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Solution and Solid-State Optical Properties of Trifluoromethylated 5-(Alkyl/aryl/heteroaryl)-2-methyl-pyrazolo[1,5-a]pyrimidine System

Felipe S. Stefanello, Jean C.B. Vieira, Juliane N. Araújo, Vitória Barbosa de Souza, Clarissa P. Frizzo, Marcos A. P. Martins, Nilo Zanatta, Bernardo A. Iglesias, Hélio G. Bonacorso

2022Photochem14 citationsDOIOpen Access PDF

Abstract

This paper describes the photophysical properties of a series of seven selected examples of 5-(alkyl/aryl/heteroaryl)-2-methyl-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidines (3), which contain alkyl, aryl, and heteroaryl substituents attached to the scaffolds of 3. Given the electron-donor groups and -withdrawing groups, the optical absorption and emission in the solid state and solution showed interesting results. Absorption UV–Vis and fluorescence properties in several solvents of a pyrazolo[1,5-a]pyrimidines series were investigated, and all derivatives were absorbed in the ultraviolet region despite presenting higher quantum emission fluorescence yields in solution and moderate emission in the solid state. Moreover, the solid-state thermal stability of compounds 3a–g was assessed using thermogravimetric analysis. The thermal decomposition profile showed a single step with almost 100% mass loss for all compounds 3. Additionally, the values of T0.05 are considerably low (72–187 °C), especially for compound 3a (72 °C), indicating low thermal stability for this series of pyrazolo[1,5-a]pyrimidines.

Topics & Concepts

ChemistryAlkylArylThermogravimetric analysisTrifluoromethylThermal stabilityPyrimidineFluorescenceAbsorption (acoustics)Thermal decompositionSolid-statePhotochemistryPhysical chemistryOrganic chemistryStereochemistryMaterials sciencePhysicsQuantum mechanicsComposite materialLuminescence and Fluorescent MaterialsOrganic Light-Emitting Diodes ResearchPhotochromic and Fluorescence Chemistry
Solution and Solid-State Optical Properties of Trifluoromethylated 5-(Alkyl/aryl/heteroaryl)-2-methyl-pyrazolo[1,5-a]pyrimidine System | Litcius