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Consequences of isosteric replacement of benzene for pyrazine in phthalocyanines

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11160%2F22%3A10458592" target="_blank" >RIV/00216208:11160/22:10458592 - isvavai.cz</a>

  • Result on the web

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=PxqO~GzPhD" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=PxqO~GzPhD</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1142/S1088424622300038" target="_blank" >10.1142/S1088424622300038</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Consequences of isosteric replacement of benzene for pyrazine in phthalocyanines

  • Original language description

    Tetrapyrazinoporphyrazines (TPyzPzs) likely represent the most investigated group of azaanalogs of phthalocyanines. This review highlights the author&apos;s contributions in this field and summarizes the most important features of these interesting macrocycles with the aim of emphasizing the differences from the parent phthalocyanines. In particular, uniqueness in synthesis, spectral, photophysical and electrochemical properties are discussed. Thanks to systematic investigation of intramolecular charge transfer with TPyzPzs as electron acceptors, detailed structure-activity relationships of this ultrafast quenching process have been disclosed. This opened the door for the use of TPyzPzs as fluorescence sensors and quenchers in oligodeoxynucleotide probes, the latter being unique for TPyzPzs, which have not been investigated with phthalocyanines. These two applications seem to be much more suitable for TPyzPzs than photodynamic therapy, where the phthalocyanines typically have superior in vitro activities.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30104 - Pharmacology and pharmacy

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2022

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Journal of Porphyrins and Phthalocyanines

  • ISSN

    1088-4246

  • e-ISSN

    1099-1409

  • Volume of the periodical

    26

  • Issue of the periodical within the volume

    12

  • Country of publishing house

    FR - FRANCE

  • Number of pages

    18

  • Pages from-to

    765-782

  • UT code for WoS article

    000849625600001

  • EID of the result in the Scopus database

    2-s2.0-85137406261