“…In the last three decades, the halogen bond , has become recognized as a valuable tool in crystal engineering. − Because of its larger directionality (as compared to the hydrogen bond) , and tunability achievable by changing the donor halogen atom in otherwise structurally equivalent donor molecules, − the halogen bond found its way into a rising number of scientific studies on the synthesis and design of functional materials − as well as organic synthesis, , solution chemistry, , pharmaceutical, − and theoretical chemistry. , The list of studied halogen bond donors and especially halogen bond acceptors grows continuously. Cyclic nitrogen atoms are the most studied and reliable acceptor species, and this is especially the case for pyridine nitrogen atoms, to the point that they are a valuable benchmark for donor evaluation ,, and studies on acceptor competitiveness. , In recent years, they have been followed by a variety of other, mostly nitrogen or oxygen atom containing species, such as methoxy, − nitro, − hydroxyl, ,, and nitrile ,− functional groups, and oxygen atoms in N -oxides. , Some recent studies also showcased the promising halogen bond acceptor potential of nitrogen atoms in piperazine and nitrogen and oxygen atoms in morpholine , as well as the carbonyl oxygen atom. ,− So far, systematic studies of halogen bonding with these moieties were mainly limited to smaller building blocks. Searching the Cambridge Structural Database, one can find a small number of larger, relatively bulky building blocks that are halogen bonded via either the ...…”