(pentamethylcyclopentadienyl)2[(i-Pr)NC(Me)N(i-Pr)-κ2N,N']U | 1203576-15-1

• 英文名称: (pentamethylcyclopentadienyl)2[(i-Pr)NC(Me)N(i-Pr)-κ2N,N']U
• 英文别名: (C5Me5)2U(MeC(N(iPr))2-κ2N,N')；(C5Me5)2[(i)PrNC(Me)N(i)Pr]U
• CAS: 1203576-15-1
• 化学式: C₂₈H₄₇N₂U
• 分子量: 649.723
• InChiKey: PUWNMJLZUWEBDE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
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• 重原子数：
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• 可旋转键数：
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• 环数：
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• sp3杂化的碳原子比例：
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• 拓扑面积：
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• 氢给体数：
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• 氢受体数：
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反应信息

• 作为反应物：
  描述：

  2,2'-二硫二吡啶 、 (pentamethylcyclopentadienyl)2[(i-Pr)NC(Me)N(i-Pr)-κ2N,N']U 以 甲基环己烷 为溶剂， 以66%的产率得到(C5Me5)2U(MeC(N(iPr))2-κ2N,N')(Spy)
  参考文献：
  名称：

  U 3+茂金属Am酸酯（C 5 Me 5）2 [ i PrNC（Me）N i Pr] U的反应化学，包括单齿乙酸铀络合物的分离

  摘要：

  U的还原化学3+在（C的金属茂配位脒环境5我5）2 [我PRNC（ME）N我镨κ 2 N，N' ] U，1，已探索。两个当量1与PhSSPh反应和2,2 ' -dithiopyridine（pySSpy）以产生（C 5我5）2 [我PRNC（ME）N我镨κ 2 N，N' ] U（SPH），2，和（C 5 Me 5）2 [ iPRNC（ME）N我镨κ 2 N，N' ] U（间谍），3，分别。配合物2和3也可以通过插入来合成我PrN═C═N我镨入甲基组中（C 5我5）2 UME（SPH）和（C 5我5）2 UME（间谍），4，分别。配合物1可以轻松还原Cu 1+试剂CuBr，CuI和CuO 2 CMe，从而生成相应的（C 5 Me 5）2 [我PRNC（ME）N我镨κ 2 N，N' ] UX复合物（X = Br的，5 ; I，6 ;○ 2 CME，7）。X射线晶体学确定络合物7为包含单齿乙酸盐

  DOI：

  10.1021/ic902141f
• 作为产物：
  描述：

  (pentamethylcyclopentadienyl)2[(i-Pr)NC(Me)N(i-Pr)-κ2N,N']UBr 在 lithium trimethylsilylmethyl 作用下， 以 氘代苯 为溶剂， 生成 (pentamethylcyclopentadienyl)2[(i-Pr)NC(Me)N(i-Pr)-κ2N,N']U
  参考文献：
  名称：

  Reactivity of Methyl Groups in Actinide Metallocene Amidinate and Triazenido Complexes with Silver and Copper Salts

  摘要：

  The effect of the heteroleptic ligand sets {(C(5)Me(5))(2)[(i)PrNC(Me)N(i)Pr]}(3-) and {(C(5)Me(5))(2)[(Me)-NNN(Ad)]}(3-) on actinide-carbon bond reactivity has been evaluated by examining the monomethyl actinide metallocene amidinate complexes (C(5)Me(5))(2)[(i)Pr-NC(Me)N(i)Pr-k(2)N,N']AnMe(An = U, 1; Th, 2) and the triazenido complex (C(5)Me(5))(2)[(Me)NNN(Ad)-k(2) N(1.3)]U Me, 3. This has led to a facile method to convert methyl groups in U(4+) and Th (4+) complexes to halide and pseudo-halide ligands. Complexes 1 and 3 react with AgOSO(2),CF(3) (AgOTf) to produce (C(5)Me(5))(2)[(i)PrNC(Me)N(i)Pr-k(2) N,N(1)]U(OTf), 4, and (C(5)Me(5))(2)[(Mc)NNN(Ad)-k(2) N(1.3)]U(OTf), 5, respectively. The methyl complexes are also reactive with copper reagents, as demonstrated by the reactions of Cul with 1 and 2 to make(C(5)Me(5))(2)[(i)PrNC(Me)N(i)Pr-k(2)N,N']UI,6, and(C(5)Me(5))2[(i)PrNC(Me)N(i)Pr-k(2) N,N']Th1,7, respectively. Similarly, reactions of CuBr with 1 and 3 generate (C(5)Me(5))2([)[(i)PrNC(Me)N(i)Pr-k(2)N,N']UBr, 8, and (C(5)MC(5))(2)[(Me)NNN(Ad)-K(2)N(1.3)] UBr, 9, respectively. These triflate and halide complexes are good precursors to other complexes with these ligand sets, as exemplified by their reactions with NaN(3), which produce (C(5)Me(5))(2)[(i)PrNC(Me)N(i)Pr-k(2) N,N']U(N(3)), 10, and (C(5)Me(5))(2)[(Me)NNN(Ad)-k(2) N(1.3)]U(N(3)), 11, respectively. However, the reactions of 4 and 6 with LiCH(2)SiMe(3) lead to reduction and the formation of the trivalent uranium heteroleptic metallocene (C(5)Me(5))2[(i)PrNC(Me)N(i)Pr-k(2)-N,N']U, 12. LiCH(2)SiMe(3) does not cause reduction with the triazenido ligand set, and the monoalkyl complex (C(5)Me(5))(2)[(Me)NNN(Ad)-k(2)N(1.3)]U(CH(2)SiMe(3)), 13, can be isolated.

  DOI：

  10.1021/om9008179