style="font-size:15px;"> 41 41 Benesi, H.A. and Hildebrand, J.H. (1948). J. Am. Chem. Soc. 70: 2832–2833.42 42 Mulliken, R.S. (1950). J. Am. Chem. Soc. 72: 600–608.
43 43 Mulliken, R.S. (1966) Spectroscopy, molecular orbitals, and chemical bonding. Nobel Lecture.
44 44 Hassel, O., Hvoslef, J., Vihovde, E.H., and Sörensen, N.A. (1954). Acta Chem. Scand. 8: 873–873.
45 45 Hassel, O., Strømme, K.O., Haraldsen, H. et al. (1958). Acta Chem. Scand. 12: 1146–1146.
46 46 Hassel, O., Strømme, K.O., Hammarsten, E. et al. (1959). Acta Chem. Scand. 13: 1781–1786.
47 47 Hassel, O., Strømme, K.O., Stenhagen, E. et al. (1959). Acta Chem. Scand. 13: 275–280.
48 48 Hassel, O. (1970) Structural aspects of interatomic charge‐transfer bonding. Nobel Lecture.
49 49 Dumas, J.M., Gomel, M., and Guerin, M. (2010). Patai Suppl. D, Chem. Halides Pseudo‐Halides Azides 2: 985–1020.
50 50 Schulz, N., Sokkar, P., Engelage, E. et al. (2018). Chem. Eur. J. 24: 3464–3473.
51 51 Legon, A.C. (1998). Chem. Eur. J.: 4, 1890–1897.
52 52 Legon, A.C. (1999). Angew. Chem. Int. Ed. 38: 2686–2714.
53 53 Weiss, R., Rechinger, M., Hampel, F., and Wolski, A. (1995). Angew. Chem. Int. Ed. 34: 441–443.
54 54 Weiss, R., Miess, G.‐E., Haller, A., and Reinhardt, W. (1986). Angew. Chem. Int. Ed. 25: 103–104.
55 55 Weiss, R., Rechinger, M., and Hampel, F. (1994). Angew. Chem. Int. Ed. 33: 893–895.
56 56 Metrangolo, P., Neukirch, H., Pilati, T., and Resnati, G. (2005). Acc. Chem. Res. 38: 386–395.
57 57 Metrangolo, P. and Resnati, G. (2001). Chem. Eur. J. 7: 2511–2519.
58 58 Li, B., Zang, S.Q., Wang, L.Y., and Mak, T.C.W. (2016). Coord. Chem. Rev. 308: 1–21.
59 59 Fourmigué, M. (2009). Curr. Opin. Solid State Mater. Sci. 13: 36–45.
60 60 Ding, X., Tuikka, M., and Haukk, M. (2012). Recent Advances in Crystallography, vol. i, 13. InTech.
61 61 Christopherson, J.C., Topić, F., Barrett, C.J., and Friščić, T. (2018). Cryst. Growth Des. 18: 1245–1259.
62 62 Mukherjee, A., Tothadi, S., and Desiraju, G.R. (2014). Acc. Chem. Res. 47: 2514–2524.
63 63 Gilday, L.C., Robinson, S.W., Barendt, T.A. et al. (2015). Chem. Rev. 115: 7118–7195.
64 64 Aakeröy, C.B. and Spartz, C.L. (2015). Halogen Bonding I: Impact on Materials Chemistry and Life Sciences (eds. P. Metrangolo and G. Resnati), 155–182. Cham: Springer International Publishing.
65 65 Metrangolo, P., Resnati, G., Pilati, T., and Biella, S. (2008). Halogen Bonding: Fundamentals and Applications (eds. P. Metrangolo and G. Resnati), 105–136. Berlin, Heidelberg: Springer Berlin Heidelberg.
66 66 Murray‐Rust, P. and Motherwell, W.D.S. (1979). J. Am. Chem. Soc. 101: 4374–4376.
67 67 Lommerse, J.P.M., Stone, A.J., Taylor, R., and Allen, F.H. (1996). J. Am. Chem. Soc. 118: 3108–3116.
68 68 Desiraju, G.R. and Parthasarathy, R. (1989). J. Am. Chem. Soc. 111: 8725–8726.
69 69 Pedireddi, V.R., Reddy, D.S., Goud, B.S. et al. (1994). J. Chem. Soc., Perkin Trans. 2: 2353.
