首页> 外文期刊>Inorganica Chimica Acta >Preparation,structure,and property of organic isothiocyanide-Fe(II) complexes,trans-[FeH(NCSR)(dppe)_2][X](dppe=Ph_2PCH_2CH_2PPh_2;R=Me,Et,Pr,i-Pr,CH_2CH=CH_2,CH_2CCH;X=I,Br,CF_3SO_3,BF_4)
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Preparation,structure,and property of organic isothiocyanide-Fe(II) complexes,trans-[FeH(NCSR)(dppe)_2][X](dppe=Ph_2PCH_2CH_2PPh_2;R=Me,Et,Pr,i-Pr,CH_2CH=CH_2,CH_2CCH;X=I,Br,CF_3SO_3,BF_4)

机译:有机异硫氰化物-Fe(II)配合物反式-[FeH(NCSR)(dppe)_2] [X](dppe = Ph_2PCH_2CH_2PPh_2; R = Me,Et,Pr,i-Pr,CH_2CH = CH_2,CH_2CCH; X = I,Br,CF_3SO_3,BF_4)

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摘要

The compound trans-[FeH(Cl)(dppe)_2](1)reacted with KSCN to give trans-[FeH(NCS)(dppe)_2](2),which underwent electrophilic attack by alkyl iodides or alkyl bromides (RX) to give organic isothiocyanide-Fe(II) complexes of the type trans-[FeH(NCSR)(dppe)_2]X{X=I:R=Me(3),Et(4),Pr(5),CH_2CH=CH_2(6),i-Pr(7);X=Br:R=Pr(8),CH_2CH=CH_2(9),CH_2C ac ident to CH(10)}.Comjpound 2 also reacted with strong electrohphiles,MeSO_3CF_3 and Me_3O·BF_4,to give trans-[FeH(NC-SMe)(dppe)_2][SO_3CF_3](11) and trans-[FeH(NCSMe)(dppe)_2][BF_4](12),respectively.Compounds 2 and 11 were characterized structurally by X-ray diffraction,in which the hydride ligand appears to be involved in the dihydrogen bonding,M-H…H-C.
机译:化合物反式-[FeH(Cl)(dppe)_2](1)与KSCN反应生成反式-[FeH(NCS)(dppe)_2](2),该化合物经历了烷基碘或烷基溴的亲电攻击(RX )得到反式-[FeH(NCSR)(dppe)_2] X {X = I:R = Me(3),Et(4),Pr(5),CH_2CH类型的有机异硫氰化物-Fe(II)配合物= CH_2(6),i-Pr(7); X = Br:R = Pr(8),CH_2CH = CH_2(9),CH_2C与CH(10)相同}。化合物2也与强亲电子试剂MeSO_3CF_3反应和Me_3O·BF_4,分别得到反式[FeH(NC-SMe)(dppe)_2] [SO_3CF_3](11)和反式[FeH(NCSMe)(dppe)_2] [BF_4](12)。图2和11的结构通过X射线衍射表征,其中氢化物配体似乎与二氢键MH…HC有关。

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