“…In this process, TM 2+ -N MOFs are usually more stable than TM 2+ -carboxylate MOFs. Tetravalent and trivalent TM cations, such as Zr 4+ and In 3+ , usually tend to form MOFs with TM-O coordination modes by forming six- to eight-coordinate environments. − However, in comparison to the number of TM 2+ - and Zr 4+ -based MOFs, In 3+ -based MOFs are comparatively fewer in number in literature reports. − In this field, the In 3+ ions were used to react with organic di-, tri-, and tetracarboxylic ligands, resulting in several In-based 2D and 3D frameworks, − which have been widely used for gas separation, pollutant removal, and catalytic reactions. , Among these structures, it could be found that most of the In 3+ centers tend to coordinate with carboxylate oxygen atoms, although several ligands contain N and S heteroatoms. ,,, To date, the design and synthesis of In-based framework materials are still in their infancy and represent a promising way to construct stable MOFs for various applications, especially for introducing polydentate ligands with both carboxylate and N-heterocyclic rings into the In-MOFs to promote the formation of In–N bonds …”