Several salicylatocopper(II) complexes with diethylnicotinamide: Preparation, structure, spectral properties and Hirshfeld surface analysis

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F19%3A39915535" target="_blank" >RIV/00216275:25310/19:39915535 - isvavai.cz</a>

Výsledek na webu

<a href="https://www.sciencedirect.com/science/article/pii/S0022286018314996?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0022286018314996?via%3Dihub</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/j.molstruc.2018.12.066" target="_blank" >10.1016/j.molstruc.2018.12.066</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Several salicylatocopper(II) complexes with diethylnicotinamide: Preparation, structure, spectral properties and Hirshfeld surface analysis

Popis výsledku v původním jazyce

The little change of the reaction conditions led to formation four monomeric copper (II) complexes of different hydrate formula [Cu(XSal)(2)(dena)(2)(H2O)(x)] (where x = 0 for XSal = 3,5-dichlorosalicylate; x = 1 for XSal = 5-methylsalicylate or x = 2 for XSal = 4-chlorosalicylate resp. 3,5-dichlorosalicylate; dena = N,N-diethylnicotinamide) and two anhydrous polymeric complexes [Cu(XSal)(2)(dena)(2)](n) (where XSal = 5-bromosalicylate or XSal = 4-methoxysalicylate). The monomeric complexes build up 1D chains and/or 2D supramolecular network. The polymeric ones constitute 1D coordination polymers. The intermolecular interactions were studied by Hirshfeld surface analysis. Four different coordination modes of anion were observed in compounds and they are in good relation to their spectral information. The EPR spectra of all the complexes were measured at room temperature. The g-factor values evaluated from the axially symmetric Cu(II) EPR spectra fulfilled an usual relation of g(//) &gt;g perpendicular to&gt; 2.0023, which is consistent with d(x)(2)-(2)(y) ground electronic state and which indicates the coordination sphere of the distorted tetragonal symmetry for copper (II) ions.

Název v anglickém jazyce

Several salicylatocopper(II) complexes with diethylnicotinamide: Preparation, structure, spectral properties and Hirshfeld surface analysis

Popis výsledku anglicky

The little change of the reaction conditions led to formation four monomeric copper (II) complexes of different hydrate formula [Cu(XSal)(2)(dena)(2)(H2O)(x)] (where x = 0 for XSal = 3,5-dichlorosalicylate; x = 1 for XSal = 5-methylsalicylate or x = 2 for XSal = 4-chlorosalicylate resp. 3,5-dichlorosalicylate; dena = N,N-diethylnicotinamide) and two anhydrous polymeric complexes [Cu(XSal)(2)(dena)(2)](n) (where XSal = 5-bromosalicylate or XSal = 4-methoxysalicylate). The monomeric complexes build up 1D chains and/or 2D supramolecular network. The polymeric ones constitute 1D coordination polymers. The intermolecular interactions were studied by Hirshfeld surface analysis. Four different coordination modes of anion were observed in compounds and they are in good relation to their spectral information. The EPR spectra of all the complexes were measured at room temperature. The g-factor values evaluated from the axially symmetric Cu(II) EPR spectra fulfilled an usual relation of g(//) &gt;g perpendicular to&gt; 2.0023, which is consistent with d(x)(2)-(2)(y) ground electronic state and which indicates the coordination sphere of the distorted tetragonal symmetry for copper (II) ions.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10402 - Inorganic and nuclear chemistry

Projekt

—

Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2019

Kód důvěrnosti údajů

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

Název periodika

Journal of Molecular Structure

ISSN

0022-2860

e-ISSN

—

Svazek periodika

1181

Číslo periodika v rámci svazku

6

Stát vydavatele periodika

NL - Nizozemsko

Počet stran výsledku

10

Strana od-do

373-382

Kód UT WoS článku

000458612300042

EID výsledku v databázi Scopus

—