Energy flow dynamics within cofacial and slip-stacked perylene-3,4-dicarboximide dimer models of π-aggregates.

Robust perylene-3,4-dicarboximide (PMI) π-aggregates provide important light-harvesting and electron-hole pair generation advantages in organic photovoltaics and related applications, but relatively few studies have focused on the electronic interactions between PMI chromophores. In contrast, structure-function relationships based on π-π stacking in the related perylene-3,4:9,10-bis(dicarboximides) (PDIs) have been widely investigated. The performance of both PMI and PDI derivatives in organic devices may be limited by the formation of low-energy excimer trap states in morphologies where interchromophore coupling is strong.

Self-Assembly of Supramolecular Light-Harvesting Arrays from Symmetric Perylene-3,4-dicarboximide Trefoils.

Unlike the widely studied perylene-3,4:9,10-bis(dicarboximide) (PDI) dyes, self-assembly of the corresponding perylene-3,4-dicarboximide (PMI) dyes into large arrays and studies of their excited state properties have received far less attention. Two symmetric PMI trefoils were synthesized by connecting the 9-position of the perylene core either directly (1) or through a phenylene linker (2) to the 1,3,5-positions of a central benzene ring. Synchrotron-based small- and wide-angle X-ray scattering measurements in methylcyclohexane show that trefoil 1 self-assembles into cofacial trimers (13) on average, while trefoil 2 forms much larger assemblies that are tridecamers (213) on average.

Triplet state formation in photoexcited slip-stacked perylene-3,4:9,10-bis(dicarboximide) dimers on a xanthene scaffold.

Two covalent perylene-3,4:9,10-bis(dicarboximide) (PDI) dimers in which the PDI molecules are attached to a xanthene (Xan) scaffold in which the long axes of the two π-π stacked PDI molecules are slipped by 4.3 and 7.9 Å were prepared.

Self-Assembly-Induced Ultrafast Photodriven Charge Separation in Perylene-3,4-dicarboximide-Based Hydrogen-Bonded Foldamers.

We report the synthesis, self-assembly characteristics, and ultrafast electron transfer dynamics of a perylene-3,4-dicarboximide (PMI) covalently linked to an N,N'-bis(3,4,5-tridodecyloxyphenyl)melamine electron donor (D) via a biphenyl spacer (PMI-Ph2-D). Synchrotron-based small- and wide-angle X-ray scattering (SAXS/WAXS) measurements in methylcyclohexane solution show that PMI-Ph2-D self-assembles into π-π stacked, hydrogen-bonded foldamers consisting of two or three hexameric rings or helices. Ultrafast transient absorption spectroscopy reveals that photoinduced charge separation within these nanostructures occurs by a unique pathway that is emergent in the assembly, whereas electron transfer does not occur in the PMI-Ph2-D monomers in tetrahydrofuran.

Bis[bis-(4-alkoxyphenyl)amino] derivatives of dithienylethene, bithiophene, dithienothiophene and dithienopyrrole: palladium-catalysed synthesis and highly delocalised radical cations.

Five diamines with thiophene-based bridges--(E)-1,2-bis{5-[bis(4-butoxyphenyl)amino]-2-thienyl}ethylene (1), 5,5'-bis[bis(4-methoxyphenyl)amino]-2,2'-bithiophene (2), 2,6-bis[bis(4-butoxyphenyl)amino]dithieno[3,2-b:2',3'-d]thiophene (3), N-(4-tert-butylphenyl)-2,6-bis[bis(4-methoxyphenyl)amino]dithieno[3,2-b:2',3'-d]pyrrole (4 a) and N-tert-butyl-2,6-bis[bis(4-methoxyphenyl)amino]dithieno[3,2-b:2',3'-d]pyrrole (4 b)--have been synthesised. The syntheses make use of the palladium(0)-catalysed coupling of brominated thiophene species with diarylamines, in some cases accelerated by microwave irradiation. The molecules all undergo facile oxidation, 4 b being the most readily oxidised at about -0.