Complex metal chalcogenides have received growing attention for secondharmonic generation (SHG) activity arising from their noncentrosymmetric structures. In this area, the impact of the Eu(II)-cation on their structures and optical properties has not been well explored. Synthetic investigations of the Eu−Ag−IV-Ch (IV = Sn or Ge; Ch = S or Se) systems have unveiled four Eu(II)-based quaternary chalcogenides exhibiting very large mid-IR SHG responses within the chemically rich systems II−I 2 -IV-Ch 4 and II 3 −I 2 -IV 2 −Ch 8 (Ch = S or Se; I, II, and IV = monovalent, divalent, and tetravalent cations, respectively). Their structures were characterized by single-crystal X-ray diffraction methods to crystallize in noncentrosymmetric space groups, I4̅ 2m for EuAg 2 GeS 4 (1) and I4̅ 3d for Eu 3 Ag 2 Ge 2 Se 8 (2) Eu 3 Ag 2 Sn 2 Se 8 (3), and Eu 3 Ag 2 Sn 2 S 8 (4). The structures consist of body-centered arrangements of (Ge/Sn)Ch 4 tetrahedra that are fully oriented and bridged by flattened AgCh 4 tetrahedra into three-dimensional (3D) networks and chargebalanced by Eu(II) cations. Their crystalline powders exhibit mid-IR (2.09 μm) SHG responses among the largest reported to date, ranging from ∼1.9 × AGS (AgGaS 2 ) for 1, to increasing activities of ∼1.9 for 3, ∼4.7 for 2, and ∼7.0 for 4 × AGS. Spin-polarized band structure calculations showed that the valence and conduction band edge states stem from interactions of the Ag-to-S/Se-based and Ge/Sn-to-S/Se-based states, respectively, with increasing contributions of the Eu(II) 4f 7 -based states in the order of 1 < 3 < 2 < 4. Interestingly, this trend correlates with the SHG activity, suggesting a potential new relationship for understanding and attaining cutting-edge SHG properties within Eu(II)-based chalcogenides. Thus, this family helps tounveil a deeper understanding of structure−optoelectronic/SHG property relationships.