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首页> 外文期刊>Inorganica Chimica Acta >REACTIVITY OF TRANS-(CO)(3)FE(PH(2)PPYM)(2) TOWARD METAL REAGENTS - SYNTHESIS AND CRYSTAL STRUCTURES OF [HGCL(PH(2)PPYM)(MU-CL)](2), TRANS-[(PH(2)PPYM)(2)RH(CO)CL]CENTER-DOT-0.5CH(2)CL(2), [PDCL(MU-PH(2)PPYM)](2)CENTER-DOT-CH2CL2, CIS-[(PH(2)PPYM)(2)
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REACTIVITY OF TRANS-(CO)(3)FE(PH(2)PPYM)(2) TOWARD METAL REAGENTS - SYNTHESIS AND CRYSTAL STRUCTURES OF [HGCL(PH(2)PPYM)(MU-CL)](2), TRANS-[(PH(2)PPYM)(2)RH(CO)CL]CENTER-DOT-0.5CH(2)CL(2), [PDCL(MU-PH(2)PPYM)](2)CENTER-DOT-CH2CL2, CIS-[(PH(2)PPYM)(2)

机译:反式-(CO)(3)FE(PH(2)PPYM)(2)对金属试剂的反应性-[HGCL(PH(2)PPYM)(MU-CL)](2)的合成和晶体结构-[((PH(2)PPYM)(2)RH(CO)CL] CENTER-DOT-0.5CH(2)CL(2),[PDCL(MU-PH(2)PPYM)](2)CENTER-DOT -CH2CL2,CIS-[[PH(2)PPYM)(2)

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The reaction of the neutral tridentate organometallic ligand trans-(CO)(3)Fe(Ph(2)Ppym)(2) with Hg-2(ClO4)(2) . xH(2)O, [(cod)RhCl](2), (cod)PdCl2, PdCl2 and Nd(SCN)(3) . xH(2)O has been studied. Five new complexes were prepared and fully characterized by single-crystal X-ray analysis: [HgCl(Ph(2)Ppym)(mu-Cl)](2) (1), space group P2(1) with a = 11.906(1), b = 11.263(1), c = 13.437(1) Angstrom, beta = 91.75(1)degrees and Z = 2; trans-[(Ph(2)Ppym)(2)Rh(CO)Cl]. 0.5CH(2)Cl(2) (2), space group C2/c with a = 12.009(1), b = 14.536(1), c = 19.093(1) Angstrom, beta = 90.00(1)degrees and Z = 4; [PdCl(mu-Ph(2)Ppym)](2) . CH2Cl2 (3), space group P2(1) with a = 12.295(1), b = 11.762(1), c = 23.919(1) Angstrom, beta = 90.00(1)degrees and Z = 4; cis-[(Ph(2)Ppym)(2)PdCl2]. 0.5CH(2)Cl(2) (4), space group P2(1) with a = 10.907(2), b = 18.525(4), c = 16.657(3) Angstrom, beta = 106.92(3)degrees and Z = 4; and cis-[Fe(NCS)(2)(Ph2P(O)pym)(2)] (5), space group P2(1)/c with a = 12.747(1), b = 11.051(1), c = 25.430(1) Angstrom, beta = 103.30(1)degrees and Z = 4. The results showed that (i) trans-(CO)(3)Fe(Ph(2)Ppym)(2) is a strong reductant, and (ii) the Ph(2)Ppym moiety weakly coordinates to the Fe(O) atom and can easily be transferred to another metal atom when the organoiron ligand reacts with various metal reagents. [References: 44]
机译:中性三齿有机金属配体反式-(CO)(3)Fe(Ph(2)Ppym)(2)与Hg-2(ClO4)(2)的反应。 xH(2)O,[(cod)RhCl](2),(cod)PdCl2,PdCl2和Nd(SCN)(3)。 xH(2)O已被研究。制备了五个新的配合物,并通过单晶X射线分析对其进行了全面表征:[HgCl(Ph(2)Ppym)(mu-Cl)](2)(1),空间群P2(1)/ n,a 11.906(1),b = 11.263(1),c = 13.437(1)埃,beta = 91.75(1)度,Z = 2;反式-[((Ph(2)Ppym)(2)Rh(CO)Cl]。 0.5CH(2)Cl(2)(2),空间组C2 / c,a = 12.009(1),b = 14.536(1),c = 19.093(1)埃,β= 90.00(1)度和Z = 4; [PdCl(mu-Ph(2)Ppym)](2)。 CH 2 Cl 2(3),空间群P2(1)/ n,a = 12.295(1),b = 11.762(1),c = 23.919(1)埃,β= 90.00(1)度,Z = 4;顺式-[(Ph(2)Ppym)(2)PdCl2]。 0.5CH(2)Cl(2)(4),空间组P2(1)/ n,a = 10.907(2),b = 18.525(4),c = 16.657(3)埃,beta = 106.92(3)度,Z = 4;和cis- [Fe(NCS)(2)(Ph2P(O)pym)(2)](5),空间群P2(1)/ c,a = 12.747(1),b = 11.051(1),c = 25.430(1)埃,β= 103.30(1)度,Z =4。结果表明(i)反式(CO)(3)Fe(Ph(2)Ppym)(2)是强还原剂, (ii)Ph(2)Ppym部分与Fe(O)原子的配位较弱,并且当有机铁配体与各种金属试剂反应时,很容易转移到另一个金属原子上。 [参考:44]

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