ArticleChemistry (Weinheim an der Bergstrasse, Germany)2026
Light-controlled 1D to 2D 2,3-Diaminophenazine Self-assembly Transformation on Cu(111) Surface.
Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Self-Assembly of Isomeric Isosceles Triangle Molecules at the Liquid-Solid Interface.ACS omega · 2026Article
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Authors and funding
10 authors.
Funding
Abstract
Controlled molecular self-assembly enables precise engineering of nanomaterials with programmable dimensionality and functionality. Conventional thermal-driven approaches, however, often struggle to achieve structural complexity due to weak intermolecular interactions and entropy-driven disorder at elevated temperatures. Here, we introduce a light-controlled methodology to realize a dimensionality transformation of carbon nitride-based architectures on a Cu(111) surface, bypassing the limitations of thermal processing. By applying ultraviolet (UV) light irradiation, we achieve the controlled conversion of 1D self-assembled nanoribbons of 2,3-diaminophenazine (DAP), a carbon nitride precursor, into ordered 2D extended frameworks. This light-driven 1D-to-2D structural evolution starkly contrasts with thermal treatments, which exclusively produce disordered aggregates under comparable conditions. Remarkably, this transformation proceeds without requiring light-reactive chemicals, underscoring the unique capability of UV light to direct molecular reorganization at interfaces. The work establishes a paradigm for manipulating nanoscale dimensionality in carbon nitride systems, circumventing conventional entropy limitations and offering a versatile platform for designing advanced 2D functional materials with applications in photocatalysis, nanoelectronics, and surface-supported molecular engineering.
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Registered trials
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