Based
on previous research, a new coassembly formed by a porphyrin
derivative (IPETPP), which contains a flexible substituent of m-phthalic acid, is observed with coronene (COR) molecules
at a higher concentration. Besides, a fresh IPETPP self-assembly formed
at a lower concentration and another new coassembly with COR molecules
are obtained. Moreover, the addition of a series of bipyridines alters
the diamond arrangement of IPETPP, which enhances the stability of
the two-component structures. It is unprecedented that bipyridine
derivatives break intermolecular hydrogen bonds containing m-phthalic acid substituents. All the coassemblies are investigated
by scanning tunneling microscopy on a highly oriented pyrolytic graphite.
Combined with density functional theory, the formation mechanism of
the assembled structures is revealed. These results would contribute
to understanding the interfacial crystal behaviors and probably provide
an efficient pathway to regulate the binary structures.