Homolysis (chemistry) (English Wikipedia)

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

refsWebsite

Global rank English rank

7doi.org

2^nd place

2acs.org

1,248^th place

1,104^th place

2nih.gov

4^th place

1iupac.org

538^th place

863^rd place

1jstor.org

26^th place

20^th place

1aip.org

2,204^th place

1,735^th place

acs.org

pubs.acs.org

Kristina Lekin, Hoa Phan, Stephen M. Winter, Joanne W. L. Wong, Alicea A. Leitch, Dominique Laniel, Wenjun Yong, Richard A. Secco, John S. Tse, Serge Desgreniers, Paul A. Dube, Michael Shatruk, and Richard T. Oakley, "Heat, Pressure and Light-Induced Interconversion of Bisdithiazolyl Radicals and Dimers", Journal of the American Chemical Society, 2014, 136 (22), 8050-8062, doi:10.1021/ja502753t.
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.

aip.org

pubs.aip.org

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.

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.
Kristina Lekin, Hoa Phan, Stephen M. Winter, Joanne W. L. Wong, Alicea A. Leitch, Dominique Laniel, Wenjun Yong, Richard A. Secco, John S. Tse, Serge Desgreniers, Paul A. Dube, Michael Shatruk, and Richard T. Oakley, "Heat, Pressure and Light-Induced Interconversion of Bisdithiazolyl Radicals and Dimers", Journal of the American Chemical Society, 2014, 136 (22), 8050-8062, doi:10.1021/ja502753t.
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

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.

pubmed.ncbi.nlm.nih.gov

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.