Bond-dissociation energy (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Bond-dissociation energy" in English language version.

refsWebsite
Global rank English rank
2nd place
2nd place
5th place
5th place
4th place
4th place
18th place
17th place
6th place
6th place
538th place
863rd place
1,712th place
1,063rd place
207th place
136th place
355th place
454th place
70th place
63rd place
11th place
8th place

archive.org

canada.ca

nrc-publications.canada.ca

doi.org

  • IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Bond-dissociation energy". doi:10.1351/goldbook.B00699
  • Mulder P, Korth HG, Pratt DA, DiLabio GA, Valgimigli L, Pedulli GF, Ingold KU (March 2005). "Critical re-evaluation of the O−H bond dissociation enthalpy in phenol". The Journal of Physical Chemistry A. 109 (11): 2647–55. Bibcode:2005JPCA..109.2647M. doi:10.1021/jp047148f. PMID 16833571.
  • Blanksby SJ, Ellison GB (April 2003). "Bond dissociation energies of organic molecules". Accounts of Chemical Research. 36 (4): 255–63. CiteSeerX 10.1.1.616.3043. doi:10.1021/ar020230d. PMID 12693923.
  • Kalescky, Robert; Kraka, Elfi; Cremer, Dieter (2013-08-30). "Identification of the Strongest Bonds in Chemistry". The Journal of Physical Chemistry A. 117 (36): 8981–8995. Bibcode:2013JPCA..117.8981K. doi:10.1021/jp406200w. ISSN 1089-5639. PMID 23927609. S2CID 11884042.
  • Miller DC, Tarantino KT, Knowles RR (June 2016). "Proton-Coupled Electron Transfer in Organic Synthesis: Fundamentals, Applications, and Opportunities". Topics in Current Chemistry. 374 (3): 30. doi:10.1007/s41061-016-0030-6. PMC 5107260. PMID 27573270.
  • Bordwell, F. G.; Cheng, Jin Pei; Harrelson, John A. (February 1988). "Homolytic bond dissociation energies in solution from equilibrium acidity and electrochemical data". Journal of the American Chemical Society. 110 (4): 1229–1231. doi:10.1021/ja00212a035.
  • Gillespie, Ronald J. (July 1998). "Covalent and Ionic Molecules: Why Are BeF2 and AlF3 High Melting Point Solids whereas BF3 and SiF4 Are Gases?". Journal of Chemical Education. 75 (7): 923. Bibcode:1998JChEd..75..923G. doi:10.1021/ed075p923. ISSN 0021-9584.
  • Grills D. C.; George M. W. (2001), "Transition metal-noble gas complexes", Advances in Inorganic Chemistry, Elsevier, pp. 113–150, doi:10.1016/s0898-8838(05)52002-6, ISBN 978-0-12-023652-7.
  • Cerpa, Erick; Krapp, Andreas; Flores-Moreno, Roberto; Donald, Kelling J.; Merino, Gabriel (2009-02-09). "Influence of Endohedral Confinement on the Electronic Interaction between He atoms: A He2@C20H20 Case Study". Chemistry – A European Journal. 15 (8): 1985–1990. doi:10.1002/chem.200801399. ISSN 0947-6539. PMID 19021178.
  • Bartmess, John E.; Scott, Judith A.; McIver, Robert T. (September 1979). "Scale of acidities in the gas phase from methanol to phenol". Journal of the American Chemical Society. 101 (20): 6046–6056. doi:10.1021/ja00514a030.
  • Connelly, Samantha J.; Wiedner, Eric S.; Appel, Aaron M. (2015-03-17). "Predicting the reactivity of hydride donors in water: thermodynamic constants for hydrogen". Dalton Transactions. 44 (13): 5933–5938. doi:10.1039/C4DT03841J. ISSN 1477-9234. PMID 25697077.

harvard.edu

ui.adsabs.harvard.edu

iupac.org

goldbook.iupac.org

  • IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Bond-dissociation energy". doi:10.1351/goldbook.B00699

loc.gov

lccn.loc.gov

nih.gov

pubmed.ncbi.nlm.nih.gov

ncbi.nlm.nih.gov

nist.gov

nvlpubs.nist.gov

psu.edu

citeseerx.ist.psu.edu

semanticscholar.org

api.semanticscholar.org

worldcat.org