| 277302-90-6

• CAS: 277302-90-6
• 化学式: BF₄*C₃₀H₅₇O₃OsP₂
• 分子量: 804.733
• InChiKey: YRRXHRLPBNQWPO-GKXFERKMSA-M

计算性质

• 辛醇/水分配系数(LogP)：
  None
• 重原子数：
  None
• 可旋转键数：
  None
• 环数：
  None
• sp3杂化的碳原子比例：
  None
• 拓扑面积：
  None
• 氢给体数：
  None
• 氢受体数：
  None

反应信息

• 作为反应物：
  描述：

  、 在 NaOMe 作用下， 以 四氢呋喃 为溶剂， 以15%的产率得到
  参考文献：
  名称：

  Hydride−Hydroxyosmacyclopropene versus Hydride−Hydroxycarbyne and Cyclic Hydroxycarbene:  Influence of the Substituents at the C(OH) Carbon Atom of the Carbon Donor Ligand

  摘要：

  The dihydride [OsH2(kappa(2)-O2CCH3)(H2O)((PPr3)-Pr-i)(2)]BF4 (1) reacts with 2-phenyl-3-butyn-2-ol and 2-methyl-3-butyn-2-ol to give isomeric mixtures of the corresponding hydride-hydroxyosmacyclopropene, [OsH(kappa(2)-O2CCH3){C[C(OH)MeR]CH2}((PPr3)-Pr-i)(2)]BF4 (R = Ph (3), Me (5)), and hydride-hydroxycarbyne, [OsH(kappa(2)-O2CCH3){=CCH2C(OH)MeR}((PPr3)-Pr-i)(2)]BF4 (R = Ph (4), Me (6)), derivatives. In solution, complexes 3 and 5 and the related compound [OsH-(kappa(2)-O2CCH3){C[C(OH)Ph-2]CH2}((PPr3)-Pr-i)(2)]BF4 (2) is isomerize into the cyclic hydroxycarbenes [Os-(kappa(2)-O2CCH3){C(Me)C(OH)RR'}((PPr3)-Pr-i)(2)]BF4 (R = R' = Ph (7); R = Ph, R' = Me (8); R = R' = Me (9)). The structure of 8 in the solid state has been determined by X-ray diffraction analysis. The geometry around the osmium center can be rationalized as a very distorted octahedron, with the phosphine ligands occupying cis positions (P-Os-P = 103.71(6)degrees). Reaction of 2 with sodium methoxide leads to the eta(2)-vinyl alkoxide derivative Os{eta(2)-CH2=CHC(Ph)(2)O}-(kappa(2)-O2CCH3)((PPr3)-Pr-i)(2) (10), which by protonation with HBF4 affords the eta(2)-1,1-diphenyl-2-propenol complex [Os(kappa(2)-O2CCH3){eta(2)-CH2=CHC(OH)Ph-2}((PPr3)-Pr-i)(2)]BF4_(11). The structure of 10 has also been determined by X-ray diffraction analysis. As for 8, the geometry around the osmium atom can be rationalized as a very distorted octahedron with the phosphine ligands occupying cis positions (P-Os-P = 106.72(4)degrees). The reaction of 8 with sodium methoxide leads to the osmaoxacyclobutene derivative Os{C(Me)C(O)MePh}(kappa(2)-O2CCH3)((PPr3)-Pr-i)(2) (12), which on protonation with HBF4. OEt2 regenerates 8. Treatment of 4 with sodium methoxide gives the hydride-vinylidene OsH(kappa(2)-O2CCH3){=C=CHC(Ph)=CH2}((PPr3)-Pr-i)(2) (13). The formation of the hydride-alkenylcarbynes [OsH(kappa(2)-O2CCH3)(=CCH=CRMe)((PPr3)-Pr-i)(2)]BF4 (R = Ph (14), Me (15)) by dehydration of 4 and 6 is also reported.

  DOI：

  10.1021/om9909542
• 作为产物：
  描述：

  2-苯基-3-丁炔-2-醇 、 以 二氯甲烷 为溶剂， 以36%的产率得到
  参考文献：
  名称：

  Hydride−Hydroxyosmacyclopropene versus Hydride−Hydroxycarbyne and Cyclic Hydroxycarbene:  Influence of the Substituents at the C(OH) Carbon Atom of the Carbon Donor Ligand

  摘要：

  The dihydride [OsH2(kappa(2)-O2CCH3)(H2O)((PPr3)-Pr-i)(2)]BF4 (1) reacts with 2-phenyl-3-butyn-2-ol and 2-methyl-3-butyn-2-ol to give isomeric mixtures of the corresponding hydride-hydroxyosmacyclopropene, [OsH(kappa(2)-O2CCH3){C[C(OH)MeR]CH2}((PPr3)-Pr-i)(2)]BF4 (R = Ph (3), Me (5)), and hydride-hydroxycarbyne, [OsH(kappa(2)-O2CCH3){=CCH2C(OH)MeR}((PPr3)-Pr-i)(2)]BF4 (R = Ph (4), Me (6)), derivatives. In solution, complexes 3 and 5 and the related compound [OsH-(kappa(2)-O2CCH3){C[C(OH)Ph-2]CH2}((PPr3)-Pr-i)(2)]BF4 (2) is isomerize into the cyclic hydroxycarbenes [Os-(kappa(2)-O2CCH3){C(Me)C(OH)RR'}((PPr3)-Pr-i)(2)]BF4 (R = R' = Ph (7); R = Ph, R' = Me (8); R = R' = Me (9)). The structure of 8 in the solid state has been determined by X-ray diffraction analysis. The geometry around the osmium center can be rationalized as a very distorted octahedron, with the phosphine ligands occupying cis positions (P-Os-P = 103.71(6)degrees). Reaction of 2 with sodium methoxide leads to the eta(2)-vinyl alkoxide derivative Os{eta(2)-CH2=CHC(Ph)(2)O}-(kappa(2)-O2CCH3)((PPr3)-Pr-i)(2) (10), which by protonation with HBF4 affords the eta(2)-1,1-diphenyl-2-propenol complex [Os(kappa(2)-O2CCH3){eta(2)-CH2=CHC(OH)Ph-2}((PPr3)-Pr-i)(2)]BF4_(11). The structure of 10 has also been determined by X-ray diffraction analysis. As for 8, the geometry around the osmium atom can be rationalized as a very distorted octahedron with the phosphine ligands occupying cis positions (P-Os-P = 106.72(4)degrees). The reaction of 8 with sodium methoxide leads to the osmaoxacyclobutene derivative Os{C(Me)C(O)MePh}(kappa(2)-O2CCH3)((PPr3)-Pr-i)(2) (12), which on protonation with HBF4. OEt2 regenerates 8. Treatment of 4 with sodium methoxide gives the hydride-vinylidene OsH(kappa(2)-O2CCH3){=C=CHC(Ph)=CH2}((PPr3)-Pr-i)(2) (13). The formation of the hydride-alkenylcarbynes [OsH(kappa(2)-O2CCH3)(=CCH=CRMe)((PPr3)-Pr-i)(2)]BF4 (R = Ph (14), Me (15)) by dehydration of 4 and 6 is also reported.

  DOI：

  10.1021/om9909542