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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
)
URL - Izvorni URL, za dostop obiščite
https://www.sciencedirect.com/science/article/pii/S0020169324004444
PDF - Predstavitvena datoteka. Vsebina dokumenta nedostopna do 01.01.2027.
MD5: FB793CB7129D52489D718AFA66491FDD
Galerija slik
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
UDK:
546.742:547.415.1
ISSN pri članku:
0020-1693
DOI:
10.1016/j.ica.2024.122353
COBISS.SI-ID:
207250179
Datum objave v RUL:
12.09.2024
Število ogledov:
174
Število prenosov:
9
Metapodatki:
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Objavi na:
Gradivo je del revije
Naslov:
Inorganica Chimica Acta
Skrajšan naslov:
Inorg. Chim. Acta
Založnik:
Elsevier
ISSN:
0020-1693
COBISS.SI-ID:
25620736
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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