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首页> 外文期刊>Organometallics >Access to alkynylpalladium(IV) and -platinum(IV) species, including triorgano(diphosphine)metal(IV) complexes and the structural study of an alkynyl(pincer)platinum(IV) complex, Pt(O2CArF)I(C CSiMe3)(NCN) (Ar-F=4-CF3C6H4, NCN = [2,6-(dimethylaminome
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Access to alkynylpalladium(IV) and -platinum(IV) species, including triorgano(diphosphine)metal(IV) complexes and the structural study of an alkynyl(pincer)platinum(IV) complex, Pt(O2CArF)I(C CSiMe3)(NCN) (Ar-F=4-CF3C6H4, NCN = [2,6-(dimethylaminome

机译:获得炔基钯(IV)和-铂(IV)物种,包括三有机(二膦)金属(IV)配合物以及炔基(钳子)铂(IV)配合物Pt(O2CArF)I(C CSiMe3)( NCN)(Ar-F = 4-CF3C6H4,NCN = [2,6-(二甲基氨基)

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摘要

New classes of alkynylplatinum(IV) complexes are described, and the first examples of alkynylpalladium(IV) complexes have been detected, including a triorganopalladium(IV) diphosphine complex. Alkynyliodine(III) triflate reagents IPh(CtCR(2))(OTf) (R-2 = SiMe3, Ph) are able to transfer alkynyl groups to diorganoplatinum(II) and "pincer" complexes Pt(O2CAr)(NCN) (NCN = [2,6-(dimethylaminomethyl)-phenyl- N,C,N](-), Ar = Ph, 4-trifluoromethylphenyl (Ar-F)); on addition of iodide ion, complexes with new alkynylplatinum(IV) kernels may be isolated: PtIMe2(C equivalent to CR2)(bpy) (1, 2, 3a) (bpy) 2,2'-bipyridine), PtI(C4H8)(C equivalent to CSiMe3)(bpy) (4a), PtIPh2(C equivalent to CSiMe3)(Bu(2)(t)bpy) (5a), and PtI(O2CAr)(C equivalent to CR2)(NCN) [Ar = Ph (14, 15), Ar-F (16, 17)]. For the reagent PtMe2(dmpe) [dmpe = 1,2-bis(dimethylphosphino)ethane], the unstable complexes PtIMe2(C equivalent to CR2)(dmpe) (6a, 8a) are detected prior to reductive elimination of ethane and isolation of PtI(C equivalent to CR2)(dmpe) (7, 9). Isomerism is exhibited by the octahedral fac-(PtR2)-R-IV- CtCR2) complexes, where complexes 1 and 2 form as a mixture of complexes with the alkynyl group opposite the bidentate ligand and cis to the iodo ligand (1a-6a, 8a), and cis to the bidentate ligand and trans to the iodo ligand (1b, 2b), complexes 3a-5a, 6a, and 8a having R groups mutually cis. An X-ray structural analysis for 16 shows distorted octahedral geometry about the metal with the iodo ligand trans to the carbon donor of the mer-pincer ligand. Studies of the reactivity of related palladium(II) substrates at low temperature allow detection of the pincer complex Pd(O2CPh)(OTf)(C equivalent to CSiMe3)(NCN) (19) and PdIMe2(C equivalent to CSiMe3)(dmpe) (18) as a model for frequently proposed "(PdXR3P2)-X-IV" species in catalytic and stoichiometric reactions.
机译:描述了新种类的炔基铂(IV)配合物,并且已经检测到炔基钯(IV)配合物的第一个实例,包括三有机钯(IV)二膦配合物。炔丙基碘(III)三氟甲磺酸盐试剂IPh(CtCR(2))(OTf)(R-2 = SiMe3,Ph)能够将炔基转移至二有机铂(II)和“钳”络合物Pt(O2CAr)(NCN)(NCN) = [2,6-(二甲基氨基甲基)-苯基-N,C,N](-),Ar = Ph,4-三氟甲基苯基(Ar-F));添加碘离子后,可以分离出具有新的炔基铂(IV)核的配合物:PtIMe2(C等同于CR2)(bpy)(1、2、3a)(bpy)2,2'-联吡啶),PtI(C4H8) (C等同于CSiMe3)(bpy)(4a),PtIPh2(C等同于CSiMe3)(Bu(2)(t)bpy)(5a)和PtI(O2CAr)(C等同于CR2)(NCN)[Ar = Ph(14,15),Ar-F(16,17)]。对于试剂PtMe2(dmpe)[dmpe = 1,2-双(二甲基膦基)乙烷],在还原性消除乙烷并分离出乙交酯之前,先检测到不稳定的络合物PtIMe2(C相当于CR2)(dmpe)(6a,8a)。 PtI(C等于CR2)(dmpe)(7,9)。八面体fac-(PtR2)-R-IV-CtCR2)配合物表现出异构性,其中配合物1和2形成为配合物的混合物,其中炔基与二齿配体相反,且与碘配体的顺式(1a-6a,具有R基团的化合物3a-5a,6a和8a相互顺式结合成顺式至二齿配体并顺式转化成碘配体(1b,2b)。对16的X射线结构分析显示,金属的扭曲八面体几何结构具有碘配体,该碘配体转移至mer-pincer配体的碳供体。对相关钯(II)底物在低温下的反应性研究使得可以检测到钳形复合物Pd(O2CPh)(OTf)(C相当于CSiMe3)(NCN)(19)和PdIMe2(C相当于CSiMe3)(dmpe) (18)作为催化和化学计量反应中经常提出的“(PdXR3P2)-X-IV”种类的模型。

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