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Multimodal switching of a redox-active macrocycle.
Payne, Daniel T; Webre, Whitney A; Matsushita, Yoshitaka; Zhu, Nianyong; Futera, Zdenek; Labuta, Jan; Jevasuwan, Wipakorn; Fukata, Naoki; Fossey, John S; D'Souza, Francis; Ariga, Katsuhiko; Schmitt, Wolfgang; Hill, Jonathan P.
Afiliação
  • Payne DT; WPI Center for Materials Nanoarchitectonics, National Institute for Materials Science, Namiki 1-1, Tsukuba, Ibaraki, 305-0044, Japan.
  • Webre WA; School of Chemistry, University of Birmingham, Edgbaston, Birmingham, West Midlands, B15 2TT, UK.
  • Matsushita Y; Department of Chemistry, University of North Texas, 1155 Union Circle, 305070 Denton, Denton, TX, 76203, USA.
  • Zhu N; Research Network and Facility Services Division, National Institute for Materials Science (NIMS), 1-2-1 Sengen, Tsukuba, Ibaraki, 305-0047, Japan.
  • Futera Z; School of Chemistry, Trinity College Dublin, The University of Dublin, College Green, Dublin 2, Ireland.
  • Labuta J; School of Chemical & Bioprocess Engineering, University College Dublin, Belfield, Dublin 4, Ireland.
  • Jevasuwan W; WPI Center for Materials Nanoarchitectonics, National Institute for Materials Science, Namiki 1-1, Tsukuba, Ibaraki, 305-0044, Japan.
  • Fukata N; WPI Center for Materials Nanoarchitectonics, National Institute for Materials Science, Namiki 1-1, Tsukuba, Ibaraki, 305-0044, Japan.
  • Fossey JS; WPI Center for Materials Nanoarchitectonics, National Institute for Materials Science, Namiki 1-1, Tsukuba, Ibaraki, 305-0044, Japan.
  • D'Souza F; School of Chemistry, University of Birmingham, Edgbaston, Birmingham, West Midlands, B15 2TT, UK.
  • Ariga K; Department of Chemistry, University of North Texas, 1155 Union Circle, 305070 Denton, Denton, TX, 76203, USA.
  • Schmitt W; WPI Center for Materials Nanoarchitectonics, National Institute for Materials Science, Namiki 1-1, Tsukuba, Ibaraki, 305-0044, Japan.
  • Hill JP; Department of Advanced Materials Science, Graduate School of Frontier Sciences, The University of Tokyo, 5-1-5 Kashiwanoha, Kashiwa, Chiba, 277-8561, Japan.
Nat Commun ; 10(1): 1007, 2019 03 01.
Article em En | MEDLINE | ID: mdl-30824697
ABSTRACT
Molecules that can exist in multiple states with the possibility of toggling between those states based on different stimuli have potential for use in molecular switching or sensing applications. Multimodal chemical or photochemical oxidative switching of an antioxidant-substituted resorcinarene macrocycle is reported. Intramolecular charge-transfer states, involving hemiquinhydrones are probed and these interactions are used to construct an oxidation-state-coupled molecular switching manifold that reports its switch-state conformation via striking variation in its electronic absorption spectra. The coupling of two different oxidation states with two different charge-transfer states within one macrocyclic scaffold delivers up to five different optical outputs. This molecular switching manifold exploits intramolecular coupling of multiple redox active substituents within a single molecule.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article