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Synthesis and characterisation of Pd(II) complexes with a derivative of aminoazobenzene. Dynamic 1H NMR study of cyclopalladation reactions in DMF


Ćurić, Manda; Babić, Darko; Marinić, Željko; Paša-Tolić, Ljiljana; Butković, Vjera; Plavec, Janez; Tušek-Božić, Ljerka
Synthesis and characterisation of Pd(II) complexes with a derivative of aminoazobenzene. Dynamic 1H NMR study of cyclopalladation reactions in DMF // Journal of organometallic chemistry, 687 (2003), 1; 85-99 doi:10.1016/j.jorganchem.2003.07.013 (međunarodna recenzija, članak, znanstveni)


Naslov
Synthesis and characterisation of Pd(II) complexes with a derivative of aminoazobenzene. Dynamic 1H NMR study of cyclopalladation reactions in DMF

Autori
Ćurić, Manda ; Babić, Darko ; Marinić, Željko ; Paša-Tolić, Ljiljana ; Butković, Vjera ; Plavec, Janez ; Tušek-Božić, Ljerka

Izvornik
Journal of organometallic chemistry (0022-328X) 687 (2003), 1; 85-99

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Palladium ; azobenzenes ; cyclopalladation ; 1H NMR study ; dynamics

Sažetak
Three new Pd(II) complexes, i.e. [PdCl_2L]_2 (A), PdCl_2L_2 (B) and [Pd(mu?Cl)(L?H)]_2 (C), each with two diethyl [alpha?(4?benzenazoanilino)?2?hydroxybenzyl]phosphonates (L) bound to either one or two palladium atoms, are synthesized and characterized by elemental analysis, by IR, UV/Vis and solid?state 13C NMR spectra. B and C are additionally characterized by 1H, 13C and 31P NMR and ES?MS studies using DMF as a solvent. In DMF solution adducts A and B undergo spontaneous rearrangement into the cyclopalladated complex C. Dynamic 1H NMR study of this rearrangement as well as of the reactions of L with PdCl_2 and Na_2PdCl_4 revealed a complex equilibrium in DMF solutions and enabled the formation mechanism of all involved species to be resolved. The complex A is immediately solvolyzed producing two molecules of intermediate M [PdCl_2(L)(DMF)]. M was also the first intermediate in the reaction of L with PdCl_2. Once present in concentration above 103^-5 mol dm^-3 M dimerizes very fast into chloro?bridged dimer [PdCl(mu?Cl)(L)]_2 (D) which undergoes cyclopalladation and converts into the complex C. The formation of C from the intermediate D is clearly demonstrated by the concentration dependence of the cyclopalladation reaction which has order greater than one. Chloride ions, released by cyclopalladation, react with D by splitting chloro?bridge and binding to metal atoms to produce byproduct [PdCl_3(L)]- (T). The same species (T) are formed in the reaction of L with Na_2PdCl_4 whereby a chloride ion is replaced by the ligand L. The complex B undergoes similar, but slower, solvolytic reaction producing M and L while further reaction steps are identical as in the solvolysis of A.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



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Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus


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