The synthesis of chiral zeolites remains a significant challenge because the primary tetrahedral building units are achiral and weak interactions exist between the guest and host frameworks. Here, we present the syntheses and characterization of three new chiral zeolitic halides, [H-3-(Dabco)(2)]Ag3X6 (X = Br (1) or I (2), Dabco = 1,4-diazabicyclo [2.2.2] octane) and [H-2(Dabco)] [(Dabco)Ag4I6] (3). Compounds 1 and 2 are isostructural, containing a 4-connected zeolitic framework built up from 3-ring units, with high-charge [H-3(Dabco)(2)](3+) located in chiral cages. compound 3 contains a similar zeolitic [Ag3I6](3-) framework to that of 2, but a [Ag(Dabco)](+) unit is incorporated in each 3-ring, with [H-2(Dabco)](2+) located in channels. These frameworks are chiral, representing the first examples of chiral zeolitic halides. The chirality transference of the frameworks for 1 and 2 was attributed to the template effect of the chiral [H-3(Dabco)(2)](3+) through strong electrostatic interactions and multiple hydrogen-bond interactions. For compound 3, direct coordination interactions play important roles in the chirality transference from the chiral Dabco ligand to the framework.