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Monodentate S-vs. bidentate 1,5-O,S-coordination of N-phosphoryl-N'-(R)-thioureas with Pd(II).
Autorzy
Rok wydania
2008
Czasopismo
Numer woluminu
27
Strony
1995-1998
DOI
10.1016/j.poly.2008.03.012
Kolekcja
Język
Angielski
Typ publikacji
Artykuł
Reaction of N-phosphorylated thioureas of common formula RNHC(S)NHP(O)(OiPr)2 (R = tBu, HLI; R = Ph, HLII; R = 4′-benzo-15-crown-5, HLIII) with Pd(PhCN)2Cl2 in acetonitrile leads to complexes of the structure Pd(HLI-S)2Cl2 (1), Pd(HLII-S)2Cl2 (2) and Pd(HLIII-S)2Cl2 (3). Reaction of N-phosphorylated thioureas of common formula RC(S)NHP(O)(OiPr)2 (R = Et2N, HLIV; R = morpholine-N-yl, HLV) in the same conditions leads to complexes Pd(LIV-O,S)2 (4) and Pd(LV-O,S)2 (5), where the palladium(II) atoms are coordinated in a square-planar fashion by the CS sulfur atoms and the PO oxygen atoms of two anionic ligands. The crystal structure of complex 1 has been investigated by X-ray crystallography. It was established that the thiourea ligands are in a trans-configuration and the palladium(II) cation is coordinated by the sulfur atoms of the CS groups and the chlorine atoms. Complex 1 is the first example of palladium(II) complex in which the potentially chelating N-phosphorylated thiourea ligand is bound through the sulfur atom only.
Adres publiczny
https://doi.org/10.1016/j.poly.2008.03.012
Strona internetowa wydawcy
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