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Formation and Dissociation of Tetrahedral Nickel(II) and Cobalt(II) Complexes of ‘Dithioimidodiphosphato’ Ligands,Measurement of Kinetically Determined Stability Constants,and Kinetic Investigations of the Rapid Formation of Tetrahedral Bis(ligand)copper(II) Complexes and Their Rates of Reduction to Trinuclear Copper(I) Species
Authors:Peter Moore  William Errington  Satindra&#x;P Sangha
Institution:Peter Moore,William Errington,Satindra P. Sangha
Abstract:The stopped‐flow technique was used to measure the rates of formation and dissociation of tetrahedral ML2] complexes (M2+=Ni2+ or Co2+) of four bidentate S2‐donor ‘dithioimidodiphosphato’ ligands L? (HL=R1R2P(?S)]NHP(?S)R3R4], R1 to R4=alkyl) at 25.0° in MeOH/H2O 95 : 5 (v/v) solution and in the presence of either MOPS (=3‐(morpholin‐4‐yl)propane‐1‐sulfonic acid) or 2,6‐lutidine (=2,6‐dimethylpyridine) buffers. The kinetically determined equilibrium formation constants for ML]+ ions (M=Ni or Co) are 10?5 K=0.50±0.01 or 1.64±0.07 l mol?1 for L=L3 (R1=R2=Me(CH2)2CH(Me), R3=R4=Me2CH), 1.27±0.02 or 7.93±0.09 l mol?1 for L=L7 (R1 to R4=Me2CHCH2), 0.88±0.04 or 3.84±0.13 l mol?1 for L=L8 (R1 to R4=Me2CH), and in case of Ni2+ 1.88±0.04 l mol?1 for L=L6 (R1=R3=Bu, R2=R4=tBu) (see Table 3; for L3 and L6–L8, see Table 1). Whereas the tetrahedral Ni2+ complexes dissociate more slowly than the analogous Co2+ species, in all cases, the Co2+ complexes are more stable than those of Ni2+ due to their larger formation rate constants (Table 3). Reactions of Cu2+ with eight ligands HL (R1 to R4=alkyl, alkoxy, aryl, and aryloxy) show that formation of intensely colored tetrahedral CuIIL2] species is too fast be measured with the available stopped‐flow apparatus (t1/2<2 ms), but the subsequent rates of reduction of CuIIL2] to give trinuclear products CuI3L3] are measurable. An X‐ray analysis establishes the structure of one of the Cu3L3] complexes, where R1=R2=Me2CHO and R3=R4=2‐(tert‐butyl)phenyl (L=L5), and a multiwavelength stopped‐flow kinetic experiment establishes the spectrum of a tetrahedral CuIIL2] species prior to the reduction reactions. The redox reactions proceed at 25.0° with first‐order rate constants in the range 0.285 s?1 (R1 to R4=PhO; L=L11) to 2.58?10?4 s?1 (R1 to R4=Me2CHCH2; L=L7) (Table 4).
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