70 70 Chopra, D. (2012). Cryst. Growth Des. 12: 541–546.
71 71 Präsang, C., Whitwood, A.C., and Bruce, D.W. (2009). Cryst. Growth Des. 9: 5319–5326.
72 72 Aakeröy, C.B., Baldrighi, M., Desper, J. et al. (2013). Chem. Eur. J. 19: 16240–16247.
73 73 Etter, M.C. (1990). Acc. Chem. Res. 23: 120–126.
74 74 Aakery, C.B., Beatty, A.M., and Helfrich, B.A. (2001). Angew. Chem. Int. Ed. 40: 3240–3242.
75 75 Aakeröy, C.B., Wijethunga, T.K., Desper, J., and Daković, M. (2016). Cryst. Growth Des. 16: 2662–2670.
76 76 Aakeröy, C.B., Spartz, C.L., Dembowski, S. et al. (2015). IUCrJ 2: 498–510.
77 77 Aakeröy, C.B., Chopade, P.D., and Desper, J. (2011). Cryst. Growth Des. 11: 5333–5336.
78 78 Aakeröy, C.B., Chopade, P.D., Ganser, C., and Desper, J. (2011). Chem. Commun. 47: 4688–4690.
79 79 Tothadi, S. and Desiraju, G.R. (2013). Chem. Commun. 49: 7791–7793.
80 80 Voth, A.R., Khuu, P., Oishi, K., and Ho, P.S. (2009). Nat. Chem. 1: 74–79.
81 81 Vasylyeva, V., Nayak, S.K., Terraneo, G. et al. (2014). CrystEngComm 16: 8102–8105.
82 82 Takemura, A., McAllister, L.J., Hart, S. et al. (2014). Chem. Eur. J. 20: 6721–6732.
83 83 Decato, D.A. and Berryman, O.B. (2018). Simultaneous halogen and hydrogen bonding to carbonyl and thiocarbonyl functionality. In: Multi‐Component Crystals, vol. 1 (eds. E. Tiekink and J. Zukerman), 272–288. Berlin, Boston: De Gruyter.
84 84 Logothetis, T.A., Meyer, F., Metrangolo, P. et al. (2004). New J. Chem. 28: 760–763.
85 85 Lisac, K. and Cinčić, D. (2018). CrystEngComm 20: 5955–5963.
86 86 Puttreddy, R., Peuronen, A., Lahtinen, M., and Rissanen, K. (2019). Cryst. Growth Des. 19: 3815–3824.
87 87 Ding, X., Tuikka, M., Rissanen, K., and Haukka, M. (2019). Crystals 9: 319.
88 88 Puttreddy, R., von Essen, C., and Rissanen, K. (2018). Eur. J. Inorg. Chem. 2018: 2393–2398.
89 89 Smart, P., Bejarano‐Villafuerte, Á., and Brammer, L. (2013). CrystEngComm 15: 3151.
90 90 Brammer, L., Mínguez Espallargas, G., and Adams, H. (2003). CrystEngComm 5: 343–345.
91 91 Mínguez Espallargas, G., Zordan, F., Arroyo Marín, L. et al. (2009). Chem. Eur. J. 15: 7554–7568.
92 92 Zordan, F., Brammer, L., and Sherwood, P. (2005). J. Am. Chem. Soc. 127: 5979–5989.
93 93 Libri, S., Jasim, N.A., Perutz, R.N., and Brammer, L. (2008). J. Am. Chem. Soc. 130: 7842–7844.
94 94 Smith, D.A., Brammer, L., Hunter, C.A., and Perutz, R.N. (2014). J. Am. Chem. Soc. 136: 1288–1291.
95 95 Ormond‐Prout, J.E., Smart, P., and Brammer, L. (2012). Cryst. Growth Des. 12: 205–216.
96 96 Carter, K.P., Kalaj, M., Surbella, R.G. et al. (2017). Chem. Eur. J. 23: 15355–15369.
97 97 Carter, K.P., Kalaj, M., Kerridge, A., and Cahill, C.L. (2018). CrystEngComm 20: 4916–4925.
98 98 Lieffrig, J., Jeannin, O., Guizouarn, T. et al. (2012). Cryst. Growth Des. 12: 4248–4257.
99 99 Lieffrig, J., Jeannin, O., Shin, K.‐S. et al.
