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Exploring Imidazole Binding Flexibility in 2D and 3D Frameworks Using Hypercoordinated Triorganotin Carboxylates Featuring a Nitrogen-Rich Ligand with Benzoic Acid, Diazenyl, and Imidazole Functionalities: Insights into Sn - N, N → Sn, and N - H⋅⋅⋅X (X = N, O) Interactions

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F62690094%3A18470%2F24%3A50021650" target="_blank" >RIV/62690094:18470/24:50021650 - isvavai.cz</a>

  • Result on the web

    <a href="https://link.springer.com/article/10.1007/s10904-024-03129-w" target="_blank" >https://link.springer.com/article/10.1007/s10904-024-03129-w</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s10904-024-03129-w" target="_blank" >10.1007/s10904-024-03129-w</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Exploring Imidazole Binding Flexibility in 2D and 3D Frameworks Using Hypercoordinated Triorganotin Carboxylates Featuring a Nitrogen-Rich Ligand with Benzoic Acid, Diazenyl, and Imidazole Functionalities: Insights into Sn - N, N → Sn, and N - H⋅⋅⋅X (X = N, O) Interactions

  • Original language description

    The multitopic heterofunctional pro-ligand 4-[(E)-(1H-imidazol-2-yl)diazenyl]benzoic acid (H &apos; HL) was synthesized by diazotization of 4-aminobenzoic acid followed by coupling with imidazole. Reactions of H &apos; HL (where H = imidazole proton and H &apos; = carboxylic acid proton) with the triorganotin precursors (Pr3SnCl)-Pr-n, ((Bu3Sn)-Bu-n)(2)O and Ph3SnOH provided three hypercoordinated triorganotin complexes, viz., [(Pr3Sn)-Pr-n(mu(4)-L)(SnPr3)-Pr-n](n)&amp; sdot;1/8nEtOH (1), [(Bu3Sn)-Bu-n(mu-HL)](n) (2) and [Ph3Sn(HL)]&amp; sdot;0.5C(6)H(6) (3), with complex 2D and 3D frameworks based on Sn - O, O -&gt; Sn, Sn - N and N -&gt; Sn metal-ligand bonds as well as N - H &amp; sdot;&amp; sdot;&amp; sdot;N, N - H &amp; sdot;&amp; sdot;&amp; sdot;O and pi-interactions. The compositions and structures of 1-3 in solution and in the solid-state were unambiguously established by NMR (H-1, C-13, Sn-119) and IR spectroscopy, UV-Vis spectral analysis, high-resolution mass spectrometry (HRMS) and single-crystal X-ray diffraction (scXRD) studies accompanied by Hirshfeld surface maps and 2D fingerprint plots.

  • 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

    10401 - Organic chemistry

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2024

  • 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 Inorganic and Organometallic Polymers and Materials

  • ISSN

    1574-1443

  • e-ISSN

    1574-1451

  • Volume of the periodical

    34

  • Issue of the periodical within the volume

    7

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    19

  • Pages from-to

    3281-3299

  • UT code for WoS article

    001234282300001

  • EID of the result in the Scopus database

    2-s2.0-85194566962