Tham khảo Phenanthroline

  1. ↑ Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013 (Blue Book).
  2. ↑ Durand, J., et al., "Long-Lived Palladium Catalysts for Co/Vinyl Arene Polyketones Synthesis: A Solution to Deactivation Problems", Chemistry – A European Journal 2006, volume 12, 7639-7651. doi:10.1002/chem.200501047
  3. ↑ C.R. Luman, F.N. Castellano "Phenanthroline Ligands" in Comprehensive Coordination Chemistry II, 2003, Elsevier. ISBN 978-0-08-043748-4
  4. ↑ B. E. Halcrow; W. O. Kermack (1946). “43. Attempts to find new antimalarials. Part XXIV. Derivatives of o-phenanthroline (7: 8: 3′: 2′-pyridoquinoline)”. J. Chem. Soc.: 155–157. doi:10.1039/jr9460000155.
  5. ↑ Teng, Qiaoqiao; Huynh, Han Vinh (2017). “A unified ligand electronic parameter based on C NMR spectroscopy of N-heterocyclic carbene complexes”. Dalton Transactions. 46 (3): 614–627. doi:10.1039/C6DT04222H.
  6. ↑ Belcher, R. "Application of chelate Compounds in Analytical Chemistry" Pure and Applied Chemistry, 1973, volume 34, pages 13-27.
  7. ↑ Bellér, G. B.; Lente, G. B.; Fábián, I. N. (2010). “Central Role of Phenanthroline Mono-N-oxide in the Decomposition Reactions of Tris(1,10-phenanthroline)iron(II) and -iron(III) Complexes”. Inorganic Chemistry. 49: 3968–3970. doi:10.1021/ic902554b. PMID 20415494.
  8. ↑ George B. Kauffman, Lloyd T. Takahashi (1966). “Resolution of the tris-(1,10-Phenanthroline)Nickel(II) Ion”. Inorg. Synth. 5: 227–232. doi:10.1002/9780470132395.ch60.
  9. ↑ Armaroli, N., "Photoactive Mono- and Polynuclear Cu(I)-Phenanthrolines.
  10. 1 2 Pallenberg, A. J.; Koenig, K. S.; Barnhart, D. M., "Synthesis and Characterization of Some Copper(I) Phenanthroline Complexes", Inorg.
  11. ↑ F. P. Dwyer; E. C. Gyarfas; W. P. Rogers; J. H. Koch (1952). “Biological Activity of Complex Ions”. Nature. 170 (4318): 190–191. doi:10.1038/170190a0. PMID 12982853.
  12. ↑ Felber, JP, Coombs, TL & Vallee, BL (1962). “The mechanism of inhibition of carboxypeptidase A by 1,10-phenanthroline”. Biochemistry. 1 (2): 231–238. doi:10.1021/bi00908a006. PMID 13892106.Quản lý CS1: nhiều tên: danh sách tác giả (liên kết)
  13. ↑ Salvesen, GS; Nagase, H (2001). “Inhibition of proteolytic enzymes”. Proteolytic enzymes: a practical approach, 2 edn. 1: 105–130. Đã bỏ qua tham số không rõ |last-author-amp= (gợi ý |name-list-style=) (trợ giúp)
  14. ↑ J. G. Leipoldt, G. J. Lamprecht, E. C.Steynberg (1991). “Kinetics of the substitution of acetylacetone in acetylactonato-1,5-cyclooctadienerhodium(I) by derivatives of 1,10-phenantrholine and 2,2′-dipyridyl”. Journal of Organometallic Chemistry. 402: 259–263. doi:10.1016/0022-328X(91)83069-G.Quản lý CS1: nhiều tên: danh sách tác giả (liên kết)
  15. ↑ eEROS. 2008. doi:10.1002/047084289X.rn00918. |title= trống hay bị thiếu (trợ giúp)
  16. ↑ Preston, H. S.; Kennard, C. H. L. (1969). “Crystal Structure of di-mu-Chloro-sym-trans-Dichloro-Bis-(2,9-Dimethyl-1,10-Phenanthroline)dinickel(II)-2-Chloroform”. J. Chem. Soc. A: 2682–2685. doi:10.1039/J19690002682.
  17. ↑ Paul J. Fagan and William A. Nugent (1998). “1-Phenyl-2,3,4,5-Tetramethylphosphole”. Organic Syntheses.; Collective Volume, 9, tr. 653
  18. ↑ Ho-Shen Lin; Leo A. Paquette (1994). “A Convenient Method for Determining the Concentration of Grignard Reagents”. Synth. Commun. 24 (17): 2503–2506. doi:10.1080/00397919408010560.

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