ArticleThe Journal of organic chemistry2017
Synthesis and Electron Spin Relaxation of Tetracarboxylate Pyrroline Nitroxides.
Article in The Journal of organic chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed.
- Exploring tunneling ESEEM beyond methyl groups in nitroxides at low temperatures.Physical chemistry chemical physics : PCCP · 2024Article
- Conformational tuning improves the stability of spirocyclic nitroxides with long paramagnetic relaxation times.Communications chemistry · 2023Article
- Quantifying methyl tunneling induced (de)coherence of nitroxides in glassyPhysical chemistry chemical physics : PCCP · 2023Article
- Bis-Spiro-Oxetane and Bis-Spiro-Tetrahydrofuran Pyrroline Nitroxide Radicals: Synthesis and Electron Spin Relaxation Studies.The Journal of organic chemistry · 2021Article
- Validation of Structural Grounds for Anomalous Molecular Mobility in Ionic Liquid Glasses.Molecules (Basel, Switzerland) · 2021Article
- Article
- Supramolecular Approach to Electron Paramagnetic Resonance Distance Measurement of Spin-Labeled Proteins.The journal of physical chemistry. B · 2020Article
- Truncated Cross Effect Dynamic Nuclear Polarization: An Overhauser Effect Doppelgänger.The journal of physical chemistry letters · 2018Article
- Reduction kinetics and electrochemistry of tetracarboxylate nitroxides.Free radical research · 2018Article
- Azaadamantyl nitroxide spin label: complexation with β-cyclodextrin and electron spin relaxation.Free radical research · 2018Article
- PEGylated, Water-Soluble, Stable Aminyl Radical.The Journal of organic chemistry · 2017Article
Corrections and comments
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Authors and funding
9 authors.
Funding
Abstract
We report the design, synthesis, and electron spin relaxation properties of hydrophilic tetracarboxylate ester pyrroline nitroxides 1 and 2, which serve as models in the search for new spin labels for DEER distance measurement at room temperature. The nitroxides are designed to have the methyl groups further away from the N-O spin site to decrease the inequivalent couplings of the unpaired electron to the methyl protons that shorten T
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