Fe 2+ is vital to O 2 transportation and photosynthesis regulated by oxidases and reductases. On the other hand, Fe 3+ is detrimental due to its irreversible binding to O 2 . Hence there is a need for selective identification of Fe 3+ from aqueous systems in the presence of Fe 2+ . However, given their close chemical nature, it is not straightforward to differentiate them. Fe 2+ and Fe 3+ are typically sensed and differentiated using magnetic measurements, Mossbauer, X-ray absorption spectroscopy, or EXAFS, which are complex and equipment intensive techniques. In comparison, the fluorescence technique is advantageous in terms of time and accessibility. Although readily available lanthanide salts exhibit fluorescence, they are weak, and to serve as an optical probe, their luminescence has to be enhanced via ligand design. Hence we have designed a chromophoric ligand that can covalently bind to lanthanides and enhance its fluorescence intensity, and it binds selectively to Fe 3+ through its nitrogen centers. It detects Fe 3+ from low concentration (∼100 μM) aqueous solutions, with fast response time (<1 min) and with a detection limit of 3.6 ppm. Importantly, the Fe 3+ adsorbed MOF can be readily reactivated for the next cycle by merely washing with an aqueous ascorbic acid solution and can be used for multiple cycles without any appreciable loss in activity. This makes the Ln-MOF an environmentally benign, cost-effective, scalable, and recyclable probe.