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A base-free terminal thorium phosphinidene metallocene and its reactivity toward selected organic molecules

机译:自由终端钍膦醚茂金属及其对选定有机分子的反应性

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摘要

The stable base-free terminal phosphinidene thorium metallocene, [(5)-1,2,4-(Me3C)(3)C5H2](2)Th?P-2,4,6-(Bu3C6H2)-Bu-t (2), can be isolated from the reaction of the thorium dichloride complex [(5)-1,2,4-(Me3C)(3)C5H2](2)ThCl2 (1) with 2 equiv. of 2,4,6-(Me3C)(3)C6H2PHK in THF. The reactivity of 2 in the activation of various small organic molecules such as diselenides, phosphines, imines, ketones, phosphine oxides, thiazole, imidazole derivatives and amines was explored. For example, when complex 2 is treated with Ph2Se2, the phosphinidene is replaced, yielding diselenido compound [(5)-1,2,4-(Me3C)(3)C5H2](2)Th(SePh)(2) (3). Moreover, E-H (E = P, N, C) bond activation occurs on exposure of 2 to 2,4,6-(Pr3C6H2PH2)-Pr-i, PhPH2, (p-tolyl)(2)C?NH, 1-indanone, cyclohexanone, Me3PO, thiazole, 1-methylimidazole and p-toluidine, resulting in the phosphido complex [(5)-1,2,4-(Me3C)(3)C5H2][(5),-C-1,2-(Me3C)(2)-4-(CH2CMe2)C5H2]Th(PH-2,4,6-(Pr3C6H2)-Pr-i) (4), the metallaheterocycle [(5)-1,2,4-(Me3C)(3)C5H2](2)Th((2)-P2Ph2) (5), the iminato phosphido complex [(5)-1,2,4-(Me3C)(3)C5H2](2)Th(PH-2,4,6-(Bu3C6H2)-Bu-t)[N?C(p-tolyl)(2)] (6), the phosphido enolyl compound [(5)-1,2,4-(Me3C)(3)C5H2](2)Th(PH-2,4,6-(Bu3C6H2)-Bu-t)(-O-1-OC9H7) (7), the enolyl complex [(5)-1,2,4-(Me3C)(3)C5H2][(5),-C-1,2-(Me3C)(2)-4-(CH2CMe2)C5H2]Th(-O-1-OC6H9) (8), the alkyl complex [(5)-1,2,4-(Me3C)(3)C5H2][(5),-C-1,2-(Me3C)(2)-4-(CH2CMe2)C5H2]Th(-O,C-OPMe2CH2) (9), the phosphido thiazolyl complex [(5)-1,2,4-(Me3C)(3)C5H2](2)Th(PH-2,4,6-(Bu3C6H2)-Bu-t)(C3H2NS) (10), the bis-imidazolyl complex [(5)-1,2,4-(Me3C)(3)C5H2](2)Th[2-(1-MeC3H2N2)](2) (11), and the imido complex [(5)-1,2,4-(Me3C)(3)C5H2](2)Th?N(p-tolyl) (12), respectively. Several spectroscopic techniques were employed for the characterisation of the new complexes 3-11, and in addition the solid-state molecular structures of compounds 3-6, 8-9 and 11 were further confirmed by X-ray diffraction analyses.
机译:稳定的游离碱末端亚膦钍金属茂,[(S)-1,2,4-(Me3C)(3)C5H2](2)的Th 2 P -2,4,6-(Bu3C6H2)-Bu-T( 2),可以从钍二氯化配合物[(5)-1,2,4-(Me3C)(3)C5H2](2反应与2当量分离)ThCl2(1)。的2,4,6-(Me3C)(3)C6H2PHK的THF溶液。 2在如diselenides,膦,亚胺,酮,氧化膦,噻唑,咪唑衍生物和胺的各种小的有机分子的活化的反应性进行了探讨。例如,当配合物2与Ph2Se2处理时,亚膦被替换,得到diselenido化合物[(S)-1,2,4-(Me3C)(3)C5H2](2)的Th(SEPH)(2)(3 )。此外,EH(E = P,N,C)键活化发生在2暴露于-2,4,6-(Pr3C6H2PH2)-Pr-I,PhPH2,(对甲苯基)(2)C 2 NH,1-茚满酮,环己酮,Me3PO,噻唑,1-甲基咪唑和对 - 甲苯胺,从而导致复杂的膦[(5)-1,2,4-(Me3C)(3)C5H2] [(5), - C-1, 2-(Me3C)(2)-4-(CH2CMe2)C5H2]的Th(PH -2,4,6-(Pr3C6H2)-Pr-i)的(4)中,metallaheterocycle [(S)-1,2,4- - (Me3C)(3)C5H2](2)个((2)-P2Ph2)(5)中,iminato膦配合物[(5)-1,2,4-(Me3C)(3)C5H2](2)第(PH -2,4,6-(Bu3C6H2)-Bu-T)[N?C(对甲苯基)(2)](6)中,膦化合物enolyl [(5)-1,2,4- (Me3C)(3)C5H2](2)的Th(PH -2,4,6-(Bu3C6H2)-Bu-T)( - O-1-OC9H7)(7),所述enolyl配合物[(5)-1 ,2,4-(Me3C)(3)C5H2] [(5), - C-1,2-(Me3C)(2)-4-(CH2CMe2)C5H2钍(-O-1-OC6H9)(8 )中,烷基络合物[(5)-1,2,4-(Me3C)(3)C5H2] [(5), - C-1,2-(Me3C)(2)-4-(CH2CMe2)C5H2]个(= O,C-OPMe2CH2)(9)中,噻唑基膦配合物[(5)-1,2,4-(Me3C)(3)C5H2](2)第(PH -2,4,6-( Bu3C6H2)-Bu-T)(C3H2NS)(10),双 - 咪唑基配合物[(5)-1,2,4-(Me3C)(3)C5H2](2)的Th [2-(1- MeC3H2N2) ](2)(11 ),以及亚氨基配合物[(5)-1,2,4-(Me3C)(3)C5H2](2)的Th 2 N(对甲苯基)(12),分别。几个光谱技术被用于该新的复合物3-11的表征,并且另外的化合物3-6,8-9和11的固态分子结构进一步通过X射线衍射分析证实。

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