cis-PtCl2(C2H4(P(C5H4N)2)2) | 244193-89-3

• 英文名称: cis-PtCl2(C2H4(P(C5H4N)2)2)
• CAS: 244193-89-3
• 化学式: C₂₂H₂₀Cl₂N₄P₂Pt
• 分子量: 668.361
• InChiKey: FVRTWRJFPNNKHQ-UHFFFAOYSA-L

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

• 作为产物：
  描述：

  1,2-二(二-2-吡啶基膦酰)乙烷 、 dichloro( 1,5-cyclooctadiene)platinum(ll) 以 二氯甲烷 为溶剂， 以70%的产率得到cis-PtCl2(C2H4(P(C5H4N)2)2)
  参考文献：
  名称：

  Coordination Chemistry of the 2-Pyridyldiphosphine Ligands, (py)₂P(CH(CH₂)₃CH)P(py)₂ and (py)₂P(CH₂)₂P(py)₂ (py = 2-Pyridyl), with Platinum(II) and Ruthenium(II). Ruthenium-Catalyzed Hydrogenation of Imines

  摘要：

  The synthesis and characterization of a range of Pt(II) and Ru(II) complexes containing the new 2-pyridyldi-phosphine ligand, d(py)pcp = (py)(2)P(CH(CH2)(3)CH)P(py)(2) (made as a racemate) and the previously reported d(py)pe = (py)(2)P(CH2)(2)P(py)(2) are given (py =2-pyridyl). The Pt complexes made were cis-PtX2(d(py)pcp) (X = Cl (1), I (2)), cis-PtX2(d(py)pe) (X = Cl (3), I (4)), [Pt(d(py)pcp)(2)][PF6](2) (5), and [Pt(d(py)pe)(2)][PF6](2) (6); these all contain P,P-bonded diphosphine ligand, as evidenced by P-31 NMR data and by crystallographic data in the case of 2 and 3. The X-ray structure of d(py)pe is also reported. The complexes RuX2(P,P,N-d(py)pcp)(PPh3) have cis-halogens and a P,P,N-bonding mode of the pyridyldiphosphine (which incorporates a four-membered P,N-chelate ring) with either a mer-arrangement (in 7a, X = Cl) or a fac-arrangement of the three P donor atoms (in 7b (X = Cl), 8 (X = Br), 9 (X = I)); cis-RuCl2(dppb)(P,N-PPh2(py)) (12) (dppb = Ph-2(CH2)(4)PPh2) is included because it has a donor set corresponding to that in 7b. Use of the purely P,P donor Ph2P(CH(CH2)(3)CH)PPh2 (dppcp), made as a racemate, affords trans-RuCl2(dppcp)(2) (10) and trans-RuCl2(dppcp)(dppb) (II). Crystallographic data for 7a, 7b, and 12 are reported together with the NMR data for all the Ru complexes. Preliminary results show that the Ru complexes 7b, 8, and 9 are effective precursors for catalytic H-2-hydrogenation of aldimines.

  DOI：

  10.1021/ic990002o