All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”

Thermal isomerization of phenylazoindoles: Inversion or rotation? That is the question

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15640%2F23%3A73622047" target="_blank" >RIV/61989592:15640/23:73622047 - isvavai.cz</a>

  • Result on the web

    <a href="https://onlinelibrary.wiley.com/doi/10.1002/qua.27120" target="_blank" >https://onlinelibrary.wiley.com/doi/10.1002/qua.27120</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/qua.27120" target="_blank" >10.1002/qua.27120</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Thermal isomerization of phenylazoindoles: Inversion or rotation? That is the question

  • Original language description

    Azoheteroarenes represent an attractive group of photochromes exhibiting a large structural variability and tunability of photoswitching characteristics. The thermal back-isomerization can proceed via inversion or rotation mechanisms, depending on the functionalization and environment. However, the distinction between the two remains a challenge for both experiment and theory. Here, four experimentally fully characterized phenylazoindoles are studied to establish the mechanism of back-reaction in solvent using density functional theory (DFT), spin-flip time-dependent (TD-)DFT, mixed-reference TD-DFT, and restricted ensemble Kohn-Sham approaches as well as CASPT2 and CCSD(T). While the inversion is consistently described by all methods, the rotation mechanism requires multireference approaches including dynamic correlation. The balanced description of both pathways becomes even more important in solvent which apparently affects the mechanism. For the present set, the range-separated functionals combined with continuum models appear to be the most consistent with experiment in terms of the substitutional and solvent effects on thermal halftimes.

  • 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

    21002 - Nano-processes (applications on nano-scale); (biomaterials to be 2.9)

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2023

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY

  • ISSN

    0020-7608

  • e-ISSN

    1097-461X

  • Volume of the periodical

    123

  • Issue of the periodical within the volume

    24

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    13

  • Pages from-to

  • UT code for WoS article

    000960460800001

  • EID of the result in the Scopus database

    2-s2.0-85151476454