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Peripheral substitution as a tool for tuning electron-accepting properties of phthalocyanine analogs in intramolecular charge transfer

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11160%2F15%3A10297699" target="_blank" >RIV/00216208:11160/15:10297699 - isvavai.cz</a>

  • Result on the web

    <a href="http://pubs.rsc.org/en/content/articlehtml/2015/dt/c5dt00400d" target="_blank" >http://pubs.rsc.org/en/content/articlehtml/2015/dt/c5dt00400d</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/c5dt00400d" target="_blank" >10.1039/c5dt00400d</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Peripheral substitution as a tool for tuning electron-accepting properties of phthalocyanine analogs in intramolecular charge transfer

  • Original language description

    The intramolecular charge transfer (ICT), which is a pathway for excited state relaxation, was studied on the newly synthesized zinc(II) complexes of tetrapyrazinoporphyrazines bearing one fixed donor (i. e., a dialkylamino substituent). The rest of theperipheral substituents on the core was designed with respect to their different electronic effects (OBu, neopentyl, StBu, COOBu). The photophysical (singlet oxygen and fluorescence quantum yields) and electrochemical (reduction potentials) properties were determined and compared within the series and with compounds that did not contain a donor moiety. The ICT efficiency correlated well with both the electron-deficient character of the core and the Hammett substituent constants sp. The most efficient ICT was observed for the core with the most electron-accepting substituent (COOBu), and the lowest ICT efficiency was detected for the least electron-deficient core (substituted by OBu). Titration of DMSO solutions of target compounds with

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CC - Organic chemistry

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/GP14-02165P" target="_blank" >GP14-02165P: Red-emitting Fluorescence Sensors Based on Azaphthalocynine Structure: Study of Aza-Crown Recognition Moiety</a><br>

  • Continuities

    S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2015

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Dalton Transactions

  • ISSN

    1477-9226

  • e-ISSN

  • Volume of the periodical

    44

  • Issue of the periodical within the volume

    15

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    11

  • Pages from-to

    6961-6971

  • UT code for WoS article

    000352271900029

  • EID of the result in the Scopus database

    2-s2.0-84926433537