氟對苯二甲酸

氟對苯二甲酸是一種有機化合物,化學式為C8H5FO4。它可由氟對二甲苯硝酸在200 °C的反應釜中反應得到。[1]它在四氫呋喃中可以被甲硫醚硼烷還原為氟對苯二甲醇。[2]它可以和金屬(ZnII[3]、CrIII[4]、ZrIV[5]等)形成配位聚合物

氟對苯二甲酸
別名 2-氟-1,4-苯二甲酸
識別
CAS號 3906-87-4  checkY
PubChem 77511
性質
化學式 C8H5FO4
摩爾質量 184.12 g·mol−1
沸點 330 °C(603 K)(升華)[1]
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. ^ 1.0 1.1 G. Valkanas; H. Hopff. 651. Fluoro- and Difluoro-benzodicarboxylic Acids and Their Anhydrides. Journal of the Chemical Society (Resumed). 1963: 3475–3476 [2022-12-16]. ISSN 0368-1769. doi:10.1039/jr9630003456. (原始內容存檔於2022-12-16) (英語). 
  2. ^ Yujia He, Tingting Fu, Yuying Li, Weiwei Xue, Mengchao Cui, Liang Wang, Mengda Niu, Zhiping Peng, Jianhua Jia. Flexible multidentate benzyldiamine derivatives with high affinity for β-amyloid in cerebral amyloid angiopathy. Molecular Diversity. 2021-02, 25 (1): 525–533 [2022-12-16]. ISSN 1381-1991. doi:10.1007/s11030-020-10098-y (英語). 
  3. ^ Scott T. Meek, John J. Perry, Stephanie L. Teich-McGoldrick, Jeffery A. Greathouse, Mark D. Allendorf. Complete Series of Monohalogenated Isoreticular Metal–Organic Frameworks: Synthesis and the Importance of Activation Method. Crystal Growth & Design. 2011-10-05, 11 (10): 4309–4312 [2022-12-16]. ISSN 1528-7483. doi:10.1021/cg201136k. (原始內容存檔於2022-12-16) (英語). 
  4. ^ Feifei Xue, Jian Cao, Xiaoting Li, Jingjing Feng, Minli Tao, Bin Xue. Continuous-flow synthesis of MIL-53(Cr) with a polar linker: probing the nanoscale piezoelectric effect. Journal of Materials Chemistry C. 2021, 9 (24): 7568–7574 [2022-12-16]. ISSN 2050-7526. doi:10.1039/D0TC06013E (英語). 
  5. ^ Qihao Yang, Yinming Wang, Xuan Tang, Qiuju Zhang, Sheng Dai, Huaitao Peng, Yichao Lin, Ziqi Tian, Zhiyi Lu, Liang Chen. Ligand Defect Density Regulation in Metal–Organic Frameworks by Functional Group Engineering on Linkers. Nano Letters. 2022-01-26, 22 (2): 838–845 [2022-12-16]. ISSN 1530-6984. doi:10.1021/acs.nanolett.1c04574. (原始內容存檔於2023-05-17) (英語).