueous Media

Abstract: International audienceThe protonation and electrochemical properties of positively charged and negatively charged porphyrins are reported in up to five different nonaqueous solvents. The positively charged porphyrins are represented by mono- and di-pyridyl derivatives having the formula Pyx(PhMe)4-xPM, where P=the dianion of the porphyrin macrocycle, PhMe is a meso-tolyl group, Py a meso-pyridyl group, x=1 or 2, and M=H2, NiII, CuII, ZnII, or CoII. The negatively charged porphyrins are comprised of meso-tetras… Show more

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Cited by 4 publications
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“…15,16,[73][74][75] Moreover, the PP-Supra-H 2 TPyP 419 nm peak redshis in z2 nm, which is a signature for the protonation of the photomodied RuCl(dppb)(5,5 ′ -Me-bipy). 16,76 In fact, a closer inspection of RuCl(dppb)(5,5 ′ -Me-bipy) intraligand bands shows that the peak at ∼327 nm is enhanced (Fig. 3a).…”
Section: Green-opa Irradiation Of Supra-h 2 Tpypmentioning
confidence: 93%
“…15,16,[73][74][75] Moreover, the PP-Supra-H 2 TPyP 419 nm peak redshis in z2 nm, which is a signature for the protonation of the photomodied RuCl(dppb)(5,5 ′ -Me-bipy). 16,76 In fact, a closer inspection of RuCl(dppb)(5,5 ′ -Me-bipy) intraligand bands shows that the peak at ∼327 nm is enhanced (Fig. 3a).…”
Section: Green-opa Irradiation Of Supra-h 2 Tpypmentioning
confidence: 93%