首页> 外文期刊>Inorganica Chimica Acta >Reactivity of alkynyl Pd(II) azido complexes toward organic isocyanides, isothiocyanates, and nitriles
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Reactivity of alkynyl Pd(II) azido complexes toward organic isocyanides, isothiocyanates, and nitriles

机译:炔基Pd(II)叠氮基络合物对有机异氰酸酯,异硫氰酸酯和腈的反应性

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Alkynyl Pd(II) azido complexes of the type [Pd(N-3)(CdropC-R)L-2] (1-3) were obtained by reactions of aqueous NaN3 with [Pd(Cl)(CdropC-R)L-2] (R = Ph or C(O)OMe). Treating compounds 1-3 with organic isocyanides (R-NC) afforded novel complexes, trans-[Pd(CdropC-Ph)(N=C=N-R)(PMe3)(2)] (R = 2,6-Me2C6H3 (4) or 2,6-Et2C6H3 (5)) and trans-[Pd(CdropC-R)(CN4-t-Bu)L-2] (6: L = PMe3, R = Ph; 7: L = PEt3, R = C(O)OMe; 8: L = PMe3 R = C(O)OMe), which contain either a carbodiimido or a C-coordinated tetrazolato group. Reactions of compounds 1 and 2 with R-N=C=S (R = 2,6-Me2C6H3 or CH2CH3) and 1,4-phenylene diisothiocyanate (C6H4(N=C=S)(2)) smoothly proceeded to give tetrazole-thiolato complexes, trans-[Pd(CdropCPh)(SCN4-R)L-2] (L = PMe3, R = Et (9) or 2,6-Me2C6H3 (10); L = PEt3, R = 2,6-Me2C6H3 (11)), and a phenylene-bridged dinuclear Pd(II) tetrazole-thiolato complex, [(PEt3)(2)(CdropCPh)Pd(SCN4-(mu-C6H4)-SCN4)Pd(CdropCPh)(PEt3)(2)] (12), respectively. Complexes 9-12 contain the Pd-S bond that is formed by the dipolar cycloaddition of the organic isothiocyanate to the Pd-azido bond. In contrast, the vcorresponding reactions of compounds land 2 with C6F5CN and Me3SiCN (organic nitriles, R-CN) gave an N-coordinated Pd(II)-tetrazolato compound {trans-[Pd(CdropC-Ph)(N4C-C6F5)(PMe3)(2)] (13)} and a mixture of Pd(II)-cyano complexes {trans[Pd(CdropC-Ph)(CN)(PEt3)(2)] (14) and [Pd(CN)2(PEt3)21 (15), respectively. Bis(phosphine) bis(cyano) complexes of Pd and Ni, [M(CN)(2)L-2] (L = PEt3, PMe3; L-2 = DEPE), could be obtained independently by the reactions of [M(N-3)(2)L-2] with excess Me3SiCN in organic solvents. (C) 2004 Elsevier B.V. All rights reserved.
机译:通过NaN3水溶液与[Pd(Cl)(CdropC-R)L的反应获得[Pd(N-3)(CdropC-R)L-2](1-3)类型的炔基Pd(II)叠氮基络合物-2](R = Ph或C(O)OMe)。用有机异氰酸酯(R-NC)处理化合物1-3可得到新型配合物,反式[Pd(CdropC-Ph)(N = C = NR)(PMe3)(2)](R = 2,6-Me2C6H3(4 )或2,6-Et2C6H3(5))和反式[Pd(CdropC-R)(CN4-t-Bu)L-2](6:L = PMe3,R = Ph; 7:L = PEt3,R = C(O)OMe; 8:L = PMe 3 R = C(O)OMe),其含有碳二亚氨基或C-配位的四唑基。化合物1和2与RN = C = S(R = 2,6-Me2C6H3或CH2CH3)和1,4-亚苯基二异硫氰酸酯(C6H4(N = C = S)(2))的反应平稳进行,得到四唑-硫醇基反式-[Pd(CdropCPh)(SCN4-R)L-2](L = PMe3,R = Et(9)或2,6-Me2C6H3(10); L = PEt3,R = 2,6-Me2C6H3 (11))和亚苯基桥连的双核Pd(II)四唑-硫醇基络合物,[(PEt3)(2)(CdropCPh)Pd(SCN4-(mu-C6H4)-SCN4)Pd(CdropCPh)(PEt3)( 2)](12)。配合物9-12含有Pd-S键,该键由有机异硫氰酸酯与Pd-叠氮基键的偶极环加成形成。相反,化合物Land 2与C6F5CN和Me3SiCN(有机腈,R-CN)的相应反应给出了N配位的Pd(II)-四唑酸酯化合物{反式-[Pd(CdropC-Ph)(N4C-C6F5)( PMe3)(2)](13)}和Pd(II)-氰基络合物的混合物{trans [Pd(CdropC-Ph)(CN)(PEt3)(2)](14)和[Pd(CN)2 (PEt3)21(15)。钯和镍的双(膦)双(氰基)配合物[M(CN)(2)L-2](L = PEt3,PMe3; L-2 = DEPE),可以通过[M (N-3)(2)L-2]和过量的Me3SiCN在有机溶剂中。 (C)2004 Elsevier B.V.保留所有权利。

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