A Comprehensive Self-Consistent Spectrophotometric Acidity Scale of Neutral Brønsted Acids in Acetonitrile

Agnes Kütt; Ivo Leito; Ivari Kaljurand; Lilli Sooväli; Vladislav M. Vlasov; Lev M. Yagupolskii; Ilmar A. Koppel

doi:10.1021/jo060031y

journal article Mar 09, 2006

A Comprehensive Self-Consistent Spectrophotometric Acidity Scale of Neutral Brønsted Acids in Acetonitrile

Agnes Kütt Ivo Leito

Ivari Kaljurand Lilli Sooväli Vladislav M. Vlasov Lev M. Yagupolskii Ilmar A. Koppel

The Journal of Organic Chemistry Vol. 71 No. 7 pp. 2829-2838 · American Chemical Society (ACS)

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References

70

[1]

Kolthoff I. M. J. Am. Chem. Soc. (1961) 10.1021/ja01480a002

[2]

Kolthoff I. M. J. Am. Chem. Soc. (1965)

[3]

Kolthoff I. M. J. Am. Chem. Soc. (1966) 10.1021/ja00975a012

[4]

Coetzee J. F. Prog. Phys. Org. Chem. (1967)

[5]

Coetzee J. F. J. Phys. Chem. (1965)

[6]

Leito I. J. Org. Chem. (1998) 10.1021/jo981124l

[7]

Vlasov V. M. Izv. Sib. Otd. Akad. Nauk SSSR, Ser. Khim. (1982)

[8]

Chantooni M. K. J. Phys. Chem. (1976) 10.1021/j100553a009

[9]

Bykova L. N. Usp. Khim. (1970) 10.1070/rc1970v039n09abeh002021

[10]

Dyumaev K. M. Usp. Khim. (1980) 10.1070/rc1980v049n11abeh002521

[11]

Izutsu K. (1990)

[12]

Tables of Rate and Equilibrium Constants of Heterolytic OrganicReactions; Palm, V., Ed.; VINITI: Moscow-Tartu, 1975−1985.

[13]

Juillard J. Acad. Sci., Ser. C. (1967)

[14]

Jasinski T. Croat. Chem. Acta (1987)

[15]

Kaljurand I. J. Org. Chem. (2005) 10.1021/jo048252w

[16]

Almerindo G. I. J. Phys. Chem. A. (2004) 10.1021/jp0361071

[17]

Vianello R. Eur. J. Org. Chem. (2005)

[18]

Vianello R. Tetrahedron Lett. (2005) 10.1016/j.tetlet.2005.03.142

[19]

Vianello R. Tetrahedron (2005) 10.1016/j.tet.2005.07.052

[20]

Chipman D. M. J. Phys. Chem. A (2002) 10.1021/jp020847c

[21]

Kolthoff I. M. J. Phys. Chem. (1968) 10.1021/j100852a082

[22]

Yagupolskii L. M. J. Chem. Soc., Perkin Trans. 2 (2002)

[23]

Bordwell F. G. J. Am. Chem. Soc. (1988)

[24]

Koppel I. A. J. Chem. Soc., Perkin Trans. 2 (2000)

[25]

Koppel I. A. Int. J. Mass Spectrom. Ion Processes. (1998) 10.1016/s0168-1176(98)00113-x

[26]

Vlasov V. M. Zh. Org. Khim. (1981)

[27]

Bordwell F. G. Acc. Chem. Res. (1988) 10.1021/ar00156a004

[28]

Ritchie C. D. J. Am. Chem. Soc. (1968) 10.1021/ja01013a018

[29]

Kolthoff I. M. J. Am. Chem. Soc. (1968)

[30]

Kolthoff I. M. J. Am. Chem. Soc. (1975) 10.1021/ja00839a015

[31]

Koppel I. A. Org. React. (1977)

[32]

Fujinaga T. J. Electroanal. Chem. (1977) 10.1016/s0022-0728(77)80163-0

[33]

Kortüm G. (1961)

[34]

Knunyants I. L. Izv. Akad. Nauk SSSR, Ser. Khim. (1966)

[35]

Bell P. H. Proc. R. Soc. London, Ser. A (1949)

[36]

Rõõm E.-I. J. Org. Chem. (2003)

