Homolysis (chemistry) (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Homolysis (chemistry)" in English language version.

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acs.org

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aip.org

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doi.org

  • IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "homolysis (homolytic)". doi:10.1351/goldbook.H02851
  • St. John, P.C., Guan, Y., Kim, Y. et al. Prediction of organic homolytic bond dissociation enthalpies at near chemical accuracy with sub-second computational cost. Nat Commun 11, 2328 (2020). https://doi.org/10.1038/s41467-020-16201-z
  • IUPAC. Compendium of Chemical Terminology, 2nd ed. (the "Gold Book"). Compiled by A. D. McNaught and A. Wilkinson. Blackwell Scientific Publications, Oxford (1997). Online version (2019-) created by S. J. Chalk. ISBN 0-9678550-9-8. https://doi.org/10.1351/goldbook.
  • Jost, Marco; Born, David A.; Cracan, Valentin; Banerjee, Ruma; Drennan, Catherine L. (2015). "Structural Basis for Substrate Specificity in Adenosylcobalamin-dependent Isobutyryl-CoA Mutase and Related Acyl-CoA Mutases". Journal of Biological Chemistry. 290 (45): 26882–26898. doi:10.1074/jbc.M115.676890. PMC 4646380. PMID 26318610.
  • Müller, Holger S. P.; Miller, Charles E.; Cohen, Edward A. (1997-11-22). "The rotational spectrum and molecular properties of bromine dioxide, OBrO". The Journal of Chemical Physics. 107 (20): 8292–8302. doi:10.1063/1.475030.
  • Gronert, Scott (2006-02-01). "An Alternative Interpretation of the C−H Bond Strengths of Alkanes". The Journal of Organic Chemistry. 71 (3): 1209–1219. doi:10.1021/jo052363t.

iupac.org

goldbook.iupac.org

  • IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "homolysis (homolytic)". doi:10.1351/goldbook.H02851

jstor.org

  • Mendenhall, G. (1978). "Long-lived free radicals". Science Progress (1933- ), 65(257), 1-18. JSTOR 43420441. Retrieved December 5, 2020.

nih.gov

ncbi.nlm.nih.gov

pubmed.ncbi.nlm.nih.gov