Synthesis and electronic properties of dinucleic octaethylporphyrin (OEP) derivatives spaced withp-phenylene group [OEP-(p-Phen)n-OEP]. A comparative study with dihexylbithiophene (DHBTh) group-spaced OEP dimers [OEP-(DHBTh)n-OEP]
Source abstract
Abstract
The dinucleic octaethylporphyrin (OEP) derivatives described as OEP-(p-Phen)n-OEP (n = 1–4) were synthesized, in each of which the porphyrin ring is spaced with p-phenylene group. Their electronic properties were studied, as compared with those of the corresponding dihexylbithiophene (DHBTh) derivatives with head-to-head (HH) and tail-to-tail (TT) orientations. It proves that OEP-(p-Phen)n-OEP possesses an in-between feature of OEP-(HH-DHBTh)n-OEP and OEP-(TT-DHBTh)n-OEP in electronic properties.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Porphyrin and Phthalocyanine Chemistry · Luminescence and Fluorescent Materials · Molecular Sensors and Ion Detection
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
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