ArticleInorganic chemistry2024
Tuning Electron-Accepting Properties of Phthalocyanines for Charge Transfer Processes.
Article in Inorganic chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
6 citing papers in PubMed.
- Isoreticular Tuning of Conductive Metal-Organic Framework Nanocrystals for the Rapid Detection and Differentiation of Toxic Gases.ACS nano · 2026Article
- Fluorescence-free single-molecule microscopy via electronic resonance stimulated Raman scattering.Nature communications · 2026Article
- Triphenylamine-Corrole Donor-Acceptor Systems: Synthesis, Spectroscopy, and Photophysical StudiesChemistry, an Asian journal · 2026Article
- Enhanced Quenching in an Azaphthalocyanine-Ferrocene Supramolecular Dyad upon Charge-Transfer Complex Formation.Inorganic chemistry · 2025Article
- CoPc/rGO and CuPc/rGO Nanocomposites: Comparative Characterization and Study of Their Gas Sensing Properties.Inorganic chemistry · 2025Article
- Water-soluble ZnPc(COOH)RSC advances · 2025Article
Corrections and comments
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Phthalocyanines play fundamental roles as electron-acceptors in many different fields; thus, the study of structural features affecting electron-accepting properties of these macrocycles is highly desirable. A series of low-symmetry zinc(II) phthalocyanines, in which one, three, or four benzene rings were replaced for pyrazines, was prepared and decorated with electron-neutral (alkylsulfanyl) or strongly electron-withdrawing (alkylsulfonyl) groups to study the role of the macrocyclic core as well as the effect of peripheral substituents. Electrochemical studies revealed that the first reduction potential (
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Registered trials
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