- 1. Building with Cubane-1,4-diyl. Synthesis of Aryl-Substituted Cubanes, p-[n]Cubyls, and Cubane-Separated Bis(arenes)
Philip E. Eaton, Kakumanu Pramod, Todd Emrick, and Richard Gilardi
J. Am. Chem. Soc., 1999, 121, (17), pp 4111–4123
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/jacsat/1999/121/i17/pdf/ja983441f.pdf- 2. Synthesis and Chemistry of 1,3,5,7-Tetranitrocubane Including Measurement of Its Acidity, Formation of o-Nitro Anions, and the First Preparations of Pentanitrocubane and Hexanitrocubane
Kirill A. Lukin, Jianchang Li, Philip E. Eaton, Nobuhiro Kanomata, Jürgen Hain, Eric Punzalan, and Richard Gilardi
J. Am. Chem. Soc., 1997, 119, (41), pp 9591–9602
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/jacsat/1997/119/i41/pdf/ja970552q.pdf- 3. A Computational Study of the Interactions among the Nitro Groups in Octanitrocubane
David A. Hrovat, Weston Thatcher Borden, Philip E. Eaton, and Bart Kahr
J. Am. Chem. Soc., 2001, 123, (7), pp 1289–1293
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/chreay/1989/89/i05/pdf/cr00095a003.pdf- 4. Synthesis and Chemistry of 1,3,5,7-Tetranitrocubane Including Measurement of Its Acidity, Formation of o-Nitro Anions, and the First Preparations of Pentanitrocubane and Hexanitrocubane
Kirill A. Lukin, Jianchang Li, Philip E. Eaton, Nobuhiro Kanomata, Jürgen Hain, Eric Punzalan, and Richard Gilardi
J. Am. Chem. Soc., 1997, 119, (41), pp 9591–9602
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http://pubs.acs.org/cgi-bin/article.cgi/jacsat/1997/119/i41/pdf/ja970552q.pdf- 5. Photolysis of cubyl iodides: access to the cubyl cation
D. Sivakumar Reddy, Gilbert P. Sollott, and Philip E. Eaton
J. Org. Chem., 1989, 54, (3), pp 722–723
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/joceah/1989/54/i03/pdf/jo00264a044.pdf- 6. Pentaprismane
Philip E. Eaton, Yat Sun Or, and Stephen J. Branca
J. Am. Chem. Soc., 1981, 103, (8), pp 2134–2136
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/jacsat/1981/103/i08/pdf/ja00398a062.pdf- 7. Formal synthesis of pentaprismane
William G. Dauben and Allan F. Cunningham
J. Org. Chem., 1983, 48, (17), pp 2842–2847
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/joceah/1983/48/i17/pdf/jo00165a012.pdf- 8. Photochemical Functionalization of Cubanes
A. Bashir-Hashemi, J. Li, Nathan Gelber, and Herman Ammon
J. Org. Chem., 1995, 60, (3), pp 698–702
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/joceah/1995/60/i03/pdf/jo00108a037.pdf- 9. Systematic substitution on the cubane nucleus. Synthesis and properties of 1,3,5-trinitrocubane and 1,3,5,7-tetranitrocubane
Philip E. Eaton, Yusheng Xiong, and Richard Gilardi
J. Am. Chem. Soc., 1993, 115, (22), pp 10195–10202
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/jacsat/1993/115/i22/pdf/ja00075a039.pdf- 10. Synthesis and Chemistry of 1,3,5,7-Tetranitrocubane Including Measurement of Its Acidity, Formation of o-Nitro Anions, and the First Preparations of Pentanitrocubane and Hexanitrocubane
Kirill A. Lukin, Jianchang Li, Philip E. Eaton, Nobuhiro Kanomata, Jürgen Hain, Eric Punzalan, and Richard Gilardi
J. Am. Chem. Soc., 1997, 119, (41), pp 9591–9602
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/jacsat/1997/119/i41/pdf/ja970552q.pdf- 11. Is N8 cubane stable?
