New learning discoveries about 1662-01-7

The synthetic route of 1662-01-7 has been constantly updated, and we look forward to future research findings.

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.1662-01-7,4,7-Diphenyl-1,10-phenanthroline,as a common compound, the synthetic route is as follows.

General procedure: The pentafluorinated beta-diketone ligand (3 mmol), NaOH(0.12 g, 3 mmol) and the auxiliary ligand (1 mmol) were dissolved in 30 mL ethanol and heated to 60 C under stirring. Then, the ethanolic solution of EuCl3¡¤6H2O(1 mmol) was added dropwise, and the reaction mixture was stirred at 60 C for 8 h. After cooling down, the yellow solid was precipitated and filtered off. The solidproduct was washed with deionized water and ethanol, and dried in vacuum. Yellow powder, yield 78%, mp 200-202 C; IR nu (KBr):3031(m), 2967 (m), 2843 (w), 1597 (s), 1572 (s), 1501 (s), 1258 (s), 1172 (s),1082 (m), 1013 (m), 930 (m), 845 (m), 789 (s), 588 (m), 508 (m) cm-1; 1H NMR(300 MHz, CDCl3):delta 3.70 (s, 3H, C=CH), 3.94 (s, 9H, OCH3),6.86 (br, 6H, Ar-H),7.61 (br, 6H, Ar-H), 7.96 (br, 2H, Bath-H), 8.17 (br, 4H, Bath-H), 8.58 (br, 2H,Bath-H), 8.73 (br, 4H, Bath-H), 9.24 (br, 2H, Bath-H), 12.10 (br, 2H, Bath-H) ppm.Anal. Calcd. for EuC60H40N2O9F15:C, 52.61; H, 2.94; N, 2.04; Eu, 11.09; Found C,52.94; H, 2.91; N, 2.09; Eu, 11.25.

The synthetic route of 1662-01-7 has been constantly updated, and we look forward to future research findings.

Reference£º
Article; Wan, Yupeng; Lyu, Heng; Du, Hengyi; Wang, Dunjia; Yin, Guodong; Research on Chemical Intermediates; vol. 45; 4; (2019); p. 1669 – 1687;,
Metal catalyst and ligand design
Ligand Template Strategies for Catalyst Encapsulation – NCBI