四(4-氟苯甲酸)二铑

四(4-氟苯甲酸)二铑
识别
CAS号	158051-44-6
SMILES	FC=1C=CC(=CC1)C2=O[Rh+2]345O=C([O-][Rh+2]5(O=C([O-]3)C=6C=CC(F)=CC6)(O=C([O-]4)C=7C=CC(F)=CC7)[O-]2)C=8C=CC(F)=CC8;
性质
化学式	C28H16F4O8Rh2
摩尔质量	762.23 g·mol−1
	若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。

四(4-氟苯甲酸)二铑是一种化合物，化学式为C₂₈H₁₆F₄O₈Rh₂。它可由四乙酸二铑和4-氟苯甲酸在碳酸钠存在下于氯苯中回流反应制得。^[1]它可以催化(2-(4-甲氧基苄氧基)苯基)(苯基)亚甲基肼和二氧化锰的氧化反应，生成(2R,3S)-2,3-二氢-2-(4-甲氧基苯基)-3-苯并呋喃。^[2]

参考文献

^ Electronic Effects in Dirhodium(II) Carboxylates. Linear Free Energy Relationships in Catalyzed Decompositions of Diazo Compounds and CO and Isonitrile Complexation. J. Am. Chem. Soc. 1994. doi:10.1021/ja00099a017.
^ Synthesis of Benzodihydrofurans by Asymmetric C−H Insertion Reactions of Donor/Donor Rhodium Carbenes. Chem A Eur J. 2017. doi:10.1002/chem.201701630.

[1] Electronic Effects in Dirhodium(II) Carboxylates. Linear Free Energy Relationships in Catalyzed Decompositions of Diazo Compounds and CO and Isonitrile Complexation. J. Am. Chem. Soc. 1994. doi:10.1021/ja00099a017.

[2] Synthesis of Benzodihydrofurans by Asymmetric C−H Insertion Reactions of Donor/Donor Rhodium Carbenes. Chem A Eur J. 2017. doi:10.1002/chem.201701630.

[1]

[2]

四(4-氟苯甲酸)二铑
识别
CAS号	158051-44-6 ^Y
SMILES	FC=1C=CC(=CC1)C2=O[Rh+2]345O=C([O-][Rh+2]5(O=C([O-]3)C=6C=CC(F)=CC6)(O=C([O-]4)C=7C=CC(F)=CC7)[O-]2)C=8C=CC(F)=CC8
性质
化学式	C₂₈H₁₆F₄O₈Rh₂
摩尔质量	762.23 g·mol⁻¹
若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。