Ray Engelke and James R. Stine
J. Phys. Chem., 1990, 94, (15), pp 5689–5694
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/jpchax/1990/94/i15/pdf/j100378a018.pdf- 12. Stability and energetics of metastable molecules: tetraazatetrahedrane (N4), hexaazabenzene (N6), and octaazacubane (N8)
Walter J. Lauderdale, John F. Stanton, Rodney J. Bartlett
J. Phys. Chem.; 1992; 96(3); 1173-1178
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/jpchax/1992/96/i03/pdf/j100182a029.pdf- 13. Protonated High Energy Density Materials: N4 Tetrahedron and N8 Octahedron
Leininger, M. L.; Van Huis, T. J.; Schaefer, H. F., III
J. Phys. Chem. A.; (Article); 1997; 101(24); 4460-4464
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/jpcafh/1997/101/i24/pdf/jp970258k.pdf- 14. New Isomers of N8 without Double Bonds
Tian, A.; Ding, F.; Zhang, L.; Xie, Y.; Schaefer, H. F., III
J. Phys. Chem. A.; (Article); 1997; 101(10); 1946-1950
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/jpcafh/1997/101/i10/pdf/jp962878b.pdf- 15. Theoretical Studies on the Potential Energy Surfaces of N8 Clusters
Li, Q. S.; Wang, L. J.
J. Phys. Chem. A.; (Article); 2001; 105(10); 1979-1982.
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/jpcafh/2001/105/i10/pdf/jp003086r.pdf- 16. Possible Reaction Pathway of HN3 + N5+ and Stability of the Products' Isomers
Wang, L. J.; Li, Q. S.; Warburton, P.; Mezey, P. G.
J. Phys. Chem. A.; (Article); 2002; 106(9); 1872-1876
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/jpcafh/2002/106/i09/pdf/jp013865n.pdf- 17. Possible Products of the End-On Addition of N3- to N5+ and Their Stability
Fau, S.; Bartlett, R. J.
J. Phys. Chem. A.; (Article); 2001; 105(16); 4096-4106
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/jpcafh/2001/105/i16/pdf/jp003970h.pdf- 18. Theoretical Prediction of the Structures and Stabilities of Azidamines
H. Harvey Michels, John Montgomery, Karl O. Christe, David A. Dixon
J. Phys. Chem.; 1995; 99(1); 187-194
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/jpchax/1995/99/i01/pdf/j100001a032.pdf- 19. N8: A Structure Analogous to Pentalene, and Other High-Energy Density Minima
Matthew L. Leininger, C. David Sherrill, Henry Schaefer
J. Phys. Chem.; 1995; 99(8); 2324-2328
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/jpchax/1995/99/i08/pdf/j100008a013.pdf- 20. Besides N2, What Is the Most Stable Molecule Composed Only of Nitrogen Atoms?
Glukhovtsev, M. N.; Jiao, H.; Schleyer, P. v. R.
Inorg. Chem.; (Article); 1996; 35(24); 7124-7133
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/inocaj/1996/35/i24/pdf/ic9606237.pdf- 21. Thermochemistry of Tetrazete and Tetraazatetrahedrane: A High-Level Computational Study
Glukhovtsev, M. N.; Laiter, S.
J. Phys. Chem.; (Article); 1996; 100(5); 1569-1577
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/jpchax/1996/100/i05/pdf/jp952026w.pdf- 22. What Makes the Cylinder-Shaped N72 Cage Stable?
Zhou, H.; Wong, N.-B.; Zhou, G.; Tian, A.
J. Phys. Chem. A.; (Article); 2006; 110(23); 7441-7446
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/jpcafh/2006/110/i23/pdf/jp062214u.pdf- 23. Cyclic D6h hexaazabenzene - a relative minimum on the hexaazabenzene potential energy hypersurface?
Paul Saxe, Henry F. Schaefer, , III
J. Am. Chem. Soc.; 1983; 105(7); 1760-1764
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/jacsat/1983/105/i07/pdf/ja00345a010.pdf- 24. Reply to comments on the stable points on the N6 energy hypersurface
Ray Engelke
J. Phys. Chem.; 1990; 94(17); 6924-6925
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/jpchax/1990/94/i17/pdf/j100380a071.pdf- 25. Theoretical Prediction on the Synthesis Reaction Pathway of N6 (C2h)
Wang, L. J.; Warburton, P.; Mezey, P. G.
J. Phys. Chem. A.; (Article); 2002; 106(11); 2748-2752
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/jpcafh/2002/106/i11/pdf/jp0141833.pdf- 26. Vibrational Spectra of the Azabenzenes Revisited: Anharmonic Force Fields
Martin, J. M. L.; Boese, A. D.
J. Phys. Chem. A.; (Article); 2004; 108(15); 3085-3096
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/jpcafh/2004/108/i15/pdf/jp0369589.pdf- 27. Five stable points on the N6 energy hypersurface: structures, energies, frequencies, and chemical shifts
Ray Engelke
J. Phys. Chem.; 1989; 93(15); 5722-5727
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http://pubs.acs.org/cgi-bin/searchRedirect.cgi/jpchax/1989/93/i15/pdf/j100352a016.pdf
