Lewis acids and bases (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Lewis acids and bases" in English language version.

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books.google.com

  • Lewis, Gilbert Newton (1923). Valence and the Structure of Atoms and Molecules. American chemical society. Monograph series. New York, New York, U.S.A.: Chemical Catalog Company. p. 142. ISBN 9780598985408. From p. 142: "We are inclined to think of substances as possessing acid or basic properties, without having a particular solvent in mind. It seems to me that with complete generality we may say that a basic substance is one which has a lone pair of electrons which may be used to complete the stable group of another atom, and that an acid substance is one which can employ a lone pair from another molecule in completing the stable group of one of its own atoms. In other words, the basic substance furnishes a pair of electrons for a chemical bond, the acid substance accepts such a pair."

doi.org

  • IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Lewis acid". doi:10.1351/goldbook.L03508
  • Lepetit, Christine; Maraval, Valérie; Canac, Yves; Chauvin, Remi (2016). "On the Nature of the Dative Bond: Coordination to Metals and Beyond. The Carbon Case". Coordination Chemistry Reviews. 308: 59–75. doi:10.1016/j.ccr.2015.07.018.
  • IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Electrophile (Electrophilic)". doi:10.1351/goldbook.E02020
  • Rowsell, Bryan D.; Gillespie, Ronald J.; Heard, George L. (1999). "Ligand Close-Packing and the Lewis Acidity of BF3 and BCl3". Inorganic Chemistry. 38 (21): 4659–4662. doi:10.1021/ic990713m. PMID 11671188.
  • Traditionally, but not precisely, H+ ions are referred as "protons". See IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "hydron". doi:10.1351/goldbook.H02904
  • Childs, R.F; Mulholland, D.L; Nixon, A. (1982). "Lewis acid adducts of α,β-unsaturated carbonyl and nitrile compounds. A nuclear magnetic resonance study". Can. J. Chem. 60 (6): 801–808. doi:10.1139/v82-117.
  • Vogel, Glenn C.; Drago, Russell S. (1996). "The ECW Model". Journal of Chemical Education. 73 (8): 701. Bibcode:1996JChEd..73..701V. doi:10.1021/ed073p701.
  • Cramer, Roger E.; Bopp, Thomas T. (1977). "Great e and C plot. Graphical display of the enthalpies of adduct formation for Lewis acids and bases". Journal of Chemical Education. 54 (10): 612. Bibcode:1977JChEd..54..612C. doi:10.1021/ed054p612.
  • Lewis, Gilbert N. (April 1916). "The atom and the molecule". Journal of the American Chemical Society. 38 (4): 762–785. doi:10.1021/ja02261a002. S2CID 95865413.
  • Brown, Herbert C.; Kanner, Bernard (1966). "Preparation and Reactions of 2,6-Di-t-butylpyridine and Related Hindered Bases. A Case of Steric Hindrance toward the Proton". Journal of the American Chemical Society. 88 (5): 986–992. doi:10.1021/ja00957a023.

harvard.edu

ui.adsabs.harvard.edu

hathitrust.org

babel.hathitrust.org

iupac.org

goldbook.iupac.org

  • IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Lewis acid". doi:10.1351/goldbook.L03508
  • IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Electrophile (Electrophilic)". doi:10.1351/goldbook.E02020
  • Traditionally, but not precisely, H+ ions are referred as "protons". See IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "hydron". doi:10.1351/goldbook.H02904

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Rowsell, Bryan D.; Gillespie, Ronald J.; Heard, George L. (1999). "Ligand Close-Packing and the Lewis Acidity of BF3 and BCl3". Inorganic Chemistry. 38 (21): 4659–4662. doi:10.1021/ic990713m. PMID 11671188.

semanticscholar.org

api.semanticscholar.org

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