7. Legon, A.C.: The interaction of dihalogens and hydrogen halides with Lewis bases in gas
phase: An experimental comparison of the halogen bond and hydrogen bond: in Structure
and Bonding, eds. P. Metrangolo, G. Restani, 126, 17–64 (2008). https://doi.org/10.1007/
430_2007_063
8. Legon, A.C.: A reduced radial potential energy function for the halogen bond and the
hydrogen bond in complexes B
…
XY and B
…
HX, where X and Y are halogen atoms. Phys.
Chem. Chem. Phys. 16, 12415–12420 (2014). https://doi.org/10.1039/c4cp01444h
9. Springer, S.D., Rivera-Rivera, L.A., McElmurry, B.A., Wang, Z., Leonov, I.I., Lucchese, R.
R. Legon, A.C., Bevan, J.W.: CMM-RS potential for characterization of the properties of the
Halogen-Bonded OC-Cl 2 Complex, and a Comparison with Hydrogen-Bonded OC-HCl.
J. Phys. Chem. A, 116, 1213–1223 (2012). dx.doi.org/https://doi.org/10.1021/jp209870x
10. Rivera-Rivera, L.A., Scott, K.W., McElmurry, B.A., Lucchese, R.R., Bevan, J.W.:
Compound modelmorphed potentials contrasting OC–79Br 35Cl with the halogen bonded
OC–35Cl2 and hydrogen-bonded OC–HX (X = 19F, 35Cl, 79Br). Chem. Phys. 425, 162–
169 (2013). https://doi.org/10.1016/j.chemphys.2013.08.016
11. Shaw, R.A., J. Hill, J.G., Legon, A.C.: Halogen bonding with phosphine: Evidence for
Mulliken Inner complexes and the importance of relaxation energy. J. Phys. Chem. A. 120,
8461–8468 (2016). https://doi.org/10.1021/acs.jpca.6b08945
12. Anable, J.P., Hird, D.E., Stephens, S.L., Zaleski, D.P., Walker, N.R., Legon, A.C.:
Characterisation of the weak halogen bond in N 2 ÁÁÁICF 3 by pure rotational spectroscopy.
Chem. Phys. Letts. 625, 179–185 (2015). https://doi.org/10.1016/j.cplett.2015.02.023
13. McIntosh, A.L., Wang, Z., Castillo-Chara, J., Lucchese, R.R., Bevan, J.W., Suenram, R.D.,
Legon, A.C.: The structure and ground state dynamics of Ar—IH. J. Chem. Phys. 111,
5764–5771 (1999). https://doi.org/10.1021/acs.jpca.6b08945
14. Walton, J.R., Rivera-Rivera, L.A., Lucchese, R.R., Bevan, J.W.: A canonical approach to
multi-dimensional van der Waals, hydrogen-bonded, and halogen-bonded potentials. Chem.
Phys. 469–470, 60–64 (2016). https://doi.org/10.1016/j.chemphys.2016.01.011
15. Walton, J.R., Rivera-Rivera, L.A., Lucchese, R.R., Bevan, J.W.: A general transformation to
canonical form for potentials in pairwise interatomic interactions. Phys. Chem. Chem. Phys.
17, 14805–14810 (2015). https://doi.org/10.1039/C5CP01543J
16. Pauling, L.: The Nature of the Chemical Bond. IV. The energy of single bonds and the
relative electronegativity of atoms. J. Amer. Chem. Soc. 54, 3570–3582 (1932)
17. Legon, A.C., Millen, D.J.: Hydrogen bonding as a probe of electron densities: Limiting
gas-phase nucleophilicities and electrophilicities of B and HX. J. Amer. Chem. Soc. 109,
356–358 (1987). https://doi.org/10.1021/ja00236a011
18. Lukashov, S., Petrov, A., Pravilov, A.: The Iodine Molecule: Insights into Intra- and
Intermolecular Perturbation in Diatomic Molecules. Springer (2018). https://doi.org/10.
1007/978-3-319-70072-4
19. Smalley, R.E., Levy, D.H., Wharton, L.: The fluorescence excitation spectrum of the HeI 2
van der Waals complex. J. Chem. Phys. 64, 3266–3275 (1976). https://doi.org/10.1063/1.
432667
20. Novick, S.E., Davis, P., Harris, S.J., Klemperer, W.: Determination of the structure of
ArHCI. J. Chem. Phys. 59, 2273–2279 (1973). https://doi.org/10.1063/1.1680332
21. Harris, S.J., Janda, K.C., Novick, S.E., Klemperer, W.: Intermolecular potential between an
atom and a linear molecule: The structure of ArOCS. J. Chem. Phys. 63, 881–884 (1975).
https://doi.org/10.1063/1.431368
22. Novick, S.: Bibliography of rotational spectra of weakly bound complexes. https://wesfiles.
wesleyan.edu/home/snovick/SN_webpage/vdW.pdf
23. Rohrbacher, A., Williams, J., Janda, K.C.: Rare gas-dihalogen potential energy surfaces.
Phys. Chem. Chem. Phys. 1, 5263–5276 (1999). https://doi.org/10.1039/A906664K
24. Chan, K.W., Power, T.D., Jai-nhuknan, J., Cybulski, S.M.: An ab initio study of He–F 2 , Ne–
F 2 , and Ar–F 2 van der Waals complexes. J. Chem. Phys. 110, 860–869 (1999). https://doi.
org/10.1063/1.478053
References
257
phase: An experimental comparison of the halogen bond and hydrogen bond: in Structure
and Bonding, eds. P. Metrangolo, G. Restani, 126, 17–64 (2008). https://doi.org/10.1007/
430_2007_063
8. Legon, A.C.: A reduced radial potential energy function for the halogen bond and the
hydrogen bond in complexes B
…
XY and B
…
HX, where X and Y are halogen atoms. Phys.
