Structural, theoretical and multinuclear NMR study of mercury(II) complexes with a new ambidentate phosphorus ylide |
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Authors: | Seyyed Javad Sabounchei Sadegh SalehzadehMarjan Hosseinzadeh Fateme Akhlaghi BagherjeriHamid Reza Khavasi |
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Affiliation: | a Faculty of Chemistry, Bu-Ali Sina University, Hamedan 65174, Iran b Department of Chemistry, Shahid Beheshti University, G.C., Evin, Tehran 1983963113, Iran |
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Abstract: | The reaction of the new ambidentate ylide, Ph3PCHCOCH2COOC2H5 (EAPPY), with HgX2 (X = Cl, Br and I) in equimolar ratios using methanol as the solvent leads to binuclear complexes of the type [EAPPY·HgX2]2 (X = Cl (1), Br (2) and I (3)). Single crystal X-ray analysis reveals the presence of a centrosymmetric dimeric structure containing the ylide and HgX2 (X = Br or I). The IR and NMR data of the product [(EAPPY)·HgCl2]2 (1), formed by the reaction of mercury(II) chloride with the same ylide, are similar to those of 2 and 3. Analytical data indicate a 1:1 stoichiometry between the ylide and Hg(II) halide in each of the three products. Theoretical studies indicate that the nature of the R group in ylides of the type Ph3PCHCOR has a weak effect on the Hg-C(ylide) bond length in binuclear Hg2L2I4 complexes. |
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Keywords: | Phosphorus ylide Mercury(II) halides complexes X-ray crystal structure Theoretical studies |
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