Two novel coumarin-embedded π-extended [5]helicene derivatives (3a and 6a) have been strategically synthesized and characterized, and the structure of 3a was determined single crystal X-ray analysis. Both of them exhibit green fluorescence in dichloromethane. In addition, molecule 3a can aggregate to form a large quantity of nanowires through the re-precipitation method. More importantly, the photoelectric conversion properties of 3a nanowire-C based films are much better than those of the thin film of bulk 3a-C, indicating that the ordered nanostructures are a crucial factor for enhancing device performance.
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Spectrochim Acta A Mol Biomol Spectrosc
December 2024
Department of Chemistry, Faculty of Science, Silpakorn University, Nakhon Pathom 73000, Thailand. Electronic address:
Gold is classified as a heavy metal, and its ion (Au) can manifest adverse impacts on ecological and human health. Thus, an effective method for Au detection is highly required. In this work, a new [5]helicene-based fluorescence sensor (M202P) was synthesized and applied for Au monitoring in near-perfect aqueous media.
View Article and Find Full Text PDFJ Hazard Mater
September 2021
Department of Chemistry, Faculty of Science, Silpakorn University, Nakhon Pathom 73000, Thailand. Electronic address:
A new fluorescence probe based on [5]helicene derivative (MT) was designed and synthesized. The chemical structure of the probe was fully characterized by NMR, mass spectrometry and X-ray crystallography. MT which is the combination of thioamide[5]helicene with Schiff base-thiophene moiety, exhibited a high selectivity to detect Hg through irreversible desulfurization reaction with "TurnON" fluorescence response and large Stokes shift of 110 nm in aqueous methanol solution.
View Article and Find Full Text PDFTalanta
January 2020
College of Materials Science and Engineering, Huaqiao University, Xiamen, 361021, China; Key Laboratory of Molecular Designing and Green Conversions (Huaqiao University), Fujian Province University, Xiamen, 361021, China.
In this paper, a tetrahydro[5]helicene-based imide dye with thienyl group (THID) was studied on its solvatochromism and aggregation-induced emission (AIE) properties by dissolved in various organic solvents. The linear relationship between Stokes shift and aprotic solvent polarity parameter was well fitted with Lippert-Mataga model. Furthermore, Stokes shift also were positively correlated with the normalized molar electronic transition energy, suggested that THID exceptionally depends on solvent polarity for twisted intramolecular charge transfer.
View Article and Find Full Text PDFACS Sens
May 2018
Department of Chemistry, Faculty of Science , Silpakorn University, Nakhon Pathom 73000 , Thailand.
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