Chem. Chem. Phys. 16, 12415–12420 (2014). https://doi.org/10.1039/c4cp01444h
9. Springer, S.D., Rivera-Rivera, L.A., McElmurry, B.A., Wang, Z., Leonov, I.I., Lucchese, R.
R. Legon, A.C., Bevan, J.W.: CMM-RS potential for characterization of the properties of the
Halogen-Bonded OC-Cl 2 Complex, and a Comparison with Hydrogen-Bonded OC-HCl.
J. Phys. Chem. A, 116, 1213–1223 (2012). dx.doi.org/https://doi.org/10.1021/jp209870x
10. Rivera-Rivera, L.A., Scott, K.W., McElmurry, B.A., Lucchese, R.R., Bevan, J.W.:
Compound modelmorphed potentials contrasting OC–79Br 35Cl with the halogen bonded
OC–35Cl2 and hydrogen-bonded OC–HX (X = 19F, 35Cl, 79Br). Chem. Phys. 425, 162–
169 (2013). https://doi.org/10.1016/j.chemphys.2013.08.016
11. Shaw, R.A., J. Hill, J.G., Legon, A.C.: Halogen bonding with phosphine: Evidence for
Mulliken Inner complexes and the importance of relaxation energy. J. Phys. Chem. A. 120,
8461–8468 (2016). https://doi.org/10.1021/acs.jpca.6b08945
12. Anable, J.P., Hird, D.E., Stephens, S.L., Zaleski, D.P., Walker, N.R., Legon, A.C.:
Characterisation of the weak halogen bond in N 2 ÁÁÁICF 3 by pure rotational spectroscopy.
Chem. Phys. Letts. 625, 179–185 (2015). https://doi.org/10.1016/j.cplett.2015.02.023
13. McIntosh, A.L., Wang, Z., Castillo-Chara, J., Lucchese, R.R., Bevan, J.W., Suenram, R.D.,
Legon, A.C.: The structure and ground state dynamics of Ar—IH. J. Chem. Phys. 111,
5764–5771 (1999). https://doi.org/10.1021/acs.jpca.6b08945
14. Walton, J.R., Rivera-Rivera, L.A., Lucchese, R.R., Bevan, J.W.: A canonical approach to
multi-dimensional van der Waals, hydrogen-bonded, and halogen-bonded potentials. Chem.
Phys. 469–470, 60–64 (2016). https://doi.org/10.1016/j.chemphys.2016.01.011
15. Walton, J.R., Rivera-Rivera, L.A., Lucchese, R.R., Bevan, J.W.: A general transformation to
canonical form for potentials in pairwise interatomic interactions. Phys. Chem. Chem. Phys.
17, 14805–14810 (2015). https://doi.org/10.1039/C5CP01543J
16. Pauling, L.: The Nature of the Chemical Bond. IV. The energy of single bonds and the
relative electronegativity of atoms. J. Amer. Chem. Soc. 54, 3570–3582 (1932)
17. Legon, A.C., Millen, D.J.: Hydrogen bonding as a probe of electron densities: Limiting
gas-phase nucleophilicities and electrophilicities of B and HX. J. Amer. Chem. Soc. 109,
356–358 (1987). https://doi.org/10.1021/ja00236a011
18. Lukashov, S., Petrov, A., Pravilov, A.: The Iodine Molecule: Insights into Intra- and
Intermolecular Perturbation in Diatomic Molecules. Springer (2018). https://doi.org/10.
1007/978-3-319-70072-4
19. Smalley, R.E., Levy, D.H., Wharton, L.: The fluorescence excitation spectrum of the HeI 2
van der Waals complex. J. Chem. Phys. 64, 3266–3275 (1976). https://doi.org/10.1063/1.
432667
20. Novick, S.E., Davis, P., Harris, S.J., Klemperer, W.: Determination of the structure of
ArHCI. J. Chem. Phys. 59, 2273–2279 (1973). https://doi.org/10.1063/1.1680332
21. Harris, S.J., Janda, K.C., Novick, S.E., Klemperer, W.: Intermolecular potential between an
atom and a linear molecule: The structure of ArOCS. J. Chem. Phys. 63, 881–884 (1975).
https://doi.org/10.1063/1.431368
22. Novick, S.: Bibliography of rotational spectra of weakly bound complexes. https://wesfiles.
wesleyan.edu/home/snovick/SN_webpage/vdW.pdf
23. Rohrbacher, A., Williams, J., Janda, K.C.: Rare gas-dihalogen potential energy surfaces.
Phys. Chem. Chem. Phys. 1, 5263–5276 (1999). https://doi.org/10.1039/A906664K
24. Chan, K.W., Power, T.D., Jai-nhuknan, J., Cybulski, S.M.: An ab initio study of He–F 2 , Ne–
F 2 , and Ar–F 2 van der Waals complexes. J. Chem. Phys. 110, 860–869 (1999). https://doi.
org/10.1063/1.478053
References
257