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  1. Article ; Online: Fluorescent Amorphous Distyrylnaphthalene-Based Polymers: Synthesis, Characterization and Thin-Film Nanomolar Sensing of Nitroaromatics in Water.

    Garay, Raúl O / Schvval, Ana B / Almassio, Marcela F / Del Rosso, Pablo G / Romagnoli, Maria J / Montani, Rosana S

    Polymers

    2018  Volume 10, Issue 12

    Abstract: Two new fluorescent segmented conjugated polymers with either 1,4- or 2,6-distyrylnaphthalene chromophores and their model compounds were synthesized and the chemosensing abilities of the polymeric thin films to detect nitroaromatics (NACs) in aqueous ... ...

    Abstract Two new fluorescent segmented conjugated polymers with either 1,4- or 2,6-distyrylnaphthalene chromophores and their model compounds were synthesized and the chemosensing abilities of the polymeric thin films to detect nitroaromatics (NACs) in aqueous media were evaluated. The structural, thermal and optical properties of the polymers were correlated with those displayed by their corresponding model compounds. Changes in the connectivity of naphthylene units caused minor differences in optical properties, morphology and quenching efficiencies. Molecular modeling highlighted the extremely bent character of polymer microstructures that explains their high solubility and amorphous character. Polymeric films are amorphous, strongly fluorescent and showed remarkable quenching efficiencies in the nanomolar range with picric acid (PA) and trinitrotoluene (TNT). Quenching experiments using either different nitroaromatic quenchers, excitation wavelengths, excitation beam path-lengths, or time of exposure of the film to the quenching solution evidenced the dominant role of inner filter effects (IFE) in the polymer response to NACs in the micromolar range. The sensing response towards PA, a quencher that strongly absorbs at the excitation wavelength, has an IFE contribution even at the nanomolar range, while the response towards the non-absorbing TNT depends only on the quenching occurring after diffusion of the analyte into the film.
    Language English
    Publishing date 2018-12-10
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2527146-5
    ISSN 2073-4360 ; 2073-4360
    ISSN (online) 2073-4360
    ISSN 2073-4360
    DOI 10.3390/polym10121366
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Chemosensing of nitroaromatics with a new segmented conjugated quaterphenylene polymer

    Del Rosso, Pablo G / Almassio, Marcela F / Garay, Raúl O

    Tetrahedron letters. 2011 Sept. 21, v. 52, no. 38

    2011  

    Abstract: A new approach for introducing porosity in fluorescent polymer films to increase sensing performance is presented. A novel segmented conjugated polymer composed of p-quaterphenylene segments tethered by their meta positions along the polymer main chain ... ...

    Abstract A new approach for introducing porosity in fluorescent polymer films to increase sensing performance is presented. A novel segmented conjugated polymer composed of p-quaterphenylene segments tethered by their meta positions along the polymer main chain by 2,2-isopropylene spacers was synthesized. The bent nature of its microstructure generates amorphous morphologies that let analytes diffuse rapidly within the films. Fluorescence quenching studies with polymer films and methanol solutions of nitroaromatics showed high sensitivity, fast response and reversibility of the fluorescence quenching. Thus, half of the maximum quench (Q₅₀%) occurred with nitrobenzene at the micromolar range in less than 1min in a reversible manner.
    Keywords chemical reactions ; chemical structure ; fluorescence ; methanol ; microstructure ; nitroaromatic compounds ; polymers ; porosity
    Language English
    Dates of publication 2011-0921
    Size p. 4911-4915.
    Publishing place Elsevier Ltd
    Document type Article
    ZDB-ID 204287-3
    ISSN 1873-3581 ; 0040-4039
    ISSN (online) 1873-3581
    ISSN 0040-4039
    DOI 10.1016/j.tetlet.2011.07.055
    Database NAL-Catalogue (AGRICOLA)

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  3. Article: Nitroaromatic compounds sensing. Synthesis, photophysical characterization and fluorescence quenching of a new amorphous segmented conjugated polymer with diphenylfluorene chromophores

    Del Rosso, Pablo G / Almassio, Marcela F / Palomar, Gerardo R / Garay, Raúl O

    Sensors & Actuators: B. Chemical. 2011 Dec. 15, v. 160, no. 1

    2011  

    Abstract: A new regularly segmented conjugated polymer bearing 2,7-diphenylfluorene chromophores tethered by isopropylidene connectors was synthesized by a relatively short synthetic route starting from easily available monomer synthons. Its photophysical ... ...

