7-hydroxy-4-trifluoromethylcoumarin has been researched along with coumarin* in 2 studies
2 other study(ies) available for 7-hydroxy-4-trifluoromethylcoumarin and coumarin
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Intermolecular proton shuttling in excited state proton transfer reactions: insights from theory.
The mechanism of base to base intermolecular proton shuttling occurring in the excited state proton transfer reaction between 7-hydroxy-4-(trifluoromethyl)coumarin (CouOH) and concentrated 1-methylimidazole base (1-MeId) in toluene solution is disclosed here by means of a computational approach based on Density Functional Theory (DFT) and Time Dependent DFT (TD-DFT). These methods allow us to characterize both the ground and excited state potential energy surfaces along the proton shuttling coordinate, and to assess the nature of the emitting species in the presence of an excess of 1-MeId. As a result, the tautomerism of CouOH is found to be photo-activated and, from a mechanistic point of view, the calculations clearly show that the overall driving force of the entire shuttling is the coumarin photoacidity, which is responsible for both the first proton transfer event and the strengthening of the following chain mechanism of base to base proton hopping. Topics: Coumarins; Imidazoles; Models, Molecular; Protons; Quantum Theory; Toluene | 2014 |
Design, synthesis, and evaluation of coumarin-based molecular probes for imaging of myelination.
Myelination represents one of the most fundamental biological processes in the vertebrate nervous system. Abnormalities and changes in myelination in the central nervous system (CNS) are seen in many neurodegenerative disorders, such as multiple sclerosis (MS). A long-standing goal has been to directly detect and quantify myelin content in order to facilitate diagnosis and therapeutic treatments of myelin-related diseases. In the course of our studies, we have developed a series of small-molecule probes (SMP) as myelin-imaging agents. Among them are coumarin derivatives, which exhibit promising brain permeability and myelin-binding properties. Herein we report a full account of the design and synthesis of coumarin-based SMPs as myelin-imaging agents. Systematic evaluation of these SMPs in both the CNS and peripheral nervous system (PNS) allowed us to identify some lead agents for potential use as fluorescent dyes for intraoperative nerve mapping in surgical operations or as radiotracers for positron emission tomography (PET) imaging of myelination. Topics: Animals; Central Nervous System; Coumarins; Drug Design; Drug Evaluation, Preclinical; Mice; Molecular Imaging; Molecular Probes; Myelin Sheath; Staining and Labeling; Structure-Activity Relationship | 2011 |