(2-Methoxy-1,3-dimethyl-1,3,2-diazaphospholidin-2-ium-2-yl)boranuide | 895578-50-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 氮杂环化合物
• 英文名称: (2-Methoxy-1,3-dimethyl-1,3,2-diazaphospholidin-2-ium-2-yl)boranuide
• 英文别名: (2-methoxy-1,3-dimethyl-1,3,2-diazaphospholidin-2-ium-2-yl)boranuide
• CAS: 895578-50-4
• 化学式: C₅H₁₆BN₂OP
• 分子量: 161.98
• InChiKey: BYSYZDDMVIUZJO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.45
• 重原子数：
  10
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  15.7
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (2-Methoxy-1,3-dimethyl-1,3,2-diazaphospholidin-2-ium-2-yl)boranuide 、 tris(carbonyl)(pentamethylcyclopentadienyl)methyltungsten 以0%的产率得到
  参考文献：
  名称：

  Molybdenum complexes bearing a diaminosubstituted-phosphiteboryl ligand: Syntheses, structures, and reactivity involving the Mo–B, B–P, and B–H activation

  摘要：

  Photoreaction of diaminosubstituted-phosphiteborane, BH3P(NMeCH2)(2)(OMe) with a methyl molybdenum complex, (eta(5)-C5R5)-Mo(CO)(3)Me (R-5 = Me-5, Me4H, H-5) yielded a phosphiteboryl molybdenum complex, (eta(5)-C5R5)Mo(CO)(3)BH2{P(NMeCH2)(2)(OMe)} (R-5 = Me-5: 2, Me4H: 3, H-5: 4). In the reaction of 2 with MeI, the Mo-B bond was activated to give (eta(5)-C5Me5)Mo(CO)(3)Me, in the reaction with PMe3, the B-P bond was activated to give (eta(5)-C5Me5)Mo(CO)(3)(BH2PMe3). Complex 2 in solution was gradually converted into (eta(5)-C5Me5)MoH(CO)(2){P(NMeCH2)(2)(OMe)} (8) via the B-H bond activation of 2. Structures of 2, 3, and 8 were determined by single crystal X-ray diffraction studies. (c) 2006 Elsevier B.V. All rights reserved.

  DOI：

  10.1016/j.jorganchem.2006.04.049
• 作为产物：
  描述：

  2-methoxy-1,3-dimethyl-1,3,2-diazaphospholane 在 硼烷四氢呋喃络合物 作用下， 以 正戊烷 为溶剂， 反应 5.0h， 以98%的产率得到(2-Methoxy-1,3-dimethyl-1,3,2-diazaphospholidin-2-ium-2-yl)boranuide
  参考文献：
  名称：

  Molybdenum complexes bearing a diaminosubstituted-phosphiteboryl ligand: Syntheses, structures, and reactivity involving the Mo–B, B–P, and B–H activation

  摘要：

  Photoreaction of diaminosubstituted-phosphiteborane, BH3P(NMeCH2)(2)(OMe) with a methyl molybdenum complex, (eta(5)-C5R5)-Mo(CO)(3)Me (R-5 = Me-5, Me4H, H-5) yielded a phosphiteboryl molybdenum complex, (eta(5)-C5R5)Mo(CO)(3)BH2{P(NMeCH2)(2)(OMe)} (R-5 = Me-5: 2, Me4H: 3, H-5: 4). In the reaction of 2 with MeI, the Mo-B bond was activated to give (eta(5)-C5Me5)Mo(CO)(3)Me, in the reaction with PMe3, the B-P bond was activated to give (eta(5)-C5Me5)Mo(CO)(3)(BH2PMe3). Complex 2 in solution was gradually converted into (eta(5)-C5Me5)MoH(CO)(2){P(NMeCH2)(2)(OMe)} (8) via the B-H bond activation of 2. Structures of 2, 3, and 8 were determined by single crystal X-ray diffraction studies. (c) 2006 Elsevier B.V. All rights reserved.

  DOI：

  10.1016/j.jorganchem.2006.04.049

文献信息

• Synthesis and Reactivity of a Phosphite−Boryl Complex of Molybdenum:  Formation of (η⁵-C₅Me₅)Mo(CO)₃(BH₂·phosphite) and Its Mo−B, B−P, and B−H Bond Reactions
  作者：Hiroshi Nakazawa、Masaharu Ohba、Masumi Itazaki

  DOI：10.1021/om0603159

  日期：2006.6.1

  The photoreaction of Cp*Mo(CO)3Me in the presence of BH3·P(OMe)(NMeCH2)2 produced the phosphite−boryl Mo complex Cp*Mo(CO)3BH2·P(OMe)(NMeCH2)2}. The complex reacts with MeI and PMe3 with Mo−B and B−P bond cleavage, respectively, and is gradually converted in solution into Cp*Mo(CO)2(H)P(OMe)(NMeCH2)2} with B−H bond cleavage.

  Cp * Mo（CO）3 Me在BH 3 ·P（OMe）（NMeCH 2）2存在下的光反应产生亚磷酸酯-硼基Mo络合物Cp * Mo（CO）3 BH 2 ·P（OMe）（ NMeCH 2）2 }。该配合物分别通过Mo-B和B-P键断裂与MeI和PMe 3反应，并在溶液中逐渐转化为Cp * Mo（CO）2（H）P（OMe）（NMeCH 2）2 } B-H键断裂。
• Molybdenum complexes bearing a diaminosubstituted-phosphiteboryl ligand: Syntheses, structures, and reactivity involving the Mo–B, B–P, and B–H activation
  作者：Hiroshi Nakazawa、Masumi Itazaki、Masaharu Ohba

  DOI：10.1016/j.jorganchem.2006.04.049

  日期：2007.1

  Photoreaction of diaminosubstituted-phosphiteborane, BH3P(NMeCH2)(2)(OMe) with a methyl molybdenum complex, (eta(5)-C5R5)-Mo(CO)(3)Me (R-5 = Me-5, Me4H, H-5) yielded a phosphiteboryl molybdenum complex, (eta(5)-C5R5)Mo(CO)(3)BH2P(NMeCH2)(2)(OMe)} (R-5 = Me-5: 2, Me4H: 3, H-5: 4). In the reaction of 2 with MeI, the Mo-B bond was activated to give (eta(5)-C5Me5)Mo(CO)(3)Me, in the reaction with PMe3, the B-P bond was activated to give (eta(5)-C5Me5)Mo(CO)(3)(BH2PMe3). Complex 2 in solution was gradually converted into (eta(5)-C5Me5)MoH(CO)(2)P(NMeCH2)(2)(OMe)} (8) via the B-H bond activation of 2. Structures of 2, 3, and 8 were determined by single crystal X-ray diffraction studies. (c) 2006 Elsevier B.V. All rights reserved.