Hydrogen bonding versus hyperconjugation in condensed-phase carbocations

Organic and Biomolecular Chemistry

Volumn 11, Issue 23, 2013, Pages 3797-3802

  Reed, Christopher A ^a   Stoyanov, Evgenii S ^a   Tham, Fook S ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GASES; POSITIVE IONS; STABILIZATION;

CARBOCATIONS; CONDENSED PHASE; CONDENSED PHASIS; COUNTERIONS; HYPERCONJUGATION; HYPERCONJUGATIVE STABILIZATION; IR SPECTRUM; POSITIVE CHARGES;

HYDROGEN BONDS;

BUTANE; CARBON; HYDROCARBON;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; COMPARATIVE STUDY; CONFORMATION; HYDROGEN BOND;

BUTANES; CARBON; HYDROCARBONS; HYDROGEN BONDING; MODELS, MOLECULAR; MOLECULAR CONFORMATION;

EID: 84888592155     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c3ob40737c     Document Type: Article

References (26)

1. G. A. Olah and A. Molnar, Hydrocarbon Chemistry, John Wiley & Sons, N.Y., 2003
2. Stable Carbocation Chemistry, ed., G. K. S. Prakash, and, P. v. R. Schleyer, John Wiley & Sons, N.Y., 1997
3. Carbocation Chemistry, ed., G. A. Olah, and, G. K. S. Prakash, John Wiley & Sons, Hoboken, N.J., 2004
4. G. A. Olah W. S. Tolgyesi S. J. Kuhn M. E. Moffatt I. J. Bastien E. B. Baker J. Am. Chem. Soc. 1963 85 1328
5. H. Feng W. Sun Y. Xie H. F. Schaefer III Chem.-Eur. J. 2011 17 10552
6. G. E. Douberly A. M. Ricks B. W. Ticknor P. v. R. Schleyer M. A. Duncan J. Am. Chem. Soc. 2007 129 13782
7. S. Sieber P. Buzek P. v. R. Schleyer W. Koch J. W. de M. Carneiro J. Am. Chem. Soc. 1993 115 259
8. G. Rasul J. L. Chen G. K. S. Prakash G. A. Olah J. Phys. Chem. A 2009 113 6795
9. G. A. Olah E. B. Baker J. C. Evans W. S. Tolgyesi J. S. McIntyre I. J. Bastien J. Am. Chem. Soc. 1964 86 1360
10. E. S. Stoyanov I. V. Stoyanova F. S. Tham C. A. Reed Angew. Chem., Int. Ed. 2012 51 9149
11. E. S. Stoyanov K.-C. Kim C. A. Reed J. Am. Chem. Soc. 2006 128 8500
12. R. Taylor O. Kennard J. Am. Chem. Soc. 1982 104 5063
13. D. R. Desiraju J. Chem. Soc., Chem. Commun. 1990 454
14. T. Steiner Angew. Chem., Int. Ed. 2002 41 48
15. J. P. Lorand J. Phys. Org. Chem. 2011 24 267
16. C. A. Reed Acc. Chem. Res. 2010 43 128
17. T. Kato C. A. Reed Angew. Chem., Int. Ed. 2004 43 2908
18. E. S. Stoyanov I. V. Stoyanova F. S. Tham C. A. Reed J. Am. Chem. Soc. 2010 132 4062
19. F. Scholz D. Himmel H. Scherer I. Krossing Chem.-Eur. J. 2013 19 109
20. J.-A. van den Berg K. R. Seddon Cryst. Growth Des. 2003 3 643
21. R. F. Howe M. J. Taylor Spectrochim. Acta, Part A 1987 43 73
22. S. Scheiner T. Kar J. Phys. Chem. A 2002 106 1784 1789
23. E. S. Stoyanov I. V. Stoyanova C. A. Reed Chem.-Eur. J. 2008 14 7880
24. M. D. Bojin D. J. Tantillo J. Phys. Chem. A 2006 110 4810 4481
25. Y. J. Hong D. J. Tantillo Chem. Sci. 2013 10.1039/c3sc50571e
26. S. Gronert Acc. Chem. Res. 2003 36 848 857