دورية أكاديمية
Photophysical, photostability, and ROS generation properties of new trifluoromethylated quinoline-phenol Schiff bases.
| العنوان: | Photophysical, photostability, and ROS generation properties of new trifluoromethylated quinoline-phenol Schiff bases. |
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| المؤلفون: | Rocha IO; 1Núcleo de Química de Heterociclos (NUQUIMHE), Departamento de Química, Universidade Federal de Santa Maria, Santa Maria, RS, 97105-900, Brazil., Kappenberg YG; 1Núcleo de Química de Heterociclos (NUQUIMHE), Departamento de Química, Universidade Federal de Santa Maria, Santa Maria, RS, 97105-900, Brazil., Rosa WC; 1Núcleo de Química de Heterociclos (NUQUIMHE), Departamento de Química, Universidade Federal de Santa Maria, Santa Maria, RS, 97105-900, Brazil., Frizzo CP; 1Núcleo de Química de Heterociclos (NUQUIMHE), Departamento de Química, Universidade Federal de Santa Maria, Santa Maria, RS, 97105-900, Brazil., Zanatta N; 1Núcleo de Química de Heterociclos (NUQUIMHE), Departamento de Química, Universidade Federal de Santa Maria, Santa Maria, RS, 97105-900, Brazil., Martins MAP; 1Núcleo de Química de Heterociclos (NUQUIMHE), Departamento de Química, Universidade Federal de Santa Maria, Santa Maria, RS, 97105-900, Brazil., Tisoco I; 1Núcleo de Química de Heterociclos (NUQUIMHE), Departamento de Química, Universidade Federal de Santa Maria, Santa Maria, RS, 97105-900, Brazil.; Laboratório de Bioinorgânica e Materiais Porfirínicos, Departamento de Química, Universidade Federal de Santa Maria, Santa Maria, RS, 97105-900, Brazil., Iglesias BA; 1Núcleo de Química de Heterociclos (NUQUIMHE), Departamento de Química, Universidade Federal de Santa Maria, Santa Maria, RS, 97105-900, Brazil.; Laboratório de Bioinorgânica e Materiais Porfirínicos, Departamento de Química, Universidade Federal de Santa Maria, Santa Maria, RS, 97105-900, Brazil., Bonacorso HG; 1Núcleo de Química de Heterociclos (NUQUIMHE), Departamento de Química, Universidade Federal de Santa Maria, Santa Maria, RS, 97105-900, Brazil. |
| المصدر: | Beilstein journal of organic chemistry [Beilstein J Org Chem] 2021 Dec 01; Vol. 17, pp. 2799-2811. Date of Electronic Publication: 2021 Dec 01 (Print Publication: 2021). |
| نوع المنشور: | Journal Article |
| اللغة: | English |
| بيانات الدورية: | Publisher: Beilstein-Institut Country of Publication: Germany NLM ID: 101250746 Publication Model: eCollection Cited Medium: Print ISSN: 1860-5397 (Print) Linking ISSN: 18605397 NLM ISO Abbreviation: Beilstein J Org Chem Subsets: PubMed not MEDLINE |
| أسماء مطبوعة: | Publication: [Frankfurt, Germany] : Beilstein-Institut Original Publication: [Frankfurt, Germany] : [London] : Beilstein-Institut ; in cooperation with BioMed Central, [2005]- |
| مستخلص: | A new series of ten examples of Schiff bases, namely ( E )-2-(((2-alkyl(aryl/heteroaryl)-4-(trifluoromethyl)quinolin-6-yl)imino)methyl)phenols 3 , was easily synthesized with yields of up to 91% from the reactions involving a series of 2-(R-substituted) 6-amino-4-(trifluoromethyl)quinolines 1 and 4(5)-R 1 -substituted salicylaldehydes 2 - in which alkyl/aryl/heteroaryl for 2-R-substituents are Me, Ph, 4-MeC (Copyright © 2021, Rocha et al.) |
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| فهرسة مساهمة: | Keywords: ROS generation; Schiff base; photophysical properties; photostability; quinoline |
| تواريخ الأحداث: | Date Created: 20211220 Latest Revision: 20211221 |
| رمز التحديث: | 20221213 |
| مُعرف محوري في PubMed: | PMC8649202 |
| DOI: | 10.3762/bjoc.17.191 |
| PMID: | 34925619 |
| قاعدة البيانات: | MEDLINE |
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