The effect of substitutents at alkylsulfanyl/arylsulfanyl non-peripherally substituted phthalocyanines: Spectral and photophysical properties, basicity and photostability
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11160%2F15%3A10317280" target="_blank" >RIV/00216208:11160/15:10317280 - isvavai.cz</a>
Výsledek na webu
<a href="http://www.worldscientific.com/doi/10.1142/S1088424615500832" target="_blank" >http://www.worldscientific.com/doi/10.1142/S1088424615500832</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1142/S1088424615500832" target="_blank" >10.1142/S1088424615500832</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
The effect of substitutents at alkylsulfanyl/arylsulfanyl non-peripherally substituted phthalocyanines: Spectral and photophysical properties, basicity and photostability
Popis výsledku v původním jazyce
A series of magnesium, zinc and metal-free derivatives of non-peripherally substituted phthalocyanines (Pcs) bearing alkylsulfanyl or arylsulfanyl groups of different bulkiness was synthesized. Their spectral and photophysical properties including also the basicity of azomethine nitrogens and photostability were compared within the series as well as with similar peripherally substituted Pcs. Non-peripheral position of substituents led to the 70 nm red-shift of Q-band in comparison to the peripherally substituted Pcs. However, unexpected blue-shift of approximately 50 nm was observed in the series of non-peripherally substituted Pcs for the most bulky tert-butylsulfanyl derivative caused probably by extreme distortion of the macrocycle. The substitutionhad no effect on photophysical properties and compounds reached Phi(Delta) values 0.74-0.76 and Phi(F) 0.053-0.080 for zinc complexes, and Phi(Delta) 0.47-0.51 and Phi(F) 0.10-0.17 for magnesium complexes following the rule of heavy atom
Název v anglickém jazyce
The effect of substitutents at alkylsulfanyl/arylsulfanyl non-peripherally substituted phthalocyanines: Spectral and photophysical properties, basicity and photostability
Popis výsledku anglicky
A series of magnesium, zinc and metal-free derivatives of non-peripherally substituted phthalocyanines (Pcs) bearing alkylsulfanyl or arylsulfanyl groups of different bulkiness was synthesized. Their spectral and photophysical properties including also the basicity of azomethine nitrogens and photostability were compared within the series as well as with similar peripherally substituted Pcs. Non-peripheral position of substituents led to the 70 nm red-shift of Q-band in comparison to the peripherally substituted Pcs. However, unexpected blue-shift of approximately 50 nm was observed in the series of non-peripherally substituted Pcs for the most bulky tert-butylsulfanyl derivative caused probably by extreme distortion of the macrocycle. The substitutionhad no effect on photophysical properties and compounds reached Phi(Delta) values 0.74-0.76 and Phi(F) 0.053-0.080 for zinc complexes, and Phi(Delta) 0.47-0.51 and Phi(F) 0.10-0.17 for magnesium complexes following the rule of heavy atom
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
CC - Organická chemie
OECD FORD obor
—
Návaznosti výsledku
Projekt
<a href="/cs/project/GA13-27761S" target="_blank" >GA13-27761S: Vývoj nových fotosensitizérů pro fotodynamickou terapii a výzkum jejich mechanismu působení na buněčné úrovni</a><br>
Návaznosti
S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2015
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Journal of Porphyrins and Phthalocyanines
ISSN
1088-4246
e-ISSN
—
Svazek periodika
19
Číslo periodika v rámci svazku
10
Stát vydavatele periodika
FR - Francouzská republika
Počet stran výsledku
12
Strana od-do
1095-1106
Kód UT WoS článku
000367814100003
EID výsledku v databázi Scopus
2-s2.0-84953635918