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Synthesis and characterization of (Ru(II), Co(III)) heterobimetallic complexes formed with a 1,10-phenanthroline based hydroxamic acid conjugate

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68081707%3A_____%2F20%3A00539536" target="_blank" >RIV/68081707:_____/20:00539536 - isvavai.cz</a>

  • Alternative codes found

    RIV/61989592:15310/20:73603655

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/pii/S0022328X20301674?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0022328X20301674?via%3Dihub</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jorganchem.2020.121265" target="_blank" >10.1016/j.jorganchem.2020.121265</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Synthesis and characterization of (Ru(II), Co(III)) heterobimetallic complexes formed with a 1,10-phenanthroline based hydroxamic acid conjugate

  • Original language description

    A novel ambidentate type hydroxamic acid derivative (phenhaH, 1) containing an (O,O) and a 1,10-phenantroline (phen) based (N,N) donoratom set together with its heterobimetallic complexes incorporating an octahedral [Co(4 N)](3+) (4 N = tris(2-aminoethyl)amine (tren) or tris(2-methylpyridyl)amine (tpa)) and a half-sandwich type [(eta(6)-p-cym)Ru](2+) entity have been synthesized and characterized using various analytical techniques. Reaction of [Co(4 N)Cl]Cl-2 with 1 proved the exclusive (O,O) coordination of the ligand to the [Co( 4 N)](3+) core to yield [Co(tpa)(phenha)](ClO4)(2), (2). Subsequent treatment of 1 with [Ru(eta(6)-p-cym)Cl-2](2) and [Co(4 N)Cl]Cl-2 in a one-pot reaction resulted in the formation of [(eta(6)-p-cym)Ru(Cl)(phenha)Co(tren)]Cl(PF6)(2) (3) and [(eta(6)-p-cym)Ru(Cl)(phenha)Co(tpa)](PF6)(3) (4) in which the organometallic Ru core is coordinated by the phen part while the Co entity by the hydroxamate part of 1. Cyclic voltammetry revealed that 4 could be reduced at a less negative potential and exhibits a reversible Co(III)/Co(II) redox process compared to 3 due to the pi-back bonding interaction between the Co(III) centre and the pyridyl-N donors of tpa in 4. Complexes 2-4 were tested for their in vitro cytotoxicity using human-derived cancer cell lines (HeLa, MCF-7, HCT116 and MDA-MB-231) and showed moderate anti-proliferative activity in the double digit micromolar concentration range, 4 being the most active. Complex 4 displayed better activity against MDA-MB-231 cells than cisplatin. (C) 2020 The Authors. Published by Elsevier B.V.

  • 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

    10402 - Inorganic and nuclear chemistry

Result continuities

  • Project

    <a href="/en/project/GA18-09502S" target="_blank" >GA18-09502S: Targeting resistance to chemotherapy of tumor cells to reinstate their susceptibility to novel, existing and unsuccessful anticancer metallodrugs</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2020

  • 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 Organometallic Chemistry

  • ISSN

    0022-328X

  • e-ISSN

  • Volume of the periodical

    916

  • Issue of the periodical within the volume

    JUN 14 2020

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    9

  • Pages from-to

    121265

  • UT code for WoS article

    000537690200011

  • EID of the result in the Scopus database

    2-s2.0-85082869532