Accelerating charge transfer in a triphenylamine-subphthalocyanine donor-acceptor system.

Chem Commun (Camb)

Departamento de Química Orgánica, C-1, Universidad Autónoma de Madrid, Cantoblanco, 28049 Madrid, Spain.

Published: April 2008

We have designed, synthesized and probed a dodecafluoro-subphthalocyaninato boron(III) unit, which bears a triphenylamine moiety in its axial position, as a novel electron donor-acceptor system.

Download full-text PDF

Source
http://dx.doi.org/10.1039/b719226fDOI Listing

Publication Analysis

Top Keywords

donor-acceptor system
8
accelerating charge
4
charge transfer
4
transfer triphenylamine-subphthalocyanine
4
triphenylamine-subphthalocyanine donor-acceptor
4
system designed
4
designed synthesized
4
synthesized probed
4
probed dodecafluoro-subphthalocyaninato
4
dodecafluoro-subphthalocyaninato boroniii
4

Similar Publications

With the rapid advancement of information technology, the need to achieve ultra-high-density data storage has become a pressing necessity. This study synthesized three hyperbranched polyimides (HBPI-TAPP, HBPI-(Zn)TAPP, and HBPI-(Cu)TAPP) by polymerizing 5,10,15,20-tetrakis(4-aminophenyl)porphyrin (TAPP), which features a cavity for metal ion coordination, with 4,4'-(hexafluoroisopropylidene)diphthalic anhydride (6FDA), to systematically investigate the effect of metal ion species on storage performance. According to the results, memory devices based on HBPI-(Zn)TAPP exhibit volatile SRAM (static random-access memory) characteristics, whereas devices employing HBPI-TAPP and HBPI-(Cu)TAPP demonstrate non-volatile WORM (write-once, read-many) characteristics.

View Article and Find Full Text PDF

The exploration of photocatalytic materials with efficient charge separation has always been a prominent area of research in photocatalysis. In the preceding years, the strategy of constructing donor-acceptor (D-A) structured materials has gradually been developed in photocatalytic systems, becoming a new research crossroads and attracting extensive interdisciplinary focus. Polymeric carbon nitride (PCN) has gradually been recognized as the primary photocatalytic material for constructing D-A structures due to its attractive exceptional physicochemical stability, electronic band structure, and cost-effectiveness.

View Article and Find Full Text PDF

A Hexavalent Tellurium-Based Chalcogen Bonding Catalysis Platform: High Catalytic Activity and Controlling of Selectivity.

J Am Chem Soc

January 2025

School of Chemistry and Chemical Engineering, Key Laboratory of Colloid and Interface Chemistry of the Ministry of Education, Shandong University, Jinan 250100, P. R. China.

Herein, we describe a hexavalent tellurium-based chalcogen bonding catalysis platform capable of addressing reactivity and selectivity issues. This research demonstrates that hexavalent tellurium salts can serve as a class of highly active chalcogen bonding catalysts for the first time. The tellurium centers in these hexavalent catalysts have only one exposed interaction site, thus providing a favorable condition for the controlling of reaction selectivity.

View Article and Find Full Text PDF

Over the last five decades, diimine rhenium(I) tricarbonyl complexes have been extensively investigated due to their remarkable and widely tuned photophysical properties. These systems are regarded as attractive targets for design functional luminescent materials and performing fundamental studies of photoinduced processes in transition metal complexes. This review summarizes the latest developments concerning Re(I) tricarbonyl complexes bearing donor-acceptor (D-A) and donor-π-acceptor (D-π-A) ligands.

View Article and Find Full Text PDF

Coumarin compounds have heterocyclic core with different properties such as high quantum yields, broad Stokes shifts, and superior photophysical and biological activity. It is known that fluorescence properties increase with increased intramolecular charge transfer in systems where electron-withdrawing or donor groups are attached to different positions of the coumarin compound. When these compounds interact with analytes in the environment, the analytes in the environment can be detected by quenching or increasing fluorescence.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!