Wide-field imaging of individual multichromophoric molecules and successive photobleaching were used to determine, accurately, the relative position of the chromophores in such systems. First, a polyphenylene dendrimer with well-defined geometry was used to establish the accuracy in localization that can be obtained by this methodology. For a signal-to-noise ratio of 20, interchromophoric distances could be measured with 4 nm accuracy. Next, the method was used to determine the end-to-end distribution of an end-capped polyfluorene polymer. From comparison between the experimental and simulated distributions, information on the conformation of the polymer could be deduced. It was found that the polymer has a nonlinear conformation. A conjugation length of six monomer units gave the best fit of the experimental data to the proposed model.
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http://dx.doi.org/10.1002/cphc.200500235 | DOI Listing |
Macromol Rapid Commun
January 2025
Polymer Science, Zernike Institute for Advanced Materials, University of Groningen, Nijenborgh 3, Groningen, 9747 AG, The Netherlands.
Conjugated polyelectrolytes (CPEs), materials that are defined by a -conjugated backbone and charged ionic functional groups, are frequently prepared through direct polymerization of charged monomer species in aqueous media. This route is, however, often accompanied by labor-intensive work-up procedures, low yields, and ultimately results in materials that are difficult to characterize. To overcome these inconveniences, in this work protection chemistry is applied on sulfonate-functionalized fluorene monomers that are polymerized under standard Suzuki polycondensation conditions to obtain protected donor-acceptor copolymers.
View Article and Find Full Text PDFPolymers (Basel)
November 2024
Division of Applied Chemistry, Graduate School of Engineering, Mie University, 1577 Kurimamachiya-cho, Tsu 514-8507, Japan.
Tetraphenylethene (TPE) is known as a molecule that exhibits aggregation-induced emission (AIE). In this study, pendant hydroxyl groups were introduced onto polyfluorene with a TPE moiety. Sol-gel reactions of polydiethoxysiloxane (PDEOS) were carried out in the presence of hydroxyl-functionalized AIE polyfluorene (TPE-PF-OH) and polydimethylsiloxane carrying pendant hydroxyl groups (PDMS-OH) to immobilize AIE polyfluorene into a PDMS/SiO hybrid in an isolated dispersion state.
View Article and Find Full Text PDFTop Curr Chem (Cham)
December 2024
Department of Chemistry, Amrita Vishwa Vidyapeetham, Amritapuri, Kollam, Kerala, 690525, India.
The keyword "Fluorene" search in SciFinder found more than 57,000 results, including high-impact journal articles, review articles, patents, books, proceedings, etc. Against this background, a detailed enquiry has been made by our group on various classes of fluorenes and their relevancy. For the past several decades, fluorene and its related compounds have experienced extensive studies, which are attributed to the vast range of applications they possess in various fields like sensors, polymers, OLED devices and even in the pharmaceutical industries.
View Article and Find Full Text PDFBiosens Bioelectron
March 2025
Key Laboratory of Luminescence Analysis and Molecular Sensing (Southwest University), Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing, 400715, PR China. Electronic address:
Dual mode detection can overcome the poor anti-interference ability of single-mode detection, and greatly improve the detection accuracy. Fluorescence/electrochemiluminescence (FL/ECL) dual mode detection combines the advantages of FL and ECL, and has a promising application in bioanalysis. Common FL/ECL dual mode detection used different signal probes.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
October 2024
Key Laboratory of Green and Precise Synthetic Chemistry and Applications, Ministry of Education; Anhui Provincial Key Laboratory of Synthetic Chemistry and Applications; College of Chemistry and Materials Science, Huaibei Normal University Huaibei, Anhui, 235000, P. R. China.
The precise preparation of hierarchical micelles is a fundamental challenge in modern materials science and chemistry. Herein, poly(di-n-hexylfluorene)-block-poly(3-tetraethylene glycol thiophene) (poly(1-b-2)) diblock copolymers and polyfluorene-block-polythiophene-block-poly(phenyl isocyanide) triblock copolymers were synthesized using a one-pot process via the sequential addition of corresponding monomers using a Ni(II) complex as a single catalyst for living/controlled polymerization. The crystallization-driven self-assembly of amphiphilic conjugated poly(1-b-2) led to the formation of nanofibers with controlled lengths and narrow dispersity.
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