Dinuclear 3D metal complexes based on a carbacylamidophosphate ligand: redetermination of the ligand crystal structure

• Published in: Transition metal chemistry (Weinheim) 2013-05, Vol.38 (4), p.473-479
• Main Authors: Litsis, Olena O., Ovchynnikov, Vladimir A., Shishkina, Svetlana V., Sliva, Tatiana Yu, Amirkhanov, Vladimir M.
• Format: Article
• Language: English
• Subjects: Catalysis; Chemistry; Chemistry and Materials Science; Inorganic Chemistry; Organometallic Chemistry; Physical Chemistry
• ISSN: 0340-4285; 1572-901X
• DOI: 10.1007/s11243-013-9713-9

Dinuclear Ni(II), Co(II) and Zn(II) complexes of general formula with a carbacylamidophosphate ligand, namely 2,2,2-trichloro- N -(dipiperidine-1-yl-phosphoryl)acetamide (CCl 3 C(O)N(H)P(O)[N(CH 2 ) 5 ] 2 ), were synthesized and characterized by physicochemical and spectroscopic methods. Electronic absorption spectra of the nickel and cobalt complexes were measured at room temperature in toluene and in the solid state. The crystal structures of HL and [Ni 2 Cl 4 (HL) 4 (i-PrOH) 2 ·2(i-PrOH)] have been determined by single-crystal XRD studies. Earlier, the structure of a monoclinic C2/c modification of HL was reported. In this paper, redetermination of the structure of HL with triclinic crystal system, P , was made. The nickel complex is a chloro-bridged dimer, in which the Ni(II) centers are in a distorted octahedral geometry and the neutral HL is coordinated via its phosphoryl oxygen atom. This coordination mode was determined for the first time for 3D metal carbacylamidophosphate complexes.