118560-99-9Relevant academic research and scientific papers
Synthesis and excited-state photodynamics of perylene-porphyrin dyads. 1: Parallel energy and charge transfer via a diphenylethyne linker
Prathapan, Sreedharan,Yang, Sung Ik,Seth, Jyoti,Miller, Mark A.,Bocian, David F.,Holten, Dewey,Lindsey, Jonathan S.
, p. 8237 - 8248 (2001)
The photophysical properties of a perylene-porphyrin dyad have been examined with the aim of using this construct for molecular photonics applications. The dyad consists of a perylene-bis(imide) dye (PDI) connected to a zinc porphyrin (Zn) via a diphenylethyne linker (pep). In both polar and nonpolar solvents, the photoexcited perylene unit (PDI*) decays very rapidly (lifetimes of 2.5 (toluene) and 2.4 ps (acetonitrile)) by energy transfer to the porphyrin, forming PDI-pep-Zn* in high yield (80%, toluene; 70% acetonitrile), and hole transfer to the porphyrin, forming PDI--pep-Zn+ in lesser yield (20%, toluene; 30% acetonitrile). In both toluene and acetonitrile, the Zn* excited state subsequently decays with a lifetime of 0.4 ns primarily (80%) by electron transfer to the perylene (forming PDI--pep-Zn+). In the nonpolar solvent (toluene), the PDI--pep-Zn+ charge-transfer product has a lifetime of > 10 ns and decays by charge recombination primarily to the ground state but also by thermal repopulation of the Zn* excited state. The occurrence of the latter process provides a direct experimental measure of the energy of the charge-separated state. In the polar solvent (acetonitrile), the PDI--pep-Zn+ charge-separated state decays much more rapidly (--pep-Zn+) that can be long- or short-lived depending on solvent polarity, indicates the versatility of the perylene-porphyrin motif for a variety of applications in molecular photonics.
Synthesis of Nonsymmetrically Substituted Perylene Fluorescent Dyes
Kaiser, Harald,Lindner, Joerg,Langhals, Heinz
, p. 529 - 535 (2007/10/02)
A general method for the preparation of perylene-3,4:9,10-tetracarboxdiimides 1 with two different substituents at the nitrogen atoms is described: The easily prepared symmetrical tetracarboxdiimides 1 (R1=R2) are transformed into carboxdiimide anhydrides 2 and condensed with primary amines to the corresponding tetracarboxdiimides 1 (R1 R2).Applications as fluorescent tracers in biochemistry and polymer chemistry are discussed.
