izpis_h1_title_alt

Synthesis and characterization of catalytically active Ni(II) complexes with bis(phenol)diamine ligands
ID Jafari, Zahra (Avtor), ID Safaei, Elham (Avtor), ID Wojtczak, Andrzej (Avtor), ID Zeinalipour-Yazdi, Constantinos D. (Avtor), ID Kozlevčar, Bojan (Avtor), ID Jagličić, Zvonko (Avtor)

URLURL - Izvorni URL, za dostop obiščite https://www.sciencedirect.com/science/article/pii/S0020169324004444 Povezava se odpre v novem oknu
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Izvleček
A novel N,N’-dimethylethylenediamine derivative of substituted bis(phenol)diamine ligands, namely 2-(tert-butyl)-4-methylphenol in H$_2$L$^1$, was synthesized by a convenient green procedure. Nickel)II) complex [NiL$^1$] 1 has been synthesized and characterized by various methods along with crystal structure determined. Ni(II) coordination center in a mononuclear complex is surrounded by two phenolate oxygen atoms and two amine nitrogen atoms of the ligand in a square planar arrangement. The magnetic susceptibility of the title complex indicates a paramagnetic behavior above 150 K, while strong ferromagnetism below 100 K. Furthermore, the cyclic voltammetry studies show two ligand-centered oxidation of the phenolate groups to phenoxyl radical and the metal-centered reduction of Ni(II) to Ni(0). The Glaser coupling reaction of phenylacetylene was also studied. A strong catalytic activity at room T in THF solvent is observed for 1 in the presence of zinc powder as a reducing agent. A full conversion rate was achieved after 7 h at 25 °C. The DFT analysis corroborates with the square-planar NiO$_2$N$_2$ chromophore of 1 being reduced in catalytically active Ni(0) by applied Zn. The calculated Gibbs free energy of the reaction leading to the formation of the substrate Ni-complex is favorable endothermic. Most of the data for 1 were obtained also for the very similar previously reported [NiL$^2$] 2, with 2,4- di tert-butylphenol in H$_2$L$^2$, which were than compared.

Jezik:Angleški jezik
Ključne besede:bisphenoldiamine, nickel complexes, Glaser reaction, coupling of phenylacetylene, ferromagnetism, green procedure
Vrsta gradiva:Članek v reviji
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:FKKT - Fakulteta za kemijo in kemijsko tehnologijo
FGG - Fakulteta za gradbeništvo in geodezijo
Status publikacije:Objavljeno
Različica publikacije:Recenzirani rokopis
Leto izida:2025
Št. strani:8 str.
Številčenje:Vol. 574, art. 122353
PID:20.500.12556/RUL-161611 Povezava se odpre v novem oknu
UDK:546.742:547.415.1
ISSN pri članku:0020-1693
DOI:10.1016/j.ica.2024.122353 Povezava se odpre v novem oknu
COBISS.SI-ID:207250179 Povezava se odpre v novem oknu
Datum objave v RUL:12.09.2024
Število ogledov:100
Število prenosov:8
Metapodatki:XML RDF-CHPDL DC-XML DC-RDF
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Gradivo je del revije

Naslov:Inorganica Chimica Acta
Skrajšan naslov:Inorg. Chim. Acta
Založnik:Elsevier
ISSN:0020-1693
COBISS.SI-ID:25620736 Povezava se odpre v novem oknu

Licence

Licenca:CC BY-NC-ND 4.0, Creative Commons Priznanje avtorstva-Nekomercialno-Brez predelav 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by-nc-nd/4.0/deed.sl
Opis:Najbolj omejujoča licenca Creative Commons. Uporabniki lahko prenesejo in delijo delo v nekomercialne namene in ga ne smejo uporabiti za nobene druge namene.

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:bisfenoldiamini, nikljevi kompleksi, Glaserjeva reakcija, sklopitev fenilacetilena, feromagnetizem, zeleni postopek

Projekti

Financer:Drugi - Drug financer ali več financerjev
Naslov:Shiraz University

Financer:Drugi - Drug financer ali več financerjev
Naslov:Center for Excellence in Research and the BRAIN interdisciplinary research group

Financer:ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:P2-0348
Naslov:Nove slikovno-analitske metode

Financer:ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:P1-0175
Naslov:Napredna anorganska kemija

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