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Singlet oxygen production by pyrano and furano 1,4-naphthoquinones in non-aqueous medium
- Source :
- RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia, instname
- Publication Year :
- 2012
- Publisher :
- Royal Society of Chemistry, 2012.
-
Abstract
- [EN] The influence of ring size on the photobehaviour of condensed 1,4-naphthoquinone systems, such as pyrano-and furano-derivatives (1 and 2, respectively) has been investigated. The absorption spectra for both families of naphthoquinones reveal clear differences; in the case of 2 they extend to longer wavelengths. A solvatochromic red shift in polar solvents is consistent with the pi,pi* character of the S-0 -> S-1 electronic transition in all cases. Theoretical (B3LYP) analysis of the HOMO and LUMO Kohn-Sham molecular orbitals of the S-0 state indicates that they are pi and pi* in nature, consistent with the experimental observation. A systematic study on the efficiency of singlet oxygen generation by these 1,4-naphthoquinones is presented, and values larger than 0.7 were found in every case. In accordance with these results, laser flash photolysis of deoxygenated acetonitrile solutions led to the formation of detectable triplet transient species with absorptions at 390 and 450 nm (1) and at 370 nm (2), with phi(ISC) close to 1. Additionally, the calculated energies for the T-1 states relative to the S-0 states at UB3LYP/6-311++G** are ca. 47 kcal mol(-1) for 1 and 43 kcal mol(-1) for 2. A comparison of the geometrical parameters for the S-0 and T-1 states reveals a marked difference with respect to the arrangement of the exocyclic phenyl ring whilst a comparison of electronic parameters revealed the change from a quinone structure to a di-dehydroquinone diradical structure.<br />This research was supported by Spanish Government MICINN (CTQ2009-13699 and PHB2008-0104-PC) and by the Brazilian agencies: CAPES (Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior), CNPq (Conselho Nacional de Desenvolvimento Cientifico e Tecnologico), FAPERJ (Fundacao de Amparo a pesquisa do Estado do Rio de Janeiro) and FAPERJ-PRONEX grant number 110.574/2010.
- Subjects :
- Triplet 2-Methyl-1,4-Naphthoquinone
Acetonitriles
Absorption spectroscopy
Beta-Lapachone Derivatives
Trypanosoma-Cruzi
Laser Flash-Photolysis
Electron-Transfer
Photochemistry
Molecular electronic transition
chemistry.chemical_compound
QUIMICA ORGANICA
QUIMICA ANALITICA
Molecular orbital
Physical and Theoretical Chemistry
HOMO/LUMO
Photolysis
Singlet Oxygen
Aqueous-Solution
Chemistry
Singlet oxygen
Diradical
Lasers
Solvatochromism
Alpha-Lapachone
Antitumor-Activity
In-Vitro
Solvents
Flash photolysis
Quantum Theory
Biological Evaluation
Naphthoquinones
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia, instname
- Accession number :
- edsair.doi.dedup.....8852e866acd1982d58f24098d09d2cb7