Mn和Re羰基与双(N,N-二烷基硒代氨基甲酸基)硒化物反应的动力学研究

Paola Deplano, Emanuele F. Trogu
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引用次数: 3

摘要

使用366 nm源,以解决方案的辐照M2 (CO) 10 (MMn, Re)和过多的(LL): 1:1的混合物RIRIINC (Se) Se (Se) CNRIRII RIRIINC (Se) Se3 (Se) CNRIRII[如果RIRIIC2H5 (LL)(Et2dsc-dscEt2),如果RIRIIN = morpholyl (LL) = (modsc-dscmo),如果国际扶轮CH3、RIIC6H5 (LL) = (Mephdsc-dscMeph)定量生产M (CO) 4 L, L = RIRIINC(−)光化学反应进行了广泛的研究,量子产量和速率常数的确定。提出了sn1型机制,包括均溶MM键裂变作为速率决定步骤。
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A kinetic study of the reaction of Mn and Re carbonyls with some bis(N,N-dialkylselenocarbamoyl) selenides

Using a 366 nm source, irradiation of a CH2Cl2 solution of M2(CO)10 (MMn, Re) and an excess of (LL):a 1:1 mixture of RIRIINC(Se)Se(Se)CNRIRII and RIRIINC(Se)Se3(Se)CNRIRII [if RI RII C2H5(LL) (Et2dsc-dscEt2), if RIRIIN = morpholyl (LL) = (modsc-dscmo), if RICH3, RIIC6H5 (LL) = (Mephdsc-dscMeph) quantitatively produces [M(CO)4L], where L = RIRIINC(−) The photochemical reaction is extensively studied, the quantum yields and the rate constants are determined. A SN1-type mechanism is proposed, involving homolytic MM bond fission as the rate determining step.

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