Halogen Bonding with Dihalogens and Interhalogens - Halogen Bonding: Fundamentals and Applications - page 75

Table 2 (continued)

S ··· I-I
REFCODE

X a (A) a -Y (A)

X a -Y ( ◦ )Mode

Compound name B d ··· d ···

BENZSI Benzyl sulfide-iodine 2.779 2.819 178.93 A

BIMMEP 4,4-Bis(methylsulfanyl)-1,3-dithiole-2-thione-diiodine 2.716 2.808 177.45 A

A

BZHTIC10 1,5-Diphenylthiocarbazone diiodine 2.663 2.917 178.49

DAXXIK Bis(benzimidazole-2-thione)iodonium (benzimidazole- 2.670 2.887 178.34 A

2-thione-diiodine) triiodide

DAXXOQ N -Methylbenzothiazole-2-thione-diiodine 2.808 2.791 176.95 A

A

DAYBOU 1,3-Dithiacyclohexane-2-thione-diiodine 2.755 2.812 175.41

DAYCIP 4,5-Ethylenedithio-1,3-dithiole-2-thione-diiodine 2.805 2.812 175.44 A

DTHINI 1,4-Dithiane bis(iodine) 178.49 2.789 177.89 A

FAJPUB Dithia(3.3.1)propellane bis(iodine) 2.825 2.797 176.71 A

2.806 2.796 176.08

FAJRAJ Dithia(3.3.2)propellane bis(iodine) 2.803 2.794 173.00 A

2.901 2.767 176.97

FOJPIE Diferrocenyl(phenyl)(diiodosulfido)phosphine 2.761 2.823 176.31 A

GEGNUB 1,3-Dimethyl-2-thioimidazolium diiodine 2.616 2.967 175.08 A

GEGNUB01 1,3-Dimethyl-2-thioimidazolium diiodine 2.607 2.984 177.11 A

GIDYOH Bis(1,3-diethylimidazolidine-2-thione-4,5-dithionato)- 2.874 2.811 179.61 A

palladium diiodine chloroform solvate

N , N -Bis(morpholino)-dithio-oxadiamide GIGLOX 2.920 2.751 175.53 A

bis(diiodine) 2.789 2.805 174.73

2.801 2.787 176.50

2.892 2.738 173.89