[37]

Vlasov V. M. Zh. Org. Khim. (1979)

[38]

Lebedeva T. I. Zh. Org. Khim. (1977)

[39]

Koppel I. A. J. Am. Chem. Soc. (1994)

[40]

Bartmess J. E. (1997)

[41]

Kebarle P. J. Am. Chem. Soc. (1977) 10.1021/ja00449a033

[42]

Taft R. W. J. Am. Chem. Soc. (1990)

[43]

Kolthoff I. M. J. Am. Chem. Soc. (1969)

[44]

Galezowski W. Can. J. Chem. (1997) 10.1139/v97-032

[45]

Webster O. W. J. Am. Chem. Soc. (1966)

[46]

A survey of Hammett substituent constants and resonance and field parameters

Corwin. Hansch, A. Leo, R. W. Taft

Chemical Reviews 1991 10.1021/cr00002a004

[47]

Kondratenko N. V. Zh. Org. Khim. (1986)

[48]

(b) Yagupolskii, L. M.Aromatic and Heterocyclic Compounds with Fluorine-ContainingSubstituents; Nauokova Dumka: Kiev, 1988; p 319.

[49]

Koppel I. A. J. Am. Chem. Soc. (2002) 10.1021/ja0255958

[50]

Yagupolskii L. M. Zh. Org. Khim. (1995)

Showing 50 of 70 references

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Details

Published: Mar 09, 2006
Vol/Issue: 71(7)
Pages: 2829-2838

Authors

A

Agnes Kütt

Institute of Chemical Physics, Department of Chemistry, University of Tartu, Jakobi 2 Str., 51014 Tartu, Estonia, Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090, Russia, and Institute of Organic Chemistry, Ukrainian National Academy of Sciences, Murmanskaya Str. 5, Kiev 02094, Ukraine

I

Ivo Leito

Institute of Chemical Physics, Department of Chemistry, University of Tartu, Jakobi 2 Str., 51014 Tartu, Estonia, Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090, Russia, and Institute of Organic Chemistry, Ukrainian National Academy of Sciences, Murmanskaya Str. 5, Kiev 02094, Ukraine

I

Ivari Kaljurand

Institute of Chemical Physics, Department of Chemistry, University of Tartu, Jakobi 2 Str., 51014 Tartu, Estonia, Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090, Russia, and Institute of Organic Chemistry, Ukrainian National Academy of Sciences, Murmanskaya Str. 5, Kiev 02094, Ukraine

L

Lilli Sooväli

Institute of Chemical Physics, Department of Chemistry, University of Tartu, Jakobi 2 Str., 51014 Tartu, Estonia, Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090, Russia, and Institute of Organic Chemistry, Ukrainian National Academy of Sciences, Murmanskaya Str. 5, Kiev 02094, Ukraine

V

Vladislav M. Vlasov

Institute of Chemical Physics, Department of Chemistry, University of Tartu, Jakobi 2 Str., 51014 Tartu, Estonia, Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090, Russia, and Institute of Organic Chemistry, Ukrainian National Academy of Sciences, Murmanskaya Str. 5, Kiev 02094, Ukraine

L

Lev M. Yagupolskii

Institute of Chemical Physics, Department of Chemistry, University of Tartu, Jakobi 2 Str., 51014 Tartu, Estonia, Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090, Russia, and Institute of Organic Chemistry, Ukrainian National Academy of Sciences, Murmanskaya Str. 5, Kiev 02094, Ukraine

I

Ilmar A. Koppel

Institute of Chemical Physics, Department of Chemistry, University of Tartu, Jakobi 2 Str., 51014 Tartu, Estonia, Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090, Russia, and Institute of Organic Chemistry, Ukrainian National Academy of Sciences, Murmanskaya Str. 5, Kiev 02094, Ukraine

Cite This Article

Agnes Kütt, Ivo Leito, Ivari Kaljurand, et al. (2006). A Comprehensive Self-Consistent Spectrophotometric Acidity Scale of Neutral Brønsted Acids in Acetonitrile. The Journal of Organic Chemistry, 71(7), 2829-2838. https://doi.org/10.1021/jo060031y

A Comprehensive Self-Consistent Spectrophotometric Acidity Scale of Neutral Brønsted Acids in Acetonitrile

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