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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 ; Online: 4'-[2-(2-Ethoxyethoxy)ethoxy]biphenyl-4-carboxylic acid: correlation between its crystalline and smectic phases.

    Montani, Rosana S / Garay, Raúl O / Cukiernik, Fabio D / Garland, Maria T / Baggio, Ricardo

    Acta crystallographica. Section C, Crystal structure communications

    2009  Volume 65, Issue Pt 3, Page(s) o81–4

    Abstract: The crystal structure of the dimeric title compound, C(19)H(22)O(5), is dominated by a head-to-head hydrogen-bonding interaction between centrosymmetrically related carboxyl groups in each monomer. The result is a dimeric axis of unusual length (ca 34 A), ...

    Abstract The crystal structure of the dimeric title compound, C(19)H(22)O(5), is dominated by a head-to-head hydrogen-bonding interaction between centrosymmetrically related carboxyl groups in each monomer. The result is a dimeric axis of unusual length (ca 34 A), but still shorter than what could be expected for a fully extended chain, owing to two turning points in the oligoethoxy ends. This allows for an explanation of the structure of the smectic mesophase exhibited by this compound and at the same time fully validates former geometric estimations based on PM3 calculations.
    Language English
    Publishing date 2009-03
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2025703-X
    ISSN 1600-5759 ; 2053-2296 ; 0108-2701
    ISSN (online) 1600-5759 ; 2053-2296
    ISSN 0108-2701
    DOI 10.1107/S0108270109001991
    Database MEDical Literature Analysis and Retrieval System OnLINE

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