溶媒効果 (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "溶媒効果" in Japanese language version.

refsWebsite

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8doi.org

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4nih.gov

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1wisc.edu

1,045^th place

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1harvard.edu

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doi.org

“Pentakis(trifluoromethyl)phenyl, a Sterically Crowded and Electron-withdrawing Group: Synthesis and Acidity of Pentakis(trifluoromethyl)benzene, -toluene, -phenol, and -aniline”. J. Org. Chem. 73 (7): 2607–2620. (2008). doi:10.1021/jo702513w. PMID 18324831.
Kütt, A.; Leito, I.; Kaljurand, I.; Sooväli, L.; Vlasov, V.M.; Yagupolskii, L.M.; Koppel, I.A. (2006). “A Comprehensive Self-Consistent Spectrophotometric Acidity Scale of Neutral Brønsted Acids in Acetonitrile”. J. Org. Chem. 71 (7): 2829–2838. doi:10.1021/jo060031y. PMID 16555839.
“Extension of the Self-Consistent Spectrophotometric Basicity Scale in Acetonitrile to a Full Span of 28 pKa Units: Unification of Different Basicity Scales”. J. Org. Chem. 70 (3): 1019–1028. (2005). doi:10.1021/jo048252w. PMID 15675863.
James T. Hynes (1985). “Chemical Reaction Dynamics in Solution”. Annu. Rev. Phys. Chem. 36 (1): 573–597. Bibcode: 1985ARPC...36..573H. doi:10.1146/annurev.pc.36.100185.003041.
Hughes, Edward D.; Ingold, Christopher K. (1935). “Mechanism of substitution at a saturated carbon atom. Part IV. A discussion of constitutional and solvent effects on the mechanism, kinetics, velocity, and orientation of substitution”. J. Chem. Soc.: 244–255. doi:10.1039/JR9350000244. https://doi.org/10.1039/JR9350000244.
Yongho, Kim.; Cramer, Christopher J.; Truhlar, Donald G. (2009). “Steric Effects and Solvent Effects on S_N2 Reactions”. J. Phys. Chem. A 113 (32): 9109–9114. doi:10.1021/jp905429p. PMID 19719294.
V. P. Ananikov; D. G. Musaev; K. Morokuma (2001). “Catalytic Triple Bond Activation and Vinyl−Vinyl Reductive Coupling by Pt(IV) Complexes. A Density Functional Study”. Organometallics 20 (8): 1652–1667. doi:10.1021/om001073u.
Grzegorz Litwinienko; A. L. J. Beckwith; K. U. Ingold (2011). “The frequently overlooked importance of solvent in free radical syntheses”. Chem. Soc. Rev. 40 (5): 2157. doi:10.1039/C1CS15007C.

harvard.edu

ui.adsabs.harvard.edu

James T. Hynes (1985). “Chemical Reaction Dynamics in Solution”. Annu. Rev. Phys. Chem. 36 (1): 573–597. Bibcode: 1985ARPC...36..573H. doi:10.1146/annurev.pc.36.100185.003041.

nih.gov

pubmed.ncbi.nlm.nih.gov

“Pentakis(trifluoromethyl)phenyl, a Sterically Crowded and Electron-withdrawing Group: Synthesis and Acidity of Pentakis(trifluoromethyl)benzene, -toluene, -phenol, and -aniline”. J. Org. Chem. 73 (7): 2607–2620. (2008). doi:10.1021/jo702513w. PMID 18324831.
Kütt, A.; Leito, I.; Kaljurand, I.; Sooväli, L.; Vlasov, V.M.; Yagupolskii, L.M.; Koppel, I.A. (2006). “A Comprehensive Self-Consistent Spectrophotometric Acidity Scale of Neutral Brønsted Acids in Acetonitrile”. J. Org. Chem. 71 (7): 2829–2838. doi:10.1021/jo060031y. PMID 16555839.
“Extension of the Self-Consistent Spectrophotometric Basicity Scale in Acetonitrile to a Full Span of 28 pKa Units: Unification of Different Basicity Scales”. J. Org. Chem. 70 (3): 1019–1028. (2005). doi:10.1021/jo048252w. PMID 15675863.
Yongho, Kim.; Cramer, Christopher J.; Truhlar, Donald G. (2009). “Steric Effects and Solvent Effects on S_N2 Reactions”. J. Phys. Chem. A 113 (32): 9109–9114. doi:10.1021/jp905429p. PMID 19719294.

wisc.edu

chem.wisc.edu

“Bordwell pKa Table (Acidity in DMSO)”. 2008年11月2日閲覧。