The oxo-functionalization of hydrocarbons is the most important type of reaction in organic chemical productions. Among various oxidizing reagents, more and more studies have focused on the employment of molecular oxygen as oxidizing species in order to realize innovative and economically advantageous process, and at the same time, move toward a sustainable chemistry. However, the reactivity of O2 with most organic molecules is inhibited by spin restriction mainly due to the triplet ground state of O2 molecule. Photosensitized oxidation holds a special promise, where O2 molecule can be efficiently activated by the excited triplet state of a photocatalyst through an energy transfer process that generates highly reactive singlet oxygen (O2). On the other hand, the production of chemicals by this type of photooxidation in a large scale is still limited. The main reasons are the stability of photosensitizers and their separation problems. Search for new photocatalysts capable of inducing high quantum yield of singlet oxygen (O2) with environment friendly and cheap reagent represents a major target from the synthetic and industrial point of view. Platinum (II) terpyridyl acetylide complex 1 (Fig. 1) is particularly attractive since it may photochemically generate O2 with a high quantum yield and absorbs light in visible region. Nevertheless, the appealing features are usually out-weighted by the relatively high costs of the catalysts, rending their application to synthesis impractical. Herein we report such a robust photosensitizer based on the silica-supported platinum (II) terpyridyl complex 1,