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1D Coordination π–d conjugated polymers with distinct structures defined by the choice of the transition metal: towards a new class of antiaromatic macrocycles

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    0541649 - FZÚ 2022 RIV DE eng J - Journal Article
    Santhini, Vijai M. - Wäckerlin, Christian - Cahlík, Aleš - Ondráček, Martin - Pascal, S. - Matěj, Adam - Stetsovych, Oleksandr - Mutombo, Pingo - Lazar, P. - Siri, O. - Jelínek, Pavel
    1D Coordination π–d conjugated polymers with distinct structures defined by the choice of the transition metal: towards a new class of antiaromatic macrocycles.
    Angewandte Chemie - International Edition. Roč. 60, č. 1 (2021), s. 439-445. ISSN 1433-7851. E-ISSN 1521-3773
    R&D Projects: GA MŠMT LM2018110; GA ČR(CZ) GX20-13692X
    Grant - others:AV ČR(CZ) AP1601
    Program: Akademická prémie - Praemium Academiae
    Institutional support: RVO:68378271
    Keywords : on surface chemistry * nc-AFM * polymers
    OECD category: Physical chemistry
    Impact factor: 16.823, year: 2021
    Method of publishing: Limited access
    https://doi.org/10.1002/anie.202011462

    Recently π–d conjugated coordination polymers have received a lot of attention owing to their unique material properties, although synthesis of long and defect‐free polymers remains challenging. Herein we introduce a novel on‐surface synthesis of coordination polymers with quinoidal ligands under ultra‐high vacuum conditions, which enables formation of flexible coordination polymers with lengths up to hundreds of nanometers. Moreover, this procedure allows the incorporation of different transition‐metal atoms with four‐ or two‐fold coordination. Remarkably, the two‐fold coordination mode revealed the formation of wires constituted by (electronically) independent 12‐membered antiaromatic macrocycles linked together through two C−C single bonds.

    Permanent Link: http://hdl.handle.net/11104/0319184

     
     
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