“…However, unlike traditional all-inorganic materials, it is challenging to impart ferroelectricity to the metal–ligand systems as structure–function relationships for them can only be drawn tentatively. , Despite the lack of highly dependable design rules, polar order in coordination networks can be achieved preferentially by systematic tuning of the nature of metal ions, coordinating ligands, counterions, and guest molecules. ,, However, attaining ferroelectricity in neutral framework materials derived from carboxylate-based ligands has thus far been a challenging task; hence, such systems are far less explored than those with charged networks. The polarity in neutral MOFs can be induced by the incorporation of polar functional groups in carboxylate ligands or via encapsulation of polar solvent molecules like water and DMF ( N , N -dimethylformamide), which interacts with the frameworks via non-covalent interactions. ,− Our group has been engaged in the design efforts of polar metal–ligand materials based on pyridyl donor ligands such as [PhPO(NHPy) 2 ], (Py = 3-pyridyl ( 3 Py) or 4-pyridyl ( 4 Py)), [PS(NH 3 Py) 3 ], and [PO(NHCH 2 3 Py) 3 ], in which the piezo- and ferroelectricity originate from their stable charge-separated structure and the low symmetry of the employed phosphoramide scaffold. − Hence, we reasoned that developing pseudo-C 2 and C 3 symmetric phsosphoramide ligands containing carboxylic acid functional groups would result in the generation of neutral noncentrosymmetric coordination networks suitable for ferro- and piezoelectric studies. In this contribution, we describe a new neutral one-dimensional zinc coordination network {[Zn( L 1 )(bpy)]·(H 2 O) 1.5∞ } ( 1 ), employing the flexible carboxylate functionalized dipodal P-N ligand [PhPO(NH-(C 6 H 4 COOH)) 2 ] ( L 1 H 2 ), which crystallizes in the polar non-centrosymmetric space group R 3 c .…”