2021-01-08

Perylene diimide (PDI), as shown in Figure 1, is an n -type organic semiconductor discovered by Kardos in 1913 [ 36 ]. Initially used as a textile dye, this high-performing pigment comes in …

PL. Photoluminescence. PPD. Polymer Photodetector. PSC. Polymer Solar Cell. Pd2(dba)3. Tris(dibenzylideneacetone)dipalladium(0).

Perylene diimide

Beilstein/REAXYS Number 4626671 . MDL number MFCD00134588. PubChem Substance ID 24848872 2018 Theses Doctoral. Perylene Diimide: A Versatile Building Block for Complex Molecular Architectures and a Stable Charge Storage Material.

The organic semiconductor 3,4,9,10-perylene tetracarboxylic diimide (PTCDI) has recently attracted attention because it can be functionalized

Perylene diimide derivatives were developed as industrial dyes due to their excellent chemical, photo, thermal, and weather stability. Nowadays, perylene dyes 18 Aug 2013 A combination of CC homocoupling and CH activation doubles the yields of perylenediimide dimers.

Herein, we report a hydrogen-bonding interfacial material, aliphatic amine-functionalized perylene-diimide (PDINN), which simultaneously down-shifts the work function of the air stable cathodes (silver and copper), and maintains good interfacial contact with the active layer.

Key Laboratory of Organic Optoelectronics and Molecular Engineering, Department of Chemistry, Tsinghua University, Beijing, 100084 P. R. China. Search for more papers by this author. Prof.

Significantly, the current of perylene diimide derivatives anion radical increased by 2∼3 orders of magnitude compared to perylene diimide derivatives under a bias of 5 V, and the maximal current of anion radical that from tetrahydrofuran solution can reach 3.6 mA.
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2021-02-15 N,N′-Bis(2,6-dimethylphenyl)perylene-3,4,9,10-tetracarboxylic diimide ≥90% Synonym: DXP CAS Number 76372-76-4. Empirical Formula (Hill Notation) C 40 H 26 N 2 O 4. Molecular Weight 598.65 . Beilstein/REAXYS Number 4626671 .

It or its derivatives may be carcinogenic, and it is considered to be a hazardous pollutant. In cell membrane cytochemistry, perylene is used as a fluorescent lipid probe.
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1,7-DIAROXY- OR 1,7-DIARYLTHIO-SUBSTITUTED PERYLENE-3,4,9,10-TETRACARBOXYLIC ACIDS AND THEIR DEREN DIANHYDRIDE UND DIIMIDE

Alberding BG(1), Brown-Xu SE, Chisholm MH, Epstein AJ, Gustafson TL, Lewis SA, Min Y. Author information: (1)The Ohio State University, 100 West 18th Avenue, Columbus, OH 43210, USA. Alkylation of perylene dianhydride to form ethylpropyl perylene diimide. The synthesis was taken from "Synthesis, Self-Assembly, and Solar Cell Performance o 2015-12-09 · We report our investigations on the potential of extended tetracationic cyclophane/perylene diimide systems as components for artificial photosynthetic applications. We show how the selection of appropriate heterocycles, as extending units, allows for tuning of the electron accumulation and photophysical properties of the extended tetracationic cyclophanes. Perylene-Diimide Helicenes: A New Molecular Architecture for Chiral Electronics Nathaniel J. Schuster Perylene-3,4,9,10-tetracarboxylic diimide (PDI) has emerged as a building block of organic materials for next generation molecular electronics. Intensely absorbing and chemically robust, Cathode engineering with perylene-diimide interlayer enabling over 17% efficiency single-junction organic solar cells June 2020 Nature Communications 11(1):2726 Keywords: perylene diimide (PDI), electronic circular dichroism (ECD), circularly polarized luminiscence (CPL), two-photon absorption, non-linear emission. Citation: Reine P, Ortuño AM, Mariz IFA, Ribagorda M, Cuerva JM, Campaña AG, Maçôas E and Miguel D (2020) Simple Perylene Diimide Cyclohexane Derivative With Combined CPL and TPA Properties. Stringing the Perylene Diimide Bow Taifeng Liu, Jingjing Yang, Florian Geyer, Felisa S. Conrad-Burton, Raﬄl Hernndez Snchez, Hexing Li, Xiaoyang Zhu, Colin P. Nuckolls,* Michael L. Steigerwald,* and Shengxiong Xiao* Abstract: This study explores a new mode of contortion in perylene diimides where the molecule is bent, like a bow, along its Perylene diimide derivatives (PDIs) with different substituents in the bay positions (Un-PDI, DFPDI and THBPDI) were chosen in this report to investigate the effect of potential on the reduction of PDIs through base (hydrazine, 1,2-ethanediamine and triethylamine)-driven keto-enol anion tautomerism.

2020-06-01 · Herein, we report a hydrogen-bonding interfacial material, aliphatic amine-functionalized perylene-diimide (PDINN), which simultaneously down-shifts the work function of the air stable cathodes

PubChem Substance ID 24848872 2018 Theses Doctoral. Perylene Diimide: A Versatile Building Block for Complex Molecular Architectures and a Stable Charge Storage Material. Milton, Margarita. Properties such as chemical robustness, potential for synthetic tunability, and superior electron-accepting character describe the chromophore perylene-3,4,9,10-tetracarboxylic diimide (PDI) and have enabled its penetration into organic The rational design and modification of the helix is of significance for fully promoting properties of configurationally stable materials for various applications in chiral science. Herein, a straightforward, sterically less demanding synthetic approach involving hybridization between two [6]helicene subunits and a perylene diimide (PDI) scaffold are presented, affording perylene diimide See how others have used N,Nprime-Bis(2,6-dimethylphenyl)perylene-3,4,9,10-tetracarboxylic diimide (CAS 76372-76-4). Click on the entry to view the PubMed entry .

Dr. Wei Jiang. IDENTIFICATION: Perylene is a yellow to colorless crystalline or plate-like solid. It is nearly insoluble in water. It is a member of a group of chemicals called polyaromatic hydrocarbons (PAHs). Perylene is a substance that occurs as a result of incomplete burning. It is found in coal, oil and gas.