“…A well‐known strategy for engineering chiral CPs consists of using chiral ligands, whose “push‐pull” effect becomes cumulative through the multiple coordination to metal centers . In that respect, camphoric acid (or 1,2,2‐trimethylcyclopentane‐1,3‐dicarboxylic acid) seems to be a good candidate to be used as organic spacer for synthesis of CPs since it presents: (i) two complexing carboxylate groups, able to coordinate cations and form multidimensional CPs, as it has been already proven, aiming the preparation of multidimensional organic–inorganic hybrid materials; (ii) conformational rigidity due to the presence of five‐membered aliphatic ring; (iii) a relative low‐cost (produced by oxidizing the naturally occurring camphor with nitric acid), envisaging large scale synthetic approaches; (iv) an environmentally friendly character, with potential therapeutic effects (antiseptic, osteoblastic differentiation, antitumor); and (v) a chiral nature, essential to build up noncentrosymmetric materials.…”