In this work, the self assembly ability of chromophores covalently linked to aliphatic dipeptides is described. Altering various parameters such as the protecting group, the solvent mixture, the dipeptide and the chromophore resulted in different nanostructures.Interestingly, a peptide-porphyrin hybrid is capable of forming a hydrogel in HFIP-water solvent mixture.Living natural systems utilize self-assembly in order to fulfil their functions; thus, understanding the basic aspects of this process takes us a step closer to the comprehension of life. 1 Numerous examples in nature have inspired supramolecular scientists to synthesize molecules with self-assembling ability aiming at the construction of materials with improved properties. 2 Self-assembled architectures that mimic chlorophylls and bacteriochlorophylls in nature are of great interest for light harvesting applications. 3 A variety of bioinspired building blocks have been explored for the fabrication of self-assembling molecules including peptides, 4,5 nucleic acids, 6,7 peptide nucleic acids, 8,9 lipids etc. Of the small peptides, diphenylalanine (FF), the basic structural motif for the Alzheimer's beta amyloid polypeptide, is an aromatic dipeptide that has been extensively investigated for its self-assembling properties. 10,11 More specifically, a great number of chromophores such as porphyrins, 12-15 boron-dipyrromethenes, 16 corroles, 17 polyoxometallates 18 and ferrocene 19 have been covalently connected to FF resulting in hybrids that retained the ability to form well-defined nanostructures. In addition, small aliphatic peptides have also been investigated for their self-assembly ability. 20 In a recent example, Yan and co-workers reported that a short peptide based on