2017
DOI: 10.1007/s11164-017-3147-5
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Comparative studies of photophysical and electrochemical properties of sulfur-containing substituted metal-free and metallophthalocyanines

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Cited by 17 publications
(6 citation statements)
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“…The herein reported Pc 3 was a more efficient 1 O 2 generator, with the Φ ∆ equal to 0.29 and 0.13 in DMF and DMSO, respectively, in comparison to Pz 7 , which revealed low Φ ∆ values equal to 0.02 and 0.09 in DMF and DMSO, respectively. These Φ ∆ values were in agreement with previous studies, in which phthalocyanines were found to be more efficient singlet oxygen generators compared to porphyrazines [ 47 , 48 ], especially sulfanyl porphyrazines [ 7 ]. Pc 3 revealed a lower singlet oxygen formation quantum yield in comparison to the reference compound—unsubstituted ZnPc.…”
Section: Resultssupporting
confidence: 92%
“…The herein reported Pc 3 was a more efficient 1 O 2 generator, with the Φ ∆ equal to 0.29 and 0.13 in DMF and DMSO, respectively, in comparison to Pz 7 , which revealed low Φ ∆ values equal to 0.02 and 0.09 in DMF and DMSO, respectively. These Φ ∆ values were in agreement with previous studies, in which phthalocyanines were found to be more efficient singlet oxygen generators compared to porphyrazines [ 47 , 48 ], especially sulfanyl porphyrazines [ 7 ]. Pc 3 revealed a lower singlet oxygen formation quantum yield in comparison to the reference compound—unsubstituted ZnPc.…”
Section: Resultssupporting
confidence: 92%
“…17 Chemical structure of substituents which are attached to the peripheral or non-peripheral positions of phthalocyanines signicantly change their properties such as absorption behavior and solubility. 9,[18][19][20][21][22][23] According to the positions of the substituents, it is readily understood that two different tetrasubstituted phthalocyanines differ signicantly in their photophysical and photochemical behaviors. Similarly, metal atoms coordinated to the phthalocyanine center are known to alter the electrochemical properties of the compound.…”
Section: Introductionmentioning
confidence: 99%
“…shows that the fluorescence excitation spectrum is blue-shifted by about 10 nm relative to that of the absorption spectrum, suggesting a change in geometry upon excitation (20) and 7). In every substituent, the complex showed similar quantum yields.…”
Section: Photophysical and Photochemical Studiesmentioning
confidence: 96%
“…(methylthio)phenylthio))phthalocyaninatogallium(III) chloride (6) were prepared according to the procedures in literature (4,19,20). Some chemicals such as dimethyl sulfoxide (DMSO) and GaCl3 were acquired from Merck and Alfa Aesar and used as received.…”
Section: +mentioning
confidence: 99%