Porphyrin as a versatile visible-light-activatable organic/metal hybrid photoremovable protecting group
| Authors | |
|---|---|
| Year of publication | 2022 |
| Type | Article in Periodical |
| Magazine / Source | Nature Communications |
| MU Faculty or unit | |
| Citation | |
| Web | https://www.nature.com/articles/s41467-022-31288-2 |
| Doi | http://dx.doi.org/10.1038/s41467-022-31288-2 |
| Keywords | OXYGEN QUANTUM YIELDS; SINGLET OXYGEN; EXCITED-STATES; TRANSIENT ABSORPTION; MECHANISMS; DYNAMICS; SPECTRA; BODIPY; PHOTOSENSITIZERS; LUMINESCENCE |
| Attached files | |
| Description | Photoremovable protecting groups (PPGs) represent one of the main contemporary implementations of photochemistry. Here, the authors show that meso-methylporphyrin unites traditionally exclusive features of organic and metal-complex PPGs within a single entity. Photoremovable protecting groups (PPGs) represent one of the main contemporary implementations of photochemistry in diverse fields of research and practical applications. For the past half century, organic and metal-complex PPGs were considered mutually exclusive classes, each of which provided unique sets of physical and chemical properties thanks to their distinctive structures. Here, we introduce the meso-methylporphyrin group as a prototype hybrid-class PPG that unites traditionally exclusive elements of organic and metal-complex PPGs within a single structure. We show that the porphyrin scaffold allows extensive modularity by functional separation of the metal-binding chromophore and up to four sites of leaving group release. The insertion of metal ions can be used to tune their spectroscopic, photochemical, and biological properties. We provide a detailed description of the photoreaction mechanism studied by steady-state and transient absorption spectroscopies and quantum-chemical calculations. Our approach applied herein could facilitate access to a hitherto untapped chemical space of potential PPG scaffolds. |
| Related projects: |