Rujukan Difenilmetana

  1. ↑ International Union of Pure and Applied Chemistry (2014). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. The Royal Society of Chemistry. m/s. 452. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.
  2. ↑ W. W. Hartman and Ross Phillips (1934). "Diphenylmethane". Organic Syntheses. 14: 34. doi:10.15227/orgsyn.014.0034.
  3. 1 2 Hauser, Charles R.; Hamrick, Phillip J. (1957). "Alkylation of Diphenylmethane with Alkyl Halides by Sodium Amide. Substitution versus β-Elimination. Relative Acidities of Diphenylmethane and Ammonia". J. Am. Chem. Soc. 79 (12): 3142–3145. doi:10.1021/ja01569a041.
  4. 1 2 Murphy, William S.; Hamrick, Phillip J.; Hauser, Charles R. (1968). "1,1-Diphenylpentane". Organic Syntheses. 48: 80. doi:10.15227/orgsyn.048.0080.
  5. ↑ Zhang, Xian-Man; Bordwell, Frederick G. (1992). "Homolytic bond dissociation energies of the benzylic carbon-hydrogen bonds in radical anions and radical cations derived from fluorenes, triphenylmethanes, and related compounds". J. Am. Chem. Soc. 114 (25): 9787–9792. doi:10.1021/ja00051a010.
  6. ↑ Blanksby, S. J.; Ellison, G. B. (2003). "Bond Dissociation Energies of Organic Molecules". Accounts of Chemical Research. 36 (4): 255–263. doi:10.1021/ar020230d. PMID 12693923.
  7. ↑ Streitwieser, Andrew; Bergman, Robert G. (2018). "Table of Bond Dissociation Energies". University of California, Berkeley. Dicapai pada December 30, 2021.