5,10,15,20-四(4-磺酸基苯基)卟啉

化合物

5,10,15,20-四(4-磺酸基苯基)卟啉是一種有機化合物,化學式為C44H30N4O12S4。它可由四苯基卟啉英語Tetraphenylporphyrin硫酸加熱反應,[1]或直接和氯磺酸反應得到。[2]它和金屬鹽反應,可以得到相應的配合物。[3][4]

5,10,15,20-四(4-磺酸基苯基)卟啉
識別
CAS號 35218-75-8  checkY
PubChem 49561
性質
化學式 C44H30N4O12S4
摩爾質量 934.99 g·mol−1
相關物質
相關化學品 5,10,15,20-四(4-羧基苯基)卟啉
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。

參考文獻

編輯
  1. ^ Belete B. Beyene, Sandeep B. Mane, Chen-Hsiung Hung. Highly efficient electrocatalytic hydrogen evolution from neutral aqueous solution by a water-soluble anionic cobalt( ii ) porphyrin. Chemical Communications. 2015, 51 (81): 15067–15070 [2021-08-24]. ISSN 1359-7345. doi:10.1039/C5CC05582B (英語). 
  2. ^ Guan Huang, Chao Yan, Jing Li Cai, Lin Qiang Mo, Shu Kai Zhao, Yong An Guo, Su Juan Wei, Yan Ling Shen. Practicably efficient ethylbenzene oxidation catalyzed by manganese tetrakis(4-sulfonatophenyl)porphyrin grafted to powdered chitosan. Journal of Porphyrins and Phthalocyanines. 2018-06, 22 (06): 481–490 [2021-08-24]. ISSN 1088-4246. doi:10.1142/S1088424618500414. (原始內容存檔於2021-08-24) (英語). 
  3. ^ Akimitsu Miyaji, Yutaka Amao. Visible‐Light Driven CO 2 Reduction to Formate with Electron Mediated Nicotinamide‐Modified Viologen in the System of Water‐Soluble Zinc Porphyrin and Formate Dehydrogenase. ChemNanoMat. 2021-06, 7 (6): 626–634 [2021-08-24]. ISSN 2199-692X. doi:10.1002/cnma.202100045 (英語). 
  4. ^ Wen-Tong Chen, Jian-Gen Hang, Xiang-Yang Lei, Rong-Hua Hu, Yun-Peng Pei, Yun-Xia Yang, Jie Zhou. A novel gadolinium tetra(4-sulfonatophenyl)porphyrin–amino acid complex with interesting photophysical and electrochemical properties. Journal of the Iranian Chemical Society. 2016-01, 13 (1): 95–101 [2021-08-24]. ISSN 1735-207X. doi:10.1007/s13738-015-0716-7 (英語).