Versatility and reactivity of salicylaldehyde S-methylisothiosemicarbazone in palladium(II) complexes
М.D. RevencoMoldova State University, ul. Matteevicha 60, Chisinau, 277009, MoldovaYu. A. SimonovInstitute of Applied Physics, Academy of Sciences of Moldova, Chisinau, MoldovaGheorghe DucaMoldova State University, ul. Matteevicha 60, Chisinau, 277009, MoldovaП. БоурошInstitute of Applied Physics, Academy of Sciences of Moldova, Chisinau, MoldovaPetru BulmagaMoldova State University, ul. Matteevicha 60, Chisinau, 277009, MoldovaVadim Yu. KukushkinSt. Petersburg State University, Universitetskaya nab. 7/9, St. Petersburg, 199164, RussiaE. JoraMoldova State University, ul. Matteevicha 60, Chisinau, 277009, MoldovaМ. GdaniecDepartment of Chemistry, Adam Mickiewicz University, Poznan, Poland
2009en
ABI
Аннотация
New palladium(II) complexes, [Pd(HL)Cl] · H2O (I) and {K[Pd(L1)(NO2)] · H2O}2, with S-methylisothiosemicarbazone of salicylaldehyde (H2L) and its derivative (H2L1) were synthesized. X-ray diffraction analysis demonstrated the ambident nature of S-alkylated thiosemicarbazone, which is attached to palladium(II) through O, N, and S donor atoms in I and through O, N, and N atoms in II. This is the first known case of metal coordination of the alkylated sulfur atom of a thiosemicarbazide moiety of the ligand. A mechanism of nitrosation of the terminal amide nitrogen atom of the H2L1 ligand during complexation was proposed.
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