    Abstract A new regularly segmented conjugated polymer bearing 2,7-diphenylfluorene chromophores tethered by isopropylidene connectors was synthesized by a relatively short synthetic route starting from easily available monomer synthons. Its photophysical properties were investigated using UV–vis absorption, steady state and time-resolved emission spectroscopies. The bent microstructure produces a highly soluble amorphous polymer and fluorescence depolarization showed that exciton mobility within the polymer film is not hindered. These properties are of practical significance in view of the high sensitivity and fast response of its fluorescence quenching by nitro aromatics. Half of the maximum quench (Q₅₀%) of a polymer film occurred with dinitrobenzene in methanol solution at the micromolar range in less than 1min in a reversible manner. We demonstrate that amorphous segmented conjugated polymers bearing relatively short chromophores can be used as sensing materials with performances comparable to those presented by conjugated polymers with more elaborate structural design.
    Keywords absorption ; fluorescence ; methanol ; microstructure ; nitroaromatic compounds ; polymers
    Language English
    Dates of publication 2011-1215
    Size p. 524-532.
    Publishing place Elsevier B.V.
    Document type Article
    ZDB-ID 1021505-0
    ISSN 0925-4005
    ISSN 0925-4005
    DOI 10.1016/j.snb.2011.08.021
    Database NAL-Catalogue (AGRICOLA)

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  4. Article: Designed suppression of aggregation in polypyrene: toward high-performance blue-light-emitting diodes.

    Figueira-Duarte, Teresa M / Del Rosso, Pablo G / Trattnig, Roman / Sax, Stefan / List, Emil J W / Müllen, Klaus

    Advanced materials (Deerfield Beach, Fla.)

    2010  Volume 22, Issue 9, Page(s) 990–993

    MeSH term(s) Colloids/chemistry ; Color ; Equipment Design ; Equipment Failure Analysis ; Lighting/instrumentation ; Macromolecular Substances/chemistry ; Pyrenes/chemistry ; Semiconductors
    Chemical Substances Colloids ; Macromolecular Substances ; Pyrenes
    Language English
    Publishing date 2010-03-10
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1474949-X
    ISSN 1521-4095 ; 0935-9648
    ISSN (online) 1521-4095
    ISSN 0935-9648
    DOI 10.1002/adma.200902744
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Nitroaromatic compounds sensing. Synthesis, photophysical characterization and fluorescence quenching of a new amorphous segmented conjugated polymer with diphenylfluorene chromophores

    Del Rosso, Pablo G. / Almassio, Marcela F. / Palomar, Gerardo R. / Garay, Raúl O.

    Sensors & Actuators: B. Chemical

    Volume v. 160,, Issue no. 1

    Abstract: A new regularly segmented conjugated polymer bearing 2,7-diphenylfluorene chromophores tethered by isopropylidene connectors was synthesized by a relatively short synthetic route starting from easily available monomer synthons. Its photophysical ... ...

    Abstract A new regularly segmented conjugated polymer bearing 2,7-diphenylfluorene chromophores tethered by isopropylidene connectors was synthesized by a relatively short synthetic route starting from easily available monomer synthons. Its photophysical properties were investigated using UV–vis absorption, steady state and time-resolved emission spectroscopies. The bent microstructure produces a highly soluble amorphous polymer and fluorescence depolarization showed that exciton mobility within the polymer film is not hindered. These properties are of practical significance in view of the high sensitivity and fast response of its fluorescence quenching by nitro aromatics. Half of the maximum quench (Q₅₀%) of a polymer film occurred with dinitrobenzene in methanol solution at the micromolar range in less than 1min in a reversible manner. We demonstrate that amorphous segmented conjugated polymers bearing relatively short chromophores can be used as sensing materials with performances comparable to those presented by conjugated polymers with more elaborate structural design.
    Keywords absorption ; fluorescence ; microstructure ; polymers ; nitroaromatic compounds ; methanol
    Language English
    Document type Article
    ISSN 0925-4005
    Database AGRIS - International Information System for the Agricultural Sciences and Technology

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