ArticleJournal of Raman spectroscopy : JRS2011
UV resonance Raman study of cation-π interactions in an indole crown ether.
Article in Journal of Raman spectroscopy : JRS, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 32 citations in OpenAlex.
- Multiphasic condensates formed with mono-component of tetrapeptides via phase separation.Nature communications · 2025Article
- Synthesis of a Novel Zwitterionic Hypercrosslinked Polymer for Highly Efficient Iodine Capture from Water.Polymers · 2024Article
- Biomolecular condensates formed by designer minimalistic peptides.Nature communications · 2023Article
- Single-droplet surface-enhanced Raman scattering decodes the molecular determinants of liquid-liquid phase separation.Nature communications · 2022Article
- Folding of the β-Barrel Membrane Protein OmpA into Nanodiscs.Biophysical journal · 2020Article
- Structural basis for substrate discrimination byRSC advances · 2018Article
- Ammonium catalyzed cyclitive additions: evidence for a cation-π interaction with alkynes.Chemical communications (Cambridge, England) · 2016Article
- UV resonance Raman study of TrpZip2 and related peptides: π-π interactions of tryptophan.Journal of Raman spectroscopy : JRS · 2012Article
- Tryptophan-lipid interactions in membrane protein folding probed by ultraviolet resonance Raman and fluorescence spectroscopy.Biophysical journal · 2011Article
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Authors and funding
4 authors at 3 institutions in 1 country.
Funding
Abstract
UV resonance Raman (UVRR) spectroscopy is used to probe changes in vibrational structure associated with cation-π interactions for the most prevalent amino acid π -donor, tryptophan. The model compound studied here is a diaza crown ether with two indole substituents. In the presence of sodium or potassium sequestered in the crown ether, or a protonated diaza group on the compound, the indole moieties participate in a cation-π interaction in which the pyrrolo group acts as the primary π-donor. Systematic shifts in relative intensity in the 760-780 cm
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