Synthesis and structural evaluation of organo-ruthenium complexes with ß-diketonates

Uršič, Matija (avtor), Lipec, Tanja (avtor), Meden, Anton (avtor), Turel, Iztok (avtor)

Four novel ruthenium organometallic complexes: [(η$^6$-p-cymene)Ru(4,4,4-trifluoro-1-(4-bromophenyl)-1,3-butanedione)Cl] (1), [(η$^6$-p-cymene)Ru(4,4,4-trifluoro-1-(4-bromophenyl)-1,3-butanedione)pta]PF$_6$ (2), [(η$^6$-p-cymene)Ru(4,4,4-trifluoro-1-(4-iodophenyl)-1,3-butanedione)Cl] (3) and [(η$^6$-p-cymene)Ru(4,4,4-trifluoro-1-(4-iodophenyl)-1,3-butanedione)pta]PF$_6$ (4) were synthesized and characterized by elemental analysis, infrared (IR), UV-Vis, NMR and mass spectroscopy and single-crystal X-ray diffraction. The crystal structures and spectroscopic data were compared to the previously published complexes [(η$^6$-p-cymene)Ru(4,4,4-trifluoro-1-(4-chloro-phenyl)-1,3-butanedione)Cl] (5) and [(η$^6$-p-cymene)Ru(4,4,4-trifluoro-1-(4-chlorophenyl)-1,3-butanedione)pta]PF$_6$ (6). The pairs of complexes 1 and 3 as well as 2 and 4 are isostructural, with the former crystallizing in triclinic P-1 and the latter in monoclinic P2$_1$/c. The ruthenium(II) ion is found in a pseudo-octahedral “piano-stool” geometry in all compounds. Bond lengths and angles are consistent with other complexes of this type. Complexes 2 and 4 exhibit some moderate dynamic disorder. The lack of hydrogen bonding and major π-π interactions means that most of intramolecular interactions are fairly weak and involve halogen atoms present. This was further confirmed by $^1$H-NMR spectra, where a significant difference is observed only on the ligand near the halogen atom, following an expected trend. The combined data show that the difference in any activity depends substantially on the type of the ligand′s substituted halogen atom.

• Jezik: Angleški jezik
• Ključne besede: organoruthenium complexes, ß-diketonate ligands, halogen substituents, 1, 3, 5-triazaphosphoadamantane (pta) ligand, disorder
• Vrsta gradiva: Članek v reviji
• Tipologija: 1.01 - Izvirni znanstveni članek
• Organizacija: FKKT - Fakulteta za kemijo in kemijsko tehnologijo
• Status publikacije: Objavljeno
• Različica publikacije: Objavljena publikacija
• Leto izida: 2017
• Št. strani: 12 str.
• Številčenje: Vol. 22, iss. 2, art. 326
• PID: 20.500.12556/RUL-131179
• UDK: 546.96:547-316
• ISSN pri članku: 1420-3049
• DOI: 10.3390/molecules22020326
• COBISS.SI-ID: 1537371075
• Datum objave v RUL: 23.09.2021

URŠIČ, Matija, LIPEC, Tanja, MEDEN, Anton in TUREL, Iztok, 2017, Synthesis and structural evaluation of organo-ruthenium complexes with ß-diketonates. Molecules [na spletu]. 2017. Vol. 22, no. 2,  326. [Dostopano 8 april 2025]. DOI 10.3390/molecules22020326. Pridobljeno s: https://repozitorij.uni-lj.si/IzpisGradiva.php?lang=slv&id=131179

Gradivo je del revije

• Naslov: Molecules
• Skrajšan naslov: Molecules
• Založnik: MDPI
• ISSN: 1420-3049
• COBISS.SI-ID: 18462981

Licence

• Licenca: CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
• Povezava: http://creativecommons.org/licenses/by/4.0/deed.sl
• Opis: To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.
• Začetek licenciranja: 20.02.2017

Sekundarni jezik

• Jezik: Slovenski jezik
• Ključne besede: organorutenijevi kompleksi, ß-diketonatni ligandi, halogenski substituenti, 1, 3, 5-triazafosfoadamantan (pta) ligand, nered

Projekti

• Financer: ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
• Program financ.: Junior Researcher Grant

• Financer: ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
• Številka projekta: P1-0175
• Naslov: Sinteza, struktura, lastnosti snovi in materialov